Narayanan Veeraraghavan
Narayanan Veeraraghavan
Rady Children's Hospital San Diego
Verified email at - Homepage
Cited by
Cited by
Heart disease and stroke statistics—2017 update: a report from the American Heart Association
EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, ...
circulation 135 (10), e146-e603, 2017
Molecular findings among patients referred for clinical whole-exome sequencing
Y Yang, DM Muzny, F Xia, Z Niu, R Person, Y Ding, P Ward, A Braxton, ...
Jama 312 (18), 1870-1879, 2014
FUSARIUM-ID v. 1.0: A DNA Sequence Database for Identifying Fusarium
DM Geiser, M del Mar Jiménez-Gasco, S Kang, I Makalowska, ...
European journal of plant pathology 110, 473-479, 2004
A cloud-compatible bioinformatics pipeline for ultrarapid pathogen identification from next-generation sequencing of clinical samples
SN Naccache, S Federman, N Veeraraghavan, M Zaharia, D Lee, ...
Genome Research, 2014
Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization
L Farnaes, A Hildreth, NM Sweeney, MM Clark, S Chowdhury, S Nahas, ...
NPJ genomic medicine 3 (1), 10, 2018
A randomized, controlled trial of the analytic and diagnostic performance of singleton and trio, rapid genome and exome sequencing in ill infants
SF Kingsmore, JA Cakici, MM Clark, M Gaughran, M Feddock, S Batalov, ...
The American Journal of Human Genetics 105 (4), 719-733, 2019
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline
JG Reid, A Carroll, N Veeraraghavan, M Dahdouli, A Sundquist, A English, ...
BMC bioinformatics 15, 1-11, 2014
Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation
MM Clark, A Hildreth, S Batalov, Y Ding, S Chowdhury, K Watkins, ...
Science translational medicine 11 (489), eaat6177, 2019
A novel rhabdovirus associated with acute hemorrhagic fever in central Africa
G Grard, JN Fair, D Lee, E Slikas, I Steffen, JJ Muyembe, T Sittler, ...
PLoS Pathogens 8 (9), 2012
Newborn sequencing in genomic medicine and public health
JS Berg, PB Agrawal, DB Bailey, AH Beggs, SE Brenner, AM Brower, ...
Pediatrics 139 (2), 2017
The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants
JE Petrikin, JA Cakici, MM Clark, LK Willig, NM Sweeney, EG Farrow, ...
NPJ Genomic Medicine 3 (1), 6, 2018
A framework for collaborative analysis of ENCODE data: making large-scale analyses biologist-friendly
D Blankenberg, J Taylor, I Schenck, J He, Y Zhang, M Ghent, ...
Genome research 17 (6), 960-964, 2007
Assessing structural variation in a personal genome—towards a human reference diploid genome
AC English, WJ Salerno, OA Hampton, C Gonzaga-Jauregui, S Ambreth, ...
BMC genomics 16, 1-15, 2015
ChloroplastDB: the chloroplast genome database
L Cui, N Veeraraghavan, A Richter, K Wall, RK Jansen, J Leebens-Mack, ...
Nucleic acids research 34 (suppl_1), D692-D696, 2006
An RCT of rapid genomic sequencing among seriously ill infants results in high clinical utility, changes in management, and low perceived harm
DP Dimmock, MM Clark, M Gaughran, JA Cakici, SA Caylor, C Clarke, ...
The American Journal of Human Genetics 107 (5), 942-952, 2020
Phytophthora database: a forensic database supporting the identification and monitoring of Phytophthora
J Park, B Park, N Veeraraghavan, K Jung, YH Lee, JE Blair, DM Geiser, ...
Plant disease 92 (6), 966-972, 2008
A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases
SF Kingsmore, LD Smith, CM Kunard, M Bainbridge, S Batalov, W Benson, ...
The American Journal of Human Genetics 109 (9), 1605-1619, 2022
Whole-exome sequencing identifies loci associated with blood cell traits and reveals a role for alternative GFI1B splice variants in human hematopoiesis
LM Polfus, RK Khajuria, UM Schick, N Pankratz, R Pazoki, JA Brody, ...
The American Journal of Human Genetics 99 (2), 481-488, 2016
Rapid sequencing-based diagnosis of thiamine metabolism dysfunction syndrome
MJ Owen, AK Niemi, DP Dimmock, M Speziale, M Nespeca, KK Chau, ...
New England Journal of Medicine 384 (22), 2159-2161, 2021
Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease
AH Li, AC Morrison, C Kovar, LA Cupples, JA Brody, LM Polfus, B Yu, ...
Nature genetics 47 (6), 640-642, 2015
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