Sarah J Garnai
2PUBLICATIONS
34CO-AUTHORS
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Publications (2)
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|Jun 29, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.Alan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb
|May 04, 2019
Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice.Sarah J Garnai, Michelle L Brinkmeier, Ben Emery
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Frequent Collaborators
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Louise C Pyle
1 joint publications
Biliana Veleva-Rotse
1 joint publications
Steven M Archer
1 joint publications
Cheng-Mao Lin
1 joint publications
Sarah Sheskey
1 joint publications
Michael Boehnke
1 joint publications
Alexander E Katz
1 joint publications
Sally A Camper
1 joint publications
Lev Prasov
1 joint publications
Silvio Alessandro Di Gioia
