Departamento de Ciencias Forenses, Anatomía Patolóxica, Xinecoloxía e Obstetricia e Pediatría
Departamento
Centre National de la Recherche Scientifique
París, FranciaPublicacións en colaboración con investigadores/as de Centre National de la Recherche Scientifique (11)
2019
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Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (Nature Genetics, (2019), 51, 3, (414-430), 10.1038/s41588-019-0358-2)
Nature Genetics
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Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Nature Genetics, Vol. 51, Núm. 3, pp. 414-430
2017
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Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci
Nature Genetics, Vol. 49, Núm. 7, pp. 993-1004
2015
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Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export
Nature Genetics, Vol. 47, Núm. 6, pp. 579-581
2013
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Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice
Nature Genetics, Vol. 45, Núm. 9, pp. 1077-1082
2012
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Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk
Neurobiology of Aging, Vol. 33, Núm. 7, pp. 1487.e21-1487.e28
2009
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Inferring the demographic history of African farmers and Pygmy hunter-gatherers using a multilocus resequencing data set
PLoS Genetics, Vol. 5, Núm. 4
2008
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Maternal traces of deep common ancestry and asymmetric gene flow between Pygmy hunter-gatherers and Bantu-speaking farmers
Proceedings of the National Academy of Sciences of the United States of America, Vol. 105, Núm. 5, pp. 1596-1601
2002
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The fingerprint of phantom mutations in mitochondrial DNA data
American Journal of Human Genetics, Vol. 71, Núm. 5, pp. 1150-1160
1996
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Cellular distribution of prolactin receptors in human digestive tissues
Journal of Clinical Endocrinology and Metabolism, Vol. 81, Núm. 5, pp. 1861-1866