Chantot-Bastaraud S - Search Results

1

Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders.

Nava C, Keren B, Mignot C, Rastetter A, Chantot-Bastaraud S, Faudet A, Fonteneau E, Amiet C, Laurent C, Jacquette A, Whalen S, Afenjar A, Périsse D, Doummar D, Dorison N, Leboyer M, Siffroi JP, Cohen D, Brice A, Héron D, Depienne C. Nava C, et al. Eur J Hum Genet. 2014 Jan;22(1):71-8. doi: 10.1038/ejhg.2013.88. Epub 2013 May 1. Eur J Hum Genet. 2014. PMID: 23632794 Free PMC article.

2

CGH and direct diagnosis of mosaic structural chromosomal abnormalities: description of a mosaic ring chromosome 17 and review of the literature.

Dupont C, Pipiras E, Chantot-Bastaraud S, Verloes A, Baumann C, Wolf JP, Benzacken B. Dupont C, et al. Eur J Hum Genet. 2003 Jun;11(6):452-6. doi: 10.1038/sj.ejhg.5200984. Eur J Hum Genet. 2003. PMID: 12774038

3

[Genetic origin of spermatogenesis impairments: clinical aspects and relationships with mouse models of infertility].

Siffroi JP, Chantot-Bastaraud S, Ravel C. Siffroi JP, et al. Gynecol Obstet Fertil. 2003 Jun;31(6):504-15. doi: 10.1016/s1297-9589(03)00133-4. Gynecol Obstet Fertil. 2003. PMID: 12865188 Review. French.

4

Structural chromosomal mosaicism and prenatal diagnosis.

Pipiras E, Dupont C, Chantot-Bastaraud S, Siffroi JP, Bucourt M, Batallan A, Largillière C, Uzan M, Wolf JP, Benzacken B. Pipiras E, et al. Prenat Diagn. 2004 Feb;24(2):101-3. doi: 10.1002/pd.797. Prenat Diagn. 2004. PMID: 14974115

5

[The future of cytogenetics after the sequencing of the human genome].

Siffroi JP, Chantot-Bastaraud S. Siffroi JP, et al. Morphologie. 2004 Apr;88(280):19-23. doi: 10.1016/s1286-0115(04)97993-3. Morphologie. 2004. PMID: 15208808 Review. French.

6

GR/GR deletions within the azoospermia factor c region on the Y chromosome might not be associated with spermatogenic failure.

Ravel C, Chantot-Bastaraud S, El Houate B, Mandelbaum J, Siffroi JP, McElreavey K. Ravel C, et al. Fertil Steril. 2006 Jan;85(1):229-31. doi: 10.1016/j.fertnstert.2005.07.1278. Fertil Steril. 2006. PMID: 16412764 Free article.

7

Y chromosome variants and male reproductive function.

McElreavey K, Ravel C, Chantot-Bastaraud S, Siffroi JP. McElreavey K, et al. Int J Androl. 2006 Feb;29(1):298-303; discussion 304-6. doi: 10.1111/j.1365-2605.2005.00637.x. Int J Androl. 2006. PMID: 16466551 Review.

8

Tail stump syndrome associated with chromosomal translocation in two brothers attempting intracytoplasmic sperm injection.

Ravel C, Chantot-Bastaraud S, Siffroi JP, Escalier D, Antoine JM, Mandelbaum J. Ravel C, et al. Fertil Steril. 2006 Sep;86(3):719.e1-7. doi: 10.1016/j.fertnstert.2005.12.078. Fertil Steril. 2006. PMID: 16952512 Free article.

9

Sperm-FISH analysis in a pericentric chromosome 1 inversion, 46,XY,inv(1)(p22q42), associated with infertility.

Chantot-Bastaraud S, Ravel C, Berthaut I, McElreavey K, Bouchard P, Mandelbaum J, Siffroi JP. Chantot-Bastaraud S, et al. Mol Hum Reprod. 2007 Jan;13(1):55-9. doi: 10.1093/molehr/gal094. Epub 2006 Oct 31. Mol Hum Reprod. 2007. PMID: 17077110

10

Mutations in the protamine 1 gene associated with male infertility.

Ravel C, Chantot-Bastaraud S, El Houate B, Berthaut I, Verstraete L, De Larouziere V, Lourenço D, Dumaine A, Antoine JM, Mandelbaum J, Siffroi JP, McElreavey K. Ravel C, et al. Mol Hum Reprod. 2007 Jul;13(7):461-4. doi: 10.1093/molehr/gam031. Epub 2007 May 9. Mol Hum Reprod. 2007. PMID: 17494104

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