Publications

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• S Palmal, K Adhikari, J Mendoza-Revilla, M Fuentes-Guajardo, CC Silva de Cerqueira, B Bonfante, JC Chacón-Duque, A Sohail, M Hurtado, V Villegas, V Granja, C Jaramillo, W Arias, RB Lozano, P Everardo-Martínez, J Gómez-Valdés, H Villamil-Ramírez, T Hünemeier, V Ramallo, ML Parolin, R Gonzalez-José, L Schüler-Faccini, MC Bortolini, V Acuña-Alonzo, S Canizales-Quinteros, C Gallo, G Poletti, G Bedoya, F Rothhammer, D. Balding, P Faux, A Ruiz-Linares. Prediction of eye, hair and skin colour in Latin Americans. Forensic Science International: Genetics, 53, 102517, 2021. doi: 10.1016/j.fsigen.2021.102517.

• Y. Chen, M André, K Adhikari, M Blin, B Bonfante, J Mendoza-Revilla, M Fuentes-Guajardo, S Palmal, JC Chacón-Duque, M Hurtado, V Villegas, V Granja, C Jaramillo, W Arias, RB Lozano, P Everardo-Martínez, J Gómez-Valdés, H Villamil-Ramírez, CCS de Cerqueira, T Hünemeier, V Ramallo, R Gonzalez-José, L Schüler-Faccini, M-C Bortolini, V Acuña-Alonzo, S Canizales-Quinteros, C Gallo, G Poletti, G Bedoya, F Rothhammer, D. Balding, DJ Tobin, S Wang, P Faux, A Ruiz-Linares. A GWAS identifies novel gene associations with facial skin wrinkling and mole count in Latin?Americans. British Journal of Dermatology, 2021. doi: 10.1111/bjd.20436.

• Betty Bonfante, Pierre Faux, Nicolas Navarro, Javier Mendoza-Revilla, Morgane Dubied, Charlotte Montillot, Emma Wentworth, Lauriane Poloni, Ceferino Varón-González, Philip Jones, Ziyi Xiong, Macarena Fuentes-Guajardo, Sagnik Palmal, Juan Camilo Chacón-Duque, Malena Hurtado, Valeria Villegas, Vanessa Granja, Claudia Jaramillo, William Arias, Rodrigo Barquera, Paola Everardo-Martínez, Mirsha Sánchez-Quinto, Jorge Gómez-Valdés, Hugo Villamil-Ramírez, Caio C Silva de Cerqueira, Tábita Hünemeier, Virginia Ramallo, Fan Liu, Seth M Weinberg, John R Shaffer, Evie Stergiakouli, Laurence J Howe, Pirro G Hysi, Timothy D Spector, Rolando Gonzalez-José, Lavinia Schüler-Faccini, Maria-Cátira Bortolini, Victor Acuña-Alonzo, Samuel Canizales-Quinteros, Carla Gallo, Giovanni Poletti, Gabriel Bedoya, Francisco Rothhammer, Christel Thauvin-Robinet, Laurence Faivre, Caroline Costedoat, D. Balding, Timothy Cox, Manfred Kayser, Laurence Duplomb, Binnaz Yalcin, Justin Cotney, Kaustubh Adhikari, Andrés Ruiz-Linares. A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.. Science advances, 7, eabc6160 (18pp), 2021. doi: 10.1126/sciadv.abc6160.

• Doug Speed, J. HOLMES, D. Balding. Evaluating and improving heritability models using summary statistics.. Nature Genetics, 458-+, 2020. doi: 10.1038/s41588-020-0600-y.

• D. Balding, Gregory S Barsh, Gregory P Copenhaver, Chengqi Yi. Mixed methods.. PLoS genetics, 16, e1008950 (2pp), 2020. doi: 10.1371/journal.pgen.1008950.

• D Taylor, D. Balding. How can courts take into account the uncertainty in a likelihood ratio?. Forensic Science International: Genetics, 48, 102361 (6pp), 2020. doi: 10.1016/j.fsigen.2020.102361.

• A. Mahmoudi, D. Balding. Inference under the coalescent with recombination. 2020.

• MM Andersen, D. Balding. Y-profile evidence: Close paternal relatives and mixtures. Forensic Science International: Genetics, 38, 48-53, 2019. doi: 10.1016/j.fsigen.2018.10.004.

• K Adhikari, J Mendoza-Revilla, A Sohail, M Fuentes-Guajardo, J Lampert, JC Chacón-Duque, M Hurtado, V Villegas, V Granja, V Acuña-Alonzo, C Jaramillo, W Arias, RB Lozano, P Everardo, J Gómez-Valdés, H Villamil-Ramírez, CC Silva de Cerqueira, T Hunemeier, V Ramallo, L Schuler-Faccini, FM Salzano, R Gonzalez-José, MC Bortolini, S Canizales-Quinteros, C Gallo, G Poletti, G Bedoya, F Rothhammer, DJ Tobin, M Fumagalli, D. Balding, A Ruiz-Linares. A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia.. Nature communications, 10, 358 (16pp), 2019. doi: 10.1038/s41467-018-08147-0.

• Maria Simonsen Speed, D. Balding, Asger Hobolth. A general framework for moment-based analysis of genetic data.. Journal of mathematical biology, 1727-1769, 2019. doi: 10.1007/s00285-018-01325-0.

• J. HOLMES, Doug Speed, D. Balding. Summary statistic analyses do not correct confounding bias: Appendix. 532069, 2019. doi: 10.1101/532069.

• Y You, D. Balding. A comparison of software for the evaluation of complex DNA profiles. Forensic Science International: Genetics, 40, 114-119, 2019. doi: 10.1016/j.fsigen.2019.02.014.

• Doug Speed, J. HOLMES, D. Balding. Evaluating and improving heritability models using summary statistics. 736496, Cold Spring Harbor Laboratory, 2019. doi: 10.1101/736496.

• J. HOLMES, Doug Speed, D. Balding. Summary statistic analyses can mistake confounding bias for heritability.. Genetic epidemiology, 930-940, 2019. doi: 10.1002/gepi.22259.

• Junaid Ashraf, D. Balding. Design of an efficient and complete elicitation decision process in contingent valuation method (Retraction of Vol 6, art no 1564164, 2019). COGENT MATHEMATICS & STATISTICS, 6, 1703298 (2pp), 2019. doi: 10.1080/25742558.2019.1703298.

• D. Balding, J. HOLMES, Doug Speed. Progress and Controversy in Analysis of Complex Phenotypes Based on Genome-wide Association Statistics. GENETIC EPIDEMIOLOGY, 43, 865-866, 2019.

• D. Balding, I Moltke, J Marioni. Handbook of statistical genomics. 1, 1-1135, Wiley, 2019. doi: 10.1002/9781119487845.

• T. Hessab, RS Aranha, RS Moura-Neto, D. Balding, CG Schrago. Evaluating DNA evidence in a genetically complex population. Forensic Science International: Genetics, 36, 141-147, 2018. doi: 10.1016/j.fsigen.2018.06.019.

• Mikkel Andersen, D. Balding. How many individuals share a mitochondrial genome?. 374686, 2018. doi: 10.1101/374686.

• Mikkel Andersen, D. Balding. Y-profile evidence: close paternal relatives and mixtures. 373423, 2018. doi: 10.1101/373423.

• Mikkel M Andersen, D. Balding. How many individuals share a mitochondrial genome?. PLoS genetics, 14, e1007774 (11pp), 2018. doi: 10.1371/journal.pgen.1007774.

• D Speed, D. Balding. SumHer better estimates the SNP heritability of complex traits from summary statistics. Nature Genetics, 277-+, 2018. doi: 10.1038/s41588-018-0279-5.

• K Heine, A Beskos, A Jasra, D. Balding, M De Iorio. Bridging trees for posterior inference on ancestral recombination graphs. Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences, 474, 20180568 (20pp), 2018. doi: 10.1098/rspa.2018.0568.

• B Abou-Khalil, P Auce, A Avbersek, M. Bahlo, D. Balding, T Bast, L Baum, AJ Becker, B Berghuis, SF Berkovic, KE Boysen, JP Bradfield, LC Brody, RJ Buono, E Campbell, GD Cascino, CB Catarino, GL Cavalleri, SS Cherny, K Chinthapalli, AJ Coffey, A Compston, A Coppola, P Cossette, JJ Craig, GJ de Haan, P De Jonghe, CGF de Kovel, N Delanty, C Depondt, O Devinsky, DJ Dlugos, CP Doherty, CE Elger, JG Eriksson, TN Ferraro, M Feucht, B Francis, A Franke, JA French, S Freytag, V Gaus, EB Geller, C Gieger, T Glauser, S Glynn, DB Goldstein, H Gui, Y Guo, KF Haas, H Hakonarson, K Hallmann, S Haut, EL Heinzen, I Helbig, C Hengsbach, H Hjalgrim, M Iacomino, A Ingason, J Jamnadas-Khoda, M. Johnson, R Kälviäinen, AM Kantanen, D KasperavičiÅ«te, D Kasteleijn-Nolst Trenite, HE Kirsch, RC Knowlton, BPC Koeleman, R Krause, M Krenn, WS Kunz, R Kuzniecky, P Kwan. Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Nature Communications, 9, 5269 (15pp), 2018. doi: 10.1038/s41467-018-07524-z.

