Oddoux C - Search Results

1

Prenatal diagnostic testing for familial dysautonomia using linked genetic markers.

Oddoux C, Reich E, Axelrod F, Blumenfeld A, Maayan C, Slaugenhaupt S, Gusella J, Ostrer H. Oddoux C, et al. Prenat Diagn. 1995 Sep;15(9):817-26. doi: 10.1002/pd.1970150905. Prenat Diagn. 1995. PMID: 8559751

2

Identification of the first non-Jewish mutation in familial Dysautonomia.

Leyne M, Mull J, Gill SP, Cuajungco MP, Oddoux C, Blumenfeld A, Maayan C, Gusella JF, Axelrod FB, Slaugenhaupt SA. Leyne M, et al. Among authors: oddoux c. Am J Med Genet A. 2003 May 1;118A(4):305-8. doi: 10.1002/ajmg.a.20052. Am J Med Genet A. 2003. PMID: 12687659

3

High-level inducible expression of visual pigments in transfected cells.

Kazmi MA, Dubin RA, Oddoux C, Ostrer H. Kazmi MA, et al. Among authors: oddoux c. Biotechniques. 1996 Aug;21(2):304-11. doi: 10.2144/96212rr05. Biotechniques. 1996. PMID: 8862817 Free article.

4

Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11.

Wistinghausen B, Reischer A, Oddoux C, Ostrer H, Nardi M, Karpatkin M. Wistinghausen B, et al. Among authors: oddoux c. Br J Haematol. 1997 Dec;99(3):575-7. doi: 10.1046/j.1365-2141.1997.4343244.x. Br J Haematol. 1997. PMID: 9401068 Free article.

5

Mendelian diseases among Roman Jews: implications for the origins of disease alleles.

Oddoux C, Guillen-Navarro E, Ditivoli C, Dicave E, Cilio MR, Clayton CM, Nelson H, Sarafoglou K, McCain N, Peretz H, Seligsohn U, Luzzatto L, Nafa K, Nardi M, Karpatkin M, Aksentijevich I, Kastner D, Axelrod F, Ostrer H. Oddoux C, et al. J Clin Endocrinol Metab. 1999 Dec;84(12):4405-9. doi: 10.1210/jcem.84.12.6268. J Clin Endocrinol Metab. 1999. PMID: 10599695 Review.

6

The genetic history of Cochin Jews from India.

Waldman YY, Biddanda A, Dubrovsky M, Campbell CL, Oddoux C, Friedman E, Atzmon G, Halperin E, Ostrer H, Keinan A. Waldman YY, et al. Among authors: oddoux c. Hum Genet. 2016 Oct;135(10):1127-43. doi: 10.1007/s00439-016-1698-y. Epub 2016 Jul 4. Hum Genet. 2016. PMID: 27377974 Free PMC article.

7

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%.

Oddoux C, Struewing JP, Clayton CM, Neuhausen S, Brody LC, Kaback M, Haas B, Norton L, Borgen P, Jhanwar S, Goldgar D, Ostrer H, Offit K. Oddoux C, et al. Nat Genet. 1996 Oct;14(2):188-90. doi: 10.1038/ng1096-188. Nat Genet. 1996. PMID: 8841192

8

The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defects.

Fitzgerald T, Duva S, Ostrer H, Pass K, Oddoux C, Ruben R, Caggana M. Fitzgerald T, et al. Among authors: oddoux c. Clin Genet. 2004 Apr;65(4):338-42. doi: 10.1111/j.1399-0004.2004.00233.x. Clin Genet. 2004. PMID: 15025729

9

The impact of Converso Jews on the genomes of modern Latin Americans.

Velez C, Palamara PF, Guevara-Aguirre J, Hao L, Karafet T, Guevara-Aguirre M, Pearlman A, Oddoux C, Hammer M, Burns E, Pe'er I, Atzmon G, Ostrer H. Velez C, et al. Among authors: oddoux c. Hum Genet. 2012 Feb;131(2):251-63. doi: 10.1007/s00439-011-1072-z. Epub 2011 Jul 26. Hum Genet. 2012. PMID: 21789512

10

The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry.

Waldman YY, Biddanda A, Davidson NR, Billing-Ross P, Dubrovsky M, Campbell CL, Oddoux C, Friedman E, Atzmon G, Halperin E, Ostrer H, Keinan A. Waldman YY, et al. Among authors: oddoux c. PLoS One. 2016 Mar 24;11(3):e0152056. doi: 10.1371/journal.pone.0152056. eCollection 2016. PLoS One. 2016. PMID: 27010569 Free PMC article.

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