
Bryn Webb
@brynwebbmd
Associate Professor @uwsmph Board-certified in Clinical Genetics, Clinical Molecular Genetics, & Pediatrics #RareDisease [email protected]
ID: 2355883720
21-02-2014 05:16:20
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731 Followers
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Are you applying to medical school or graduate school & you’re seeking wet lab experience? My lab at University of Wisconsin Department of Pediatrics UW School of Medicine and Public Health studies rare genetic disease. We have some exciting projects & I’m happy to mentor! If interested, please send your resume to [email protected]



Attn: Clinical Geneticists (MDs)🧬🩺- Come join our growing team in Madison, Wisconsin UW School of Medicine and Public Health! Some positives here: very collegial team; opportunities for basic, translational, and clinical research; low-cost of living; & many outdoor activities. Reach out if you have questions!

join us for our 1st Annual Precision Medicine Symposium UW–Madison UW School of Medicine and Public Health Center for Human Genomics and Precision Medicine Abstract submission ends 8/31. Dr. Paul Lambert will be keynote speaker. We have 6 x $500 travel awards for best abstracts and a $50,000 collaborative grant to give out bit.ly/3pzrwqp


Confirmed speakers include: Paul Lambert and Wei Xu (McArdle Laboratory), Angela Gibson and Hau Le (UW-Madison Department of Surgery @AngGibson01), David Beebe (UW-Madison BME UW Dept of Pathology and Laboratory Medicine), Corinne Engelman (UW Pop Health Sci), Kim Keppler-Noreuil and Bryn Webb (University of Wisconsin Department of Pediatrics Bryn Webb)


🚀 PUBLISHED Nature Genetics 📰 Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis 🧑🤝🧑 Elizabeth C. Engle, Alan P. Tenney, Silvio Alessandro Di Gioia, Bryn D. Webb and team 👇🏼 go.nature.com/3Not8i0

Researchers at Boston Children's, in collaboration with National Human Genome Research Institute and Mount Sinai Department of Medicine, have found variants in the human genome associated with hereditary congenital facial paresis type 1 (HCFP1).

A great collaborative project to gain insight into the cause of #HCFP. Congrats to @Engle_lab Bryn Webb @alexdigiox for leading this work. And thank you for allowing us to contribute; Proud to be part of this! ElkedB Hans van Bokhoven Solve-RD Radboudumc Human Genetics Nijmegen, Radboudumc


Led by Engle Lab Alessandro Di Gioia Bryn Webb & Alan Tenney, in collaboration with Solve-RD partners ElkedB Lisenka Vissers Hans van Bokhoven and many others. Read 🧵below ⤵️








Solving elusive diagnoses & giving families long-sought answers = joy for Dr. Bryn Webb, Laboratory Genetics and Genomics Editor for ACMG's flagship journal, Genetics in Medicine. She serves as PI for the University of Wisconsin Undiagnosed Disease Program. #MedicalGeneticsAwareness