Rebecca Schüle

Also affiliated with University Hospital Heidelberg

NeuroscienceMedicine

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 100%percentile

0Author DataRank

Indexed papers

1in 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 1 indexed paper 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 →

Papers

Driven by 20 papers. Top paper: “BiP inactivation due to loss of the deAMPylation function of FICD causes a motor neuron disease”.

BiP inactivation due to loss of the deAMPylation function of FICD causes a motor neuron disease

Genetics in Medicine(2022)10.1016/j.gim.2022.08.019

N/A

1.0DataRank · unranked

30 citations

Ariel Ruiz, Maike F. Dohrn, Melanie Wayand, Amjad Farooq, Matt C. Danzi +14 more

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

New England Journal of Medicine(2022)10.1056/nejmoa2207406

N/A

0.831DataRank · unranked

253 citations

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

Do Not Trust the Pedigree: Reduced and Sex-Dependent Penetrance at a Novel Mutation Hotspot in ATL1 Blurs Autosomal Dominant Inheritance of Spastic Paraplegia

Human Mutation(2013)10.1002/humu.22309

N/A

0.489DataRank · unranked

25 citations

Rebecca Schüle, Hicham Fadel, Irene Valenzuela, Fiorella Speziani, Michael Gonzalez +11 more

Early‐Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST

Movement Disorders(2022)10.1002/mds.29225

N/A

0.464DataRank · unranked

21 citations

Afshin Saffari, Melanie Kellner, Marion Döbler‐Neumann, Catherine Jordan, Siddharth Srivastava +13 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

0.345DataRank · unranked

9 citations

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

0.165DataRank · unranked

2 citations

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

Serum Neurofilament Light Chain and Glial Fibrillary Acidic Protein as Biomarkers in Primary Progressive Multiple Sclerosis and Hereditary Spastic Paraplegia Type 4

International Journal of Molecular Sciences(2022)10.3390/ijms232113466

N/A

0DataRank · unranked

9 citations

Christoph Ruschil, Ahmed Abdelhak, Carlo Wilke, Aleksandra Maleska, Jens Kühle +4 more

The kinesin motor KIF1C is a putative transporter of the exon junction complex in neuronal cells

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.08.24.505074

N/A

0DataRank · unranked

1 citations

Marvin Noß, Jishu Xu, Nicola Horn, Marius Ueffing, Karsten Boldt +2 more

Loss of Fic causes progressive neurodegeneration in a Drosophila model of hereditary spastic paraplegia

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease(2024)10.1016/j.bbadis.2024.167348

N/A

0DataRank · unranked

10 citations

Natalie Ortiz-Vega, Tijana Canic, Xianzun Tao, Nika Bucan, Kai Ruan +6 more

Unraveling Axonal Transcriptional Landscapes: Insights from iPSC-Derived Cortical Neurons and Implications for Motor Neuron Degeneration

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.26.586780

N/A

0DataRank · unranked

3 citations

Michaela Hörner, Maike Nagel, Perwin Perhat, Milena Korneck, Marvin Noß +6 more

Long-read RNA-sequencing reveals transcript-specific regulation in human-derived cortical neurons

Open Biology(2025)10.1098/rsob.250200

N/A

0DataRank · unranked

4 citations

Michaela Hörner, Elena Buena‐Atienza, Kalaivani Manibarathi, Maike Nagel, Stefan Hauser +5 more

Serum NfL, but not GFAP, differentiates primary lateral sclerosis from adrenomyeloneuropathy and hereditary spastic paraplegia type 4

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration(2025)10.1080/21678421.2025.2557936

N/A

0DataRank · unranked

0 citations

Carlo Wilke, Holger Hengel, Tim W. Rattay, Aleksandra Maleska Maceski, Jens Kühle +3 more

The kinesin motor KIF1C is a putative transporter of the exon junction complex in neuronal cells

RNA(2022)10.1261/rna.079426.122

N/A

0DataRank · unranked

13 citations

Marvin Noß, Jishu Xu, Nicola Horn, Marius Ueffing, Karsten Boldt +2 more

Confirmation of TACO1 as a Leigh Syndrome Disease Gene in Two Additional Families

Journal of Neuromuscular Diseases(2020)10.3233/jnd-200510

N/A

0DataRank · unranked

19 citations

Serdal Güngör, Lena Zeltner, Sarah Wiethoff, Lüdger Schöls, Ece Sönmezler +16 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

Generation of the CRISPR/Cas9-mediated KIF1C knock-out human iPSC line HIHRSi003-A-1

Stem Cell Research(2020)10.1016/j.scr.2020.102059

N/A

0DataRank · unranked

7 citations

Sandra Müßig, Philip Höflinger, Lüdger Schöls, Stefan Hauser, Rebecca Schüle +1 more

Neurofilament light chain is a cerebrospinal fluid biomarker in hereditary spastic paraplegia

Annals of Clinical and Translational Neurology(2021)10.1002/acn3.51358

N/A

0DataRank · unranked

18 citations

Lina María Serna-Higuita, Tim W. Rattay, Walter Maetzler, Isabel Wurster, Stefanie N. Hayer +8 more

The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15

Brain(2022)10.1093/brain/awac391

N/A

0DataRank · unranked

24 citations

Melanie Kellner, Catherine Jordan, Helena Rosengarten, Alisa Mo, Bo Zhang +29 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