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Genes|April 3, 2021
Evaluation of a Custom Design Gene Panel as a Diagnostic Tool for Human Non-Syndromic InfertilityOzlem Okutman, Julien Tarabeux, Jean Muller, et al.Journal of Assisted Reproduction and Genetics|September 28, 2018
Genetic evaluation of patients with non-syndromic male infertilityOzlem Okutman, Maroua Ben Rhouma, Moncef Benkhalifa, et al.Human Reproduction (Oxford, England)|December 16, 2022
A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrestOzlem Okutman, Manon Boivin, Jean Muller, et al.Molecular Human Reproduction|October 31, 2015
Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermiaHouda Ghédir, Samira Ibala-Romdhane, Ozlem Okutman, et al.The Turkish Journal of Pediatrics|August 19, 2003
Achondroplasia in Turkey is defined by recurrent G380R mutation of the FGFR3 geneSacide Pehlivan, Ferda Ozkinay, Ozlem Okutman, et al.Journal of Assisted Reproduction and Genetics|April 18, 2016
A new mutation identified in SPATA16 in two globozoospermic patientsElias ElInati, Camille Fossard, Ozlem Okutman, et al.G3 (Bethesda, Md.)|October 15, 2020
Programmed Cell Death 2-Like (Pdcd2l) Is Required for Mouse Embryonic DevelopmentBrendan J Houston, Manon S Oud, Daniel M Aguirre, et al.Human Molecular Genetics|July 23, 2015
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish familyOzlem Okutman, Jean Muller, Yoni Baert, et al.Journal of Assisted Reproduction and Genetics|February 5, 2026
Disruption of meiotic double-strand break dynamics provokes germline human infertility in both sexesOzlem Okutman, Asma Sassi, Ahmet Salvarci, et al.Journal of Assisted Reproduction and Genetics|April 13, 2017
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish familyOzlem Okutman, Jean Muller, Valerie Skory, et al.Pageof 1