Shengru Guo

Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior

Andrea Ganna, Karin J. H. Verweij, Michel G. Nivard et al. · Science · 2019 · 407 citations · Full text

Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia

Michail Spiliopoulos, Francesco Brancati, Eric Powell et al. · The American Journal of Human Genetics · 2011 · 256 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

Güney Bademci, Joseph Foster, Nejat Mahdieh et al. · Genetics in Medicine · 2015 · 158 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +11

Genome-wide scan demonstrates significant linkage for male sexual orientation

Alan R. Sanders, Eden R. Martin, Gary W. Beecham et al. · Psychological Medicine · 2014 · 142 citations

Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents

Denise Yan, Demet Tekin, Güney Bademci et al. · Human Genetics · 2016 · 136 citations · Full text

Allelic Variant, Multiple Continents, Mendelian Disorder +12