Fundación Pública Galega de Medicina Xenómica
Centro de investigación
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National Institute for Health and Welfare
Helsinki, FinlandiaPublicacións en colaboración con investigadores/as de National Institute for Health and Welfare (9)
2024
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Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes
Nature Communications, Vol. 15, Núm. 1
2020
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Association between DNA methylation and ADHD symptoms from birth to school age: a prospective meta-analysis
Translational Psychiatry, Vol. 10, Núm. 1
2019
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Association analyses identify 31 new risk loci for colorectal cancer susceptibility
Nature Communications, Vol. 10, Núm. 1
2014
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Common variant at 16p11.2 conferring risk of psychosis
Molecular Psychiatry, Vol. 19, Núm. 1, pp. 108-114
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Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Nature Genetics, Vol. 46, Núm. 8, pp. 826-836
2013
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Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
Nature Genetics, Vol. 45, Núm. 8, pp. 868-876
2011
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Common variants at VRK2 and TCF4 conferring risk of schizophrenia
Human Molecular Genetics, Vol. 20, Núm. 20, pp. 4076-4081
2009
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Common variants conferring risk of schizophrenia
Nature, Vol. 460, Núm. 7256, pp. 744-747