Literature DB >> 7081294

Neural tube defects in France: segregation analysis.

F Demenais, M Le Merrer, M L Briard, R C Elston.   

Abstract

Segregation analysis was performed on a subset of a large body of French data comprising 298 nuclear families. Two models were used in this analysis: the transmission probability model [Elston and Stewart, 1971; Elston, 1981] and the mixed model [Morton and MacLean, 1974]. Both models are consistent with familial aggregation of neural tube defects, in this sample, being due to either the segregation of a recessive major gene or a sibling environmental effect, or both factors. In each case, other environmental factors are also involved. These results were compared to the findings of other studies and discussed in respect to the diversity of the epidemiological features displayed by different populations. Some observations of vertical transmission in a British study and the proportion of affected first cousins, in both France and Great Britain, lead us to reject a possible absence of transmission. We propose a monogenic component with a large influence of environmental factors, some of which may be common to sibs, to explain the occurrence of neural tube defects in this sample.

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Year:  1982        PMID: 7081294     DOI: 10.1002/ajmg.1320110305

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  9 in total

1.  Complex segregation analysis of nonsyndromic cleft lip and palate.

Authors:  J T Hecht; P Yang; V V Michels; K H Buetow
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025

2.  Missing genetic risk in neural tube defects: can exome sequencing yield an insight?

Authors:  Deidre R Krupp; Karen L Soldano; Melanie E Garrett; Heidi Cope; Allison E Ashley-Koch; Simon G Gregory
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2014-07-21

Review 3.  Genetic epidemiology of neural tube defects.

Authors:  Philip J Lupo; A J Agopian; Heidi Castillo; Jonathan Castillo; Gerald H Clayton; Nienke P Dosa; Betsy Hopson; David B Joseph; Brandon G Rocque; William O Walker; John S Wiener; Laura E Mitchell
Journal:  J Pediatr Rehabil Med       Date:  2017-12-11

4.  Genetic study of indirect inguinal hernia.

Authors:  Y Gong; C Shao; Q Sun; B Chen; Y Jiang; C Guo; J Wei; Y Guo
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

Review 5.  Human neural tube defects: developmental biology, epidemiology, and genetics.

Authors:  Eric R Detrait; Timothy M George; Heather C Etchevers; John R Gilbert; Michel Vekemans; Marcy C Speer
Journal:  Neurotoxicol Teratol       Date:  2005-03-05       Impact factor: 3.763

6.  On the possibility of pleiotropic monogenic control of hereditary polyposis and primary cancer of the colon.

Authors:  E K Ginsburg; T I Axenovich; B A Altshouler; M D Bazhenova
Journal:  Am J Hum Genet       Date:  1989-02       Impact factor: 11.025

7.  Mapping a chromosomal locus for valproic acid-induced exencephaly in mice.

Authors:  Yunxia Wang Lundberg; Robert M Cabrera; Kimberly A Greer; Jian Zhao; Rohit Garg; Richard H Finnell
Journal:  Mamm Genome       Date:  2004-05       Impact factor: 2.957

8.  Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects.

Authors:  Kristen L Deak; Deborah G Siegel; Timothy M George; Simon Gregory; Allison Ashley-Koch; Marcy C Speer
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2008-10

9.  Absence of linkage between familial neural tube defects and PAX3 gene.

Authors:  S Chatkupt; F A Hol; Y Y Shugart; M P Geurds; E S Stenroos; M R Koenigsberger; B C Hamel; W G Johnson; E C Mariman
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

  9 in total

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