Tanya Stojkovic

11.3k citations

200 papers · 5.3k indexed · h-index 42

Neurology top 0.5%
- Peripheral Neuropathies and Disorders 30
Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases 48
- Hereditary Neurological Disorders 36
Pathology and Forensic Medicine top 1%
- Multiple Sclerosis Research Studies 22
Rheumatology top 1%
Genetics top 2%
- Neurogenetic and Muscular Disorders Research 15
Molecular Biology
- Muscle Physiology and Disorders 40
- Mitochondrial Function and Pathology 21
Cardiology and Cardiovascular Medicine
- Cardiomyopathy and Myosin Studies 29

Co-authors: Patrick Vermersch J. de Sèze D. Ferriby Pascal Laforêt Jean‐Pierre Pruvo Anthony Béhin S. Delalande Thierry Maisonobe
Cited by: Neurology Cellular and Molecular Neuroscience Pathology and Forensic Medicine
Partner nations: France United States United Kingdom

In The Last Decade

Tanya Stojkovic

193 papers receiving 5.1k citations

Peers

Countries citing papers authored by Tanya Stojkovic

Since Specialization

Citations

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

Fields of papers citing papers by Tanya Stojkovic

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Tanya Stojkovic, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Tanya Stojkovic Line = papers co-authored together Tanya Stojkovic links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	REGISTRE SMA FRANCE: A nationwide observational registry of patients with spinal muscular atrophy in France Lamiae Grimaldi‐Bensouda,Rocio García-Uzquiano,Marta Gómez‐García de la Banda,Amal Oulhissane-Omar,Céline Tard,Pascale Saugier-Véber,Vincent Laugel,I. Desguerre,Pascal Cintas,Carole Vuillerot,Frédérique Audic,Claude Cancés,Tanya Stojkovic,Jon Andoni Urtizberea,Shahram Attarian,Juliette Ropars,Susana Quijano‐Roy,(unknown)	2025	0
2	Comparative Analysis of CRISPR/Cas9-targeted Nanopore Sequencing Approaches in Repeat Expansion Disorders Louise Benarroch,Pierre‐Yves Boëlle,Hélène Madry,Badreddine Mohand Oumoussa,Nobuyuki Eura,Ichizo Nishino,Karim Labrèche,V. N. Gorbunova,Guillaume Bassez,Tanya Stojkovic,Geneviève Gourdon,Gisèle Bonne,Stéphanie Tomé	2025	0
3	Recurrent “outsider” intronic variation in the SLC5A6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb Lamisse Mansour‐Hendili,Cyril Gitiaux,Madeleine Harion,Céline Latouche,Bénédicte Héron,Tanya Stojkovic,Mélanie Rama,Thomas Smol,A.‐S. Jourdain,Karine Mention,Yann Nadjar,Manuel Schiff,Julie Lemale,Jamal Ghoumid,Frédèric Gottrand,Cécile Talbotec,Agnès Rötig,Benoît Funalot,Isabelle Desguerre	2024	1
4	Severe Respiratory and Swallowing Disorders in Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease Type 1 Édouard Berling,Philippe Latour,Klervie Loiselet,Clément Guémy,Léo Vidoni,Norma B. Romero,Emmanuelle Lacène,Teresinha Evangelista,Tanya Stojkovic	2024	0
5	Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort Édouard Berling,Camille Verebi,Nadia Venturelli,Stéphane Vassilopoulos,Anthony Béhin,Céline Tard,Maud Michaud,Rocío N. Villar‐Quiles,Savine Vicart,Marion Masingue,Robert‐Yves Carlier,Norma B. Romero,Emmanuelle Lacène,France Leturcq,B. Eymard,Pascal Laforêt,Tanya Stojkovic	2023	4
6	Clinical and electrophysiological characteristics of women with X‐linked Charcot–Marie–Tooth disease Luce Barbat du Closel,Nathalie Bonello‐Palot,Yann Péréon,Andoni Echaniz‐Laguna,Jean‐Philippe Camdessanché,Aleksandra Nadaj-Pakleza,Jean‐Baptiste Chanson,Simon Frachet,Laurent Magy,Julien Cassereau,Pascal Cintas,(unknown),Perrine Devic,Sarah Louis,Robinson Gravier Dumonceau,Émilien Delmont,Emmanuelle Salort‐Campana,Françoise Bouhour,Philippe Latour,Tanya Stojkovic,Shahram Attarian	2023	1
7	Expanding the phenotypic variability of MORC2 gene mutations: From Charcot‐Marie‐Tooth disease to late‐onset pure motor neuropathy Arnaud Jacquier,Shams Ribault,Michel Mendes,Nicolas Lacoste,Valérie Risson,Julien Carras,Philippe Latour,Aleksandra Nadaj‐Pakleza,Tanya Stojkovic,Laurent Schaeffer	2022	6
8	A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency Aurélien Perrin,Corinne Métay,Marcello Villanova,Robert‐Yves Carlier,Elena Pegoraro,Raúl Juntas‐Morales,Tanya Stojkovic,Isabelle Richard,Pascale Richard,Norma B. Romero,Henk Granzier,M. Kœnig,Edoardo Malfatti,Mireille Cossée	2020	9
9	Assessment of diaphragm motion using ultrasonography in a patient with facio-scapulo-humeral dystrophy Abdallah Fayssoil,Tanya Stojkovic,Adam Ogna,Pascal Laforêt,Hélène Prigent,Frédéric Lofaso,David Orlikowski,Guillaume Bassez,B. Eymard,Anthony Béhin	2019	3
