Alexis Brice

Centre National de la Recherche Scientifique

Also affiliated with Inserm, Sorbonne Université, Institut de Psychiatrie et Neurosciences de Paris, Institut du Cerveau

MedicineNeuroscienceBiochemistry, Genetics and Molecular Biology

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 1%percentile

9.9Author DataRank

Indexed papers

9in 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 9 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.

Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database

PLoS Genetics(2012)10.1371/journal.pgen.1002548

Top 3%

6.9DataRank

Top 3%543 citations

Johannes T. Roehr, Matthew B. McQueen, Fotini K. Kavvoura, Sachin Bagade, Brit-Maren M. Schjeide +61 more

Papers

Driven by 68 papers — median percentile 80. Top paper: “Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database”.

Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database

PLoS Genetics(2012)10.1371/journal.pgen.1002548

Top 3%

6.9DataRank

Top 3%543 citations

Johannes T. Roehr, Matthew B. McQueen, Fotini K. Kavvoura, Sachin Bagade, Brit-Maren M. Schjeide +61 more

Large-scale replication and heterogeneity in Parkinson disease genetic loci

Neurology(2012)10.1212/wnl.0b013e318264e353

N/A

6.6DataRank · unranked

132 citations

Grazia Annesi, Alexis Brice, Christine Van Broeckhoven, Muin J. Khoury, Maria Bozi +160 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

Differences in the Presentation and Progression of Parkinson's Disease by Sex

Movement Disorders(2020)10.1002/mds.28312

N/A

3.5DataRank · unranked

102 citations

Cornelis Blauwendraat, Hampton L. Leonard, Mary B. Makarious, Jonggeol J. Kim, Ganqiang Liu +43 more

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

Journal of Medical Genetics(2012)10.1136/jmedgenet-2012-101155

N/A

3.1DataRank · unranked

108 citations

John P. A. Ioannidis, Grazia Annesi, Alexis Brice, Muin J. Khoury, Maria Bozi +67 more

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

Neurobiology of Aging(2011)10.1016/j.neurobiolaging.2011.05.024

N/A

1.8DataRank · unranked

33 citations

Demetrius M. Maraganore, Peter Nuernberg, Grazia Annesi, Nadine Abahuni, Anna Rita Bentivoglio +42 more

Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort

Frontiers in Neurology(2020)10.3389/fneur.2020.00682

Top 14%

1.4DataRank

Top 14%47 citations

Marion Houot, Graziella Mangone, Christelle Tesson, Hélène Bertrand, Sylvie Forlani +21 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 meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

Nature Genetics(2014)10.1038/ng.3043

N/A

1.1DataRank · unranked

1956 citations

NeuroGenetics Research Consortium (NGRC), The Ashkenazi Jewish Dataset Investigator, Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE), Alzheimer Genetic Analysis Group, Nathan Pankratz +49 more

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

The Lancet Neurology(2008)10.1016/s1474-4422(08)70117-0

N/A

1.1DataRank · unranked

1574 citations

Mario Falchi, Sean S O'Sullivan, Vincenzo Bonifati, Alexandra Durr, Susan Bressman +20 more

Brain atrophy in prodromal synucleinopathy is shaped by structural connectivity and gene expression

Brain(2022)10.1093/brain/awac187

N/A

1.0DataRank · unranked

52 citations

Christina Tremblay, Andrew Vo, Ying Qiu Zheng, Stéphane Lehéricy, Isabelle Arnulf +55 more

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

The Lancet Neurology(2011)10.1016/s1474-4422(11)70175-2

N/A

0.876DataRank · unranked

343 citations

Michael G. Heckman, Nadine Abahuni, Grazia Annesi, Justin A. Bacon, Soraya Bardien +60 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

Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers

Movement Disorders(2023)10.1002/mds.29337

Top 25%

0.809DataRank

Top 25%28 citations

Elise A. Lucotte, Cloé Domenighetti, Matthew H. Law, Mark M. Iles, Kevin M. Brown +89 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

Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson’s Disease

Journal of Parkinson s Disease(2021)10.3233/jpd-212851

N/A

0.663DataRank · unranked

82 citations

Pierre‐Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover, Océane Mohamed +74 more

Characterization of Recessive Parkinson Disease in a Large Multicenter Study

Annals of Neurology(2020)10.1002/ana.25787

N/A

0.663DataRank · unranked

82 citations

Ariane Lunati, Marion Houot, Sawssan Ben Romdhan, Fabienne Clot, Christelle Tesson +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

Reduced synaptic activity and dysregulated extracellular matrix pathways in midbrain neurons from Parkinson’s disease patients

npj Parkinson s Disease(2022)10.1038/s41531-022-00366-z

N/A

0.621DataRank · unranked

62 citations

Shong Lau, Andreea Manole, Idan Rosh, Menachem Mendel Percia, Ran Ben Ezer +28 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

Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort

Movement Disorders(2023)10.1002/mds.29288

N/A

0.590DataRank · unranked

50 citations

Susen Schaake, Katja Lohmann, Shalini Padmanabhan, Alexis Brice, Suzanne Lesage +95 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

