Tania Fuchs

1.7k total citations
18 papers, 1.1k citations indexed

About

Tania Fuchs is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Tania Fuchs has authored 18 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Neurology, 12 papers in Cellular and Molecular Neuroscience and 4 papers in Molecular Biology. Recurrent topics in Tania Fuchs's work include Neurological disorders and treatments (13 papers), Genetic Neurodegenerative Diseases (8 papers) and Parkinson's Disease Mechanisms and Treatments (7 papers). Tania Fuchs is often cited by papers focused on Neurological disorders and treatments (13 papers), Genetic Neurodegenerative Diseases (8 papers) and Parkinson's Disease Mechanisms and Treatments (7 papers). Tania Fuchs collaborates with scholars based in United States, Israel and Germany. Tania Fuchs's co-authors include Laurie J. Ozelius, Susan Bressman, Rachel Saunders‐Pullman, Deborah Raymond, Michelle E. Ehrlich, Sophie Gavarini, Doron Lancet, Gary A. Heiman, Marta San Luciano and Nutan Sharma and has published in prestigious journals such as Nature Genetics, Annals of Neurology and The Lancet Neurology.

In The Last Decade

Tania Fuchs

18 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tania Fuchs United States	16	718	659	297	157	121	18	1.1k
Yaroslav Tsytsyura Germany	12	129 0.2×	319 0.5×	701 2.4×	46 0.3×	85 0.7×	20	1.0k
D.L. Browne United States	16	200 0.3×	575 0.9×	977 3.3×	250 1.6×	25 0.2×	31	1.3k
Richard Pellegrino United States	11	61 0.1×	331 0.5×	400 1.3×	36 0.2×	324 2.7×	21	889
Jennifer Spaethling United States	12	124 0.2×	320 0.5×	464 1.6×	69 0.4×	16 0.1×	12	847
Véronique Pellier‐Monnin France	12	71 0.1×	298 0.5×	283 1.0×	42 0.3×	124 1.0×	18	670
Zhigao Long China	14	77 0.1×	174 0.3×	358 1.2×	206 1.3×	52 0.4×	42	673
Kazuho Hirata Japan	16	70 0.1×	356 0.5×	214 0.7×	17 0.1×	47 0.4×	32	674
Gabriela Sekerková Slovakia	6	53 0.1×	186 0.3×	278 0.9×	44 0.3×	198 1.6×	9	581
Noam D. Rudnick United States	9	154 0.2×	129 0.2×	443 1.5×	116 0.7×	21 0.2×	16	764

Countries citing papers authored by Tania Fuchs

Since Specialization

Citations

This map shows the geographic impact of Tania Fuchs'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 Tania Fuchs with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tania Fuchs more than expected).

Fields of papers citing papers by Tania Fuchs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tania Fuchs. 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 Tania Fuchs. The network helps show where Tania Fuchs may publish in the future.

Co-authorship network of co-authors of Tania Fuchs

This figure shows the co-authorship network connecting the top 25 collaborators of Tania Fuchs. A scholar is included among the top collaborators of Tania Fuchs 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 Tania Fuchs. Tania Fuchs is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

Gusmão, Claudio M. de, Tania Fuchs, Trisha Multhaupt‐Buell, et al.. (2016). Dystonia‐Causing Mutations as a Contribution to the Etiology of Spasmodic Dysphonia. Otolaryngology. 155(4). 624–628. 9 indexed citations

Putzel, Gregory, Tania Fuchs, Giovanni Battistella, et al.. (2016). GNAL mutation in isolated laryngeal dystonia. Movement Disorders. 31(5). 750–755. 17 indexed citations

Ruiz, Marta, Maitane Ortiz‐Virumbrales, Aurélie Méneret, et al.. (2015). Abnormalities of motor function, transcription and cerebellar structure in mouse models ofTHAP1dystonia. Human Molecular Genetics. 24(25). 7159–7170. 44 indexed citations

Saunders‐Pullman, Rachel, Tania Fuchs, Marta San Luciano, et al.. (2014). Heterogeneity in primary dystonia: Lessons from THAP1, GNAL, and TOR1A in Amish‐Mennonites. Movement Disorders. 29(6). 812–818. 27 indexed citations

Fuchs, Tania & Laurie J. Ozelius. (2013). Genetics in Dystonia: An Update. Current Neurology and Neuroscience Reports. 13(12). 410–410. 9 indexed citations

Fuchs, Tania, Rachel Saunders‐Pullman, Ikuo Masuho, et al.. (2012). Mutations in GNAL cause primary torsion dystonia. Nature Genetics. 45(1). 88–92. 207 indexed citations

Panov, Fedor, Michele Tagliati, Laurie J. Ozelius, et al.. (2011). Pallidal deep brain stimulation for DYT6 dystonia. Journal of Neurology Neurosurgery & Psychiatry. 83(2). 182–187. 60 indexed citations

Fuchs, Tania & Laurie J. Ozelius. (2011). Genetics of Dystonia. Seminars in Neurology. 31(5). 441–448. 17 indexed citations

Gavarini, Sophie, Corinne Cayrol, Tania Fuchs, et al.. (2010). Direct interaction between causative genes of DYT1 and DYT6 primary dystonia. Annals of Neurology. 68(4). 549–553. 59 indexed citations

10.

Aguiar, Patrícia de Carvalho, Tania Fuchs, Vanderci Borges, et al.. (2010). Screening of Brazilian families with primary dystonia reveals a novel THAP1 mutation and a de novo TOR1A GAG deletion. Movement Disorders. 25(16). 2854–2857. 15 indexed citations

11.

Sharma, Nutan, Ramon A. Franco, John K. Kuster, et al.. (2010). Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia. Movement Disorders. 25(13). 2183–2187. 24 indexed citations

12.

Bressman, Susan, Deborah Raymond, Tania Fuchs, et al.. (2009). Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study. The Lancet Neurology. 8(5). 441–446. 119 indexed citations

13.

Fuchs, Tania, Sophie Gavarini, Rachel Saunders‐Pullman, et al.. (2009). Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia. Nature Genetics. 41(3). 286–288. 207 indexed citations

14.

Djarmati, Ana, Susanne A. Schneider, Katja Lohmann, et al.. (2009). Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study. The Lancet Neurology. 8(5). 447–452. 94 indexed citations

15.

Olender, Tsviya, Tania Fuchs, Chaim Linhart, et al.. (2003). The canine olfactory subgenome. Genomics. 83(3). 361–372. 89 indexed citations

16.

Fuchs, Tania, Barbora Malecová, Chaim Linhart, et al.. (2002). DEFOG: A Practical Scheme for Deciphering Families of Genes. Genomics. 80(3). 295–302. 18 indexed citations

17.

Fuchs, Tania, Gustavo Glusman, Shirley Horn‐Saban, Doron Lancet, & Yitzhak Pilpel. (2001). The human olfactory subgenome: from sequence to structure and evolution. Human Genetics. 108(1). 1–13. 55 indexed citations

18.

Dantes, Ada, et al.. (1996). Removal of proteasomes from the nucleus and their accumulation in apoptotic blebs during programmed cell death. FEBS Letters. 394(1). 47–50. 47 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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