Research center
Fundación Pública Galega de Medicina Xenómica
Publications (72) Publications in which a researcher has participated
2012
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'Costa da Morte' ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization
Brain, Vol. 135, Núm. 5, pp. 1423-1435
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A method for the analysis of 32 X chromosome insertion deletion polymorphisms in a single PCR
International Journal of Legal Medicine, Vol. 126, Núm. 1, pp. 97-105
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A missense mutation in PKD1 attenuates the severity of renal disease
Kidney International, Vol. 81, Núm. 4, pp. 412-417
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A new SNP assay for identification of highly degraded human DNA
Forensic Science International: Genetics, Vol. 6, Núm. 3, pp. 341-349
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Activity of β2-adrenergic receptor in oral squamous cell carcinoma is mediated by overexpression of the ADRBK2 gene: A pilot study
Biotechnic and Histochemistry, Vol. 87, Núm. 3, pp. 179-186
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Actualización en la base genética de las distonías
Revista española de trastornos del movimiento, Vol. 4, Núm. 4, pp. 22-32
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Allele frequencies of 20 STRs from Northwest Spain (Galicia)
Forensic Science International: Genetics
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Analysis of a claimed distant relationship in a deficient pedigree using high density SNP data
Forensic Science International: Genetics, Vol. 6, Núm. 3, pp. 350-353
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Analysis of the SNPforID 52-plex markers in four native American populations from Venezuela
Forensic Science International: Genetics, Vol. 6, Núm. 5
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Association of a XRCC3 polymorphism and rectum mean dose with the risk of acute radio-induced gastrointestinal toxicity in prostate cancer patients
Radiotherapy and Oncology, Vol. 105, Núm. 3, pp. 321-328
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Axonal neuropathy, long limbs and bumpy tongue: Think of MEN2B
Muscle and Nerve, Vol. 46, Núm. 6, pp. 961-964
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BCL10 expression is unrelated to clinico-pathological parameters or prognoses for oral squamous cell carcinomas
Biotechnic and Histochemistry, Vol. 87, Núm. 6, pp. 423-427
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Breast feeding, parity and breast cancer subtypes in a Spanish cohort
PLoS ONE, Vol. 7, Núm. 7
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COGENT (COlorectal cancer GENeTics) revisited
Mutagenesis, Vol. 27, Núm. 2, pp. 143-151
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Characterization of BRCA1 and BRCA2 splicing variants: A collaborative report by ENIGMA consortium members
Breast Cancer Research and Treatment, Vol. 132, Núm. 3, pp. 1009-1023
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Characterization of TGM1 c.984+1G>A mutation identified in a homozygous carrier of lamellar ichthyosis
International Journal of Dermatology, Vol. 51, Núm. 4, pp. 427-430
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Characterization of single nucleotide polymorphisms of cytochrome P450 in an Australian deceased sample
Current Drug Metabolism, Vol. 13, Núm. 5, pp. 679-692
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Clinical and molecular classification of ichthyosis
Piel
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Cognitive functioning in children and adults with Smith-Magenis syndrome
European Journal of Medical Genetics, Vol. 55, Núm. 6-7, pp. 394-399
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Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer
Gut, Vol. 61, Núm. 6, pp. 865-872