Çiğdem Köroğlu

540 total citations
20 papers, 361 citations indexed

About

Çiğdem Köroğlu is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Çiğdem Köroğlu has authored 20 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Physiology. Recurrent topics in Çiğdem Köroğlu's work include Neurological diseases and metabolism (3 papers), RNA regulation and disease (2 papers) and Autoimmune Bullous Skin Diseases (2 papers). Çiğdem Köroğlu is often cited by papers focused on Neurological diseases and metabolism (3 papers), RNA regulation and disease (2 papers) and Autoimmune Bullous Skin Diseases (2 papers). Çiğdem Köroğlu collaborates with scholars based in United States, Türkiye and Mexico. Çiğdem Köroğlu's co-authors include Aslıhan Tolun, Hatice Karasoy, Leyla Baysal-Kıraç, Murat Çetinkaya, Mehmet Seven, Yusuf K. Durlu, Fatih Yıldız, Eren Erken, Bozkurt Gülek and Elif Kocasoy Orhan and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Çiğdem Köroğlu

19 papers receiving 358 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Çiğdem Köroğlu United States 11 151 115 101 91 58 20 361
Meyke Schouten Netherlands 10 221 1.5× 60 0.5× 126 1.2× 124 1.4× 49 0.8× 19 420
Natasa Schiza Cyprus 8 190 1.3× 370 3.2× 67 0.7× 167 1.8× 74 1.3× 9 578
Léna Guillot‐Noël France 8 134 0.9× 148 1.3× 39 0.4× 37 0.4× 74 1.3× 10 325
Hana Friedman Canada 12 250 1.7× 49 0.4× 63 0.6× 208 2.3× 74 1.3× 20 493
Christoph Ott Germany 5 137 0.9× 278 2.4× 56 0.6× 108 1.2× 65 1.1× 7 504
Jean Christophe Antoine France 7 118 0.8× 179 1.6× 38 0.4× 106 1.2× 67 1.2× 10 384
Shelley Kennedy Canada 13 241 1.6× 95 0.8× 241 2.4× 172 1.9× 82 1.4× 18 612
Bader Alhaddad Germany 15 331 2.2× 54 0.5× 174 1.7× 69 0.8× 43 0.7× 29 516
Elisabetta Indelicato Austria 12 202 1.3× 161 1.4× 71 0.7× 221 2.4× 31 0.5× 40 397
Kristina Gotovac Croatia 9 205 1.4× 114 1.0× 34 0.3× 74 0.8× 32 0.6× 25 382

Countries citing papers authored by Çiğdem Köroğlu

Since Specialization
Citations

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

Fields of papers citing papers by Çiğdem Köroğlu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Çiğdem Köroğlu

