| Comprehensive molecular characterization of human colon and rectal cancer Cancer Genome Atlas Network Nature 487 (7407), 330, 2012 | 7524 | 2012 |
| Integrated genomic characterization of endometrial carcinoma DA Levine, ... Nature 497 (7447), 67-73, 2013 | 4934 | 2013 |
| Genomic classification of cutaneous melanoma R Akbani, KC Akdemir, B áArman Aksoy, M Albert, A Ally, SB Amin, ... Cell 161 (7), 1681-1696, 2015 | 2715 | 2015 |
| De novo mutations in histone-modifying genes in congenital heart disease S Zaidi, M Choi, H Wakimoto, L Ma, J Jiang, JD Overton, ... Nature 498 (7453), 220-223, 2013 | 951 | 2013 |
| Prospective, randomized, controlled clinical trial comparing traditional versus reduced tidal volume ventilation in acute respiratory distress syndrome patients RG Brower, CB Shanholtz, HE Fessler, DM Shade, P White, CM Wiener, ... Critical care medicine 27 (8), 1492-1498, 1999 | 790 | 1999 |
| Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes J Elia, X Gai, HM Xie, JC Perin, E Geiger, JT Glessner, M D'arcy, ... Molecular psychiatry 15 (6), 637-646, 2010 | 623 | 2010 |
| Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification. C Fong, NC Dracopoli, PS White, PT Merrill, RC Griffith, DE Housman, ... Proceedings of the National Academy of Sciences 86 (10), 3753-3757, 1989 | 492 | 1989 |
| High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications TH Shaikh, X Gai, JC Perin, JT Glessner, H Xie, K Murphy, R O'Hara, ... Genome research 19 (9), 1682-1690, 2009 | 434 | 2009 |
| Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder J Elia, JT Glessner, K Wang, N Takahashi, CJ Shtir, D Hadley, ... Nature genetics 44 (1), 78-84, 2012 | 421 | 2012 |
| Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia) S Nicole, CS Davoine, H Topaloglu, L Cattolico, D Barral, P Beighton, ... Nature genetics 26 (4), 480-483, 2000 | 340 | 2000 |
| Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas C Guo, PS White, MJ Weiss, MD Hogarty, PM Thompson, DO Stram, ... Oncogene 18 (35), 4948-4957, 1999 | 322 | 1999 |
| Biology and genetics of human neuroblastomas GM Brodeur, JM Maris, DJ Yamashiro, MD Hogarty, PS White Journal of pediatric hematology/oncology 19 (2), 93-101, 1997 | 321 | 1997 |
| A region of consistent deletion in neuroblastoma maps within human chromosome 1p36. 2-36.3. PS White, JM Maris, C Beltinger, E Sulman, HN Marshall, M Fujimori, ... Proceedings of the National Academy of Sciences 92 (12), 5520-5524, 1995 | 318 | 1995 |
| Pancreatic β cells require NeuroD to achieve and maintain functional maturity C Gu, GH Stein, N Pan, S Goebbels, H Hörnberg, KA Nave, P Herrera, ... Cell metabolism 11 (4), 298-310, 2010 | 303 | 2010 |
| Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data JT Glessner, AG Bick, K Ito, JG Homsy, L Rodriguez-Murillo, M Fromer, ... Circulation research 115 (10), 884-896, 2014 | 277 | 2014 |
| A combined linkage-physical map of the human genome X Kong, K Murphy, T Raj, C He, PS White, TC Matise The American Journal of Human Genetics 75 (6), 1143-1148, 2004 | 272 | 2004 |
| Integrated annotation for biomedical information extraction S Kulick, A Bies, M Liberman, M Mandel, R McDonald, M Palmer, ... HLT-NAACL 2004 workshop: linking biological literature, ontologies and …, 2004 | 237 | 2004 |
| CHD5 , a Tumor Suppressor Gene Deleted From 1p36.31 in Neuroblastomas T Fujita, J Igarashi, ER Okawa, T Gotoh, J Manne, V Kolla, J Kim, H Zhao, ... JNCI: Journal of the National Cancer Institute 100 (13), 940-949, 2008 | 229 | 2008 |
| Definition and characterization of a region of 1p36. 3 consistently deleted in neuroblastoma PS White, PM Thompson, T Gotoh, ER Okawa, J Igarashi, M Kok, C Winter, ... Oncogene 24 (16), 2684-2694, 2005 | 223 | 2005 |
| Loss of heterozygosity at 1p36 independently predicts for disease progression but not decreased overall survival probability in neuroblastoma patients: a Children’s Cancer … JM Maris, MJ Weiss, C Guo, RB Gerbing, DO Stram, PS White, ... Journal of clinical oncology 18 (9), 1888-1899, 2000 | 215 | 2000 |
