Exome sequencing and the genetic basis of complex traits - Wikidata - awgldk - TriplyDB

Exome sequencing and the genetic basis of complex traits

Exome sequencing and the genetic basis of complex traits

http://www.wikidata.org/entity/Q37056084

about

OTX2 duplication is implicated in hemifacial microsomia Association claims in the sequencing era Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic Epidemiology AP1S3 mutations are associated with pustular psoriasis and impaired Toll-like receptor 3 trafficking Emerging Genomic Tools for Legume Breeding: Current Status and Future Prospects Genetic studies of rheumatoid arthritis Interrogating the major histocompatibility complex with high-throughput genomics Challenges in medical applications of whole exome/genome sequencing discoveries Medical genomics: The intricate path from genetic variant identification to clinical interpretation Exome sequencing and complex disease: practical aspects of rare variant association studies Genetic Risk Factors for Ischemic and Hemorrhagic Stroke Mutations and altered expression of SERPINF1 in patients with familial otosclerosis Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes Connectivity Homology Enables Inter-Species Network Models of Synthetic Lethality Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models Guidelines for investigating causality of sequence variants in human disease Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project.Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis.The impact of host genetic variation on infection with HIV-1.Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks Fine-scale patterns of population stratification confound rare variant association tests.Association of exome sequences with plasma C-reactive protein levels in >9000 participants.Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.A practical method to detect SNVs and indels from whole genome and exome sequencing data.Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.Effective filtering strategies to improve data quality from population-based whole exome sequencing studies.Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data.Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations.Likelihood-based complex trait association testing for arbitrary depth sequencing data.The Use of Non-Variant Sites to Improve the Clinical Assessment of Whole-Genome Sequence Data.Prioritization Of Nonsynonymous Single Nucleotide Variants For Exome Sequencing Studies Via Integrative Learning On Multiple Genomic Data.Global inference of disease-causing single nucleotide variants from exome sequencing data The next generation of complex lung genetic studies.Association study between SNP rs150689919 in the DNA demethylation gene, TET1, and Parkinson's disease in Chinese Han population.708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.The impact of population demography and selection on the genetic architecture of complex traits.Sequencing your genome: what does it mean?Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.Genetic architecture of retinal and macular degenerative diseases: the promise and challenges of next-generation sequencing.

