Tayfun Özçelık

21.4k total citations
59 papers, 3.1k citations indexed

About

Tayfun Özçelık is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Tayfun Özçelık has authored 59 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 23 papers in Genetics and 8 papers in Oncology. Recurrent topics in Tayfun Özçelık's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and DNA Repair Mechanisms (4 papers). Tayfun Özçelık is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and DNA Repair Mechanisms (4 papers). Tayfun Özçelık collaborates with scholars based in Türkiye, United States and France. Tayfun Özçelık's co-authors include Uta Francke, Onur Emre Onat, Cemaliye Boylu Akyerli, Philip M. Murphy, Gökçe Törüner, Elif Uz, Richard L. Sidman, Andrew A. Welcher, Eric M. Shooter and Ueli Suter and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Tayfun Özçelık

58 papers receiving 3.1k citations

Peers

Countries citing papers authored by Tayfun Özçelık

Since Specialization

Citations

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

Fields of papers citing papers by Tayfun Özçelık

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tayfun Özçelık

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	The genetic structure of the Turkish population reveals high levels of variation and admixture 2021 ·Proceedings of the National Academy of Sciences ·(unknown), A. Nazlı Başak, Onur Emre Onat, Kaya Bilgüvar, Jungmin Choi, Yuval Itan, Caner Çağlar, (unknown), Jean‐Laurent Casanova, D.N. Cooper, Peter D. Stenson, Alper Yavuz, Hakan Buluş, Murat Günel, Jeffrey M. Friedman, Tayfun Özçelık	47
2	Human CRY1 variants associate with attention deficit/hyperactivity disorder 2020 ·Journal of Clinical Investigation ·Onur Emre Onat, (unknown), Şeref Gül, Kaya Bilgüvar, Yiming Wu, (unknown), Cihan Aydın, A. Nazlı Başak, (unknown), Arianna Goracci, Chiara Fallerini, Alessandra Renieri, Jean‐Laurent Casanova, Yuval Itan, Cem Atbaşoğlu, Meram Can Saka, İbrahim Halil Kavaklı, Tayfun Özçelık	33
3	Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder 2017 ·Cell ·Alina Patke, Patricia Murphy, Onur Emre Onat, Ana C. Krieger, Tayfun Özçelık, Scott S. Campbell, Michael W. Young	249
4	Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ) 2015 ·BMC Neuroscience ·(unknown), Mehmet Neset Özel, Süleyman Gülsüner, Ayşe B. Tekinay, Tayfun Özçelık, Özlen Konu, Michelle M. Adams	4
5	Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair 2014 ·Journal of Medical Genetics ·(unknown), Bekir Ergüner, Mahmut Şamil Sağıroğlu, Bayram Yüksel, Onur Emre Onat, Can Alkan, Tayfun Özçelık	38
6	Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion 2012 ·European Journal of Human Genetics ·Onur Emre Onat, Süleyman Gülsüner, Kaya Bilgüvar, A. Nazlı Başak, Haluk Topaloğlu, Meli̇ha Tan, Üner Tan, Murat Günel, Tayfun Özçelık	100
7	Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred 2011 ·Genome Research ·Süleyman Gülsüner, Ayşe B. Tekinay, Katja Doerschner, Hüseyin Boyacı, Kaya Bilgüvar, (unknown), (unknown), Onur Emre Onat, Ergin Atalar, A. Nazlı Başak, Haluk Topaloğlu, Tülay Kansu, Meli̇ha Tan, Üner Tan, Murat Günel, Tayfun Özçelık	51
