Publicaciones en las que colabora con José Augusto García-Agúndez Pérez-Coca (12)

2021

  1. Exome-wide rare variant analysis in familial essential tremor

    Parkinsonism and Related Disorders, Vol. 82, pp. 109-116

2017

  1. Delta-amino-levulinic acid dehydratase gene and essential tremor

    European Journal of Clinical Investigation, Vol. 47, Núm. 5, pp. 348-356

  2. Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

    Journal of Neural Transmission, Vol. 124, Núm. 3, pp. 285-291

2016

  1. A family study of DRD3 rs6280, SLC1A2 rs3794087 and MAPT rs1052553 variants in essential tremor

    Neurological Research, Vol. 38, Núm. 10, pp. 880-887

  2. Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis

    Scientific Reports, Vol. 6

2015

  1. Association between Vitamin D receptor rs731236 (Taq1) polymorphism and risk for restless legs syndrome in the Spanish caucasian population

    Medicine (United States), Vol. 94, Núm. 47, pp. e2125

  2. Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor

    Medicine, Vol. 94, Núm. 24, pp. e968

  3. Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome

    Medicine (United States), Vol. 94, Núm. 34, pp. e1448

  4. Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor

    Human Molecular Genetics, Vol. 24, Núm. 20, pp. 5677-5686

  5. TREM2 R47H variant and risk of essential tremor: A cross-sectional international multicenter study

    Parkinsonism and Related Disorders, Vol. 21, Núm. 3, pp. 306-309

2013

  1. Fused in sarcoma (FUS) gene mutations are not a frequent cause of essential tremor in europeans

    Neurobiology of Aging, Vol. 34, Núm. 10, pp. 2441.e9-2441.e11

  2. No association of the SLC1A2 rs3794087 allele with risk for essential tremor in the Spanish population

    Pharmacogenetics and Genomics, Vol. 23, Núm. 11, pp. 587-590