Mina Ryten

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 3%percentile

1.6Author DataRank

Indexed papers

3in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 3 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

A data-driven single-cell and spatial transcriptomic map of the human prefrontal cortex

Science(2024)10.1126/science.adh1938

Top 18%

1.2DataRank

Top 18%69 citations

Abby Spangler, Nicholas J. Eagles, Kelsey D. Montgomery, Sang Ho Kwon, Boyi Guo +90 more

Papers

Driven by 71 papers — median percentile 71. Top paper: “Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli”.

Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli

Nature(2020)10.1038/s41586-020-2080-8

N/A

8.3DataRank · unranked

1184 citations

Jens Puschhof, Axel Rosendahl Huber, Arne van Hoeck, Henry M. Wood, Jason Nomburg +95 more

Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

JAMA Neurology(2021)10.1001/jamaneurol.2020.5257

N/A

4.5DataRank · unranked

205 citations

David Zhang, Sebastian Guelfi, Claudia Manzoni, Leon Hubbard, Regina Hertfelder Reynolds +85 more

Heritability Enrichment Implicates Microglia in Parkinson's Disease Pathogenesis

Annals of Neurology(2021)10.1002/ana.26032

N/A

1.7DataRank · unranked

73 citations

Sara Bandrés‐Ciga, Regina Hertfelder Reynolds, John Hardy, Mina Ryten, Lynne Krohn +4 more

Genome sequence analyses identify novel risk loci for multiple system atrophy

Neuron(2024)10.1016/j.neuron.2024.04.002

N/A

1.7DataRank · unranked

45 citations

Anindita Ray, Zalak Shah, Jinhui Ding, Paola Ruffo, Masashi Fujita +95 more

Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects

Nature Communications(2022)10.1038/s41467-022-34732-5

N/A

1.7DataRank · unranked

95 citations

Karl Heilbron, Cornelis Blauwendraat, Regina Hertfelder Reynolds, Eric Yu, Konstantin Senkevich +95 more

Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups

Brain(2021)10.1093/brain/awab402

N/A

1.4DataRank · unranked

66 citations

Zalak Shah, Ruth Chia, Sandra E. Black, Ziv Gan‐Or, Julia Keith +81 more

Large-scale rare variant burden testing in Parkinson's disease

Brain(2023)10.1093/brain/awad214

N/A

1.4DataRank · unranked

52 citations

Julie Lake, Vanessa Pitz, Allen Ye Fu, Joseph L. Guidubaldi, Caroline Warly Solsberg +31 more

A data-driven single-cell and spatial transcriptomic map of the human prefrontal cortex

Science(2024)10.1126/science.adh1938

Top 18%

1.2DataRank

Top 18%69 citations

Abby Spangler, Nicholas J. Eagles, Kelsey D. Montgomery, Sang Ho Kwon, Boyi Guo +90 more

Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome

Nature Communications(2021)10.1038/s41467-021-26280-1

N/A

0.808DataRank · unranked

217 citations

Demis A. Kia, Mona M. Almramhi, Sara Bandres-Ciga, Chris Finan, Alastair J. Noyce +170 more

Human and mouse essentiality screens as a resource for disease gene discovery

Nature Communications(2020)10.1038/s41467-020-14284-2

N/A

0.730DataRank · unranked

129 citations

Violeta Muñoz‐Fuentes, Stephen A. Murray, Mary E. Dickinson, Maja Bućan, Lauryl M. J. Nutter +95 more

RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses

The Lancet Neurology(2024)10.1016/s1474-4422(24)00121-2

N/A

0.706DataRank · unranked

110 citations

Jordan Follett, Joanne Trinh, Sandeep Kumar Barodia, Raquel Real, Zhiyong Liu +31 more

A systems‐level analysis highlights microglial activation as a modifying factor in common epilepsies

Neuropathology and Applied Neurobiology(2021)10.1111/nan.12758

N/A

0.601DataRank · unranked

54 citations

Mina Ryten, Martina Di Nunzio, Teresa Ravizza, Daniele Tolomeo, Regina Hertfelder Reynolds +95 more

Using deep long-read RNAseq in Alzheimer’s disease brain to assess medical relevance of RNA isoform diversity

