Detalhe da pesquisa
1.
The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families.
Am J Hum Genet
; 110(12): 2029-2041, 2023 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38006881
2.
Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program.
Genet Med
; 26(1): 101011, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37897232
3.
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.
Genet Med
; 25(9): 100880, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37158195
4.
Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program.
Clin Genet
; 104(2): 210-225, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37334874
5.
Detection of mosaic variants using genome sequencing in a large pediatric cohort.
Am J Med Genet A
; 191(3): 699-710, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36563179
6.
Integration of stakeholder engagement from development to dissemination in genomic medicine research: Approaches and outcomes from the CSER Consortium.
Genet Med
; 24(5): 1108-1119, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35227608
7.
Establishing the value of genomics in medicine: the IGNITE Pragmatic Trials Network.
Genet Med
; 23(7): 1185-1191, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33782552
8.
Are Parental Perceptions of Child Activity Levels and Overall Health More Important than Perceptions of Weight?
Matern Child Health J
; 20(7): 1456-63, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27010551
9.
Phosphosite Scanning reveals a complex phosphorylation code underlying CDK-dependent activation of Hcm1.
Nat Commun
; 14(1): 310, 2023 01 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36658165
10.
pH-Selective Reactions to Selectively Reduce Cancer Cell Proliferation: Effect of CaS Nanostructures in Human Skin Melanoma and Benign Fibroblasts.
Biochem (Basel)
; 3(1): 15-30, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37035583
11.
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.
medRxiv
; 2023 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36993157
12.
The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing.
Pilot Feasibility Stud
; 9(1): 47, 2023 Mar 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36949526
13.
The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families.
medRxiv
; 2023 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37461450
14.
Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals: A Randomized Clinical Trial.
JAMA Netw Open
; 5(3): e221048, 2022 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35244702
15.
Creating accessible Spanish language materials for Clinical Sequencing Evidence-Generating Research consortium genomic projects: challenges and lessons learned.
Per Med
; 18(5): 441-454, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34448595
16.
Strategies to Integrate Genomic Medicine into Clinical Care: Evidence from the IGNITE Network.
J Pers Med
; 11(7)2021 Jul 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34357114
17.
The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children.
Trials
; 22(1): 56, 2021 Jan 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-33446240
18.
Lessons learned about harmonizing survey measures for the CSER consortium.
J Clin Transl Sci
; 4(6): 537-546, 2020 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-33948230
19.
Comprehensive examination of the multilevel adverse risk and protective factors for cardiovascular disease among hypertensive African Americans.
J Clin Hypertens (Greenwich)
; 21(6): 794-803, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31125186
20.
Views Of Primary Care Providers On Testing Patients For Genetic Risks For Common Chronic Diseases.
Health Aff (Millwood)
; 37(5): 793-800, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29733703