A flexible approach for the analysis of rare variants allowing for a mixture of effects on binary or quantitative traits. by Geraldine M Clarke, Manuel A Rivas, Andrew P Morris

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The use of class imbalanced learning methods on ULSAM data to predict the case–control status in genome-wide association studies by R. Onur Öztornaci, Hamzah Syed, Andrew P. Morris, Bahar Taşdelen

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Two-stage two-locus models in genome-wide association. by David M Evans, Jonathan Marchini, Andrew P Morris, Lon R Cardon

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What Can Machine Learning Approaches in Genomics Tell Us about the Molecular Basis of Amyotrophic Lateral Sclerosis? by Christina Vasilopoulou, Andrew P. Morris, George Giannakopoulos, Stephanie Duguez, William Duddy

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Bridging the diversity gap: Analytical and study design considerations for improving the accuracy of trans-ancestry genetic prediction by Ozvan Bocher, Arthur Gilly, Young-Chan Park, Eleftheria Zeggini, Andrew P. Morris

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Leveraging information between multiple population groups and traits improves fine-mapping resolution by Feng Zhou, Opeyemi Soremekun, Tinashe Chikowore, Segun Fatumo, Inês Barroso, Andrew P. Morris, Jennifer L. Asimit

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Genomic insights into the comorbidity between type 2 diabetes and schizophrenia by Ana Luiza Arruda, Golam M. Khandaker, Andrew P. Morris, George Davey Smith, Laura M. Huckins, Eleftheria Zeggini

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Evaluating the Performance of Fine-Mapping Strategies at Common Variant GWAS Loci. by Martijn van de Bunt, Adrian Cortes, IGAS Consortium, Matthew A Brown, Andrew P Morris, Mark I McCarthy

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Genome-Wide Gene-Set Analysis Identifies Molecular Mechanisms Associated with ALS by Christina Vasilopoulou, Sarah L. McDaid-McCloskey, Gavin McCluskey, Stephanie Duguez, Andrew P. Morris, William Duddy

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Genetic and methylation variation in the CYP2B6 gene is related to circulating p,p′-dde levels in a population-based sample by Lars Lind, Esther Ng, Erik Ingelsson, Cecilia Lindgren, Samira Salihovic, Bert van Bavel, Anubha Mahajan, Erik Lampa, Andrew P. Morris, P. Monica Lind

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Analysis of chromatin organization and gene expression in T cells identifies functional genes for rheumatoid arthritis by Jing Yang, Amanda McGovern, Paul Martin, Kate Duffus, Xiangyu Ge, Peyman Zarrineh, Andrew P. Morris, Antony Adamson, Peter Fraser, Magnus Rattray, Stephen Eyre

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Multi-ancestry meta-analysis of host genetic susceptibility to tuberculosis identifies shared genetic architecture by Haiko Schurz, Vivek Naranbhai, Tom A Yates, James J Gilchrist, Tom Parks, Peter J Dodd, Marlo Möller, Eileen G Hoal, Andrew P Morris, Adrian VS Hill, International Tuberculosis Host Genetics Consortium

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The inheritance of resistance alleles in multiple sclerosis. by Sreeram V Ramagopalan, Andrew P Morris, David A Dyment, Blanca M Herrera, Gabriele C DeLuca, Matthew R Lincoln, Sarah M Orton, Michael J Chao, A Dessa Sadovnick, George C Ebers

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Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to... by Esteban J Parra, Andrew Mazurek, Christopher R Gignoux, Alexandra Sockell, Michael Agostino, Andrew P Morris, Lauren E Petty, Craig L Hanis, Nancy J Cox, Adan Valladares-Salgado, Jennifer E Below, Miguel Cruz

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Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study by Bridget M. Lin, Girish N. Nadkarni, Girish N. Nadkarni, Ran Tao, Ran Tao, Mariaelisa Graff, Myriam Fornage, Steven Buyske, Tara C. Matise, Heather M. Highland, Lynne R. Wilkens, Christopher S. Carlson, Christopher S. Carlson, S. Lani Park, V. Wendy Setiawan, Jose Luis Ambite, Gerardo Heiss, Eric Boerwinkle, Dan-Yu Lin, Andrew P. Morris, Andrew P. Morris, Ruth J. F. Loos, Ruth J. F. Loos, Charles Kooperberg, Kari E. North, Christina L. Wassel, Nora Franceschini

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Variability of genome-wide DNA methylation and mRNA expression profiles in reproductive and endocrine disease related tissues by Nilufer Rahmioglu, Alexander W Drong, Helen Lockstone, Thomas Tapmeier, Karin Hellner, Merli Saare, Triin Laisk-Podar, Christine Dew, Emily Tough, George Nicholson, Maire Peters, Andrew P Morris, Cecilia M Lindgren, Christian M Becker, Krina T Zondervan

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The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. by Thomas S Scerri, Fahimeh Darki, Dianne F Newbury, Andrew J O Whitehouse, Myriam Peyrard-Janvid, Hans Matsson, Qi W Ang, Craig E Pennell, Susan Ring, John Stein, Andrew P Morris, Anthony P Monaco, Juha Kere, Joel B Talcott, Torkel Klingberg, Silvia Paracchini

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Genome-wide association analysis of cystatin-C kidney function in continental AfricaResearch in context by Richard Mayanja, Tafadzwa Machipisa, Opeyemi Soremekun, Abram B. Kamiza, Christopher Kintu, Allan Kalungi, Robert Kalyesubula, Obondo J. Sande, Daudi Jjingo, June Fabian, Cassianne Robinson-Cohen, Nora Franceschini, Dorothea Nitsch, Moffat Nyirenda, Eleftheria Zeggini, Andrew P. Morris, Tinashe Chikowore, Segun Fatumo

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Functional genomics atlas of synovial fibroblasts defining rheumatoid arthritis heritability by Xiangyu Ge, Mojca Frank-Bertoncelj, Kerstin Klein, Amanda McGovern, Tadeja Kuret, Miranda Houtman, Blaž Burja, Raphael Micheroli, Chenfu Shi, Miriam Marks, Andrew Filer, Christopher D. Buckley, Gisela Orozco, Oliver Distler, Andrew P. Morris, Paul Martin, Stephen Eyre, Caroline Ospelt

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Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. by William M Brandler, Andrew P Morris, David M Evans, Thomas S Scerri, John P Kemp, Nicholas J Timpson, Beate St Pourcain, George Davey Smith, Susan M Ring, John Stein, Anthony P Monaco, Joel B Talcott, Simon E Fisher, Caleb Webber, Silvia Paracchini

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