8	Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy 2010 ·Neurogenetics ·Luis Kolb, Zülfikar Arlıer, Cengiz Yalçınkaya, Ali K. Ozturk, Jennifer Moliterno, Özdem Ertürk Çetin, Fatih Bayraklı, Barış Korkmaz, Michael L. DiLuna, Katsuhito Yasuno, Kaya Bilgüvar, Tayfun Özçelık, Beyhan Tüysüz, Matthew W. State, Murat Günel	18
9	DNA repair gene polymorphisms and bladder cancer susceptibility in a Turkish population. 2007 ·PubMed ·Bensu Karahalıl, Neslihan Aygün Kocabaş, Tayfun Özçelık	42
10	Skewed X-Chromosome Inactivation in Scleroderma 2007 ·Clinical Reviews in Allergy & Immunology ·Elif Uz, Laurence Loubière, Vijayakrishna K. Gadi, Zeynep Özbalkan, Jeffrey J Stewart, J. Lee Nelson, Tayfun Özçelık	39
11	The SOCS‐1 gene methylation in chronic myeloid leukemia patients 2007 ·American Journal of Hematology ·Özden Hatırnaz Ng, (unknown), Muhlis Cem Ar, Cemaliye Boylu Akyerli, Teoman Soysal, Burhan Ferhanoğlu, Tayfun Özçelık, Uğur Özbek	29
12	Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity 2006 ·European Journal of Human Genetics ·Tayfun Özçelık, Elif Uz, Cemaliye Boylu Akyerli, Sevgi Baǧışlar, (unknown), Alptekin Gürsoy, Nurten Akarsu, Gökçe Törüner, Nuri Kamel, Sevim Güllü	90
13	Extremely skewed X‐chromosome inactivation patterns in women with recurrent spontaneous abortion 2006 ·Australian and New Zealand Journal of Obstetrics and Gynaecology ·Sevgi Baǧışlar, İşık Üstüner, (unknown), Feride Söylemez, Cemaliye Boylu Akyerli, Serdar Ceylaner, (unknown), (unknown), Tayfun Özçelık	16
14	Skewed X chromosome inactivation in blood cells of women with scleroderma 2005 ·Arthritis & Rheumatism ·Zeynep Özbalkan, Sevgi Baǧışlar, Sedat Kiraz, Cemaliye Boylu Akyerli, Hüseyin Özer, Şule Yavuz, Merih Bırlık, Meral Çalgünerı, Tayfun Özçelık	124
15	Germline mutations in theBRCA1andBRCA2genes in Turkish breast/ovarian cancer patients 2003 ·Human Mutation ·(unknown), Güven Lüleci, Tayfun Özçelık, Tahsin Çolak, Hagit Schayek, M Akaydın, Eitan Friedman	18
16	Concomitant inactivation of p53 and Chk2 in breast cancer 2002 ·Oncogene ·Alexandra Sullivan, Martin Yuille, Claire E. Repellin, (unknown), Olivier Reelfs, Alexandra Bell, Barbara Dunne, Barry A. Gusterson, Peter Osin, Paul J. Farrell, Işık G. Yuluğ, Abigail Evans, Tayfun Özçelık, Milena Gasco, Tim Crook	67
17	A retrospective comparison of allogeneic peripheral blood stem cell and bone marrow transplantation results from a single center: A focus on the incidence of graft-vs.-host disease and relapse 1999 ·Biology of Blood and Marrow Transplantation ·Celalettin Üstün, Önder Arslan, Meral Beksac, (unknown), Günhan Gürman, Tayfun Özçelık, (unknown), (unknown), Hamdi Akan, Muhıt Özcan, Taner Demirer, (unknown), Nahıde Konuk, Mutlu Arat, İmdat Dılek, Harika Çelebi, H.Ş. Çoşkun	28
18	Reply to Rivera. 1993 ·The American Journal of Human Genetics ·Valerie Lindgren, Christine R. Bryke, Tayfun Özçelık, Teresa L. Yang‐Feng, Uta Francke	1
19	Molecular evolution of the human interleukin–8 receptor gene cluster 1992 ·Nature Genetics ·Sunil K. Ahuja, Tayfun Özçelık, (unknown), Uta Francke, Philip M. Murphy	90
20	Chromosomal mapping of brain-derived neurotrophic factor and neurotrophin-3 genes in man and mouse 1991 ·Genomics ·Tayfun Özçelık, Arnon Rosenthal, Uta Francke	34

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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