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.08.06.552162

N/A

0.557DataRank · unranked

14 citations

J. Anthony Brandon, Madeline L. Page, Kayla A. Nations, Ketsile I. Dikobe, Brendan J. White +18 more

Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

Cell Genomics(2023)10.1016/j.xgen.2023.100316

N/A

0.524DataRank · unranked

32 citations

Ruth Chia, Jinhui Ding, Memoona Rasheed, Masashi Fujita, Vilas Menon +88 more

Integrated single cell and unsupervised spatial transcriptomic analysis defines molecular anatomy of the human dorsolateral prefrontal cortex

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.02.15.528722

N/A

0.520DataRank · unranked

31 citations

Abby Spangler, Nicholas J. Eagles, Kelsey D. Montgomery, Sang Ho Kwon, Boyi Guo +18 more

Rare disease gene association discovery in the 100,000 GenomesProject

Nature(2025)10.1038/s41586-025-08623-w

N/A

0.515DataRank · unranked

18 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

IntroVerse: a comprehensive database of introns across human tissues

Nucleic Acids Research(2022)10.1093/nar/gkac1056

Top 39%

0.484DataRank

Top 39%13 citations

Emil K. Gustavsson, David Zhang, Regina Hertfelder Reynolds, Zhongbo Chen, Aine Fairbrother-Browne +5 more

African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1

Nature Structural & Molecular Biology(2024)10.1038/s41594-024-01423-2

N/A

0.425DataRank · unranked

16 citations

Peter Wild Crea, Daniel M. Ramos, Emil K. Gustavsson, Mandy Radefeldt, Andrey Damianov +36 more

Investigation of the genetic aetiology of Lewy body diseases with and without dementia

Brain Communications(2024)10.1093/braincomms/fcae190

N/A

0.385DataRank · unranked

12 citations

Raquel Real, Alejandro Martínez-Carrasco, Ruth Chia, Michael Lawton, Maryam Shoai +93 more

Genome-wide Analysis of Motor Progression in Parkinson Disease

Neurology Genetics(2023)10.1212/nxg.0000000000200092

N/A

0.345DataRank · unranked

9 citations

Raquel Real, Michael Lawton, Regina Hertfelder Reynolds, Manuela Tan, Lesley Wu +16 more

Profiling the NOTCH2NLC GGC Repeat Expansion in Parkinson's Disease in the European Population

Movement Disorders(2022)10.1002/mds.29155

N/A

0.312DataRank · unranked

7 citations

Pilar Álvarez Jerez, Francis P. Grenn, Sara Bandrés‐Ciga, Laksh Malik, Dena Hernandez +16 more

Association of cardiovascular disease management drugs with Lewy body dementia: a case–control study

Brain Communications(2023)10.1093/braincomms/fcad346

N/A

0.292DataRank · unranked

6 citations

Brian Moroz, Sara Sáez-Atiénzar, Ruth Chia, Elizabeth K. Cahoon, Clifton L. Dalgard +93 more

Large-scale pathway-specific polygenic risk, transcriptomic community networks and functional inferences in Parkinson disease

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.05.079228

N/A

0.208DataRank · unranked

3 citations

Sara Sáez-Atiénzar, JJ Kim, MB Makarious, Faraz Faghri, Mónica Díez-Fairén +21 more

A pathogenic variant in RAB32 causes autosomal dominant Parkinson’s disease and activates LRRK2 kinase

medRxiv(2024)10.1101/2024.01.17.24300927

N/A

0.208DataRank · unranked

3 citations

Jordan Follett, Joanne Trinh, Sandeep Kumar Barodia, Raquel Real, Zhiyong Liu +32 more

Identification of GGC Repeat Expansions in ZFHX3 among Chilean Movement Disorder Patients

Movement Disorders(2025)10.1002/mds.30242

N/A

0.208DataRank · unranked

3 citations

Abraham Moller, Kensuke Daida, Pilar Álvarez Jerez, Zhongbo Chen, Zachary B. Anderson +18 more

Characterizing a complex CT-rich haplotype in intron 4 of SNCA using large-scale targeted amplicon long-read sequencing

npj Parkinson s Disease(2024)10.1038/s41531-024-00749-4

N/A

0.104DataRank · unranked

1 citations

Kensuke Daida, Francis P. Grenn, Laksh Malik, Abigail Miano‐Burkhardt, Mary B. Makarious +17 more

Leveraging sex-genetic interactions to understand brain disorders: recent advances and current gaps

Brain Communications(2024)10.1093/braincomms/fcae192

N/A

0.104DataRank · unranked

1 citations

Frida Lona-Durazo, Mina Ryten, Sarah A. Gagliano Taliun, Frida Lona‐Durazo, Nikita Neale

