Narayanan Veeraraghavan

Also affiliated with Rady Children's Hospital-San Diego

Biochemistry, Genetics and Molecular BiologyImmunology and MicrobiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 9 papers. Top paper: “An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm”.

An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.10.003

N/A

0DataRank · unranked

191 citations

Michelle M. Clark, Mary Gaughran, Julie A. Cakici, Sara Caylor, Christina Clarke +62 more

Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskCLINICAL PERSPECTIVE

UNC Libraries(2020)10.17615/ttpw-sn86

N/A

0DataRank · unranked

0 citations

Alex P. Reiner, Donna M. Muzny, Shih‐Jen Hwang, Christopher Newton‐Cheh, Leslie J. Raffel +30 more

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

UNC Libraries(2020)10.17615/vn1s-8a35

N/A

0DataRank · unranked

0 citations

Frank J.A. van Rooij, Raha Pazoki, Albert Hofman, Nathan Pankratz, Richard A. Gibbs +51 more

Newborn Sequencing in Genomic Medicine and Public Health

UNC Libraries(2020)10.17615/p3y4-3s09

N/A

0DataRank · unranked

0 citations

Stacey Pereira, Sean D. Mooney, Anastasia L. Wise, Jennifer M. Puck, Timothy W. Yu +37 more

Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

npj Genomic Medicine(2021)10.1038/s41525-021-00192-x

N/A

0DataRank · unranked

76 citations

Shareef Nahas, Shimul Chowdhury, Serge Batalov, Michelle M. Clark, Sara Caylor +8 more

Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

npj Genomic Medicine(2021)10.1038/s41525-021-00206-8

N/A

0DataRank · unranked

6 citations

Shareef Nahas, Shimul Chowdhury, Serge Batalov, Michelle M. Clark, Sara Caylor +8 more

Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

npj Genomic Medicine(2021)10.1038/s41525-021-00205-9

N/A

0DataRank · unranked

5 citations

Shareef Nahas, Shimul Chowdhury, Serge Batalov, Michelle M. Clark, Sara Caylor +8 more

A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.003

N/A

0DataRank · unranked

171 citations

Laurie D. Smith, Chris M. Kunard, Matthew Bainbridge, Sergey Batalov, Wendy Benson +46 more

Response to Grosse et al.

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.05.004

N/A

0DataRank · unranked

1 citations

Laurie D. Smith, Chris M. Kunard, Matthew Bainbridge, Serge Batalov, Wendy Benson +46 more