About: Cathryn Lewis

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Professor of Genetic Epidemiology and Statistics

Attributes	Values
rdf:type	Item
description	հետազոտող (hy) hulumtuese (sq) psycholoog (nl) Professor of Genetic Epidemiology and Statistics (en)
rdfs:label	Cathryn Lewis (de) Cathryn Lewis (en) Cathryn Lewis (es) Cathryn Lewis (nl) Cathryn Lewis (sl) Cathryn Lewis (sq) Cathryn Lewis (tr) Cathryn Lewis (ast)
skos:prefLabel	Cathryn Lewis (de) Cathryn Lewis (en) Cathryn Lewis (es) Cathryn Lewis (nl) Cathryn Lewis (sl) Cathryn Lewis (sq) Cathryn Lewis (tr) Cathryn Lewis (ast)
name	Cathryn Lewis (de) Cathryn Lewis (en) Cathryn Lewis (es) Cathryn Lewis (nl) Cathryn Lewis (sl) Cathryn Lewis (sq) Cathryn Lewis (tr) Cathryn Lewis (ast)
Freebase ID	wds:Q16731445-90EC5ECB-0E79-4E3A-BA87-B10437009A51
Freebase ID	/m/0_frh6_
Scopus author ID	wds:Q16731445-58E8F648-F783-4DD1-B70E-529EC3873D0C wds:Q16731445-B41D12AE-F52D-4B4E-9FFA-AA130C0D9C22
Scopus author ID	57201864389 7402975073
given name	wds:Q16731445-91B00BCD-93C5-42D1-BC5C-C0BB55E2E964
given name	Cathryn
image	wds:Q16731445-B9A212EC-359C-4826-8364-2A35BBE9297D
instance of	wds:Q16731445-A2FA44B0-2DE0-4A48-A46C-FCD82747EDBD
image
instance of	Homo sapiens
Commons category	wds:Q16731445-3e1671c7-0fd1-4fec-8671-af74ff0d0faa
Commons category	Cathryn Lewis
skos:altLabel	Cathryn M Lewis (en) Cathryn M. Lewis (en) Cathryn M. Lewis (nl) Lewis CM (en)
occupation	wds:Q16731445-5E649775-39C5-4733-80C0-54D6DC422BD5 wds:Q16731445-A8EFD650-84FC-4B4C-B4C8-F273C7529A3A
employer	wds:Q16731445-6362CF47-BBB7-4D61-A492-DE282C8B1B5A wds:Q16731445-AE9AB13E-9631-42D3-92A6-FAB7FB23974B wds:Q16731445-B8516D7B-8D8D-4BAE-991F-597AA77F4737
sex or gender	wds:Q16731445-308BDAF0-2281-4786-BB3D-E89E945FE453
educated at	wds:Q16731445-560ee8a7-c928-48b2-9364-c8550f236ba5
family name	wds:Q16731445-9B908775-DDF3-4307-AF85-DC7C1640ACD5
official website	wds:Q16731445-B97088B3-1469-4612-9C7B-0D6CD9E60822
occupation	psychologist geneticist
employer	King's College London
sex or gender	female organism
educated at	University of Oxford
family name	Lewis
official website	https://kclpure.kcl.ac.uk/portal/en/persons/cathryn-lewis(c24b651a-a53b-4370-9a65-ae96800fab7b).html
ORCID iD	wds:Q16731445-05C8D81B-6894-418F-AA17-6DEA18A9EEDC
ORCID iD	https://orcid.org/0000-0002-8249-8476
ORCID iD	0000-0002-8249-8476
Gateway to Research person ID	wds:Q16731445-E4C85EA6-DA2E-461B-B868-524DEAB8EADE
Gateway to Research person ID	2C8449A4-22C8-4857-A9A3-BF4A17360F53
ResearcherID	wds:Q16731445-3988BD2A-8E95-45A8-9F72-307F127EECFF
Publons author ID	wds:Q16731445-daeabe02-5162-43b2-b080-861c618fa395
ResearcherID	A-5225-2010
Publons author ID	2849048
is owl:sameAs of	Cathryn Lewis
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q16731445 Cathryn Lewis Category:Cathryn Lewis
is author of	Meta-Analysis of Genome-wide Linkage Studies in BMI and Obesity* Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations Power of the TDT to detect association: effect of linkage disequilibrium between genetic markers and an unobserved disease mutation Genetic association studies: design, analysis and interpretation Establishing the characteristics of an effective pharmacogenetic test for clozapine-induced agranulocytosis Genetic Modeling of Abnormal Photosensitivity in Families with Polymorphic Light Eruption and Actinic Prurigo Standardization and statistical approaches to therapeutic trials in the R6/2 mouse Introduction to genetic association studies A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis Predicting the risk of rheumatoid arthritis and its age of onset through modelling genetic risk variants with smoking Meta-analysis of the association of urbanicity with schizophrenia Advances in the genetics of schizophrenia: will high-risk copy number variants be useful in clinical genetics or diagnostics? Estimating risks of common complex diseases across genetic and environmental factors: the example of Crohn disease. Apolipoprotein E polymorphisms influence effect of pravastatin on survival after myocardial infarction in a Mediterranean population: the GISSI-Prevenzione study Tumor necrosis factor and its targets in the inflammatory cytokine pathway are identified as putative transcriptomic biomarkers for escitalopram response. Genetic Factors Influencing Coagulation Factor XIII B-Subunit Contribute to Risk of Ischemic Stroke Investigating the genetic variation underlying episodicity in major depressive disorder: suggestive evidence for a bipolar contribution Pharmacogenetic variants in the DPYD, TYMS, CDA and MTHFR genes are clinically significant predictors of fluoropyrimidine toxicity Genetics of inflammatory bowel disease: progress and prospects Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship Multipoint linkage analysis of a candidate gene locus in rheumatoid arthritis demonstrates significant evidence of linkage and association with the corticotropin-releasing hormone genomic region Modelling the effects of penetrance and family size on rates of sporadic and familial disease. A Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5 Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

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