| 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 | 17712 | 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 | 1515 | 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 | 1385 | 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 | 508 | 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 | 406 | 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 | 307 | 2019 |
| 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 | 266 | 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 | 258 | 2014 |
| 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 | 249 | 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 | 247 | 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 | 207 | 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 | 172 | 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 | 160 | 2015 |
| 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 | 140 | 2020 |
| 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 | 137 | 2006 |
| 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 | 109 | 2022 |
| 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 | 97 | 2021 |
| 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 | 81 | 2008 |
| 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 | 69 | 2021 |
| 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 | 64 | 2016 |
Kerry O'DonnellResearch Microbiologist, NCAUR-ARS-USDAכתובת אימייל מאומתת בדומיין ars.usda.gov