Narayanan Veeraraghavan
5PUBLICATIONS
34CO-AUTHORS
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Publications (5)
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|Feb 14, 2023
Scalable, high quality, whole genome sequencing from archived, newborn, dried blood spots.Yan Ding, Mallory Owen, Jennie Le
|May 27, 2021
Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury
|May 27, 2021
Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury
|Apr 23, 2021
Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury
|Apr 26, 2019
Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation.Michelle M Clark, Amber Hildreth, Sergey Batalov
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Frequent Collaborators
5 joint publications
Sergey Batalov
4 joint publications
Michelle M Clark
4 joint publications
Stephen F Kingsmore
4 joint publications
David Dimmock
3 joint publications
Julie Cakici
3 joint publications
Nathaly M Sweeney
1 joint publications
Amber Hildreth
1 joint publications
Kelly Watkins
1 joint publications
Katarzyna Ellsworth
1 joint publications
Margaret Bray
