| Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family O Okutman, J Muller, Y Baert, M Serdarogullari, M Gultomruk, A Piton, ... Human molecular genetics 24 (19), 5581-5588, 2015 | 133 | 2015 |
| Genetic evaluation of patients with non-syndromic male infertility O Okutman, MB Rhouma, M Benkhalifa, J Muller, S Viville Journal of Assisted Reproduction and Genetics 35, 1939-1951, 2018 | 55 | 2018 |
| A new mutation identified in SPATA16 in two globozoospermic patients E ElInati, C Fossard, O Okutman, H Ghédir, S Ibala-Romdhane, PF Ray, ... Journal of assisted reproduction and genetics 33, 815-820, 2016 | 54 | 2016 |
| Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia MS Oud, L Ramos, MK O'Bryan, RI McLachlan, Ö Okutman, S Viville, ... Human Mutation 38 (11), 1592-1605, 2017 | 48 | 2017 |
| A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family O Okutman, J Muller, V Skory, JM Garnier, A Gaucherot, Y Baert, ... Journal of assisted reproduction and genetics 34, 683-694, 2017 | 48 | 2017 |
| Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia MS Oud, Ö Okutman, LAJ Hendricks, PF de Vries, BJ Houston, L Vissers, ... Human reproduction 35 (1), 240-252, 2020 | 42 | 2020 |
| Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermia H Ghedir, S Ibala-Romdhane, O Okutman, G Viot, A Saad, S Viville MHR: Basic science of reproductive medicine 22 (1), 35-45, 2016 | 39 | 2016 |
| Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect Ö Okutman, C Demirel, F Tülek, V Pfister, U Büyük, J Muller, ... Genes 11 (4), 382, 2020 | 21 | 2020 |
| Genetic aspects of male infertility: From bench to clinic B Rhouma, O Okutman, J Muller, M Benkhalifa, H Bahri, B Rhouma, ... Gynecologie, obstetrique, fertilite & senologie 47 (1), 54-62, 2018 | 9 | 2018 |
| A systematic review and evidence assessment of monogenic gene–disease relationships in human female infertility and differences in sex development A Van Der Kelen, Ö Okutman, E Javey, M Serdarogullari, C Janssens, ... Human Reproduction Update 29 (2), 218-232, 2023 | 8 | 2023 |
| Achondroplasia in Turkey is defined by recurrent G380R mutation of the FGFR3 gene S Pehlivan, F Ozkinay, O Okutman, O Coğulu, A Ozcan, T Çankaya, ... The Turkish Journal of Pediatrics 45 (2), 99-101, 2003 | 7 | 2003 |
| Evaluation of a custom design gene panel as a diagnostic tool for human non-syndromic infertility O Okutman, J Tarabeux, J Muller, S Viville Genes 12 (3), 410, 2021 | 5 | 2021 |
| Programmed Cell Death 2-Like (Pdcd2l) Is Required for Mouse Embryonic Development BJ Houston, MS Oud, DM Aguirre, DJ Merriner, AE O’Connor, O Okutman, ... G3: Genes, Genomes, Genetics 10 (12), 4449-4457, 2020 | 3 | 2020 |
| Genetics of male infertility: genes implicated in non-obstructive azoospermia and severe oligozoospermia Ö Okutman Université de Strasbourg, 2015 | 3 | 2015 |
| A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest O Okutman, M Boivin, J Muller, N Charlet-Berguerand, S Viville Human Reproduction 38 (2), 306-314, 2023 | 2 | 2023 |
| Aspect génétique de l’infertilité masculine: de la recherche à la clinique MB Rhouma, O Okutman, J Muller, M Benkhalifa, H Bahri, KB Rhouma, ... Gynécologie Obstétrique Fertilité & Sénologie 47 (1), 54-62, 2019 | 2 | 2019 |
| Genetics of infertility: a paradigm shift for medically assisted reproduction W Verpoest, Ö Okutman, A Van Der Kelen, K Sermon, S Viville Human Reproduction 38 (12), 2289-2295, 2023 | 1 | 2023 |
| Early cleavage is associated with pregnancy success: an opportunity for replacing less embryos A Demircan, O Okutman, G Sarac, S Nebioglu, E Kervancioglu Human Reproduction 15, 122-122, 2000 | 1 | 2000 |
| Does cleavage at 27 h predict pregnancy in ICSI? A Demircan, O Okutman, S Yaylagul, E Kervancioglu Human Reproduction 14, 339-339, 1999 | 1 | 1999 |
| Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility F Tüttelmann, B Stallmeyer, C Bühlmann, R Stakaitis, AK Dicke, F Gieh, ... | | 2024 |
