Pervin Dinçer
Impact in
- Cell Biology top 5%
- Calpain Protease Function and Regulation
-
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Papers in
-
- Muscle Physiology and Disorders 25
- Nuclear Structure and Function 7
- Ubiquitin and proteasome pathways 6
- RNA Research and Splicing 5
- Cell Biology 11
- Calpain Protease Function and Regulation 6
- Skin and Cellular Biology Research 4
- Co-authors
- Haluk Topaloğlu (17 shared papers)Beril Talim (14 shared papers)Hülya Gündeşli (7 shared papers)Burcu Balcı-Hayta (9 shared papers)Tobias Willer (3 shared papers)Petek Korkusuz (4 shared papers)Göknur Haliloğlu (4 shared papers)Kevin P. Campbell (3 shared papers)
- Journals
- Neuromuscular Disorders (8 papers)Prenatal Diagnosis (2 papers)Journal of Medical Genetics (2 papers)Scientific Reports (1 paper)Cell Biology International (1 paper)
- Partner nations
- TürkiyeUnited StatesUnited Kingdom
In The Last Decade
Pervin Dinçer
41 papers receiving 922 citations
Peers
Comparison fields: 5 of 75
- Cell Biology 313
- Cellular and Molecular Neuroscience 258
- Genetics 135
- Molecular Biology 825
- Cardiology and Cardiovascular Medicine 176
Countries citing papers authored by Pervin Dinçer
This map shows the geographic impact of Pervin Dinçer'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 Pervin Dinçer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pervin Dinçer more than expected).
Fields of papers citing papers by Pervin Dinçer
This network shows the impact of papers produced by Pervin Dinçer. 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 Pervin Dinçer. The network helps show where Pervin Dinçer may publish in the future.
Co-authors
The 25 scholars most cited alongside Pervin Dinçer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 45 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 178 | |
| 2 | 2005 | 120 | |
| 3 | 1997 | 87 | |
| 4 | Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins. | 1997 | 87 |
| 5 | 2010 | 79 | |
| 6 | 2014 | 59 | |
| 7 | 2013 | 50 | |
| 8 | 2003 | 32 | |
| 9 | 2006 | 31 | |
| 10 | 1997 | 30 | |
| 11 | 2000 | 23 | |
| 12 | 2021 | 17 | |
| 13 | 2021 | 17 | |
| 14 | 2000 | 15 | |
| 15 | 2022 | 13 | |
| 16 | 2009 | 13 | |
| 17 | 2009 | 12 | |
| 18 | 2022 | 8 | |
| 19 | 1996 | 8 | |
| 20 | Identification of an ancestral haplotype of the 35delG mutation in the GJB2 (connexin 26) gene responsible for autosomal recessive non-syndromic hearing loss in families from the Eastern Black Sea Region in Turkey. | 2005 | 8 |
About Pervin Dinçer
Pervin Dinçer is a scholar working on Molecular Biology, Cell Biology, Cardiology and Cardiovascular Medicine, Cellular and Molecular Neuroscience and Oncology, having authored 45 papers that have together received 947 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (25 papers), Nuclear Structure and Function (7 papers), Genetic Neurodegenerative Diseases (6 papers), Calpain Protease Function and Regulation (6 papers), Ubiquitin and proteasome pathways (6 papers), Cardiomyopathy and Myosin Studies (5 papers), RNA Research and Splicing (5 papers) and Skin and Cellular Biology Research (4 papers). The work is most often cited by research in Cell Biology (313 citations), Cellular and Molecular Neuroscience (258 citations), Genetics (135 citations), Molecular Biology (825 citations) and Cardiology and Cardiovascular Medicine (176 citations). Pervin Dinçer has collaborated with scholars based in Türkiye, United States and United Kingdom. Frequent co-authors include Haluk Topaloğlu, Beril Talim, Hülya Gündeşli, Burcu Balcı-Hayta, Tobias Willer, Petek Korkusuz, Göknur Haliloğlu, Kevin P. Campbell, Gülsev Kale and Francesco Muntoni. Their work appears in journals such as Neuromuscular Disorders, Prenatal Diagnosis, Journal of Medical Genetics, Scientific Reports and Cell Biology International.
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.