(Q34549400)

3 August 2017

0 references

Case-control association mapping by proxy using family history of disease (English)

1 reference

3 August 2017

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28092683%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

author name string

Yaniv Erlich

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28092683%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Joseph K Pickrell

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28092683%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

language of work or name

English

0 references

publication date

16 January 2017

1 reference

3 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28092683%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

volume

49

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28092683%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28092683%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

page(s)

325-331

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28092683%20AND%20SRC:MED&resulttype=core&format=json

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age

10 June 2020

cites work

1 reference

Web-based, participant-driven studies yield novel genetic associations for common traits

21 January 2018

1 reference

Invited review: Genomic selection in dairy cattle: progress and challenges

21 January 2018

1 reference

Deregressing estimated breeding values and weighting information for genomic regression analyses

21 January 2018

1 reference

Distribution and location of genetic effects for dairy traits.

21 January 2018

1 reference

The value of relatives with phenotypes but missing genotypes in association studies for quantitative traits

21 January 2018

1 reference

Family-based association tests for genomewide association scans

21 January 2018

1 reference

Unique lipoprotein phenotype and genotype associated with exceptional longevity

21 January 2018

1 reference

Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan

21 January 2018

1 reference

Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants

21 January 2018

1 reference

Power assessment for genetic association study of human longevity using offspring of long-lived subjects

21 January 2018

1 reference

Many sequence variants affecting diversity of adult human height

21 January 2018

1 reference

Parental origin of sequence variants associated with complex diseases

21 January 2018

1 reference

Case-control association testing with related individuals: a more powerful quasi-likelihood score test

21 January 2018

1 reference

Alzheimer Disease in the US Population

21 January 2018

1 reference

Epidemiology of Parkinson's disease

21 January 2018

1 reference

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

21 January 2018

1 reference

Lipoprotein(a) and coronary heart disease. Meta-analysis of prospective studies

21 January 2018

1 reference

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

21 January 2018

1 reference

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

21 January 2018

1 reference

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

21 January 2018

1 reference

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

21 January 2018

1 reference

A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25

21 January 2018

1 reference

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

21 January 2018

1 reference

From genotypes to genes: doubling the sample size

21 January 2018

1 reference

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

21 January 2018

1 reference

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

21 January 2018

1 reference

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

21 January 2018

1 reference

A mega-analysis of genome-wide association studies for major depressive disorder

21 January 2018

1 reference

Consensus analysis of signal peptide peptidase and homologous human aspartic proteases reveals opposite topology of catalytic domains compared with presenilins

21 January 2018

1 reference

CD33 modulates TREM2: convergence of Alzheimer loci.

21 January 2018

1 reference

Conserved epigenomic signals in mice and humans reveal immune basis of Alzheimer's disease

21 January 2018

1 reference

FGD5 mediates proangiogenic action of vascular endothelial growth factor in human vascular endothelial cells.

21 January 2018

1 reference

Vascular endothelial growth factor in heart failure

21 January 2018

1 reference

Phosphatidylinositol transfer protein, cytoplasmic 1 (PITPNC1) binds and transfers phosphatidic acid

21 January 2018

1 reference

Mixed model with correction for case-control ascertainment increases association power

21 January 2018

1 reference

Accurate liability estimation improves power in ascertained case-control studies

21 January 2018

1 reference

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

21 January 2018

1 reference

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

21 January 2018

1 reference

The UK10K project identifies rare variants in health and disease

21 January 2018

1 reference

A global reference for human genetic variation

21 January 2018

1 reference

Mutations in BRIP1 confer high risk of ovarian cancer

21 January 2018

1 reference

In silico method for inferring genotypes in pedigrees

21 January 2018

1 reference

Second-generation PLINK: rising to the challenge of larger and richer datasets

21 January 2018

1 reference

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

21 January 2018

1 reference

Efficient Bayesian mixed-model analysis increases association power in large cohorts.

21 January 2018

1 reference

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

21 January 2018

1 reference

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

21 January 2018

1 reference

7 January 2021

Personalized investigation

1 reference

7 January 2021

Genome hacker uncovers largest-ever family tree

1 reference

7 January 2021

Software for generating liability distributions for pedigrees conditional on their observed disease states and covariates

1 reference

7 January 2021

An atlas of genetic correlations across human diseases and traits

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG.3766

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28092683%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

1 reference