Ignacio Rubio‐Agusti

Author

University College London

Also Known As

Ignacio Rubio-Agusti, Ignacio Rubio-Agustí, Ignacio Rubio‐Agusti, Ignacio Rubio‐Agustí

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

University College London Hospital Universitari i Politècnic La Fe National Hospital for Neurology and Neurosurgery University of Ljubljana Sobell House

About

Ignacio Rubio‐Agusti is an author at University College London specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	277
2	Neurology	3	3	102
3	Health Sciences	2	2	248
4	Diabetes	1	1	73
5	Kinesiology	1	1	175

Ignacio Rubio‐Agusti

Publications

Citations

H-Index

Page 1

	Year	Citations
Mutations in ANO3 Cause Dominant Craniocervical Dystonia: Ion Channel Implicated in Pathogenesis Gavin Charlesworth, Vincent Plagnol, Kira M. Holmström, The American Journal of Human Genetics	2012	254
Physical precipitating factors in functional movement disorders Isabel Pareés, Maja Kojović, Carolina Pires, Journal of the Neurological Sciences Physical Precipitating FactorsPhysical ActivityKinesiologyMotor ControlRehabilitation	2014	175
A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia Niccolò E. Mencacci, Ignacio Rubio‐Agusti, Anselm A. Zdebik, The American Journal of Human Genetics	2015	139
The phenotypic spectrum of DYT24 due to ANO3 mutations María Stamelou, Gavin Charlesworth, Carla Cordivari, Movement Disorders	2014	111
Transcranial magnetic stimulation follow‐up study in early Parkinson's disease: A decline in compensation with disease progression? Maja Kojović, Panagiotis Kassavetis, Matteo Bologna, Movement Disorders	2015	76
Movement Disorders in Adult Patients With Classical Galactosemia Ignacio Rubio‐Agusti, Miryam Carecchio, Kailash P. Bhatia, Movement Disorders Electrolyte DisorderMotor DysfunctionMetabolic DisorderProgressive WorseningPhysiology	2013	73
Functional (psychogenic) symptoms in Parkinson's disease Isabel Pareés, Tabish A. Saifee, Maja Kojović, Movement Disorders	2013	69
The syndrome of deafness‐dystonia: Clinical and genetic heterogeneity Maja Kojović, Isabel Pareés, Tânia Lampreia, Movement Disorders	2013	31
Expanding the Phenotype and Genetic Defects Associated with the <i> <scp>GOSR</scp> 2 </i> Gene Roman Praschberger, Bettina Balint, Niccolò E. Mencacci, Movement Disorders Clinical Practice	2015	23
Lack of validation of variants associated with cervical dystonia risk: A GWAS replication study Pilar Gómez‐Garre, Ismael Huertas‐Fernández, María Teresa Cáceres‐Redondo, Movement Disorders	2014	18

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