Brian L. Yaspan

Functional impact of global rare copy number variation in autism spectrum disorders

Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei et al. · Nature · 2010 · 2K citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus et al. · Neuron · 2011 · 1.3K citations · Full text

Medicine, Genetics, Molecular Genetics +17

A genome-wide scan for common alleles affecting risk for autism

Richard Anney, Lambertus Klei, Dalila Pinto et al. · Human Molecular Genetics · 2010 · 588 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

Patrick Sulem, Andrei Manolescu, Daníel F. Guðbjartsson et al. · Nature Genetics · 2008 · 373 citations

Medicine, Genetics, Molecular Genetics +11

Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis

Richard J. Allen, Beatriz Guillén‐Guío, Justin M. Oldham et al. · American Journal of Respiratory and Critical Care Medicine · 2019 · 341 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17