N Weaver
14PUBLICATIONS
49CO-AUTHORS
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Publications (14)
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|Nov 04, 2024
RMND1 and PLN variants are the underlying cause of Perrault-like syndrome and cardiac anomalies in a patient.Xiaoli Du, Cara L Barnett, Kimberly M Widmeyer
|Oct 18, 2023
Phenotypes and genotypes in a cohort of children with single-ventricle CHD.Elizabeth K Baker, Amy Shikany, David S Winlaw
|Sep 29, 2023
Prenatal and infantile diagnosis of craniosynostosis in individuals with RASopathies.Carolyn R Serbinski, April Vanderwal, Sarah E Chadwell
|May 15, 2023
ARF1-related disorder: phenotypic and molecular spectrum.Jean-Madeleine de Sainte Agathe, Ben Pode-Shakked, Sophie Naudion
|Dec 01, 2022
Central nervous system involvement in individuals with RASopathies.K Nicole Weaver, Karen W Gripp
|Nov 26, 2022
Further expansion and confirmation of phenotype in rare loss of YWHAE gene distinct from Miller-Dieker syndrome.Elizabeth K Baker, Casey J Brewer, Leonardo Ferreira
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Frequent Collaborators
4 joint publications
Elizabeth K Baker
2 joint publications
Yuri A Zarate
1 joint publications
Katherine Abell
1 joint publications
Kelly Smallwood
1 joint publications
Dan Doherty
1 joint publications
Jing Chen
1 joint publications
Amy Shikany
1 joint publications
Pete S White
1 joint publications
Carlos E Prada
1 joint publications
Bruce D Gelb