SARA captures disparate progression and responsiveness in spinocerebellar ataxias

Journal of Neurology(2024)10.1007/s00415-024-12475-1

N/A

0.540DataRank · unranked

16 citations

Tanja Schmitz‐Hübsch, Giulia Coarelli, Heike Jacobi, Anna Heinzmann, Karla P. Figueroa +21 more

Mitochondrial function-associated genes underlie cortical atrophy in prodromal synucleinopathies

Brain(2023)10.1093/brain/awad044

N/A

0.538DataRank · unranked

35 citations

Christina Tremblay, Andrew Vo, Bratislav Misic, Stéphane Lehéricy, Isabelle Arnulf +57 more

Population‐specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO‐PD) consortium

Movement Disorders(2013)10.1002/mds.25600

N/A

0.538DataRank · unranked

35 citations

Alexandra I. Soto‐Ortolaza, Nadine Abahuni, Grazia Annesi, Justin A. Bacon, Soraya Bardien +65 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

Evidence for apolipoprotein E ϵ4 association in early‐onset Alzheimer's patients with late‐onset relatives

American Journal of Medical Genetics(1995)10.1002/ajmg.1320600613

N/A

0.500DataRank · unranked

27 citations

Dominique Campion, Maria Martinez, Alexis Brice, Sandrine Tardieu, Didier Hannequin +5 more

De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia

Movement Disorders(2022)10.1002/mds.28959

N/A

0.494DataRank · unranked

26 citations

Jonathan De Winter, Danique Beijer, Giulia Coarelli, Melanie Wayand, Robin Palvadeau +33 more

Distinct brain atrophy progression subtypes underlie phenoconversion in isolated REM sleep behaviour disorder

EBioMedicine(2025)10.1016/j.ebiom.2025.105753

N/A

0.442DataRank · unranked

18 citations

Aline Delva, Christina Tremblay, Andrew Vo, Marie Filiatrault, Max Tweedale +77 more

Somatic instability of the FGF14 -SCA27B GAA•TTC repeat reveals a marked expansion bias in the cerebellum

Brain(2024)10.1093/brain/awae312

N/A

0.425DataRank · unranked

16 citations

Jean‐Loup Méreaux, Susana Boluda, Matt C. Danzi, Marie-Josée Dicaire, Claire-Sophie Davoine +32 more

The Interaction between HLA‐DRB1 and Smoking in Parkinson's Disease Revisited

Movement Disorders(2022)10.1002/mds.29133

N/A

0.416DataRank · unranked

15 citations

Venceslas Douillard, Pierre‐Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover +75 more

Association of Body Mass Index and Parkinson Disease

Neurology(2024)10.1212/wnl.0000000000209620

N/A

0.385DataRank · unranked

12 citations

Pierre‐Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover, Berta Portugal +72 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 association studies of LRRK2 modifiers of Parkinson's disease

medRxiv(2020)10.1101/2020.12.14.20224378

N/A

0.360DataRank · unranked

10 citations

Babak Alipanahi, Pierre Fontanillas, Tae‐Hwi Schwantes‐An, Jan Aasly, Roy N. Alcalay +55 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

Proxy-analysis of the genetics of cognitive decline in Parkinson’s disease through polygenic scores

npj Parkinson s Disease(2024)10.1038/s41531-023-00619-5

N/A

0.330DataRank · unranked

8 citations

Manuela Tan, Fanny Casse, Suzanne Lesage, Christelle Tesson, Alexis Brice +7 more

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into the complex genetic architecture

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.06.185066

N/A

0.312DataRank · unranked

7 citations

Marya S. Sabir, Sara Bandrés‐Ciga, Sara Sáez-Atiénzar, Regina Hertfelder Reynolds, Emil K. Gustavsson +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

Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data

Cell Genomics(2024)10.1016/j.xgen.2024.100679

N/A

0.292DataRank · unranked

6 citations

Cleide Dos Santos Souza, Ruth Chia, Selina N. Beal, Ileana Lorenzini, Ruili Huang +92 more

Impact of Y chromosome loss on the risk of Parkinson's disease and progression

EBioMedicine(2025)10.1016/j.ebiom.2025.105769

N/A

0.241DataRank · unranked

4 citations

Xinyi Chen, Wenxuan Du, Cha Lin, Liao Yu, Jean‐Christophe Corvol +43 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

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

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 an age-related Parkinson's disease risk factor that regulates sulfur metabolism

Research Square(2021)10.21203/rs.3.rs-1168396/v1

N/A

0.208DataRank · unranked

3 citations

Shani Stern, Sara B. Linker, Diogo H. Da Silva, Nako Nakatsuka, Juliane Tampé +12 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

Investigation of Autosomal Genetic Sex Differences in Parkinson’s disease

medRxiv(2021)10.1101/2021.02.09.21250262

N/A

0.104DataRank · unranked

1 citations

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

Alternative Translation Initiation in PRKN Delays the Onset of Parkinson's Disease and Offers a Therapeutic Target

