About: Tom R. Gaunt

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

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) investigador (es) chercheur (fr) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl) researcher (en-ca) researcher (en-gb) researcher (en-us) investigador (ca) investigador (gl) investigador (ast) investigador (pt)
rdfs:label	Tom R Gaunt (nl) Tom R Gaunt (sl) Tom R. Gaunt (de) Tom R. Gaunt (en) Tom R. Gaunt (es)
skos:prefLabel	Tom R Gaunt (nl) Tom R Gaunt (sl) Tom R. Gaunt (de) Tom R. Gaunt (en) Tom R. Gaunt (es)
name	Tom R Gaunt (nl) Tom R Gaunt (sl) Tom R. Gaunt (de) Tom R. Gaunt (en) Tom R. Gaunt (es)
given name	wds:Q37390320-9704CD72-E686-4D70-A692-094B396CBC2D
given name	Tom
instance of	wds:Q37390320-DDACFB15-C3C0-4A97-8FF3-F708C67BCA2D
instance of	Homo sapiens
Semantic Scholar author ID	wds:Q37390320-9a7dfd31-4121-4b92-84ef-af219a8259f2
Semantic Scholar author ID	2261094
skos:altLabel	T R Gaunt (en) Tom Gaunt (en) Tom R Gaunt (en)
occupation	wds:Q37390320-1EDB6DFC-DA14-44A2-8E9B-1F4B5CC30ABA
employer	wds:Q37390320-566244A7-526E-42FE-ADDB-B6A2583F0FD5
sex or gender	wds:Q37390320-4DADE471-7850-4209-AC71-2BBA633F9F47
VIAF ID	wds:Q37390320-b2702ec6-9feb-41a2-88cc-3748bd1b3008
DBLP author ID	wds:Q37390320-6FC13EE2-9337-416C-8AC2-62340140A8FE
IdRef ID	wds:Q37390320-2E7FA6B3-071D-49BA-AA79-3ECE17950F41
educated at	wds:Q37390320-53D25256-3819-448A-850C-E1580F573638
family name	wds:Q37390320-B348F5DB-B646-46C1-9805-42AF280E4E38
official website	wds:Q37390320-1EF2F733-52E9-42E5-AAF5-26311A5D5C26
VIAF ID	http://viaf.org/viaf/70146573903038101610
DBLP author ID	https://dblp.org/pid/63/2162.rdf
IdRef ID	http://www.idref.fr/193031612/id
occupation	researcher
employer	University of Bristol
sex or gender	male
VIAF ID	70146573903038101610
DBLP author ID	63/2162
IdRef ID	193031612
educated at	University of Southampton
family name	Gaunt
official website	http://research-information.bristol.ac.uk/en/persons/tom-r-gaunt(f4d3d2e8-dcc0-412e-9fee-91847127513b).html
ORCID iD	wds:Q37390320-A77B9B5D-499E-4F48-A9F9-DC0E3842A1A5
ORCID iD	https://orcid.org/0000-0003-0924-3247
ORCID iD	0000-0003-0924-3247
Gateway to Research person ID	wds:Q37390320-C2D5650F-CCED-4DCC-9085-1CDA49E4C323
Gateway to Research person ID	8A645CAB-3E47-417D-B03E-07A54237F360
ResearcherID	wds:Q37390320-ACF32217-0EE9-4359-91E4-2A6324AFC1F6
Publons author ID	wds:Q37390320-ee92cdbf-d08f-4ae0-ae84-9b0f07b823a5
ResearcherID	O-3918-2014
Publons author ID	2463544
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37390320
is author of	Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4,610 cases amongst 18,637 participants The relationship between plasma angiopoietin-like protein 4 levels, angiopoietin-like protein 4 genotype, and coronary heart disease risk Loci influencing blood pressure identified using a cardiovascular gene-centric array Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia. From a single whole exome read to notions of clinical screening: primary ciliary dyskinesia and RSPH9 p.Lys268del in the Arabian Peninsula A pathway-based data integration framework for prediction of disease progression Variants of ADRA2A are associated with fasting glucose, blood pressure, body mass index and type 2 diabetes risk: meta-analysis of four prospective studies Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study Sixty-five common genetic variants and prediction of type 2 diabetes Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci Metabolite profiling and cardiovascular event risk: a prospective study of 3 population-based cohorts MIDAS: software for analysis and visualisation of interallelic disequilibrium between multiallelic markers Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX' Positive associations between single nucleotide polymorphisms in the IGF2 gene region and body mass index in adult males TAS2R38 (phenylthiocarbamide) haplotypes, coronary heart disease traits, and eating behavior in the British Women's Heart and Health Study Whole-genome sequence-based analysis of thyroid function. Importance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene Functions Proxy molecular diagnosis from whole-exome sequencing reveals Papillon-Lefevre syndrome caused by a missense mutation in CTSC Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process. An integrative approach to predicting the functional effects of non-coding and coding sequence variation Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models

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