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- 2018
- Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
- 2017
- Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression : identification of a modifier of breast cancer risk at locus 11q22.3
-
Gaia Data Release 1 : Open cluster astrometry: Performance, limitations, and future prospects
van Leeuwen, F. ; Vallenari, A ; Jordi, C ; Lindegren, L. LU
; Bastian, U.
; Prusti, T.
; de Bruijne, J.H.J.
; Brown, A. G. A.
; Babusiaux, C.
and Bailer-Jones, C. A L
, et al.
(2017)
In Astronomy and Astrophysics
601.
Mark
- 2016
- Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women
- Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
- BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
- Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
- No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
- Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
- 2015
- Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers.
- An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers.
- Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
- Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.
- 2014
- Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study.
- DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
- 2013
- Assessment of Fusion Gene Status in Sarcomas Using a Custom Made Fusion Gene Microarray
- 2010
- Genomic Changes in Chromosomes 10, 16, and X in Malignant Peripheral Nerve Sheath Tumors Identify a High-Risk Patient Group.
- 2008
-
Heterogeneous genetic profiles in soft tissue myoepitheliomas
Hansén Nord, Karolin LU ; Teixeira, Manuel R. ; Fletcher, Christopher D. M. ; Bizarro, Susana ; Staaf, Johan LU
; Domanski, Henryk
LU
; Vult von Steyern, Fredrik
LU
; Panagopoulos, Ioannis
LU
; Mandahl, Nils
LU
and Mertens, Fredrik
LU
(2008)
In Modern Pathology
21(11).
p.1311-1319
Mark
- 2004
- Genome characteristics of primary carcinomas, local recurrences, carcinomatoses, and liver metastases from colorectal cancer patients