Jacqueline A. Odgis
Jacqueline A. Odgis
Verified email at mssm.edu
Title
Cited by
Cited by
Year
The IGNITE network: a model for genomic medicine implementation and research
KW Weitzel, M Alexander, BA Bernhardt, N Calman, DJ Carey, ...
BMC medical genomics 9 (1), 1-13, 2015
1622015
Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system
GM Belbin, J Odgis, EP Sorokin, MC Yee, S Kohli, BS Glicksberg, ...
Elife 6, e25060, 2017
512017
Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank
NS Abul-Husn, ER Soper, JA Odgis, S Cullina, D Bobo, A Moscati, ...
Genome medicine 12 (1), 1-12, 2020
332020
The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children
JA Odgis, KM Gallagher, SA Suckiel, KE Donohue, MA Ramos, NR Kelly, ...
Trials 22 (1), 1-14, 2021
52021
GUÍA: a digital platform to facilitate result disclosure in genetic counseling
SA Suckiel, JA Odgis, KM Gallagher, JE Rodriguez, D Watnick, G Bertier, ...
Genetics in Medicine 23 (5), 942-949, 2021
42021
A review and definition of ‘usual care’in genetic counseling trials to standardize use in research
BB Biesecker, SE Lillie, LM Amendola, KE Donohue, KM East, ...
Journal of Genetic Counseling 30 (1), 42-50, 2021
22021
“Is that something that should concern me?”: a qualitative exploration of parent understanding of their child’s genomic test results
D Watnick, JA Odgis, SA Suckiel, KM Gallagher, N Teitelman, ...
Human Genetics and Genomics Advances 2 (2), 100027, 2021
12021
Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium
SA Suckiel, JM O’Daniel, KE Donohue, KM Gallagher, MJ Gilmore, ...
Journal of Personalized Medicine 11 (3), 202, 2021
12021
Hope versus reality: parent expectations of genomic testing
KE Donohue, SM Dolan, D Watnick, KM Gallagher, JA Odgis, SA Suckiel, ...
Patient Education and Counseling, 2021
12021
GenomeDiver: a platform for phenotype-guided medical genomic diagnosis
NM Pearson, C Stolte, K Shi, F Beren, NS Abul-Husn, G Bertier, K Brown, ...
Genetics in Medicine, 1-5, 2021
2021
Correction to: The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children
JA Odgis, KM Gallagher, SA Suckiel, KE Donohue, MA Ramos, NR Kelly, ...
Trials 22, 2021
2021
Exome Sequencing Reveals a High Prevalence ofBRCA1andBRCA2Founder Variants in a Diverse Population-Based Biobank
NS Abul-Husn, ER Soper, JA Odgis, S Cullina, D Bobo, A Moscati, ...
2019
Leveraging Electronic Health Records to Explore Clinical Features of Carriers of a Rare Monogenic Disease
JA Odgis
Icahn School of Medicine at Mount Sinai, 2017
2017
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Articles 1–13