Sevim Balcı

2.1k citations

70 papers · 1.3k · h-index 18

Impact in

Developmental Biology top 2%
- Congenital limb and hand anomalies
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research

Papers in

Genetics 29
- Genomic variations and chromosomal abnormalities 10
- Craniofacial Disorders and Treatments 5
Molecular Biology 22
- Hedgehog Signaling Pathway Studies 9

Co-authors: Nurten Akarsu (4 shared papers)Burhan Say (10 shared papers)Hülya Kayserili (2 shared papers)Nilgün Atakan (1 shared paper)Bernd Wollnik (3 shared papers)Han G. Brunner (1 shared paper)Ellen van Beusekom (1 shared paper)E. Ferda Perçin (1 shared paper)
Journals: Clinical Genetics (5 papers)Acta Obstetricia Et Gynecologica Scandinavica (2 papers)Human Genetics (2 papers)European Journal of Human Genetics (2 papers)The Lancet (2 papers)
Partner nations: Türkiye United States Germany

In The Last Decade

Sevim Balcı

67 papers receiving 1.1k citations

Peers

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-authors

The 25 scholars most cited alongside Sevim Balcı, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sevim Balcı Line = papers co-authored together Sevim Balcı links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 70 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome Nature Genetics ·Hans van Bokhoven, Jacopo Celli, Hülya Kayserili, Ellen van Beusekom, Sevim Balcı, Wim Brussel, F Skovby, Bronwyn Kerr, E. Ferda Perçin, Nurten Akarsu, Han G. Brunner	2000	207
2	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 ·Elif Uz, Yasemin Alanay, Dilek Aktaş, İbrahim Vargel, Şafak Güçer, Gökhan Tunçbi̇lek, Ferdinand von Eggeling, Engin Yılmaz, Özgür Deren, Nicole Posorski, Hi̇lal Özdağ, Thomas Liehr, Sevim Balcı, Mehmet Alikaşifoğlu, Bernd Wollnik, Nurten Akarsu	2010	111
3	A specific mutation in the distant sonic hedgehog (SHH)cis-regulator (ZRS) causes Werner mesomelic syndrome (WMS) while complete ZRS duplications underlie Haas type polysyndactyly and preaxial polydactyly (PPD) with or without triphalangeal thumb Human Mutation ·Dagmar Wieczorek, Barbara Pawlik, Yun Li, Nurten Akarsu, Almuth Caliebe, Klaus May, Bernd Schweiger, Fernando Regla Vargas, Sevim Balcı, Gabriele Gillessen‐Kaesbach, Bernd Wollnik	2009	97
4	ALX4 dysfunction disrupts craniofacial and epidermal development Human Molecular Genetics ·Hülya Kayserili, Elif Uz, Carien M. Niessen, İbrahim Vargel, Yasemin Alanay, Gökhan Tunçbi̇lek, Gökhan Yigit, Zehra Oya Uyguner, Şükrü Candan, Hamza Okur, Serkan Kaygin, Sevim Balcı, Emin Mavili, Mehmet Alikaşifoğlu, Ingo Haase, Bernd Wollnik, Nurten Akarsu	2009	93
5	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 ·Oliver Bartsch, Annett Wagner, Georg Klaus Hinkel, Petra Krebs, Markus Stümm, Bernhard Schmalenberger, Sabine Böhm, Sevim Balcı, Frank Majewski	1999	69
6	Dermatological manifestations of 71 Down syndrome children admitted to a clinical genetics unit Clinical Genetics ·M. Erics, Sevim Balcı, Nilgün Atakan	1996	62
7	Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1–11.2;p13.3) Developmental Medicine & Child Neurology ·Sevim Balcı, Aysun Ünal, Özlem Engiz, Dilek Aktaş, Thomas Liehr, Madelaine Gross, Kristin Mrasek, Serap Saygı	2007	35
8	Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies American Journal of Medical Genetics Part A ·Sevim Balcı, Özlem Engiz, Dilek Aktaş, İbrahim Vargel, Mehmet Sinan Beksaç, Kristin Mrasek, Joris Vermeesch, Thomas Liehr	2006	34
9	Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy American Journal of Medical Genetics Part A ·Yasemin Soysal, Sevim Balcı, Kuyaş Hekimler, Thomas Liehr, Elisabeth Ewers, Jacqueline Schoumans, The‐Hung Bui, Fadime Mutlu İçduygu, Nadezda Kosyakova, Necat İmirzalıoğlu	2009	29
