Amanda Thomas-Wilson
5PUBLICATIONS
18CO-AUTHORS
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Publications (5)
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|Jun 13, 2025
Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell-Silver Syndrome in Infancy.Amanda Thomas-Wilson, Mythily Ganapathi, Nina Harkavy
|Jul 07, 2023
Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease.Thomas Hays, Rebecca Hernan, Michele Disco
|Apr 09, 2023
Biallelic variants in TUBGCP6 result in microcephaly and chorioretinopathy 1: Report of four cases and a literature review.Amanda Thomas-Wilson, John P Schacht, David Chitayat
|Dec 23, 2022
Detection of mosaic variants using genome sequencing in a large pediatric cohort.Jacqueline A Odgis, Katie M Gallagher, Atteeq U Rehman
|Dec 19, 2018
SCAPER-associated nonsyndromic autosomal recessive retinitis pigmentosa.Ruben Jauregui, Amanda L Thomas, Benjamin Liechty
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Frequent Collaborators
1 joint publications
Stephen H Tsang
1 joint publications
Thomas Hays
1 joint publications
Rebecca Hernan
1 joint publications
Emily L Griffin
1 joint publications
Nimrod Goldshtrom
1 joint publications
Diana Vargas
1 joint publications
Volkan Okur
1 joint publications
Vaidehi Jobanputra
1 joint publications
Wendy K Chung
1 joint publications
Jacqueline A Odgis