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

All Works

20 of 20 papers shown
1.
Köroğlu, Çiğdem, Michael Traurig, Yunhua L. Muller, et al.. (2024). Identification and functional validation of rare coding variants in genes linked to monogenic obesity. Obesity. 32(9). 1769–1777. 1 indexed citations
2.
Muller, Yunhua L., Michael S. Saporito, Çiğdem Köroğlu, et al.. (2022). Functional characterization of a novel p.Ser76Thr variant in IGFBP4 that associates with body mass index in American Indians. European Journal of Human Genetics. 30(10). 1159–1166. 1 indexed citations
3.
Shan, Yue, Shelley A. Cole, Karin Haack, et al.. (2022). Association of protein function-altering variants with cardiometabolic traits: the strong heart study. Scientific Reports. 12(1). 9317–9317.
4.
Traurig, Michael, Pankaj Kumar, Paolo Piaggi, et al.. (2022). Functional variants in cytochrome b5 type A (CYB5A) are enriched in Southwest American Indian individuals and associate with obesity. Obesity. 30(2). 546–552. 4 indexed citations
5.
Muller, Yunhua L., Çiğdem Köroğlu, Sayuko Kobes, et al.. (2021). Exome Sequencing of 21 Bardet‐Biedl Syndrome (BBS) Genes to Identify Obesity Variants in 6,851 American Indians. Obesity. 29(4). 748–754. 9 indexed citations
6.
Williams, Robert C., Çiğdem Köroğlu, William C. Knowler, et al.. (2021). Next generation sequencing for HLA loci in full heritage Pima Indians of Arizona, Part II: HLA-A, -B, and -C with selected non-classical loci at 4-field resolution from whole genome sequences. Human Immunology. 82(6). 385–403. 1 indexed citations
7.
Muller, Yunhua L., Çiğdem Köroğlu, Sayuko Kobes, et al.. (2021). A missense variant Arg611Cys in LIPE which encodes hormone sensitive lipase decreases lipolysis and increases risk of type 2 diabetes in American Indians. Diabetes/Metabolism Research and Reviews. 38(3). e3504–e3504. 4 indexed citations
8.
Kim, Hye In, Bin Ye, Nehal Gosalia, et al.. (2020). Characterization of Exome Variants and Their Metabolic Impact in 6,716 American Indians from the Southwest US. The American Journal of Human Genetics. 107(2). 251–264. 10 indexed citations
9.
Piaggi, Paolo, Çiğdem Köroğlu, Yunhua L. Muller, et al.. (2020). Exome Sequencing Identifies A Nonsense Variant inDAOAssociated With Reduced Energy Expenditure in American Indians. The Journal of Clinical Endocrinology & Metabolism. 105(11). e3989–e4000. 8 indexed citations
10.
Köroğlu, Çiğdem, Marci E. Gluck, Michael Traurig, et al.. (2020). Assessing established BMI variants for a role in nighttime eating behavior in robustly phenotyped Southwestern American Indians. European Journal of Clinical Nutrition. 74(12). 1718–1724. 1 indexed citations
11.
Köroğlu, Çiğdem, et al.. (2017). GNE missense mutation in recessive familial amyotrophic lateral sclerosis. Neurogenetics. 18(4). 237–243. 13 indexed citations
12.
Kara, Bülent, Çiğdem Köroğlu, Karita Peltonen, et al.. (2017). Severe neurodegenerative disease in brothers with homozygous mutation in POLR1A. European Journal of Human Genetics. 25(3). 315–323. 20 indexed citations
13.
Erken, Eren, Çiğdem Köroğlu, Fatih Yıldız, et al.. (2014). A novel recessive 15-hydroxyprostaglandin dehydrogenase mutation in a family with primary hypertrophic osteoarthropathy. Modern Rheumatology. 25(2). 315–321. 17 indexed citations
14.
Durlu, Yusuf K., Çiğdem Köroğlu, & Aslıhan Tolun. (2014). Novel Recessive Cone-Rod Dystrophy Caused byPOC1BMutation. JAMA Ophthalmology. 132(10). 1185–1185. 22 indexed citations
15.
Yıldırım, Yeşerin, et al.. (2013). A homozygous 237-kb deletion at 1p31 identified as the locus for midline cleft of the upper and lower lip in a consanguineous family. European Journal of Human Genetics. 22(3). 333–337. 12 indexed citations
16.
Erken, Eren, Çiğdem Köroğlu, Fatih Yıldız, et al.. (2013). A novel recessive 15-hydroxyprostaglandin dehydrogenase mutation in a family with primary hypertrophic osteoarthropathy. Modern Rheumatology. 25(2). 315–21. 18 indexed citations
17.
Köroğlu, Çiğdem, Mehmet Seven, & Aslıhan Tolun. (2013). Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism. Journal of Medical Genetics. 50(8). 515–520. 49 indexed citations
18.
Köroğlu, Çiğdem, Leyla Baysal-Kıraç, Murat Çetinkaya, Hatice Karasoy, & Aslıhan Tolun. (2012). DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability. Parkinsonism & Related Disorders. 19(3). 320–324. 128 indexed citations
19.
Lohmann, Ebba, et al.. (2011). A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood. Parkinsonism & Related Disorders. 18(2). 191–193. 11 indexed citations
20.
Köroğlu, Çiğdem, et al.. (2009). Autosomal recessive spastic paraplegia (SPG45) with mental retardation maps to 10q24.3–q25.1. Neurogenetics. 10(4). 325–331. 32 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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