10	Is the novel SCKL3 at 14q23 the predominant Seckel locus? European Journal of Human Genetics ·(unknown), Vasiliki Ninis, Sı̇bel Aylı̇n Uğur İşerı̇, Beyhan Tüysüz, Mehmet Seven, Sevim Balcı, Judith Goodship, Aslıhan Tolun	2003	24
11	A NEW SYNDROME OF DYSMORPHOGENESIS: IMPERFORATE‐ANUS ASSOCIATED WITH POLY‐OLIGODACTYLY AND SKELETAL (MAINLY VERTEBRAL) ANOMALIES Acta Paediatrica ·Burhan Say, Sevim Balcı, Tuğrul Pırnar, Ergül Tunçbılek	1971	23
12	Incidence of Congenital Malformations in a Sample of the Turkish Population Human Heredity ·Burhan Say, Ergül Tunçbılek, Sevim Balcı, Zehra Muluk, Talat Gögüs, Muhsin Saraçlar, Cevat Koçal	1973	22
13	Familial ring (18) mosaicism in a 23‐year‐old young adult with 46,XY,r(18) (::p11→q21::)/46,XY karyotype, intellectual disability, motor retardation and single maxillary incisor and in his phenotypically normal mother, karyotype 47,XX,+r(18)(::p11→q21::)/46,XX American Journal of Medical Genetics Part A ·Sevim Balcı, Celal Tümer, Ç. Karaca, Oliver Bartsch	2011	20
14	Noonan syndrome and systemic lupus erythematosus: presentation in childhood Clinical Dysmorphology ·Yasemin Alanay, Sevim Balcı, Seza Özen	2004	19
15	BIRTH DEFECTS AND ORAL CONTRACEPTIVES The Lancet ·Sevim Balcı, Burhan Say, Tuğrul Pırnar, Akgün Hiçsönmez	1973	19
16	Imperforate anus/polydactyly/vertebral anomalies syndrome: A hereditary trait? The Journal of Pediatrics ·Burhan Say, Sevim Balcı, Tuğrul Pırnar, Akgün Hiçsönmez	1971	19
17	Aberrant splicing is a common mutational mechanism inMKS1, a key player in Meckel-Gruber syndrome Human Mutation ·Valeska Frank, Nadina Ortiz Brüchle, Silke Mager, Suzanna G.M. Frints, Axel Bohring, Gabriele du Bois, Irmgard Debatin, Heide Seidel, Jan Senderek, Nesrin Beşbaş, Unda Todt, Christian Kubisch, T. Grimm, Fulya Tekşen, Sevim Balcı, Klaus Zerres, Carsten Bergmann	2007	18
18	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 ·Mehmet Sinan Beksaç, (unknown), Ömer Faruk Özkan, Ayşe Nur Çakar, Sevim Balcı, Ümit Karakaş, Yahya Lâleli	1995	18
19	Formation of a familial ring chromosome 18 investigated by SNP‐array analysis American Journal of Medical Genetics Part A ·Sevim Balcı, Johannes Zschocke, Dieter Kotzot, Mehmet Ali Ergün, Ana Spreiz	2014	16
20	Unusual calcium deposition in cartilage associated with short stature and peculiar facial features: A case report Pediatric Radiology ·Burhan Say, Sevim Balcı, Tuğrul Pırnar, R. G. Israel, M Atasu	1973	14

About Sevim Balcı

Sevim Balcı is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Developmental Biology, having authored 70 papers that have together received 1.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (16 papers), Congenital limb and hand anomalies (11 papers), Genomic variations and chromosomal abnormalities (10 papers), Hedgehog Signaling Pathway Studies (9 papers), Congenital Anomalies and Fetal Surgery (7 papers), Urological Disorders and Treatments (7 papers), Fetal and Pediatric Neurological Disorders (5 papers) and Craniofacial Disorders and Treatments (5 papers). The work is most often cited by research in Developmental Biology (160 citations), Genetics (479 citations), Pediatrics, Perinatology and Child Health (191 citations), Genetics (84 citations) and Molecular Biology (544 citations). Sevim Balcı has collaborated with scholars based in Türkiye, United States and Germany. Frequent co-authors include Nurten Akarsu, Burhan Say, Hülya Kayserili, Nilgün Atakan, Bernd Wollnik, Han G. Brunner, Ellen van Beusekom, E. Ferda Perçin, Wim Brussel and Bronwyn Kerr. Their work appears in journals such as Clinical Genetics, Acta Obstetricia Et Gynecologica Scandinavica, Human Genetics, European Journal of Human Genetics and The Lancet.

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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