Detalhe da pesquisa
1.
Germline evaluation of patients undergoing tumor genomic profiling: An academic cancer center's experience with implementing a germline review protocol.
J Genet Couns
; 30(3): 900-910, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33754402
2.
Screening guidelines and recommendations for patients at high risk of developing endocrine cancers.
J Surg Oncol
; 121(6): 975-983, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32090344
3.
Detection of germline variants using expanded multigene panels in patients with localized pancreatic cancer.
HPB (Oxford)
; 22(12): 1745-1752, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32354656
4.
Implementation of a quality improvement project for universal genetic testing in women with ovarian cancer.
Gynecol Oncol
; 149(3): 565-569, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29653687
5.
Stat5 is critical for the development and maintenance of myeloproliferative neoplasm initiated by Nf1 deficiency.
Haematologica
; 101(10): 1190-1199, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27418650
6.
Nf1 mutant mice with p19ARF gene loss develop accelerated hematopoietic disease resembling acute leukemia with a variable phenotype.
Am J Hematol
; 86(7): 579-85, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21681782
7.
Cost-effectiveness analysis of universal germline testing for patients with pancreatic cancer.
Surgery
; 169(3): 629-635, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32826069
8.
Inherited syndromes involving pancreatic neuroendocrine tumors.
J Gastrointest Oncol
; 11(3): 559-566, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32655935
9.
Does Supply Equal Demand? The Workforce of Direct Patient Care Genetic Counselors in Wisconsin.
WMJ
; 119(3): 158-164, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33091282
10.
HEREDITARY ENDOCRINE TUMOURS: CURRENT STATE-OF-THE-ART AND RESEARCH OPPORTUNITIES: Challenges and opportunities in genetic counseling for hereditary endocrine neoplasia syndromes.
Endocr Relat Cancer
; 27(8): T65-T75, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32106089
11.
Splicing profile by capture RNA-seq identifies pathogenic germline variants in tumor suppressor genes.
NPJ Precis Oncol
; 4: 4, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32133419
12.
Gene mutations and genomic rearrangements in the mouse as a result of transposon mobilization from chromosomal concatemers.
PLoS Genet
; 2(9): e156, 2006 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-17009875
13.
OVARIAN GRANULOSA CELL TUMOR IN A PATIENT WITH A PATHOGENIC VARIANT IN THE CDC73 GENE (HYPERPARATHYROIDISM-JAW TUMOR SYNDROME).
AACE Clin Case Rep
; 5(3): e222-e225, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31967039
14.
Risk reduction and survival benefit of prophylactic surgery in BRCA mutation carriers, a systematic review.
Am J Surg
; 212(4): 660-669, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27649974
15.
Challenges to clinical utilization of hereditary cancer gene panel testing: perspectives from the front lines.
Fam Cancer
; 14(4): 641-9, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26108897
16.
Beta common receptor inactivation attenuates myeloproliferative disease in Nf1 mutant mice.
Blood
; 109(4): 1687-91, 2007 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17090653
17.
RNA as a source of transposase for Sleeping Beauty-mediated gene insertion and expression in somatic cells and tissues.
Mol Ther
; 13(3): 625-30, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16368272
18.
Sleeping Beauty-mediated transposition and long-term expression in vivo: use of the LoxP/Cre recombinase system to distinguish transposition-specific expression.
Mol Ther
; 13(3): 617-24, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16356773