Author details

Full Name

John Blangero

Affiliation

ORCID

Career Start Year

1982

Papers

712

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
38029722	Riemannian frameworks for the harmonization of resting-state functional MRI scans.		2024
37425772	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.	medRxiv	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
37805498	Metabolic phenotyping of BMI to characterize cardiometabolic risk: evidence from large population-based cohorts.	Nat Commun	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
37886476	A Scan of Pleiotropic Immune Mediated Disease Genes Identifies Novel Determinants of Baseline FVIII Inhibitor Status in Hemophilia-A.		2023
37795246	Genotype-by-socioeconomic status interaction influences heart disease risk scores and carotid artery thickness in Mexican Americans: the predominant role of education in comparison to household income and socioeconomic index.		2023
37961350	A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.	bioRxiv	2023
37961304	Functional characterization of the disease-associated rs1024611G-rs13900T haplotype: The role of the RNA-binding protein HuR.		2023
36970519	Cocktail-party listening and cognitive abilities show strong pleiotropy.		2023
36778386	Structural variation across 138,134 samples in the TOPMed consortium.	Res Sq	2023
37398003	Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.	medRxiv	2023
36882501	Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population.	Mol Psychiatry	2023
36702996	Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.	Nat Genet	2023
37126548	The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.	Sci Adv	2023
36747810	Structural variation across 138,134 samples in the TOPMed consortium.	bioRxiv	2023
36469193	Co-alteration Network Architecture of Major Depressive Disorder: A Multi-modal Neuroimaging Assessment of Large-scale Disease Effects.	Neuroinformatics	2023
37046083	Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.	Nature	2023
36927883	Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function: A Meta-analysis of Community-Based Cohorts.	Neurology	2023
34645953	Genetic determinants of metabolic biomarkers and their associations with cardiometabolic traits in Hispanic/Latino adolescents.	Pediatr Res	2022
36111257	The Genetic contribution to solving the cocktail-party problem.	iScience	2022
35845438	Non-alcoholic Fatty Liver Disease and Depression: Evidence for Genotype Ã¿ Environment Interaction in Mexican Americans.	Frontiers in Psychiatry	2022
35592775	The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.	Front Endocrinol (Lausanne)	2022
35652341	Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.	Hypertension	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
35498404	Burden of Type 2 Diabetes and Associated Cardiometabolic Traits and Their Heritability Estimates in Endogamous Ethnic Groups of India: Findings From the INDIGENIUS Consortium.	Frontiers in Endocrinology	2022
36151472	Publisher Correction: Brain charts for the human lifespan.	Nature	2022
36268164	Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
36204553	Metabolic syndrome predictors of brain gray matter volume in an age-stratified community sample of 776 Mexican- American adults: Results from the genetics of brain structure image archive.	Frontiers in Aging Neuroscience	2022
35734277	Influence of the Human Lipidome on Epicardial Fat Volume in Mexican American Individuals.	Frontiers in Cardiovascular Medicine	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022
35668104	Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease.	Nat Commun	2022
35853479	Lipidomic profiling in the Strong Heart Study identified American Indians at risk of chronic kidney disease.	Kidney Int	2022
36185993	Chronic neuropsychiatric sequelae of SARS-CoV-2: Protocol and methods from the Alzheimer's Association Global Consortium.	Alzheimers Dement (N Y)	2022
35399580	Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
36481753	Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program.	Nat Commun	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
33772461	Efficient Generation of Functional Hepatocytes from Human Induced Pluripotent Stem Cells for Disease Modeling and Disease Gene Discovery.	Methods in Molecular Biology	2022
34553764	Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.	Hum Mol Genet	2022
30644433	Genetic influence on cognitive development between childhood and adulthood.	Mol Psychiatry	2021
33805011	Disease Modeling and Disease Gene Discovery in Cardiomyopathies: A Molecular Study of Induced Pluripotent Stem Cell Generated Cardiomyocytes.	International Journal of Molecular Sciences	2021
34291061	Association of HIV-1 Infection and Antiretroviral Therapy With Type 2 Diabetes in the Hispanic Population of the Rio Grande Valley, Texas, USA.	Frontiers in Medicine	2021
33479282	Further evidence supporting a potential role for ADH1B in obesity.	Sci Rep	2021
33846329	Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.	Nat Commun	2021
33785081	Genetic influences on externalizing psychopathology overlap with cognitive functioning and show developmental variation.	Eur Psychiatry	2021
33622655	Searching for Imaging Biomarkers of Psychotic Dysconnectivity.	Biol Psychiatry Cogn Neurosci Neuroimaging	2021
34108472	Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.	Nat Commun	2021
33887960	Identifying the Lipidomic Effects of a Rare Loss-of-Function Deletion in .	Circulation. Genomic and precision medicine	2021