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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
Подтвержден адрес электронной почты в домене cchmc.org
Название
Процитировано
Процитировано
Год
Integrated genomic characterization of endometrial carcinoma
DA Levine, ...
Nature 497 (7447), 67-73, 2013
45082013
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
25422015
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
9252013
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
7711999
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
6092010
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
4811989
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
4282009
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
4152012
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
3292000
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
3161995
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
3131997
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
3121999
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
2922010
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
2732004
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
2542014
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
2342004
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
2242008
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
2182005
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
2141992
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
2132003
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Статьи 1–20