Author details

Full Name

Dexter Hadley

Affiliation

ORCID

Career Start Year

1994

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37539132	Characterization of monoclonal gammopathy of undetermined significance progression to multiple myeloma through meta-analysis of GEO data.		2023
34697751	Empowering study of breast cancer data with application of artificial intelligence technology: promises, challenges, and use cases.	Clinical and Experimental Metastasis	2022
35585177	Prediction of future healthcare expenses of patients from chest radiographs using deep learning: a pilot study.	Sci Rep	2022
36158924	Transcriptome changes in stages of non-alcoholic fatty liver disease.	World Journal of Hepatology	2022
36268056	Probing predilection to Crohn's disease and Crohn's disease flares: A crowd-sourced bioinformatics approach.	Journal of Pathology Informatics	2022
35612107	An Ontology for Cardiothoracic Surgical Education and Clinical Data Analytics.	Stud Health Technol Inform	2022
36505372	Gender-based time discrepancy in diagnosis of coronary artery disease based on data analytics of electronic medical records.		2022
34837585	Opal: an implementation science tool for machine learning clinical decision support in anesthesia.	J Clin Monit Comput	2022
34648530	Meta-Analysis illustrates possible role of lipopolysaccharide (LPS)-induced tissue injury in nasopharyngeal carcinoma (NPC) pathogenesis.	PLoS ONE	2021
33492921	Meta-Analysis Reveals the Prognostic Relevance of Nuclear and Membrane-Associated Bile Acid Receptors in Gastric Cancer.	Clinical and Translational Gastroenterology	2021
33262303	Metaanalysis Reveals Genetic Correlates of Osteoporosis Pathogenesis.	Journal of Rheumatology	2021
34381057	A merged microarray meta-dataset for transcriptionally profiling colorectal neoplasm formation and progression.	Scientific data	2021
34604507	Machine Learning Prediction of Liver Allograft Utilization From Deceased Organ Donors Using the National Donor Management Goals Registry.	Transplant Direct	2021
33015383	Investigating genetic drivers of dermatomyositis pathogenesis using meta-analysis.	Heliyon	2020
35949665	From cirrhosis to hepatocellular carcinoma: An investigation into hepatitis C viral oncogenesis.		2020
31937769	Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.	Nat Commun	2020
30465142	Automatic Labeling of Special Diagnostic Mammography Views from Images and DICOM Headers.	J Digit Imaging	2019
31615985	Tracing diagnosis trajectories over millions of patients reveal an unexpected risk in schizophrenia.	Sci Data	2019
30398430	A Deep Learning Model to Predict a Diagnosis of Alzheimer Disease by Using [18]F-FDG PET of the Brain.	Radiology	2019
30128778	Large Scale Semi-Automated Labeling of Routine Free-Text Clinical Records for Deep Learning.	J Digit Imaging	2019
29317701	A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth.	Sci Rep	2018
30646095	Development and Validation of an Electronic Health Record-Based Machine Learning Model to Estimate Delirium Risk in Newly Hospitalized Patients Without Known Cognitive Impairment.	JAMA network open	2018
29351777	Are minor alleles more likely to be risk alleles?	BMC Med Genomics	2018
29366600	Translational Radiomics: Defining the Strategy Pipeline and Considerations for Application-Part 1: From Methodology to Clinical Implementation.	Journal of the American College of Radiology	2018
29366598	Translational Radiomics: Defining the Strategy Pipeline and Considerations for Application-Part 2: From Clinical Implementation to Enterprise.	Journal of the American College of Radiology	2018
29191242	Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders.	Genome Med	2017
28815132	Precision Diagnosis Of Melanoma And Other Skin Lesions From Digital Images.		2017
28936969	Systematic integration of biomedical knowledge prioritizes drugs for repurposing.	Elife	2017
28362817	Cis-eQTL-based trans-ethnic meta-analysis reveals novel genes associated with breast cancer risk.	PLoS Genet	2017
28925997	Precision annotation of digital samples in NCBI's gene expression omnibus.	Sci Data	2017
28832883	Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum Disorders.	JAMA Psychiatry	2017
27860440	Integrating Clinical Phenotype and Gene Expression Data to Prioritize Novel Drug Uses.	CPT Pharmacometrics Syst Pharmacol	2016
26879370	Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos Syndrome variant.	BMC Musculoskelet Disord	2016
26535158	Relating Chemical Structure to Cellular Response: An Integrative Analysis of Gene Expression, Bioactivity, and Structural Data Across 11,000 Compounds.	CPT Pharmacometrics Syst Pharmacol	2015
25533614	Improved serotype-specific dengue virus detection in Trinidad and Tobago using a multiplex, real-time RT-PCR.	Diagnostic Microbiology and Infectious Disease	2015
26043652	Relating hepatocellular carcinoma tumor samples and cell lines using gene expression data in translational research.	BMC Med Genomics	2015
24927284	The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism.	Nat Commun	2014
24467814	Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.	Mol Autism	2014
23341896	Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.	PLoS One	2013
24166486	GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus.	Sci Rep	2013
21878851	Association between high-risk disease loci and response to anti-vascular endothelial growth factor treatment for wet age-related macular degeneration.	Retina	2012
23159250	Copy-number disorders are a common cause of congenital kidney malformations.	Am J Hum Genet	2012
22138692	Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.	Nat Genet	2011
19933195	Analysis of six genetic risk factors highly associated with AMD in the region surrounding ARMS2 and HTRA1 on chromosome 10, region q26.	Invest Ophthalmol Vis Sci	2010
20385819	Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.	Proc Natl Acad Sci U S A	2010
19557195	Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.	PLoS Genet	2009
17921354	PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.	Genome Res	2007
17096848	Patterns of sequence conservation in presynaptic neural genes.	Genome Biol	2006
8731455	Analysis of chromosome 18 DNA markers in multiplex pedigrees with manic depression.	Biol Psychiatry	1996
7615302	Manic-depression and the norepinephrine transporter gene.	Hum Hered	1995