Stephanie L. Sherman

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Daniel Taliun, Daniel Harris, Michael D. Kessler et al. · Nature · 2021 · 2.2K citations · Full text

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Alexander G. Bick, Joshua S. Weinstock, Satish K. Nandakumar et al. · Nature · 2020 · 698 citations · Full text

Genetic Disorder, Genetics, Hematology +3

Association of FMR1 repeat size with ovarian dysfunction

Amy K. Sullivan, Michele Marcus, Michael P. Epstein et al. · Human Reproduction · 2004 · 496 citations · Full text

Association and Linkage of the Dopamine Transporter Gene and Attention-Deficit Hyperactivity Disorder in Children: Heterogeneity owing to Diagnostic Subtype and Severity

Irwin D. Waldman, David Rowe, Ann Abramowitz et al. · The American Journal of Human Genetics · 1998 · 462 citations · Full text

Adhd, Neuropsychology, Psychiatry +11

Incidence of Fragile X Syndrome by Newborn Screening for Methylated FMR1 DNA

Bradford Coffee, Krayton Keith, Igor Albizua et al. · The American Journal of Human Genetics · 2009 · 432 citations · Full text

Fragile X Syndrome, Genetic Testing, Newborn Screening +11