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Peter White
Peter White
Chair and Riveschl Professor, Department of Biomedical Informatics, University of Cincinnati and Cincinnati Children's Hospital Medical Center
Verified email at cchmc.org
Title
Cited by
Cited by
Year
Comprehensive molecular characterization of human colon and rectal cancer
Cancer Genome Atlas Network
Nature 487 (7407), 330, 2012
75312012
Integrated genomic characterization of endometrial carcinoma
DA Levine, ...
Nature 497 (7447), 67-73, 2013
49372013
Genomic classification of cutaneous melanoma
R Akbani, KC Akdemir, B áArman Aksoy, M Albert, A Ally, SB Amin, ...
Cell 161 (7), 1681-1696, 2015
27172015
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
9512013
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
7901999
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
6242010
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
4921989
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
4342009
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
4222012
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
3402000
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
3221999
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
3211997
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
3181995
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
3032010
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
2772014
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
2722004
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
2372004
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
2292008
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
2232005
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
2152000
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