Sevim Balcı

2.1k total citations
70 papers, 1.2k citations indexed

About

Sevim Balcı is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sevim Balcı has authored 70 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 22 papers in Molecular Biology and 21 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sevim Balcı's work include Prenatal Screening and Diagnostics (16 papers), Congenital limb and hand anomalies (11 papers) and Genomic variations and chromosomal abnormalities (10 papers). Sevim Balcı is often cited by papers focused on Prenatal Screening and Diagnostics (16 papers), Congenital limb and hand anomalies (11 papers) and Genomic variations and chromosomal abnormalities (10 papers). Sevim Balcı collaborates with scholars based in Türkiye, United States and Germany. Sevim Balcı's co-authors include Nurten Akarsu, Burhan Say, Hülya Kayserili, Bernd Wollnik, F Skovby, Han G. Brunner, Wim Brussel, Nilgün Atakan, Jacopo Celli and Ellen van Beusekom and has published in prestigious journals such as The Lancet, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Sevim Balcı

68 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sevim Balcı Türkiye 17 552 463 200 181 160 70 1.2k
Frank Majewski Germany 16 579 1.0× 755 1.6× 200 1.0× 271 1.5× 118 0.7× 26 1.3k
Fahed Halal Canada 18 462 0.8× 564 1.2× 332 1.7× 151 0.8× 82 0.5× 50 1.2k
Laurence Taine France 21 428 0.8× 398 0.9× 147 0.7× 274 1.5× 86 0.5× 46 924
Florence Petit France 20 610 1.1× 461 1.0× 107 0.5× 105 0.6× 92 0.6× 61 1.0k
Maria Teresa Divizia Italy 17 541 1.0× 464 1.0× 135 0.7× 63 0.3× 89 0.6× 46 1.1k
J. Herrmann United States 21 388 0.7× 645 1.4× 261 1.3× 334 1.8× 162 1.0× 50 1.2k
Robert W. Marion United States 19 520 0.9× 460 1.0× 138 0.7× 111 0.6× 37 0.2× 47 1.2k
R. Sid Wilroy United States 21 635 1.2× 778 1.7× 166 0.8× 275 1.5× 44 0.3× 53 1.3k
Fernando Regla Vargas Brazil 24 805 1.5× 480 1.0× 215 1.1× 204 1.1× 121 0.8× 83 2.0k
M. Preus Canada 19 412 0.7× 443 1.0× 102 0.5× 122 0.7× 71 0.4× 44 966

Countries citing papers authored by Sevim Balcı

Since Specialization
Citations

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

Fields of papers citing papers by Sevim Balcı

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sevim Balcı

This figure shows the co-authorship network connecting the top 25 collaborators of Sevim Balcı. A scholar is included among the top collaborators of Sevim Balcı 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 Sevim Balcı. Sevim Balcı 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.
Uz, Elif, Yasemin Alanay, Dilek Aktaş, et al.. (2010). Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia. The American Journal of Human Genetics. 86(5). 789–796. 101 indexed citations
2.
Soysal, Yasemin, Sevim Balcı, Thomas Liehr, et al.. (2009). Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy. American Journal of Medical Genetics Part A. 149A(12). 2782–2787. 13 indexed citations
3.
Kayserili, Hülya, Elif Uz, Carien M. Niessen, et al.. (2009). ALX4 dysfunction disrupts craniofacial and epidermal development. Human Molecular Genetics. 18(22). 4357–4366. 86 indexed citations
4.
Frank, Valeska, Nadina Ortiz Brüchle, Suzanna G.M. Frints, et al.. (2007). Aberrant splicing is a common mutational mechanism inMKS1, a key player in Meckel-Gruber syndrome. Human Mutation. 28(6). 638–639. 17 indexed citations
5.
Beksaç, Mehmet Sinan, Sevim Balcı, Emine Seda Güvendağ Güven, Süleyman Güven, & Süheyla Özkutlu. (2007). Complex conotruncal cardiac anomalies consecutively in three siblings from a consanguineous family possibly associated with maternal hyperhomocysteinemia. Archives of Gynecology and Obstetrics. 276(5). 547–549. 7 indexed citations
6.
Tezcan, İlhan, Fügen Ersoy, Özden Sanal, et al.. (2005). Long-term survival in severe combined immune deficiency: The role of persistent maternal engraftment. The Journal of Pediatrics. 146(1). 137–140. 13 indexed citations
7.
Ekinci, Gazanfer, Sevim Balcı, & Canan Erzen. (2005). An anencephalic monocephalus diprosopus "headed twin": postmortem and CT findings with emphasis on the cranial bones. The Turkish Journal of Pediatrics. 47(2). 195–198. 8 indexed citations
8.
9.
Zorlu, Pelin, et al.. (2003). Is it a new syndrome or a clinical variability in cerebro‐oculo‐nasal syndrome?. American Journal of Medical Genetics Part A. 120A(2). 253–255. 3 indexed citations
10.
Derbent, Murat, et al.. (2001). Popliteal pterygium associated with neonatal Marfan syndrome: case report*. Clinical Dysmorphology. 10(3). 209–213. 4 indexed citations
11.
Tekinalp, Gülsevin, S. Ümit Sarící, A. Seval Özgü-Erdinç, et al.. (2001). LETHAL HYDROPS FETALIS DUE TO CONGENITAL DYSERYTHROPOIETIC ANEMIA IN A NEWBORN: Association of a New Skeletal Abnormality. Pediatric Hematology and Oncology. 18(8). 537–542. 12 indexed citations
12.
Balcı, Sevim, et al.. (2000). Three sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cysts. American Journal of Medical Genetics. 90(3). 185–187. 21 indexed citations
13.
Bokhoven, Hans van, Jacopo Celli, Hülya Kayserili, et al.. (2000). Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome. Nature Genetics. 25(4). 423–426. 195 indexed citations
14.
Atalay, Figen, et al.. (2000). Sister chromatid exchange rate from pleural fluid cells in patients with malignant mesothelioma. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 465(1-2). 159–163. 8 indexed citations
15.
Bartsch, Oliver, et al.. (1999). FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy. European Journal of Human Genetics. 7(7). 748–756. 65 indexed citations
16.
Beksaç, Mehmet Sinan, et al.. (1995). An artificial intelligent diagnostic system with neural networks to determine genetical disorders and fetal health by using maternal serum markers. European Journal of Obstetrics & Gynecology and Reproductive Biology. 59(2). 131–136. 18 indexed citations
17.
Balcı, Sevim, et al.. (1995). Familial intestinal polyatresia syndrome. Clinical Genetics. 47(5). 245–247. 11 indexed citations
18.
Bakkaloğlu, Ayşı̇n, Seza Özen, Nesrin Beşbaş, U Saatçi, & Sevim Balcı. (1994). Down syndrome associated with systemic lupus erythematosus: a mere coincidence or a significant association?. Clinical Genetics. 46(4). 322–323. 8 indexed citations
19.
Balcı, Sevim, et al.. (1991). Familial short rib syndrome, type Beemer, with pyloric stenosis and short intestine, one case diagnosed prenatally. Clinical Genetics. 39(4). 298–303. 10 indexed citations
20.
Say, Burhan, et al.. (1973). Incidence of Congenital Malformations in a Sample of the Turkish Population. Human Heredity. 23(5). 434–441. 21 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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