Serap Emre

3.0k total citations
8 papers, 400 citations indexed

About

Serap Emre is a scholar working on Molecular Biology, Cell Biology and Biochemistry. According to data from OpenAlex, Serap Emre has authored 8 papers receiving a total of 400 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Cell Biology and 4 papers in Biochemistry. Recurrent topics in Serap Emre's work include Lipid metabolism and biosynthesis (4 papers), Skin and Cellular Biology Research (3 papers) and Ubiquitin and proteasome pathways (2 papers). Serap Emre is often cited by papers focused on Lipid metabolism and biosynthesis (4 papers), Skin and Cellular Biology Research (3 papers) and Ubiquitin and proteasome pathways (2 papers). Serap Emre collaborates with scholars based in Türkiye, Algeria and France. Serap Emre's co-authors include Devrim Gözüaçık, Özlem Kutlu, Ayşen Karaduman, Judith Fischer, B. Bouadjar, Isabelle Thomas, Susan Cure, Meral Özgüç, Jean-François Prud’homme and Banu Nur and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Investigative Dermatology and Journal of Dermatological Science.

In The Last Decade

Serap Emre

8 papers receiving 393 citations

Peers

Serap Emre

MB

BIOCH

CB

PHYSI

EPIDE

Anne G. Ostermeyer‐Fay United States

Armella Zadoorian Australia

Yulia V. Shulga Canada

Katlyn R. Gabriel United States

F. Lermé France

Haiping Wang China

Rotem Tidhar Israel

Liping Hu China

LeAnn C. Rogers United States

Quanhai Chen United States

Anne G. Ostermeyer‐Fay United States

Serap Emre

337 ×1.6

MB

214 ×1.2

BIOCH

133 ×1.0

CB

136 ×2.1

PHYSI

44 ×0.8

EPIDE

Citations per year, relative to Serap Emre Serap Emre (= 1×) peers Anne G. Ostermeyer‐Fay

Countries citing papers authored by Serap Emre

Since Specialization

Citations

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

Fields of papers citing papers by Serap Emre

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Serap Emre

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

All Works

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8 of 8 papers shown

1.

Kutlu, Özlem, et al.. (2018). Impairment of lipophagy by PNPLA1 mutations causes lipid droplet accumulation in primary fibroblasts of Autosomal Recessive Congenital Ichthyosis patients. Journal of Dermatological Science. 93(1). 50–57. 10 indexed citations

2.

Kutlu, Özlem, et al.. (2017). Lipid Droplets in Health and Disease. Lipids in Health and Disease. 16(1). 128–128. 238 indexed citations

3.

Nur, Banu, et al.. (2015). Chanarin-Dorfman syndrome: Genotype-Phenotype Correlation. European Journal of Medical Genetics. 58(4). 238–242. 27 indexed citations

4.

Emre, Serap, Neşe Ünver, Sibel Ersoy Evans, et al.. (2010). Molecular analysis of Chanarin-Dorfman syndrome (CDS) patients: Identification of novel mutations in the ABHD5 gene. European Journal of Medical Genetics. 53(3). 141–144. 18 indexed citations

5.

Evans, Sibel Ersoy, et al.. (2007). Multiple endocrine neoplasia type 2b associated with lichen nitidus.. PubMed. 17(4). 292–4. 1 indexed citations

6.

Lesueur, Fabienne, B. Bouadjar, Caroline Lefèvre, et al.. (2006). Novel Mutations in ALOX12B in Patients with Autosomal Recessive Congenital Ichthyosis and Evidence for Genetic Heterogeneity on Chromosome 17p13. Journal of Investigative Dermatology. 127(4). 829–834. 33 indexed citations

7.

Fischer, Judith, B. Bouadjar, C Blanchet‐Bardon, et al.. (2000). Two New Loci for Autosomal Recessive Ichthyosis on Chromosomes 3p21 and 19p12-q12 and Evidence for Further Genetic Heterogeneity. The American Journal of Human Genetics. 66(3). 904–913. 59 indexed citations

8.

Nohutçu, Rahime M., et al.. (1991). Sister chromatid exchange in lymphocytes of patients with cancer of the larynx. American Journal of Otolaryngology. 12(2). 101–103. 14 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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