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Ivarsdottir EV, Gudmundsson J, Tragante V, Sveinbjornsson G, Kristmundsdottir S, Stacey SN, Halldorsson GH, Magnusson MI, Oddsson A, Walters GB, Sigurdsson A, Saevarsdottir S, Beyter D, Thorleifsson G, Halldorsson BV, Melsted P, Stefansson H, Jonsdottir I, Sørensen E, Pedersen OB, Erikstrup C, Bøgsted M, Pøhl M, Røder A, Stroomberg HV et al. (2024)
Gene-based burden tests of rare germline variants identify six cancer susceptibility genes
Nat Genet, 56 (11), 2422-2433
DOI 10.1038/s41588-024-01966-6, PubMed 39472694

Møller P, Seppälä TT, Dominguez-Valentin M, Sampson J (2024)
Commentary on Estimating cancer risk in carriers of Lynch syndrome variants in UK Biobank
J Med Genet (in press)
DOI 10.1136/jmg-2024-110385, PubMed 39375027

Fernández-Ramires R, Margarit S, Morales S, Lazaro C, Álvarez S, Martin ES, Benavides C, Cammarata F, Encina G, Berkovits A, Gischkow G, Dominguez M, Espinosa-Parrilla Y, Echeverría C, Zapata-Contreras D, Soto G, Calegaro-Nassif M, Espinoza K, Sullcahuaman Y, Palmero E (2023)
[Consensus for Oncology Genetic Counseling and Molecular Diagnosis: The Punta Arenas Statement]
Rev Med Chil, 151 (9), 1262-1263
DOI 10.4067/s0034-98872023000901262, PubMed 39093165