Detalhe da pesquisa
1.
Impact of an Expanded Definition of Family History on Outcomes of Active Surveillance for Prostate Cancer.
J Urol
; 209(6): 1112-1119, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36951811
2.
Motivation and family communication in hereditary prostate cancer genetic testing: Survey of patients from a US tertiary medical center.
J Genet Couns
; 32(1): 79-89, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35941805
3.
Transition to telephone genetic counseling services during the COVID-19 pandemic.
J Genet Couns
; 30(4): 984-988, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33277765
4.
The contribution of de novo coding mutations to autism spectrum disorder.
Nature
; 515(7526): 216-21, 2014 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-25363768
5.
Factors associated with referral and completion of genetic counseling in women with epithelial ovarian cancer.
Int J Gynecol Cancer
; 30(9): 1397-1403, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32447294
6.
SMASH, a fragmentation and sequencing method for genomic copy number analysis.
Genome Res
; 26(6): 844-51, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27197213
7.
Universal screening of both endometrial and colon cancers increases the detection of Lynch syndrome.
Cancer
; 124(15): 3145-3153, 2018 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29750335
8.
Optimizing sparse sequencing of single cells for highly multiplex copy number profiling.
Genome Res
; 25(5): 714-24, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25858951
9.
A tailored approach to BRAF and MLH1 methylation testing in a universal screening program for Lynch syndrome.
Mod Pathol
; 30(3): 440-447, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28059100
10.
Tumour evolution inferred by single-cell sequencing.
Nature
; 472(7341): 90-4, 2011 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21399628
11.
Gastric cancer in Lynch syndrome is associated with underlying immune gastritis.
J Med Genet
; 56(12): 844-845, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31055502
12.
Clinical applications of melanoma genetics.
Curr Treat Options Oncol
; 15(2): 336-50, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24652319
13.
Magnetic Resonance Imaging-based Prostate Cancer Screening in Carriers of Pathogenic Germline Mutations: Interim Results from the Initial Screening Round of the Prostate Cancer Genetic Risk Evaluation and Screening Study.
Eur Urol Oncol
; 2024 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38453598
14.
Inferring tumor progression from genomic heterogeneity.
Genome Res
; 20(1): 68-80, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19903760
15.
Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing.
Elife
; 92020 05 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32401198
16.
Utility of Single-Cell Genomics in Diagnostic Evaluation of Prostate Cancer.
Cancer Res
; 78(2): 348-358, 2018 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29180472
17.
Whole-genome single-cell copy number profiling from formalin-fixed paraffin-embedded samples.
Nat Med
; 23(3): 376-385, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28165479
18.
The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.
J Child Neurol
; 30(14): 1947-53, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26391891
19.
Genome-wide copy number analysis of single cells.
Nat Protoc
; 7(6): 1024-41, 2012 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-22555242
20.
De novo gene disruptions in children on the autistic spectrum.
Neuron
; 74(2): 285-99, 2012 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-22542183