Huw R. Morris

National Hospital for Neurology and Neurosurgery

Also affiliated with University College London

MedicineNeuroscience

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 2%percentile

1.8Author DataRank

Indexed papers

8in 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 8 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.

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

npj Parkinson s Disease(2023)10.1038/s41531-023-00533-w

Top 26%

0.769DataRank

Top 26%39 citations

Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar +95 more

Papers

Driven by 70 papers — median percentile 40. Top paper: “Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets”.

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

Exenatide once a week versus placebo as a potential disease-modifying treatment for people with Parkinson's disease in the UK: a phase 3, multicentre, double-blind, parallel-group, randomised, placebo-controlled trial

The Lancet(2025)10.1016/s0140-6736(24)02808-3

N/A

2.3DataRank · unranked

131 citations

Christine Girges, Grace Auld, Rachel McComish, Alexa King, Simon S. Skene +32 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

Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study

The Lancet Neurology(2015)10.1016/s1474-4422(15)00178-7

N/A

0.811DataRank · unranked

222 citations

Cory Y. McLean, Jacqueline Rick, Shirley Eberly, Samantha J. Hutten, Katrina Gwinn +40 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

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

npj Parkinson s Disease(2023)10.1038/s41531-023-00533-w

Top 26%

0.769DataRank

Top 26%39 citations

Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar +95 more

Polygenic risk of Parkinson disease is correlated with disease age at onset

Annals of Neurology(2015)10.1002/ana.24335

N/A

0.747DataRank · unranked

144 citations

Mike A. Nalls, Huw R. Morris, Steven Lubbe, Alexis Brice, Thomas Gasser +6 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

Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy

Molecular Neurodegeneration(2024)10.1186/s13024-024-00747-3

N/A

0.665DataRank · unranked

26 citations

Timothy S. Chang, Beth A. Dombroski, Po‐Liang Cheng, Vishakha Patil, Leopoldo Valiente‐Banuet +57 more

NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

medRxiv(2023)10.1101/2023.11.06.23298176

N/A

0.658DataRank · unranked

23 citations

Faraz Faghri, Elisa Majounie, Mathew J. Koretsky, Jeffrey Kim, Kristin Levine +29 more

Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease

Annals of Neurology(2021)10.1002/ana.26090

N/A

0.628DataRank · unranked

65 citations

Hirotaka Iwaki, Mary B. Makarious, Sara Bandrés‐Ciga, Hampton L. Leonard, Francis P. Grenn +32 more

Genotype–phenotype correlation in PRKN-associated Parkinson’s disease

npj Parkinson s Disease(2024)10.1038/s41531-024-00677-3

N/A

0.612DataRank · unranked

58 citations

Sara Sambin, Baptiste Crinière‐Boizet, Thomas Courtin, Christelle Tesson, Fanny Casse +49 more

Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes

Neurology Genetics(2021)10.1212/nxg.0000000000000557

N/A

0.568DataRank · unranked

43 citations

Rami Al‐Ouran, Rainer von Coelln, Cornelis Blauwendraat, Emily J. Hill, Lan Luo +17 more

Genome-wide determinants of mortality and motor progression in Parkinson’s disease

npj Parkinson s Disease(2024)10.1038/s41531-024-00729-8

N/A

0.565DataRank · unranked

15 citations

Michael Lawton, Miriam I. Pollard, Emmeline Brown, Raquel Real, Alejandro Martínez-Carrasco +35 more

Polygenic Parkinson's Disease Genetic Risk Score as Risk Modifier of Parkinsonism in Gaucher Disease

Movement Disorders(2023)10.1002/mds.29342

N/A

0.457DataRank · unranked

20 citations

Nahid Tayebi, Elizabeth Geena Woo, Grisel Lopez, Luca Fierro, Marco Toffoli +15 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

Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy

medRxiv(2023)10.1101/2023.12.28.23300612

N/A

0.351DataRank · unranked

8 citations

Timothy S. Chang, Beth A. Dombroski, Po‐Liang Cheng, Vishakha Patil, Leopoldo Valiente‐Banuet +56 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

