Sevim Balcı

2.1k citations

82 papers · 1.6k · h-index 18

Impact in

Developmental Biology top 0.5%
- Congenital limb and hand anomalies
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Genomics and Rare Diseases
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research

Papers in

Developmental Biology 23
- Congenital limb and hand anomalies 23
Genetics 32
- Craniofacial Disorders and Treatments 9
- Genomic variations and chromosomal abnormalities 9
- Congenital Ear and Nasal Anomalies 7
- Connective tissue disorders research 7
- Genomics and Rare Diseases 6

Co-authors: Nurten Ayse Akarsu (4 shared papers)Burhan Say (10 shared papers)Hülya Kayserili (2 shared papers)Bernd Wollnik (3 shared papers)Nilgün Atakan (1 shared paper)Yasemin Alanay (3 shared papers)Dilek Aktaş (4 shared papers)Han G. Brunner (1 shared paper)
Journals: Clinical Genetics (5 papers)The Lancet (3 papers)Human Genetics (3 papers)Human Mutation (2 papers)Acta Paediatrica (2 papers)
Partner nations: Türkiye Germany Netherlands

In The Last Decade

Sevim Balcı

77 papers receiving 1.4k 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 82 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, Flemming Skovby, Bronwyn A. Kerr	2000	214
2	Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis The American Journal of Human Genetics ·Sandra Hanks, Sarah Adams, Jenny B. Douglas, Laura T. Arbour, David J. Atherton, Sevim Balcı, Harald Bode, Mary Ellen Campbell	2003	181
3	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	2010	117
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	2009	104
5	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 Ayse Akarsu, Almuth Caliebe, Bernd Schweiger, Fernando Regla Vargas, Sevim Balcı	2009	102
6	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, Sevim Balcı, Frank Majewski +1 other	1999	72
7	Dermatological manifestations of 71 Down syndrome children admitted to a clinical genetics unit Clinical Genetics ·M. Erics, Sevim Balcı, Nilgün Atakan	1996	59
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 Robert Vermeesch, Thomas Liehr	2006	36
9	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
10	Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy American Journal of Medical Genetics Part A ·Yasemin Dilek Soysal, Sevim Balcı, Kuyaş Hekimler, Thomas Liehr, Elisabeth Ewers, Jacqueline Schoumans, The‐Hung Bui, Fadime Mutlu İçduygu	2009	30
11	Is the novel SCKL3 at 14q23 the predominant Seckel locus? European Journal of Human Genetics ·Vasiliki Ninidu Ninis, Sı̇bel Aylı̇n Uğur İşerı̇, Beyhan Tüysüz, Mehmet Seven, Sevim Balcı, Judith Goodship, Aslıhan Tolun +1 other	2003	25
12	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	24
13	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	24
14	Imperforate anus/polydactyly/vertebral anomalies syndrome: A hereditary trait? The Journal of Pediatrics ·Burhan Say, Sevim Balcı, Tuğrul Pırnar, Akgün Hiçsönmez	1971	22
15	Noonan syndrome and systemic lupus erythematosus: presentation in childhood Clinical Dysmorphology ·Yasemin Alanay, Sevim Balcı, Seza Özen	2004	21
16	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	21
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	2007	20
18	BIRTH DEFECTS AND ORAL CONTRACEPTIVES The Lancet ·Sevim Balcı, Burhan Say, Tuğrul Pırnar, Akgün Hiçsönmez	1973	18
19	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, Ayşe Nur Çakar, Sevim Balcı, Ümit Karakaş, Yahya Rauf Laleli +2 others	1995	17
20	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	15

About Sevim Balcı

Sevim Balcı is a scholar working on Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health, Genetics and Surgery, having authored 82 papers that have together received 1.6k indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (23 papers), Craniofacial Disorders and Treatments (9 papers), Genomic variations and chromosomal abnormalities (9 papers), Fetal and Pediatric Neurological Disorders (8 papers), Congenital Ear and Nasal Anomalies (7 papers), Connective tissue disorders research (7 papers), Genomics and Rare Diseases (6 papers) and Spinal Dysraphism and Malformations (6 papers). The work is most often cited by research in Developmental Biology (269 citations), Genetics (666 citations), Pediatrics, Perinatology and Child Health (158 citations), Genetics (80 citations) and Pharmacy (27 citations). Sevim Balcı has collaborated with scholars based in Türkiye, Germany and Netherlands. Frequent co-authors include Nurten Ayse Akarsu, Burhan Say, Hülya Kayserili, Bernd Wollnik, Nilgün Atakan, Yasemin Alanay, Dilek Aktaş, Han G. Brunner, Thomas Liehr and Wim Brussel. Their work appears in journals such as Clinical Genetics, The Lancet, Human Genetics, Human Mutation and Acta Paediatrica.

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