BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 20667163)

  • 1. 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]  

  • 2. 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]  

  • 3. Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.
    Lamb NE; Feingold E; Savage A; Avramopoulos D; Freeman S; Gu Y; Hallberg A; Hersey J; Karadima G; Pettay D; Saker D; Shen J; Taft L; Mikkelsen M; Petersen MB; Hassold T; Sherman SL
    Hum Mol Genet; 1997 Sep; 6(9):1391-9. PubMed ID: 9285774
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Parental origin, nondisjunction, and recombination of the extra chromosome 21 in Down syndrome: a study in a sample of the Colombian population.
    Ramírez NJ; Belalcázar HM; Yunis JJ; Quintero LN; Arboleda GH; Arboleda H
    Biomedica; 2007 Mar; 27(1):141-8. PubMed ID: 17546231
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21.
    Sherman SL; Lamb NE; Feingold E
    Biochem Soc Trans; 2006 Aug; 34(Pt 4):578-80. PubMed ID: 16856865
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Origin and mechanisms of non-disjunction in human autosomal trisomies.
    Nicolaidis P; Petersen MB
    Hum Reprod; 1998 Feb; 13(2):313-9. PubMed ID: 9557829
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II.
    Lamb NE; Freeman SB; Savage-Austin A; Pettay D; Taft L; Hersey J; Gu Y; Shen J; Saker D; May KM; Avramopoulos D; Petersen MB; Hallberg A; Mikkelsen M; Hassold TJ; Sherman SL
    Nat Genet; 1996 Dec; 14(4):400-5. PubMed ID: 8944019
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome.
    Vorsanova SG; Iourov IY; Beresheva AK; Demidova IA; Monakhov VV; Kravets VS; Bartseva OB; Goyko EA; Soloviev IV; Yurov YB
    Tsitol Genet; 2005; 39(6):30-6. PubMed ID: 16396318
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.
    Ballesta F; Queralt R; Gómez D; Solsona E; Guitart M; Ezquerra M; Moreno J; Oliva R
    Ann Genet; 1999; 42(1):11-5. PubMed ID: 10214502
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Young mothers and higher incidence of maternal meiosis-I non- disjunction: Interplay of environmental exposure and genetic alterations during halt phase in trisomy 21.
    Saiyed N; Bakshi S; Muthuswamy S; Agarwal S
    Reprod Toxicol; 2018 Aug; 79():1-7. PubMed ID: 29702247
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Parental age and the origin of extra chromosome 21 in Down syndrome.
    Jyothy A; Kumar KS; Mallikarjuna GN; Babu Rao V; Uma Devi B; Sujatha M; Reddy PP
    J Hum Genet; 2001; 46(6):347-50. PubMed ID: 11393539
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.