Matthis Synofzik

German Center for Neurodegenerative Diseases

Also affiliated with Hertie Institute for Clinical Brain Research

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 4%percentile

0.642Author DataRank

Indexed papers

2in 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 2 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.

Progression of biological markers in spinocerebellar ataxia type 3: longitudinal analysis of prospective data from the ESMI cohort

The Lancet Regional Health - Europe(2025)10.1016/j.lanepe.2025.101339

Top 51%

0.345DataRank

Top 51%9 citations

Héctor García‐Moreno, Mónica Ferreira, Jeannette Hübener‐Schmid, Tamara Schaprian, Philipp Wegner +47 more

Papers

Driven by 47 papers — median percentile 47. Top paper: “Plasma Neurofilament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar Degeneration”.

Plasma Neurofilament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar Degeneration

Neurology(2021)10.1212/wnl.0000000000011848

N/A

1.7DataRank · unranked

108 citations

Ping Wang, Adam M. Staffaroni, Carolin Heller, Yann Cobigo, Amy Wolf +88 more

Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3

Movement Disorders(2021)10.1002/mds.28610

N/A

1.2DataRank · unranked

59 citations

Tamara Schaprian, Koyak Berkan, Kathrin Reetz, Marcondes C. França, Thiago Junqueira Ribeiro de Rezende +26 more

LifeTime and improving European healthcare through cell-based interceptive medicine

Nature(2020)10.1038/s41586-020-2715-9

N/A

0.747DataRank · unranked

144 citations

Geneviève Almouzni, Stanislaw A. Gorski, Stein Aerts, Ido Amit, Michela G. Bertero +178 more

Progression of biological markers in spinocerebellar ataxia type 3: longitudinal analysis of prospective data from the ESMI cohort

The Lancet Regional Health - Europe(2025)10.1016/j.lanepe.2025.101339

Top 51%

0.345DataRank

Top 51%9 citations

Héctor García‐Moreno, Mónica Ferreira, Jeannette Hübener‐Schmid, Tamara Schaprian, Philipp Wegner +47 more

Anatomical progression of genetic frontotemporal lobar degeneration across the lifespan

Brain(2025)10.1093/brain/awaf195

Top 55%

0.296DataRank

Top 55%6 citations

Boris Mansencal, Vladimir S. Fonov, José V. Manjón, Thomas Tourdias, Arabella Bouzigues +95 more

MRI data-driven algorithm for the diagnosis of behavioural variant frontotemporal dementia

Journal of Neurology Neurosurgery & Psychiatry(2021)10.1136/jnnp-2020-324106

N/A

0DataRank · unranked

25 citations

Mahsa Dadar, John C. van Swieten, Barbara Borroni, Raquel Sánchez‐Valle, Fermín Moreno +25 more

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

New England Journal of Medicine(2022)10.1056/nejmoa2207406

N/A

0DataRank · unranked

251 citations

Matt C. Danzi, Carlo Wilke, M. Renaud, Sarah Fazal, Marie‐Josée Dicaire +46 more

Temporal order of clinical and biomarker changes in familial frontotemporal dementia

Nature Medicine(2022)10.1038/s41591-022-01942-9

N/A

0DataRank · unranked

138 citations

Melanie Quintana, Barbara Wendelberger, Hilary W. Heuer, Lucy L. Russell, Yann Cobigo +95 more

Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementia

Brain(2022)10.1093/brain/awac069

N/A

0DataRank · unranked

92 citations

Vincent Bazinet, Mahsa Dadar, Ana L. Manera, D. Louis Collins, Alain Dagher +95 more

Tau and neurofilament light‐chain as fluid biomarkers in spinocerebellar ataxia type 3

European Journal of Neurology(2022)10.1111/ene.15373

N/A

0DataRank · unranked

50 citations

Mercedes Prudencio, Gilbert Thomas‐Black, Nita Solanky, Karen Jansen‐West, Rana Hanna Al‐Shaikh +22 more

Progressive Spinal Cord Degeneration in Friedreich's Ataxia: Results from ENIGMA‐Ataxia

