(Q35524572)

8 August 2017

title

Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms (English)

1 reference

8 August 2017

3

Sumantra Chatterjee

1 reference

8 August 2017

Ashish Kapoor

1

1 reference

8 August 2017

Qian Jiang

2

1 reference

8 August 2017

Prakash Chakraborty

4

1 reference

8 August 2017

Maria X Sosa

5

1 reference

8 August 2017

Courtney Berrios

6

1 reference

8 August 2017

Aravinda Chakravarti

7

1 reference

8 August 2017

publication date

9 February 2015

1 reference

8 August 2017

published in

Human Molecular Genetics

1 reference

8 August 2017

volume

24

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8 August 2017

issue

10

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8 August 2017

page(s)

2997-3003

1 reference

describes a project that uses

8 August 2017

Bayes' theorem

1 reference

18 June 2022

https://europepmc.org/article/PMC/4406299

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

Contribution of rare and common variants determine complex diseases-Hirschsprung disease as a model

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

Mutational spectrum of semaphorin 3A and semaphorin 3D genes in Spanish Hirschsprung patients

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

Comprehensive analysis of NRG1 common and rare variants in Hirschsprung patients

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

Hirschsprung disease, associated syndromes and genetics: a review

27 July 2018

1 reference

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

27 July 2018

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The neuregulin-I/ErbB signaling system in development and disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

Semaphorins command cells to move

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

Genetics of Hirschsprung disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

The semaphorin genes encode a family of transmembrane and secreted growth cone guidance molecules

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

A genetic study of Hirschsprung disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

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.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4406299

Population genetics--making sense out of sequence

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25666438

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Semaphorin 3A expression in the colon of Hirschsprung disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25666438

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDV051

1 reference

8 August 2017

1 reference

8 August 2017

1 reference