Fundación Pública Galega de Medicina Xenómica
Centro de investigación
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QIMR Berghofer Medical Research Institute
Brisbane, AustraliaPublicacións en colaboración con investigadores/as de QIMR Berghofer Medical Research Institute (6)
2022
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Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
Communications biology, Vol. 5, Núm. 1, pp. 1061
2020
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Nature Genetics, Vol. 52, Núm. 1, pp. 56-73
2019
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The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
npj Breast Cancer, Vol. 5, Núm. 1
2018
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Genetic testing and clinical management practices for variants in non-BRCA1/2 breast (and breast/ovarian) cancer susceptibility genes: An international survey by the Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) clinical working group
JCO Precision Oncology, Vol. 2
2015
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Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk
Human Molecular Genetics, Vol. 24, Núm. 5, pp. 1478-1492
2014
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Common variant at 16p11.2 conferring risk of psychosis
Molecular Psychiatry, Vol. 19, Núm. 1, pp. 108-114