132 related articles for article (PubMed ID: 36447056)
1. Genetic aetiology of Down syndrome birth: novel variants of maternal DNMT3B and RFC1 genes increase risk of meiosis II nondisjunction in the oocyte.
Halder P; Pal U; Ganguly A; Ghosh P; Ray A; Sarkar S; Ghosh S
Mol Genet Genomics; 2023 Jan; 298(1):293-313. PubMed ID: 36447056
[TBL] [Abstract][Full Text] [Related]
2. The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte.
Pal U; Halder P; Ray A; Sarkar S; Datta S; Ghosh P; Ghosh S
PLoS Genet; 2021 Mar; 17(3):e1009462. PubMed ID: 33750944
[TBL] [Abstract][Full Text] [Related]
3. Risk of Down syndrome birth: Consanguineous marriage is associated with maternal meiosis-II nondisjunction at younger age and without any detectable recombination error.
Ray A; Oliver TR; Halder P; Pal U; Sarkar S; Dutta S; Ghosh S
Am J Med Genet A; 2018 Nov; 176(11):2342-2349. PubMed ID: 30240118
[TBL] [Abstract][Full Text] [Related]
4. Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations.
Ghosh S; Feingold E; Dey SK
Am J Med Genet A; 2009 Jul; 149A(7):1415-20. PubMed ID: 19533770
[TBL] [Abstract][Full Text] [Related]
5. A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.
Chernus JM; Allen EG; Zeng Z; Hoffman ER; Hassold TJ; Feingold E; Sherman SL
PLoS Genet; 2019 Dec; 15(12):e1008414. PubMed ID: 31830031
[TBL] [Abstract][Full Text] [Related]
6. New insights into human nondisjunction of chromosome 21 in oocytes.
Oliver TR; Feingold E; Yu K; Cheung V; Tinker S; Yadav-Shah M; Masse N; Sherman SL
PLoS Genet; 2008 Mar; 4(3):e1000033. PubMed ID: 18369452
[TBL] [Abstract][Full Text] [Related]
7. The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.
Antonarakis SE; Petersen MB; McInnis MG; Adelsberger PA; Schinzel AA; Binkert F; Pangalos C; Raoul O; Slaugenhaupt SA; Hafez M
Am J Hum Genet; 1992 Mar; 50(3):544-50. PubMed ID: 1347192
[TBL] [Abstract][Full Text] [Related]
8. Understanding etiology of chromosome 21 nondisjunction from gene × environment models.
Halder P; Pal U; Ganguly A; Ghosh P; Ray A; Sarkar S; Ghosh S
Sci Rep; 2021 Nov; 11(1):22390. PubMed ID: 34789805
[TBL] [Abstract][Full Text] [Related]
9. Telomere length is associated with types of chromosome 21 nondisjunction: a new insight into the maternal age effect on Down syndrome birth.
Ghosh S; Feingold E; Chakraborty S; Dey SK
Hum Genet; 2010 Apr; 127(4):403-9. PubMed ID: 20063167
[TBL] [Abstract][Full Text] [Related]
10. Nondisjunction in trisomy 21: origin and mechanisms.
Petersen MB; Mikkelsen M
Cytogenet Cell Genet; 2000; 91(1-4):199-203. PubMed ID: 11173856
[TBL] [Abstract][Full Text] [Related]
11. Chromosome 21 non-disjunction and Down syndrome birth in an Indian cohort: analysis of incidence and aetiology from family linkage data.
Ghosh S; Bhaumik P; Ghosh P; Dey SK
Genet Res (Camb); 2010 Jun; 92(3):189-97. PubMed ID: 20667163
[TBL] [Abstract][Full Text] [Related]
12. The association between maternal occupation and down syndrome: A report from the national Down syndrome project.
Keen C; Hunter JE; Allen EG; Rocheleau C; Waters M; Sherman SL
Int J Hyg Environ Health; 2020 Jan; 223(1):207-213. PubMed ID: 31519426
[TBL] [Abstract][Full Text] [Related]
13. Maternal risk for down syndrome and polymorphisms in the promoter region of the DNMT3B gene: a case-control study.
Jaiswal SK; Sukla KK; Kumari N; Lakhotia AR; Kumar A; Rai AK
Birth Defects Res A Clin Mol Teratol; 2015 Apr; 103(4):299-305. PubMed ID: 25656965
[TBL] [Abstract][Full Text] [Related]
14. The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project.
Hunter JE; Allen EG; Shin M; Bean LJ; Correa A; Druschel C; Hobbs CA; O'Leary LA; Romitti PA; Royle MH; Torfs CP; Freeman SB; Sherman SL
Genet Med; 2013 Sep; 15(9):698-705. PubMed ID: 23558253
[TBL] [Abstract][Full Text] [Related]
15. Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project.
Hollis ND; Allen EG; Oliver TR; Tinker SW; Druschel C; Hobbs CA; O'Leary LA; Romitti PA; Royle MH; Torfs CP; Freeman SB; Sherman SL; Bean LJ
Am J Med Genet A; 2013 Mar; 161A(3):438-44. PubMed ID: 23401135
[TBL] [Abstract][Full Text] [Related]
16. Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.
Stewart GD; Hassold TJ; Berg A; Watkins P; Tanzi R; Kurnit DM
Am J Hum Genet; 1988 Feb; 42(2):227-36. PubMed ID: 2893544
[TBL] [Abstract][Full Text] [Related]
17. Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defects.
Zittergruen MM; Murray JC; Lauer RM; Burns TL; Sheffield VC
Circulation; 1995 Nov; 92(10):2803-10. PubMed ID: 7586245
[TBL] [Abstract][Full Text] [Related]
18. Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects.
Allen EG; Freeman SB; Druschel C; Hobbs CA; O'Leary LA; Romitti PA; Royle MH; Torfs CP; Sherman SL
Hum Genet; 2009 Feb; 125(1):41-52. PubMed ID: 19050929
[TBL] [Abstract][Full Text] [Related]
19. Association between maternal age and meiotic recombination for trisomy 21.
Lamb NE; Yu K; Shaffer J; Feingold E; Sherman SL
Am J Hum Genet; 2005 Jan; 76(1):91-9. PubMed ID: 15551222
[TBL] [Abstract][Full Text] [Related]
20. The genetics of folate metabolism and maternal risk of birth of a child with Down syndrome and associated congenital heart defects.
Coppedè F
Front Genet; 2015; 6():223. PubMed ID: 26161087
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
