Seher Başaran
Impact in
Papers in
- Genetics 33
- Genomic variations and chromosomal abnormalities 15
- Neurogenetic and Muscular Disorders Research 5
- Genetic Syndromes and Imprinting 5
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- Prenatal Screening and Diagnostics 20
- Co-authors
- Birsen Karaman (35 shared papers)Zehra Oya Uyguner (29 shared papers)Hülya Kayserili (20 shared papers)Toshitaka Kawarai (1 shared paper)Peter St George‐Hyslop (1 shared paper)Carla Babalini (1 shared paper)Gaetano Bernardi (1 shared paper)Antonio Orlacchio (1 shared paper)
- Journals
- Prenatal Diagnosis (4 papers)Clinical Genetics (4 papers)Fetal Diagnosis and Therapy (4 papers)European Journal of Medical Genetics (3 papers)Hereditas (2 papers)
- Partner nations
- TürkiyeGermanyUnited States
In The Last Decade
Seher Başaran
66 papers receiving 802 citations
Peers
Comparison fields: 5 of 63
- Genetics 161
- Neurology 94
- Pediatrics, Perinatology and Child Health 184
- Neurology 145
- Genetics 269
Countries citing papers authored by Seher Başaran
This map shows the geographic impact of Seher Başaran'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 Seher Başaran with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Seher Başaran more than expected).
Fields of papers citing papers by Seher Başaran
This network shows the impact of papers produced by Seher Başaran. 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 Seher Başaran. The network helps show where Seher Başaran may publish in the future.
Co-authors
The 25 scholars most cited alongside Seher Başaran, 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 72 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 187 | |
| 2 | 1996 | 47 | |
| 3 | 2004 | 39 | |
| 4 | 2007 | 37 | |
| 5 | 1990 | 27 | |
| 6 | 2011 | 25 | |
| 7 | 2008 | 24 | |
| 8 | 1995 | 23 | |
| 9 | 2003 | 22 | |
| 10 | 2018 | 22 | |
| 11 | 1992 | 19 | |
| 12 | 2018 | 19 | |
| 13 | 1988 | 18 | |
| 14 | 1994 | 18 | |
| 15 | 2007 | 17 | |
| 16 | 2009 | 16 | |
| 17 | 2019 | 16 | |
| 18 | 2001 | 15 | |
| 19 | 2018 | 14 | |
| 20 | 2002 | 11 |
About Seher Başaran
Seher Başaran is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Surgery and Genetics, having authored 72 papers that have together received 826 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (15 papers), RNA modifications and cancer (8 papers), Chromosomal and Genetic Variations (7 papers), Neurogenetic and Muscular Disorders Research (5 papers), Genetic Syndromes and Imprinting (5 papers), Sexual Differentiation and Disorders (4 papers) and Congenital Anomalies and Fetal Surgery (4 papers). The work is most often cited by research in Genetics (161 citations), Neurology (94 citations), Pediatrics, Perinatology and Child Health (184 citations), Neurology (145 citations) and Genetics (269 citations). Seher Başaran has collaborated with scholars based in Türkiye, Germany and United States. Frequent co-authors include Birsen Karaman, Zehra Oya Uyguner, Hülya Kayserili, Toshitaka Kawarai, Peter St George‐Hyslop, Carla Babalini, Gaetano Bernardi, Antonio Orlacchio, H. Ermiş and Antonella Borreca. Their work appears in journals such as Prenatal Diagnosis, Clinical Genetics, Fetal Diagnosis and Therapy, European Journal of Medical Genetics and Hereditas.
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.