• Juan-Camilo Chacón-Duque, Kaustubh Adhikari, Macarena Fuentes-Guajardo, Javier Mendoza-Revilla, Victor Acuña-Alonzo, Rodrigo Barquera, Mirsha Quinto-Sánchez, Jorge Gómez-Valdés, Paola Everardo Martínez, Hugo Villamil-Ramírez, Tábita Hünemeier, Virginia Ramallo, Caio C Silva de Cerqueira, Malena Hurtado, Valeria Villegas, Vanessa Granja, Mercedes Villena, René Vásquez, Elena Llop, José R Sandoval, Alberto A Salazar-Granara, Maria-Laura Parolin, Rosenda I Peñaloza-Espinosa, Hector Rangel-Villalobos, Cheryl A Winkler, William Klitz, Claudio Bravi, Julio Molina, Daniel Corach, Ramiro Barrantes, Verónica Gomes, Carlos Resende, Leonor Gusmão, Antonio Amorim, Yali Xue, Jean-Michel Dugoujon, Pedro Moral, Rolando González-José, Lavinia Schuler-Faccini, Francisco M Salzano, Maria-Cátira Bortolini, Samuel Canizales-Quinteros, Giovanni Poletti, Carla Gallo, Gabriel Bedoya, Francisco Rothhammer, D. Balding, Garrett Hellenthal, Andrés Ruiz-Linares. Latin Americans show wide-spread Converso ancestry and imprint of local Native ancestry on physical appearance.. Nat Commun, 9, 5388 (13pp), 2018. doi: 10.1038/s41467-018-07748-z.

• J Mendoza-Revilla, K Adhikari, M Fumagalli, V Acuna-Alonzo, S Canizales-Quinteros, C Gallo, G Poletti, F Rothhammer, M Bortolini, G Bedoya, R Gonzalez-Jose, F Balloux, D. Balding, A Ruiz-Linares. Genetic signals of selection in Native and admixed populations of Latin America. EUROPEAN JOURNAL OF HUMAN GENETICS, 26, 783-784, 2018.

• Debbie A Kennett, Adrian Timpson, D. Balding, Mark G Thomas. The Rise and Fall of BritainsDNA: A Tale of Misleading Claims, Media Manipulation and Threats to Academic Freedom. Genealogy, 2, 47 (26pp), 2018. doi: 10.3390/genealogy2040047.

• Doug Speed, D. Balding. Re-Evaluation of SNP Heritability in Complex Human Traits. Genetic Epidemiology, 41, 686 (1pp), 2017.

• Mikkel M Andersen, D. Balding. How convincing is a matching Y-chromosome profile?. PLOS Genetics, 13, e1007028 (16pp), 2017. doi: 10.1371/journal.pgen.1007028.

• Roberto Salvatori, Serban Radian, Yoan Diekmann, Donato Iacovazzo, Alessia David, Plamena Gabrovska, Giorgia Grassi, Anna-Marie Bussell, Karen Stals, Astrid Weber, Richard Quinton, Elizabeth C Crowne, Valentina Corazzini, Lou Metherell, Tara Kearney, Daniel Du Plessis, Ajay Kumar Sinha, Atik Baborie, Anne-Lise Lecoq, Philippe Chanson, Olaf Ansorge, Sian Ellard, Peter J Trainer, D. Balding, Mark G Thomas, Marta Korbonits. In-frame seven amino-acid duplication in AIP arose over the last 3000 years, disrupts protein interaction and stability and is associated with gigantism. European Journal of Endocrinology, 177, 257-266, 2017. doi: 10.1530/EJE-17-0293.

• Joshua Traynelis, Michael Silk, Quanli Wang, Samuel F Berkovic, Liping Liu, David B Ascher, D. Balding, Slave Petrovski. Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation. Genome Research, 27, 1715-1729, 2017. doi: 10.1101/gr.226589.117.

• Alexandre Fournier-Level, Charles Robin, D. Balding. GWAlpha: genome-wide estimation of additive effects (alpha) based on trait quantile distribution from pool-sequencing experiments. Bioinformatics, 33, 1246-1247, 2017. doi: 10.1093/bioinformatics/btw805.

• Geoffrey Stewart Morrison, David H Kaye, D. Balding, D. Taylor, Philip Dawid, Colin GG Aitken, Simone Gittelson, Grzegorz Zadora, Bernard Robertson, Sheila Willis, Susan Pope, Martin Neil, Kristy A Martire, Amanda Hepler, Richard D Gill, Allan Jamieson, Jacob de Zoete, R Brent Ostrum, Amke Caliebe. A comment on the PCAST report: Skip the "match"/"non-match" stage. Forensic Science International, 272, E7-E9, 2017. doi: 10.1016/j.forsciint.2016.10.018.

• D. Speed, Na Cai, M. Johnson, Sergey Nejentsev, D. Balding, UCLEB Consortium. Reevaluation of SNP heritability in complex human traits. Nature Genetics, 49, 986-+, 2017. doi: 10.1038/ng.3865.

• Serban Radian, Yoan Diekmann, Plamena Gabrovska, Brendan Holland, Lisa Bradley, Helen Wallace, Karen Stals, Anna-Marie Bussell, Karen McGurren, Martin Cuesta, Anthony W Ryan, Maria Herincs, Laura C Hernandez-Ramirez, Jade Samuels, Elena Daniela Aflorei, Sayka Barry, Judit Denes, Ida Pernicova, Craig E Stiles, Giampaolo Trivellin, Ronan McCloskey, Michal Ajzensztejn, Noina Abid, Scott A Akker, Moises Mercado, Mark Cohen, Rajesh V Thakker, Stephanie Baldeweg, Ariel Barkan, Madalina Musat, Miles Levy, Stephen M Orme, Martina Unterlaender, Joachim Burger, A. Kumar, Sian Ellard, Joseph McPartlin, Ross McManus, Gerard J Linden, Brew Atkinson, D. Balding, Amar Agha, C. Thompson, Steven J Hunter, Mark G Thomas, Patrick J Morrison, Marta Korbonits, LC Hernández-Ramírez, J Dénes, M Unterländer. Increased Population Risk of AIP-Related Acromegaly and Gigantism in Ireland. Human Mutation, 38, 78-85, 2017. doi: 10.1002/humu.23121.

• Mikkel Andersen, D. Balding. How Convincing Is A Matching Y-Chromosome Profile?. 2017. doi: 10.1101/131920.

• K Ryan, D Gareth Williams, D. Balding. Probabilistic evaluation of low-quality DNA profiles. 2016.

• Marco Scutari, Ian Mackay, D. Balding. Using Genetic Distance to Infer the Accuracy of Genomic Prediction. PLOS Genetics, 12, e1006288 (19pp), 2016. doi: 10.1371/journal.pgen.1006288.

• K Ryan, D Gareth Williams, D. Balding. Encoding of low-quality DNA profiles as genotype probability matrices for improved profile comparisons, relatedness evaluation and database searches. Forensic Science International-Genetics, 25, 227-239, 2016. doi: 10.1016/j.fsigen.2016.09.004.

• C. Steele, Matthew Greenhalgh, D. Balding. Evaluation of low-template DNA profiles using peak heights. Statistical Applications in Genetics and Molecular Biology, 15, 431-445, 2016. doi: 10.1515/sagmb-2016-0038.

• Kaustubh Adhikari, Tania Fontanil, Santiago Cal, Javier Mendoza-Revilla, Macarena Fuentes-Guajardo, Juan-Camilo Chacon-Duque, Farah Al-Saadi, Jeanette A Johansson, Mirsha Quinto-Sanchez, Victor Acuna-Alonzo, Claudia Jaramillo, William Arias, Rodrigo Barquera Lozano, Gaston Macin Perez, Jorge Gomez-Valdes, Hugo Villamil-Ramirez, Tabita Hunemeier, Virginia Ramallo, Caio C Silva de Cerqueira, Malena Hurtado, Valeria Villegas, Vanessa Granja, Carla Gallo, Giovanni Poletti, Lavinia Schuler-Faccini, Francisco M Salzano, Maria-Catira Bortolini, Samuel Canizales-Quinteros, Francisco Rothhammer, Gabriel Bedoya, Rolando Gonzalez-Jose, Denis Headon, Carlos Lopez-Otin, Desmond J Tobin, D. Balding, Andres Ruiz-Linares, JC Chacón-Duque, V Acuña-Alonzo, GM Pérez, J Gómez-Valdés, H Villamil-Ramírez, R Gonzalez-José, C López-Otín, Gastón Macín Pérez. A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features. Nature Communications, 7, 10815 (12pp), 2016. doi: 10.1038/ncomms10815.

• Kaustubh Adhikari, Macarena Fuentes-Guajardo, Mirsha Quinto-Sanchez, Javier Mendoza-Revilla, Juan Camilo Chacon-Duque, Victor Acuna-Alonzo, Claudia Jaramillo, William Arias, Rodrigo Barquera Lozano, Gaston Macin Perez, Jorge Gomez-Valdes, Hugo Villamil-Ramirez, Tabita Hunemeier, Virginia Ramallo, Caio C Silva de Cerqueira, Malena Hurtado, Valeria Villegas, Vanessa Granja, Carla Gallo, Giovanni Poletti, Lavinia Schuler-Faccini, Francisco M Salzano, Maria-Catira Bortolini, Samuel Canizales-Quinteros, Michael Cheeseman, Javier Rosique, Gabriel Bedoya, Francisco Rothhammer, Denis Headon, Rolando Gonzalez-Jose, D. Balding, Andres Ruiz-Linares, M Quinto-Sánchez, J Camilo Chacón-Duque, V Acuña-Alonzo, GM Pérez, J Gómez-Valdés, H Villamil-Ramírez, R González-José. A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation. Nature Communications, 7, 11616 (11pp), 2016. doi: 10.1038/ncomms11616.

• Dace Ruklisa, James S Ware, Roddy Walsh, D. Balding, Stuart A Cook. Bayesian models for syndrome- and gene-specific probabilities of novel variant pathogenicity. Genome Medicine, 7, 5 (16pp), 2015. doi: 10.1186/s13073-014-0120-4.

• Lucy van Dorp, D. Balding, Simon Myers, Luca Pagani, Chris Tyler-Smith, Endashaw Bekele, Ayele Tarekegn, Mark G Thomas, Neil Bradman, Garrett Hellenthal. Evidence for a Common Origin of Blacksmiths and Cultivators in the Ethiopian Ari within the Last 4500 Years: Lessons for Clustering-Based Inference. PLOS Genetics, 11, e1005397 (49pp), 2015. doi: 10.1371/journal.pgen.1005397.

