About: Marylyn D. Ritchie

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

Professor of Genetics

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) 研究者 (ja) investigador (es) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) Professor of Genetics (en) biochemicus (nl)
rdfs:label	Marylyn D. Ritchie (en) Marylyn D. Ritchie (es) Marylyn D. Ritchie (sq) Marylyn D. Ritchie (ast) Marylyn Ritchie (nl)
skos:prefLabel	Marylyn D. Ritchie (en) Marylyn D. Ritchie (es) Marylyn D. Ritchie (sq) Marylyn D. Ritchie (ast) Marylyn Ritchie (nl)
name	Marylyn D. Ritchie (en) Marylyn D. Ritchie (es) Marylyn D. Ritchie (sq) Marylyn D. Ritchie (ast) Marylyn Ritchie (nl)
Freebase ID	wds:Q18631934-9300E4EA-2549-4607-87BE-03596A401D69
Freebase ID	/m/0128rjmc
given name	wds:Q18631934-DAE3048D-32F9-4AB2-93F3-1EBC423D745E
given name	Marylyn
instance of	wds:Q18631934-168A4279-D3B5-436D-BB10-974C7E03459C
instance of	Homo sapiens
Academic Tree ID	wds:Q18631934-c8b1a460-4406-ebf0-b01c-3d5432376414
Academic Tree ID	713033
Google Scholar author ID	wds:Q18631934-FC46ADB3-7B56-4F30-91EC-8D09410D04A2
Google Scholar author ID	cfuoZagAAAAJ
skos:altLabel	Marylyn DeRiggi Ritchie (en) Marylyn Ritchie (en)
occupation	wds:Q18631934-5983cdf2-e351-46eb-afa1-d2cd2dc1f10b wds:Q18631934-ADE62F92-47C9-48AA-AA42-4B29541614AA
employer	wds:Q18631934-107735A1-9942-4783-A8B6-840523DDEDFA wds:Q18631934-32009691-999F-425D-9735-E0FF9BC2BAC9 wds:Q18631934-6CA3CDD2-BC21-4E25-A777-F3D123045E14
NUKAT ID	wds:Q18631934-2E0AC931-9EE9-48CA-B1A2-0DA9AE06B57F
sex or gender	wds:Q18631934-FF799FED-D62E-48E8-9779-83C7A556DDD6
ISNI	wds:Q18631934-6ACC844D-53D1-4463-9061-6C885FDDB44A
VIAF ID	wds:Q18631934-4f8a8dd3-4928-03d7-40c8-544ff277b088
GND ID	wds:Q18631934-829f1fda-5573-46a3-bb48-edc82699dfca
Library of Congress authority ID	wds:Q18631934-6e02d9da-4c50-9b9d-0437-e0c8b3950126
DBLP author ID	wds:Q18631934-E0BF3E64-F9A9-4ADD-B485-2DA46C5CD072
openMLOL author ID	wds:Q18631934-3842BAEE-1A2D-4F02-B53B-BBDB693B592C wds:Q18631934-8030C35F-BB63-47EB-AA08-D9AFF38DAEF7
family name	wds:Q18631934-E05C8E6B-E533-4DC9-9287-B034ECA331CB
VIAF ID	http://viaf.org/viaf/163356832
GND ID	https://d-nb.info/gnd/1250930855
Library of Congress authority ID	http://id.loc.gov/authorities/names/no2005011936
DBLP author ID	https://dblp.org/pid/65/714.rdf
occupation	researcher biochemist
employer	Vanderbilt University Pennsylvania State University University of Pennsylvania
NUKAT ID	n2010120387
sex or gender	female organism
ISNI	0000000112174137
VIAF ID	163356832
GND ID	1250930855
Library of Congress authority ID	no2005011936
DBLP author ID	65/714
openMLOL author ID	296599 294618
family name	Ritchie
ORCID iD	wds:Q18631934-93185753-41d8-2b19-b36e-0d02c567e389
ORCID iD	https://orcid.org/0000-0002-1208-1720
ORCID iD	0000-0002-1208-1720
is owl:sameAs of	Marylyn D. Ritchie
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q18631934 Marylyn D. Ritchie
is author of	Genetic studies of body mass index yield new insights for obesity biology Meta-analysis identifies six new susceptibility loci for atrial fibrillation Interaction between interleukin 3 and dystrobrevin-binding protein 1 in schizophrenia Power of multifactor dimensionality reduction for detecting gene-gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneity A novel method to identify gene-gene effects in nuclear families: the MDR-PDT. A general framework for formal tests of interaction after exhaustive search methods with applications to MDR and MDR-PDT. Identifying the genotype behind the phenotype: a role model found in VKORC1 and its association with warfarin dosing Assessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical records The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network Using prior knowledge and genome-wide association to identify pathways involved in multiple sclerosis Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgery Polymorphism modulates symptomatic response to antiarrhythmic drug therapy in patients with lone atrial fibrillation Model-based multifactor dimensionality reduction for detecting epistasis in case-control data in the presence of noise Exploring the performance of Multifactor Dimensionality Reduction in large scale SNP studies and in the presence of genetic heterogeneity among epistatic disease models A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains Effects of smoking on the genetic risk of obesity: the population architecture using genomics and epidemiology study A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. Association of the FTO obesity risk variant rs8050136 with percentage of energy intake from fat in multiple racial/ethnic populations: the PAGE study Optimizing drug outcomes through pharmacogenetics: a case for preemptive genotyping The Challenges of Whole-Genome Approaches to Common Diseases

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