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
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
13562015
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
6452013
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
5242010
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
4581989
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
3922009
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
3242012
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
3011997
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
2901995
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
2832000
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
2681999
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
2622004
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
2102010
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
2011992
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
1932008
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
1881992
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
1872005
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
1871995
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
1852000
Chromosome 1
PS White
eLS, 1973
184*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
1802003
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