Shannon Rego
6PUBLICATIONS
32CO-AUTHORS
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Publications (6)
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|May 04, 2021
New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder.Justin O Szot, Anne Slavotinek, Karen Chong
|Sep 21, 2020
Candidate variants in TUB are associated with familial tremor.M Reza Sailani, Fereshteh Jahanbani, Charles W Abbott
|Sep 09, 2020
The expanding spectrum of NFIB-associated phenotypes in a diverse patient population-A report of two new patients.Kathleen Barrus, Shannon Rego, Tiffany Yip
|Mar 06, 2019
Much ado about nothing: A qualitative study of the experiences of an average-risk population receiving results of exome sequencing.Shannon Rego, Orit Dagan-Rosenfeld, Stephanie A Bivona
|Nov 30, 2018
High-frequency actionable pathogenic exome variants in an average-risk cohort.Shannon Rego, Orit Dagan-Rosenfeld, Wenyu Zhou
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Frequent Collaborators
2 joint publications
Kelly E Ormond
1 joint publications
Megan E Grove
1 joint publications
Mildred K Cho
1 joint publications
M Reza Sailani
1 joint publications
Fereshteh Jahanbani
1 joint publications
Charles W Abbott
1 joint publications
Hayan Lee
1 joint publications
Tahir N Khan
1 joint publications
Stefanie H Müller
1 joint publications
Katherine M Lyman