The Global Landscape of Genetic Variation in Parkinson’s disease: Multi-Ancestry Insights into Established Disease Genes and their Translational Relevance

medRxiv(2025)10.1101/2025.07.08.25330815

N/A

0.312DataRank · unranked

7 citations

Zih‐Hua Fang, Mary B. Makarious, Nicole Kuznetsov, Kajsa Brolin, Shannon Ballard +41 more

Large-scale genetic characterization of Parkinson’s disease in the African and African admixed populations

medRxiv(2025)10.1101/2025.01.14.25320205

Top 55%

0.301DataRank

Top 55%4 citations

Kimberly Paquette, Peter Wild Crea, Paula Saffie Awad, Charles Achoru, Funmilola Taiwo +95 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 genetic characterization of Parkinson’s disease in the African and African admixed populations

Brain(2025)10.1093/brain/awaf379

Top 56%

0.288DataRank

Top 56%3 citations

Kimberly Paquette, Peter Wild Crea, Kathryn Step, Emily Waldo, Mathew J. Koretsky +95 more

The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population

npj Parkinson s Disease(2025)10.1038/s41531-025-00896-2

N/A

0.241DataRank · unranked

4 citations

Kristin Levine, Susan H. Fox, Connie Marras, Nazish Ahmed, Nicole Kuznetsov +95 more

Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells

Movement Disorders(2025)10.1002/mds.30150

N/A

0.241DataRank · unranked

4 citations

Timothy S. Chang, Beth A. Dombroski, Po‐Liang Cheng, Yaqin Si, Albert Tucci +62 more

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

medRxiv(2022)10.1101/2022.11.25.22282764

Top 63%

0.217DataRank

Top 63%3 citations

Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar +19 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

Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy

Molecular Neurodegeneration(2024)10.1186/s13024-024-00763-3

N/A

0.189DataRank · unranked

2 citations

Timothy S. Chang, Beth A. Dombroski, Po‐Liang Cheng, Vishakha Patil, Leopoldo Valiente‐Banuet +57 more

Rare but Relevant? Assessing Variants in Dystonia‐Linked Genes in Parkinson's Disease

Movement Disorders(2025)10.1002/mds.70073

Top 70%

0.165DataRank

Top 70%2 citations

Zih‐Hua Fang, Laurel A. Screven, Ai Huey Tan, Roy N. Alcalay, Rim Amouri +33 more

Genome-wide association study of REM sleep behavior disorder in Parkinson’s disease

npj Parkinson s Disease(2025)10.1038/s41531-025-01078-w

N/A

0.165DataRank · unranked

2 citations

Karl Heilbron, Pierre Fontanillas, Lucy Norcliffe‐Kaufmann, Eric Yu, Uladzislau Rudakou +26 more

ASSESSING THE RELATIONSHIP BETWEEN MONOALLELIC PARK2 MUTATIONS AND PARKINSON’S RISK

medRxiv(2020)10.1101/2020.06.26.20138172

N/A

0.149DataRank · unranked

1 citations

Bernabé I. Bustos, Jing Hu, Dimitri Krainc, Theresita Joseph, Jason Hehir +8 more

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

Genome-wide assessment identifies novel runs of homozygosity linked to Parkinson’s disease etiology across diverse ancestral populations

medRxiv(2025)10.1101/2025.05.21.25328076

Top 78%

0.104DataRank

Top 78%1 citations

Carlos F. Hernández, Esraa Eltaraifee, Ana J. Hernández-Medrano, Pin‐Jui Kung, Miriam Ostrožovičová +11 more

NeuroBooster Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

Movement Disorders(2024)10.1002/mds.29902

N/A

0DataRank · unranked

38 citations

Faraz Faghri, Elisa Majounie, Mathew J. Koretsky, Jeffrey Kim, Kristin Levine +29 more

Genome‐Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease

Movement Disorders(2020)10.1002/mds.28342

N/A

0DataRank · unranked

173 citations

Michael Lawton, Edwin Jabbari, Regina Hertfelder Reynolds, Hirotaka Iwaki, Cornelis Blauwendraat +23 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

