Serkan Erdin

10.1k total citations · 2 hit papers
63 papers, 5.8k citations indexed

About

Serkan Erdin is a scholar working on Molecular Biology, Genetics and Atomic and Molecular Physics, and Optics. According to data from OpenAlex, Serkan Erdin has authored 63 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 15 papers in Genetics and 9 papers in Atomic and Molecular Physics, and Optics. Recurrent topics in Serkan Erdin's work include Bioinformatics and Genomic Networks (10 papers), Protein Structure and Dynamics (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Serkan Erdin is often cited by papers focused on Bioinformatics and Genomic Networks (10 papers), Protein Structure and Dynamics (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Serkan Erdin collaborates with scholars based in United States, United Kingdom and Italy. Serkan Erdin's co-authors include Diego L. Medina, Andrea Ballabio, Francesco Vetrini, Tuong Huynh, Carmine Settembre, Pasqualina Colella, Marco Sardiello, Vinicia Assunta Polito, Chiara Di Malta and Moisés Garcı́a-Arencibia and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Physical Review Letters.

In The Last Decade

Serkan Erdin

61 papers receiving 5.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

TFEB Links Autophagy to Lysosomal Biogenesis

2011 2.5k citations Carmine Settembre, Chiara Di Malta et al. Science profile →
A lysosome-to-nucleus signalling mechanism senses and regulates the lysosome via mTOR and TFEB

2012 1.5k citations Carmine Settembre, Diego L. Medina et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Serkan Erdin United States	23	3.1k	2.6k	949	836	761	63	5.8k
Juan Marugán United States	42	2.5k 0.8×	900 0.4×	898 0.9×	1.2k 1.4×	675 0.9×	167	5.7k
Alessandro Fraldi Italy	25	1.9k 0.6×	1.6k 0.6×	1.1k 1.2×	1.6k 1.9×	865 1.1×	39	4.4k
Andrew P. Lieberman United States	43	3.2k 1.0×	1.2k 0.5×	935 1.0×	1.5k 1.8×	797 1.0×	106	6.5k
Shawn M. Ferguson United States	43	4.3k 1.4×	1.5k 0.6×	3.0k 3.2×	1.3k 1.6×	819 1.1×	78	7.5k
Paola Pizzo Italy	52	5.7k 1.8×	961 0.4×	1.6k 1.6×	1.8k 2.1×	1.3k 1.7×	115	8.7k
Andrea Raimondi Italy	36	2.7k 0.9×	954 0.4×	2.1k 2.2×	550 0.7×	297 0.4×	68	4.6k
Ye Tian China	28	3.2k 1.0×	1.5k 0.6×	787 0.8×	627 0.8×	244 0.3×	82	5.2k
Volkmar Gieselmann Germany	48	3.9k 1.3×	1.5k 0.6×	1.8k 1.9×	3.7k 4.4×	696 0.9×	187	7.4k
Toshiyuki Nakagawa Japan	27	4.3k 1.4×	1.3k 0.5×	2.7k 2.9×	793 0.9×	260 0.3×	84	7.0k
Roman Polishchuk Italy	54	6.2k 2.0×	2.2k 0.9×	4.6k 4.8×	2.0k 2.4×	1.3k 1.8×	118	10.9k

Countries citing papers authored by Serkan Erdin

Since Specialization

Citations

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

Fields of papers citing papers by Serkan Erdin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Serkan Erdin

This figure shows the co-authorship network connecting the top 25 collaborators of Serkan Erdin. A scholar is included among the top collaborators of Serkan Erdin 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 Serkan Erdin. Serkan Erdin 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:

20 of 20 papers shown

Li, Haobo, Serkan Erdin, Matthew J. Smith, et al.. (2025). Whole-blood transcriptomic analysis reveals preoperative complement inhibitor deficiencies linked to postoperative delirium. Molecular Psychiatry. 30(10). 4690–4699.

Szkop, Krzysztof J., Françis Robert, Roberta L. Beauchamp, et al.. (2025). TSC2 loss in neural progenitor cells suppresses mRNA translation of neurodevelopmental genes. Brain. 148(8). 2935–2950.

