| Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1 L Li, ID Krantz, YU Deng, A Genin, AB Banta, CC Collins, M Qi, BJ Trask, ... Nature genetics 16 (3), 243-251, 1997 | 1482 | 1997 |
| Mutations in the human Jagged1 gene are responsible for Alagille syndrome T Oda, AG Elkahloun, BL Pike, K Okajima, ID Krantz, A Genin, DA Piccoli, ... Nature genetics 16 (3), 235-242, 1997 | 1326 | 1997 |
| NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway R McDaniell, DM Warthen, PA Sanchez-Lara, A Pai, ID Krantz, DA Piccoli, ... The American Journal of Human Genetics 79 (1), 169-173, 2006 | 867 | 2006 |
| Features of Alagille syndrome in 92 patients: frequency and relation to prognosis KM Emerick, EB Rand, E Goldmuntz, ID Krantz, NB Spinner, DA Piccoli Hepatology 29 (3), 822-829, 1999 | 719 | 1999 |
| Common variants at five new loci associated with early-onset inflammatory bowel disease M Imielinski, RN Baldassano, A Griffiths, RK Russell, V Annese, ... Nature genetics 41 (12), 1335-1340, 2009 | 586 | 2009 |
| Diet in the pathogenesis and treatment of inflammatory bowel diseases D Lee, L Albenberg, C Compher, R Baldassano, D Piccoli, JD Lewis, ... Gastroenterology 148 (6), 1087-1106, 2015 | 485 | 2015 |
| Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease S Kugathasan, RN Baldassano, JP Bradfield, PMA Sleiman, M Imielinski, ... Nature genetics 40 (10), 1211-1215, 2008 | 423 | 2008 |
| Vascular anomalies in Alagille syndrome: a significant cause of morbidity and mortality BM Kamath, NB Spinner, KM Emerick, AE Chudley, C Booth, DA Piccoli, ... Circulation 109 (11), 1354-1358, 2004 | 390 | 2004 |
| Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease K Wang, H Zhang, S Kugathasan, V Annese, JP Bradfield, RK Russell, ... The American Journal of Human Genetics 84 (3), 399-405, 2009 | 363 | 2009 |
| Analysis of Cardiovascular Phenotype and Genotype-Phenotype Correlation in Individuals With a JAG1 Mutation and/or Alagille Syndrome DB McElhinney, ID Krantz, L Bason, DA Piccoli, KM Emerick, NB Spinner, ... Circulation 106 (20), 2567-2574, 2002 | 356 | 2002 |
| Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity LN Bull, VE Carlton, NL Stricker, S Baharloo, JA DeYoung, NB Freimer, ... Hepatology 26 (1), 155-164, 1997 | 312 | 1997 |
| Inflammatory bowel disease in pediatric and adolescent patients RN Baldassano, DA Piccoli Gastroenterology Clinics of North America 28 (2), 445-458, 1999 | 300 | 1999 |
| Detection of group C rotavirus in infants with extrahepatic biliary atresia M Riepenhoff-Talty, V Gouvea, MJ Evans, L Svensson, E Hoffenberg, ... Journal of Infectious Diseases 174 (1), 8-15, 1996 | 295 | 1996 |
| Inflammatory bowel disease in children 5 years of age and younger P Mamula, GW Telega, JE Markowitz, KA Brown, PA Russo, DA Piccoli, ... Official journal of the American College of Gastroenterology| ACG 97 (8 …, 2002 | 276 | 2002 |
| Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families ID Krantz, RP Colliton, A Genin, EB Rand, L Li, DA Piccoli, NB Spinner The American Journal of Human Genetics 62 (6), 1361-1369, 1998 | 264 | 1998 |
| Alagille syndrome. ID Krantz, DA Piccoli, NB Spinner Journal of medical genetics 34 (2), 152-157, 1997 | 258 | 1997 |
| NOTCH2 mutations in Alagille syndrome BM Kamath, RC Bauer, KM Loomes, G Chao, J Gerfen, A Hutchinson, ... Journal of medical genetics 49 (2), 138-144, 2012 | 254 | 2012 |
| Jagged1 (JAG1) mutations in Alagille syndrome: increasing the mutation detection rate DM Warthen, EC Moore, BM Kamath, JJD Morrissette, P Sanchez, ... Human mutation 27 (5), 436-443, 2006 | 235 | 2006 |
| Vitamin D status in children, adolescents, and young adults with Crohn disease TA Sentongo, EJ Semaeo, N Stettler, DA Piccoli, VA Stallings, BS Zemel The American journal of clinical nutrition 76 (5), 1077-1081, 2002 | 233 | 2002 |
| Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects K Wang, R Baldassano, H Zhang, HQ Qu, M Imielinski, S Kugathasan, ... Human molecular genetics 19 (10), 2059-2067, 2010 | 223 | 2010 |
Nancy SpinnerProfessor, The University of Pennsylvania and The Children's Hospital of PhiladelphiaEmail được xác minh tại chop.edu