P2860

Q21090627-610BEC48-408C-4C85-9A1B-35115D5BB355 Q24273315-5F394349-5557-4901-B1BE-99719EA292C2 Q24273406-73C2E87E-0965-4E7D-A481-9933F2E3A7C7 Q24296788-02935AAF-903F-4527-9078-264D7C394B6B Q26747385-7D0E2FF1-5866-487D-925D-E4F959A29ECE Q26783892-18F55787-614E-4EFA-92BC-BB4252C8716E Q26822705-C8B86B9D-FF3B-4187-8317-E17BE1A80390 Q26824047-225C542E-EE87-479B-8AD3-9EEDBBC15459 Q26824974-8BA28BDB-8BBB-427B-A06F-BE1DB25E1B83 Q27027055-B2826A71-6E41-41AC-8E59-77D6874F8353 Q28079249-F36C4CD9-1CB5-4CF4-AF52-F21E92671F37 Q28397220-8EB339F7-1DC8-405F-9321-C24943948741 Q28546038-A1A91267-7B66-4146-BEC5-07C3EA8F0998 Q28550178-12FA3E1D-22C9-4C8A-AAE3-CF57F65583C2 Q28647065-C1AF3441-3E4C-4AAF-9026-2ADA303030BD Q28655218-30682097-D0F4-4899-A9B2-672A0261F0DB Q30275850-8683FC9C-1C28-4EC9-BAA5-7325D4D51F08 Q30278692-6C07DCC2-419B-4601-BD87-330F77DAF3B5 Q30373501-73AD7BA6-EA09-4C0A-8513-FB61C784F1DC Q30374810-0AE7CA0D-5D25-4CE9-9F3D-4DB394B989E8 Q30411387-82E18608-8FBE-48FD-9234-27EF70504A4B Q30418221-E0B4EC7E-8274-4CE2-8D65-1307AF6F79C5 Q30459027-9B6F6466-B376-41C0-A13B-CE332ECF0C27 Q30490228-AF96AD82-F86F-4831-AFB0-1AD09CD49748 Q30653786-76D85EA3-A003-444F-B3A8-76C8BAF33861 Q30809578-5DA11D02-6B7E-4879-90CD-0900BFBD095D Q30828110-662FC38F-EF5D-42B2-A1EB-09DFE63E8967 Q30832807-1DB3E292-2810-48C5-90CA-DB47B351FA4D Q30884606-4D8E4DD9-D9EE-484A-B73E-A4A635AA4322 Q30952543-A2FEB915-5DA0-4C6E-B9E7-5BDABEA34C33 Q30978835-2E2C33E9-C684-43E5-AC62-E7DB609A8B8C Q31004569-59423DB6-DB23-4D1E-BBE8-71A51E274A5F Q31159221-04565739-561A-4020-A21D-449D1B56FBB1 Q33354240-FA04B8BA-503B-4F35-951A-E0502F926C96 Q33641207-A8AA2324-D740-4DF3-B13D-06828EB98212 Q33652520-2335AE58-8009-47AB-8BF2-07DABBEA5142 Q33686100-01FE01AC-7249-4263-B357-7614798E5725 Q33732868-49011C32-FD2E-4905-BE93-797FDD4A9A32 Q33747916-EF4D1468-7345-446C-A95A-28C8D09D4C51 Q33790443-2FAA7466-6657-4733-83ED-A7DBE7266BBC

P2860

Exome sequencing and the genetic basis of complex traits

http://www.wikidata.org/entity/Q37056084

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 29 May 2012

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Exome sequencing and the genetic basis of complex traits

@en

Exome sequencing and the genetic basis of complex traits.

@nl

type

label

Exome sequencing and the genetic basis of complex traits

@en

Exome sequencing and the genetic basis of complex traits.

@nl

prefLabel

Exome sequencing and the genetic basis of complex traits

@en

Exome sequencing and the genetic basis of complex traits.

