| 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 | 38 | 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 ‘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 | 17 | 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 |
| 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 |
| 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 | 11 | 2022 |
| “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 |
