Publicacións en colaboración con investigadores/as de Universidade de Santiago de Compostela (22)

2020

  1. Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36)

    Cerebellum, Vol. 19, Núm. 4, pp. 501-509

2017

  1. PET and MRI detection of early and progressive neurodegeneration in spinocerebellar ataxia type 36

    Movement Disorders, Vol. 32, Núm. 2, pp. 264-273

2016

  1. Synaptotagmin XI in Parkinson's disease: New evidence from an association study in Spain and Mexico

    Journal of the Neurological Sciences, Vol. 362, pp. 321-325

2015

  1. Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

    Nature Genetics, Vol. 47, Núm. 6, pp. 579-581

  2. No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 168, Núm. 1, pp. 54-65

2014

  1. Medical genomics: The intricate path from genetic variant identification to clinical interpretation

    Applied and Translational Genomics, Vol. 3, Núm. 3, pp. 60-67

2012

  1. 'Costa da Morte' ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization

    Brain, Vol. 135, Núm. 5, pp. 1423-1435

  2. Revisiting genotype-phenotype overlap in neurogenetics: Triplet-repeat expansions mimicking spastic paraplegias

    Human Mutation, Vol. 33, Núm. 9, pp. 1315-1323

2011

  1. A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy

    Neuromuscular Disorders, Vol. 21, Núm. 4, pp. 254-262

  2. sesoramiento genético en Neurología: un problema complejo que necesita regulación

    Neurologia, Vol. 26, Núm. 3, pp. 129-136

2009

  1. New population and phylogenetic features of the internal variation within mitochondrial DNA macro-haplogroup R0

    PLoS ONE, Vol. 4, Núm. 4

2005

  1. SNaPshot typing of mitochondrial DNA coding region variants.

    Methods in molecular biology (Clifton, N.J.), Vol. 297, pp. 197-208

2004

  1. A new rare mutation (691delCC/insAAA) in exon 17 of the PYGM gene causing McArdle disease

    Archives of Neurology, Vol. 61, Núm. 7, pp. 1108-1110

  2. Micro-geographical differentiation in Northern Iberia revealed by Y-chromosomal DNA analysis

    Gene, Vol. 329, Núm. 1-2, pp. 17-25

  3. Microgeographic substructure of NW Iberian Y chromosome STR haplotypes

    International Congress Series, Vol. 1261, Núm. C, pp. 296-298

  4. Typing mtDNA SNPs of forensic and population interest with snapshot

    International Congress Series, Vol. 1261, Núm. C, pp. 419-421

  5. Typing of mitochondrial DNA coding region SNPs of forensic and anthropological interest using SNaPshot minisequencing

    Forensic Science International, Vol. 140, Núm. 2-3, pp. 251-257

2003

  1. Microgeographic patterns of highly informative Y-chromosome haplotypes (using biallelic markers and STRs) in Galicia (NW Spain): Forensic and anthropological implications

    International Congress Series, Vol. 1239, Núm. C, pp. 61-66

  2. Population data of Galicia (NW Spain) on the new Y-STRs DYS437, DYS438, DYS439, GATA A10, GATA A7.1, GATA A7.2, GATA C4 and GATA H4

    Forensic Science International, Vol. 131, Núm. 2-3, pp. 220-224

  3. Results of the GEP-ISFG collaborative study on the Y chromosome STRs GATA A10, GATA C4, GATA H4, DYS437, DYS438, DYS439, DYS460 and DYS461: Population data

    Forensic Science International, Vol. 135, Núm. 2, pp. 150-157