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Prospective Graduate Students / Postdocs
This faculty member is currently not looking for graduate students or Postdoctoral Fellows. Please do not contact the faculty member with any such requests.
Carles Vilarino-Guell
Assistant Professor
Research Classification
Research Interests
Genetic Diseases
multiple sclerosis
Neurological disorders
Neuromyelitis optica
Relevant Thesis-Based Degree Programs
Affiliations to Research Centres, Institutes & Clusters
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Research Methodology
Familial genetics
Population genetics
Next generation sequencing
Genotyping
Neuroscience
Publications
- (2022)
JAMA neurology, - (2021)
Parkinsonism & Related Disorders, - (2021)
Molecular Psychiatry, - (2021)
- (2020)
Brain Research Bulletin, 165, 63--69 - (2020)
Immunogenetics, 72 (6-7), 381--385 - (2020)
Neurology - Neuroimmunology Neuroinflammation, - (2020)
Neurology(R) neuroimmunology & neuroinflammation, - (2019)
The Pharmacogenomics Journal, 19 (6), 499--500 - (2019)
PLOS Genetics, - (2019)
PLoS biology, - (2019)
Unpublished, - (2019)
Frontiers in Neurology, - (2018)
Mol Neurobiol, - (2018)
Mult Scler, , 1352458518803789 - (2018)
Immunogenetics, - (2018)
J Neuroinflammation, 15 (1), 265 - (2018)
Neurol Genet, 4 (6), e285 - (2018)
J Gerontol A Biol Sci Med Sci, - (2017)
Human Genetics, - (2017)
Clinical Immunology, 180, 100--105 - (2017)
Brain, 140, 98-117 - (2017)
Neurol Genet, 3 (5), e195 - (2017)
Hum Mutat, - (2017)
Brain, - (2017)
Movement Disorders, 32 (2), 292-295 - (2016)
Journal of Neuroimmunology, 291, 70--72 - (2016)
G3: Genes, Genomes, Genetics, 6 (7), 2073-2079 - (2016)
Neuron, 92 (2), 339-341 - (2016)
The Lancet Neurology, 15 (12), 1248-1256 - (2016)
Brain, 139, 3163-3169 - (2016)
Neuron, 90 (5), 948-954 - (2015)
Journal of Human Genetics, 60 (8), 405-406 - (2015)
Annals of Neurology, 77 (3), 458-468 - (2015)
Movement Disorders, 30 (2), 273-278 - (2015)
European Journal of Neurology, 22 (9), 1323-1325 - (2015)
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 42 (4), 235-41 - (2015)
European Journal of Human Genetics, 23 (6), 887-888 - (2014)
Neurobiology of Aging, 35 (5), 1125-1131 - (2014)
Movement Disorders, 29 (9), 1201-1204 - (2014)
Journal of Neuroimmunology, 266 (1-2), 64-66 - (2014)
PLoS ONE, 9 (11) - (2014)
Movement Disorders, - (2014)
Hum Mol Genet, 23 (7), 1794-801 - (2014)
Parkinsonism and Related Disorders, 20 (6), 659-661 - (2014)
Neurogenetics, 15 (3), 165-169 - (2014)
European Journal of Neurology, 21 (2), 361-363 - (2014)
Multiple Sclerosis Journal, 20 (6), 766-767 - SLC1A2 rs3794087 does not associate with essential tremor (2014)
Neurobiology of Aging, 35 (4) - (2014)
Neurobiology of Aging, 35 (1) - (2014)
European Journal of Neurology, 21 (11), e91-e92 - (2013)
Movement Disorders, 28 (6), 811-813 - (2013)
European Journal of Neurology, 20 (9) - (2013)
Movement Disorders, 28 (12), 1740-1744 - (2013)
Acta Neuropathologica, 125 (3), 425-438 - (2013)
Parkinsonism and Related Disorders, 19 (5), 563-565 - (2012)
Journal of Medical Genetics, 49 (11), 721-726 - (2012)
