(Q34213357)

English

High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35. (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

neural tube defect

1 reference

based on heuristic

inferred from title

author name string

Demetra S Stamm

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Evadnie Rampersaud

2

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31 July 2017

Susan H Slifer

3

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31 July 2017

Lorraine Mehltretter

4

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31 July 2017

Deborah G Siegel

5

1 reference

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31 July 2017

Jianzhen Xie

6

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Diane Hu-Lince

7

1 reference

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31 July 2017

David W Craig

8

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31 July 2017

Dietrich A Stephan

9

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31 July 2017

Timothy M George

10

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31 July 2017

John R Gilbert

11

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31 July 2017

Marcy C Speer

12

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31 July 2017

NTD Collaborative Group

13

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31 July 2017

language of work or name

1 reference

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publication date

1 June 2006

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Europe PubMed Central

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31 July 2017

Birth Defects Research Part A: Clinical and Molecular Teratology

1 reference

Europe PubMed Central

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31 July 2017

76

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31 July 2017

6

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31 July 2017

499-505

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Europe PubMed Central

PubMed publication ID

31 July 2017

A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous family.

1 reference

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5 July 2018

Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing

1 reference

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A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis

1 reference

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Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10.

1 reference

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5 July 2018

Non-multifactorial neural tube defects

1 reference

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Current perspectives on the causes of neural tube defects resulting from diabetic pregnancy

1 reference

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Mouse models of neural tube defects: investigating preventive mechanisms.

1 reference

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Comparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility Loci

1 reference

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Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis

1 reference

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5 July 2018

Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps

1 reference

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5 July 2018

Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites

1 reference

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5 July 2018

Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.

1 reference

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5 July 2018

Fumonisins disrupt sphingolipid metabolism, folate transport, and neural tube development in embryo culture and in vivo: a potential risk factor for human neural tube defects among populations consuming fumonisin-contaminated maize

1 reference

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5 July 2018

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

1 reference

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5 July 2018

Mutation of MEF2A in an inherited disorder with features of coronary artery disease

1 reference

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Dorsal closure and convergent extension: two polarised morphogenetic movements controlled by similar mechanisms?

1 reference

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The genetic basis of mammalian neurulation.

1 reference

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The concerted action of Meox homeobox genes is required upstream of genetic pathways essential for the formation, patterning and differentiation of somites

1 reference

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5 July 2018

Epidemiology of neural tube defects

1 reference

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5 July 2018

Neural tube closure requires Dishevelled-dependent convergent extension of the midline

1 reference

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5 July 2018

A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter

1 reference

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5 July 2018

New frontiers in Alzheimer's disease genetics

1 reference

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5 July 2018

Improved inference of relationship for pairs of individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4169147

5 July 2018

Allegro, a new computer program for multipoint linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4169147

5 July 2018

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4169147

5 July 2018

Allele-sharing models: LOD scores and accurate linkage tests

1 reference

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5 July 2018

Accurate inference of relationships in sib-pair linkage studies

1 reference

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Is maternal obesity a risk factor for anencephaly and spina bifida?

1 reference

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5 July 2018

Aneuploidy among prenatally detected neural tube defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4169147

5 July 2018

Etiology and pathogenesis of human neural tube defects: insights from mouse models.

1 reference

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Epidemiological evaluation of the use of genetics to improve the predictive value of disease risk factors.

1 reference

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Clues to the Aetiology of Neural Tube Malformations*

1 reference

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Neural tube defects: a review of human and animal studies on the etiology of neural tube defects

1 reference

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Estimating the power of a proposed linkage study: a practical computer simulation approach

1 reference

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1 reference

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In-utero exposure to valproate and neural tube defects.

1 reference

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1 reference

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Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

1 reference

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1 reference

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Risk of neural tube defect-affected pregnancies among obese women

1 reference

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1 reference

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1 reference

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Valproic acid and spina bifida

1 reference

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1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible teratogenicity of valproic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/16933213

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inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/16933213

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1 reference

https://pubmed.ncbi.nlm.nih.gov/16933213

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inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/16933213

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inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/16933213

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Identifiers

10.1002/BDRA.20272

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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