Umut Altunoğlu

2.8k total citations
54 papers, 572 citations indexed

About

Umut Altunoğlu is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Umut Altunoğlu has authored 54 papers receiving a total of 572 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 26 papers in Genetics and 9 papers in Genetics. Recurrent topics in Umut Altunoğlu's work include RNA Research and Splicing (6 papers), Genomics and Rare Diseases (5 papers) and Sexual Differentiation and Disorders (5 papers). Umut Altunoğlu is often cited by papers focused on RNA Research and Splicing (6 papers), Genomics and Rare Diseases (5 papers) and Sexual Differentiation and Disorders (5 papers). Umut Altunoğlu collaborates with scholars based in Türkiye, Germany and United States. Umut Altunoğlu's co-authors include Hülya Kayserili, Zehra Oya Uyguner, Seher Başaran, Güven Toksoy, Birsen Karaman, Bruno Reversade, Firdevs Baş, Şükran Poyrazoğlu, Şahin Avcı and Yeliz Güven and has published in prestigious journals such as Neuron, The Journal of Experimental Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

Umut Altunoğlu

51 papers receiving 568 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Umut Altunoğlu Türkiye 14 377 162 67 56 55 54 572
Cordula Surmann‐Schmitt Germany 13 390 1.0× 151 0.9× 51 0.8× 138 2.5× 40 0.7× 16 761
Ekim Z. Taşkıran Türkiye 15 329 0.9× 195 1.2× 84 1.3× 89 1.6× 37 0.7× 70 739
Jiansu Shao United States 9 578 1.5× 192 1.2× 118 1.8× 125 2.2× 63 1.1× 15 823
Chalurmpon Srichomthong Thailand 16 342 0.9× 356 2.2× 29 0.4× 74 1.3× 35 0.6× 49 676
Muhammad Faiyaz‐Ul‐Haque Canada 13 291 0.8× 300 1.9× 41 0.6× 44 0.8× 129 2.3× 31 636
Daniel Horbelt Germany 9 342 0.9× 102 0.6× 64 1.0× 59 1.1× 56 1.0× 10 593
Julia Etich Germany 16 276 0.7× 78 0.5× 42 0.6× 36 0.6× 51 0.9× 25 557
F. Conte-Auriol France 10 311 0.8× 140 0.9× 32 0.5× 111 2.0× 39 0.7× 14 591
Naomi Pode‐Shakked Israel 16 731 1.9× 105 0.6× 162 2.4× 83 1.5× 42 0.8× 35 913
Hiroko Meguro Japan 3 355 0.9× 63 0.4× 88 1.3× 48 0.9× 24 0.4× 4 525

Countries citing papers authored by Umut Altunoğlu

Since Specialization
Citations

This map shows the geographic impact of Umut Altunoğlu'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 Umut Altunoğlu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Umut Altunoğlu more than expected).

Fields of papers citing papers by Umut Altunoğlu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Umut Altunoğlu. 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 Umut Altunoğlu. The network helps show where Umut Altunoğlu may publish in the future.

