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Narayanan Veeraraghavan
Narayanan Veeraraghavan
Rady Children's Hospital San Diego
Verified email at rchsd.org - Homepage
Title
Cited by
Cited by
Year
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
170482017
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
14632014
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
13492004
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
4862014
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
3692018
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
2752019
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
2462014
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
2452012
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
2442019
Newborn sequencing in genomic medicine and public health
JS Berg, PB Agrawal, DB Bailey, AH Beggs, SE Brenner, AM Brower, ...
Pediatrics 139 (2), 2017
2282017
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
1842018
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
1682007
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
1592015
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
1352006
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
1192020
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
822022
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
802008
Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases
FM De La Vega, S Chowdhury, B Moore, E Frise, J McCarthy, ...
Genome Medicine 13, 1-19, 2021
732021
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
632016
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
612021
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