Catherine Keegan
9PUBLICATIONS
38CO-AUTHORS
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Publications (9)
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|Feb 24, 2025
Long-read sequencing resolves the clinically relevant <i>CYP21A2</i> locus, supporting a new clinical test for Congenital Adrenal Hyperplasia.Jean Monlong, Xiao Chen, Hayk Barseghyan
|Feb 19, 2025
Variants in KLF4 affecting residue Asp441 cause an autosomal dominant syndromic ichthyosis.Zijuan Wang, Jun Liu, Oded Wechsberg
|Aug 12, 2022
An Interdisciplinary Approach to Müllerian Outflow Tract Obstruction Associated with Cloacal Malformation and Cloacal Exstrophy.Bryan S Sack, K Elizabeth Speck, Anastasia L Hryhorczuk
|Oct 14, 2021
Differential impact of a dyskeratosis congenita mutation in TPP1 on mouse hematopoiesis and germline.Jacqueline V Graniel, Kamlesh Bisht, Ann Friedman
|Jun 24, 2020
Author Correction: Mutually suppressive roles of KMT2A and KDM5C in behaviour, neuronal structure, and histone H3K4 methylation.Christina N Vallianatos, Brynne Raines, Robert S Porter
|Jun 03, 2020
Mutually suppressive roles of KMT2A and KDM5C in behaviour, neuronal structure, and histone H3K4 methylation.Christina N Vallianatos, Brynne Raines, Robert S Porter
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Frequent Collaborators
3 joint publications
David E Sandberg
2 joint publications
Christina N Vallianatos
2 joint publications
Brynne Raines
2 joint publications
Robert S Porter
2 joint publications
Michael C Wu
2 joint publications
Patricia M Garay
2 joint publications
Natalie C Tronson
2 joint publications
Shigeki Iwase
1 joint publications
Heather M Byers
1 joint publications
Elizabeth A McCauley
