Seher Başaran

1.7k citations

73 papers · 814 indexed · h-index 17

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
Neurology top 10%
- Amyotrophic Lateral Sclerosis Research
- Neurological diseases and metabolism

Papers in ⓘ

Developmental Biology 4
Pediatrics, Perinatology and Child Health 27
- Prenatal Screening and Diagnostics 23

Co-authors: Birsen Karaman (35 shared papers)Hülya Kayserili (22 shared papers)Zehra Oya Uyguner (29 shared papers)Carla Babalini (1 shared paper)Ekaterina Rogaeva (1 shared paper)Antonella Borreca (1 shared paper)Roberto Massa (1 shared paper)Carlo Patrono (1 shared paper)
Journals: Fetal Diagnosis and Therapy (4 papers)Prenatal Diagnosis (4 papers)Clinical Genetics (4 papers)European Journal of Medical Genetics (3 papers)Hereditas (2 papers)
Partner nations: Türkiye Germany United States

In The Last Decade

Seher Başaran

67 papers receiving 789 citations

Peers

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-authors

The 25 scholars most cited alongside Seher Başaran, 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 Seher Başaran Line = papers co-authored together Seher Başaran 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 73 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis Brain ·Antonio Orlacchio, Carla Babalini, Antonella Borreca, Carlo Patrono, Roberto Massa, Seher Başaran, Renato P. Munhoz, Ekaterina Rogaeva, Peter St George‐Hyslop, Gaetano Bernardi, Toshitaka Kawarai	2010	182
2	Isochromosome 18p Results from Maternal Meiosis II Nondisjunction European Journal of Human Genetics ·Dieter Kotzot, Gertrud Bundscherer, Fabiana Bernasconi, Lukrecija Brečević, Iosif W. Lurie, Seher Başaran, Carlo Baccicchetti, Adelheid Höller, Claudio Castellan, C Braun-Quentin, Rudolph A. Pfeiffer, Albert Schinzel	1996	47
3	Dandy-Walker Malformation: A Review of 78 Cases Diagnosed by Prenatal Sonography Fetal Diagnosis and Therapy ·Recep Has, H. Ermiş, Atıl Yüksel, L. İbrahimoğlu, Alkan Yıldırım, Hande Delier Sezer, Seher Başaran	2004	39
4	MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation American Journal of Medical Genetics Part A ·Ersan Kalay, Abdullah Üzümcü, Elmar Krieger, Refik Çaylan, Zehra Oya Uyguner, Melike Ulubil‐Emiroglu, Hidayet Erdöl, Hülya Kayserili, Günter Hafız, Nermin Başerer, Angelien Heister, Hans Christian Hennies, Peter Nürnberg, Seher Başaran, Han G. Brunner, Cor W. R. J. Cremers, Ahmet Karagüzel, Bernd Wollnik, Hannie Kremer	2007	38
5	Molecular basis of ?-thalassemia in Turkey: detection of rare mutations by direct sequencing Human Genetics ·C. Aulehla‐Scholz, Seher Başaran, Leyla Ağaoğlu, Ayten Arcasoy, Wolfgang Holzgreve, Peter Miny, F. Ridolfi, J. Horst	1990	27
6	Congenital heart disease in children with Downs syndrome: Turkish experience of 13 years Acta Cardiologica ·Kemal Nişli, Naci Öner, Şükrü Candan, Hülya Kayserili, Türkan Tansel, Emin Tirelı, Birsen Karaman, Rukiye Eker Ömeroğlu, Aygün Dindar, Ümrah Aydoğan, Seher Başaran, Türkân Ertuğrul	2008	26
7	Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutations American Journal of Medical Genetics Part A ·Hülya Kayserili, Umut Altunoğlu, H. Ozgur, Seher Başaran, Zehra Oya Uyguner	2011	23
8	Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatally American Journal of Medical Genetics ·Peter Miny, B. Koppers, Bernd Dworniczak, Nadia Bogdanova, Wolfgang Holzgreve, Sevgi Tercanli, Seher Başaran, Helga Rehder, Rita Exeler, J. Horst	1995	23
9	Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity BMC Pregnancy and Childbirth ·Halıl Aslan, Nilay Karaca, Seher Başaran, H. Ermiş, Yavuz Ceylan	2003	22
10	A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations Journal of Clinical Research in Pediatric Endocrinology ·Aslı Derya Kardelen, Güven Toksoy, Firdevs Baş, Zehra Yavaş Abalı, Ali Genco Gençay, Şükran Poyrazoğlu, Rüveyde Bundak, Umut Altunoğlu, Şahin Avcı, Adam Najaflı, Zehra Oya Uyguner, Birsen Karaman, Seher Başaran, Feyza Darendelıler	2018	21
