Mina Ryten

30.3k total citations · 2 hit papers
80 papers, 4.5k citations indexed

About

Mina Ryten is a scholar working on Molecular Biology, Neurology and Neurology. According to data from OpenAlex, Mina Ryten has authored 80 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 22 papers in Neurology and 17 papers in Neurology. Recurrent topics in Mina Ryten's work include RNA Research and Splicing (14 papers), Parkinson's Disease Mechanisms and Treatments (13 papers) and Bioinformatics and Genomic Networks (13 papers). Mina Ryten is often cited by papers focused on RNA Research and Splicing (14 papers), Parkinson's Disease Mechanisms and Treatments (13 papers) and Bioinformatics and Genomic Networks (13 papers). Mina Ryten collaborates with scholars based in United Kingdom, United States and Spain. Mina Ryten's co-authors include John Hardy, Daniah Trabzuni, Michael E. Weale, Colin Smith, Robert Walker, Geoffrey Burnstock, Adaikalavan Ramasamy, Mark Cookson, Regina H. Reynolds and Sebastian Guelfi and has published in prestigious journals such as Nature, Nucleic Acids Research and Nature Communications.

In The Last Decade

Mina Ryten

74 papers receiving 4.4k 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 Daniah Trabzuni, Sebastian Guelfi et al. profile →
ggtranscript : an R package for the visualization and interpretation of transcript isoforms using ggplot2

2022 245 citations Emil K. Gustavsson, David Zhang et al. Bioinformatics profile →