ATP10B and the risk for Parkinson’s disease

Acta Neuropathologica(2020)10.1007/s00401-020-02172-4

N/A

0DataRank · unranked

16 citations

Anni Moore, Cornelis Blauwendraat, Huw R. Morris, Sara Bandrés‐Ciga, Raquel Real

The Cortical Basal ganglia Functional Scale (CBFS): Development and preliminary validation

Parkinsonism & Related Disorders(2020)10.1016/j.parkreldis.2020.08.021

N/A

0DataRank · unranked

26 citations

Glenn T. Stebbins, Ping Wang, Edwin Jabbari, Ruth Lamb, Huw R. Morris +25 more

Genome-wide association studies of cognitive and motor progression in Parkinson's disease

medRxiv(2020)10.1101/2020.05.07.20084343

N/A

0DataRank · unranked

21 citations

Michael Lawton, Edwin Jabbari, Regina Hertfelder Reynolds, Hirotaka Iwaki, Cornelis Blauwendraat +23 more

Genome-Wide Association Study Meta-Analysis for Parkinson’s Disease Motor Subtypes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.26.174276

N/A

0DataRank · unranked

0 citations

Rami Al‐Ouran, Rainer von Coelln, Cornelis Blauwendraat, Emily J. Hill, Lan Luo +16 more

Longitudinal risk factors for developing depressive symptoms in Parkinson's disease

Journal of the Neurological Sciences(2021)10.1016/j.jns.2021.117615

N/A

0DataRank · unranked

8 citations

Huw R. Morris, Faraz Faghri, Hampton L. Leonard, Mike A. Nalls, Andrew Singleton +2 more

The impact of Type 2 diabetes in Parkinson’s disease

medRxiv(2021)10.1101/2021.10.21.21265308

N/A

0DataRank · unranked

3 citations

James R. Evans, Anna I. Wernick, Gurvir S. Virdi, Minee Liane-Choi, Michael Lawton +9 more

Investigation of Autosomal Genetic Sex Differences in Parkinson’s disease

medRxiv(2021)10.1101/2021.02.09.21250262

N/A

0DataRank · unranked

1 citations

Hirotaka Iwaki, Mary B. Makarious, Sara Bandrés‐Ciga, Hampton L. Leonard, Francis P. Grenn +32 more

Longitudinal Risk Factors For Developing Depression in Parkinson’s Disease

medRxiv(2021)10.1101/2021.06.29.21259714

N/A

0DataRank · unranked

0 citations

Huw R. Morris, Faraz Faghri, Hampton L. Leonard, Mike A. Nalls, Andrew Singleton +2 more

Multi-modality machine learning predicting Parkinson’s disease

npj Parkinson s Disease(2022)10.1038/s41531-022-00288-w

N/A

0DataRank · unranked

156 citations

Hampton L. Leonard, Dan Vitale, Hirotaka Iwaki, Lana Sargent, Anant Dadu +22 more

A data-driven model of brain volume changes in progressive supranuclear palsy

Brain Communications(2022)10.1093/braincomms/fcac098

N/A

0DataRank · unranked

25 citations

Martina Bocchetta, Emily Todd, David M. Cash, Neil P. Oxtoby, L. VandeVrede +8 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

Polygenic Parkinson’s disease genetic risk score as risk modifier of parkinsonism in Gaucher disease

medRxiv(2022)10.1101/2022.12.19.22280175

N/A

0DataRank · unranked

1 citations

Nahid Tayebi, Elizabeth Geena Woo, Grisel Lopez, Luca Fierro, Marco Toffoli +15 more

Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study

The Lancet Neurology(2023)10.1016/s1474-4422(23)00283-1

N/A

0DataRank · unranked

157 citations

Sara Bandrés‐Ciga, Mary B. Makarious, Oluwadamilola O. Ojo, Peter Wild Crea, Oladunni Abiodun +72 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

0DataRank · unranked

32 citations

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

Uncovering spatiotemporal patterns of atrophy in progressive supranuclear palsy using unsupervised machine learning

