Oates RD - Search Results

1

Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the Y chromosome, and of 18 children conceived via ICSI.

Oates RD, Silber S, Brown LG, Page DC. Oates RD, et al. Hum Reprod. 2002 Nov;17(11):2813-24. doi: 10.1093/humrep/17.11.2813. Hum Reprod. 2002. PMID: 12407032

2

Azoospermic men with deletion of the DAZ gene cluster are capable of completing spermatogenesis: fertilization, normal embryonic development and pregnancy occur when retrieved testicular spermatozoa are used for intracytoplasmic sperm injection.

Mulhall JP, Reijo R, Alagappan R, Brown L, Page D, Carson R, Oates RD. Mulhall JP, et al. Among authors: oates rd. Hum Reprod. 1997 Mar;12(3):503-8. doi: 10.1093/humrep/12.3.503. Hum Reprod. 1997. PMID: 9130751

3

AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes.

Rozen SG, Marszalek JD, Irenze K, Skaletsky H, Brown LG, Oates RD, Silber SJ, Ardlie K, Page DC. Rozen SG, et al. Among authors: oates rd. Am J Hum Genet. 2012 Nov 2;91(5):890-6. doi: 10.1016/j.ajhg.2012.09.003. Epub 2012 Oct 25. Am J Hum Genet. 2012. PMID: 23103232 Free PMC article.

4

The pituitary-testicular axis in Klinefelter's syndrome and in oligo-azoospermic patients with and without deletions of the Y chromosome long arm.

Tomasi PA, Oates R, Brown L, Delitala G, Page DC. Tomasi PA, et al. Clin Endocrinol (Oxf). 2003 Aug;59(2):214-22. doi: 10.1046/j.1365-2265.2003.01828.x. Clin Endocrinol (Oxf). 2003. PMID: 12864799

5

Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure.

Repping S, Skaletsky H, Lange J, Silber S, Van Der Veen F, Oates RD, Page DC, Rozen S. Repping S, et al. Among authors: oates rd. Am J Hum Genet. 2002 Oct;71(4):906-22. doi: 10.1086/342928. Epub 2002 Sep 20. Am J Hum Genet. 2002. PMID: 12297986 Free PMC article.

6

Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection.

Repping S, Skaletsky H, Brown L, van Daalen SK, Korver CM, Pyntikova T, Kuroda-Kawaguchi T, de Vries JW, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Repping S, et al. Among authors: oates rd. Nat Genet. 2003 Nov;35(3):247-51. doi: 10.1038/ng1250. Epub 2003 Oct 5. Nat Genet. 2003. PMID: 14528305

7

A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region.

Repping S, van Daalen SK, Korver CM, Brown LG, Marszalek JD, Gianotten J, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Repping S, et al. Among authors: oates rd. Genomics. 2004 Jun;83(6):1046-52. doi: 10.1016/j.ygeno.2003.12.018. Genomics. 2004. PMID: 15177557

8

Genetic characterization of a missense mutation in the X-linked TAF7L gene identified in an oligozoospermic man†.

Ling L, Li F, Yang P, Oates RD, Silber S, Kurischko C, Luca FC, Leu NA, Zhang J, Yue Q, Skaletsky H, Brown LG, Rozen SG, Page DC, Wang PJ, Zheng K. Ling L, et al. Among authors: oates rd. Biol Reprod. 2022 Jul 25;107(1):157-167. doi: 10.1093/biolre/ioac093. Biol Reprod. 2022. PMID: 35554494 Free PMC article.

9

The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.

Kuroda-Kawaguchi T, Skaletsky H, Brown LG, Minx PJ, Cordum HS, Waterston RH, Wilson RK, Silber S, Oates R, Rozen S, Page DC. Kuroda-Kawaguchi T, et al. Nat Genet. 2001 Nov;29(3):279-86. doi: 10.1038/ng757. Nat Genet. 2001. PMID: 11687796

10

TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.

Yang F, Silber S, Leu NA, Oates RD, Marszalek JD, Skaletsky H, Brown LG, Rozen S, Page DC, Wang PJ. Yang F, et al. Among authors: oates rd. EMBO Mol Med. 2015 Sep;7(9):1198-210. doi: 10.15252/emmm.201404967. EMBO Mol Med. 2015. PMID: 26136358 Free PMC article.

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