Şahin Avcı

463 total citations
21 papers, 103 citations indexed

About

Şahin Avcı is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Şahin Avcı has authored 21 papers receiving a total of 103 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Genetics. Recurrent topics in Şahin Avcı's work include Sexual Differentiation and Disorders (4 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Genomics and Rare Diseases (2 papers). Şahin Avcı is often cited by papers focused on Sexual Differentiation and Disorders (4 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Genomics and Rare Diseases (2 papers). Şahin Avcı collaborates with scholars based in Türkiye, United States and Cyprus. Şahin Avcı's co-authors include Umut Altunoğlu, Zehra Oya Uyguner, Seher Başaran, Güven Toksoy, Birsen Karaman, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Hülya Kayserili, Firdevs Baş and Feyza Darendelıler and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and The Journal of Steroid Biochemistry and Molecular Biology.

In The Last Decade

Şahin Avcı

16 papers receiving 103 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Şahin Avcı Türkiye 6 83 41 35 14 14 21 103
Aziz Mhanni Canada 6 50 0.6× 54 1.3× 10 0.3× 14 1.0× 5 0.4× 10 102
Paul-Martin Holterhus Germany 5 99 1.2× 50 1.2× 88 2.5× 8 0.6× 2 0.1× 6 132
Flavia Amanda Costa‐Barbosa Brazil 8 113 1.4× 96 2.3× 100 2.9× 22 1.6× 18 1.3× 13 225
Michel Polak France 7 45 0.5× 72 1.8× 79 2.3× 41 2.9× 10 0.7× 16 171
F Kurtz France 4 92 1.1× 52 1.3× 71 2.0× 10 0.7× 2 0.1× 6 155
Jazmín Arteaga‐Vázquez Mexico 6 50 0.6× 26 0.6× 5 0.1× 12 0.9× 5 0.4× 20 86
Fanny Laffargue France 5 47 0.6× 37 0.9× 11 0.3× 43 3.1× 6 0.4× 9 89
Abigail R. Benkert United States 7 72 0.9× 41 1.0× 18 0.5× 27 1.9× 3 0.2× 17 139
Yanning Song China 8 124 1.5× 62 1.5× 32 0.9× 6 0.4× 5 0.4× 22 171
Emregül Işık Türkiye 5 29 0.3× 28 0.7× 42 1.2× 18 1.3× 4 0.3× 6 91

Countries citing papers authored by Şahin Avcı

Since Specialization
Citations

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

Fields of papers citing papers by Şahin Avcı

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Şahin Avcı

This figure shows the co-authorship network connecting the top 25 collaborators of Şahin Avcı. A scholar is included among the top collaborators of Şahin Avcı 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 Şahin Avcı. Şahin Avcı 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.
Avcı, Şahin, et al.. (2024). A genetic cause for intractable seizures: Atypical Gaucher disease with a novel pathological variant. Epileptic Disorders. 26(3). 392–394.
2.
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
3.
4.
Avcı, Şahin, et al.. (2023). Revisiting TOP2B‐related phenotypes: Three new cases and literature review. Clinical Genetics. 104(2). 251–258. 2 indexed citations
5.
Baş, Firdevs, Birsen Karaman, Güven Toksoy, et al.. (2023). PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency. Journal of Clinical Research in Pediatric Endocrinology. 15(4). 338–347. 2 indexed citations
6.
Avcı, Şahin, et al.. (2023). Successful Kidney Transplantation in MYH-9-Related Disease Presenting with Severe Macrothrombocytopenia. Turkish Journal of Hematology. 40(3). 232–233.
7.
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.
8.
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
9.
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
10.
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
11.
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
12.
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. 2 indexed citations
13.
Samancı, Bedia, Murat Kürtüncü, Umut Altunoğlu, et al.. (2021). Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. SHILAP Revista de lepidopterología. 27(3). 240–247. 3 indexed citations
14.
Avcı, Şahin, et al.. (2020). Clinical exome sequencing in neuromuscular diseases: an experience from Turkey. Neurological Sciences. 41(8). 2157–2164. 9 indexed citations
15.
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
16.
Toksoy, Güven, Hacer Durmuş, Seher Başaran, et al.. (2019). Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling. Neuromuscular Disorders. 29(8). 601–613. 16 indexed citations
17.
Toksoy, Güven, Birsen Karaman, Seher Başaran, et al.. (2019). MOLECULAR ANALYSIS OF FGFR1-3, TWIST1, MSX2, POR, FREM1 AND RAB23 GENES IN SYNDROMIC AND NON-SYNDROMIC CRANIOSYNOSTOSIS CASES. Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi. 82(2).
18.
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
19.
Toksoy, Güven, Firdevs Baş, Zehra Yavaş Abalı, et al.. (2018). A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations. Journal of Clinical Research in Pediatric Endocrinology. 10(3). 206–215. 21 indexed citations
20.
Baş, Firdevs, Güven Toksoy, Berrin Ergun-Longmire, et al.. (2018). Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene. The Journal of Steroid Biochemistry and Molecular Biology. 181. 88–97. 19 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.

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