Vaidehi Jobanputra
10PUBLICATIONS
71CO-AUTHORS
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Publications (10)
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|Feb 26, 2024
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders.Kristen M Wigby, Deanna Brockman, Gregory Costain
|Jul 07, 2023
Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease.Thomas Hays, Rebecca Hernan, Michele Disco
|Feb 21, 2023
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study.Emily L Griffin, Shannon N Nees, Sarah U Morton
|Dec 08, 2022
Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care.Edwin Cuppen, Olivier Elemento, Richard Rosenquist
|Oct 31, 2022
A novel biallelic loss-of-function variant in DAND5 causes heterotaxy syndrome.Mythily Ganapathi, Christie M Buchovecky, Fernando Cristo
|Apr 09, 2022
Best practices for the interpretation and reporting of clinical whole genome sequencing.Christina A Austin-Tse, Vaidehi Jobanputra, Denise L Perry
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Frequent Collaborators
4 joint publications
Stacie Taylor
3 joint publications
Wendy K Chung
3 joint publications
David Dimmock
3 joint publications
David Bick
3 joint publications
Emily L Griffin
2 joint publications
Christian R Marshall
2 joint publications
Elizabeth Goldmuntz
2 joint publications
Jane W Newburger
2 joint publications
Yufeng Shen
2 joint publications
John W Belmont
