Author details

Full Name

Laura M Raffield

Affiliation

ORCID

Career Start Year

2013

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37533140	Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait.	Clin J Am Soc Nephrol	2023
35567697	Assay-related differences in SuPAR levels: implications for measurement and data interpretation.	Journal of Nephrology	2023
36342131	Prolonged, physiologically relevant nicotine concentrations in the airways of smokers.	American Journal of Physiology - Lung Cellular and Molecular Physiology	2023
36444934	Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.	Hum Mol Genet	2023
37849304	Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression.	Am J Psychiatry	2023
37756531	Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk.	Diabetes Care	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
37905118	Determinants of mosaic chromosomal alteration fitness.	medRxiv	2023
37648373	Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.	Open Heart	2023
37558590	Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19.	Blood Cells Mol Dis	2023
37872285	Metabolomic epidemiology offers insights into disease aetiology.	Nat Metab	2023
37609271	The Relationship of Duffy Gene Polymorphism, High Sensitivity C-Reactive Protein, and Long-term Outcomes.	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
37148359	The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes.	Diabetologia	2023
37398003	Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.	medRxiv	2023
36702996	Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.	Nat Genet	2023
36812475	DNAmFitAge: biological age indicator incorporating physical fitness.	Aging (Albany NY)	2023
37046083	Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.	Nature	2023
36791419	Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.	Diabetes	2023
35138379	Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits.	Hum Mol Genet	2022
35701873	Genome Wide Association Studies of Variant-by-Thiazide Interaction on Lipids Identifies a Novel Low-Density Lipoprotein Cholesterol Locus.	Circulation Research	2022
35504290	TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data.	Am J Hum Genet	2022
36198314	MagicalRsq: Machine-learning-based genotype imputation quality calibration.	Am J Hum Genet	2022
36481753	Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program.	Nat Commun	2022
34789503	Obesity Partially Mediates the Diabetogenic Effect of Lowering LDL Cholesterol.	Diabetes Care	2022
34553764	Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.	Hum Mol Genet	2022
34779012	A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.	Genet Epidemiol	2022
34582791	Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.	Am J Hum Genet	2021
34050697	Clonal hematopoiesis associated with epigenetic aging and clinical outcomes.	Aging Cell	2021
34107879	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	BMC Genomics	2021
33887194	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.	Am J Hum Genet	2021
33619371	Malaria is a cause of iron deficiency in African children.	Nat Med	2021
34210413	Supplemental Association of Clonal Hematopoiesis With Incident HeartÂ Failure.	J Am Coll Cardiol	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
33931109	Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci.	Genome Med	2021
34347846	Genetic underpinnings of regional adiposity distribution in African Americans: Assessments from the Jackson Heart Study.	PLoS One	2021
34356065	Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations.	Genes (Basel)	2021
34021356	Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche.	Hum Reprod	2021
33137338	Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.	Kidney Int	2021
33418499	Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.	EBioMedicine	2021
33434830	Optimism and telomere length among African American adults in the Jackson Heart Study.	Psychoneuroendocrinology	2021
33268503	Effect of Sickle Cell Trait and <i>APOL1</i> Genotype on the Association of Soluble uPAR with Kidney Function Measures in Black Americans.	Clin J Am Soc Nephrol	2021
34517814	Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study.	BMC Genomics	2021
35036986	Association of mitochondrial DNA copy number with cardiometabolic diseases.	Cell Genom	2021
34604815	Genetic discovery and risk characterization in type 2 diabetes across diverse populations.	HGG Adv	2021
32888493	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Cell	2020
32171239	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	BMC Genomics	2020
31883642	Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.	Am J Hum Genet	2020
31985870	Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome-wide analysis in African Americans.	J Thromb Haemost	2020
32386347	Comparison of Proteomic Assessment Methods in Multiple Cohort Studies.	Proteomics	2020