Annals of Neurology(2026)10.1002/ana.78180

N/A

0.104DataRank · unranked

1 citations

Katja Lohmann, Manabu Funayama, Poornima J. Menon, Eva‐Juliane Vollstedt, Teresa Kleinz +10 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

SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration

Brain(2021)10.1093/brain/awab171

N/A

0DataRank · unranked

26 citations

Agnès Camuzat, Khalid El Hachimi, Justine Guégan, Daisy Rinaldi, Serena Lattante +40 more

Exploration of Neurodegenerative Diseases Using Long‐Read Sequencing and Optical Genome Mapping Technologies

Movement Disorders(2025)10.1002/mds.30151

N/A

0DataRank · unranked

9 citations

Kensuke Daida, Cornelis Blauwendraat, Kimberley J. Billingsley, Alexis Brice, Guillaume Cogan

Classification of GBA1 variants and their impact on Parkinson’s disease: an in silico score analysis

npj Parkinson s Disease(2025)10.1038/s41531-025-01060-6

N/A

0DataRank · unranked

5 citations

Christelle Tesson, Aymeric Basset, François-Xavier Lejeune, Guillaume Cogan, Graziella Mangone +93 more

Screening of Hidden Pathogenic Structural Variants in PRKN

Movement Disorders(2025)10.1002/mds.30267

N/A

0DataRank · unranked

0 citations

Guillaume Cogan, Christelle Tesson, Suzanne Lesage, Susen Schaake, Alexander Balck +15 more

Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease

Annals of Neurology(2021)10.1002/ana.26094

N/A

0DataRank · unranked

50 citations

Babak Alipanahi, Pierre Fontanillas, Tae‐Hwi Schwantes‐An, Jan Aasly, Roy N. Alcalay +56 more

Clinical Variability of SYNJ1-Associated Early-Onset Parkinsonism

Frontiers in Neurology(2021)10.3389/fneur.2021.648457

N/A

0DataRank · unranked

39 citations

Graziella Mangone, Christelle Tesson, Hélène Bertrand, Mustapha Benmahdjoub, Selma Kesraoui +5 more

Differential early subcortical involvement in genetic FTD within the GENFI cohort

NeuroImage Clinical(2021)10.1016/j.nicl.2021.102646

N/A

0DataRank · unranked

66 citations

Emily Todd, Georgia Peakman, David M. Cash, Rhian S. Convery, Lucy L. Russell +95 more

CAG repeat mosaicism is gene specific in spinocerebellar ataxias

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.015

N/A

0DataRank · unranked

26 citations

François‐Xavier Lejeune, Isabelle David, Susana Boluda, Giulia Coarelli, Sabrina Leclère-Turbant +14 more

Reduced synaptic activity and dysregulated extracellular matrix pathways are common phenotypes in midbrain neurons derived from sporadic and mutation-associated Parkinson’s disease patients

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2021.12.31.474654

N/A

0DataRank · unranked

7 citations

Shong Lau, Andreea Manole, Idan Rosh, Menahem Percia, Ran Ben Ezer +24 more

Mitochondrial haplogroups and cognitive progression in Parkinson’s disease

Brain(2022)10.1093/brain/awac327

N/A

0DataRank · unranked

24 citations

Chunming Ni, Jiamin Zhan, Weimin Li, Junfeng Luo, Zhixiang Liao +42 more

PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability

Brain(2022)10.1093/brain/awac326

N/A

0DataRank · unranked

33 citations

Christelle Tesson, Ana Carreras Mascaro, Thomas Courtin, Riaan van Coller, Salma Sakka +91 more

Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study

Movement Disorders(2022)10.1002/mds.28902

N/A

0DataRank · unranked

45 citations

Pierre‐Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover, Océane Mohamed +74 more

Long‐Read Sequencing Unravels the Complexity of Structural Variants in PRKN in Two Individuals with Early‐Onset Parkinson's Disease

Movement Disorders(2024)10.1002/mds.29914

N/A

0DataRank · unranked

9 citations

Kensuke Daida, Kimberley J. Billingsley, Christelle Tesson, Sylvie Forlani, Ludmila Jornéa +10 more

Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions

EBioMedicine(2023)10.1016/j.ebiom.2023.104931

N/A

0DataRank · unranked

58 citations

Claire-Sophie Davoine, David Pellerin, Giulia Coarelli, Marie Coutelier, Claire Ewenczyk +42 more

Somatic instability of the FGF14 -SCA27B GAA•TTC repeat reveals a marked expansion bias in the cerebellum

medRxiv(2024)10.1101/2024.07.01.24309777

N/A

0DataRank · unranked

3 citations

Jean‐Loup Méreaux, Susana Boluda, Matt C. Danzi, Marie-Josée Dicaire, Claire-Sophie Davoine +32 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

Alexis Brice

Indexed papers

Top data-sharing exemplar

Papers