About: Chris Wallace

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

British genonomic statistician

Attributes	Values
rdf:type	Item
description	Biochemikerin (de) 연구원 (ko) গবেষক (bn) 研究者 (ja) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl) British genonomic statistician (en)
exact match	wds:Q37624906-FF06B3D9-E645-4ABC-AE1E-193B2F2AAE7E
exact match	https://scigraph.springernature.com/person.0766204577.10
rdfs:label	Chris Wallace (de) Chris Wallace (en) Chris Wallace (es) Chris Wallace (it) Chris Wallace (nl) Chris Wallace (sl) Chris Wallace (ast) ক্রিস ওয়ালেস (bn) Chris Wallace (sq)
skos:prefLabel	Chris Wallace (de) Chris Wallace (en) Chris Wallace (es) Chris Wallace (it) Chris Wallace (nl) Chris Wallace (sl) Chris Wallace (ast) ক্রিস ওয়ালেস (bn) Chris Wallace (sq)
name	Chris Wallace (de) Chris Wallace (en) Chris Wallace (es) Chris Wallace (it) Chris Wallace (nl) Chris Wallace (sl) Chris Wallace (ast) ক্রিস ওয়ালেস (bn) Chris Wallace (sq)
Scopus author ID	wds:Q37624906-42300622-4A34-4B6C-818B-A433DA29A9C7
Scopus author ID	8931612300
given name	wds:Q37624906-E8174265-62A1-4C11-A63F-450A7899FCDA
given name	Chris
instance of	wds:Q37624906-150CE9F7-CE76-4CB7-8972-8392A9E0B36A
instance of	Homo sapiens
Google Scholar author ID	wds:Q37624906-2bc56440-43a5-11e0-abb7-07dd94c8ffe6
Google Scholar author ID	PB2gO4MAAAAJ
occupation	wds:Q37624906-25F6FFB0-83E3-4E49-A9CB-78819835E194 wds:Q37624906-bd83af68-4372-8c53-6bb9-631d4c235723
employer	wds:Q37624906-22E8C541-255A-4629-90B7-1F7015093EFA wds:Q37624906-2352F408-8421-4709-8C89-F79E986E9CBE
GitHub username	wds:Q37624906-A16A32A2-79BD-4B79-A26D-7905F4A07983
sex or gender	wds:Q37624906-73A82993-0096-4C12-8139-A6AFD4F88332
DBLP author ID	wds:Q37624906-9EFCDAD3-B8B9-4DB2-A448-CAE974152BAC
educated at	wds:Q37624906-77F4CEC8-A127-4545-ADB0-0FD933DB8F2B
family name	wds:Q37624906-B4C50A97-6776-4298-8F9D-0F252F11E2BF
DBLP author ID	https://dblp.org/pid/05/1626-2.rdf
occupation	statistician biochemist
employer	John Ffowcs Williams Queen Mary University of London
GitHub username	chr1swallace
sex or gender	female organism
DBLP author ID	05/1626-2
educated at	London School of Hygiene & Tropical Medicine
family name	Wallace
ORCID iD	wds:Q37624906-E2A270E7-699A-4B29-A3CB-F0077E3C73C6
Dimensions author ID	wds:Q37624906-5D4B7C1E-16EC-4E22-BCB8-F426014C476D
ORCID iD	https://orcid.org/0000-0001-9755-1703
ORCID iD	0000-0001-9755-1703
Dimensions author ID	0766204577.10
Gateway to Research person ID	wds:Q37624906-2C53CDFC-4F07-4B76-A34E-FE2AFB5CE908
Gateway to Research person ID	073675CC-FCDE-4CA2-8BD4-45569089D060
AcademiaNet ID	wds:Q37624906-41CA1657-A5D0-41F9-9EB5-5535D275424F
AcademiaNet ID	1216995
is owl:sameAs of	Chris Wallace
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37624906
is author of	Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations Common variants near MC4R are associated with fat mass, weight and risk of obesity Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Plasma concentrations of soluble IL-2 receptor α (CD25) are increased in type 1 diabetes and associated with reduced C-peptide levels in young patients. Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension An allele of IKZF1 (Ikaros) conferring susceptibility to childhood acute lymphoblastic leukemia protects against type 1 diabetes Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls Genetic loci influencing kidney function and chronic kidney disease SLC2A9 is a high-capacity urate transporter in humans Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension Extreme clonality in lymphoblastoid cell lines with implications for allele specific expression analyses A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma Haplotypes of the beta-2 adrenergic receptor associate with high diastolic blood pressure in the Caerphilly prospective study

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