Co-authorship network of co-authors of Umut Altunoğlu

This figure shows the co-authorship network connecting the top 25 collaborators of Umut Altunoğlu. A scholar is included among the top collaborators of Umut Altunoğlu 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 Umut Altunoğlu. Umut Altunoğlu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Altunoğlu, Umut, Güven Toksoy, Şahin Avcı, et al.. (2024). Clinical and molecular characteristics of 26 fetuses with lethal multiple congenital contractures. Clinical Genetics. 105(6). 596–610. 2 indexed citations
2.
Karaman, Birsen, et al.. (2024). Association of Antenatal Evaluations with Postmortem and Genetic Findings in the Series of Fetal Osteogenesis Imperfecta. Fetal Diagnosis and Therapy. 51(3). 285–299. 1 indexed citations
3.
Theil, Arjan F., Alex Pines, José María Heredia‐Genestar, et al.. (2023). Trichothiodystrophy‐associated MPLKIP maintains DBR1 levels for proper lariat debranching and ectodermal differentiation. EMBO Molecular Medicine. 15(11). e17973–e17973. 8 indexed citations
4.
Güleç, Elif Yılmaz, Alper Gezdirici, Şahin Avcı, et al.. (2022). Clinical and molecular genetic findings of Crisponi/cold‐induced sweating syndrome (CS/CISS) spectrum in patients from Turkey. Clinical Genetics. 102(3). 201–217.
5.
Altunoğlu, Umut, Güven Toksoy, Şahin Avcı, et al.. (2022). Functional loss of ubiquitin‐specific protease 14 may lead to a novel distal arthrogryposis phenotype. Clinical Genetics. 101(4). 421–428. 2 indexed citations
6.
Altunoğlu, Umut, et al.. (2022). A New Family with a Novel <b><i>OTUD6B</i></b> Mutation: Practicing Whole Exome Sequencing for Antenatal Diagnosis of Tetralogy of Fallot. Molecular Syndromology. 13(3). 206–211. 1 indexed citations
7.
Altunoğlu, Umut, Zehra Yavaş Abalı, Şahin Avcı, et al.. (2022). Evaluation of growth, puberty, osteoporosis, and the response to long‐term bisphosphonate therapy in four patients with osteoporosis‐pseudoglioma syndrome. American Journal of Medical Genetics Part A. 188(7). 2061–2070. 2 indexed citations
8.
Marais, Anett, Aida M. Bertoli‐Avella, Christian Beetz, et al.. (2022). Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease. European Journal of Medical Genetics. 65(8). 104537–104537. 4 indexed citations
9.
Altunoğlu, Umut, Aytül Çorbacıoğlu Esmer, Şahin Avcı, et al.. (2022). Fetal skeletal dysplasia cohort of a single tertiary referral center in Istanbul, Turkey. American Journal of Medical Genetics Part A. 191(2). 498–509. 3 indexed citations
10.
Uyguner, Zehra Oya, Firdevs Baş, Umut Altunoğlu, et al.. (2022). Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD. Journal of Clinical Research in Pediatric Endocrinology. 14(2). 153–171. 3 indexed citations
11.
Adami, Eleonora, Sivakumar Viswanathan, Anissa A. Widjaja, et al.. (2021). IL11 is elevated in systemic sclerosis and IL11-dependent ERK signalling underlies TGFβ-mediated activation of dermal fibroblasts. Lara D. Veeken. 60(12). 5820–5826. 42 indexed citations
12.
Altunoğlu, Umut, Anju Shukla, Nathalie Escande‐Beillard, et al.. (2021). Expanding the spectrum of syndromic PPP2R3C ‐related XY gonadal dysgenesis to XX gonadal dysgenesis. Clinical Genetics. 101(2). 221–232. 5 indexed citations
13.
Toksoy, Güven, Şahin Avcı, Nilay Güneş, et al.. (2020). Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey. Molecular Syndromology. 11(4). 183–196. 6 indexed citations
14.
Bonnard, Carine, Naveenan Navaratnam, Thong Teck Tan, et al.. (2020). A loss-of-function NUAK2 mutation in humans causes anencephaly due to impaired Hippo-YAP signaling. The Journal of Experimental Medicine. 217(12). 35 indexed citations
15.
Yıldırım, Zeynep Yürük, Güven Toksoy, Zehra Oya Uyguner, et al.. (2019). Primary coenzyme Q10 Deficiency-6 (COQ10D6): Two siblings with variable expressivity of the renal phenotype. European Journal of Medical Genetics. 63(1). 103621–103621. 11 indexed citations
16.
Avcı, Şahin, Güven Toksoy, Umut Altunoğlu, et al.. (2018). RADİYAL IŞIN DEFEKTLERİNİN KLİNİK SINIFLANDIRMASI VE ETYOPATOGENEZİNİN ARAŞTIRILMASI. Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi. 81(4). 127–138. 1 indexed citations
17.
Lehalle, Daphné, Umut Altunoğlu, Ange‐Line Bruel, et al.. (2017). Clinical delineation of a subtype of frontonasal dysplasia with creased nasal ridge and upper limb anomalies: Report of six unrelated patients. American Journal of Medical Genetics Part A. 173(12). 3136–3142. 5 indexed citations
18.
Bögershausen, Nina, Umut Altunoğlu, Filippo Beleggia, et al.. (2016). An unusual presentation of Kabuki syndrome with orbital cysts, microphthalmia, and cholestasis with bile duct paucity. American Journal of Medical Genetics Part A. 170(12). 3282–3288. 13 indexed citations
19.
Güven, Yeliz, Firdevs Baş, Umut Altunoğlu, et al.. (2016). Cleidocranial dysplasia: Clinical, endocrinologic and molecular findings in 15 patients from 11 families. European Journal of Medical Genetics. 60(3). 163–168. 30 indexed citations
20.
Coşkun, Salih, Y. Yildirim, Abdullah Çim, et al.. (2015). Romano-Ward sendromunda KCNQ1 geninde bir duplikasyon mutasyonu. Clinical Genetics. 1(1). 25–28. 11 indexed citations

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Cordula Surmann‐Schmitt Breakdown of academic impact, for papers by Ekim Z. Taşkıran Breakdown of academic impact, for papers by Jiansu Shao Breakdown of academic impact, for papers by Chalurmpon Srichomthong Breakdown of academic impact, for papers by Muhammad Faiyaz‐Ul‐Haque Breakdown of academic impact, for papers by Daniel Horbelt Breakdown of academic impact, for papers by Julia Etich Breakdown of academic impact, for papers by F. Conte-Auriol Breakdown of academic impact, for papers by Naomi Pode‐Shakked Breakdown of academic impact, for papers by Hiroko Meguro
Rankless by CCL
2026