(Q21202163)

17 August 2022

8

Donna K Arnett

Donna K

Arnett

1 reference

17 August 2022

Nathan E Wineinger

1

Nathan E

Wineinger

1 reference

17 August 2022

Amit Patki

2

Amit

Patki

1 reference

17 August 2022

Kristin J Meyers

3

Kristin J

Meyers

1 reference

17 August 2022

Ulrich Broeckel

4

Ulrich

Broeckel

1 reference

17 August 2022

Charles C Gu

5

Charles C

Gu

1 reference

17 August 2022

D C Rao

6

DC

Rao

1 reference

17 August 2022

Hemant K Tiwari

9

Hemant K

Tiwari

1 reference

Finding the missing heritability of complex diseases

17 August 2022

language of work or name

English

0 references

publication date

2011

0 references

published in

BMC Medical Genomics

0 references

volume

4

0 references

issue

1

0 references

page(s)

4

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Novel genetic variants contributing to left ventricular hypertrophy: the HyperGEN study

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

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

6 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

A whole genome scan for pulse pressure/stroke volume ratio in African Americans: the HyperGEN study

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

A haplotype map of the human genome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Control of confounding of genetic associations in stratified populations

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

The transmission/disequilibrium test: history, subdivision, and admixture

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Principal components analysis corrects for stratification in genome-wide association studies

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Origins and functional impact of copy number variation in the human genome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

On the allelic spectrum of human 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=3027088

Tackling the widespread and critical impact of batch effects in high-throughput data

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Mixed linear model approach adapted for genome-wide association studies

10 May 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Copy number variation in African Americans

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Lack of adrenomedullin in the mouse brain results in behavioral changes, anxiety, and lower survival under stress conditions.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Aortic root diameter and longitudinal blood pressure tracking

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Genomewide rapid association using mixed model and regression: a fast and simple method for genomewide pedigree-based quantitative trait loci association analysis

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Genome-wide association studies: theoretical and practical concerns

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Measuring and using admixture to study the genetics of complex diseases

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Population admixture may appear to mask, change or reverse genetic effects of genes underlying complex traits

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

CGRP-RCP, a novel protein required for signal transduction at calcitonin gene-related peptide and adrenomedullin receptors.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Replication of the Wellcome Trust genome-wide association study on essential hypertension in a Korean population

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Aortic root dilatation as a cause of isolated, severe aortic regurgitation. Prevalence, clinical and echocardiographic patterns, and relation to left ventricular hypertrophy and function

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Two-dimensional echocardiographic aortic root dimensions in normal children and adults

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Determinants of echocardiographic aortic root size. The Framingham Heart Study

30 May 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-4

Aortic root dilatation at sinuses of valsalva and aortic regurgitation in hypertensive and normotensive subjects: The Hypertension Genetic Epidemiology Network Study .

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-4

Effect of hypertension on aortic root size and prevalence of aortic regurgitation

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-4

A genome scan for linkage with aortic root diameter in hypertensive African Americans and whites in the Hypertension Genetic Epidemiology Network (HyperGEN) study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-4

A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-4

Ambulatory blood pressure, target organ damage and aortic root size in never-treated essential hypertensive patients

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Alteration of the adrenomedullin receptor components gene expression associated with the blood pressure in pregnancy-induced hypertension

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Prognostic significance of the pattern of aortic root dilation in the Marfan syndrome

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027088

Impedance progress: aortic diameter rears its head again?

29 November 2018

1 reference

12 December 2020

Pulse pressure is inversely related to aortic root diameter implications for the pathogenesis of systolic hypertension

1 reference

12 December 2020

Prodynorphin gene promoter polymorphism and temporal lobe epilepsy

1 reference

12 December 2020

Central pulse pressure is a major determinant of ascending aorta dilation in Marfan syndrome

1 reference

12 December 2020

Dominant inheritance in two families with familial Mediterranean fever (FMF)

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-4

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1186/1755-8794-4-4

1 reference

0 references

1 reference

1 reference

PubMed publication ID

21223598

1 reference