(Q36716183)

English

Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate

scientific article published on 12 January 2012

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate (English)

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

0 references

passive smoking

1 reference

based on heuristic

1 reference

based on heuristic

Ethylin Wang Jabs

object named as

Ethylin Wang Jabs

13

0 references

Mary L. Marazita

18

object named as

Mary L Marazita

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Philip Kuo-Ting Chen

12

object named as

Philip K Chen

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

author name string

Tao Wu

1

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

M Daniele Fallin

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Min Shi

3

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Ingo Ruczinski

4

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Kung Yee Liang

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Jacqueline B Hetmanski

6

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Hong Wang

7

1 reference

Europe PubMed Central

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15 August 2017

Roxann G Ingersoll

8

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Shangzhi Huang

9

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Xiaoqian Ye

10

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Yah-Huei Wu-Chou

11

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Bing Shi

14

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Richard Redett

15

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Alan F Scott

16

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Jeffrey C Murray

17

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Ronald G Munger

19

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Terri H Beaty

20

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

publication date

12 January 2012

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Birth Defects Research Part A: Clinical and Molecular Teratology

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

94

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

76-83

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Regulation of bone development and extracellular matrix protein genes by RUNX2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Importance of gene-environment interactions in the etiology of selected birth defects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Folate intake, markers of folate status and oral clefts: is the evidence converging?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Epidemiology underpinning research in the aetiology of orofacial clefts.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Identification of risk-related haplotypes with the use of multiple SNPs from nuclear families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Mitotic retention of gene expression patterns by the cell fate-determining transcription factor Runx2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Asian oral-facial cleft birth prevalence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Runx2 regulates the expression of GNAS on SaOs-2 cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Runx2: a master organizer of gene transcription in developing and maturing osteoblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Assessing maternal genetic associations: a comparison of the log-linear approach to case-parent triad data and a case-control approach.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Minireview: GNAS: normal and abnormal functions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Phenotypic changes in dentition of Runx2 homozygote-null mutant mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

The genetic basis for skeletal diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Nonsyndromic cleft lip and palate: complex genetics and environmental effects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Methods for detection of parent-of-origin effects in genetic studies of case-parents triads

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Achondroplasia is defined by recurrent G380R mutations of FGFR3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

30 September 2017

Association among polymorphisms at MYH9, environmental factors, and nonsyndromic orofacial clefts in western China

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

28 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

28 June 2018

Testing for linkage disequilibrium, maternal effects, and imprinting with (In)complete case-parent triads, by use of the computer program LEM.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

28 June 2018

Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

28 June 2018

General score tests for associations of genetic markers with disease using cases and their parents.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

28 June 2018

Analysis of interactions between genetic variants of BMP4 and environmental factors with nonsyndromic cleft lip with or without cleft palate susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

Genetic susceptibilities in the association between maternal exposure to tobacco smoke and the risk of nonsyndromic oral cleft.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

Testing and estimating gene-environment interactions in family-based association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

snp.plotter: an R-based SNP/haplotype association and linkage disequilibrium plotting package.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

Gene-environment interactions in rare diseases that include common birth defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

Cigarette smoking and exposure to environmental tobacco smoke in China: the international collaborative study of cardiovascular disease in Asia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

Duplicate zebrafish runx2 orthologues are expressed in developing skeletal elements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

Runx2 integrates estrogen activity in osteoblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

A natural history of cleidocranial dysplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

Identification of a stop codon mutation in the CBFA1 runt domain from a patient with cleidocranial dysplasia and cleft lip.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

Infant TGF-alpha genotype, orofacial clefts, and maternal periconceptional multivitamin use.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3608124

5 September 2018

Cleft lip and palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/22241686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testing candidate genes for non-syndromic oral clefts using a case-parent trio design

1 reference

https://pubmed.ncbi.nlm.nih.gov/22241686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6

1 reference

https://pubmed.ncbi.nlm.nih.gov/22241686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/22241686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exploiting gene-environment interaction to detect genetic associations

1 reference

https://pubmed.ncbi.nlm.nih.gov/22241686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/BDRA.22885

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

0 references

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