Andreas Roos

479 total citations
9 papers, 77 citations indexed

About

Andreas Roos is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Andreas Roos has authored 9 papers receiving a total of 77 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Cell Biology and 4 papers in Genetics. Recurrent topics in Andreas Roos's work include Cellular transport and secretion (3 papers), Myasthenia Gravis and Thymoma (2 papers) and RNA regulation and disease (2 papers). Andreas Roos is often cited by papers focused on Cellular transport and secretion (3 papers), Myasthenia Gravis and Thymoma (2 papers) and RNA regulation and disease (2 papers). Andreas Roos collaborates with scholars based in Germany, Canada and United Kingdom. Andreas Roos's co-authors include Ulrike Schara‐Schmidt, Andreas Hentschel, Albert Sickmann, Hanns Lochmüller, Ute Münchberg, Erik Freier, Jens Reimann, Angela Abicht, Adela Della Marina and Andrea Gangfuß and has published in prestigious journals such as Human Molecular Genetics, Frontiers in Human Neuroscience and Human Mutation.

In The Last Decade

Andreas Roos

9 papers receiving 75 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Andreas Roos Germany	6	46	27	20	18	11	9	77
Andrea Gangfuß Germany	6	51 1.1×	14 0.5×	19 0.9×	12 0.7×	14 1.3×	23	84
İbrahim Öncel Türkiye	7	87 1.9×	20 0.7×	27 1.4×	18 1.0×	30 2.7×	23	153
Raoul F. V. Germano Belgium	3	76 1.7×	26 1.0×	10 0.5×	4 0.2×	12 1.1×	4	115
Julie Steffann France	8	100 2.2×	18 0.7×	6 0.3×	26 1.4×	13 1.2×	22	142
Willem De Ridder Belgium	6	32 0.7×	11 0.4×	12 0.6×	7 0.4×	18 1.6×	16	68
Karen Gaudon France	3	30 0.7×	34 1.3×	67 3.4×	13 0.7×	6 0.5×	6	88
Rawan Almass Saudi Arabia	7	77 1.7×	23 0.9×	9 0.5×	24 1.3×	16 1.5×	14	102
Lucile Pinson France	6	68 1.5×	14 0.5×	32 1.6×	34 1.9×	22 2.0×	8	116
Cristiane Araújo Martins Moreno Brazil	9	73 1.6×	43 1.6×	48 2.4×	14 0.8×	23 2.1×	28	143
Mai Thao Bui France	5	59 1.3×	47 1.7×	8 0.4×	8 0.4×	23 2.1×	10	108

Countries citing papers authored by Andreas Roos

Since Specialization

Citations

This map shows the geographic impact of Andreas Roos's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Andreas Roos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Roos more than expected).

Fields of papers citing papers by Andreas Roos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andreas Roos. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Andreas Roos. The network helps show where Andreas Roos may publish in the future.

Co-authorship network of co-authors of Andreas Roos

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Roos. A scholar is included among the top collaborators of Andreas Roos based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Andreas Roos. Andreas Roos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

Gangfuß, Andrea, Tomás Ferreira, Andreas Hentschel, et al.. (2024). A Homozygous NDUFS6 Variant Associated with Neuropathy and Optic Atrophy. Journal of Neuromuscular Diseases. 11(2). 485–491. 3 indexed citations

Hentschel, Andreas, Nancy Meyer, Nicolai Kohlschmidt, et al.. (2023). A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function. Molecular Neurobiology. 60(5). 2602–2618. 5 indexed citations

Kohlschmidt, Nicolai, Andreas Hentschel, Enrika Bartels, et al.. (2022). Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects. Orphanet Journal of Rare Diseases. 17(1). 29–29. 5 indexed citations

Gangfuß, Andrea, Andreas Hentschel, Albert Sickmann, et al.. (2022). Identification of a novel homozygous synthesis of cytochrome c oxidase 2 variant in siblings with early‐onset axonal Charcot‐Marie‐Tooth disease. Human Mutation. 43(4). 477–486. 7 indexed citations

Gangfuß, Andrea, Gökhan Yigit, Janine Altmüller, et al.. (2021). Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal study. American Journal of Medical Genetics Part A. 185(4). 1216–1221. 5 indexed citations

Gangfuß, Andrea, Petra Stöbe, Tobias B. Haack, et al.. (2021). Expansion of the mutational spectrum of BMPER leading to diaphanospondylodysostosis and description of the associated disease process. Molecular Genetics & Genomic Medicine. 9(12). e1767–e1767. 2 indexed citations

Hentschel, Andreas, Ute Münchberg, Erik Freier, et al.. (2021). Protein signature of human skin fibroblasts allows the study of the molecular etiology of rare neurological diseases. Orphanet Journal of Rare Diseases. 16(1). 73–73. 24 indexed citations

Marina, Adela Della, Angela Abicht, Heike Kölbel, et al.. (2020). Long Term Follow-Up on Pediatric Cases With Congenital Myasthenic Syndromes—A Retrospective Single Centre Cohort Study. Frontiers in Human Neuroscience. 14. 560860–560860. 13 indexed citations

Cordts, Isabell, et al.. (2018). MYO9A deficiency in motor neurons is associated with reduced neuromuscular agrin secretion. Human Molecular Genetics. 27(8). 1434–1446. 13 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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