Author details

Full Name

Namrata Gupta

Affiliation

ORCID

Career Start Year

2010

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37425716	Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects.	bioRxiv	2023
37763321	Validating the Nutraceutical Significance of Minor Millets by Employing Nutritional-Antinutritional Profiling.		2023
37601969	Multiset correlation and factor analysis enables exploration of multi-omics data.	Cell Genom	2023
37749248	Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.	Nat Genet	2023
37662416	Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association Studies.	bioRxiv	2023
37868038	The functional impact of rare variation across the regulatory cascade.	Cell Genom	2023
36960714	Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.	Circ Genom Precis Med	2023
36463326	Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis.	Int J Obes (Lond)	2023
37231098	Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture.	Nat Genet	2023
35385699	Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.	Am J Hum Genet	2022
36180445	Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.	Nat Commun	2022
36042188	Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.	Nat Commun	2022
35389749	Monogenic and Polygenic Contributions to QTc Prolongation in the Population.	Circulation	2022
35647563	Accounting for population structure in genetic studies of cystic fibrosis.	HGG Adv	2022
34373650	Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans.	Nature	2021
33536627	Author Correction: A structural variation reference for medical and population genetics.	Nature	2021
33536625	Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans.	Nature	2021
33822779	Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.	PLoS Genet	2021
34914532	Pangenomics enables genotyping of known structural variants in 5202 diverse genomes.	Science	2021
32862661	Heterozygous <i>ABCG5</i> Gene Deficiency and Risk of Coronary Artery Disease.	Circ Genom Precis Med	2020
32303876	Infantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction.	J Clin Immunol	2020
31998013	Goal-directed fluid therapy using transoesophageal echocardiographic inferior venacaval index in patients with low left ventricular ejection fraction undergoing major cytoreductive surgery: A clinical trial.	Saudi Journal of Anaesthesia	2020
31707836	Genetic Interleukin 6 Signaling Deficiency Attenuates Cardiovascular Risk in Clonal Hematopoiesis.	Circulation	2020
32461654	The mutational constraint spectrum quantified from variation in 141,456 humans.	Nature	2020
30718883	Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genes.	Eur J Hum Genet	2019
31869403	Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.	PLoS Genet	2019
30586733	Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction.	Circulation	2019
30389748	DNA Sequence Variation in <i>ACVR1C</i> Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 Diabetes.	Diabetes	2019
29857119	Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.	Genomics	2019
30970187	Molecular Genetic Anatomy and Risk Profile of Hirschsprung's Disease.	N Engl J Med	2019
30914438	Impaired human hematopoiesis due to a cryptic intronic <i>GATA1</i> splicing mutation.	J Exp Med	2019
30735661	The Genetic Landscape of Diamond-Blackfan Anemia.	Am J Hum Genet	2019
27625029	A Novel Mutation in Helical Domain 2 of NOD2 in Sporadic Blau Syndrome.	Ocular Immunology and Inflammation	2018
28982690	Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling.	Circulation	2018
29892015	Multi-ethnic genome-wide association study for atrial fibrillation.	Nat Genet	2018
30503522	The Genetic Landscape of Diamond-Blackfan Anemia.	Am J Hum Genet	2018
30535219	Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation.	JAMA	2018
29861106	Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum.	Am J Hum Genet	2018
29691411	Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease.	Nat Commun	2018
28118524	A Multinational Arab Genome-Wide Association Study Identifies New Genetic Associations for Rheumatoid Arthritis.	Arthritis Rheumatol	2017
28506971	Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease.	Circ Res	2017
28385496	ANGPTL3 Deficiency and Protection Against Coronary Artery Disease.	J Am Coll Cardiol	2017
28636844	Clonal Hematopoiesis and Risk of Atherosclerotic Cardiovascular Disease.	N Engl J Med	2017
28794525	Utility of non-invasive haemoglobin monitoring in oncosurgery patients.	Indian Journal of Anaesthesia	2017
28406212	Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity.	Nature	2017
28968755	Evaluating the Impact of Functional Genetic Variation on HIV-1 Control.	J Infect Dis	2017
29074945	Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology.	Nat Genet	2017
28283061	Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation.	Cell	2017
28267856	Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease.	JAMA	2017
28110127	Bacteriophage application on red meats and poultry: Effects on Salmonella population in final ground products.	Meat Science	2017