Detalhe da pesquisa
1.
The role of family history in predicting germline pathogenic variant carriers who develop pancreatic cancer: Results of a multicenter collaboration.
Cancer
; 2024 May 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38809542
2.
Validation of a clinical breast cancer risk assessment tool combining a polygenic score for all ancestries with traditional risk factors.
Genet Med
; : 101128, 2024 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38829299
3.
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
BMC Med
; 19(1): 199, 2021 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34404389
4.
Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
Genome Res
; 25(3): 305-15, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25637381
5.
Correction to: Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
BMC Med
; 19(1): 288, 2021 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34732190
6.
SNPs and breast cancer risk prediction for African American and Hispanic women.
Breast Cancer Res Treat
; 154(3): 583-9, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26589314
7.
BRCA-mutated Invasive Breast Carcinomas: Immunohistochemical Analysis of Insulin-like Growth Factor II mRNA-binding Protein (IMP3), Cytokeratin 8/18, and Cytokeratin 14.
Breast J
; 21(6): 596-603, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26390986
8.
Acupuncture for Chronic Radiation-Induced Xerostomia in Head and Neck Cancer: A Multicenter Randomized Clinical Trial.
JAMA Netw Open
; 7(5): e2410421, 2024 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38739392
9.
Impact of family history on choosing risk-reducing surgery among BRCA mutation carriers.
Am J Obstet Gynecol
; 208(4): 329.e1-6, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23333547
10.
Participation in genetic screening: testing different outreach methods across a diverse hospital system based patient population.
Front Genet
; 14: 1272931, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37900185
11.
Development and Validation of a Breast Cancer Polygenic Risk Score on the Basis of Genetic Ancestry Composition.
JCO Precis Oncol
; 6: e2200084, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36331239
12.
Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations.
Hum Mutat
; 32(2): 152-67, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20848652
13.
Painting a portrait: Analysis of national health survey data for cancer genetic counseling.
Cancer Med
; 8(3): 1306-1314, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30734520
14.
Exome sequencing for the diagnosis of 46,XY disorders of sex development.
J Clin Endocrinol Metab
; 100(2): E333-44, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25383892
15.
Connective tissue disorders with spontaneous spinal cerebrospinal fluid leaks and intracranial hypotension: a prospective study.
Neurosurgery
; 54(1): 65-70; discussion 70-1, 2004 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-14683542
16.
Absence of TGFBR2 mutations in patients with spontaneous spinal CSF leaks and intracranial hypotension.
J Headache Pain
; 9(2): 99-102, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18264665
17.
Capturing the power of the family history.
Virtual Mentor
; 11(9): 690-6, 2009 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23199465