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Author Details
Full Name
Jonathan D Mosley
Affiliation
Vanderbilt University Medical Center
ORCID
Career Start Year
1995
Papers
104
H Index
27
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35895516
White blood cell ranges and frequency of neutropenia by Duffy genotype status.
Blood Adv
2023
37961155
Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves cross-ancestry prediction.
medRxiv
2023
37662324
Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count genetics.
medRxiv
2023
37522172
Genetics of Pulmonary Pressure and Right Ventricle Stress Identify Diabetes as a Causal Risk Factor.
J Am Heart Assoc
2023
37930895
Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomics.
Bioinformatics
2023
37536150
Polygenic risk score in comparison with C-reactive protein for predicting incident coronary heart disease.
Atherosclerosis
2023
37353859
Variant-based heritability assessment of dexmedetomidine and fentanyl clearance in pediatric patients.
Clin Transl Sci
2023
37219552
Coronary Artery Calcium Score and Polygenic Risk Score for the Prediction of Coronary Heart Disease Events.
JAMA
2023
37041293
Genetic susceptibility for autoimmune diseases and white blood cell count.
Sci Rep
2023
37105192
<i>APOL1</i> and the risk of adverse renal outcomes in patients of African ancestry with systemic lupus erythematosus.
Lupus
2023
37205487
Transcriptome-Wide Association Analysis Identifies Novel Candidate Susceptibility Genes for Prostate-Specific Antigen Levels in Men Without Prostate Cancer.
medRxiv
2023
37264206
Genetically adjusted PSA levels for prostate cancer screening.
Nat Med
2023
36877498
A Polygenic Risk Score for Prostate Cancer Risk Prediction.
JAMA Intern Med
2023
36524479
Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization.
Circulation
2023
34625956
Identifying Potential Therapeutic Applications and Diagnostic Harms of Increased Bilirubin Concentrations: A Clinical and Genetic Approach.
Clin Pharmacol Ther
2022
35384379
Obesity influences composition of salivary and fecal microbiota and impacts the interactions between bacterial taxa.
Physiol Rep
2022
35377938
ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia.
Blood
2022
35642720
Frequency of benign neutropenia among Black versus White individuals undergoing a bone marrow assessment.
J Cell Mol Med
2022
35724382
Race, Genotype, and Azathioprine Discontinuation : A Cohort Study.
Ann Intern Med
2022
35751511
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.
Eur Heart J
2022
35749358
Microbiome-associated human genetic variants impact phenome-wide disease risk.
Proc Natl Acad Sci U S A
2022
35656995
Genetic Determinants of Body Mass Index and Fasting Glucose Are Mediators of Grade 1 Diastolic Dysfunction.
J Am Heart Assoc
2022
35621206
Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol.
J Am Heart Assoc
2022
36315951
Web Exclusive. Annals On Call - Understanding Benign Neutropenia.
Ann Intern Med
2022
36271344
Limited clinical utility for GWAS or polygenic risk score for postoperative acute kidney injury in non-cardiac surgery in European-ancestry patients.
BMC Nephrol
2022
36378922
Leveraging Genetics to Dissect a Triglyceride-Blood Pressure Association.
Hypertension
2022
36376015
Ancestry, <i>ACKR1</i> and leucopenia in patients with systemic lupus erythematosus.
Lupus Sci Med
2022
34930020
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.
Circulation
2022
32712226
BMI Is Causally Associated With Pulmonary Artery Pressure But Not Hemodynamic Evidence of Pulmonary Vascular Remodeling.
Chest
2021
33647223
Predictive Accuracy of a Polygenic Risk Score for Postoperative Atrial Fibrillation After Cardiac Surgery.
Circ Genom Precis Med
2021
33591955
Proteomic profiling reveals biomarkers and pathways in type 2 diabetes risk.
JCI Insight
2021
33895829
Genetic Thyrotropin Regulation of Atrial Fibrillation Risk Is Mediated Through an Effect on Height.
J Clin Endocrinol Metab
2021
34521746
Using genetics to detangle the relationships between red cell distribution width and cardiovascular diseases: a unique role for body mass index.
Open Heart
2021
34463132
Polygenic Risk Score to Identify Subclinical Coronary Heart Disease Risk in Young Adults.
Circ Genom Precis Med
2021
34545125
Heart failure clinical care analysis uncovers risk reduction opportunities for preserved ejection fraction subtype.
Sci Rep
2021
34180972
Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.
JAMA Intern Med
2021
34151428
Genome-Wide Approach to Measure Variant-Based Heritability of Drug Outcome Phenotypes.
Clin Pharmacol Ther
2021
34097045
A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease Phenotypes.
JAMA Netw Open
2021
34341450
The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene.
Sci Rep
2021
34057579
A metabolome and microbiome wide association study of healthy eating index points to the mechanisms linking dietary pattern and metabolic status.
Eur J Nutr
2021
33977795
Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis.
Lupus
2021
34309407
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare <i>KCNH2</i> Variants.
Circ Genom Precis Med
2021
31796895
Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease.
Mol Psychiatry
2021
33420026
Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics.
Nat Commun
2021
33441150
Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease.
Genome Med
2021
32372017
The polygenic architecture of left ventricular mass mirrors the clinical epidemiology.
Sci Rep
2020
32068817
Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease.
JAMA
2020
32586526
Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome.
J Pediatr
2020
32307929
Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome-Wide Association Study and Inverse Variance-Weighted Meta-Analysis.
Arthritis Rheumatol
2020
30608875
Unbiased Phenome-Wide Association Studies of Red Cell Distribution Width Identifies Key Associations with Pulmonary Hypertension.
Ann Am Thorac Soc
2019
1 - 50 of 104
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John S Witte
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Eric Farber-Eger
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Nancy J Cox
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David R Crosslin
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Thomas J Wang
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