Publications:50
Bryn D Webb, MD
About Me
Dr. Bryn Webb is a clinical geneticist, clinical molecular geneticist, and pediatrician specializing in genetic studies of rare, congenital anomalies. She is Assistant Professor for the Department of Genetics and Genomic Sciences and Pediatrics, Co-Director of the Multi-Disciplinary Cleft and Craniofacial Program at the Icahn School of Medicine at Mount Sinai and Co-Director of the Mitochondrial Medicine Program in the Division of Medical Genetics at Mount Sinai. She is also Director of the Mindich Child Health and Development Institute (MCHDI) Undiagnosed Disease Program.
Language
English
Position
ADJUNCT ASSISTANT PROFESSOR | Genetics and Genomic Sciences
Research Topics
Gene Discovery, Genetics, Human Genetics and Genetic Disorders
Clinical Focus
- Birth Defects
- Mitochondrial Myopathy
- Oral-Facial Clefts
Publications
Selected Publications
- Data-driven consideration of genetic disorders for global genomic newborn screening programs. Thomas Minten, Sarah Bick, Sophia Adelson, Nils Gehlenborg, Laura M. Amendola, François Boemer, Alison J. Coffey, Nicolas Encina, Alessandra Ferlini, Janbernd Kirschner, Bianca E. Russell, Laurent Servais, Kristen L. Sund, Ryan J. Taft, Petros Tsipouras, Hana Zouk, Aldona Zygmunt, Athina Ververi, Carol Siu, Emanuela Ponzi, Enrico Bertini, Huang Xinwen, Jovanka King, Karin Kassahn, Maria Koutsogianni, Maria Luisa Valente, Matthew J. Pelo, Mattia Gentile, Paola Orsini, Romina Ficarella, Stefaan Sansen, Xiao Rui, Zhao Zhengyan, David Bick, Aaron Goldenberg, Aditi Satija, Alberte Lundquist, Alessandra Ferlini, Alexandra Wiedemann, Alice Tuff-Lacey, Aljazi Al-Maraghi, Amanda Pichini, Ammira Alshabeeb Akil, Amy Brower, Amy Gaviglio, Amy Ponte, Andrea Oza, Andreas Posch, Bryn Webb, Melissa Wasserstein. Genetics in Medicine
- Familial RPL26 Variant Causing Congenital Anomalies Without Hematological Features of Diamond Blackfan Anemia. Lisa M. Karger, Bryn D. Webb, Lisa Edelmann, Jun Liao, Lakshmi Mehta. American Journal of Medical Genetics, Part A
- Sequence variants in HECTD1 result in a variable neurodevelopmental disorder. Gazelle Zerafati-Jahromi, Elias Oxman, Hieu D. Hoang, Wu Lin Charng, Tanvitha Kotla, Weimin Yuan, Keito Ishibashi, Sonia Sebaoui, Kathryn Luedtke, Bryce Winrow, Rebecca D. Ganetzky, Anna Ruiz, Carmen Manso-Basúz, Nino Spataro, Peter Kannu, Taryn Athey, Christina Peroutka, Caitlin Barnes, Richard Sidlow, George Anadiotis, Kari Magnussen, Irene Valenzuela, Alejandro Moles-Fernandez, Seth Berger, Christina L. Grant, Eric Vilain, Gudny A. Arnadottir, Patrick Sulem, Telma S. Sulem, Kari Stefansson, Shavonne Massey, Natalie Ginn, Annapurna Poduri, Alissa M. D'Gama, Rozalia Valentine, Sara K. Trowbridge, Chaya N. Murali, Rachel Franciskovich, Yen Tran, Bryn D. Webb, Kim M. Keppler-Noreuil, April L. Hall, Bobbi McGivern, Kristin G. Monaghan, Maria J. Guillen Sacoto, Dustin Baldridge, Gary A. Silverman, Sonika Dahiya, Tychele N. Turner, Tim Schedl, Joshua G. Corbin, Stephen C. Pak, Irene E. Zohn, Christina A. Gurnett. American Journal of Human Genetics
Industry Relationships
Physicians and scientists on the faculty of the Icahn School of Medicine at Mount Sinai often interact with pharmaceutical, device, biotechnology companies, and other outside entities to improve patient care, develop new therapies and achieve scientific breakthroughs. In order to promote an ethical and transparent environment for conducting research, providing clinical care and teaching, Mount Sinai requires that salaried faculty inform the School of their outside financial relationships.
Dr. Webb has not yet completed reporting of Industry relationships.
Mount Sinai’s faculty policies relating to faculty collaboration with industry are posted on our website. Patients may wish to ask their physician about the activities they perform for companies.