About: Anubha Mahajan

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Anubha Mahajan Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Human genetics researcher

Attributes	Values
rdf:type	Item
owl:sameAs	Anubha Mahajan
description	forskare (sv) ikertzailea (eu) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідниця (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtuese (sq) Human genetics researcher (en)
rdfs:label	Anubha Mahajan (en) Anubha Mahajan (es) Anubha Mahajan (nl) Anubha Mahajan (sl) Anubha Mahajan (ast)
skos:prefLabel	Anubha Mahajan (en) Anubha Mahajan (es) Anubha Mahajan (nl) Anubha Mahajan (sl) Anubha Mahajan (ast)
name	Anubha Mahajan (en) Anubha Mahajan (es) Anubha Mahajan (nl) Anubha Mahajan (sl) Anubha Mahajan (ast)
instance of	wds:Q47502230-ABD5E9EB-6794-439F-97EA-1AA05469B9FE
instance of	Homo sapiens
Google Knowledge Graph ID	wds:Q47502230-B5445EFF-B433-4AE9-AD8D-B84117A3A5EA
Google Knowledge Graph ID	http://g.co/kg/g/11h1m5hh_f
Google Knowledge Graph ID	/g/11h1m5hh_f
skos:altLabel	A Mahajan (en) Mahajan A (en)
occupation	wds:Q47502230-FD697E95-DDE7-4003-80C0-EBD925B700D1
employer	wds:Q47502230-8B4D5E9B-E8E8-4AA8-A87B-3D68378DE8C1
sex or gender	wds:Q47502230-518b454e-426b-a404-7979-0e9bb7c4934a
date of birth	wds:Q47502230-38A6A060-728E-4989-8A05-ABC6DF8A110F
family name	wds:Q47502230-37FEA386-A916-4722-B666-D068459DCD61
occupation	researcher
employer	University of Oxford
sex or gender	female organism
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
family name	Mahajan
ORCID iD	wds:Q47502230-D1B6534F-E143-4411-8F70-977F1B4C1FE2
ORCID iD	https://orcid.org/0000-0001-5585-3420
ORCID iD	0000-0001-5585-3420
is owl:sameAs of	Anubha Mahajan Anubha Mahajan
is about of	Anubha Mahajan https://www.wikidata.org/wiki/Special:EntityData/Q47502230 Anubha Mahajan
is author of	Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility Genetic studies of body mass index yield new insights for obesity biology Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways Mining literature for a comprehensive pathway analysis: a case study for retrieval of homocysteine related genes for genetic and epigenetic studies Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism Common variants of FTO and the risk of obesity and type 2 diabetes in Indians A novel common variant in DCST2 is associated with length in early life and height in adulthood Obesity-dependent association of TNF-LTA locus with type 2 diabetes in North Indians Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus FTO genotype is associated with phenotypic variability of body mass index PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study New genetic loci link adipose and insulin biology to body fat distribution Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. Association of variants in genes involved in pancreatic β-cell development and function with type 2 diabetes in North Indians Loss-of-function mutations in SLC30A8 protect against type 2 diabetes Defining the role of common variation in the genomic and biological architecture of adult human height Impact of common variants of PPARG, KCNJ11, TCF7L2, SLC30A8, HHEX, CDKN2A, IGF2BP2, and CDKAL1 on the risk of type 2 diabetes in 5,164 Indians. Genetic loci associated with heart rate variability and their effects on cardiac disease risk Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk Evaluation of DOK5 as a susceptibility gene for type 2 diabetes and obesity in North Indian population High-sensitivity C-reactive protein levels and type 2 diabetes in urban North Indians The genetic architecture of type 2 diabetes Rare and low-frequency coding variants alter human adult height Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease A reference panel of 64,976 haplotypes for genotype imputation Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index Elevated levels of C-reactive protein as a risk factor for metabolic syndrome in Indians Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation The impact of low-frequency and rare variants on lipid levels Genome-wide associations for birth weight and correlations with adult disease Genome-wide association study of toxic metals and trace elements reveals novel associations New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk Common variants in CRP and LEPR influence high sensitivity C-reactive protein levels in North Indians Clinical and genetic correlates of growth differentiation factor 15 in the community Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease Evaluation of type 2 diabetes genetic risk variants in Chinese adults: findings from 93,000 individuals from the China Kadoorie Biobank. Genome-wide DNA methylation study identifies genes associated with the cardiovascular biomarker GDF-15 Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 196 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software