Movement Disorders(2022)10.1002/mds.29261

N/A

0DataRank · unranked

27 citations

Isaac Adanyeguh, Filippo Arrigoni, Benjamin Bender, Fernando Cendes, Louise A. Corben +27 more

Longitudinal Cognitive Changes in Genetic Frontotemporal Dementia Within the GENFI Cohort

Neurology(2022)10.1212/wnl.0000000000200384

N/A

0DataRank · unranked

29 citations

Amy MacDougall, Esther van den Berg, Lize C. Jiskoot, Janne M. Papma, Emma L. van der Ende +94 more

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

Movement Disorders(2022)10.1002/mds.28959

N/A

0DataRank · unranked

26 citations

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

Adult‐Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERDND): Time to Move Beyond the Skin

Movement Disorders(2022)10.1002/mds.29071

N/A

0DataRank · unranked

22 citations

Demet Önder, Andreas Traschütz, Xenia Kobeleva, Ivan Karin, Martina Minnerop +25 more

Repeat expansions nested within tandem CNVs: a unique structural change in GLS exemplifies the diagnostic challenges of non-coding pathogenic variation

Human Molecular Genetics(2022)10.1093/hmg/ddac173

N/A

0DataRank · unranked

13 citations

Matt C. Danzi, André B. P. Kuilenburg, Selina Reich, Andreas Traschütz, Benjamin Bender +13 more

Expanding PRDX3 disease: broad range of onset age and infratentorial MRI signal changes

Brain(2022)10.1093/brain/awac240

N/A

0DataRank · unranked

8 citations

Benjamin Bender, Tobias B. Haack, Stephan Züchner, A. Nazlı Başak, Matthis Synofzik +1 more

Characteristics of serum neurofilament light chain as a biomarker in hereditary spastic paraplegia type 4

Annals of Clinical and Translational Neurology(2022)10.1002/acn3.51518

N/A

0DataRank · unranked

9 citations

Lina María Serna-Higuita, Carlo Wilke, Tim W. Rattay, Holger Hengel, Jennifer Reichbauer +8 more

Spinal cord damage in Friedreich’s ataxia: Results from the ENIGMA-Ataxia

medRxiv(2022)10.1101/2022.04.20.22273878

N/A

0DataRank · unranked

1 citations

Isaac Adanyeguh, Filippo Arrigoni, Benjamin Bender, Fernando Cendes, Louise A. Corben +27 more

Stage‐Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3

Annals of Neurology(2023)10.1002/ana.26824

N/A

0DataRank · unranked

28 citations

Moritz Berger, Carlo Wilke, Jeannette Hübener‐Schmid, Tamara Schaprian, Magda M. Santana +34 more

Structural MRI predicts clinical progression in presymptomatic genetic frontotemporal dementia: findings from the GENetic Frontotemporal dementia Initiative cohort

Brain Communications(2023)10.1093/braincomms/fcad061

N/A

0DataRank · unranked

22 citations

Emily Todd, Arabella Bouzigues, David M. Cash, Jennifer Nicholas, Rhian S. Convery +95 more

Recurrentde-novo gain-of-functionmutation inSPTLC2confirms dysregulated sphingolipid production to cause juvenile amyotrophic lateral sclerosis

Journal of Neurology Neurosurgery & Psychiatry(2023)10.1136/jnnp-2023-332130

N/A

0DataRank · unranked

14 citations

Danique Beijer, Museer A. Lone, Elif Bayraktar, Piraye Oflazer, Rotem Orbach +15 more

Stage-dependent biomarker changes in spinocerebellar ataxia type 3

medRxiv(2023)10.1101/2023.04.21.23287817

N/A

0DataRank · unranked

10 citations

Moritz Berger, Carlo Wilke, Jeannette Hübener‐Schmid, Tamara Schaprian, Magda M. Santana +34 more

Intronic FGF14 GAA repeat expansions are a common cause of downbeat nystagmus syndromes: frequency, phenotypic profile, and 4-aminopyridine treatment response

medRxiv(2023)10.1101/2023.07.30.23293380

N/A

0DataRank · unranked

10 citations

Felix Heindl, Carlo Wilke, Matt C. Danzi, Andreas Traschütz, Catherine Ashton +12 more

