Detalles de la búsqueda
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-38006881
2.
Patient and Provider Experiences and Views on the Use of Telehealth in Genetics Clinics in Response to the COVID-19 Pandemic.
Telemed J E Health
; 30(1): 118-125, 2024 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37294555
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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| MEDLINE | ID: mdl-36563179
6.
GUÍA: a digital platform to facilitate result disclosure in genetic counseling.
Genet Med
; 23(5): 942-949, 2021 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33531665
7.
Pharmacogenomic education among genetic counseling training programs in North America.
J Genet Couns
; 30(5): 1500-1508, 2021 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-33882174
8.
The evolution of genetic counseling graduate education in New York City during the COVID-19 pandemic: In the eye of the storm.
J Genet Couns
; 30(4): 1057-1068, 2021 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-34218495
9.
Impact of Genomic Counseling on Informed Decision-Making among ostensibly Healthy Individuals Seeking Personal Genome Sequencing: the HealthSeq Project.
J Genet Couns
; 25(5): 1044-53, 2016 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-26898680
10.
How do students react to analyzing their own genomes in a whole-genome sequencing course?: outcomes of a longitudinal cohort study.
Genet Med
; 17(11): 866-74, 2015 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-25634025
11.
The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.
Genet Med
; 15(10): 761-71, 2013 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-23743551
12.
The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families.
medRxiv
; 2023 Jul 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-37461450
13.
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.
medRxiv
; 2023 Mar 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-36993157
14.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-36949526
15.
Commentary: "My Identical Twin Sequenced Our Genome".
J Genet Couns
; 26(2): 281-282, 2017 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-28124750
16.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-33446240
17.
Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years.
BMC Med Genomics
; 11(1): 5, 2018 01 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-29382336
18.
Race, Genomics and Chronic Disease: What Patients with African Ancestry Have to Say.
J Health Care Poor Underserved
; 28(1): 248-260, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28238999
19.
Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project.
Eur J Hum Genet
; 25(3): 280-292, 2017 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-28051073
20.
Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
Eur J Hum Genet
; 24(1): 14-20, 2016 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-26036856