Sebastian Guelfi

6.9k total citations · 1 hit paper
12 papers, 1.1k citations indexed

About

Sebastian Guelfi is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Sebastian Guelfi has authored 12 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Cancer Research and 3 papers in Genetics. Recurrent topics in Sebastian Guelfi's work include Cancer-related molecular mechanisms research (5 papers), Bioinformatics and Genomic Networks (4 papers) and RNA Research and Splicing (4 papers). Sebastian Guelfi is often cited by papers focused on Cancer-related molecular mechanisms research (5 papers), Bioinformatics and Genomic Networks (4 papers) and RNA Research and Splicing (4 papers). Sebastian Guelfi collaborates with scholars based in United Kingdom, United States and Spain. Sebastian Guelfi's co-authors include John Hardy, Mina Ryten, Michael E. Weale, Daniah Trabzuni, Robert Walker, Adaikalavan Ramasamy, Colin Smith, Juan A. Botía, Andrew B. Singleton and Tisham De and has published in prestigious journals such as Nature Communications, Nature Neuroscience and Brain.

In The Last Decade

Sebastian Guelfi

12 papers receiving 1.1k 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.

Genetic variability in the regulation of gene expression in ten regions of the human brain

2014 410 citations Adaikalavan Ramasamy, Daniah Trabzuni et al. Nature Neuroscience profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sebastian Guelfi United Kingdom	9	529	283	246	246	131	12	1.1k
Julia TCW United States	15	633 1.2×	119 0.4×	302 1.2×	394 1.6×	210 1.6×	25	1.1k
José V. Sánchez‐Mut Spain	17	1.1k 2.1×	459 1.6×	120 0.5×	262 1.1×	157 1.2×	25	1.6k
Mickaël Audrain France	14	432 0.8×	168 0.6×	380 1.5×	461 1.9×	175 1.3×	28	1.1k
Koen L.I. van Gassen Netherlands	22	564 1.1×	407 1.4×	159 0.6×	122 0.5×	319 2.4×	42	1.3k
Elizabeta Gjoneska United States	8	1.1k 2.0×	252 0.9×	213 0.9×	361 1.5×	172 1.3×	8	1.4k
Mahdi Ghani Canada	16	459 0.9×	249 0.9×	153 0.6×	366 1.5×	133 1.0×	30	960
Heike Rebholz United States	18	1.2k 2.3×	110 0.4×	125 0.5×	199 0.8×	203 1.5×	27	1.6k
Ram Madabhushi United States	12	1.3k 2.4×	280 1.0×	110 0.4×	204 0.8×	250 1.9×	17	1.7k
Birger Victor Dieriks New Zealand	19	503 1.0×	111 0.4×	189 0.8×	274 1.1×	173 1.3×	41	1.1k

Countries citing papers authored by Sebastian Guelfi

Since Specialization

Citations

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

Fields of papers citing papers by Sebastian Guelfi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sebastian Guelfi

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

All Works

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12 of 12 papers shown

García-Ruiz, Sonia, David Zhang, Emil K. Gustavsson, et al.. (2025). Splicing accuracy varies across human introns, tissues, age and disease. Nature Communications. 16(1). 1068–1068. 1 indexed citations

Martirosyan, Araks, Rizwan Ansari, Katja Hebestreit, et al.. (2024). Unravelling cell type-specific responses to Parkinson’s Disease at single cell resolution. Molecular Neurodegeneration. 19(1). 7–7. 40 indexed citations

D’Sa, Karishma, Sebastian Guelfi, Jana Vandrovcová, et al.. (2023). Analysis of subcellular RNA fractions demonstrates significant genetic regulation of gene expression in human brain post-transcriptionally. Scientific Reports. 13(1). 13874–13874. 1 indexed citations

Sethi, Siddharth, David Zhang, Sebastian Guelfi, et al.. (2022). Leveraging omic features with F3UTER enables identification of unannotated 3’UTRs for synaptic genes. Nature Communications. 13(1). 2270–2270. 3 indexed citations

Zhang, David, Sebastian Guelfi, Sonia García-Ruiz, et al.. (2020). Incomplete annotation has a disproportionate impact on our understanding of Mendelian and complex neurogenetic disorders. Science Advances. 6(24). 26 indexed citations

Augustus, Meena, Jean-Philippe Villemin, Sebastian Guelfi, et al.. (2020). Transformation Foci in IDH1-mutated Gliomas Show STAT3 Phosphorylation and Downregulate the Metabolic Enzyme ETNPPL, a Negative Regulator of Glioma Growth. Scientific Reports. 10(1). 35 indexed citations

Guelfi, Sebastian, Juan A. Botía, Maria Thom, et al.. (2019). Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsy. Brain. 142(6). 1616–1630. 42 indexed citations

Salih, Derviş A., Sevinç Bayram, Sebastian Guelfi, et al.. (2019). Genetic variability in response to amyloid beta deposition influences Alzheimer’s disease risk. Brain Communications. 1(1). fcz022–fcz022. 75 indexed citations

Botía, Juan A., Jana Vandrovcová, Paola Forabosco, et al.. (2017). An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks. BMC Systems Biology. 11(1). 47–47. 186 indexed citations

10.

Blauwendraat, Cornelis, et al.. (2017). Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson’s disease on chromosome 7p15.3. Neurogenetics. 18(3). 121–133. 46 indexed citations

11.

Matarín, Mar, Derviş A. Salih, Marina V. Yasvoina, et al.. (2015). A Genome-wide Gene-Expression Analysis and Database in Transgenic Mice during Development of Amyloid or Tau Pathology. Cell Reports. 10(4). 633–644. 193 indexed citations

12.

Ramasamy, Adaikalavan, Daniah Trabzuni, Sebastian Guelfi, et al.. (2014). Genetic variability in the regulation of gene expression in ten regions of the human brain. Nature Neuroscience. 17(10). 1418–1428. 410 indexed citations breakdown →

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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