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Plos One|July 11, 2015
Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological SenseSabine Siegert, Andreas Wolf, David N Cooper, et al.Human Mutation|February 20, 2004
Gross Rearrangement Breakpoint Database (GRaBD)Shaun S Abeysinghe, Peter D Stenson, Michael Krawczak, et al.Human Genetics|December 7, 2016
The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesisHildegard Kehrer-Sawatzki, Said Farschtschi, Victor-Felix Mautner, et al.Human Genetics|June 29, 2005
A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic diseaseJian-Min Chen, Peter D Stenson, David N Cooper, et al.Nucleic Acids Research|April 17, 2016
Translocation and deletion breakpoints in cancer genomes are associated with potential non-B DNA-forming sequencesAlbino Bacolla, John A Tainer, Karen M Vasquez, et al.Human Genomics|December 14, 2011
Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesisSebastian Laycock-van Spyk, Nick Thomas, David N Cooper, et al.Human Genomics|July 24, 2010
Characterisation of a functional intronic polymorphism in the human growth hormone (GH1) geneDavid S Millar, Martin Horan, Nadia A Chuzhanova, et al.Human Genomics|December 19, 2012
Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?Adila Alkindy, Nadia Chuzhanova, Usha Kini, et al.American Journal of Human Genetics|August 24, 2004
Transmission-ratio distortion and allele sharing in affected sib pairs: a new linkage statistic with reduced bias, with application to chromosome 6q25.3Mathieu Lemire, Nicole M Roslin, Catherine Laprise, et al.Diabetes|March 31, 2007
Toward further mapping of the association between the IL2RA locus and type 1 diabetesHui-Qi Qu, Alexander Montpetit, Bing Ge, et al.Pageof 57