• D. Speed, D. Balding. Relatedness in the post-genomic era: is it still useful?. Nature Reviews Genetics, 16, 33-44, 2015. doi: 10.1038/nrg3821.

• Julie Bertrand, Maria De Iorio, D. Balding. Integrating dynamic mixed-effect modelling and penalized regression to explore genetic association with pharmacokinetics. Pharmacogenetics and Genomics, 25, 231-238, 2015. doi: 10.1097/FPC.0000000000000127.

• Adam Persing, Ajay Jasra, Alexandros Beskos, D. Balding, Maria De Iorio. A Simulation Approach for Change-Points on Phylogenetic Trees. Journal of Computational Biology, 22, 10-24, 2015. doi: 10.1089/cmb.2014.0218.

• Kaustubh Adhikari, Guillermo Reales, A. Smith, Esra Konka, Jutta Palmen, Mirsha Quinto-Sanchez, Victor Acuna-Alonzo, Claudia Jaramillo, William Arias, Macarena Fuentes, Maria Pizarro, Rodrigo Barquera Lozano, Gaston Macin Perez, Jorge Gomez-Valdes, Hugo Villamil-Ramirez, Tabita Hunemeier, Virginia Ramallo, Caio C Silva de Cerqueira, Malena Hurtado, Valeria Villegas, Vanessa Granja, Carla Gallo, Giovanni Poletti, Lavinia Schuler-Faccini, Francisco M Salzano, Maria-Catira Bortolini, Samuel Canizales-Quinteros, Francisco Rothhammer, Gabriel Bedoya, Rosario Calderon, Javier Rosique, Michael Cheeseman, Mahmood F Bhutta, Steve E Humphries, Rolando Gonzalez-Jose, Denis Headon, D. Balding, Andres Ruiz-Linares, V Acuña-Alonzo, G MacÍn Pérez, J Gómez-Valdés, H Villamil-Ramírez, R Calderón, R Gonzalez-José, Gastón Macín Pérez. A genome-wide association study identifies multiple loci for variation in human ear morphology. Nature Communications, 6, 7500 (10pp), 2015. doi: 10.1038/ncomms8500.

• Daniel C Jeffares, Charalampos Rallis, Adrien Rieux, D. Speed, Martin Prevorovsky, Tobias Mourier, Francesc X Marsellach, Zamin Iqbal, Winston Lau, Tammy MK Cheng, Rodrigo Pracana, Michael Muelleder, Jonathan LD Lawson, Anatole Chessel, Sendu Bala, Garrett Hellenthal, Thomas Keane, Jared T Simpson, Leanne Bischof, Bartlomiej Tomiczek, Danny A Bitton, Theodora Sideri, Sandra Codlin, Josephine EEU Hellberg, Laurent van Trigt, Linda Jeffery, Juan-Juan Li, Sophie Atkinson, Malte Thodberg, Melanie Febrer, Kirsten McLay, Nizar Drou, William Brown, Jacqueline Hayles, Rafael E Carazo Salas, Markus Ralser, Nikolas Maniatis, D. Balding, Francois Balloux, Richard Durbin, Juerg Baehler, M PÅ™evorovský, M Mülleder, J Bähler. The genomic and phenotypic diversity of Schizosaccharomyces pombe. Nature Genetics, 47, 235-+, 2015. doi: 10.1038/ng.3215.

• D. Speed, Aarno Palotie, Kirill Shkura, Anthony G Marson, D. Balding, M. Johnson, Terence J O’Brien. Describing the genetic architecture of epilepsy through heritability analysis. Brain, 137, 2680-2689, 2014. doi: 10.1093/brain/awu206.

• C. Steele, Denise Syndercombe Court, D. Balding. Worldwide F-ST Estimates Relative to Five Continental-Scale Populations. Annals of Human Genetics, 78, 468-477, 2014. doi: 10.1111/ahg.12081.

• C. Steele, Matthew Greenhalgh, D. Balding. Verifying likelihoods for low template DNA profiles using multiple replicates. Forensic Science International-Genetics, 13, 82-89, 2014. doi: 10.1016/j.fsigen.2014.06.018.

• Pascale Gerbault, Robin G Allaby, Nicole Boivin, Anna Rudzinski, Ilaria M Grimaldi, J Chris Pires, Cynthia Climer Vigueira, Keith Dobney, Kristen J Gremillion, Loukas Barton, Manuel Arroyo-Kalin, Michael D Purugganan, Rafael Rubio de Casas, Ruth Bollongino, Joachim Burger, Dorian Q Fuller, Daniel G Bradley, D. Balding, Peter J Richerson, M Thomas P Gilbert, Greger Larson, Mark G Thomas. Storytelling and story testing in domestication. Proceedings of the National Academy of Sciences of the United States of America, 111, 6159-6164, 2014. doi: 10.1073/pnas.1400425111.

• C. Steele, D. Balding. Statistical Evaluation of Forensic DNA Profile Evidence. Annual Review of Statistics and its Applications, 1, 361-384, 2014. doi: 10.1146/annurev-statistics-022513-115602.

• Marco Scutari, Phil Howell, D. Balding, Ian Mackay. Multiple Quantitative Trait Analysis Using Bayesian Networks. Genetics, 198, 129-137, 2014. doi: 10.1534/genetics.114.165704.

• D. Speed, D. Balding. MultiBLUP: improved SNP-based prediction for complex traits. Genome Research, 24, 1550-1557, 2014. doi: 10.1101/gr.169375.113.

• Andre FS Amaral, Adaikalavan Ramasamy, Francesc Castro-Giner, Cosetta Minelli, Simone Accordini, Inga-Cecilie Sorheim, Isabelle Pin, Manolis Kogevinas, Rain Jogi, D. Balding, Dan Norback, Giuseppe Verlato, Mario Olivieri, Nicole Probst-Hensch, Christer Janson, Jan-Paul Zock, Joachim Heinrich, Deborah L Jarvis, IC Sørheim, R Jõgi, D Norbäck. Interaction between gas cooking and GSTM1 null genotype in bronchial responsiveness: results from the European Community Respiratory Health Survey. Thorax, 69, 558-564, 2014. doi: 10.1136/thoraxjnl-2013-204574.

• T. King, Gloria Gonzalez Fortes, Patricia Balaresque, Mark G Thomas, D. Balding, Pierpaolo Maisano Delser, Rita Neumann, Walther Parson, Michael Knapp, S. Walsh, Laure Tonasso, John Holt, Manfred Kayser, Jo Appleby, Peter Forster, David Ekserdjian, Michael Hofreiter, Kevin Schuerer, K Schürer. Identification of the remains of King Richard III. Nature Communications, 5, 5631 (8pp), 2014. doi: 10.1038/ncomms6631.

• C. Steele, D. Balding. Choice of population database for forensic DNA profile analysis. Science & Justice, 54, 487-493, 2014. doi: 10.1016/j.scijus.2014.10.004.

• Alison R Bentley, Marco Scutari, Nicolas Gosman, Sebastien Faure, Felicity Bedford, Phil Howell, James Cockram, Gemma A Rose, Tobias Barber, Jose Irigoyen, Richard Horsnell, Claire Pumfrey, Emma Winnie, Johannes Schacht, Katia Beauchene, Sebastien Praud, Andy Greenland, D. Balding, Ian J Mackay, K Beauchêne. Applying association mapping and genomic selection to the dissection of key traits in elite European wheat. Theoretical and Applied Genetics, 127, 2619-2633, 2014. doi: 10.1007/s00122-014-2403-y.

• Richard JL Anney, Andreja Avbersek, D. Balding, Larry Baum, Felicitas Becker, Samuel F Berkovic, Jonathan P Bradfield, Lawrence C Brody, Russell J Buono, Claudia B Catarino, Gianpiero L Cavalleri, Stacey S Cherny, Krishna Chinthapalli, Alison J Coffey, Alastair Compston, Patrick Cossette, Gerrit-Jan de Haan, Peter De Jonghe, Carolien GF de Kovel, Norman Delanty, Chantal Depondt, Dennis J Dlugos, Colin P Doherty, Christian E Elger, Thomas N Ferraro, Martha Feucht, Andre Franke, Jacqueline French, Verena Gaus, David B Goldstein, Hongsheng Gui, Y. Guo, Hakon Hakonarson, Kerstin Hallmann, Erin L Heinzen, Ingo Helbig, Helle Hjalgrim, Margaret Jackson, Jennifer Jamnadas-Khoda, Dieter Janz, M. Johnson, Reetta Kaelviaeinen, Anne-Mari Kantanen, Dalia Kasperaviciute, Dorothee Kasteleijn-Nolst Trenite, Bobby PC Koeleman, Wolfram S Kunz, Patrick Kwan, Y. Lau, Anna-Elina Lehesjoki, Holger Lerche, Costin Leu, Wolfgang Lieb, Dick Lindhout, Warren Lo, Daniel H Lowenstein, Alberto Malovini, Anthony G Marson, Mark McCormack, J. Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies. Lancet Neurology, 13, 893-903, 2014. doi: 10.1016/S1474-4422(14)70171-1.

• Andres Ruiz-Linares, Kaustubh Adhikari, Victor Acuna-Alonzo, Mirsha Quinto-Sanchez, Claudia Jaramillo, William Arias, Macarena Fuentess, Maria Pizarro, Paola Everardo, Francisco de Avila, Jorge Gomez-Valdes, Paola Leon-Mimila, Tabita Hunemeier, Virginia Ramallo, Caio C Silva de Cerqueira, Mari-Wyn Burley, Esra Konca, Marcelo Zagonel de Oliveira, Mauricio Roberto Veronez, Marta Rubio-Codina, Orazio Attanasio, Sahra Gibbon, Nicolas Ray, Carla Gallo, Giovanni Poletti, Javier Rosique, Lavinia Schuler-Faccini, Francisco M Salzano, Maria-Catira Bortolini, Samuel Canizales-Quinteros, Francisco Rothhammers, Gabriel Bedoya, D. Balding, Rolando Gonzalez-Jose, V Acuña-Alonzo, M Fuentes, J Gómez-Valdés, P León-Mimila, F Rothhammer, R Gonzalez-José. Admixture in Latin America: Geographic Structure, Phenotypic Diversity and Self-Perception of Ancestry Based on 7,342 Individuals. PLOS Genetics, 10, e1004572 (13pp), 2014. doi: 10.1371/journal.pgen.1004572.