Brain Communications(2023)10.1093/braincomms/fcad048

N/A

0DataRank · unranked

31 citations

Cameron Shand, Emily Todd, Martina Bocchetta, David M. Cash, Lawren VandeVrede +26 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

Active elite rugby participation is associated with altered precentral cortical thickness

Brain Communications(2023)10.1093/braincomms/fcad257

N/A

0DataRank · unranked

6 citations

Karl Zimmerman, Etienne Laverse, Niall Bourke, Neil Graham, Emma‐Jane Mallas +6 more

Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson’s Disease in African and African Admixed Populations

medRxiv(2023)10.1101/2023.05.05.23289529

N/A

0DataRank · unranked

18 citations

Sara Bandrés‐Ciga, Mary B. Makarious, Oluwadamilola O. Ojo, Peter Wild Crea, Oladunni Abiodun +74 more

Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.09.565552

N/A

0DataRank · unranked

11 citations

Jack Humphrey, Timothy S. Chang, Yi Zhao, Yuk Yee Leung, Pavel P. Kuksa +42 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

Uncovering the genetic basis of Parkinson's disease globally: from discoveries to the clinic

The Lancet Neurology(2024)10.1016/s1474-4422(24)00378-8

N/A

0DataRank · unranked

73 citations

Ai Huey Tan, Azlina Ahmad, Njideka Ulunma Okubadejo, Katja Lohmann, Huw R. Morris +16 more

Genome sequence analyses identify novel risk loci for multiple system atrophy

Neuron(2024)10.1016/j.neuron.2024.04.002

N/A

0DataRank · unranked

44 citations

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

Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes

Nature Communications(2024)10.1038/s41467-024-52025-x

N/A

0DataRank · unranked

41 citations

Jack Humphrey, Timothy S. Chang, Yi Zhao, Yuk Yee Leung, Pavel P. Kuksa +55 more

Evaluation of Cerebrospinal Fluid α‐Synuclein Seed Amplification Assay in Progressive Supranuclear Palsy and Corticobasal Syndrome

Movement Disorders(2024)10.1002/mds.30019

N/A

0DataRank · unranked

28 citations

Riona Fumi, Marte Theilmann Jensen, Megan Hodgson, Tatiana Georgiades, Lesley Wu +19 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

MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

The Lancet Neurology(2024)10.1016/s1474-4422(24)00083-8

N/A

0DataRank · unranked

23 citations

William J. Scotton, Shanu F. Roemer, Tammaryn Lashley, Michael G. Heckman, Maryam Shoai +95 more

Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.05.017

N/A

0DataRank · unranked

14 citations

Demis A. Kia, Raffaele Ferrari, Ganna Leonenko, Beatrice Costa, Valentina Saba +95 more

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

Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypes

medRxiv(2024)10.1101/2024.02.26.24303379

N/A

0DataRank · unranked

0 citations

Timothy S. Chang, Beth A. Dombroski, Po‐Liang Cheng, Yaqin Si, Albert Tucci +59 more

Tackling a disease on a global scale, the Global Parkinson’s Genetics Program, GP2: A new generation of opportunities

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.07.014

N/A

0DataRank · unranked

6 citations

Alastair J. Noyce, Ignácio F. Mata, Laurel A. Screven, J Solle, Sonya B. Dumanis +7 more

Distinct spatiotemporal atrophy patterns in corticobasal syndrome are associated with different underlying pathologies

Brain Communications(2025)10.1093/braincomms/fcaf066

N/A

0DataRank · unranked

1 citations

Cameron Shand, Emily Todd, Martina Bocchetta, Christopher Kobylecki, David M. Cash +31 more

Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson’s Disease

medRxiv(2025)10.1101/2025.07.10.25330831

N/A

0DataRank · unranked

0 citations

Zih‐Hua Fang, Laurel A. Screven, Ai Huey Tan, Roy N. Alcalay, Rim Amouri +33 more

Huw R. Morris

Indexed papers

Top data-sharing exemplar

Papers