Bayram Toraman

469 total citations
10 papers, 199 citations indexed

About

Bayram Toraman is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Bayram Toraman has authored 10 papers receiving a total of 199 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Genetics. Recurrent topics in Bayram Toraman's work include Moyamoya disease diagnosis and treatment (1 paper), Hearing, Cochlea, Tinnitus, Genetics (1 paper) and Corneal Surgery and Treatments (1 paper). Bayram Toraman is often cited by papers focused on Moyamoya disease diagnosis and treatment (1 paper), Hearing, Cochlea, Tinnitus, Genetics (1 paper) and Corneal Surgery and Treatments (1 paper). Bayram Toraman collaborates with scholars based in Türkiye, Netherlands and United States. Bayram Toraman's co-authors include Ersan Kalay, Nurten Akarsu, Yakup Aslan, Ayşegül Cansu, Ebtesam Abdalla, Shiv Pillai, Orhan Sezgın, Mehmet Mutlu, Hülya Kayserili and Vasant Chellappa and has published in prestigious journals such as The American Journal of Human Genetics, Gene and British Journal of Ophthalmology.

In The Last Decade

Bayram Toraman

10 papers receiving 197 citations

Peers

Countries citing papers authored by Bayram Toraman

Since Specialization

Citations

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

Fields of papers citing papers by Bayram Toraman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bayram Toraman

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

#	Work	Indexed citations
1	A novel homozygous RIPK4 variant in a family with severe Bartsocas‐Papas syndrome 2021 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Bayram Toraman, (unknown), (unknown), Zafer Yüksel, Ersan Kalay	2
2	Finding underlying genetic mechanisms of two patients with autism spectrum disorder carrying familial apparently balanced chromosomal translocations 2021 ·The Journal of Gene Medicine ·Bayram Toraman, (unknown), Selma Tural Hesapçıoğlu, (unknown), (unknown), Bekir Ergüner, (unknown), (unknown), (unknown), (unknown), (unknown), Ersan Kalay	3
3	Klinik Enterobacterales İzolatlarında Plazmit Aracılı mcr Kolistin Direnç Geninin Araştırılması 2020 ·Mikrobiyoloji Bulteni ·(unknown), Celal Kurtuluş Buruk, İlknur Tosun, Bayram Toraman, Neşe Kaklıkkaya, Faruk Aydın	2
4	RIPK4 suppresses the TGF‐β1 signaling pathway in HaCaT cells 2019 ·Cell Biology International ·(unknown), (unknown), (unknown), Bayram Toraman, (unknown), Ersan Kalay	8
5	HLA-E0101/0103X is Associated with Susceptibility to Pemphigus Vulgaris: A Case-control Study. 2017 ·PubMed* ·(unknown), Savaş Yaylı, Bayram Toraman, (unknown), Ersan Kalay, (unknown), Sevgi Bahadır	3
6	Analysis of centrosome and DNA damage response in PLK4 associated Seckel syndrome 2017 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), (unknown), Yavuz Dodurga, (unknown), Bayram Toraman, Adem Yıldırım, Nuran Sabir, Nurten Akarsu, (unknown), Ersan Kalay	21
7	Novel splice-site and missense mutations in theALDH1A3gene underlying autosomal recessive anophthalmia/microphthalmia 2014 ·British Journal of Ophthalmology ·(unknown), Ersan Kalay, Cem Yıldırım, (unknown), (unknown), Bayram Toraman, (unknown), (unknown), Volkan Okur, N. Lale Şatıroğlu-Tufan, Nurten Akarsu	17
8	Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation 2012 ·Gene ·Bayram Toraman, Ayşenur Ökten, Ersan Kalay, Gülay Karagüzel, (unknown), (unknown), Ahmet Karagüzel	9
9	Mutations in RIPK4 Cause the Autosomal-Recessive Form of Popliteal Pterygium Syndrome 2011 ·The American Journal of Human Genetics ·Ersan Kalay, Orhan Sezgın, Vasant Chellappa, Mehmet Mutlu, Heba Morsy, Hülya Kayserili, (unknown), Ayşegül Cansu, Bayram Toraman, Ebtesam Abdalla, Yakup Aslan, Shiv Pillai, Nurten Akarsu	72
10	Involvement ofDFNB59 mutations in autosomal recessive nonsyndromic hearing impairment 2007 ·Human Mutation ·Rob W.J. Collin, Ersan Kalay, Jaap Oostrik, Refik Çaylan, Bernd Wollnik, Selçuk Arslan, Anneke I. den Hollander, (unknown), Peter Lichtner, Tim M. Strom, Bayram Toraman, Lies H. Hoefsloot, Cor W. R. J. Cremers, Han G. Brunner, Frans P.M. Cremers, Ahmet Karagüzel, Hannie Kremer	62

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