Lim, Elaine T., Yingleong Chan, Xiaoge Guo, et al.. (2022). Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorder. Nature Communications. 13(1). 3243–3243. 14 indexed citations

Morini, Elisabetta, Dadi Gao, Monica Salani, et al.. (2021). Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage. Journal of genetics and genomics. 49(7). 654–665. 6 indexed citations

Kovalenko, Marina, Serkan Erdin, Jason St. Claire, et al.. (2020). Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease mice. eLife. 9. 8 indexed citations

Beauchamp, Roberta L., Serkan Erdin, Justin T. Jordan, et al.. (2020). mTOR kinase inhibition disrupts neuregulin 1-ERBB3 autocrine signaling and sensitizes NF2-deficient meningioma cellular models to IGF1R inhibition. Journal of Biological Chemistry. 296. 100157–100157. 7 indexed citations

Tebaldi, Toma, Toshimi Yoshida, Serkan Erdin, et al.. (2019). Hypomorphic mutation of the mouse Huntington’s disease gene orthologue. PLoS Genetics. 15(3). e1007765–e1007765. 13 indexed citations

Jordan, Justin T., Miriam J. Smith, James A. Walker, et al.. (2018). LZTR1 mutations associated with greater pain among patients with schwannomatosis (P6.142). Neurology. 90(15_supplement). 1 indexed citations

Seabra, Catarina M., Serkan Erdin, Ashok Ragavendran, et al.. (2017). A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings. American Journal of Medical Genetics Part A. 173(9). 2478–2484. 5 indexed citations

10.

Hennig, Krista M., Daniel M. Fass, Wen‐Ning Zhao, et al.. (2017). WNT/β-Catenin Pathway and Epigenetic Mechanisms Regulate the Pitt-Hopkins Syndrome and Schizophrenia Risk Gene TCF4. PubMed. 3(1). 53–71. 21 indexed citations

11.

Karaca, Ender, Özge Özalp Yüreğir, Sevcan Tuğ Bozdoğan, et al.. (2015). Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel–Feil syndrome. American Journal of Medical Genetics Part A. 167(11). 2795–2799. 38 indexed citations

12.

Karaca, Ender, Ramazan Büyükkaya, Davut Pehli̇van, et al.. (2014). Whole-Exome Sequencing Identifies Homozygous GPR161 Mutation in a Family with Pituitary Stalk Interruption Syndrome. The Journal of Clinical Endocrinology & Metabolism. 100(1). E140–E147. 60 indexed citations

13.

Blumenthal, Ian, Ashok Ragavendran, Serkan Erdin, et al.. (2014). Transcriptional Consequences of 16p11.2 Deletion and Duplication in Mouse Cortex and Multiplex Autism Families. The American Journal of Human Genetics. 94(6). 870–883. 88 indexed citations

14.

Bayram, Yavuz, Davut Pehli̇van, Ender Karaca, et al.. (2014). Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome. American Journal of Medical Genetics Part A. 164(9). 2328–2334. 17 indexed citations

15.

Erdin, Serkan, et al.. (2013). Prediction and experimental validation of enzyme substrate specificity in protein structures. Proceedings of the National Academy of Sciences. 110(45). E4195–202. 31 indexed citations

16.

Wilkins, Angela D., Eric Venner, David C. Marciano, et al.. (2013). Accounting for epistatic interactions improves the functional analysis of protein structures. Bioinformatics. 29(21). 2714–2721. 19 indexed citations

17.

Komurov, Kakajan, et al.. (2012). NetWalker: a contextual network analysis tool for functional genomics. BMC Genomics. 13(1). 282–282. 74 indexed citations

18.

Settembre, Carmine, Chiara Di Malta, Vinicia Assunta Polito, et al.. (2011). TFEB Links Autophagy to Lysosomal Biogenesis. Science. 332(6036). 1429–1433. 2496 indexed citations breakdown →

19.

Wilkins, Angela D., Serkan Erdin, Rhonald C. Lua, & Olivier Lichtarge. (2011). Evolutionary Trace for Prediction and Redesign of Protein Functional Sites. Methods in molecular biology. 819. 29–42. 50 indexed citations

20.

Wilkins, Angela D., Rhonald C. Lua, Serkan Erdin, R. Matthew Ward, & Olivier Lichtarge. (2010). Sequence and structure continuity of evolutionary importance improves protein functional site discovery and annotation. Protein Science. 19(7). 1296–1311. 17 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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