Bryan Paeper

The contribution of de novo coding mutations to autism spectrum disorder

Ivan Iossifov, Brian J. O’Roak, Stephan Sanders et al. · Nature · 2014 · 2.7K citations · Full text

Neurodevelopmental Disorders, Spectrum Disorder, Syndromic Autism +8

Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse

Mary E. Brunkow, Eric W. Jeffery, Kathryn A. Hjerrild et al. · Nature Genetics · 2001 · 2.6K citations

New Forkhead/winged-helix Protein, Immunology, Pathology +6

Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein

Mary E. Brunkow, Jessica C. Gardner, Jeff Van Ness et al. · The American Journal of Human Genetics · 2001 · 999 citations · Full text

Bone Disease, Sclerostin, Bone Morphogenic Protein +9

A 52‐kb deletion in the <i>SOST‐MEOX1</i> intergenic region on 17q12‐q21 is associated with van Buchem disease in the Dutch population

Karen Staehling-Hampton, Sean Proll, Bryan Paeper et al. · American Journal of Medical Genetics · 2002 · 299 citations

Sclerostin, Genetics, Genetic Epidemiology +19

Polymorphisms in the Sclerosteosis/van Buchem Disease Gene (SOST) Region Are Associated with Bone-Mineral Density in Elderly Whites

André G. Uitterlinden, Pascal Arp, Bryan Paeper et al. · The American Journal of Human Genetics · 2004 · 131 citations · Full text

Bone Disease, Bone-mineral Density, Region Are Associated +10