(Q21145019)

22

object named as

Christopher Newton-Cheh

Christopher

Newton-Cheh

1 reference

17 August 2022

3

Itsik Pe'er

Itsik

Pe'er

1 reference

17 August 2022

5

Jacqueline Salit

Jacqueline

Salit

1 reference

17 August 2022

Eimear E Kenny

6

Eimear E

Kenny

1 reference

17 August 2022

Julian B Maller

2

Julian B

Maller

1 reference

17 August 2022

Jia Nee Foo

12

Jia Nee

Foo

1 reference

17 August 2022

Ralph Burkhardt

8

Ralph

Burkhardt

1 reference

17 August 2022

David M Altshuler

26

David M

Altshuler

1 reference

17 August 2022

25

Mark J Daly

Mark J

Daly

1 reference

17 August 2022

4

Benjamin M Neale

Benjamin M

Neale

1 reference

17 August 2022

19

Hope

Ferdowsian

Hope Ferdowsian

1 reference

17 August 2022

7

Jessica L

Shea

Jessica L Shea

1 reference

17 August 2022

9

J Gustav

Smith

J Gustav Smith

1 reference

17 August 2022

27

Jeffrey M

Friedman

Jeffrey M Friedman

1 reference

17 August 2022

Jennifer K Lowe

1

Jennifer K

Lowe

1 reference

17 August 2022

Weizhen Ji

10

Weizhen

Ji

1 reference

17 August 2022

Martha Noel

11

Martha

Noel

1 reference

17 August 2022

Maude L Blundell

13

Maude L

Blundell

1 reference

17 August 2022

Vita Skilling

14

Vita

Skilling

1 reference

17 August 2022

Laura Garcia

15

Laura

Garcia

1 reference

17 August 2022

Marcia L Sullivan

16

Marcia L

Sullivan

1 reference

17 August 2022

Heather E Lee

17

Heather E

Lee

1 reference

17 August 2022

Anna Labek

18

Anna

Labek

1 reference

17 August 2022

Steven B Auerbach

20

Steven B

Auerbach

1 reference

17 August 2022

Richard P Lifton

21

Richard P

Lifton

1 reference

17 August 2022

Jan L Breslow

23

Jan L

Breslow

1 reference

17 August 2022

Markus Stoffel

24

Markus

Creative Commons Attribution 4.0 International

Stoffel

1 reference

17 August 2022

language of work or name

English

0 references

publication date

February 2009

0 references

published in

PLOS Genetics

0 references

volume

5

0 references

page(s)

e1000365

0 references

issue

2

0 references

copyright license

start time

6 February 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Estimation of significance thresholds for genomewide association scans

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

PLINK: a tool set for whole-genome association and population-based linkage analyses

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Structural mechanism for statin inhibition of HMG-CoA reductase

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Many sequence variants affecting diversity of adult human height

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Identification of ten loci associated with height highlights new biological pathways in human growth

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Worldwide human relationships inferred from genome-wide patterns of variation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Genomic control for association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Genotype, haplotype and copy-number variation in worldwide human populations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Linkage analysis of quantitative traits for obesity, diabetes, hypertension, and dyslipidemia on the island of Kosrae, Federated States of Micronesia

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Proteome of H-411E (liver) cells exposed to insulin and tumor necrosis factor-alpha: analysis of proteins involved in insulin resistance

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Complex trait mapping in isolated populations: Are specific statistical methods required?

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Gene finding in genetically isolated populations

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Genetics of population isolates.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Role of the apolipoprotein E polymorphism in determining normal plasma lipid and lipoprotein variation

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Diabetes incidence and prevalence in Pima Indians: a 19-fold greater incidence than in Rochester, Minnesota

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Type 2 diabetes in native Hawaiians and Pacific Islanders in Hawaii.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Implementing a unified approach to family-based tests of association.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

Epidemiology and factor analysis of obesity, type II diabetes, hypertension, and dyslipidemia (syndrome X) on the Island of Kosrae, Federated States of Micronesia

30 May 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000365

High-resolution mapping of crossovers reveals extensive variation in fine-scale recombination patterns among humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000365

Optimal two-stage testing for family-based genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000365

Optimal designs for two-stage genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000365

Qualitative and quantitative effects of APOE genetic variation on plasma C-reactive protein, LDL-cholesterol, and apoE protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000365

Polymorphisms associated with cholesterol and risk of cardiovascular events.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000365

A multivariate family-based association test using generalized estimating equations: FBAT-GEE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000365

Ethnic differences in the prevalence of new and known diabetes mellitus, impaired glucose tolerance, and impaired fasting glucose. Diabetes Heart and Health Survey (DHAH) 2002-2003, Auckland New Zealand.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2628735

The value of isolated populations

29 November 2018

1 reference

12 December 2020

Are common disease susceptibility alleles the same in outbred and founder populations?

1 reference

12 December 2020

Late adolescent growth in stature

1 reference

12 December 2020

Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia

1 reference

12 December 2020

10.1371/JOURNAL.PGEN.1000365

Identifiers

DOI

1 reference

660614

660614

1 reference

1 reference

1 reference