Journal of Neurology, Neurosurgery and Psychiatry, 83 (4), 424-429 - (2012)
Parkinsonism and Related Disorders, 18 (4), 332-338 - Large-scale replication and heterogeneity in Parkinson disease genetic loci (2012)
Neurology, 79 (7), 659-667 - (2011)
Neurology, 76 (19), 1623-1630 - (2011)
Lancet Neurology, 10 (10), 898-908 - (2011)
European Journal of Neurology, 18 (8), 1090-1093 - (2011)
Movement Disorders, 26 (14), 2552-2556 - (2011)
PLoS Genetics, 7 (7) - (2011)
Parkinsonism and Related Disorders, 17 (1), 55-57 - (2011)
Annals of Neurology, 69 (5), 778-792 - (2011)
Neuropathology and Applied Neurobiology, 37 (7), 777-790 - (2011)
Parkinsonism & Related Disorders, 17 (8), 629-631 - (2011)
Neurology, 76 (7), 670-672 - (2011)
European Journal of Neurology, 18 (6), 876-881 - (2011)
American Journal of Human Genetics, 89 (3), 398-406 - (2011)
American Journal of Human Genetics, 89 (1), 162-167 - (2010)
Journal of Neurology, Neurosurgery and Psychiatry, 81 (4), 391-395 - (2010)
Neurology, 75 (24), 2248-2249 - (2010)
Annals of Neurology, 67 (3), 409-411 - (2010)
European Journal of Neurology, 17 (3), 483-486 - (2010)
Archives of Neurology, 67 (8), 970-975 - (2010)
European Journal of Neurology, 17 (2), 208-211 - (2010)
Movement Disorders, 25 (13), 2052-2058 - (2010)
Parkinsonism and Related Disorders, 16 (10), 686-687 - (2010)
Neuroscience Letters, 477 (2), 57-60 - (2010)
Mechanisms of Ageing and Development, 131 (3), 210-214 - (2010)
Parkinsonism and Related Disorders, 16 (2), 112-114 - (2010)
Neurogenetics, 11 (4), 401-408 - (2010)
Parkinsonism and Related Disorders, 16 (2), 109-111 - (2010)
Movement Disorders, 25 (12), 1973-1992 - (2010)
Neuroscience Letters, 486 (3), 228-230 - (2010)
Movement Disorders, 25 (13), 2156-2163 - (2010)
Annals of Neurology, 67 (3), 414-415 - (2009)
Parkinsonism and Related Disorders, 15 (9), 627-632 - (2009)
Movement Disorders, 24 (16), 2411-2414 - (2009)
Human Mutation, 30 (3), 406-410 - (2009)
Neurology, 72 (23), 2024-2028 - (2009)
Mayo Clinic Proceedings, 84 (2), 134-138 - (2009)
Nature Genetics, 41 (2), 163-165 - (2009)
Neuroscience Letters, 461 (2), 74-75 - (2009)
Neurology, 73 (3), 243-245 - (2009)
Movement Disorders, 24 (12), 1868-1869 - (2009)
Movement Disorders, 24 (4), 619-620 - (2008)
New England Journal of Medicine, 358 (4), 425-427 - (2008)
Journal of Neural Transmission, 115 (9), 1279-1284 - (2008)
Parkinsonism and Related Disorders, 14 (7), 544-547 - (2008)
Rheumatology, 47 (12), 1761-1767 - (2008)
Parkinsonism and Related Disorders, 14 (7), 539-543 - (2008)
Neurology, 71 (3), 222-223 - (2007)
Journal of Clinical Endocrinology and Metabolism, 92 (6), 2286-2291 - (2007)
Journal of Clinical Endocrinology and Metabolism, 92 (2), 641-647 - (2007)
Calcified Tissue International, 81 (4), 270-278 - (2007)
Calcified Tissue International, 81 (1), 1-9 - (2003)
Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 526 (1-2), 63-73 - (2000)
Genomics, 68 (2), 220-228 - Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension (2000)
Nature Genetics, 26 (1), 81-84
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