• D. Balding. Kinship, Heritability, and Prediction. Human Heredity, 76, 87 (1pp), 2014.

• D. Speed, D. Balding. MultiBLUP: Improved Prediction for Complex Traits. Human Heredity, 76, 90 (1pp), 2014.

• Doug Speed, Clive Hoggart, Slave Petrovski, Ioanna Tachmazidou, Alison Coffey, Andrea Jorgensen, Hariklia Eleftherohorinou, Maria De Iorio, Marian Todaro, Tisham De, David Smith, Margaret Jackson, Paul Cooper, Mark Kellett, Stephen Howell, Mark Newton, Raju Yerra, Meng Tan, Chris French, Markus Reuber, Graeme E Sills, David Chadwick, Munir Pirmohamed, David Bentley, Ingrid Scheffer, Samuel Berkovic, D. Balding, Aarno Palotie, Anthony Marson, M. Johnson. A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy.. Human molecular genetics, 23, 247-258, 2014. doi: 10.1093/hmg/ddt403.

• D. Balding, Michael Krawczak, John S Buckleton, James M Curran. Decision-making in familial database searching: KI alone or not alone?. Forensic Science International-Genetics, 7, 52-54, 2013. doi: 10.1016/j.fsigen.2012.06.001.

• Roberto Puch-Solis, Lauren Rodgers, Anjali Mazumder, Susan Pope, Ian Evett, James Curran, D. Balding. Evaluating forensic DNA profiles using peak heights, allowing for multiple donors, allelic dropout and stutters. Forensic Science International-Genetics, 7, 555-563, 2013. doi: 10.1016/j.fsigen.2013.05.009.

• D. Balding. Evaluation of mixed-source, low-template DNA profiles in forensic science. Proceedings of the National Academy of Sciences of the United States of America, 110, 12241-12246, 2013. doi: 10.1073/pnas.1219739110.

• Peter Bauer, D. Balding, Hans H Kluenemann, David EJ Linden, Daniel S Ory, Merce Pineda, Josef Priller, Frederic Sedel, Audrey Muller, Harbajan Chadha-Boreham, Richard WD Welford, Daniel S Strasser, Marc C Patterson, HH Klünemann, HH Klunemann. Genetic screening for NiemannPick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM study. Human Molecular Genetics, 22, 4349-4356, 2013. doi: 10.1093/hmg/ddt284.

• Marco Scutari, Ian Mackay, D. Balding. Improving the efficiency of genomic selection. Statistical Applications in Genetics and Molecular Biology, 12, 517-527, 2013. doi: 10.1515/sagmb-2013-0002.

• Xiayi Ke, Mario Cortina-Borja, Bruno Cesar Silva, Robert Lowe, Vardhman Rakyan, D. Balding. Integrated analysis of genome-wide genetic and epigenetic association data for identification of disease mechanisms. Epigenetics, 8, 1236-1244, 2013. doi: 10.4161/epi.26407.

• Doug Speed, Gibran Hemani, M. Johnson, D. Balding. Response to Lee et al.: SNP-Based Heritability Analysis with Dense Data. The American Journal of Human Genetics, 93, 1155-1157, 2013. doi: 10.1016/j.ajhg.2013.10.016.

• Julie Bertrand, D. Balding. Multiple single nucleotide polymorphism analysis using penalized regression in nonlinear mixed-effect pharmacokinetic models.. Pharmacogenetics and genomics, 23, 167-174, 2013. doi: 10.1097/FPC.0b013e32835dd22c.

• Alexessander Couto Alves, Soren Bruhn, Adaikalavan Ramasamy, Hui Wang, John W Holloway, Anna-Liisa Hartikainen, Marjo-Riitta Jarvelin, Mikael Benson, D. Balding, Lachlan JM Coin. Dysregulation of complement system and CD4+ T cell activation pathways implicated in allergic response.. PloS one, 8, e74821 (15pp), 2013. doi: 10.1371/journal.pone.0074821.

• AJ Walley, P Jacobson, M Falchi, L Bottolo, JC Andersson, E Petretto, A Bonnefond, E Vaillant, C Lecoeur, V Vatin, M Jernas, D. Balding, M Petteni, YS Park, T Aitman, S Richardson, L Sjostrom, LMS Carlsson, P Froguel. Differential coexpression analysis of obesity-associated networks in human subcutaneous adipose tissue. International Journal of Obesity, 36, 137-147, 2012. doi: 10.1038/ijo.2011.22.

• Luca Pagani, Toomas Kivisild, Ayele Tarekegn, Rosemary Ekong, Chris Plaster, Irene Gallego Romero, Qasim Ayub, S Qasim Mehdi, Mark G Thomas, Donata Luiselli, Endashaw Bekele, Neil Bradman, D. Balding, Chris Tyler-Smith, Irene Gallego Romero. Ethiopian Genetic Diversity Reveals Linguistic Stratification and Complex Influences on the Ethiopian Gene Pool. American Journal of Human Genetics, 91, 83-96, 2012. doi: 10.1016/j.ajhg.2012.05.015.

• Simon Mead, James Uphill, John Beck, Mark Poulter, T. Campbell, Jessica Lowe, Gary Adamson, Holger Hummerich, Norman Klopp, Ina-Maria Rueckert, H-Erich Wichmann, Dhoyazan Azazi, Vincent Plagnol, Wandagi H Pako, Jerome Whitfield, Michael P Alpers, John Whittaker, D. Balding, Inga Zerr, Hans Kretzschmar, John Collinge, IM Rückert. Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. Human Molecular Genetics, 21, 1897-1906, 2012. doi: 10.1093/hmg/ddr607.

• D. Speed, Gibran Hemani, M. Johnson, D. Balding. Improved Heritability Estimation from Genome-wide SNPs. American Journal of Human Genetics, 91, 1011-1021, 2012. doi: 10.1016/j.ajhg.2012.10.010.

• D. Speed, D. Balding. Understanding complex traits: from farmers to pharmas. 4, 59 (3pp), BIOMED CENTRAL LTD, 2012. doi: 10.1186/gm360.

• D. Balding. Invited Speaker: Evaluation of low-copy number forensic DNA profiles. Annals of Human Genetics, 76, 410 (1pp), 2012.

• Audrey Muller, D. Balding, Hans H Kluenemann, David Linden, Daniel Ory, Marc C Patterson, Merce Pineda, Josef Priller, Frederic Sedel, Harbajan Chadha-Boreham, James E Wraith, Peter Bauer. Challenges in Screening Rare Diseases: The ZOOM Experience. Pharmacoepidemiology and Drug Safety, 21, 202 (1pp), 2012.

• Vardhman K Rakyan, Thomas A Down, D. Balding, Stephan Beck. Epigenome-wide association studies for common human diseases. Nature Reviews Genetics, 12, 529-541, 2011. doi: 10.1038/nrg3000.

• D. Balding. Inference in complex systems INTRODUCTION. 1, 805-806, Royal Society, 2011. doi: 10.1098/rsfs.2011.0074.

• Marc Patterson, Peter Bauer, Hans Kluenemann, Frederic Sedel, David Linden, Ed Wraith, Mercedes Pineda, Josef Priller, Audrey Muller, Harbajan Chadha-Boreham, Christine Remy, D. Balding, Hans Klünemann. ZOOM: Observational genetic screening study of Niemann-Pick Disease Type C in adults with neurological and psychiatric signs. 102, S34 (1pp), Academic Press Inc Elsevier Science, 2011. doi: 10.1016/j.ymgme.2010.11.114.

• Adaikalavan Ramasamy, Ivan Curjuric, Lachlan J Coin, A. Kumar, Wendy L McArdle, Medea Imboden, Benedicte Leynaert, Manolis Kogevinas, Peter Schmid-Grendelmeier, Juha Pekkanen, Matthias Wjst, Andreas J Bircher, Ulla Sovio, Thierry Rochat, Anna-Liisa Hartikainen, D. Balding, Marjo-Riitta Jarvelin, Nicole Probst-Hensch, David P Strachan, Deborah L Jarvis. A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order. Journal of Allergy and Clinical Immunology, 128, 996-1005, 2011. doi: 10.1016/j.jaci.2011.08.030.

• Charlotte M Vignal, Aruna T Bansal, D. Balding. Using Penalised Logistic Regression to Fine Map HLA Variants for Rheumatoid Arthritis. Annals of Human Genetics, 75, 655-664, 2011. doi: 10.1111/j.1469-1809.2011.00670.x.

• MPH Stumpf, D. Balding, M Girolami. Handbook of Statistical Systems Biology. 1-508, 2011. doi: 10.1002/9781119970606.

• MPH Stumpf, D. Balding, M Girolami. Preface. 2011. doi: 10.1002/9781119970606.

• P Bauer, MC Patterson, F Sedel, D Linden, JE Wraith, M Pineda, J Priller, A Muller, H Chadha-Boreham, C Remy, DS Ory, D. Balding, HH Kluenemann. ZOOM: a genetic screening study of Niemann-Pick disease type C in adults with neurological and psychiatric signs. Journal of Neurology, 258, 164 (1pp), 2011.

• D. Balding, PF O'Reilly. Admixture provides new insights into recombination.. 43, 819-820, NATURE PUBLISHING GROUP, 2011. doi: 10.1038/ng.918.

