Articles with public access mandates - Peter WhiteLearn more
Not available anywhere: 4
Analysis of chromosomal structural variation in patients with congenital left‐sided cardiac lesions
PS White, HM Xie, P Werner, J Glessner, B Latney, H Hakonarson, ...
Birth Defects Research Part A: Clinical and Molecular Teratology 100 (12 …, 2014
Mandates: US National Institutes of Health
Sharpening up your spectra: broadband homonuclear decoupling in HSQC by real-time pure shift acquisition
P Kiraly, GA Morris, L Quanxiu, M Nilsson
Synlett 30 (09), 1015-1025, 2019
Mandates: UK Engineering and Physical Sciences Research Council
Long‐read whole genome sequencing reveals HOXD13 alterations in synpolydactyly
M Melas, EA Kautto, SJ Franklin, M Mori, KL McBride, TM Mosher, ...
Human Mutation 43 (2), 189-199, 2022
Mandates: US National Institutes of Health
A Novel In Vitro Human Model Of Sarcoidosis
ED Crouser, E Guirado, MW Julian, W Sadee, A Papp, A Friedman, ...
C101. SARCOIDOSIS, A6189-A6189, 2016
Mandates: US National Institutes of Health
Available somewhere: 73
Comprehensive molecular characterization of human colon and rectal cancer
Cancer Genome Atlas Network
Nature 487 (7407), 330, 2012
Mandates: US National Institutes of Health
Integrated genomic characterization of endometrial carcinoma
DA Levine, ...
Nature 497 (7447), 67-73, 2013
Mandates: US National Institutes of Health
Genomic classification of cutaneous melanoma
R Akbani, KC Akdemir, B áArman Aksoy, M Albert, A Ally, SB Amin, ...
Cell 161 (7), 1681-1696, 2015
Mandates: US National Institutes of Health, Cancer Research UK
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
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
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
Mandates: US National Institutes of Health
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
Mandates: US National Institutes of Health
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
Mandates: US National Institutes of Health
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
Mandates: US National Institutes of Health
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
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
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
Mandates: US National Institutes of Health
Rare structural variation of synapse and neurotransmission genes in autism
X Gai, HM Xie, JC Perin, N Takahashi, K Murphy, AS Wenocur, M D'arcy, ...
Molecular psychiatry 17 (4), 402-411, 2012
Mandates: US National Institutes of Health
The congenital heart disease genetic network study: rationale, design, and early results
Pediatric Cardiac Genomics Consortium, Writing Committee:, B Gelb, ...
Circulation research 112 (4), 698-706, 2013
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Male-biased autosomal effect of 16p13. 11 copy number variation in neurodevelopmental disorders
M Tropeano, JW Ahn, RJB Dobson, G Breen, J Rucker, A Dixit, DK Pal, ...
PloS one 8 (4), e61365, 2013
Mandates: Wellcome Trust
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
CA Brownstein, AH Beggs, N Homer, B Merriman, TW Yu, KC Flannery, ...
Genome biology 15, 1-18, 2014
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies
E Goldmuntz, P Paluru, J Glessner, H Hakonarson, JA Biegel, PS White, ...
Congenital heart disease 6 (6), 592-602, 2011
Mandates: US National Institutes of Health
An interactive online dashboard for tracking COVID-19 in US counties, cities, and states in real time
BD Wissel, PJ Van Camp, M Kouril, C Weis, TA Glauser, PS White, ...
Journal of the American Medical Informatics Association 27 (7), 1121-1125, 2020
Mandates: US National Institutes of Health
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