about
sameAs
Rarity of the Alzheimer disease-protective APP A673T variant in the United StatesInflammatory response after influenza vaccination in men with and without carotid artery diseaseFunctional genomic of the paraoxonase (PON1) polymorphisms: effects on pesticide sensitivity, cardiovascular disease, and drug metabolismPharmacogenomic considerations of the paraoxonase polymorphismsA common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease riskRole of paraoxonase (PON1) status in pesticide sensitivity: genetic and temporal determinantsDetectable clonal mosaicism from birth to old age and its relationship to cancerConfirmation of the reported association of clonal chromosomal mosaicism with an increased risk of incident hematologic cancerConducting a large, multi-site survey about patients' views on broad consent: challenges and solutionsPerformance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research ConsortiumThe phenotypic legacy of admixture between modern humans and NeandertalsCharacterizing genetic variants for clinical actionReturn of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) NetworkThe Electronic Medical Records and Genomics (eMERGE) Network: past, present, and futureInformed Consent in Genome-Scale Research: What Do Prospective Participants Think?Genomic research and wide data sharing: views of prospective participantsThe eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studiesCommon variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project.Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.Actionable exomic incidental findings in 6503 participants: challenges of variant classificationRare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing ProjectWhole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes lociExome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families.WNT1 mutations in families affected by moderately severe and progressive recessive osteogenesis imperfecta.Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association studyToll-like receptor 1 polymorphisms affect innate immune responses and outcomes in sepsis.Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6qPolymorphisms of the IL1-receptor antagonist gene (IL1RN) are associated with multiple markers of systemic inflammation.Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the USGenetic and nongenetic sources of variation in phospholipid transfer protein activityGenetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk.Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).Return of results in the genomic medicine projects of the eMERGE networkPLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activityJoint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia.Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS dataSummary report: Missing data and pedigree and genotyping errors.
P50
Q27346292-56D2AFE1-AE13-4994-9B6A-EE22C44FF880Q28200616-48E82C82-6FE4-471F-AB44-419A72BD4FF6Q28202894-97F7A7DA-20DB-4401-8F85-84AC4CC36C09Q28203018-C6F981BF-B9D7-43C4-A973-C29142FFA9DBQ28259831-920C2F52-B687-4601-AC66-1918BFC84ACDQ28268258-511E7D64-9A6D-4FD4-903E-F4B94F87BC9AQ28385149-7D115040-0CF6-4E8B-897A-B310BB681189Q28396075-CE469025-2A2C-4251-8B33-1C81BC1435E0Q28593352-074677D7-02B4-48AC-B01D-6EC6BCAAEB41Q28601251-3E233CAE-601E-4E56-8F2D-8CC7F132B521Q28603615-4823B921-EDBA-4072-BAA5-5425ECD766B4Q28655937-8BE97F75-1292-4D1F-A026-1F46C4BFC090Q28673413-12AF0813-970F-4FFB-98E4-A371CE85B135Q28674604-8570B6E2-8825-4986-A3D3-D6F7F64547E6Q28704258-143DDE43-7666-4282-B63F-0BAE62E3F289Q28742349-C0294AF0-2255-4E3C-AEB2-C23F8B11EC20Q28742793-DD207718-2129-4FA1-BACC-5E016DD1E569Q28943325-A1E9707C-2440-4E2F-8E8B-D458267302CEQ30276732-CA52FD99-A29B-4A4A-BE67-37DF4054AA45Q30299967-F9768EC8-9F24-4B54-A918-B0E900133B93Q30300875-04B6F493-E0C8-4A77-AF02-55E8EA534247Q30393812-2E31B8C2-1CBC-4080-8359-0D7B3603DF5FQ30411390-7081568C-82E7-4DA5-B1D4-14B2010FD7FAQ30419436-D759CB1C-5D18-49D7-935D-CBA232B41F63Q30425020-87387B60-23C8-4EAE-B541-34739399B822Q30426901-459E2080-579E-4BA6-9099-5312EE5CC03AQ30448491-04E17B74-1B21-42BA-B57D-AE91634C156EQ30459046-8201647D-500B-431F-8062-60248AF31C14Q30483818-363F29CD-42D5-4D43-A971-DE70DF04C83DQ30486850-81D0A156-5F65-47EF-83C2-E6EBB1298368Q30490407-B96185E3-D9E2-4763-B77C-FF4DE4DFF6B4Q30490882-00DC0340-0C3D-497E-8636-EDF39F9CE92AQ30494062-32395E25-FF15-4E67-BDAE-520BA367DA83Q30497894-BAD0C1FE-EE92-4A37-B064-FEB7B3E65C3FQ30557139-9DD12C25-29D5-402F-B24C-97EA7BAF9716Q30575241-516FDF7A-5C74-4BE7-B1CD-6D44039DE7EEQ30655573-F7A88E39-55F5-440B-A877-921B6F7B01A9Q30700100-4FCF007B-636C-4CA9-9B99-6E8AC09F74FAQ30717783-1E40E89C-8507-4208-88A0-75CD692DAB88Q30884666-EE44846A-D11F-40B7-BB26-2E3493809064
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
ricercatrice
@it
հետազոտող
@hy
name
Gail Jarvik
@es
Gail Jarvik
@nl
Gail Jarvik
@sl
Gail P. Jarvik
@en
type
label
Gail Jarvik
@es
Gail Jarvik
@nl
Gail Jarvik
@sl
Gail P. Jarvik
@en
altLabel
Gail Jarvik
@en
Gail P Jarvik
@en
prefLabel
Gail Jarvik
@es
Gail Jarvik
@nl
Gail Jarvik
@sl
Gail P. Jarvik
@en
P973
P214
P244
P2671
P166
P21
P214
P2381
P244
no2015039430
P2671
/g/11f3jy6pyv
P31
P496
0000-0002-6710-8708
P569
1959-02-08T00:00:00Z
P734
P7859
lccn-no2015039430