Birsen Karaman

828 total citations
58 papers, 345 citations indexed

About

Birsen Karaman is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Birsen Karaman has authored 58 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 27 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Birsen Karaman's work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (11 papers) and RNA modifications and cancer (9 papers). Birsen Karaman is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (11 papers) and RNA modifications and cancer (9 papers). Birsen Karaman collaborates with scholars based in Türkiye, United States and Germany. Birsen Karaman's co-authors include Seher Başaran, Hülya Kayserili, Zehra Oya Uyguner, Güven Toksoy, Umut Altunoğlu, Şahin Avcı, Bernd Wollnik, Şükrü Candan, Firdevs Baş and Kemal Nişli and has published in prestigious journals such as SHILAP Revista de lepidopterología, Allergy and Clinical Endocrinology.

In The Last Decade

Birsen Karaman

51 papers receiving 334 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Birsen Karaman Türkiye 12 180 157 64 57 44 58 345
Daniele De Brasi Italy 14 224 1.2× 256 1.6× 73 1.1× 86 1.5× 43 1.0× 44 478
Barbara Delle Chiaie Belgium 7 195 1.1× 251 1.6× 30 0.5× 136 2.4× 48 1.1× 10 423
Moira Blyth United Kingdom 12 139 0.8× 162 1.0× 57 0.9× 51 0.9× 68 1.5× 22 379
Claire Turner United Kingdom 13 304 1.7× 414 2.6× 61 1.0× 183 3.2× 19 0.4× 14 578
Daniela Bettio Italy 12 169 0.9× 277 1.8× 49 0.8× 235 4.1× 17 0.4× 35 535
Susan J. Kirkpatrick United States 10 154 0.9× 211 1.3× 122 1.9× 120 2.1× 15 0.3× 13 430
Naoaki Hori Japan 10 191 1.1× 131 0.8× 110 1.7× 18 0.3× 20 0.5× 24 425
Cristina Molinatto Italy 10 270 1.5× 296 1.9× 43 0.7× 196 3.4× 27 0.6× 12 472
Rachel Michaelson‐Cohen Israel 12 201 1.1× 170 1.1× 36 0.6× 81 1.4× 32 0.7× 39 525
S Gough United Kingdom 9 132 0.7× 198 1.3× 79 1.2× 19 0.3× 27 0.6× 16 512

Countries citing papers authored by Birsen Karaman

Since Specialization
Citations

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

Fields of papers citing papers by Birsen Karaman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Birsen Karaman

This figure shows the co-authorship network connecting the top 25 collaborators of Birsen Karaman. A scholar is included among the top collaborators of Birsen Karaman 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 Birsen Karaman. Birsen Karaman 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.
Kalelioğlu, İbrahim, et al.. (2025). Diagnostic contribution of conventional and molecular karyotyping in congenital diaphragmatic hernia related copy number variations. Taiwanese Journal of Obstetrics and Gynecology. 64(4). 678–686.
2.
Uyguner, Zehra Oya, Birsen Karaman, Can Baykal, et al.. (2024). Genotype-Phenotype Correlation in Lipoid Proteinosis: 15 Cases from Turkiye. Molecular Syndromology. 16(4). 327–334.
3.
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
4.
Karaman, Birsen, et al.. (2024). Seeing Clowns with a Ring 20 Chromosome. SHILAP Revista de lepidopterología. 30(1). 31–35. 1 indexed citations
5.
Karaman, Birsen, et al.. (2024). Association of Antenatal Evaluations with Postmortem and Genetic Findings in the Series of Fetal Osteogenesis Imperfecta. Fetal Diagnosis and Therapy. 51(3). 285–299. 1 indexed citations
6.
Theil, Arjan F., Alex Pines, José María Heredia‐Genestar, et al.. (2023). Trichothiodystrophy‐associated MPLKIP maintains DBR1 levels for proper lariat debranching and ectodermal differentiation. EMBO Molecular Medicine. 15(11). e17973–e17973. 8 indexed citations
7.
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
8.
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
9.
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
10.
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
11.
Kalelioğlu, İbrahim, et al.. (2022). Fibular Agenesis and Ball-Like Toes Mimicking Preaxial Polydactyly: Prenatal Presentation of Du Pan Syndrome. Molecular Syndromology. 14(2). 152–157.
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. 3 indexed citations
13.
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
14.
Karaman, Birsen, et al.. (2020). Three Offspring with Cri-du-Chat Syndrome from Phenotypically Normal Parents. Molecular Syndromology. 11(2). 97–103. 3 indexed citations
15.
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
16.
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
17.
Yüksel, Atıl, et al.. (2016). P01.06: False‐positive and false‐negative results of cell‐free DNA testing. Ultrasound in Obstetrics and Gynecology. 48(S1). 168–169. 1 indexed citations
18.
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
19.
Çetin, Zafer, et al.. (2011). Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1). SHILAP Revista de lepidopterología. 14(1). 57–60. 2 indexed citations
20.
Karaman, Birsen, Bernd Wollnik, H. Ermiş, Memnune Yüksel‐Apak, & Seher Başaran. (2003). A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish family. Prenatal Diagnosis. 23(4). 336–339. 3 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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