Özlem Okutman

615 total citations
18 papers, 353 citations indexed

About

Özlem Okutman is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Özlem Okutman has authored 18 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 11 papers in Molecular Biology and 11 papers in Reproductive Medicine. Recurrent topics in Özlem Okutman's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), Sperm and Testicular Function (10 papers) and Reproductive Biology and Fertility (9 papers). Özlem Okutman is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), Sperm and Testicular Function (10 papers) and Reproductive Biology and Fertility (9 papers). Özlem Okutman collaborates with scholars based in France, Türkiye and Belgium. Özlem Okutman's co-authors include Stéphane Viville, Jean Muller, Moncef Benkhalifa, Saad Hasan Mohammed Ali, Samira Ibala‐Romdhane, Münevver Serdarogullari, Moira K. O’Bryan, Emre Bakırcıoğlu, Yoni Baert and Mustafa Bahçeci and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and Human Reproduction.

In The Last Decade

Özlem Okutman

16 papers receiving 346 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Özlem Okutman France 8 226 207 179 161 44 18 353
Sélima Fourati Ben Mustapha France 7 239 1.1× 184 0.9× 137 0.8× 191 1.2× 35 0.8× 13 338
Thassadite Dirami France 6 141 0.6× 94 0.5× 113 0.6× 115 0.7× 24 0.5× 7 284
Manon S. Oud Netherlands 11 352 1.6× 337 1.6× 325 1.8× 228 1.4× 75 1.7× 22 608
T.K. Yoon South Korea 10 217 1.0× 71 0.3× 155 0.9× 257 1.6× 56 1.3× 22 413
Denise R. Archambeault United States 8 109 0.5× 99 0.5× 196 1.1× 79 0.5× 13 0.3× 8 267
Can Dai China 11 209 0.9× 122 0.6× 234 1.3× 310 1.9× 94 2.1× 22 446
Jianteng Zhou China 10 130 0.6× 106 0.5× 108 0.6× 100 0.6× 16 0.4× 23 222
Capucine Hyon France 12 89 0.4× 262 1.3× 210 1.2× 64 0.4× 98 2.2× 21 376
Yung Ming Lin Taiwan 11 181 0.8× 195 0.9× 185 1.0× 63 0.4× 19 0.4× 15 323

Countries citing papers authored by Özlem Okutman

Since Specialization
Citations

This map shows the geographic impact of Özlem Okutman's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Özlem Okutman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Özlem Okutman more than expected).

Fields of papers citing papers by Özlem Okutman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Özlem Okutman. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Özlem Okutman. The network helps show where Özlem Okutman may publish in the future.

Co-authorship network of co-authors of Özlem Okutman

This figure shows the co-authorship network connecting the top 25 collaborators of Özlem Okutman. A scholar is included among the top collaborators of Özlem Okutman based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Özlem Okutman. Özlem Okutman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Okutman, Özlem, Éléonore Réal, Kirsley Chennen, et al.. (2024). Pathogenic missense variation in PABPC1L/EPAB causes female infertility due to oocyte maturation arrest at the germinal vesicle stage. Journal of Assisted Reproduction and Genetics. 41(2). 311–322.
2.
Okutman, Özlem, Timur Gürgan, Julien Tarabeux, et al.. (2024). Evaluation of an Updated Gene Panel as a Diagnostic Tool for Both Male and Female Infertility. Reproductive Sciences. 31(8). 2309–2317. 1 indexed citations
3.
Verpoest, Willem, et al.. (2023). Genetics of infertility: a paradigm shift for medically assisted reproduction. Human Reproduction. 38(12). 2289–2295. 3 indexed citations
4.
Okutman, Özlem, Münevver Serdarogullari, Ingrid Segers, et al.. (2022). A systematic review and evidence assessment of monogenic gene–disease relationships in human female infertility and differences in sex development. Human Reproduction Update. 29(2). 218–232. 18 indexed citations
5.
Okutman, Özlem, et al.. (2022). A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest. Human Reproduction. 38(2). 306–314. 5 indexed citations
6.
Okutman, Özlem, Julien Tarabeux, Jean Muller, & Stéphane Viville. (2021). Evaluation of a Custom Design Gene Panel as a Diagnostic Tool for Human Non-Syndromic Infertility. Genes. 12(3). 410–410. 7 indexed citations
7.
Okutman, Özlem, et al.. (2020). Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect. Genes. 11(4). 382–382. 16 indexed citations
8.
Houston, Brendan J., Manon S. Oud, D. Jo Merriner, et al.. (2020). Programmed Cell Death 2-Like (Pdcd2l) Is Required for Mouse Embryonic Development. G3 Genes Genomes Genetics. 10(12). 4449–4457. 3 indexed citations
9.
Oud, Manon S., Özlem Okutman, Petra F. de Vries, et al.. (2019). Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia. Human Reproduction. 35(1). 240–252. 46 indexed citations
10.
Okutman, Özlem, Jean Muller, Moncef Benkhalifa, et al.. (2018). Aspect génétique de l’infertilité masculine : de la recherche à la clinique. Gynécologie Obstétrique Fertilité & Sénologie . 47(1). 54–62. 4 indexed citations
11.
Okutman, Özlem, et al.. (2018). Genetic evaluation of patients with non-syndromic male infertility. Journal of Assisted Reproduction and Genetics. 35(11). 1939–1951. 34 indexed citations
12.
Oud, Manon S., Liliana Ramos, Moira K. O’Bryan, et al.. (2017). Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia. Human Mutation. 38(11). 1592–1605. 44 indexed citations
13.
Elinati, Elias, Özlem Okutman, Samira Ibala‐Romdhane, et al.. (2016). A new mutation identified in SPATA16 in two globozoospermic patients. Journal of Assisted Reproduction and Genetics. 33(6). 815–820. 39 indexed citations
14.
Okutman, Özlem, Jean Muller, Yoni Baert, et al.. (2015). Exome sequencing reveals a nonsense mutation inTEX15causing spermatogenic failure in a Turkish family. Human Molecular Genetics. 24(19). 5581–5588. 93 indexed citations
15.
Ibala‐Romdhane, Samira, et al.. (2015). Identification of a newDPY19L2mutation and a better definition ofDPY19L2deletion breakpoints leading to globozoospermia. Molecular Human Reproduction. 22(1). 35–45. 29 indexed citations
16.
Okutman, Özlem, et al.. (2004). Screening of Y chromosome microdeletion which contains AZF regions in 71 Turkish azoospermic men.. PubMed. 15(2). 199–205. 7 indexed citations
17.
Pehlıvan, Sacide, et al.. (2003). Achondroplasia in Turkey is defined by recurrent G380R mutation of the FGFR3 gene.. SHILAP Revista de lepidopterología. 45(2). 99–101. 4 indexed citations
18.
Pehlıvan, Sacide, et al.. (2001). Akondroplazi'de moleküler genetik analizler: Bir ön çalışma. 8(4). 205–208.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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