Author details

Full Name

Braxton D Mitchell

Affiliation

ORCID

Career Start Year

1986

Papers

511

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37495379	Neglected Mendelian causes of stroke in adult Chinese patients who had an ischaemic stroke or transient ischaemic attack.	Stroke Vasc Neurol	2024
37846209	Causal Factors for Osteoarthritis: A Scoping Review of Mendelian Randomization Studies.	Arthritis Care Res (Hoboken)	2024
37916415	Polygenic Risk Score Associates With Atherosclerotic Plaque Characteristics at Autopsy.	Arterioscler Thromb Vasc Biol	2024
37425772	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.	medRxiv	2023
35698853	Frontal white matter association with sleep quality and the role of stress.	Journal of Sleep Research	2023
36401354	Evaluating the causal effect of tobacco smoking on white matter brain aging: a two-sample Mendelian randomization analysis in UK Biobank.	Addiction	2023
36444934	Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.	Hum Mol Genet	2023
37608471	Pharmacogenetics of sodium-glucose co-transporter-2 inhibitors: Validation of a sex-agnostic pharmacodynamic biomarker.	Diabetes Obes Metab	2023
37745480	Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium.	bioRxiv	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
38014529	Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.	Circ Genom Precis Med	2023
37913995	Missense variants in SORT1 are associated with LDL-C in an Amish population.	J Lipid Res	2023
37808823	Acute pharmacodynamic responses to sitagliptin: Drug-induced increase in early insulin secretion in oral glucose tolerance test.	medRxiv	2023
37905118	Determinants of mosaic chromosomal alteration fitness.	medRxiv	2023
37904051	Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.	Nat Genet	2023
38094903	Genomic risk scores and oral contraceptive-associated ischemic stroke risk: a call for collaboration.		2023
37802043	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.	Am J Hum Genet	2023
37634742	An in-depth association analysis of genetic variants within nicotine-related loci: Meeting in middle of GWAS and genetic fine-mapping.		2023
38076909	Evidence of survival bias in the association between and age of ischemic stroke onset.		2023
37961350	A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.	bioRxiv	2023
37961161	<i>APOE4</i> poses opposite effects of plasma LDL on white matter integrity in older adults.	bioRxiv	2023
37348055	Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.	Genetics	2023
37159869	Association of parity with body mass index and cardiometabolic risk in high-parous women.	Menopause	2023
36778406	Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.	bioRxiv	2023
37461703	Polygenic Risk Score Associates with Atherosclerotic Plaque Characteristics at Autopsy.	bioRxiv	2023
37398003	Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.	medRxiv	2023
37268629	Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.	Nat Commun	2023
37078962	Evidence of Neurovascular Water Exchange and Endothelial Vascular Dysfunction in Schizophrenia: An Exploratory Study.	Schizophr Bull	2023
37330925	Deciphering the causal relationship between blood pressure and regional white matter integrity: A two-sample Mendelian randomization study.	J Neurosci Res	2023
37264484	Acute pharmacodynamic responses to exenatide: Drug-induced increases in insulin secretion and glucose effectiveness.	Diabetes Obes Metab	2023
36882501	Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population.	Mol Psychiatry	2023
37011072	Decoding Hypertension Through Primary Aldosteronism.		2023
36945579	Pharmacogenetics of SGLT2 Inhibitors: Validation of a sex-agnostic pharmacodynamic biomarker.	medRxiv	2023
36941539	Associations of genome-wide and regional autozygosity with 96 complex traits in old order Amish.	BMC Genomics	2023
36993363	Acute pharmacodynamic responses to exenatide: Drug-induced increases in insulin secretion and glucose effectiveness.	medRxiv	2023
36606600	Depression, stress and regional cerebral blood flow.	J Cereb Blood Flow Metab	2023
34935254	Biallelic truncating variants in the muscular A-type lamin-interacting protein (MLIP) gene cause myopathy with hyperCKemia.	Eur J Neurol	2022
36180445	Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.	Nat Commun	2022
35527502	Polygenic Risk Scores for Blood Pressure to Assess the Risk of Severe Bevacizumab-Induced Hypertension in Cancer Patients (Alliance).	Clin Pharmacol Ther	2022
36042188	Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.	Nat Commun	2022
35654975	A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.	Nat Genet	2022
36240095	Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke.	Neurology	2022
35963506	Cerebral blood flow and cardiovascular risk effects on resting brain regional homogeneity.	Neuroimage	2022
35652341	Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.	Hypertension	2022
35513726	Polygenic risk scores for CARDINAL study.	Nat Genet	2022
35389749	Monogenic and Polygenic Contributions to QTc Prolongation in the Population.	Circulation	2022
35442562	Impact of parental relatedness on reproductive outcomes among the Old Order Amish of Lancaster County.	Am J Med Genet A	2022
35385311	Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.	Sci Adv	2022
36220816	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.	Nat Commun	2022
36055577	Selective adipocyte loss of Angiopoietin-2 prompts female-specific obesity and metabolic syndrome.	Molecular Metabolism	2022