Abdullah Üzümcü

402 total citations
5 papers, 87 citations indexed

About

Abdullah Üzümcü is a scholar working on Surgery, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Abdullah Üzümcü has authored 5 papers receiving a total of 87 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Surgery, 2 papers in Molecular Biology and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Abdullah Üzümcü's work include Pectus Deformity Diagnosis and Treatment (2 papers), Head and Neck Anomalies (2 papers) and Hearing, Cochlea, Tinnitus, Genetics (1 paper). Abdullah Üzümcü is often cited by papers focused on Pectus Deformity Diagnosis and Treatment (2 papers), Head and Neck Anomalies (2 papers) and Hearing, Cochlea, Tinnitus, Genetics (1 paper). Abdullah Üzümcü collaborates with scholars based in Türkiye, Germany and Netherlands. Abdullah Üzümcü's co-authors include Zehra Oya Uyguner, Hülya Kayserili, Bernd Wollnik, Peter Nürnberg, Seher Başaran, Angelien Heister, Şükrü Candan, Han G. Brunner, Cynthia F. Bartels and Christian Netzer and has published in prestigious journals such as Human Mutation, American Journal of Medical Genetics Part A and Journal of genetics and genomics.

In The Last Decade

Abdullah Üzümcü

5 papers receiving 85 citations

Peers

Countries citing papers authored by Abdullah Üzümcü

Since Specialization

Citations

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

Fields of papers citing papers by Abdullah Üzümcü

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Abdullah Üzümcü

This figure shows the co-authorship network connecting the top 25 collaborators of Abdullah Üzümcü. A scholar is included among the top collaborators of Abdullah Üzümcü 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 Abdullah Üzümcü. Abdullah Üzümcü is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

5 of 5 papers shown

#	Work	Indexed citations
1	A mutation in the signal sequence ofLRP5in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats 2009 ·Human Mutation ·(unknown), Hülya Kayserili, Minrong Ai, Jan Freudenberg, Abdullah Üzümcü, Zehra Oya Uyguner, Cynthia F. Bartels, Stefan Höning, Alfredo Ramı́rez, Franz‐Georg Hanisch, Gudrun Nürnberg, Peter Nürnberg, Matthew L. Warman, Bernd Wollnik, Christian Kubisch, Christian Netzer	24
2	Ataxia with vitamin E deficiency associated with deafness. 2009 ·PubMed ·Bülent Kara, Abdullah Üzümcü, Zehra Oya Uyguner, Rasim Özgür Rosti, (unknown), Meral Özmen, Hülya Kayserili	6
3	Mutational screening of BASP1 and transcribed processed pseudogene TPΨg-BASP1 in patients with Möbius syndrome 2009 ·Journal of genetics and genomics ·Abdullah Üzümcü, Şükrü Candan, Güven Toksoy, Zehra Oya Uyguner, Birsen Karaman, (unknown), Burak Tatlı, Hülya Kayserili, Adnan Yüksel, (unknown), Memnune Yüksel‐Apak, Seher Başaran	3
4	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 2009 ·European Journal of Medical Genetics ·Abdullah Üzümcü, Birsen Karaman, Güven Toksoy, Zehra Oya Uyguner, Şükrü Candan, (unknown), Burak Tatlı, (unknown), Adnan Yüksel, Hülya Kayserili, Seher Başaran	16
5	MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation 2007 ·American Journal of Medical Genetics Part A ·Ersan Kalay, Abdullah Üzümcü, Elmar Krieger, Refik Çaylan, Zehra Oya Uyguner, (unknown), 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	38

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.

Explore authors with similar magnitude of impact