Stephen W. Scherer

发表

Global variation in copy number in the human genome

D. Conrad, R. Redon, L. Feuk, 2006, Nature.

Nature Genetics Advance Online Publication Genetic Association Study of Qt Interval Highlights Role for Calcium Signaling Pathways in Myocardial Repolarization

Michael J Ackerman, Christian Gieger, Thomas Meitinger, 2022 .

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development.

S. Scherer, L. Tsui, J. Rommens, 1996, Human molecular genetics.

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2021 .

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2021 .

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

R. Schmidt, Candace Patterson, Stephan J. Sanders, 2021 .

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2021 .

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2021 .