| Prediction of complicated disease course for children newly diagnosed with Crohn's disease: a multicentre inception cohort study S Kugathasan, LA Denson, TD Walters, MO Kim, UM Marigorta, ... The Lancet 389 (10080), 1710-1718, 2017 | 585 | 2017 |
| Transcriptional risk scores link GWAS to eQTLs and predict complications in Crohn's disease. UM Marigorta, LA Denson, JS Hyams, K Mondal, J Prince, TD Walters, ... Nature genetics 49 (10), 1517, 2017 | 174 | 2017 |
| Blood-Derived DNA Methylation Signatures of Crohn's Disease and Severity of Intestinal Inflammation HK Somineni, S Venkateswaran, V Kilaru, UM Marigorta, A Mo, DT Okou, ... Gastroenterology 156 (8), 2254-2265. e3, 2019 | 115 | 2019 |
| NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease T Schwerd, RV Bryant, S Pandey, M Capitani, L Meran, JB Cazier, J Jung, ... Mucosal immunology 11 (2), 562-574, 2018 | 83 | 2018 |
| Design of temperature-sensitive mutants solely from amino acid sequence G Chakshusmathi, K Mondal, GS Lakshmi, G Singh, A Roy, RB Ch, ... Proceedings of the National Academy of Sciences 101 (21), 7925-7930, 2004 | 78 | 2004 |
| Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn’s Disease LA Denson, I Jurickova, R Karns, KA Shaw, DJ Cutler, DT Okou, A Dodd, ... Gastroenterology 154 (8), 2097-2110, 2018 | 74 | 2018 |
| Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel disease DT Okou, K Mondal, WA Faubion, LJ Kobrynski, LA Denson, JG Mulle, ... Journal of pediatric gastroenterology and nutrition 58 (5), 561, 2014 | 63 | 2014 |
| Dissecting allele architecture of early onset IBD using high-density genotyping DJ Cutler, ME Zwick, DT Okou, S Prahalad, T Walters, SL Guthery, ... PloS one 10 (6), e0128074, 2015 | 47 | 2015 |
| SeqAnt: a web service to rapidly identify and annotate DNA sequence variations AC Shetty, P Athri, K Mondal, VL Horner, KM Steinberg, V Patel, ... BMC bioinformatics 11 (1), 1-8, 2010 | 47 | 2010 |
| Excess Variants in AFF2 Detected by Massively Parallel Sequencing of Males with Autism Spectrum Disorder K Mondal, D Ramachandran, VC Patel, KR Hagen, P Bose, DJ Cutler, ... Human Molecular Genetics, 2012 | 44 | 2012 |
| Design and isolation of temperature-sensitive mutants of Gal4 in yeast and Drosophila K Mondal, AG Dastidar, G Singh, S Madhusudhanan, SL Gande, ... Journal of molecular biology 370 (5), 939-950, 2007 | 43 | 2007 |
| The effect of early-life environmental exposures on disease phenotype and clinical course of Crohn's disease in children L Lindoso, K Mondal, S Venkateswaran, HK Somineni, C Ballengee, ... American Journal of Gastroenterology 113 (10), 1524-1529, 2018 | 37 | 2018 |
| Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse M Sun, K Mondal, V Patel, VL Horner, AB Long, DJ Cutler, T Caspary, ... G3: Genes| Genomes| Genetics 2 (1), 143-150, 2012 | 28 | 2012 |
| Variation in Care in the Management of Children With Crohn’s Disease: Data From a Multicenter Inception Cohort Study C Krishnakumar, CR Ballengee, C Liu, MO Kim, SS Baker, ... Inflammatory bowel diseases 25 (7), 1208-1217, 2019 | 24 | 2019 |
| Targeted sequencing of the human X chromosome exome K Mondal, AC Shetty, V Patel, DJ Cutler, ME Zwick Genomics 98 (4), 260-265, 2011 | 23 | 2011 |
| Association between plasma level of collagen type III alpha 1 chain and development of strictures in pediatric patients with Crohn’s disease CR Ballengee, RW Stidham, C Liu, MO Kim, J Prince, K Mondal, ... Clinical Gastroenterology and Hepatology 17 (9), 1799-1806, 2019 | 21 | 2019 |
| Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder JK Bedoyan, VM Schaibley, W Peng, Y Bai, K Mondal, AC Shetty, ... Journal of Medical Genetics 49 (5), 332-340, 2012 | 20 | 2012 |
| Evolution of Pediatric Inflammatory Bowel Disease Unclassified (IBD-U): Incorporated With Serological and Gene Expression Profiles R Chandradevan, T Hofmekler, K Mondal, N Harun, S Venkateswaran, ... Inflammatory bowel diseases 24 (10), 2285-2290, 2018 | 19 | 2018 |
| Variant ATRX Syndrome with Dysfunction of ATRX and MAGT1 Genes Y Qiao, K Mondal, V Trapani, J Wen, G Carpenter, R Wildin, EM Price, ... Human mutation 35 (1), 58-62, 2014 | 15 | 2014 |
| Design and utility of temperature-sensitive Gal4 mutants for conditional gene expression in Drosophila K Mondal, K VijayRaghavan, R Varadarajan Fly 1 (5), 282-286, 2007 | 14 | 2007 |
kugathasan, sProfessor of Pediatrics and Human Genetics, Marcus Professor of Pediatric Gastroenterology在 emory.edu 的电子邮件经过验证
