Emine Bolat

767 total citations
6 papers, 246 citations indexed

About

Emine Bolat is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Emine Bolat has authored 6 papers receiving a total of 246 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Oncology. Recurrent topics in Emine Bolat's work include Genetic and Kidney Cyst Diseases (3 papers), Cancer-related Molecular Pathways (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Emine Bolat is often cited by papers focused on Genetic and Kidney Cyst Diseases (3 papers), Cancer-related Molecular Pathways (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Emine Bolat collaborates with scholars based in Netherlands, Germany and Australia. Emine Bolat's co-authors include Hans Scheffer, Ronald Roepman, Tuula Rinne, Hans van Bokhoven, Dorus A. Mans, Sylvia E. C. van Beersum, Heleen H. Arts, Liesbeth Spruijt, Janneke Schuurs-Hoeijmakers and Ernie M.H.F. Bongers and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and Clinical Chemistry.

In The Last Decade

Emine Bolat

6 papers receiving 246 citations

Peers

Emine Bolat

MB

GENET

ONCOL

CB

PPCH

Jennifer M. Huang United States

Marika Zanotti Italy

Pola Smirin‐Yosef Israel

Laura C. Collopy United Kingdom

Christian Osterburg Germany

Dominique Meunier Austria

Irina Lagovsky Israel

Sylvia Redon France

Francesco Cucco Italy

Hannah Carlson-Donohoe United States

Jennifer M. Huang United States

Emine Bolat

256 ×1.2

MB

160 ×0.9

GENET

38 ×0.5

ONCOL

47 ×1.3

CB

64 ×3.6

PPCH

Citations per year, relative to Emine Bolat Emine Bolat (= 1×) peers Jennifer M. Huang

Countries citing papers authored by Emine Bolat

Since Specialization

Citations

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

Fields of papers citing papers by Emine Bolat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emine Bolat

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

All Works

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6 of 6 papers shown

1.

Coene, Karlien L. M., Karsten Boldt, Jeroen van Reeuwijk, et al.. (2012). The lebercilin-like protein is embedded in a ciliary protein network and is preferentially expressed in motile cilia. SHILAP Revista de lepidopterología. 1(S1). 1 indexed citations

2.

Arts, Heleen H., Ernie M.H.F. Bongers, Dorus A. Mans, et al.. (2011). C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome. Journal of Medical Genetics. 48(6). 390–395. 102 indexed citations

3.

Coene, Karlien L. M., Dorus A. Mans, Karsten Boldt, et al.. (2011). The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase. Human Molecular Genetics. 20(18). 3592–3605. 52 indexed citations

4.

Rinne, Tuula, et al.. (2009). Spectrum of p63 mutations in a selected patient cohort affected with ankyloblepharon‐ectodermal defects‐cleft lip/palate syndrome (AEC). American Journal of Medical Genetics Part A. 149A(9). 1948–1951. 43 indexed citations

5.

Rinne, Tuula, Evert N. Lamme, Pascal H. G. Duijf, et al.. (2008). A novel translation re-initiation mechanism for the p63 gene revealed by amino-terminal truncating mutations in Rapp-Hodgkin/Hay-Wells-like syndromes. Human Molecular Genetics. 17(13). 1968–1977. 46 indexed citations

6.

Demacker, Pierre N.M., Emine Bolat, Helga Toenhake-Dijkstra, & Lambertus J.H. van Tits. (2004). Factors Influencing Isoprotein Dependency of Polyclonal Apolipoprotein(a) Assays. Clinical Chemistry. 50(11). 2161–2163. 2 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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