Peers

Countries citing papers authored by Mina Ryten

Since Specialization

Citations

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

Fields of papers citing papers by Mina Ryten

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mina Ryten

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Splicing accuracy varies across human introns, tissues, age and disease 2025 ·Nature Communications ·Sonia García-Ruiz, David Zhang, Emil K. Gustavsson, (unknown), (unknown), (unknown), Regina H. Reynolds, Jonathan Brenton, (unknown), Zhongbo Chen, Donald C. Rio, Juan A. Botía, Sebastian Guelfi, Leonardo Collado‐Torres, Mina Ryten	1
2	Evidence for divergent cortical organisation in Parkinson’s disease and Lewy Body Dementia 2025 ·Nature Communications ·Angeliki Zarkali, George E. Thomas, (unknown), (unknown), (unknown), Martina F. Callaghan, Mina Ryten, Rimona S. Weil	0
3	RASP: Optimal Single Puncta Detection in Complex Cellular Backgrounds 2024 ·The Journal of Physical Chemistry B ·(unknown), (unknown), Rebecca Andrews, (unknown), (unknown), Christina E. Toomey, (unknown), Tammaryn Lashley, Mina Ryten, Nicholas Wood, Michele Vendruscolo, Sonia Gandhi, Lucien E. Weiss, Joseph S. Beckwith, Steven F. Lee	1
4	ensemblQueryR: fast, flexible and high-throughput querying of Ensembl LD API endpoints in R 2023 ·SHILAP Revista de lepidopterología ·(unknown), Sonia García-Ruiz, Regina H. Reynolds, Mina Ryten, Alan Hodgkinson	2
5	The non-specific lethal complex regulates genes and pathways genetically linked to Parkinson’s disease 2023 ·Brain ·(unknown), Regina H. Reynolds, Benjamin O’Callaghan, Sonia García-Ruiz, (unknown), Juan A. Botía, Hélène Plun‐Favreau, Mina Ryten	2
6	Genome-wide Analysis of Motor Progression in Parkinson Disease 2023 ·Neurology Genetics ·Alejandro Martínez-Carrasco, Raquel Real, Michael Lawton, Regina H. Reynolds, Manuela Tan, (unknown), Nigel Williams, Camille Carroll, Jean‐Christophe Corvol, (unknown), Donald G. Grosset, John Hardy, Mina Ryten, Yoav Ben‐Shlomo, Maryam Shoai, Huw R. Morris	5
7	PhenoExam: gene set analyses through integration of different phenotype databases 2022 ·BMC Bioinformatics ·(unknown), Aurora González-Vidal, (unknown), Jordí Ortiz, (unknown), Zhongbo Chen, Mike A. Nalls, Faraz Faghri, John Hardy, (unknown), Paolo Maietta, Sara Álvarez, Mina Ryten, Juan A. Botía	1
8	Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia 2022 ·Brain ·Raquel Real, Alejandro Martínez-Carrasco, Regina H. Reynolds, Michael Lawton, Manuela Tan, Maryam Shoai, Jean‐Christophe Corvol, Mina Ryten, Catherine Bresner, Leon Hubbard, Alexis Brice, Suzanne Lesage, Johann Faouzi, Alexis Elbaz, Fanny Artaud, Nigel Williams, (unknown), Yoav Ben‐Shlomo, Donald G. Grosset, John Hardy, Huw R. Morris	31
9	ggtranscript : an R package for the visualization and interpretation of transcript isoforms using ggplot2 breakdown → 2022 ·Bioinformatics ·Emil K. Gustavsson, David Zhang, Regina H. Reynolds, Sonia García-Ruiz, Mina Ryten	245
10	Modeling multifunctionality of genes with secondary gene co-expression networks in human brain provides novel disease insights 2021 ·Bioinformatics ·Juan A. Sánchez, (unknown), (unknown), Sonia García-Ruiz, (unknown), Regina H. Reynolds, Mike A. Nalls, John Hardy, Mina Ryten, Juan A. Botía	3
11	Mitochondrial-nuclear cross-talk in the human brain is modulated by cell type and perturbed in neurodegenerative disease 2021 ·Communications Biology ·(unknown), (unknown), Regina H. Reynolds, Sonia García-Ruiz, David Zhang, Zhongbo Chen, Mina Ryten, Alan Hodgkinson	13
12	Regional brain iron and gene expression provide insights into neurodegeneration in Parkinson’s disease 2021 ·Brain ·George E. Thomas, Angeliki Zarkali, Mina Ryten, Karin Shmueli, (unknown), Louise‐Ann Leyland, Peter McColgan, Julio Acosta‐Cabronero, Andrew J. Lees, Rimona S. Weil	72
13	A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene 2021 ·Brain ·(unknown), Andrew Graham, Thomas M. Piers, (unknown), (unknown), Maryam Shoai, Regina H. Reynolds, Juan A. Botía, Keeley J. Brookes, Tamar Guetta‐Baranes, Eftychia Bellou, Sevinç Bayram, Dimitra Sokolova, Mina Ryten, Carlo Sala Frigerio, Valentina Escott‐Price, Kevin Morgan, Jennifer M. Pocock, John Hardy, Derviş A. Salih	75
14	Heritability Enrichment Implicates Microglia in Parkinson's Disease Pathogenesis 2021 ·Annals of Neurology ·(unknown), Sara Bandrés‐Ciga, Regina H. Reynolds, John Hardy, Mina Ryten, Lynne Krohn, Ziv Gan‐Or, Inge R. Holtman, Lasse Pihlstrøm	36
15	Differences in network controllability and regional gene expression underlie hallucinations in Parkinson’s disease 2020 ·Brain ·Angeliki Zarkali, Peter McColgan, Mina Ryten, Regina H. Reynolds, Louise‐Ann Leyland, Andrew J. Lees, Geraint Rees, Rimona S. Weil	35
16	Incomplete annotation has a disproportionate impact on our understanding of Mendelian and complex neurogenetic disorders 2020 ·Science Advances ·David Zhang, Sebastian Guelfi, Sonia García-Ruiz, (unknown), Regina H. Reynolds, Karishma D’Sa, Wenfei Liu, Thomas Courtin, Amy Peterson, Andrew E. Jaffe, John Hardy, Juan A. Botía, Leonardo Collado‐Torres, Mina Ryten	26
17	Pathogenic PTPN11 variants involving the poly‐glutamine Gln ²⁵⁵ ‐Gln ²⁵⁶ ‐Gln ²⁵⁷ stretch highlight the relevance of helix B in SHP2's functional regulation 2020 ·Human Mutation ·Simone Martinelli, Luca Pannone, Christina Lißewski, Julia Brinkmann, Elisabetta Flex, Denny Schanze, Paolo Calligari, Massimiliano Anselmi, Francesca Pantaleoni, (unknown), Francesca Clementina Radio, Adonis S. Ioannides, Nils Rahner, Ina Schanze, Dragana Josifova, Gianfranco Bocchinfuso, Mina Ryten, Lorenzo Stella, Marco Tartaglia, Martin Zenker	1
18	An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks 2017 ·BMC Systems Biology ·Juan A. Botía, Jana Vandrovcová, Paola Forabosco, Sebastian Guelfi, Karishma D’Sa, John Hardy, Cathryn M. Lewis, Mina Ryten, Michael E. Weale	186
19	Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy 2013 ·Journal of Neurology Neurosurgery & Psychiatry ·Arianna Tucci, (unknown), Elisavet Preza, Robert D. S. Pitceathly, Annapurna Chalasani, Vincent Plagnol, (unknown), Daniah Trabzuni, Mina Ryten, (unknown), Zane Jaunmuktane, Mary M. Reilly, Sebastian Brandner, Iain P. Hargreaves, John Hardy, (unknown), Andrey Y. Abramov, Henry Houlden	34
20	Investigating the utility of human embryonic stem cell‐derived neurons to model ageing and neurodegenerative disease using whole‐genome gene expression and splicing analysis 2012 ·Journal of Neurochemistry ·Rickie Patani, Patrick A. Lewis, Daniah Trabzuni, Clare A. Puddifoot, David J. A. Wyllie, Robert Walker, Colin Smith, Giles E. Hardingham, Michael E. Weale, John Hardy, Siddharthan Chandran, Mina Ryten	45

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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