| 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, 1-13, 2015 | 211 | 2015 |
| 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, 1-12, 2020 | 91 | 2020 |
| 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 | 73 | 2017 |
| Returning integrated genomic risk and clinical recommendations: The eMERGE study JE Linder, A Allworth, HT Bland, PJ Caraballo, RL Chisholm, EW Clayton, ... Genetics in Medicine 25 (4), 100006, 2023 | 40 | 2023 |
| 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, 1-14, 2021 | 24 | 2021 |
| 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 | 20 | 2021 |
| A review and definition of Ħusual 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 | 18 | 2021 |
| Regeneron Genetics Center; Loos, RJF; et al NS Abul-Husn, ER Soper, JA Odgis, S Cullina, D Bobo, A Moscati, ... Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder …, 2019 | 14 | 2019 |
| Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients NS Abul-Husn, PN Marathe, NR Kelly, KE Bonini, M Sebastin, JA Odgis, ... Genetics in Medicine 25 (9), 100880, 2023 | 13 | 2023 |
| Perspectives of diverse Spanish-and English-speaking patients on the clinical use of polygenic risk scores SA Suckiel, GT Braganza, KL Aguiñiga, JA Odgis, KE Bonini, EE Kenny, ... Genetics in Medicine 24 (6), 1217-1226, 2022 | 12 | 2022 |
| Hope versus reality: Parent expectations of genomic testing KE Donohue, SM Dolan, D Watnick, KM Gallagher, JA Odgis, SA Suckiel, ... Patient education and counseling 104 (8), 2073-2079, 2021 | 12 | 2021 |
| “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), 2021 | 9 | 2021 |
| 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 | 8 | 2021 |
| The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing M Sebastin, JA Odgis, SA Suckiel, KE Bonini, M Di Biase, K Brown, ... Pilot and Feasibility Studies 9 (1), 47, 2023 | 6 | 2023 |
| Detection of mosaic variants using genome sequencing in a large pediatric cohort JA Odgis, KM Gallagher, AU Rehman, PN Marathe, KE Bonini, ... American Journal of Medical Genetics Part A 191 (3), 699-710, 2023 | 6 | 2023 |
| 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 23 (10), 1998-2002, 2021 | 3 | 2021 |
| Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program KE Bonini, A Thomas‐Wilson, PN Marathe, M Sebastin, JA Odgis, ... Clinical Genetics 104 (2), 210-225, 2023 | 1 | 2023 |
| Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program A Berkalieva, NR Kelly, A Fisher, SF Hohmann, M Sebastin, M Di Biase, ... Genetics in Medicine 26 (1), 101011, 2024 | | 2024 |
| The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families SA Suckiel, NR Kelly, JA Odgis, KM Gallagher, M Sebastin, KE Bonini, ... The American Journal of Human Genetics 110 (12), 2029-2041, 2023 | | 2023 |
| The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families SA Suckiel, NR Kelly, JA Odgis, KM Gallagher, M Sebastin, KE Bonini, ... medRxiv, 2023 | | 2023 |