Digital gait measures capture 1-year progression in early-stage spinocerebellar ataxia type 2

medRxiv(2023)10.1101/2023.10.08.23296692

N/A

0DataRank · unranked

10 citations

Lina Daghsen, Mathieu Cazier, Jean‐Charles Lamy, Marie‐Laure Welter, Martin A. Giese +5 more

A common flanking variant is associated with enhanced meiotic stability of the FGF14 -SCA27B locus

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.05.11.540430

N/A

0DataRank · unranked

9 citations

Giulia Gobbo, Madeline Couse, Egor Dolzhenko, Marie‐Josée Dicaire, Stephan Züchner +18 more

Blood neurofilament light chain levels are associated with disease progression in a transgenic SCA3 mouse model

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.02.28.530463

N/A

0DataRank · unranked

0 citations

Isabel G. Wellik, Kristen H. Schuster, Sabrina I. Jarrah, Madeleine Wacker, Naila S. Ashraf +5 more

Sensitivity and specificity of a seed amplification assay for diagnosis of multiple system atrophy: a multicentre cohort study

The Lancet Neurology(2024)10.1016/s1474-4422(24)00395-8

N/A

0DataRank · unranked

73 citations

Carly M. Farris, Sandrina Weber, Sebastian Schade, Hieu Nguyen, Alexandra Pérez‐Soriano +29 more

GAA-FGF14 disease: defining its frequency, molecular basis, and 4-aminopyridine response in a large downbeat nystagmus cohort

EBioMedicine(2024)10.1016/j.ebiom.2024.105076

N/A

0DataRank · unranked

66 citations

Felix Heindl, Carlo Wilke, Matt C. Danzi, Andreas Traschütz, Catherine Ashton +12 more

A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus

Nature Genetics(2024)10.1038/s41588-024-01808-5

N/A

0DataRank · unranked

34 citations

Giulia Gobbo, Madeline Couse, Egor Dolzhenko, Sathiji Nageshwaran, Warren Cheung +95 more

Digital Gait Measures Capture 1‐Year Progression in Early‐Stage Spinocerebellar Ataxia Type 2

Movement Disorders(2024)10.1002/mds.29757

N/A

0DataRank · unranked

25 citations

Lina Daghsen, Matthieu Cazier, Jean‐Charles Lamy, Marie‐Laure Welter, Martin A. Giese +5 more

Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study

Journal of Neurology Neurosurgery & Psychiatry(2024)10.1136/jnnp-2023-332696

N/A

0DataRank · unranked

16 citations

Isaac Adanyaguh, Orlando Graziani Póvoas Barsottini, Benjamin Bender, Fernando Cendes, Léo Coutinho +28 more

An iPSC model for POLR3A-associated spastic ataxia: Generation of three unrelated patient cell lines

Stem Cell Research(2024)10.1016/j.scr.2024.103363

N/A

0DataRank · unranked

2 citations

Tam Pham, Holger Hengel, Matthis Synofzik, Maike Nagel, Rebecca Schüle +1 more

Neuroradiological findings in GAA- FGF14 ataxia (SCA27B): more than cerebellar atrophy

medRxiv(2024)10.1101/2024.02.16.24302945

N/A

0DataRank · unranked

9 citations

Catherine Ashton, Rawan Sakalla, Guillemette Clément, Sophie Planel, Céline Bonnet +22 more

The Pattern and Staging of Brain Atrophy in Spinocerebellar Ataxia Type 2 (SCA2): MRI Volumetrics from ENIGMA-Ataxia

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.16.613281

N/A

0DataRank · unranked

3 citations

Isaac Adanyeguh, Benjamin Bender, Sylvia Boesch, Arturo Brunetti, Sirio Cocozza +31 more

Disease stage–specific atrophy markers in Alzheimer's disease

Alzheimer s & Dementia(2025)10.1002/alz.70482

N/A

0DataRank · unranked

11 citations

Helena M. Gellersen, Sarah E. Polk, René Lattmann, Anika Wuestefeld, Laura E.M. Wisse +47 more

