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1.
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.
Am J Hum Genet
; 108(10): 1907-1923, 2021 10 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-34597585
2.
Altered regulation of BRCA1 exon 11 splicing is associated with breast cancer risk in carriers of BRCA1 pathogenic variants.
Hum Mutat
; 42(11): 1488-1502, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34420246
3.
Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation.
Breast Cancer Res
; 23(1): 79, 2021 08 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34344426
4.
Gene- and pathway-level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility.
Int J Cancer
; 148(8): 1895-1909, 2021 04 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-33368296
5.
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing.
Int J Cancer
; 144(8): 1962-1974, 2019 04 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-30303537
6.
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
Hum Mol Genet
; 24(18): 5345-55, 2015 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-26130695
7.
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.
Breast Cancer Res Treat
; 161(1): 117-134, 2017 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27796716
8.
Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.
BMC Cancer
; 17(1): 328, 2017 05 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-28499365
9.
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
J Med Genet
; 53(5): 298-309, 2016 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-26921362
10.
GENESIS: a French national resource to study the missing heritability of breast cancer.
BMC Cancer
; 16: 13, 2016 Jan 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-26758370
11.
Mutation analysis of PALB2 gene in French breast cancer families.
Breast Cancer Res Treat
; 154(3): 463-71, 2015 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-26564480
12.
Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population.
BMC Genet
; 16: 22, 2015 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-25879635
13.
Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study.
Breast Cancer Res
; 16(3): R58, 2014 Jun 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-24894818
14.
Contribution of ATM and FOXE1 (TTF2) to risk of papillary thyroid carcinoma in Belarusian children exposed to radiation.
Int J Cancer
; 134(7): 1659-68, 2014 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-24105688
15.
COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration.
Breast Cancer Res
; 15(3): 402, 2013 Jun 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-23809231
16.
Usefulness of an RNA extraction-free test for the multiplexed detection of ALK, ROS1, and RET Gene Fusions in Real Life FFPE Specimens of Non-Small Cell Lung Cancers.
Expert Rev Mol Diagn
; 23(12): 1283-1291, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37906110
17.
Multiomic analysis of malignant pleural mesothelioma identifies molecular axes and specialized tumor profiles driving intertumor heterogeneity.
Nat Genet
; 55(4): 607-618, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36928603
18.
Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study.
Breast Cancer Res
; 13(1): R6, 2011 Jan 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-21244692
19.
Selected highlights of the 2019 Pulmonary Pathology Society Biennial Meeting: PD-L1 test harmonization studies.
Transl Lung Cancer Res
; 9(3): 906-916, 2020 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-32676356
20.
New molecular classification of large cell neuroendocrine carcinoma and small cell lung carcinoma with potential therapeutic impacts.
Transl Lung Cancer Res
; 9(5): 2233-2244, 2020 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-33209646