Detalhe da pesquisa
1.
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
Am J Hum Genet
; 98(5): 801-817, 2016 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27153395
2.
Collaborative science in the next-generation sequencing era: a viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genes.
Brief Bioinform
; 17(4): 672-7, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26358132
3.
Mutant SF3B1 promotes malignancy in PDAC.
Elife
; 122023 10 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37823551
4.
Mutation Rates in Cancer Susceptibility Genes in Patients With Breast Cancer With Multiple Primary Cancers.
JCO Precis Oncol
; 42020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32954205
5.
Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genes.
Eur J Hum Genet
; 27(5): 824-828, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30718883
6.
Erratum: Author Correction: The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk.
NPJ Breast Cancer
; 3: 44, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29119134
7.
The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk.
NPJ Breast Cancer
; 3: 22, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28649662
8.
Avulsion of a bronchial blocker cuff in the trachea when using a Parker Flex-Tip endotracheal tube.
J Cardiothorac Vasc Anesth
; 25(2): 391-2, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20573519
9.
Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA.
JAMA Oncol
; 2(1): 104-11, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26556299
10.
A Recurrent ERCC3 Truncating Mutation Confers Moderate Risk for Breast Cancer.
Cancer Discov
; 6(11): 1267-1275, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27655433
11.
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins.
Nat Commun
; 5: 4835, 2014 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-25203624
12.
Genome Sequencing of Multiple Primary Tumors Reveals a Novel PALB2 Variant.
J Clin Oncol
; 34(8): e61-7, 2016 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-24982446