Investigation of the genetic aetiology of Lewy body diseases with and without dementia

medRxiv(2023)10.1101/2023.10.17.23297157

N/A

0.104DataRank · unranked

1 citations

Raquel Real, Alejandro Martínez-Carrasco, Ruth Chia, Michael Lawton, Maryam Shoai +14 more

Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia

medRxiv(2022)10.1101/2022.05.23.22275465

N/A

0.104DataRank · unranked

1 citations

Alejandro Martínez-Carrasco, Regina Hertfelder Reynolds, Michael Lawton, Manuela Tan, Maryam Shoai +16 more

CoExp Web, a web tool for the exploitation of co-expression networks

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.29.176057

N/A

0.104DataRank · unranked

1 citations

Ana Luisa Gil-Martínez, Alejandro Cisterna‐García, Francisco Jurado, Regina Romano Reynolds, Mark Cookson +4 more

Genome-wide association study of REM sleep behavior disorder identifies novel loci with distinct polygenic and brain expression effects

medRxiv(2021)10.1101/2021.09.08.21254232

N/A

0DataRank · unranked

8 citations

Karl Heilbron, Cornelis Blauwendraat, Regina Hertfelder Reynolds, Eric Yu, Konstantin Senkevich +53 more

Genome‐Wide Analysis of Structural Variants in Parkinson Disease

Annals of Neurology(2023)10.1002/ana.26608

N/A

0DataRank · unranked

37 citations

Jinhui Ding, Pilar Álvarez Jerez, Anastasia Illarionova, Kristin Levine, Francis P. Grenn +35 more

Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy

Brain(2021)10.1093/brain/awab417

N/A

0DataRank · unranked

3 citations

Sara Larivière, Raúl Rodríguez‐Cruces, Jessica Royer, Shahin Tavakol, Yezhou Wang +82 more

Local genetic correlations exist among neurodegenerative and neuropsychiatric diseases

npj Parkinson s Disease(2023)10.1038/s41531-023-00504-1

N/A

0DataRank · unranked

23 citations

Aaron Z. Wagen, Frida Lona‐Durazo, Sonja W. Scholz, Maryam Shoai, John Hardy +3 more

Genetic meta-analysis of levodopa induced dyskinesia in Parkinson’s disease

npj Parkinson s Disease(2023)10.1038/s41531-023-00573-2

N/A

0DataRank · unranked

12 citations

Raquel Real, Michael Lawton, Hirotaka Iwaki, Manuela Tan, Lesley Wu +11 more

Regional genetic correlations highlight relationships between neurodegenerative disease loci and the immune system

Communications Biology(2023)10.1038/s42003-023-05113-5

N/A

0DataRank · unranked

10 citations

Regina Hertfelder Reynolds, Sonja W. Scholz, Mina Ryten, Sarah A. Gagliano Taliun, Frida Lona‐Durazo

Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia

New England Journal of Medicine(2023)10.1056/nejmc2301605

N/A

0DataRank · unranked

15 citations

Arianna Tucci, Mina Ryten, Zhongbo Chen

An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of α-synuclein

Cell Reports(2021)10.1016/j.celrep.2021.109189

N/A

0DataRank · unranked

13 citations

Alessandro Crimi, Anne Wiedmer, Marc Emmenegger, C. Manzoni, Sara Bandrés‐Ciga +28 more

Mitochondrial-nuclear cross-talk in the human brain is modulated by cell type and perturbed in neurodegenerative disease

Communications Biology(2021)10.1038/s42003-021-02792-w

N/A

0DataRank · unranked

20 citations

Aminah T. Ali, Regina Hertfelder Reynolds, Sonia García-Ruiz, David Zhang, Zhongbo Chen +3 more

Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types

Science Advances(2021)10.1126/sciadv.abd9036

N/A

0DataRank · unranked

100 citations

Sara Bandrés‐Ciga, Rebekah G. Langston, Jonggeol J. Kim, Shing Wan Choi, Regina Hertfelder Reynolds +12 more

Splicing accuracy varies across human introns, tissues and age

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.03.29.534370

N/A

0DataRank · unranked

5 citations

David Zhang, Emil K. Gustavsson, G Rocamora-Perez, Melissa Grant‐Peters, Aine Fairbrother-Browne +10 more

