Author details

Full Name

Kari E North

Affiliation

ORCID

Career Start Year

1999

Papers

492

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36917487	A Gene-Acculturation Study of Obesity Among US Hispanic/Latinos: The Hispanic Community Health Study/Study of Latinos.		2023
36444934	Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.	Hum Mol Genet	2023
38028628	Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.	Front Genet	2023
37666943	Correction: Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes.	Leukemia	2023
37932662	Epigenome-wide methylation and progression to high-grade cervical intraepithelial neoplasia (CIN2+): a prospective cohort study in the United States.		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
38017291	Branched chain amino acids harbor distinct and often opposing effects on health and disease.		2023
37658231	Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts.	Hum Genet	2023
37817410	Mendelian randomization with incomplete measurements on the exposure in the Hispanic Community Health Study/Study of Latinos.		2023
37653519	Sex-specific associations between adipokine profiles and carotid-intima media thickness in the Cameron County Hispanic Cohort (CCHC).	Cardiovasc Diabetol	2023
37648373	Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.	Open Heart	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
37875120	Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics.	Am J Hum Genet	2023
37217495	Selenomonas sputigena acts as a pathobiont mediating spatial structure and biofilm virulence in early childhood caries.		2023
37470492	Investigating Associations of Omega-3 Fatty Acids, Lung Function Decline, and Airway Obstruction.	Am J Respir Crit Care Med	2023
37090648	MUSSEL: Enhanced Bayesian Polygenic Risk Prediction Leveraging Information across Multiple Ancestry Groups.	bioRxiv	2023
36775672	Physical activity and diet associations with the gut microbiota in the Coronary Artery Risk Development in Young Adults (CARDIA) study.	J Nutr	2023
36711663	Investigating associations of omega-3 fatty acids, lung function decline, and airway obstruction.	medRxiv	2023
36574663	Natural selection of immune and metabolic genes associated with health in two lowland Bolivian populations.		2023
36702996	Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.	Nat Genet	2023
37131817	Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics.	bioRxiv	2023
36941441	Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals.	Nat Genet	2023
36791419	Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.	Diabetes	2023
37168250	Cumulative socioeconomic status and incident type 2 diabetes among African American adults from the Jackson heart study.		2023
37528943	Challenges and strategies for recruitment of minorities to clinical research and trials.	J Clin Transl Sci	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
35157052	Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes.	Hum Mol Genet	2022
35592775	The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.	Front Endocrinol (Lausanne)	2022
35654413	Extended Human Papillomavirus Genotyping to Predict Progression to High-Grade Cervical Precancer: A Prospective Cohort Study in the Southeastern United States.	Cancer Epidemiol Biomarkers Prev	2022
35653334	A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program.	PLoS Genet	2022
35652341	Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.	Hypertension	2022
36235682	Novel Insights into the Effects of Genetic Variants on Serum Urate Response to an Acute Fructose Challenge: A Pilot Study.	Nutrients	2022
35448546	Metabolomic Associations of Asthma in the Hispanic Community Health Study/Study of Latinos.	Metabolites	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
36088317	Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations.	BMC Med Genomics	2022
35500859	Gaseous air pollutants and DNA methylation in a methylome-wide association study of an ethnically and environmentally diverse population of U.S. adults.	Environ Res	2022
36000800	Phenotype Harmonization in the GLIDE2 Oral Health Genomics Consortium.	J Dent Res	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
36268164	Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022
36055210	Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience.	Am J Hum Genet	2022
35536696	Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis.	Am J Respir Crit Care Med	2022
35349783	Enrichment analyses identify shared associations for 25 quantitative traits in over 600,000 individuals from seven diverse ancestries.	Am J Hum Genet	2022
35915156	Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.	Nat Med	2022
35533073	Strengthening Causal Inference in Exposomics Research: Application of Genetic Data and Methods.	Environmental Health Perspectives	2022
35467716	Infant Growth Trajectories and Lipid Levels in Adolescence: Evidence From a Chilean Infancy Cohort.	Am J Epidemiol	2022
35399580	Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022