Andreas Roos

Also affiliated with BG University Hospital Bergmannsheil Bochum, University of Duisburg-Essen

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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

4in 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 4 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 →

Papers

Driven by 14 papers. Top paper: “NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and mice”.

NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and mice

Brain(2022)10.1093/brain/awac055

N/A

0.553DataRank · unranked

39 citations

Leen Vendredy, Emily L. Spaulding, Marina Stavrou, Denisa Hathazi, Anika Grüneboom +12 more

Mitochondrial damage is associated with an early immune response in inclusion body myositis

Brain(2025)10.1093/brain/awaf118

N/A

0.538DataRank · unranked

17 citations

Emily S. Cross, Daniel Lagos, Sara Walli, Benedikt Schoser, Andreas Hentschel +17 more

Brain malformations and seizures by impaired chaperonin function of TRiC

Science(2024)10.1126/science.adp8721

N/A

0.489DataRank · unranked

25 citations

Piere Rodriguez-Aliaga, Weimin Yuan, Lena Franken, Kamil K. Zajt, Dimah Hasan +82 more

Serum miRNAs as biomarkers for the rare types of muscular dystrophy

Neuromuscular Disorders(2022)10.1016/j.nmd.2022.03.003

N/A

0.425DataRank · unranked

16 citations

Demetris Koutalianos, Kristia Georgiou, Andrea C. Kakouri, Anastasis Oulas, Marios Tomazou +10 more

Modulation of the Acetylcholine Receptor Clustering Pathway Improves Neuromuscular Junction Structure and Muscle Strength in a Mouse Model of Congenital Myasthenic Syndrome

Frontiers in Molecular Neuroscience(2020)10.3389/fnmol.2020.594220

N/A

0.416DataRank · unranked

15 citations

Rachel Howarth, Grace McMacken, Tracey Davey, Kaitlyn Quinlan, Emily O’Connor +7 more

Weight loss with GLP-1 medicines does not result in a disproportionate loss of muscle mass or function in obese mice and humans

Cell Reports Medicine(2026)10.1016/j.xcrm.2026.102665

N/A

0.330DataRank · unranked

8 citations

Natalie K. Gilmore, Christopher M.T. Hayden, Julien Roux, Bruno Bariohay, Thaïs Rouquet +17 more

Giant axonal neuropathy (GAN): cross-sectional data on phenotypes, genotypes, and proteomic signature from a German cohort

Journal of Neurology(2025)10.1007/s00415-024-12744-z

N/A

0.241DataRank · unranked

4 citations

Guido Goj, Silke Polz, Adela Della Marina, Andreas Hentschel, Katja Ahlbory +14 more

Galactose treatment rescues neuromuscular junction transmission in glutamine-fructose-6-phosphate transaminase 1 (Gfpt1) deficient mice

Human Molecular Genetics(2025)10.1093/hmg/ddaf140

N/A

0.208DataRank · unranked

3 citations

Ricardo Carmona-Martinez, Daniel O’Neil, Kelly Ho, Kaela O’Connor, Yoshiteru Azuma +4 more

Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis

Nature Medicine(2021)10.1038/s41591-021-01346-1

N/A

0DataRank · unranked

153 citations

Sandra Donkervoort, Museer A. Lone, Matthew Nalls, Kenneth Gable, Sita D. Gupta +41 more

Cardiovascular Risk Across Myocardial Injury and Infarction Categories Using the Universal Definition

Journal of the American College of Cardiology(2025)10.1016/j.jacc.2025.11.043

N/A

0DataRank · unranked

2 citations

Pedro López‐Ayala, Alexander J F Thurston, Kuan Ken Lee, Yong Yong Tew, Dimitrios Doudesis +78 more

Molecular pathophysiology of human MICU1 deficiency

Neuropathology and Applied Neurobiology(2021)10.1111/nan.12694

N/A

0DataRank · unranked

33 citations

Miriam Elbracht, Artur Czech, Martin Häusler, Vietxuan Phan, Ana Töpf +13 more

TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy

European Journal of Human Genetics(2020)10.1038/s41431-019-0563-6

N/A

0DataRank · unranked

41 citations

Pietro Spitali, Irina Zaharieva, Stefan Böhringer, Monika Hiller, Amina Chaouch +19 more

Dysregulation of FLVCR1a-dependent mitochondrial calcium handling in neural progenitors causes congenital hydrocephalus

Cell Reports Medicine(2024)10.1016/j.xcrm.2024.101647

N/A

0DataRank · unranked

7 citations

Dibyanti Mukherjee, Massimo Bonora, Christoph P. Bagowski, Jeannette Nardelli, Livia Metani +34 more

A Deficiency in Glutamine-Fructose-6-Phosphate Transaminase 1 (Gfpt1) in Skeletal Muscle Results in Reduced Glycosylation of the Delta Subunit of the Nicotinic Acetylcholine Receptor (AChRδ)

Biomolecules(2024)10.3390/biom14101252

N/A

0DataRank · unranked

7 citations

Ricardo Carmona-Martinez, Kaela O’Connor, Daniel O’Neil, Andreas Roos, Sally Spendiff +2 more