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data

medRxiv(2023)10.1101/2023.12.20.23300294

N/A

0DataRank · unranked

3 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

Genetic meta-analysis of levodopa induced dyskinesia in Parkinson’s disease

medRxiv(2023)10.1101/2023.05.24.23290362

N/A

0DataRank · unranked

2 citations

Raquel Real, Michael Lawton, Hirotaka Iwaki, Manuela Tan, Lesley Wu +11 more

Systematic visualisation of molecular QTLs reveals variant mechanisms at GWAS loci

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.06.535816

N/A

0DataRank · unranked

1 citations

Ralf Tambets, James Hayhurst, Ida Rahu, Peep Kolberg, Uku Raudvere +18 more

Modelling population genetic screening in rare neurodegenerative diseases

medRxiv(2023)10.1101/2023.07.03.23292187

N/A

0DataRank · unranked

1 citations

Alfredo Iacoangeli, Mina Ryten, Francesca Forzano, Neil Pearce, Ammar Al‐Chalabi +1 more

Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies

UNC Libraries(2020)10.17615/ng8x-wz67

N/A

0DataRank · unranked

0 citations

John Hardy, Daniah Trabzuni, Dena G. Hernandez, Mark Cookson, Mina Ryten +11 more

Mapping medically relevant RNA isoform diversity in the aged human frontal cortex with deep long-read RNA-seq

Nature Biotechnology(2024)10.1038/s41587-024-02245-9

N/A

0DataRank · unranked

53 citations

J. Anthony Brandon, Madeline L. Page, Kayla A. Nations, Ketsile I. Dikobe, Brendan J. White +18 more

Adaptive Long‐Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4

Movement Disorders(2024)10.1002/mds.29704

N/A

0DataRank · unranked

49 citations

Emil K. Gustavsson, Hannah Macpherson, Claire Anderson, Chris Clarkson, Clarissa Rocca +19 more

Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.20.211276

N/A

0DataRank · unranked

9 citations

Sara Bandrés‐Ciga, Rebekah G. Langston, Jonggeol J. Kim, Shing Wan Choi, Regina Hertfelder Reynolds +11 more

Repeat expansion disorders

Practical Neurology(2024)10.1136/pn-2023-003938

N/A

0DataRank · unranked

22 citations

Huw R. Morris, James Polke, Nicholas Wood, Sonia Gandhi, Mina Ryten +3 more

The ENIGMA‐Epilepsy working group: Mapping disease from large data sets

Human Brain Mapping(2020)10.1002/hbm.25037

N/A

0DataRank · unranked

79 citations

Christopher D. Whelan, Sean N. Hatton, Khoa H Huynh, André Altmann, Mina Ryten +67 more

Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease

Acta Neuropathologica(2020)10.1007/s00401-020-02181-3

N/A

0DataRank · unranked

119 citations

Sara Sáez-Atiénzar, Jeff Kim, Mary B. Makarious, Faraz Faghri, Mónica Díez-Fairén +23 more

The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder

Movement Disorders(2024)10.1002/mds.30077

N/A

0DataRank · unranked

5 citations

Pilar Álvarez Jerez, Claire Anderson, Martin Paucar, Jasmaine Lee, Daniel Nilsson +19 more

RNApysoforms: fast rendering interactive visualization of RNA isoform structure and expression in Python

Bioinformatics Advances(2024)10.1093/bioadv/vbaf057

N/A

0DataRank · unranked

2 citations

Madeline L. Page, Emil K. Gustavsson, Mina Ryten, Mark Ebbert, Bernardo Aguzzoli Heberle

A Population‐Wide Exploration of the THAP11 CAG Repeat Size and Structure in the 100,000 Genomes Project and UK Biobank

Movement Disorders(2024)10.1002/mds.30073

N/A

0DataRank · unranked

3 citations

Zhongbo Chen, Clarissa Rocca, Bharati Jadhav, Kristina Ibáñez, Mina Ryten +4 more

A worldwide ENIGMA study on epilepsy-related gray and white matter compromise across the adult lifespan

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.02.583073

N/A

0DataRank · unranked

6 citations

Alexander Ngo, Raúl Rodríguez‐Cruces, Jessica Royer, Maria Eugenia Caligiuri, Antonio Gambardella +83 more

Long-Read epigenetic clocks identify improved brain aging predictions

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.09.30.679553

N/A

0DataRank · unranked

1 citations

Mary B. Makarious, Melissa Meredith, Abraham Moller, Melissa Grant‐Peters, Amy R. Hicks +13 more