• Harvinder S Chahal, Karen Stals, Martina Unterlander, D. Balding, Mark G Thomas, A. Kumar, G Michael Besser, A Brew Atkinson, Patrick J Morrison, Trevor A Howlett, Miles J Levy, Steve M Orme, Scott A Akker, Richard L Abel, Ashley B Grossman, Joachim Burger, Sian Ellard, Marta Korbonits, Martina Unterländer. Brief Report: AIP Mutation in Pituitary Adenomas in the 18th Century and Today.. The New England journal of medicine, 364, 43-50, 2011. doi: 10.1056/NEJMoa1008020.

• H Kluenemann, F Sedel, D Linden, D. Balding, JE Wraith, MC Patterson, M Pineda, J Priller, C Remy, P Bauer. ZOOM: observational genetic screening study of Niemann-Pick disease type C in adults with neurological/psychiatric signs. European Neuropsychopharmcology, 20, S569 (1pp), 2010.

• Federico CF Calboli, Federica Tozzi, Nicholas W Galwey, Athos Antoniades, Vincent Mooser, Martin Preisig, Peter Vollenweider, Dawn Waterworth, Gerard Waeber, M. Johnson, Pierandrea Muglia, D. Balding. A Genome-Wide Association Study of Neuroticism in a Population-Based Sample. PLoS One, 5, e11504 (7pp), 2010. doi: 10.1371/journal.pone.0011504.

• D. Balding, M Weale, M Richards, M Thomas. Genetic and isotopic analysis and the UK Border Agency. Significance, 7, 58-61, 2010. doi: 10.1111/j.1740-9713.2010.00419.x.

• D. Balding. Animal Research: Reporting In Vivo Experiments: The ARRIVE guidelines. Journal of Physiology, 588, 2519-2521, 2010. doi: 10.1113/jphysiol.2010.192278.

• D. Balding. Animal Research: Reporting In Vivo Experiments: The ARRIVE guidelines. Experimental Physiology, 95, 842-844, 2010. doi: 10.1113/expphysiol.2010.053793.

• Carol Kilkenny, William Browne, Innes C Cuthill, Michael Emerson, Douglas G Altmans, Douglas G Altman, D. Balding. Animal Research: Reporting In Vivo Experiments: The ARRIVE Guidelines. Journal of Gene Medicine, 12, 561-563, 2010. doi: 10.1002/jgm.1473.

• Carol Kilkenny, William Browne, Innes C Cuthill, Michael Emerson, Douglas G Altman, D. Balding. Animal research: Reporting in vivo experiments: The ARRIVE guidelines. British Journal of Pharmacology, 160, 1577-1579, 2010. doi: 10.1111/j.1476-5381.2010.00872.x.

• Delilah Zabaneh, D. Balding. A genome-wide association study of the metabolic syndrome in Indian Asian men.. PloS one, 5, e11961 (6pp), 2010. doi: 10.1371/journal.pone.0011961.

• Lachlan JM Coin, Julian E Asher, Robin G Walters, Julia S El-Sayed Moustafa, Adam J de Smith, Rob Sladek, D. Balding, Philippe Froguel, Alexandra IF Blakemore. cnvHap: an integrative population and haplotype–based multiplatform model of SNPs and CNVs. Nature methods, 7, 541-U85, 2010. doi: 10.1038/NMETH.1466.

• James Cockram, Jon White, Diana L Zuluaga, David Smith, Jordi Comadran, Malcolm Macaulay, Zewei Luo, Mike J Kearsey, Peter Werner, David Harrap, Chris Tapsell, Hui Liu, Peter E Hedley, Nils Stein, Daniela Schulte, Burkhard Steuernagel, David F Marshall, William TB Thomas, Luke Ramsay, Ian Mackay, D. Balding, Robbie Waugh, AGOUEB Consortium, C Booer, S Pike, G Hamilton, G Jellis, N Davies, A Ross, P Bury, R Habgood, S Klose, D Vequaud, T Christerson, J Brosnan, A Newton, J Russell, P Shaw, R Bayles, M Wang. Genome-wide association mapping to candidate polymorphism resolution in the unsequenced barley genome.. Proceedings of the National Academy of Sciences of the United States of America, 107, 21611-21616, 2010. doi: 10.1073/pnas.1010179107.

• Mark A Beaumont, Rasmus Nielsen, Christian Robert, Jody Hey, Oscar Gaggiotti, Lacey Knowles, Arnaud Estoup, Mahesh Panchal, Jukka Corander, Mike Hickerson, Scott A Sisson, Nelson Fagundes, Lounes Chikhi, Peter Beerli, Renaud Vitalis, Jean-Marie Cornuet, John Huelsenbeck, Matthieu Foll, Ziheng Yang, Francois Rousset, D. Balding, Laurent Excoffier. In defence of model-based inference in phylogeography.. Molecular ecology, 19, 436-446, 2010. doi: 10.1111/j.1365-294X.2009.04515.x.

• Matthew A Nunes, D. Balding. On optimal selection of summary statistics for approximate bayesian computation. Statistical applications in genetics and molecular biology, 9, Article34 (16pp), 2010. doi: 10.2202/1544-6115.1576.

• Shu-Yi Su, Julian E Asher, Marjo-Riita Jarvelin, Phillipe Froguel, Alexandra IF Blakemore, D. Balding, Lachlan JM Coin. Inferring combined CNV/SNP haplotypes from genotype data.. Bioinformatics (Oxford, England), 26, 1437-1445, 2010. doi: 10.1093/bioinformatics/btq157.

• Miriam F Moffatt, Ivo G Gut, Florence Demenais, David P Strachan, Emmanuelle Bouzigon, Simon Heath, Erika von Mutius, Martin Farrall, Mark Lathrop, William OCM Cookson, A. Kumar, Peter Burney, Debbie Jarvis, Matthias Wjst, Manolis Kogevinas, Rain Jogi, Christer Janson, Karl A Franklin, Ernst Omenaas, Benedicte Leynaert, Isabelle Pin, Joachim Heinrich, Nicole M Probst-Hensch, Josep M Anto, Jordi Sunyer, Jose-Antonio Maldonado, Jesus Martinez-Moratalla, Isabel Urrutia, Felix Payo, Francine Kauffmann, Marie-Helene Dizier, Valerie Siroux, Andrzej Boznanski, Charlotte Braun-Fahrlaender, Jon Genuneit, Juergen Glas, Elisabeth Horak, Michael Kabesch, Sreekumar G Pillai, Peter J Helms, Karin Carlsen, Jorrit Gerritsen, Michael Silverman, Peter Sly, John Tsanakas, Andrea Von Berg, Moira Whyte, Malcolm Blumenthal, Medea Imboden, Thierry Rochat, Gian Andri Thun, Margaret W Gerbase, Ivan Curjuric, Jean-Michel Gaspoz, Lee-Jane S Liu, Inge M Wouters, Torben Sigsgaard, Dick Heederik, Ioannis Basinas, Vivi Schlunssen, Oyvind O. A large-scale, consortium-based genomewide association study of asthma.. The New England journal of medicine, 363, 1211-1221, 2010. doi: 10.1056/NEJMoa0906312.

• Joao S Lopes, D. Balding, Mark A Beaumont. PopABC: a program to infer historical demographic parameters. Bioinformatics, 25, 2747-2749, 2009. doi: 10.1093/bioinformatics/btp487.

• Hariklia Eleftherohorinou, Victoria Wright, Clive Hoggart, Anna-Liisa Hartikainen, Marjo-Riitta Jarvelin, D. Balding, Lachlan Coin, Michael Levin. Pathway Analysis of GWAS Provides New Insights into Genetic Susceptibility to 3 Inflammatory Diseases. PLoS One, 4, e8068 (11pp), 2009. doi: 10.1371/journal.pone.0008068.

• D. Balding, John Buckleton. Interpreting low template DNA profiles. Forensic Science International-Genetics, 4, 1-10, 2009. doi: 10.1016/j.fsigen.2009.03.003.

• David Meyre, Jerome Delplanque, Jean-Claude Chevre, Cecile Lecoeur, Stephane Lobbens, Sophie Gallina, Emmanuelle Durand, Vincent Vatin, Franck Degraeve, Christine Proenca, Stefan Gaget, Antje Koerner, Peter Kovacs, Wieland Kiess, Jean Tichet, Michel Marre, Anna-Liisa Hartikainen, Fritz Horber, Natascha Potoczna, Serge Hercberg, Claire Levy-Marchal, Francois Pattou, Barbara Heude, Maithe Tauber, Mark I McCarthy, Alexandra IF Blakemore, Alexandre Montpetit, Constantin Polychronakos, Jacques Weill, Lachlan JM Coin, Julian Asher, Paul Elliott, Marjo-Riitta Jarvelin, Sophie Visvikis-Siest, Beverley Balkau, Rob Sladek, D. Balding, Andrew Walley, Christian Dina, Philippe Froguel, JC Chèvre, C Proença, A Körner, MR Järvelin. Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. Nature Genetics, 41, 157-159, 2009. doi: 10.1038/ng.301.

• John C Chambers, Weihua Zhang, Delilah Zabaneh, Joban Sehmi, Piyush Jain, Mark I McCarthy, Philippe Froguel, Aimo Ruokonen, D. Balding, Marjo-Riitta Jarvelin, James Scott, Paul Elliott, Jaspal S Kooner, Z Weihua. Common Genetic Variation Near Melatonin Receptor MTNR1B Contributes to Raised Plasma Glucose and Increased Risk of Type 2 Diabetes Among Indian Asians and European Caucasians. Diabetes, 58, 2703-2708, 2009. doi: 10.2337/db08-1805.

• Charlotte Vignal, Aruna T Bansal, D. Balding, Michael H Binks, Marion C Dickson, Doug S Montgomery, Anthony G Wilson. Challenges in mapping non-HLA-DRB1 major histocompatibility genes in rheumatoid arthritis: comment on the article by Vignal et al Reply. Arthritis and Rheumatism, 60, 2207-2208, 2009. doi: 10.1002/art.24808.