The Pattern and Stages of Atrophy in Spinocerebellar Ataxia Type 2: Volumetrics from ENIGMA‐Ataxia

Movement Disorders(2025)10.1002/mds.30143

N/A

0DataRank · unranked

4 citations

Isaac Adanyeguh, Benjamin Bender, Sylvia Boesch, Arturo Brunetti, Sirio Cocozza +31 more

Thalamus involvement in genetic frontotemporal dementia assessed using structural and diffusion MRI: a GENFI study

Brain Communications(2025)10.1093/braincomms/fcaf420

N/A

0DataRank · unranked

2 citations

Henry F. J. Tregidgo, Emily Todd, Arabella Bouzigues, David M. Cash, Lucy L. Russell +95 more

Brain atrophy staging in spinocerebellar ataxia type 3 for clinical prognosis and trial enrichment

EBioMedicine(2025)10.1016/j.ebiom.2025.106090

N/A

0DataRank · unranked

2 citations

Philipp Wegner, Mónica Ferreira, Tamara Schaprian, Marcondes C. França, Thiago Junqueira Ribeiro Rezende +73 more

A new FTLD-TDP subtype with annexin A11 co-pathology

Acta Neuropathologica(2025)10.1007/s00401-025-02962-8

N/A

0DataRank · unranked

1 citations

Marleen Van den Broeck, Sarah Wynants, Simon Cheung, Johannes Prudlo, Andreas Hermann +6 more

Content Validity of the Friedreich Ataxia Rating Scale in Patients with Spinocerebellar Ataxia

Neurology and Therapy(2025)10.1007/s40120-024-00704-8

N/A

0DataRank · unranked

1 citations

K. Rüdell, Naomi Suminski, Rinchen Doma, Maggie Heinrich, Linda Abetz‐Webb +14 more

A Core Pattern of Cerebellar and Brainstem Degeneration and Reduced Cerebrocerebellar Structural Covariance in Spinocerebellar Ataxia Type 3 (SCA3): MRI Volumetrics from ENIGMA-Ataxia

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.08.08.669370

N/A

0DataRank · unranked

1 citations

Isaac Adanyeguh, David J. Arpin, Tetsuo Ashizawa, Benjamin Bender, Fernando Cendes +39 more

Disease stage-specific atrophy markers in Alzheimer’s disease

medRxiv(2025)10.1101/2025.03.13.25323904

N/A

0DataRank · unranked

0 citations

Helena M. Gellersen, Sarah E. Polk, René Lattmann, Anika Wuestefeld, Laura E.M. Wisse +47 more

Neurodevelopmental effects of genetic frontotemporal dementia mutations revealed by total intracranial volume differences

Journal of Alzheimer s Disease(2025)10.1177/13872877251393414

N/A

0DataRank · unranked

0 citations

Arabella Bouzigues, Lucy L. Russell, Phoebe H. Foster, Eve Ferry‐Bolder, John C. van Swieten +37 more

Clinico‐Genetic, Imaging and Molecular Delineation of COQ8A‐Ataxia: A Multicenter Study of 59 Patients

Annals of Neurology(2020)10.1002/ana.25751

N/A

0DataRank · unranked

77 citations

Tommaso Schirinzi, Lucia Laugwitz, Nathan H. Murray, C.A. Bingman, Selina Reich +37 more

ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy

Annals of Neurology(2020)10.1002/ana.25723

N/A

0DataRank · unranked

53 citations

Stefania Magri, Andrea Legati, Valentina Del Dotto, Francesca Tagliavini, Francesca Balistreri +26 more

The genetic landscape of axonal neuropathies in the middle-aged and elderly

Neurology(2020)10.1212/wnl.0000000000011132

N/A

0DataRank · unranked

31 citations

Petra Laššuthová, Dagmara Kabzińska, Lisa Abreu, Jonathan Baets, Christian Beetz +52 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

Matthis Synofzik

Indexed papers

Top data-sharing exemplar

Papers