11	Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene The Journal of Steroid Biochemistry and Molecular Biology ·Firdevs Baş, Güven Toksoy, Berrin Ergun-Longmire, Zehra Oya Uyguner, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Volkan Karaman, Şahin Avcı, Umut Altunoğlu, Rüveyde Bundak, Birsen Karaman, Seher Başaran, Feyza Darendelıler	2018	19
12	No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangements PubMed ·Albert Schinzel, P A Adelsberger, Franz Binkert, Seher Başaran, Stylianos E. Antonarakis	1992	19
13	Tetra‐amelia, lung hypo‐/aplasia, cleft lip‐palate, and heart defect: A new syndrome? American Journal of Medical Genetics ·Seher Başaran, Adnan Yüksel, H. Ermiş, Faik Kuseyri, Brian K. Agan, Memnune Yüksel‐Apak	1994	18
14	Rapid karyotyping for prenatal diagnosis in the second and third trimesters of pregnancy Prenatal Diagnosis ·Seher Başaran, Peter Miny, Ivar‐Harry Pawlowitzki, Jürgen Horst, Wolfgang Holzgreve	1988	18
15	A new locus for autosomal recessive non‐syndromic mental retardation maps to 1p21.1–p13.3 Clinical Genetics ·Zehra Oya Uyguner, Hülya Kayserili, Y. Li, Birsen Karaman, Gudrun Nürnberg, HC Hennies, C. Becker, Peter Nürnberg, Seher Başaran, MY Apak, Bernd Wollnik	2007	17
16	Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling Neuromuscular Disorders ·Güven Toksoy, Hacer Durmuş, Agharza Aghayev, Г. Г. Багирова, B Sevinc Rustemoglu, Seher Başaran, Şahin Avcı, Birsen Karaman, Yeşim Parman, Umut Altunoğlu, Zühal Yapıcı, Pınar Tektürk, Feza Deymeer, Haluk Topaloğlu, Hülya Kayserili, Piraye Oflazer, Zehra Oya Uyguner	2019	16
17	Molecular genetic screening of MBS1 locus on chromosome 13 for microdeletions and exclusion of FGF9, GSH1 and CDX2 as causative genes in patients with Moebius syndrome European Journal of Medical Genetics ·Abdullah Üzümcü, Birsen Karaman, Güven Toksoy, Zehra Oya Uyguner, Şükrü Candan, Hacer Eris, Burak Tatlı, Bilge Geçkinli, Adnan Yüksel, Hülya Kayserili, Seher Başaran	2009	16
18	Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS) Journal of Medical Genetics ·Hülya Kayserili, Timothy C. Cox, Liza L. Cox, Seher Başaran, G. Kilic, Andrea Ballabio, Memnune Yüksel‐Apak	2001	15
19	Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases Molecular Cytogenetics ·Birsen Karaman, Hülya Kayserili, Asadollah Ghanbari, Zehra Oya Uyguner, Güven Toksoy, Umut Altunoğlu, Seher Başaran	2018	13
20	Prenatal Diagnosis of 13q-Syndrome in a Fetus With Dandy-Walker Malformation Obstetrics and Gynecology ·Ahmet Gül, Altan Cebeci, Onur Erol, Yavuz Ceylan, Seher Başaran, Atıl Yüksel	2005	11

About Seher Başaran

Seher Başaran is a scholar working on Developmental Biology, Pediatrics, Perinatology and Child Health, Genetics, Research and Theory and Issues, ethics and legal aspects, having authored 73 papers that have together received 814 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (23 papers), Genomic variations and chromosomal abnormalities (17 papers), RNA modifications and cancer (8 papers), Chromosomal and Genetic Variations (8 papers), Genetic Syndromes and Imprinting (5 papers), Sexual Differentiation and Disorders (5 papers), Tumors and Oncological Cases (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). The work is most often cited by research in Genetics (177 citations), Neurology (104 citations), Pediatrics, Perinatology and Child Health (215 citations), Genetics (305 citations) and Neurology (149 citations). Seher Başaran has collaborated with scholars based in Türkiye, Germany and United States. Frequent co-authors include Birsen Karaman, Hülya Kayserili, Zehra Oya Uyguner, Carla Babalini, Ekaterina Rogaeva, Antonella Borreca, Roberto Massa, Carlo Patrono, Toshitaka Kawarai and H. Ermiş. Their work appears in journals such as Fetal Diagnosis and Therapy, Prenatal Diagnosis, Clinical Genetics, European Journal of Medical Genetics and Hereditas.

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