Peter White
Peter White
Chair and Riveschl Professor, Department of Biomedical Informatics, University of Cincinnati and Cincinnati Children's Hospital Medical Center
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Cited by
Cited by
Genomic classification of cutaneous melanoma
R Akbani, KC Akdemir, BA Aksoy, M Albert, A Ally, SB Amin, H Arachchi, ...
Cell 161 (7), 1681-1696, 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
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
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
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
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
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
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
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
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
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
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
Loss of heterozygosity for chromosomes 1 or 14 defines subsets of advanced neuroblastomas
C Fong, PS White, K Peterson, C Sapienza, WK Cavenee, SE Kern, ...
Cancer research 52 (7), 1780-1785, 1992
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
Neuroblastoma: effect of genetic factors on prognosis and treatment
GM Brodeur, C Azar, M Brother, J Hiemstra, B Kaufman, H Marshall, ...
Cancer 70 (S4), 1685-1694, 1992
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
Significance of chromosome 1p loss of heterozygosity in neuroblastoma
JM Maris, PS White, CP Beltinger, EP Sulman, RP Castleberry, JJ Shuster, ...
Cancer research 55 (20), 4664-4669, 1995
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
Chromosome 1
PS White
eLS, 1973
CHD5, a new member of the chromodomain gene family, is preferentially expressed in the nervous system
PM Thompson, T Gotoh, M Kok, PS White, GM Brodeur
Oncogene 22 (7), 1002-1011, 2003
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