• Matthew Stephens, D. Balding. Bayesian statistical methods for genetic association studies. Nature Reviews Genetics, 10, 681-690, 2009. doi: 10.1038/nrg2615.

• William Astle, D. Balding. Population Structure and Cryptic Relatedness in Genetic Association Studies. Statistical Science, 24, 451-471, 2009. doi: 10.1214/09-STS307.

• D. Balding, Pablo A Ferrari, Ricardo Fraiman, Mariela Sued. Limit theorems for sequences of random trees. Test, 18, 302-315, 2009. doi: 10.1007/s11749-008-0092-z.

• D Zabaneh, JC Chambers, P Elliott, J Scott, D. Balding, JS Kooner. Heritability and genetic correlations of insulin resistance and component phenotypes in Asian Indian families using a multivariate analysis. Diabetologia, 52, 2585-2589, 2009. doi: 10.1007/s00125-009-1504-7.

• Charlotte Vignal, Aruna T Bansal, D. Balding, Michael H Binks, Marion C Dickson, Doug S Montgomery, Anthony G Wilson. Genetic Association of the Major Histocompatibility Complex With Rheumatoid Arthritis Implicates Two Non-DRB1 Loci. Arthritis and Rheumatism, 60, 53-62, 2009. doi: 10.1002/art.24138.

• Suzanne A Al-Bustan, Moussa Alkhalaf, Ibrahim Al-Rashdan, Salwa Al-Otaibi, Eman Al-Baker, D. Balding, Majed A Alnaqeeb. Apolipoprotein E, CI and B Gene Polymorphisms in a Sample of Patients with Coronary Heart Disease in the Kuwaiti Population. Medical Principles and Practice, 18, 294-299, 2009. doi: 10.1159/000215727.

• DE Krane, V Bahn, D. Balding, B Barlow, H Cash, BL Desportes, K Devlin, TE Doom, I Dror, S Ford, C Funk, J Gilder, G Hampikian, K Inman, A Jamieson, PE Kent, R Koppl, I Kornfield, S Krimsky, J Mnookin, L Mueller, E Murphy, DR Paoletti, DA Petrov, M Raymer, DM Risinger, A Roth, N Rudin, W Shields, JA Siegel, M Slatkin, YS Song, T. Speed, C Spiegelman, P Sullivan, AR Swienton, T Tarpey, WC Thompson, E Ungvarsky, S Zabell. Time for DNA Disclosure. 326, 1631-1632, Amer Assoc Advancement Science, 2009. doi: 10.1126/science.326.5960.1631.

• D. Balding. Genetic Policing: The Use of DNA in Criminal Investigations. Canadian Journal of Criminology and Criminal Justice, 51, 271 (1pp), 2009.

• W Zhang, D Zabaneh, D. Balding, MI McCarthy, P Elliott, J Scott, JS Kooner, JC Chambers. Are Indian Asians genetically homogeneous? Implications for genetic association studies. Heart, 94, A65 (1pp), 2008.

• JC Chambers, W Zhang, D Zabaneh, D. Balding, MI McCarthy, J Scott, P Elliott, JS Kooner. Does genetic variation in FTO account for the increased risk of obesity and type 2 diabetes in UK Indian Asians?. Heart, 94, A58-A59, 2008.

• D. Balding, F Calboli. Analysing complex canine pedigrees. Annals of Human Genetics, 72, 693 (1pp), 2008.

• D. Balding. Statistical approaches for genome-wide association studies. 6, 187 (1pp), Pergamon-Elsevier Science Ltd, 2008. doi: 10.1016/S1359-6349(08)71841-X.

• Clive J Hoggart, John C Whittaker, Maria De Iorio, D. Balding. Simultaneous Analysis of All SNPs in Genome-Wide and Re-Sequencing Association Studies. PLOS Genetics, 4, e1000130 (8pp), 2008. doi: 10.1371/journal.pgen.1000130.

• Federico CF Calboli, Jeff Sampson, Neale Fretwell, D. Balding. Population structure and inbreeding from pedigree analysis of purebred dogs. Genetics, 179, 593-601, 2008. doi: 10.1534/genetics.107.084954.

• Jean-Marie Cornuet, Filipe Santos, Mark A Beaumont, Christian P Robert, Jean-Michel Marin, D. Balding, Thomas Guillemaud, Arnaud Estoup. Inferring population history with DIY ABC: a user-friendly approach to approximate Bayesian computation. Bioinformatics, 24, 2713-2719, 2008. doi: 10.1093/bioinformatics/btn514.

• S. Su, Jonathan White, D. Balding, Lachlan JM Coin. Inference of haplotypic phase and missing genotypes in polyploid organisms and variable copy number genomic regions. BMC Bioinformatics, 9, 513 (9pp), 2008. doi: 10.1186/1471-2105-9-513.

• Clive J Hoggart, Taane G Clark, Maria De Lorio, John C Whittaker, D. Balding, M De Iorio. Genome-wide significance for dense SNP and resequencing data. Genetic Epidemiology, 32, 179-185, 2008. doi: 10.1002/gepi.20292.

• Marc Chadeau-Hyam, Clive J Hoggart, John C Whittaker, Maria De Iorio, D. Balding. Fregene: Simulation of realistic sequence-level data in populations and ascertained samples. BMC Bioinformatics, 9, 364 (11pp), 2008. doi: 10.1186/1471-2105-9-364.

• Ewan Birney, D. Balding. Confounding between recombination and selection, and the Ped/Pop method for detecting selection. Genome Research, 18, 1304-1313, 2008. doi: 10.1101/gr.067181.107.

• John C Chambers, Paul Elliott, Delilah Zabaneh, Weihua Zhang, Y. Li, Philippe Froguel, D. Balding, James Scott, Jaspal S Kooner. Common genetic variation near MC4R is associated with waist circumference and insulin resistance. Nature Genetics, 40, 716-718, 2008. doi: 10.1038/ng.156.

• S. Su, D. Balding, Lachlan JM Coin. Disease association tests by inferring ancestral haplotypes using a hidden markov model. Bioinformatics, 24, 972-978, 2008. doi: 10.1093/bioinformatics/btn071.

• John PA Ioannidis, Paolo Boffetta, Julian Little, Andre G Uitterlinden, Paolo Vineis, D. Balding, Anand Chokkalingam, Siobhan M Dolan, W Dana Flanders, Julian PT Higgins, Mark I McCarthy, David H McDermott, Grier P Page, Timothy R Rebbeck, Daniela Seminara, Muin J Khoury. Assessment of cumulative evidence on genetic associations: interim guidelines. International Journal of Epidemiology, 37, 120-132, 2008. doi: 10.1093/ije/dym159.

• D. Balding, M Bishop, C Cannings. Handbook of Statistical Genetics: Third Edition. 1, 1-1476, 2008. doi: 10.1002/9780470061619.

• D. Balding, M Bishop, C Cannings. Editor's Preface to the Third Edition. 1, 2008. doi: 10.1002/9780470061619.

• C Vignal, A Bansal, D. Balding. A shrinkage regression approach to tackle the HLA region. Genetic Epidemiology, 31, 613-614, 2007.

• JR Vaughan, M. Johnson, C Maddison, D. Balding, RS Shakir. Alopecia-hypogonadism-extrapyramidal disorder in a new family? A novel gene. Journal of Neurology, Neurosurgery and Psychiatry, 79, 357-358, 2007.

• E Birney, D. Balding. Confounding between recombination and selection, and a novel genome-wide method for detecting selection. Genetic Epidemiology, 31, 611 (1pp), 2007.

• Rob Sladek, Ghislain Rocheleau, Johan Rung, Christian Dina, Lishaung Shen, David Serre, Philippe Boutin, Marc Prentki, Barry I Posner, D. Balding, David Meyre, Constantin Polychronakos, Philippe Froguel. A high density genome-wide association study identifies novel susceptibility genes for type 2 diabetes mellitus and reveals new mechanisms for glucose intolerance. Diabetes, 56, A94 (1pp), 2007.

• LJ Astle, CC Holmes, D. Balding. Turbo Genomic Control. Genetic Epidemiology, 31, 605 (1pp), 2007. doi: 10.1002/gepi.20262.

• Guy D Leschziner, Toby Andrew, John Paul Leach, David Chadwick, Alison J Coffey, D. Balding, David R Bentley, Munir Pirmohamed, M. Johnson. Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach. Pharmacogenetics and Genomics, 17, 217-220, 2007. doi: 10.1097/01.fpc.0000230408.23146.b1.

• M Fazil Baksh, D. Balding, Timothy J Vyse, John C Whittaker. Family-based association analysis with ordered categorical phenotypes, covariates and interactions. Genetic Epidemiology, 31, 1-8, 2007. doi: 10.1002/gepi.20183.

• Taane G Clark, Toby Andrew, Gregory M Cooper, Elliott H Margulies, James C Mullikin, D. Balding. Functional constraint and small insertions and deletions in the ENCODE regions of the human genome. Genome Biology, 8, R180 (14pp), 2007. doi: 10.1186/gb-2007-8-9-r180.

• Clive J Hoggart, Marc Chadeau-Hyam, Taane G Clark, Riccardo Lampariello, John C Whittaker, Maria De Iorio, D. Balding. Sequence-level population simulations over large genomic regions. Genetics, 177, 1725-1731, 2007. doi: 10.1534/genetics.106.069088.

• Jan Graffelman, D. Balding, Anna Gonzalez-Neira, Jaume Bertranpetit. Variation in estimated recombination rates across human populations. Human Genetics, 122, 301-310, 2007. doi: 10.1007/s00439-007-0391-6.

• Robert Sladek, Ghislain Rocheleau, Johan Rung, Christian Dina, Lishuang Shen, David Serre, Philippe Boutin, Daniel Vincent, Alexandre Belisle, Samy Hadjadj, Beverley Balkau, Barbara Heude, Guillaume Charpentier, Thomas J Hudson, Alexandre Montpetit, Alexey V Pshezhetsky, Marc Prentki, Barry I Posner, D. Balding, David Meyre, Constantin Polychronakos, Philippe Froguel. A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature, 445, 881-885, 2007. doi: 10.1038/nature05616.