10	Molecular diagnosis of inherited peripheral neuropathies by targeted next-generation sequencing: molecular spectrum delineation Juliette Bacquet,Tanya Stojkovic,Amandine Boyer,Nathalie Martini,Frédérique Audic,B. Chabrol,Emmanuelle Salort‐Campana,Émilien Delmont,Jean‐Pierre Desvignes,Annie Verschueren,Shahram Attarian,Annabelle Chaussenot,Valérie Delague,Nicolas Lévy,Nathalie Bonello‐Palot	2018	40
11	Cryptic amyloidogenic elements in mutant NEFH causing Charcot-Marie-Tooth 2 trigger aggresome formation and neuronal death Arnaud Jacquier,Cécile Delorme,Edwige Belotti,Raoul Juntas-Morales,Guilhem Solé,O. Dubourg,Marianne Giroux,Claude-Alain Maurage,Valérie Castellani,Adriana Rebelo,Alexander J. Abrams,Stephan Züchner,Tanya Stojkovic,Laurent Schaeffer,Philippe Latour	2017	18
12	216th ENMC international workshop: Clinical readiness in FKRP related myopathies January 15–17, 2016 Naarden, The Netherlands Isabelle Richard,Jean‐Pierre Laurent,Sebahattin Çirak,John Vissing,S. Brown,Kevin P. Campbell,Evelyne Gicquel,Jean‐Yves Hogrel,Géraldine Honnet,Nynke Koelma,Jean‐Pierre Laurent,Katherine D. Mathews,Francesco Muntoni,Susana Quijano‐Roy,Agata Robertson,Herb Stevenson,Tanya Stojkovic,Volker Straub,Haluk Topaloğlu,Jiri Vajsar,Maggie C. Walter	2016	13
13	Respiratory muscle dysfunction in facioscapulohumeral muscular dystrophy Dante Brasil Santos,Ghilas Boussaïd,Tanya Stojkovic,David Orlikowski,Nadège Letilly,Anthony Béhin,Sandrine Butel,Frédéric Lofaso,Hélène Prigent	2015	19
14	Neutral lipid storage disease with myopathy: A whole-body nuclear MRI and metabolic study Pascal Laforêt,Tanya Stojkovic,Guillaume Bassez,Pierre G. Carlier,Karine Clément,Karim Wahbi,François Petit,B. Eymard,Robert‐Yves Carlier	2012	26
15	Permanent muscle weakness in MCArdle disease Aleksandra Nadaj‐Pakleza,C. Vincitorio,Pascal Laforêt,B. Eymard,Élisabeth Dion,Susana Teijeira,Irene Vietez,Marc Jeanpierre,Carmen Navarro,Tanya Stojkovic	2009	46
16	Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study Kristl G. Claeys,Peter F. M. van der Ven,Anthony Béhin,Tanya Stojkovic,B. Eymard,O. Dubourg,Pascal Laforêt,Georgine Faulkner,Pascale Richard,Patrick Vicart,Norma B. Romero,G. Stoltenburg,Bjarne Udd,Michel Fardeau,Thomas Voït,Dieter O. Fürst	2009	54
17	Patients with Familial Partial Lipodystrophy of the Dunnigan Type Due to aLMNAR482W Mutation Show Muscular and Cardiac Abnormalities Marie‐Christine Vantyghem,P. Pigny,C. A. Maurage,Nathalie Rouaix‐Emery,Tanya Stojkovic,Jean‐Marie Cuisset,A Millaire,Olivier Lascols,Patrick Vermersch,Jean-Louis Wémeau,Jacqueline Capeau,Corinne Vigouroux	2004	93
18	Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene Tanya Stojkovic,Philippe Latour,Ghislaine Viet,J. de Sèze,Jean‐François Hurtevent,Antoon Vandenberghe,Patrick Vermersch	2004	34
19	Autonomic and respiratory dysfunction in Charcot–Marie–Tooth disease due to Thr124Met mutation in the myelin protein zero gene Tanya Stojkovic,J. de Sèze,Olivier Dubourg,Marie‐Christine Arné‐Bes,Sandrine Tardieu,J C Hache,Patrick Vermersch	2003	31
20	Phrenic nerve palsy as a feature of chronic inflammatory demyelinating polyradiculoneuropathy Tanya Stojkovic,J. de Sèze,Jean‐François Hurtevent,François Fourrier,Patrick Vermersch	2003	21

About Tanya Stojkovic

Tanya Stojkovic is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 200 papers that have together received 5.3k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (48 papers), Muscle Physiology and Disorders (40 papers), Hereditary Neurological Disorders (36 papers), Peripheral Neuropathies and Disorders (30 papers), Cardiomyopathy and Myosin Studies (29 papers), Multiple Sclerosis Research Studies (22 papers), Mitochondrial Function and Pathology (21 papers) and Neurogenetic and Muscular Disorders Research (15 papers). The work is most often cited by research in Neurology (1.7k citations), Cellular and Molecular Neuroscience (1.5k citations) and Pathology and Forensic Medicine (1.0k citations). Tanya Stojkovic has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Patrick Vermersch, J. de Sèze, D. Ferriby, Pascal Laforêt, Jean‐Pierre Pruvo, Anthony Béhin, S. Delalande, Thierry Maisonobe, B. Eymard and Karim Wahbi.

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.

Explore authors with similar magnitude of impact