@nl

P1433

Q37056084-98D03622-7BA6-4672-B842-F506ECCF67AA

P1476

Q37056084-E9DAE327-6BD4-4802-A12D-A11E0F6FF0D3

P2093

Q37056084-01992FBC-A8F5-4117-9A49-97A4AF3B36C6

Q37056084-1AF01C11-0F88-4EC3-93B7-283937ECB526

Q37056084-42FFD349-1DB2-44DC-87EC-24A4F0BBE62A

Q37056084-4C667F46-6CF9-4490-B09B-9CFA1E2789C7

Q37056084-7A71990D-F098-4D43-B3C4-04526780472E

Q37056084-8D8DE301-10FA-4BF2-AEBC-FB4E22BF839E

Q37056084-9F7057FA-A5C8-4C11-B3A8-10ECEE95D1BA

Q37056084-A05FB0FE-D952-48D6-8E19-D149B2740B92

Q37056084-A98E0285-E5E9-4355-97CE-E418E3252DF0

Q37056084-B6B322E9-A276-4EA7-9754-915A7D1C7FF1

P2860

Q37056084-0347AC72-4B4D-4488-991A-DC028D3F6DAD

Q37056084-03753B95-501D-4EC8-9E56-60975B16B983

Q37056084-07FD581D-193C-4D1D-87F1-C5473A6486D8

Q37056084-0A4418EE-8087-4838-BD9F-B86C93686DDA

Q37056084-1261A72A-22C7-4136-B491-8F52C3C9D9C5

Q37056084-128E7C0D-CB3A-4BB7-9C41-1548423456DF

Q37056084-14D23BD6-C8B0-412F-9DC4-983A97C55C8D

Q37056084-18216E6F-2338-4C64-85F6-DB4651E93C05

Q37056084-24EB4877-ED9C-41CA-8F68-BF2EC2BD0372

Q37056084-27748305-5546-4D0B-B995-35A7916BC2E6

P2888

Q37056084-061670F8-C9E0-4AF3-AE4C-C4524BB0D1DD

P304

Q37056084-2BC6A7DD-DC6D-457D-A24F-E38824C84A23

P31

Q37056084-7D2FB71C-B781-4BB3-A965-C9686F8CCE62

P356

Q37056084-6A3DDDC0-13F7-4761-94A2-6F873867ECC5

P407

Q37056084-D18AAF3C-1980-441E-907F-84C2CEAE8D76

P433

Q37056084-C80657CB-A544-4794-87C8-2A87FD782EC8

P478

Q37056084-DD10CB80-F6CC-44F5-98E9-D32B97CA1AE0

P50

Q37056084-1028843C-544F-41AB-9E18-AEDCA3AC0F70

Q37056084-6D14F40E-F7FE-4D17-A3B2-F326BA27F20D

Q37056084-775A7524-5964-4640-9761-F71DCDBB21FB

Q37056084-91BB9C2A-42E5-49C6-A890-A4D70847EDBC

Q37056084-98663BAF-07E8-473C-915F-E5D6335D14CE

Q37056084-CF35D965-AD20-40BB-838F-4780465819EF

P577

Q37056084-FB522D9D-9361-4061-92DC-3E79F055540C

P5875

Q37056084-035CF432-B9A1-4C07-9871-9F5A4964E70E

P6179

Q37056084-A2C36C19-11E5-4D1C-A0B8-B8891225F1D7

P698

Q37056084-F38C53CB-90AE-49F7-87DC-8A32C2948EAD

P932

Q37056084-A599C546-2AD8-47A9-AC5D-4B92EC43304A

P356

P1433

Nature Genetics

P1476

Exome sequencing and the genetic basis of complex traits

@en

P2093

Adam Kiezun

http://www.w3.org/2001/XMLSchema#string

Alkes L Price

http://www.w3.org/2001/XMLSchema#string

Benjamin M Neale

http://www.w3.org/2001/XMLSchema#string

Kiran Garimella

http://www.w3.org/2001/XMLSchema#string

Namrata Gupta

http://www.w3.org/2001/XMLSchema#string

Pamela Sklar

http://www.w3.org/2001/XMLSchema#string

Patrick F Sullivan

http://www.w3.org/2001/XMLSchema#string

Paul I W de Bakker

http://www.w3.org/2001/XMLSchema#string

Ron Do

http://www.w3.org/2001/XMLSchema#string

Shamil R Sunyaev

http://www.w3.org/2001/XMLSchema#string

P2860

The distribution of fitness effects of new deleterious amino acid mutations in humans

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

The allelic architecture of human disease genes: common disease-common variant... or not?

Are rare variants responsible for susceptibility to complex diseases?

Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

Inference of population structure using multilocus genotype data

Estimate of the mutation rate per nucleotide in humans

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Targeted capture and massively parallel sequencing of 12 human exomes

P2888

P304

623-630

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/NG.2303

http://www.w3.org/2001/XMLSchema#string

P407

P433

6

http://www.w3.org/2001/XMLSchema#string

P478

44

http://www.w3.org/2001/XMLSchema#string

P50

Patrik K E Magnusson

Jennifer L. Moran

Paul J. McLaren

Nathan O Stitziel

Paul Lichtenstein

Christina M. Hultman

P577

2012-05-29T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

225068993

http://www.w3.org/2001/XMLSchema#string

P6179

1000345582

http://www.w3.org/2001/XMLSchema#string

P698

22641211

http://www.w3.org/2001/XMLSchema#string

P932

3727622

http://www.w3.org/2001/XMLSchema#string