Dexter Hadley
Dexter Hadley
Chief of AI, University of Central Florida, College of Medicine
Verified email at - Homepage
Cited by
Cited by
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
K Wang, M Li, D Hadley, R Liu, J Glessner, SFA Grant, H Hakonarson, ...
Genome research 17 (11), 1665-1674, 2007
A Deep Learning Model to Predict a Diagnosis of Alzheimer Disease by Using 18F-FDG PET of the Brain
Y Ding, JH Sohn, MG Kawczynski, H Trivedi, R Harnish, NW Jenkins, ...
Radiology 290 (2), 456-464, 2019
Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration
W Chen, D Stambolian, AO Edwards, KE Branham, M Othman, ...
Proceedings of the National Academy of Sciences 107 (16), 7401-7406, 2010
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
M Bucan, BS Abrahams, K Wang, JT Glessner, EI Herman, LI Sonnenblick, ...
PLoS genetics 5 (6), e1000536, 2009
Systematic integration of biomedical knowledge prioritizes drugs for repurposing
DS Himmelstein, A Lizee, C Hessler, L Brueggeman, SL Chen, D Hadley, ...
Elife 6, e26726, 2017
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
Copy-number disorders are a common cause of congenital kidney malformations. Source: American journal of human genetics (0002-9297) 91 (2012); 987-997
S Sanna-Cherchi, K Kiryluk, KE Burgess, M Bodria, MG Sampson, ...
American journal of human genetics 91 (2012), 987-997, 2012
Common variants at 6q22 and 17q21 are associated with intracranial volume
Nature genetics 44 (5), 539-544, 2012
Common variants at 12q15 and 12q24 are associated with infant head circumference
HR Taal, B St Pourcain, E Thiering, S Das, DO Mook-Kanamori, ...
Nature genetics 44 (5), 532-538, 2012
Development and validation of an electronic health record–based machine learning model to estimate delirium risk in newly hospitalized patients without known cognitive impairment
A Wong, AT Young, AS Liang, R Gonzales, VC Douglas, D Hadley
JAMA network open 1 (4), e181018-e181018, 2018
Relating hepatocellular carcinoma tumor samples and cell lines using gene expression data in translational research
B Chen, M Sirota, H Fan-Minogue, D Hadley, AJ Butte
BMC medical genomics 8, 1-10, 2015
The impact of COVID-19 on African American communities in the United States
E Cyrus, R Clarke, D Hadley, Z Bursac, MJ Trepka, JG Dévieux, U Bagci, ...
Health Equity 4 (1), 476-483, 2020
Association between high-risk disease loci and response to anti–vascular endothelial growth factor treatment for wet age-related macular degeneration
A Orlin, D Hadley, W Chang, AC Ho, G Brown, RS Kaiser, CD Regillo, ...
Retina 32 (1), 4-9, 2012
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population
N Matsunami, D Hadley, CH Hensel, GB Christensen, C Kim, E Frackelton, ...
PloS one 8 (1), e52239, 2013
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index
A Hinney, M Kesselmeier, S Jall, AL Volckmar, M Föcker, J Antel, IM Heid, ...
Molecular psychiatry 22 (2), 192-201, 2017
Are minor alleles more likely to be risk alleles?
T Kido, W Sikora-Wohlfeld, M Kawashima, S Kikuchi, N Kamatani, ...
BMC medical genomics 11, 1-11, 2018
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism
D Hadley, Z Wu, C Kao, A Kini, A Mohamed-Hadley, K Thomas, ...
Nature communications 5 (1), 4074, 2014
Association between mitochondrial DNA haplogroup variation and autism spectrum disorders
D Chalkia, LN Singh, J Leipzig, M Lvova, O Derbeneva, A Lakatos, ...
JAMA psychiatry 74 (11), 1161-1168, 2017
Cis-eQTL-based trans-ethnic meta-analysis reveals novel genes associated with breast cancer risk
JD Hoffman, RE Graff, NC Emami, CG Tai, MN Passarelli, D Hu, ...
PLoS genetics 13 (3), e1006690, 2017
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations
YR Li, JT Glessner, BP Coe, J Li, M Mohebnasab, X Chang, J Connolly, ...
Nature communications 11 (1), 255, 2020
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