RNApysoforms: Fast rendering interactive visualization of RNA isoform structure and expression in Python

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.11.06.622357

N/A

0DataRank · unranked

1 citations

Madeline L. Page, Emil K. Gustavsson, Mina Ryten, Mark Ebbert, Bernardo Aguzzoli Heberle

African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1

medRxiv(2024)10.1101/2024.02.20.24302827

N/A

0DataRank · unranked

1 citations

Peter Wild Crea, Daniel M. Ramos, Emil K. Gustavsson, Mandy Radefeldt, Mary B. Makarious +33 more

Ancestry-specific gene expression in peripheral monocytes mediates risk of neurodegenerative disease

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.11.20.624489

N/A

0DataRank · unranked

0 citations

Regina Hertfelder Reynolds, Jia Nee Foo, Aine Fairbrother-Browne, Emil K. Gustavsson, Sarah Galgiano-Turin +4 more

Splicing accuracy varies across human introns, tissues, age and disease

Nature Communications(2025)10.1038/s41467-024-55607-x

N/A

0DataRank · unranked

22 citations

David Zhang, Emil K. Gustavsson, G Rocamora-Perez, Melissa Grant‐Peters, Aine Fairbrother-Browne +10 more

Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study

The Lancet Neurology(2020)10.1016/s1474-4422(20)30394-x

N/A

0DataRank · unranked

120 citations

Shunsuke Koga, Rebecca R. Valentino, Regina Hertfelder Reynolds, Raffaele Ferrari, Manuela Tan +51 more

Advances in the genetics and pathology of Lewy body dementia

The Lancet Neurology(2025)10.1016/s1474-4422(25)00363-1

N/A

0DataRank · unranked

6 citations

Njideka Okubadejo, Priya Prakash, Shane A. Liddelow, Mina Ryten, Glenda M. Halliday +1 more

Modelling Population Genetic Screening in Rare Neurodegenerative Diseases

Biomedicines(2025)10.3390/biomedicines13051018

N/A

0DataRank · unranked

1 citations

Alfredo Iacoangeli, Mina Ryten, Francesca Forzano, Neil Pearce, Ammar Al‐Chalabi +1 more

Identification of 4 novel human ocular coloboma genes ANK3, BMPR1B, PDGFRA, and CDH4 through evolutionary conserved vertebrate gene analysis

Genetics in Medicine(2022)10.1016/j.gim.2021.12.014

N/A

0DataRank · unranked

13 citations

Maria Toms, Rodrigo Young, Jonathan Eintracht, Hajrah Sarkar, Brian P. Brooks +70 more

Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.16.452643

N/A

0DataRank · unranked

1 citations

Branduff McAllister, Mia McDade‐Kumar, G. Bernhard Landwehrmeyer, Michael Orth, Anne Rosser +13 more

Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1

npj Genomic Medicine(2022)10.1038/s41525-022-00317-w

N/A

0DataRank · unranked

21 citations

Branduff McAllister, Mia McDade‐Kumar, G. Bernhard Landwehrmeyer, Michael Orth, Anne Rosser +13 more

Local genetic correlations exist among neurodegenerative and neuropsychiatric diseases

medRxiv(2022)10.1101/2022.05.30.22275781

N/A

0DataRank · unranked

1 citations

Aaron Z. Wagen, Frida Lona‐Durazo, Sonja W. Scholz, Maryam Shoai, John Hardy +3 more

Association of genetic variation at the GJA5/ACP6 locus with motor progression in Parkinson’s

medRxiv(2022)10.1101/2022.10.28.22281645

N/A

0DataRank · unranked

1 citations

Raquel Real, Michael Lawton, Regina Hertfelder Reynolds, Manuela Tan, Lesley Wu +11 more

Regional genetic correlations highlight relationships between neurodegenerative diseases and the immune system

medRxiv(2022)10.1101/2022.12.07.22283179

N/A

0DataRank · unranked

1 citations

Regina Hertfelder Reynolds, Sonja W. Scholz, Mina Ryten, Sarah A. Gagliano Taliun, Frida Lona‐Durazo

Normal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosis

Brain(2023)10.1093/brain/awad240

N/A

0DataRank · unranked

72 citations

Stefania Magri, Riccardo Curró, Elena Abati, Stefano Facchini, Marinella Corbetta +95 more

Mina Ryten

Indexed papers

Top data-sharing exemplar

Papers