MARÍA ISABEL
TEJADA MÍNGUEZ
Chercheuse jusqu' 2019
KU Leuven
Lovaina, BélgicaPublications en collaboration avec des chercheurs de KU Leuven (5)
2023
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Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes
The Lancet. Oncology, Vol. 24, Núm. 1, pp. 91-106
2017
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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Nature Genetics, Vol. 49, Núm. 12, pp. 1767-1778
2015
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Infectious and Immunologic Phenotype of MECP2 Duplication Syndrome
Journal of Clinical Immunology, Vol. 35, Núm. 2, pp. 168-181
2011
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A child with mild X-linked intellectual disability and a microduplication at Xp22.12 including RPS6KA3
Pediatrics, Vol. 128, Núm. 4
2009
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A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
Nature Genetics, Vol. 41, Núm. 5, pp. 535-543