Gökhan Yigit

3.2k total citations
24 papers, 355 citations indexed

About

Gökhan Yigit is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Gökhan Yigit has authored 24 papers receiving a total of 355 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Gökhan Yigit's work include Hedgehog Signaling Pathway Studies (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Gökhan Yigit is often cited by papers focused on Hedgehog Signaling Pathway Studies (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Gökhan Yigit collaborates with scholars based in Germany, Türkiye and Switzerland. Gökhan Yigit's co-authors include Bernd Wollnik, Peter Nürnberg, Hülya Kayserili, Zehra Oya Uyguner, Yun Li, Filippo Beleggia, Janine Altmüller, Esther Pohl, Gudrun Nürnberg and Nina Bögershausen and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

Gökhan Yigit

19 papers receiving 353 citations

Peers

Countries citing papers authored by Gökhan Yigit

Since Specialization

Citations

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

Fields of papers citing papers by Gökhan Yigit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gökhan Yigit

This figure shows the co-authorship network connecting the top 25 collaborators of Gökhan Yigit. A scholar is included among the top collaborators of Gökhan Yigit 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 Gökhan Yigit. Gökhan Yigit 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	Phenotypes Linked to Duplication Upstream of SOX9: New Insights Into Presentation and Diagnosis 2025 ·The Journal of Clinical Endocrinology & Metabolism ·Edip Ünal, (unknown), Atilla Çayır, Esra Deniz Papatya Çakır, (unknown), (unknown), (unknown), Gökhan Yigit, Arne Zibat, Bernd Wollnik, Hüseyin Demirbilek, Tülay Güran	1
2	Functional characterization of PI3K C2 domain mutations detected in breast cancer circulating tumor cells and metastatic cells 2024 ·Cellular Signalling ·Daniel J. Smit, (unknown), Stefan Horn, Gökhan Yigit, Marie‐Therese Haider, Vivian Pogenberg, Udo Schumacher, Klaus Pantel, Manfred Jücker	2
3	The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued 2023 ·Orphanet Journal of Rare Diseases ·Simone Schröder, Gökhan Yigit, Yun Li, Janine Altmüller, (unknown), Barbara Fiedler, (unknown), Peter Nürnberg, Jürgen Seeger, (unknown), Enza Maria Valente, Bernd Wollnik, Eugen Boltshauser, Knut Brockmann	2
4	Lysinuric protein intolerance caused by a homozygous SLC7A7 deletion and presented with hyperferritinemia and osteoporosis in two siblings 2023 ·Molecular Genetics and Metabolism Reports ·(unknown), (unknown), (unknown), Gökhan Yigit, Bernd Wollnik	0
5	MFSD2A-associated primary microcephaly - Expanding the clinical and mutational spectrum of this ultra-rare disease 2021 ·European Journal of Medical Genetics ·(unknown), Gökhan Yigit, (unknown), Janine Altmüller, Hölger Thiele, Peter Nürnberg, Nursel Elçioğlu, (unknown), Ute Hehr, Anja Stein, Adela Della Marina, Angela Köninger, Christel Depienne, Frank J. Kaiser, Bernd Wollnik, Alma Kuechler	6
6	Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state 2021 ·Journal of Medical Genetics ·Gökhan Yigit, Ruth Sheffer, (unknown), Yun Li, (unknown), (unknown), Janine Altmüller, Peter Nürnberg, Liza Douiev, Silke Kaulfuß, Peter Burfeind, Bernd Wollnik, Knut Brockmann	10
7	Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal study 2021 ·American Journal of Medical Genetics Part A ·Andrea Gangfuß, Gökhan Yigit, Janine Altmüller, Peter Nürnberg, Johanna Christina Czeschik, Bernd Wollnik, Nina Bögershausen, Peter Burfeind, Dagmar Wieczorek, Frank J. Kaiser, Andreas Roos, Heike Kölbel, Ulrike Schara‐Schmidt, Alma Kuechler	5
8	Survey of germline variants in cancer‐associated genes in young adults with colorectal cancer 2021 ·Genes Chromosomes and Cancer ·(unknown), Joanne Young, Yun Li, Eric Smith, (unknown), (unknown), Gonzalo Tapia Rico, Nicola Poplawski, Jennifer E. Hardingham, Yoko Tomita, Amanda Townsend, Jinghua Feng, Arne Zibat, Silke Kaulfuß, Christian Müller, Gökhan Yigit, Bernd Wollnik, Timothy Price	8
