Seher Başaran

1.7k total citations
73 papers, 814 citations indexed

About

Seher Başaran is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Seher Başaran has authored 73 papers receiving a total of 814 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Genetics, 27 papers in Pediatrics, Perinatology and Child Health and 23 papers in Molecular Biology. Recurrent topics in Seher Başaran's work include Prenatal Screening and Diagnostics (23 papers), Genomic variations and chromosomal abnormalities (17 papers) and RNA modifications and cancer (8 papers). Seher Başaran is often cited by papers focused on Prenatal Screening and Diagnostics (23 papers), Genomic variations and chromosomal abnormalities (17 papers) and RNA modifications and cancer (8 papers). Seher Başaran collaborates with scholars based in Türkiye, Germany and United States. Seher Başaran's co-authors include Birsen Karaman, Hülya Kayserili, Zehra Oya Uyguner, Roberto Massa, Carlo Patrono, Antonella Borreca, Ekaterina Rogaeva, Renato P. Munhoz, Toshitaka Kawarai and Peter St George‐Hyslop and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Obstetrics and Gynecology.

In The Last Decade

Seher Başaran

67 papers receiving 789 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Seher Başaran Türkiye 17 305 278 215 177 149 73 814
Julie T. Parke United States 12 355 1.2× 304 1.1× 108 0.5× 133 0.8× 212 1.4× 14 1.0k
Katja Eggermann Germany 20 527 1.7× 703 2.5× 360 1.7× 399 2.3× 81 0.5× 44 1.2k
Hélène Bruyèrè Canada 17 401 1.3× 462 1.7× 137 0.6× 164 0.9× 37 0.2× 44 1.0k
Stavit A. Shalev Israel 19 416 1.4× 519 1.9× 84 0.4× 59 0.3× 49 0.3× 44 962
Rena E. Falk United States 19 447 1.5× 408 1.5× 174 0.8× 55 0.3× 71 0.5× 39 1.0k
Chia‐Cheng Hung Taiwan 19 181 0.6× 310 1.1× 146 0.7× 165 0.9× 22 0.1× 38 785
Eric A. M. Hennekam Netherlands 11 200 0.7× 408 1.5× 33 0.2× 230 1.3× 332 2.2× 14 957
Chiharu Torii Japan 16 243 0.8× 313 1.1× 106 0.5× 43 0.2× 54 0.4× 42 721
Fabiola Quintero‐Rivera United States 16 907 3.0× 634 2.3× 357 1.7× 96 0.5× 28 0.2× 54 1.4k
Emmanuelle Lemyre Canada 22 879 2.9× 550 2.0× 276 1.3× 63 0.4× 63 0.4× 52 1.3k

Countries citing papers authored by Seher Başaran

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Seher Başaran

This figure shows the co-authorship network connecting the top 25 collaborators of Seher Başaran. A scholar is included among the top collaborators of Seher Başaran 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 Seher Başaran. Seher Başaran 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.
Bostancı, Hayrani Eren, Ravikumar Kapavarapu, Fatih Çelik, et al.. (2025). Synthesis and in silico study of novel benzimidazole derivatives bearing oxadiazole moiety as potential carbonic anhydrase inhibitors, anticancer and antioxidant agents. Journal of Molecular Structure. 1342. 142750–142750. 1 indexed citations
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.
Toksoy, Güven, et al.. (2023). Novel GALT variations and genetic spectrum in Turkish population with the correlation of genotype and phenotype. Annals of Human Genetics. 87(6). 285–294.
4.
Karaman, Birsen, et al.. (2023). A rare ring chromosome 21 abnormality is associated with azoospermia in two different phenotypically normal cases. Systems Biology in Reproductive Medicine. 69(5). 387–393. 1 indexed citations
5.
Toksoy, Güven, et al.. (2022). INTER-POPULATION COMPARISONS AND THE IMPORTANCE IN INFECTIOUS DISEASES OF THE IRF7, TBK1, IFNAR1, IFNAR2 AND TLR3 GENE VARIANTS IN TURKISH INDIVIDUALS. SHILAP Revista de lepidopterología. 85(3). 344–354. 1 indexed citations
6.
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
7.
Uyguner, Zehra Oya, et al.. (2022). A new enrichment approach for candidate gene detection in unexplained recurrent pregnancy loss and implantation failure. Molecular Genetics and Genomics. 298(1). 253–272. 2 indexed citations
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.
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
10.
Toksoy, Güven, İbrahim Kalelioğlu, Selma Demır, et al.. (2021). NOONAN SENDROMU’NUN PRENATAL TANISINDA PTPN11 GEN ANALİZLERİNİN ETKİNLİĞİ. SHILAP Revista de lepidopterología. 84(1). 34–39. 1 indexed citations
11.
Samancı, Bedia, Güven Toksoy, Zeynep Tüfekçıoğlu, et al.. (2021). Clinical and molecular genetic findings of hereditary Parkinson's patients from Turkey. Parkinsonism & Related Disorders. 93. 35–39. 3 indexed citations
12.
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
13.
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
14.
Başaran, Seher & Sergül Duygulu. (2015). Hemşirelikte Güç Kavramının Analizi. DergiPark (Istanbul University). 1(3). 62–73. 1 indexed citations
15.
Ergül, Yakup, Kemal Nişli, Hülya Kayserili, et al.. (2012). Evaluation of coronary artery abnormalities in Williams syndrome patients using myocardial perfusion scintigraphy and CT angiography. Cardiology Journal. 19(3). 301–308. 11 indexed citations
16.
Has, Recep, İbrahim Kalelioğlu, H. Ermiş, et al.. (2006). Screening for Fetal Chromosomal Abnormalities with Nuchal Translucency Measurement in the First Trimester. Fetal Diagnosis and Therapy. 21(4). 355–359. 8 indexed citations
17.
Aslan, Halıl, et al.. (2003). Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity. BMC Pregnancy and Childbirth. 3(1). 1–1. 22 indexed citations
18.
Uyguner, Zehra Oya, Bernd Wollnik, Hülya Kayserili, et al.. (2000). Establishment of a Nonradioactive Molecular Diagnosis of Fragile-X Syndrome. DergiPark (Istanbul University). 3 indexed citations
19.
Artan, Sevilhan, et al.. (1999). FISH analysis with locus‐specific probes in sperm from two translocation carrier men. Clinical Genetics. 56(2). 129–135. 4 indexed citations
20.
Kotzot, Dieter, Lukrecija Brečević, Iosif W. Lurie, et al.. (1996). Isochromosome 18p Results from Maternal Meiosis II Nondisjunction. European Journal of Human Genetics. 4(3). 168–174. 47 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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