• Guy D Leschziner, Andrea L Jorgensen, Toby Andrews, P. Williamson, Anthony G Marson, Alison J Coffey, Claire Middleditch, D. Balding, Jane Roger, David R Bentley, David Chadwick, M. Johnson, Munir Pirmohamed, T Andrew, J Rogers. The association between polymorphisms in RLIP76 and drug response in epilepsy. Pharmacogenomics, 8, 1715-1722, 2007. doi: 10.2217/14622416.8.12.1715.

• D. Balding. Reply: On the value of haplotype-based genotype-phenotype analysis and on data transformation in pharmacogenetics and -genomics. Nature Reviews Genetics, 8, 2007. doi: 10.1038/nrg1916-c2.

• D Zabaneh, JC Chambers, P Elliott, R Baliga, J Scott, D. Balding, JS Kooner. Estimating heritabilities and genetic correlations of insulin resistance and related metabolic traits in Indian families using a multivariate maximum likelihood approach. Genetic Epidemiology, 31, 651 (1pp), 2007.

• Clive Hoggart, Maria De Iorio, John Whittakker, D. Balding. Bayesian shrinkage priors for detecting multiple causal variants from genome-wide association studies. Annals of Human Genetics, 71, 557 (1pp), 2007.

• CJ Hoggart, M De Iorio, JC Whittaker, D. Balding. Simultaneous analysis of genome-wide SNP data. Genetic Epidemiology, 31, 609 (1pp), 2007.

• Ewan Birney, D. Balding. The interplay between recombination and selection can confound their inference from population data - But suggests a novel genome-wide method for detecting selection. Annals of Human Genetics, 71, 551-552, 2007.

• William Astle, Chris Holmes, D. Balding. Turbo Genomic Control. Annals of Human Genetics, 71, 553-554, 2007.

• S. Su, D. Balding, L Coin. Using haplotype clustering techniques to perform genome-wide disease association studies. Genetic Epidemiology, 31, 612 (1pp), 2007.

• Z Yang, D. Balding. Adaptive Molecular Evolution. 375-406, John Wiley & Sons, Ltd, 2007. doi: 10.1002/9780470061619.ch12.

• E Setakis, H Stirnadel, D. Balding. Logistic regression protects against population structure in genetic association studies. Genome Research, 16, 290-296, 2006. doi: 10.1101/gr.4346306.

• Guy Leschziner, Delilah Zabaneh, M Pirmohamed, Andrew Owen, Jane Rogers, Alison J Coffey, D. Balding, David B Bentley, M. Johnson. Exon sequencing and high resolution haplotype analysis of ABC transporter genes implicated in drug resistance. Pharmacogenetics and Genomics, 16, 439-450, 2006. doi: 10.1097/01.fpc.0000197467.21964.67.

• D. Balding. A tutorial on statistical methods for population association studies. Nature Reviews Genetics, 7, 781-791, 2006. doi: 10.1038/nrg1916.

• Guy Leschziner, Andrea L Jorgensen, Toby Andrew, Munir Pirmohaomed, P. Williamson, Anthony G Marson, Alison J Coffey, Claire Middleditch, Jane Rogers, David R Bentley, David W Chadwick, D. Balding, M. Johnson, M Pirmohamed. Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort study. Lancet Neurology, 5, 668-676, 2006. doi: 10.1016/S1474-4422(06)70500-2.

• Lianne R Mayor, D. Balding. Discrimination of half-siblings when maternal genotypes are known. Forensic Science International, 159, 141-147, 2006. doi: 10.1016/j.forsciint.2005.07.007.

• ERB Waldron, JC Whittaker, D. Balding. Fine mapping of disease genes via haplotype clustering. Genetic Epidemiology, 30, 170-179, 2006. doi: 10.1002/gepi.20134.

• MF Baksh, D. Balding, TJ Vyse, JC Whittaker. A likelihood ratio approach to family-based association studies with covariates. Annals of Human Genetics, 70, 131-139, 2006. doi: 10.1111/j.1529-8817.2005.00189.x.

• C Vignal, A Bansal, D. Balding. Disentangling HLA associations: Multivariate association study using Bayesian logistic regression. Genetic Epidemiology, 31, 502 (1pp), 2006.

• D. Balding, C. Phillips. Relatedness. John Wiley & Sons Ltd, 2005.

• D. Balding. Typing technologies. 43-55, John Wiley & Sons Ltd, 2005.

• D. Balding. Some population genetics for DNA evidence. 56-81, John Wiley & Sons Ltd, 2005.

• D. Balding. Solutions to exercises. 157-174, John Wiley & Sons Ltd, 2005.

• D. Balding. Other approaches to weight of evidence. 135-144, John Wiley & Sons Ltd, 2005.

• D. Balding. Issues for the courtroom. 145-156, John Wiley & Sons Ltd, 2005.

• D. Balding. Identification. 82-110, John Wiley & Sons Ltd, 2005.

• D. Balding. Crime on an island. 7-21, John Wiley & Sons Ltd, 2005.

• D. Balding. Assessing evidence via likelihood ratios. 22-42, John Wiley & Sons Ltd, 2005.

• KL Ayres, D. Balding. Paternity index calculations when some individuals share common ancestry. Forensic Science International, 151, 101-103, 2005. doi: 10.1016/j.forsciint.2004.10.007.

• D. Balding. Weight-of-Evidence for Forensic DNA Profiles. 1-185, John Wiley & Sons Ltd, 2005. doi: 10.1002/9780470867693.

• D. Balding. A question of identity. Significance, 2, 20-23, 2005. doi: 10.1111/j.1740-9713.2005.00079.x.

• D. Balding, T Clark, CJ Hoggart. Sequence-level population genomic simulations. Genetic Epidemiology, 29, 235-236, 2005.

• ERB Waldron, JC Whittaker, D. Balding. A spatial clustering approach to fine-mapping of disease genes. Genetic Epidemiology, 29, 283 (1pp), 2005.

• MF Baksh, D. Balding, TJ Vyse, JC Whittaker. A family-based association test with a complex phenotype, covariates and interactions: assessing CRP and lupus. Annals of Human Genetics, 69, 764 (1pp), 2005.

• AP Morris, JC Whittaker, D. Balding. Little loss of information due to unknown phase for fine-scale linkage-disequilibrium mapping with single-nucleotide-polymorphism genotype data. American Journal of Human Genetics, 74, 945-953, 2004. doi: 10.1086/420773.

• LR Mayor, KP Fleming, A Muller, D. Balding, MJE Sternberg, A Müller. Clustering of protein domains in the human genome. Journal of Molecular Biology, 340, 991-1004, 2004. doi: 10.1016/j.jmb.2004.05.036.

• MA Beaumont, D. Balding. Identifying adaptive genetic divergence among populations from genome scans. Molecular Ecology, 13, 969-980, 2004. doi: 10.1111/j.1365-294X.2004.02125.x.

• IJ Wilson, ME Weale, D. Balding. Inferences from DNA data: population histories, evolutionary processes and forensic match probabilities. Journal of the Royal Statistical Society Series A: Statistics in Society, 166, 155-188, 2003. doi: 10.1111/1467-985X.00264.

• MS Phillips, R Lawrence, R Sachidanandam, AP Morris, D. Balding, MA Donaldson, JF Studebaker, WM Ankener, SV Alfisi, FS Kuo, AL Camisa, V Pazorov, KE Scott, BJ Carey, J Faith, G Katari, HA Bhatti, JM Cyr, V Derohannessian, C Elosua, AM Forman, NM Grecco, CR Hock, JM Kuebler, JA Lathrop, MA Mockler, EP Nachtman, SL Restine, SA Varde, MJ Hozza, CA Gelfand, J Broxholme, GR Abecasis, MT Boyce-Jacino, LR Cardon. Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots. Nature Genetics, 33, 382-387, 2003. doi: 10.1038/ng1100.

• AP Morris, JC Whittaker, CF Xu, LK Hosking, D. Balding. Multipoint linkage-disequilibrium mapping narrows location interval and identifies mutation heterogeneity. Proceedings of the National Academy of Sciences of the United States of America, 100, 13442-13446, 2003. doi: 10.1073/pnas.2235031100.

• D. Balding. Likelihood-based inference for genetic correlation coefficients. Theoretical Population Biology, 63, 221-230, 2003. doi: 10.1016/S0040-5809(03)00007-8.

• D. Balding, JL Gastwirth. International Statistical Review: Introduction. 71, 469-471, 2003.

• L Excoffier, G Laval, D. Balding. Gametic phase estimation over large genomic regions using an adaptive window approach. Human Genomics, 1, 7-19, 2003. doi: 10.1186/1479-7364-1-1-7.

• D. Balding, JL Gastwirth. Featuring a collection of papers on forensic statistics - Introduction. International Statistical Review, 71, 469-471, 2003.

• D. Balding, AP Morris, JC Whittaker, LK Hosking, CF Xu. Coalescent-based LD fine-mapping narrows location interval and identifies mutation heterogeneity.. American Journal of Human Genetics, 73, 196 (1pp), 2003.

• AP Morris, JC Whittaker, D. Balding. Fine-scale mapping of disease loci via shattered coalescent modeling of genealogies. American Journal of Human Genetics, 70, 686-707, 2002. doi: 10.1086/339271.

• KL Ayres, J Chaseling, D. Balding. Implications for DNA identification arising from an analysis of Australian forensic databases. Forensic Science International, 129, 90-98, 2002. doi: 10.1016/S0379-0738(02)00232-3.

