Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations (Q37383875)

20 August 2017

Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations (English)

1 reference

20 August 2017

Ethylin W Jabs

14

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Sun Ha Jee

object named as

Sun Ha Jee

13

0 references

Philip Kuo-Ting Chen

8

object named as

Philip K Chen

1 reference

20 August 2017

12

Beyoung Yun Park

1 reference

20 August 2017

Jae Woong Sull

1

1 reference

20 August 2017

Kung-Yee Liang

2

1 reference

20 August 2017

Jacqueline B Hetmanski

3

1 reference

20 August 2017

Margaret Daniele Fallin

4

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20 August 2017

Roxanne G Ingersoll

5

1 reference

20 August 2017

Jiwan Park

6

1 reference

20 August 2017

Yah-Huei Wu-Chou

7

1 reference

20 August 2017

Samuel S Chong

9

1 reference

20 August 2017

Felicia Cheah

10

1 reference

20 August 2017

Vincent Yeow

11

1 reference

20 August 2017

Richard Redett

15

1 reference

20 August 2017

Alan F Scott

16

1 reference

20 August 2017

Terri H Beaty

17

1 reference

20 August 2017

14 January 2009

1 reference

European Journal of Human Genetics

20 August 2017

1 reference

20 August 2017

17

1 reference

20 August 2017

6

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20 August 2017

831-839

1 reference

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

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Human genetic factors in nonsyndromic cleft lip and palate: an update

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Rhabdomyosarcomas in adults and children: an update

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Specification of the neural crest occurs during gastrulation and requires Pax7

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

A hybrid design for studying genetic influences on risk of diseases with onset early in life

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

A Pax3/Pax7-dependent population of skeletal muscle progenitor cells

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Haploview: analysis and visualization of LD and haplotype maps

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Maximum-likelihood estimation of haplotype frequencies in nuclear families

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

The complex genetics of cleft lip and palate

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

What good is genomic imprinting: the function of parent-specific gene expression

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Glial cells generate neurons: the role of the transcription factor Pax6.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Genetic and biochemical diversity in the Pax gene family

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Transmission/disequilibrium tests using multiple tightly linked markers

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

In vivo amplification of the PAX3-FKHR and PAX7-FKHR fusion genes in alveolar rhabdomyosarcoma

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Parental-origin-specific epigenetic modification of the mouse H19 gene

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Achondroplasia is defined by recurrent G380R mutations of FGFR3

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Missense mutations in the DNA-binding region and termination codon in PAX6.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Pax genes and their roles in cell differentiation and development

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Hau-Pax3/7A is an early marker of leech mesoderm involved in segmental morphogenesis, nephridial development, and body cavity formation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

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

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

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

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Sex ratio and cleft lip with or without cleft palate.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palate

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Upstream CpG island methylation of the PAX3 gene in human rhabdomyosarcomas.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Highly parallel SNP genotyping

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

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.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate?

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

The conflict theory of genomic imprinting: how much can be explained?

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760446

BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping

2 September 2018

1 reference

12 December 2020

Testing for genetic associations with the PAX gene family in a spina bifida population

1 reference

12 December 2020

Sex ratio and associated risk factors for 50 congenital anomaly types: clues for causal heterogeneity

1 reference

12 December 2020

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

1 reference

12 December 2020

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

1 reference

12 December 2020

Evaluation of Nyholt's procedure for multiple testing correction

1 reference

12 December 2020

PAX9 and TGFB3 are linked to susceptibility to nonsyndromic cleft lip with or without cleft palate in the Japanese: population-based and family-based candidate gene analyses

1 reference

12 December 2020

Detection of parent-of-origin effects in nuclear families using haplotype analysis

1 reference

12 December 2020

Dense SNP association study for bipolar I disorder on chromosome 18p11 suggests two loci with excess paternal transmission

1 reference

12 December 2020

Identifiers

DOI

10.1038/EJHG.2008.250

1 reference

20 August 2017

1 reference

20 August 2017

PubMed publication ID

19142206

1 reference