Author details

Full Name

Diane M Becker

Affiliation

ORCID

Career Start Year

1985

Papers

210

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36702996	Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.	Nat Genet	2023
37770635	Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.	Nat Genet	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022
35621212	Association of Vascular Properties With the Brain White Matter Hyperintensity in Middle-Aged Population.	Journal of the American Heart Association	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
35232957	Correction: Association of low-frequency and rare coding variants with information processing speed.	Transl Psychiatry	2022
33829634	Gene and protein expression in human megakaryocytes derived from induced pluripotent stem cells.	J Thromb Haemost	2021
33713608	Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.	Am J Hum Genet	2021
33279889	White Matter Injury Is Associated with Reduced Manual Dexterity and Elevated Serum Ceramides in Subjects with Cerebral Small Vessel Disease.	Cerebrovascular Diseases	2021
34864818	Association of low-frequency and rare coding variants with information processing speed.	Transl Psychiatry	2021
34139692	Cerebral Small-Vessel Disease in Individuals with a Family History of Coronary Heart Disease: The Atherosclerosis Risk in Communities Study.	Neuroepidemiology	2021
34000829	Association of Coronary Artery Atherosclerosis With Brain White Matter Hyperintensity.	Stroke	2021
33876560	FGL1 as a modulator of plasma D-dimer levels: Exome-wide marker analysis of plasma tPA, PAI-1, and D-dimer.	J Thromb Haemost	2021
33186364	Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.	PLoS One	2020
29185836	Exome-chip meta-analysis identifies association between variation in ANKRD26 and platelet aggregation.	Platelets	2019
31127295	A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.	Hum Mol Genet	2019
30942856	Evolution of Hominin Polyunsaturated Fatty Acid Metabolism: From Africa to the New World.	Genome Biology and Evolution	2019
29875064	The relationship of family history and risk of type 2 diabetes differs by ancestry.		2019
29553866	Targeted deep sequencing of the PEAR1 locus for platelet aggregation in European and African American families.	Platelets	2019
31719535	Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.	Nat Commun	2019
29455858	A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.	Am J Hum Genet	2018
28520984	Genome-Wide Association Study of Heavy Smoking and Daily/Nondaily Smoking in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).	Nicotine Tob Res	2018
30442693	Hypertension Is Associated with White Matter Disruption in Apparently Healthy Middle-Aged Individuals.		2018
30388399	Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.	Am J Hum Genet	2018
30265320	Diabetes and Platelet Response to Low-Dose Aspirin.	Journal of Clinical Endocrinology and Metabolism	2018
30258056	Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume.	Nat Commun	2018
30002152	Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging.	Stroke	2018
29912962	Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.	PLoS One	2018
29750786	Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.	PLoS Genet	2018
29030599	Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity.	Nat Commun	2017
28850949	White Matter Lesion Progression and Cognitive Function Over 5 Years in a Young Susceptible Population.	Neuroepidemiology	2017
28498854	Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.	PLoS Genet	2017
28430825	Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.	PLoS Genet	2017
28300864	Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation.	Thromb Haemost	2017
28107356	Integrity of Induced Pluripotent Stem Cell (iPSC) Derived Megakaryocytes as Assessed by Genetic and Transcriptomic Analysis.	PLoS One	2017
28098162	Novel genetic loci associated with hippocampal volume.	Nat Commun	2017
28017375	Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.	Am J Hum Genet	2017
27321945	Trans-ethnic Meta-analysis and Functional Annotation Illuminates theÂ Genetic Architecture of Fasting Glucose and Insulin.	Am J Hum Genet	2016
26561523	A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.	Hum Mol Genet	2016
27872105	Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis.	Circ Cardiovasc Genet	2016
27855341	The relationship of fasting hyperglycemia to changes in fat and muscle mass after exercise training in type 2 diabetes.	Diabetes Res Clin Pract	2016
27694991	Novel genetic loci underlying human intracranial volume identified through genome-wide association.	Nat Neurosci	2016
27651445	SCARB1 Gene Variants Are Associated With the Phenotype of Combined High High-Density Lipoprotein Cholesterol and High Lipoprotein (a).	Circulation: Cardiovascular Genetics	2016
27536930	Impact of Self-Preference Community Fitness Interventions in High-Risk African Americans.	Fam Community Health	2016
27530333	Relation of Plasma Lipoprotein(a) to Subclinical Coronary Plaque Volumes, Three-Vessel and Left Main Coronary Disease, and Severe Coronary Stenoses in Apparently Healthy African-Americans With a Family History of Early-Onset Coronary Artery Disease.	American Journal of Cardiology	2016
27346689	Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.	Am J Hum Genet	2016
27346686	Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.	Am J Hum Genet	2016