• C Romualdi, D. Balding, IS Nasidze, G Risch, M Robichaux, ST Sherry, M Stoneking, MA Batzer, G Barbujani. Patterns of human diversity, within and among continents, inferred from biallelic DNA polymorphisms. Genome Research, 12, 602-612, 2002. doi: 10.1101/gr.214902.

• MA Beaumont, WY Zhang, D. Balding. Approximate Bayesian computation in population genetics. Genetics, 162, 2025-2035, 2002.

• D. Balding. The DNA database search controversy. Biometrics, 58, 241-244, 2002. doi: 10.1111/j.0006-341X.2002.00241.x.

• D. Balding, AD Carothers, JL Marchini, LR Cardon, A Vetta, B Griffiths, BS Weir, WG Hill, D Goldstein, K Strimmer, S Myers, MA Beaumont, CA Glasbey, CD Mayer, S Richardson, C Marshall, R Durrett, R Nielsen, PM Visscher, SA Knott, CS Haley, RD Ball, CA Hackett, S. Holmes, D Husmeier, RC Jansen, CJF ter Braak, CA Maliepaard, MP Boer, P Joyce, N. Li, M Stephens, GA Marcoulides, Z Drezner, K Mardia, G McVean, XL Meng, MF Ochs, M Pagel, N Sha, M Vannucci, MJ Sillanpaa, S Sisson, BS Yandell, CF Jin, JM Satagopan, PJ Gaffney, ZB Zeng, KW Broman, T. Speed, P Fearnhead, P Donnelly, B Larget, DL Simon, JB Kadane, G Nicholson, A. Smith, F Jonsson, O Gustafsson, K Stefansson, G Parmigiani, ES Garrett, R Anbazhagan, E Gabrielson, MJ Sillanpää, F Jónsson, O Gústafsson, K Stefánsson. Discussion on the meeting on 'Statistical modelling and analysis of genetic data'. 64, 737-775, WILEY-BLACKWELL, 2002. doi: 10.1111/1467-9868.00359.

• G McGuire, MC Denham, D. Balding. MAC5: Bayesian inference of phylogenetic trees from DNA sequences incorporating gaps. Bioinformatics, 17, 479-480, 2001. doi: 10.1093/bioinformatics/17.5.479.

• KL Ayres, D. Balding. Measuring gametic disequilibrium from multilocus data. Genetics, 157, 413-423, 2001.

• G McGuire, MC Denham, D. Balding. Models of sequence evolution for DNA sequences containing gaps. Molecular Biology and Evolution, 18, 481-490, 2001. doi: 10.1093/oxfordjournals.molbev.a003827.

• D. Balding, JC Whittaker, AP Morris. Linkage disequilibrium mapping via coalescent modelling.. American Journal of Human Genetics, 69, 530 (1pp), 2001.

• D. Balding, NG Becker, M Eerola, D Mollison. Analyses of infectious disease data from household outbreaks by Markov chain Monte Carlo methods. Journal of the Royal Statistical Society Series C: Applied Statistics, 49, 517-542, 2000. doi: 10.1111/1467-9876.00210.

• D. Balding, S Richardson. Special issue: Modern statistical methods for disease gene mapping. 68, 1-3, Int Statistical Inst, 2000. doi: 10.1111/j.1751-5823.2000.tb00383.x.

• AP Morris, JC Whittaker, D. Balding. Bayesian fine-scale mapping of disease loci, by hidden Markov models. American Journal of Human Genetics, 67, 155-169, 2000. doi: 10.1086/302956.

• D. Balding. When can a DNA profile be regarded as unique?. Science & Justice, 39, 257-260, 1999. doi: 10.1016/S1355-0306(99)72057-5.

• KL Ayres, D. Balding. Measuring departures from Hardy-Weinberg: a Markov chain Monte Carlo method for estimating the inbreeding coefficient. Heredity, 80, 769-777, 1998. doi: 10.1046/j.1365-2540.1998.00360.x.

• IJ Wilson, D. Balding. Genealogical inference from microsatellite data. Genetics, 150, 499-510, 1998.

• D. Balding. Bayesian analysis of DNA profiling data in forensic identification applications - Discussion. Journal of the Royal Statistical Society Series A: Statistics in Society, 160, 459-460, 1997.

• D. Balding, RA Nichols. Significant genetic correlations among Caucasians at forensic DNA loci. Heredity, 78, 583-589, 1997. doi: 10.1038/sj.hdy.6881750.

• D. Balding, DC Torney. The design of pooling experiments for screening a clone map. Fungal Genetics and Biology, 21, 302-307, 1997. doi: 10.1006/fgbi.1997.0985.

• S Tavare, D. Balding, RC Griffiths, P Donnelly, S Tavaré. Inferring coalescence times from DNA sequence data. Genetics, 145, 505-518, 1997.

• D. Balding, M Greenhalgh, RA Nichols. Population genetics of STR loci in Caucasians. International Journal of Legal Medicine, 108, 300-305, 1996. doi: 10.1007/BF02432124.

• D. Balding, P Donnelly. Evaluating DNA profile evidence when the suspect is identified through a database search. Journal of Forensic Sciences, 41, 603-607, 1996.

• D. Balding, DC Torney. Optimal pooling designs with error detection. Journal of Combinatorial Theory Series A, 74, 131-140, 1996. doi: 10.1006/jcta.1996.0041.

• Y. Fu, W. Li, P Donnelly, S Tavare, D. Balding, RC Griffiths, G. Weiss, A Von Haeseler, J Rogers, PB Samollow, AG Comuzzie, RL Dorit, H Akashi, W Gilbert, S Tavar ;, RC Griffiths;, A von Haeseler;, AG Comuzzie;. Estimating the age of the common ancestor of men from the ZFY intron. Science, 272, 1356-1357, 1996. doi: 10.1126/science.272.5266.1356.

• D. Balding, P Donnelly. Inferring identity from DNA profile evidence. Proceedings of the National Academy of Sciences of the United States of America, 92, 11741-11745, 1995. doi: 10.1073/pnas.92.25.11741.

• WJ Bruno, E Knill, D. Balding, DC Bruce, NA Doggett, WW Sawhill, RL Stallings, CC Whittaker, DC Torney. Efficient pooling designs for library screening. Genomics, 26, 21-30, 1995. doi: 10.1016/0888-7543(95)80078-Z.

• D. Balding, RA Nichols. A method for quantifying differentiation between populations at multi-allelic loci and its implications for investigating identity and paternity. Genetica, 96, 3-12, 1995. doi: 10.1007/BF01441146.

• D. Balding. Estimating products in forensic identification using dna profiles. Journal of the American Statistical Association, 90, 839-844, 1995. doi: 10.1080/01621459.1995.10476582.

• D. Balding, P Donnelly. Inference in forensic identification. Journal of the Royal Statistical Society Series A: Statistics in Society, 158, 21-53, 1995. doi: 10.2307/2983402.

• D. Balding. Design and analysis of chromosome physical mapping experiments. Philosophical Transactions of the Royal Society of London Series B-Biological Sciences, 344, 329-335, 1994. doi: 10.1098/rstb.1994.0071.

• D. Balding, P Donnelly. How convincing is DNA evidence. Nature, 368, 285-286, 1994. doi: 10.1038/368285a0.

• D. Balding, RA Nichols. DNA profile match probability calculation - how to allow for population stratification, relatedness, database selection and single bands. Forensic Science International, 64, 125-140, 1994. doi: 10.1016/0379-0738(94)90222-4.

• D. Balding, P Donnelly, RA Nichols. Comment: Some causes for concern about DNA profiles. Statistical Science, 9, 248-252, 1994. doi: 10.1214/ss/1177010489.

• D. Balding, P Donnelly, RA Nichols. Some causes for concern about DNA profiles - comment. Statistical Science, 9, 248-251, 1994. doi: 10.1214/ss/1177010489.

• D. Balding, P Donnelly. The prosecutors fallacy and dna evidence. Criminal Law Review, 711-721, 1994.

• CC Whittaker, M Mundt, V Faber, D. Balding, RL Dougherty, RL Stallings, SW White, DC Torney. Computations for mapping genomes with clones. International Journal of Genome Research, 1, 195-226, 1993.

• D. Balding, RA Nichols, DM HUNT. Detecting gene conversion - primate visual pigment genes. Proceedings of the Royal Society B-Biological Sciences, 249, 275-280, 1992. doi: 10.1098/rspb.1992.0114.

• D. Balding, D Torney. Statistical analysis of DNA fingerprint data for ordered clone physical mapping of human chromosomes. Bulletin of Mathematical Biology, 53, 853-879, 1991. doi: 10.1016/S0092-8240(05)80411-2.

• RA Nichols, D. Balding. Effects of population-structure on dna fingerprint analysis in forensic-science. Heredity, 66, 297-302, 1991. doi: 10.1038/hdy.1991.37.

• D. Balding, DC Torney. Statistical-analysis of DNA fingerprint data for ordered clone physical mapping of human-chromosomes. Bulletin of Mathematical Biology, 53, 853-879, 1991. doi: 10.1007/BF02461488.

• D. Balding, NJB Green. Diffusion-controlled reactions in one dimension - exact-solutions and deterministic approximations. Physical Review A, 40, 4585-4592, 1989. doi: 10.1103/PhysRevA.40.4585.

• D. Balding, P Clifford, NJB Green. Invasion processes and binary annihilation in one dimension. Physics Letters A, 126, 481-483, 1988. doi: 10.1016/0375-9601(88)90043-6.

• D. Balding. Diffusion-reaction in one dimension. Journal of Applied Probability, 25, 733-743, 1988. doi: 10.2307/3214294.

• HM Alexander, D. Balding, AJ DOBSON, RW Gibberd, DM Lloyd, SR LEEDER. Risk-factors and heart-disease mortality - a regional perspective. Medical Journal of Australia, 144, 20-22, 1986.

• D. Balding, DL Sean McElwain. A mathematical-model of tumor-induced capillary growth. Journal of Theoretical Biology, 114, 53-73, 1985. doi: 10.1016/S0022-5193(85)80255-1.