Detalhe da pesquisa
1.
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Artigo
em Inglês
| MEDLINE | ID: mdl-31412182
2.
Development of the Initial Surveys for the All of Us Research Program.
Epidemiology
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Artigo
em Inglês
| MEDLINE | ID: mdl-31045611
3.
Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health.
PLoS Med
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Artigo
em Inglês
| MEDLINE | ID: mdl-30114233
4.
A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health.
PLoS Med
; 15(8): e1002631, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30071015
5.
National Institute on Drug Abuse symposium report: drugs of abuse, dopamine, and HIV-associated neurocognitive disorders/HIV-associated dementia.
J Neurovirol
; 19(2): 119-22, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23456951
6.
A framework for assessing clinical trial site readiness.
J Clin Transl Sci
; 7(1): e151, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37456265
7.
The NIH-led research response to COVID-19.
Science
; 379(6631): 441-444, 2023 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36730407
8.
Gene-environment interplay in common complex diseases: forging an integrative modelrecommendations from an NIH workshop.
Genet Epidemiol
; 35(4): 217-25, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21308768
9.
Advancing translational science education.
Clin Transl Sci
; 15(11): 2555-2566, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36045637
10.
The IDeaS initiative: pilot study to assess the impact of rare diseases on patients and healthcare systems.
Orphanet J Rare Dis
; 16(1): 429, 2021 10 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34674728
11.
Diversity and inclusion for the All of Us research program: A scoping review.
PLoS One
; 15(7): e0234962, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32609747
12.
Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan.
Radiat Res
; 171(1): 77-88, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19138047
13.
The Bespoke Gene Therapy Consortium: facilitating development of AAV gene therapies for rare diseases.
Nat Rev Drug Discov
; 23(3): 157-158, 2024 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38321319
14.
The All of Us Research Program is an opportunity to enhance the diversity of US biomedical research.
Nat Med
; 30(2): 330-333, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38374344
15.
Similar prevalence of founder BRCA1 and BRCA2 mutations among Ashkenazi and non-Ashkenazi men with breast cancer: evidence from 261 cases in Israel, 1976-1999.
Eur J Med Genet
; 51(2): 141-7, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18158280
16.
An ontology-driven semantic mashup of gene and biological pathway information: application to the domain of nicotine dependence.
J Biomed Inform
; 41(5): 752-65, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18395495
17.
Diversity, equity, inclusion, and access are necessary for clinical trial site readiness.
J Clin Transl Sci
; 7(1): e268, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38380391
18.
Identification and characterization of novel human transcripts embedded within HMGA2 in t(12;14)(q15;q24.1) uterine leiomyoma.
Mutat Res
; 602(1-2): 43-53, 2006 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17045619
19.
Evidence generation and reproducibility in cell and gene therapy research: A call to action.
Mol Ther Methods Clin Dev
; 22: 11-14, 2021 Sep 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34377737
20.
CDKN2A point mutations D153spl(c.457G>T) and IVS2+1G>T result in aberrant splice products affecting both p16INK4a and p14ARF.
Oncogene
; 22(28): 4444-8, 2003 Jul 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-12853981