(Q53388910)

English

Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations.

scientific article published in July 2009

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scholarly article

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations. (English)

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

1 reference

based on heuristic

inferred from title

Eleanor Feingold

2

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

author name string

Sujoy Ghosh

1

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

Subrata Kumar Dey

3

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

language of work or name

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publication date

1 July 2009

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

American Journal of Medical Genetics

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

149A

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

7

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

1415-1420

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

New insights into human nondisjunction of chromosome 21 in oocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Epidemiology of Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Polymorphic variation in human meiotic recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

The National Down Syndrome Project: design and implementation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Effect of meiotic recombination on the production of aneuploid gametes in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

The roles of MAD1, MAD2 and MAD3 in meiotic progression and the segregation of nonexchange chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Association between maternal age and meiotic recombination for trisomy 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

A genome-wide screen identifies genes required for centromeric cohesion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Association between spindle assembly checkpoint expression and maternal age in human oocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Spontaneous X chromosome MI and MII nondisjunction events in Drosophila melanogaster oocytes have different recombinational histories.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Recombination and nondisjunction in humans and flies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Exchanges are not equally able to enhance meiotic chromosome segregation in yeast

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Mutant rec-1 eliminates the meiotic pattern of crossing over in Caenorhabditis elegans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

First meiotic division abnormalities in human oocytes: mechanism of trisomy formation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

The yeast med1 mutant undergoes both meiotic homolog nondisjunction and precocious separation of sister chromatids.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Separation anxiety: the etiology of nondisjunction in flies and people.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

Trisomy 21: association between reduced recombination and nondisjunction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

22 May 2018

BubR1 insufficiency causes early onset of aging-associated phenotypes and infertility in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

13 August 2018

Maternal age and trisomy--a unifying mechanism of formation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2732749

13 August 2018

The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination

1 reference

https://pubmed.ncbi.nlm.nih.gov/19533770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiotic nondisjunction does the two-step

1 reference

https://pubmed.ncbi.nlm.nih.gov/19533770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II

1 reference

https://pubmed.ncbi.nlm.nih.gov/19533770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/19533770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal age-specific rates of numerical chromosome abnormalities with special reference to trisomy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19533770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms. Down Syndrome Collaborative Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/19533770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/AJMG.A.32932

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

1 reference

Europe PubMed Central

13 May 2018

http://europepmc.org/abstract/PMC/2732749

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