Jacqueline A. Odgis
Jacqueline A. Odgis
Verified email at mssm.edu
Cited by
Cited by
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
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
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
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, 2020
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
GenomeDiver: A platform for phenotype-guided medical genomic diagnosis.
N Pearson, C Stolte, K Shi, F Beren, NS Abul-Husn, G Bertier, K Brown, ...
medRxiv, 2020
GUÍA: a digital platform to facilitate result disclosure in genetic counseling
SA Suckiel, JA Odgis, KM Gallagher, JE Rodriguez, D Watnick, G Bertier, ...
medRxiv, 2020
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, ...
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
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Articles 1–9