Author details

Full Name

Joseph M Devaney

Affiliation

ORCID

Career Start Year

1994

Papers

111

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
33846581	Interference of nuclear mitochondrial DNA segments in mitochondrial DNA testing resembles biparental transmission of mitochondrial DNA in humans.	Genet Med	2021
32562017	Correction to: Comparative multidimensional molecular analyses of pediatric diffuse intrinsic pontine glioma reveals distinct molecular subtypes.	Acta Neuropathol	2020
30711709	Interactive effect of 5-HTTLPR and BDNF polymorphisms on amygdala intrinsic functional connectivity and anxiety.	Psychiatry Res Neuroimaging	2019
30556326	PAC1R Genotype to Phenotype Correlations in Autism Spectrum Disorder.	Autism Research	2019
30124928	TNF-Î± Stress Response Is Reduced Following Load Carriage Training.	Military Medicine	2019
29624921	A genetic variant in IL-15RÎ± correlates with physical activity among European-American adults.	Molecular genetics & genomic medicine	2018
28177749	Genetic characterization of physical activity behaviours in university students enrolled in kinesiology degree programs.	Appl Physiol Nutr Metab	2017
28944236	The angiotensin-converting enzyme insertion/deletion polymorphism rs4340 associates with habitual physical activity among European American adults.	Molecular genetics & genomic medicine	2017
27797444	Hereditary fructose intolerance mimicking a biochemical phenotype of mucolipidosis: A review of the literature of secondary causes of lysosomal enzyme activity elevation in serum.	American Journal of Medical Genetics, Part A	2017
28027286	Relationship of the Middle Ear Effusion Microbiome to Secretory Mucin Production in Pediatric Patients With Chronic Otitis Media.	Pediatric Infectious Disease Journal	2017
27159321	Whole exome sequencing in patients with white matter abnormalities.	Ann Neurol	2016
27078692	Proteomic Characterization of Middle Ear Fluid Confirms Neutrophil Extracellular Traps as a Predominant Innate Immune Response in Chronic Otitis Media.	PLoS ONE	2016
26821164	Glucocorticoid Receptor (NR3C1) Variants Associate with the Muscle Strength and Size Response to Resistance Training.	PLoS ONE	2016
25250560	Identification of novel mutations by exome sequencing in African American colorectal cancer patients.	Cancer	2015
25864488	Genome-wide differentially methylated genes in prostate cancer tissues from African-American and Caucasian men.	Epigenetics	2015
25682967	Circulating and urinary microRNA profile in focal segmental glomerulosclerosis: a pilot study.	Eur J Clin Invest	2015
26264609	A clinicopathologic study of diencephalic pediatric low-grade gliomas with BRAF V600 mutation.	Acta Neuropathol	2015
26495240	Obesity-Related Genetic Variants and their Associations with Physical Activity.	Sports Med Open	2015
26107372	The ACTN3 R577X Polymorphism Is Associated with Cardiometabolic Fitness in Healthy Young Adults.	PLoS One	2015
26327553	CK-MM Polymorphism is Associated With Physical Fitness Test Scores in Military Recruits.	Military Medicine	2015
26670709	Are Immune Modulating Single Nucleotide Polymorphisms Associated with Necrotizing Enterocolitis?	Sci Rep	2015
26526994	Age-Associated Methylation Suppresses SPRY1, Leading to a Failure of Re-quiescence and Loss of the Reserve Stem Cell Pool in Elderly Muscle.	Cell Reports	2015
23968837	Resting-state striato-frontal functional connectivity is sensitive to DAT1 genotype and predicts executive function.	Cerebral Cortex	2015
25138607	Multi-omic integrated networks connect DNA methylation and miRNA with skeletal muscle plasticity to chronic exercise in Type 2 diabetic obesity.	Physiological Genomics	2014
24297113	Comparative multidimensional molecular analyses of pediatric diffuse intrinsic pontine glioma reveals distinct molecular subtypes.	Acta Neuropathol	2014
24101675	SLC30A8 nonsynonymous variant is associated with recovery following exercise and skeletal muscle size and strength.		2014
24757210	Response to Comment on Sprouse et al. SLC30A8 nonsynonymous variant is associated with recovery following exercise and skeletal muscle size and strength. Diabetes 2014;63:363-368.		2014
25143582	Single-molecule long-read 16S sequencing to characterize the lung microbiome from mechanically ventilated patients with suspected pneumonia.	J Clin Microbiol	2014
24516231	DNA methylation profile associated with rapid decline in kidney function: findings from the CRIC study.	Nephrol Dial Transplant	2014
24598548	Genomics in premature infants: a non-invasive strategy to obtain high-quality DNA.	Sci Rep	2014
23582646	A de novo mutation in the Î²-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum.	Am J Hum Genet	2013
22275169	Rationality and emotionality: serotonin transporter genotype influences reasoning bias.	Social Cognitive and Affective Neuroscience	2013
24455711	Highlights from the functional single nucleotide polymorphisms associated with human muscle size and strength or FAMuSS study.	BioMed Research International	2013
23896626	Identification of novel DNA-methylated genes that correlate with human prostate cancer and high-grade prostatic intraepithelial neoplasia.	Prostate Cancer and Prostatic Diseases	2013
23895809	Racial disparity with on-treatment platelet reactivity in patients undergoing percutaneous coronary intervention.	American Heart Journal	2013
23847500	Individual differences in emotion-cognition interactions: emotional valence interacts with serotonin transporter genotype to influence brain systems involved in emotional reactivity and cognitive control.	Frontiers in Human Neuroscience	2013
23967293	An exploration of heat tolerance in mice utilizing mRNA and microRNA expression analysis.	PLoS ONE	2013
24011578	Epigenetics of progression of chronic kidney disease: fact or fantasy?	Seminars in Nephrology	2013
23274598	Alterations in osteopontin modify muscle size in females in both humans and mice.	Medicine and Science in Sports and Exercise	2013
22047966	Effect of dopamine transporter genotype on intrinsic functional connectivity depends on cognitive state.	Cerebral Cortex	2012
22580979	Variants of the ankyrin repeat domain 6 gene (ANKRD6) and muscle and physical activity phenotypes among European-derived American adults.	Journal of Strength and Conditioning Research	2012
22421340	The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis.	Lancet	2012
22613962	Genetic influences on vitamin D status and forearm fracture risk in African American children.	J Investig Med	2012
22607825	Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study.	Lancet	2012
22975643	Leptin and leptin receptor genetic variants associate with habitual physical activity and the arm body composition response to resistance training.	Gene	2012
23122333	Polymorphisms in dipeptidyl peptidase IV gene are associated with the risk of myocardial infarction in patients with atherosclerosis.	Neuropeptides	2012
23024164	Association between albuminuria, kidney function, and inflammatory biomarker profile in CKD in CRIC.	Clin J Am Soc Nephrol	2012
21606135	A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.	Circ Cardiovasc Genet	2011
22303337	Pathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation.	Front Genet	2011
21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Nat Genet	2011