9	Heterozygous Truncating Variants in SUFU Cause Congenital Ocular Motor Apraxia 2021 ·Neuropediatrics ·Simone Schröder, (unknown), Gökhan Yigit, Eugen Boltshauser, Anja Uhmann, Bernd Wollnik, Knut Brockmann, (unknown)	0
10	Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia 2020 ·Genetics in Medicine ·Simone Schröder, Yun Li, Gökhan Yigit, Janine Altmüller, Ingrid Bader, Andrea Bevot, Saskia Biskup, Steffi Dreha‐Kulaczewski, Georg Christoph Korenke, Raimund Kottke, Johannes A. Mayr, (unknown), Sandra P. Toelle, (unknown), Saskia B. Wortmann, Heidi Hahn, Eugen Boltshauser, Anja Uhmann, Bernd Wollnik, Knut Brockmann	10
11	Neugeborenes mit Nasenagenesie: Neonatologische Herausforderungen bei der Versorgung eines Neugeborenen mit Bosma-Arhinie-Mikrophthalmie-Syndrom (BAMS) 2020 ·Zeitschrift für Geburtshilfe und Neonatologie ·(unknown), (unknown), Gökhan Yigit, (unknown), Franz Bahlmann, Robert Sader, (unknown), Marc Lüchtenberg, Kay Latta, Chie Hee Cho, Bernd Wollnik, Steffen Kunzmann	2
12	Novel compound heterozygous mutations in TELO2 in a patient with severe expression of You-Hoover-Fong syndrome 2017 ·Molecular Genetics & Genomic Medicine ·Shahida Moosa, Janine Altmüller, Troels Lyngbye, Rikke Christensen, Yun Li, Peter Nürnberg, Gökhan Yigit, Ida Vogel, Bernd Wollnik	11
13	An unusual presentation of Kabuki syndrome with orbital cysts, microphthalmia, and cholestasis with bile duct paucity 2016 ·American Journal of Medical Genetics Part A ·Nina Bögershausen, Umut Altunoğlu, Filippo Beleggia, Gökhan Yigit, Hülya Kayserili, Peter Nürnberg, Yun Li, Janine Altmüller, Bernd Wollnik	13
14	Smith–Kingsmore syndrome: A third family with the MTOR mutation c.5395G>A p.(Glu1799Lys) and evidence for paternal gonadal mosaicism 2016 ·American Journal of Medical Genetics Part A ·Shahida Moosa, (unknown), Janine Altmüller, Filippo Beleggia, Peter Nürnberg, Yun Li, Gökhan Yigit, Bernd Wollnik	13
15	Mutations in CDK 5 RAP 2 cause Seckel syndrome 2015 ·Molecular Genetics & Genomic Medicine ·Gökhan Yigit, Karen E. Brown, Hülya Kayserili, Esther Pohl, Almuth Caliebe, (unknown), Elisabeth Rosser, Nina Bögershausen, Zehra Oya Uyguner, Umut Altunoğlu, Gudrun Nürnberg, Peter Nürnberg, Anita Rauch, Yun Li, Christian T. Thiel, Bernd Wollnik	44
16	A novel mutation in RNU4ATAC in a patient with microcephalic osteodysplastic primordial dwarfism type I 2015 ·American Journal of Medical Genetics Part A ·Esra KAYA KILIÇ, Gökhan Yigit, Gülen Eda Ütine, Bernd Wollnik, Ercan Mıhçı, Banu Nur, Koray Boduroğlu	10
17	A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome 2013 ·Human Genetics ·Esther Pohl, Ayça Aykut, Filippo Beleggia, Emin Karaca, Burak Durmaz, Katharina Keupp, (unknown), Melis Palamar, Gökhan Yigit, Ferda Özkınay, Bernd Wollnik	42
18	Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies 2012 ·European Journal of Human Genetics ·Bodo B. Beck, Anne Baasner, Anja Buescher, Sandra Habbig, (unknown), Markus J. Kemper, Przemysław Sikora, Christoph J. Mache, Martin Pöhl, Mirjam Stahl, Burkhard Toenshoff, Lars Pape, Henry Fehrenbach, Dorrit E. Jacob, Bernd Grohe, Matthias T. F. Wolf, Gudrun Nürnberg, Gökhan Yigit, Eduardo Salido, Bernd Höppe	58
19	Epstein-Barr virus LMP2A signaling in statu nascendi mimics a B cell antigen receptor-like activation signal 2012 ·Cell Communication and Signaling ·Niklas Engels, Gökhan Yigit, Christoph H. Emmerich, Dirk Czesnik, Detlev Schild, Jürgen Wienands	21
20	ALX4 dysfunction disrupts craniofacial and epidermal development 2009 ·Human Molecular Genetics ·Hülya Kayserili, Elif Uz, Carien M. Niessen, İbrahim Vargel, Yasemin Alanay, Gökhan Tunçbįlek, Gökhan Yigit, Zehra Oya Uyguner, Şükrü Candan, Hamza Okur, (unknown), Sevim Balcı, Emin Mavili, Mehmet Alikaşifoğlu, Ingo Haase, Bernd Wollnik, Nurten Akarsu	86

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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