McElreavey K - Search Results

1

New technologies for the identification of novel genetic markers of disorders of sex development (DSD).

Bashamboo A, Ledig S, Wieacker P, Achermann JC, McElreavey K. Bashamboo A, et al. Among authors: mcelreavey k. Sex Dev. 2010 Sep;4(4-5):213-24. doi: 10.1159/000314917. Epub 2010 Jul 3. Sex Dev. 2010. PMID: 20820110 Free PMC article. Review.

2

The genetic basis of murine and human sex determination: a review.

McElreavey K, Barbaux S, Ion A, Fellous M. McElreavey K, et al. Heredity (Edinb). 1995 Dec;75 ( Pt 6):599-611. doi: 10.1038/hdy.1995.179. Heredity (Edinb). 1995. PMID: 8575930 Review.

3

Sex determination and the Y chromosome.

McElreavey K, Fellous M. McElreavey K, et al. Am J Med Genet. 1999 Dec 29;89(4):176-85. doi: 10.1002/(sici)1096-8628(19991229)89:4<176::aid-ajmg2>3.0.co;2-b. Am J Med Genet. 1999. PMID: 10727993 Review.

4

Identification of a Y chromosome haplogroup associated with reduced sperm counts.

Krausz C, Quintana-Murci L, Rajpert-De Meyts E, Jørgensen N, Jobling MA, Rosser ZH, Skakkebaek NE, McElreavey K. Krausz C, et al. Among authors: mcelreavey k. Hum Mol Genet. 2001 Sep 1;10(18):1873-7. doi: 10.1093/hmg/10.18.1873. Hum Mol Genet. 2001. PMID: 11555623

5

Mutations in NR5A1 associated with ovarian insufficiency.

Lourenço D, Brauner R, Lin L, De Perdigo A, Weryha G, Muresan M, Boudjenah R, Guerra-Junior G, Maciel-Guerra AT, Achermann JC, McElreavey K, Bashamboo A. Lourenço D, et al. Among authors: mcelreavey k. N Engl J Med. 2009 Mar 19;360(12):1200-10. doi: 10.1056/NEJMoa0806228. Epub 2009 Feb 25. N Engl J Med. 2009. PMID: 19246354 Free PMC article.

6

Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility.

Vinci G, Brauner R, Tar A, Rouba H, Sheth J, Sheth F, Ravel C, McElreavey K, Bashamboo A. Vinci G, et al. Among authors: mcelreavey k. Fertil Steril. 2009 Oct;92(4):1347-1350. doi: 10.1016/j.fertnstert.2009.04.009. Epub 2009 May 21. Fertil Steril. 2009. PMID: 19463995 Free article.

7

Lack of association between genetic polymorphisms in enzymes associated with folate metabolism and unexplained reduced sperm counts.

Ravel C, Chantot-Bastaraud S, Chalmey C, Barreiro L, Aknin-Seifer I, Pfeffer J, Berthaut I, Mathieu EE, Mandelbaum J, Siffroi JP, McElreavey K, Bashamboo A. Ravel C, et al. Among authors: mcelreavey k. PLoS One. 2009 Aug 6;4(8):e6540. doi: 10.1371/journal.pone.0006540. PLoS One. 2009. PMID: 19657388 Free PMC article.

8

Novel human pathological mutations. Gene symbol: SRY. Disease: XY sex reversal.

Ravel C, Lakhal B, Elghezal H, Braham R, Saad A, Bashamboo A, Siffroi JP, McElreavey K, Christin-Maitre S. Ravel C, et al. Among authors: mcelreavey k. Hum Genet. 2009 Aug;126(2):333. Hum Genet. 2009. PMID: 19694000 No abstract available.

9

[NR5A1 and ovarian failure].

Bashamboo A, Ravel C, Brauner R, McElreavey K. Bashamboo A, et al. Among authors: mcelreavey k. Med Sci (Paris). 2009 Oct;25(10):809-13. doi: 10.1051/medsci/20092510809. Med Sci (Paris). 2009. PMID: 19849982 Free article. Review. French.

10

NR5A1/SF-1 and development and function of the ovary.

Bashamboo A, McElreavey K. Bashamboo A, et al. Among authors: mcelreavey k. Ann Endocrinol (Paris). 2010 May;71(3):177-82. doi: 10.1016/j.ando.2010.02.013. Epub 2010 Apr 14. Ann Endocrinol (Paris). 2010. PMID: 20394914 Review.

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