Elif Uz

1.3k total citations
13 papers, 659 citations indexed

About

Elif Uz is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Elif Uz has authored 13 papers receiving a total of 659 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Elif Uz's work include Craniofacial Disorders and Treatments (4 papers), Amino Acid Enzymes and Metabolism (1 paper) and Congenital Ear and Nasal Anomalies (1 paper). Elif Uz is often cited by papers focused on Craniofacial Disorders and Treatments (4 papers), Amino Acid Enzymes and Metabolism (1 paper) and Congenital Ear and Nasal Anomalies (1 paper). Elif Uz collaborates with scholars based in Türkiye, United States and United Kingdom. Elif Uz's co-authors include Tayfun Özçelık, Nurten Akarsu, Yasemin Alanay, İbrahim Vargel, Gökhan Tunçbįlek, Sevim Balcı, Bernd Wollnik, Mehmet Alikaşifoğlu, Üner Tan and Gökçe Törüner and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Elif Uz

13 papers receiving 649 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elif Uz Türkiye	11	304	293	126	71	59	13	659
Zeynep Coban‐Akdemir United States	18	396 1.3×	544 1.9×	131 1.0×	53 0.7×	86 1.5×	50	965
Yangzhu Du United States	13	366 1.2×	611 2.1×	110 0.9×	49 0.7×	47 0.8×	20	979
Tomoko Uehara Japan	14	275 0.9×	358 1.2×	82 0.7×	29 0.4×	34 0.6×	79	733
José Elías García‐Ortíz Mexico	14	463 1.5×	443 1.5×	96 0.8×	37 0.5×	44 0.7×	48	944
Irene Bottillo Italy	18	253 0.8×	531 1.8×	98 0.8×	114 1.6×	74 1.3×	65	1.1k
Jörg Seidel Germany	8	284 0.9×	505 1.7×	112 0.9×	30 0.4×	93 1.6×	18	767
Silvia Majore Italy	16	319 1.0×	427 1.5×	59 0.5×	63 0.9×	29 0.5×	48	808
Jennifer Hebert United States	13	274 0.9×	640 2.2×	86 0.7×	34 0.5×	40 0.7×	19	910
Diane Beysen Belgium	12	357 1.2×	397 1.4×	45 0.4×	121 1.7×	27 0.5×	20	951
Seval Türkmen Germany	17	474 1.6×	752 2.6×	87 0.7×	56 0.8×	98 1.7×	36	1.3k

Countries citing papers authored by Elif Uz

Since Specialization

Citations

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

Fields of papers citing papers by Elif Uz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elif Uz

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

All Works

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13 of 13 papers shown

Yılmaz, Mustafa Sertaç, et al.. (2020). Intracerebroventricularly injected nesfatin-1 activates central cyclooxygenase and lipoxygenase pathways. Autonomic Neuroscience. 226. 102670–102670. 4 indexed citations

Çağdaş, Deniz, Baran Erman, Elif Uz, et al.. (2015). STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation. Clinical Immunology. 161(2). 316–323. 55 indexed citations

Alanay, Yasemin, Bekir Ergüner, Eda Ütine, et al.. (2013). TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia. American Journal of Medical Genetics Part A. 164(2). 291–304. 23 indexed citations

Bonnard, Carine, Mohammad Shboul, Hane Lee, et al.. (2012). Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1. Nature Genetics. 44(6). 709–713. 53 indexed citations

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

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

Uz, Elif, Rezan Topaloğlu, Yelda Bilginer, et al.. (2009). Increased frequency of extremely skewed X chromosome inactivation in juvenile idiopathic arthritis. Arthritis & Rheumatism. 60(11). 3410–3412. 15 indexed citations

Uz, Elif, Ahmed Rebaï, Mouna Mnif, et al.. (2009). Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases. Arthritis Research & Therapy. 11(4). 73 indexed citations

Plagnol, Vincent, Elif Uz, Chris Wallace, et al.. (2008). Extreme Clonality in Lymphoblastoid Cell Lines with Implications for Allele Specific Expression Analyses. PLoS ONE. 3(8). e2966–e2966. 45 indexed citations

10.

Özçelık, Tayfun, Nurten Akarsu, Elif Uz, et al.. (2008). Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans. Proceedings of the National Academy of Sciences. 105(11). 4232–4236. 71 indexed citations

11.

Uz, Elif, Laurence Loubière, Vijayakrishna K. Gadi, et al.. (2007). Skewed X-Chromosome Inactivation in Scleroderma. Clinical Reviews in Allergy & Immunology. 34(3). 352–355. 39 indexed citations

12.

Özçelık, Tayfun, Elif Uz, Cemaliye Boylu Akyerli, et al.. (2006). Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity. European Journal of Human Genetics. 14(6). 791–797. 90 indexed citations

13.

Uz, Elif, İsmail Dölen, Ragıp Atakan Al, & Tayfun Özçelık. (2006). Extremely skewed X-chromosome inactivation is increased in pre-eclampsia. Human Genetics. 121(1). 101–105. 4 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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