Rajkovic A - Search Results

1

Gene variants identified by whole-exome sequencing in 33 French women with premature ovarian insufficiency.

Yang X, Touraine P, Desai S, Humphreys G, Jiang H, Yatsenko A, Rajkovic A. Yang X, et al. Among authors: rajkovic a. J Assist Reprod Genet. 2019 Jan;36(1):39-45. doi: 10.1007/s10815-018-1349-4. Epub 2018 Nov 7. J Assist Reprod Genet. 2019. PMID: 30406445 Free PMC article.

2

Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency.

Ochalski ME, Engle N, Wakim A, Ravnan BJ, Hoffner L, Rajkovic A, Surti U. Ochalski ME, et al. Among authors: rajkovic a. Fertil Steril. 2011 Jun;95(7):2433.e9-15. doi: 10.1016/j.fertnstert.2011.03.082. Epub 2011 Apr 29. Fertil Steril. 2011. PMID: 21530964 Free article.

3

Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas.

McGuire MM, Yatsenko A, Hoffner L, Jones M, Surti U, Rajkovic A. McGuire MM, et al. Among authors: rajkovic a. PLoS One. 2012;7(3):e33251. doi: 10.1371/journal.pone.0033251. Epub 2012 Mar 12. PLoS One. 2012. PMID: 22428002 Free PMC article.

4

High quality RNA in semen and sperm: isolation, analysis and potential application in clinical testing.

Georgiadis AP, Kishore A, Zorrilla M, Jaffe TM, Sanfilippo JS, Volk E, Rajkovic A, Yatsenko AN. Georgiadis AP, et al. Among authors: rajkovic a. J Urol. 2015 Jan;193(1):352-9. doi: 10.1016/j.juro.2014.07.107. Epub 2014 Aug 1. J Urol. 2015. PMID: 25088949 Free PMC article.

5

Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability.

AlAsiri S, Basit S, Wood-Trageser MA, Yatsenko SA, Jeffries EP, Surti U, Ketterer DM, Afzal S, Ramzan K, Faiyaz-Ul Haque M, Jiang H, Trakselis MA, Rajkovic A. AlAsiri S, et al. Among authors: rajkovic a. J Clin Invest. 2015 Jan;125(1):258-62. doi: 10.1172/JCI78473. Epub 2014 Dec 1. J Clin Invest. 2015. PMID: 25437880 Free PMC article.

6

MCM9 mutations are associated with ovarian failure, short stature, and chromosomal instability.

Wood-Trageser MA, Gurbuz F, Yatsenko SA, Jeffries EP, Kotan LD, Surti U, Ketterer DM, Matic J, Chipkin J, Jiang H, Trakselis MA, Topaloglu AK, Rajkovic A. Wood-Trageser MA, et al. Among authors: rajkovic a. Am J Hum Genet. 2014 Dec 4;95(6):754-62. doi: 10.1016/j.ajhg.2014.11.002. Am J Hum Genet. 2014. PMID: 25480036 Free PMC article.

7

Novel Inactivating Mutation of the FSH Receptor in Two Siblings of Indian Origin With Premature Ovarian Failure.

Katari S, Wood-Trageser MA, Jiang H, Kalynchuk E, Muzumdar R, Yatsenko SA, Rajkovic A. Katari S, et al. Among authors: rajkovic a. J Clin Endocrinol Metab. 2015 Jun;100(6):2154-7. doi: 10.1210/jc.2015-1401. Epub 2015 Apr 15. J Clin Endocrinol Metab. 2015. PMID: 25875778 Free PMC article.

8

X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.

Yatsenko AN, Georgiadis AP, Röpke A, Berman AJ, Jaffe T, Olszewska M, Westernströer B, Sanfilippo J, Kurpisz M, Rajkovic A, Yatsenko SA, Kliesch S, Schlatt S, Tüttelmann F. Yatsenko AN, et al. Among authors: rajkovic a. N Engl J Med. 2015 May 28;372(22):2097-107. doi: 10.1056/NEJMoa1406192. Epub 2015 May 13. N Engl J Med. 2015. PMID: 25970010 Free PMC article.

9

Prenatal whole-exome sequencing: parental attitudes.

Kalynchuk EJ, Althouse A, Parker LS, Saller DN Jr, Rajkovic A. Kalynchuk EJ, et al. Among authors: rajkovic a. Prenat Diagn. 2015 Oct;35(10):1030-6. doi: 10.1002/pd.4635. Epub 2015 Jul 6. Prenat Diagn. 2015. PMID: 26151551

10

High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacy.

Yatsenko SA, Bakos HA, Vitullo K, Kedrov M, Kishore A, Jennings BJ, Surti U, Wood-Trageser MA, Cercone S, Yatsenko AN, Rajkovic A, Iannaccone A. Yatsenko SA, et al. Among authors: rajkovic a. Clin Genet. 2016 Jan;89(1):82-7. doi: 10.1111/cge.12638. Epub 2015 Jul 28. Clin Genet. 2016. PMID: 26153062 Free PMC article.

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