Coskun S - Search Results

1

Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease.

Kaya N, Imtiaz F, Colak D, Al-Sayed M, Al-Odaib A, Al-Zahrani F, Al-Mubarak BR, Al-Owain M, Al-Dhalaan H, Chedrawi A, Al-Hassnan Z, Coskun S, Sakati N, Ozand P, Meyer BF. Kaya N, et al. Among authors: coskun s. Genet Med. 2008 Sep;10(9):675-84. doi: 10.1097/gim.0b013e31818337a8. Genet Med. 2008. PMID: 18978679 Free article.

2

Pregnancy after preimplantation genetic diagnosis for Sanjad-Sakati syndrome.

Hellani A, Aqueel A, Jaroudi K, Ozand P, Coskun S. Hellani A, et al. Among authors: coskun s. Prenat Diagn. 2004 Apr;24(4):302-6. doi: 10.1002/pd.841. Prenat Diagn. 2004. PMID: 15065107

3

Multiple displacement amplification on single cell and possible PGD applications.

Hellani A, Coskun S, Benkhalifa M, Tbakhi A, Sakati N, Al-Odaib A, Ozand P. Hellani A, et al. Among authors: coskun s. Mol Hum Reprod. 2004 Nov;10(11):847-52. doi: 10.1093/molehr/gah114. Epub 2004 Oct 1. Mol Hum Reprod. 2004. PMID: 15465849

4

Preimplantation genetic diagnosis for Niemann-Pick disease type B.

Hellani A, Schuchman EH, Al-Odaib A, Al Aqueel A, Jaroudi K, Ozand P, Coskun S. Hellani A, et al. Among authors: coskun s. Prenat Diagn. 2004 Dec 15;24(12):943-8. doi: 10.1002/pd.1050. Prenat Diagn. 2004. PMID: 15612058

5

Transcriptional profiling of granulosa cells from a patient with recurrent empty follicle syndrome.

Inan MS, Al-Hassan S, Ozand P, Coskun S. Inan MS, et al. Among authors: coskun s. Reprod Biomed Online. 2006 Oct;13(4):481-91. doi: 10.1016/s1472-6483(10)60634-7. Reprod Biomed Online. 2006. PMID: 17007665

6

Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemia.

Kaya N, Al-Owain M, Albakheet A, Colak D, Al-Odaib A, Imtiaz F, Coskun S, Al-Sayed M, Al-Hassnan Z, Al-Zaidan H, Meyer B, Ozand P. Kaya N, et al. Among authors: coskun s. Eur J Med Genet. 2008 Nov-Dec;51(6):558-65. doi: 10.1016/j.ejmg.2008.08.001. Epub 2008 Aug 26. Eur J Med Genet. 2008. PMID: 18790721

7

Preimplantation genetic diagnosis of Morquio disease.

Qubbaj W, Al-Aqeel AI, Al-Hassnan Z, Al-Duraihim A, Awartani K, Al-Rejjal R, Coskun S. Qubbaj W, et al. Among authors: coskun s. Prenat Diagn. 2008 Oct;28(10):900-3. doi: 10.1002/pd.2081. Prenat Diagn. 2008. PMID: 18792995

8

Gene expression profiling of granulosa cells from PCOS patients following varying doses of human chorionic gonadotropin.

Coskun S, Otu HH, Awartani KA, Al-Alwan LA, Al-Hassan S, Al-Mayman H, Kaya N, Inan MS. Coskun S, et al. J Assist Reprod Genet. 2013 Mar;30(3):341-52. doi: 10.1007/s10815-013-9935-y. Epub 2013 Feb 5. J Assist Reprod Genet. 2013. PMID: 23381551 Free PMC article.

9

Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro.

Natesan SA, Bladon AJ, Coskun S, Qubbaj W, Prates R, Munne S, Coonen E, Dreesen JC, Stevens SJ, Paulussen AD, Stock-Myer SE, Wilton LJ, Jaroudi S, Wells D, Brown AP, Handyside AH. Natesan SA, et al. Among authors: coskun s. Genet Med. 2014 Nov;16(11):838-45. doi: 10.1038/gim.2014.45. Epub 2014 May 8. Genet Med. 2014. PMID: 24810687 Free PMC article.

10

Cell-free DNA levels of twins and sibling pairs indicate individuality and possible use as a personalized biomarker.

Alghofaili L, Almubarak H, Gassem K, Islam SS, Coskun S, Kaya N, Karakas B. Alghofaili L, et al. Among authors: coskun s. PLoS One. 2019 Oct 10;14(10):e0223470. doi: 10.1371/journal.pone.0223470. eCollection 2019. PLoS One. 2019. PMID: 31600277 Free PMC article.

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