MARIA DE LOS ANGELES
MARTINEZ DE PANCORBO GOMEZ
Forscher/in in der Zeit 2004-2023
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Hospital Universitario de Donostia
San Sebastián, EspañaPublikationen in Zusammenarbeit mit Forschern von Hospital Universitario de Donostia (12)
2021
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Long runs of homozygosity are associated with Alzheimer’s disease
Translational Psychiatry, Vol. 11, Núm. 1
2019
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Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project
Alzheimer's and Dementia, Vol. 15, Núm. 10, pp. 1333-1347
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Single nucleotide polymorphisms associated with susceptibility for development of colorectal cancer: Case-control study in a Basque population
PLoS ONE, Vol. 14, Núm. 12
2016
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Luminal B breast cancer subtype displays a dicotomic epigenetic pattern
SpringerPlus, Vol. 5, Núm. 1
2015
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MAPT H1 haplotype is associated with late-onset Alzheimer's disease risk in APOE ε 4 noncarriers: Results from the dementia genetics Spanish consortium
Journal of Alzheimer's Disease, Vol. 49, Núm. 2, pp. 343-352
2013
2011
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Progression from amnesic mild cognitive impairment to alzheimer's disease: ESR1 and ESR2 polymorphisms and APOE gene
Dementia and Geriatric Cognitive Disorders, Vol. 32, Núm. 5, pp. 332-341
2010
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Cardiac sympathetic denervation precedes nigrostriatal loss in the E46K mutation of the α-synuclein gene (SNCA)
Clinical Autonomic Research, Vol. 20, Núm. 4, pp. 267-269
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DNA methylation epigenotypes in breast cancer molecular subtypes
Breast Cancer Research, Vol. 12, Núm. 5
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Somatic mosaicism in a case of apparently sporadic Creutzfeldt-Jakob disease carrying a de novo D178N mutation in the PRNP gene
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 153, Núm. 7, pp. 1283-1291
2009
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The COMT Val158 met polymorphism as an associated risk factor for Alzheimer disease and mild cognitive impairment in APOE 4 carriers
BMC Neuroscience, Vol. 10, pp. 125
2005
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Ancestral origins of the prion protein gene D178N mutation in the Basque Country
Human Genetics, Vol. 117, Núm. 1, pp. 61-69