| Bioinspired nanoparticulate medical glues for minimally invasive tissue repair Y Lee, C Xu, M Sebastin, A Lee, N Holwell, C Xu, D Miranda Nieves, L Mu, ... Advanced healthcare materials 4 (16), 2587-2596, 2015 | 42 | 2015 |
| 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 |
| Biallelic variants in SLC38A3 encoding a glutamine transporter cause epileptic encephalopathy D Marafi, JM Fatih, R Kaiyrzhanov, MP Ferla, C Gijavanekar, A Al-Maraghi, ... Brain 145 (3), 909-924, 2022 | 19 | 2022 |
| 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 |
| 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 |
| Genetic screening of relatives of decedents experiencing sudden unexpected death: medical examiner’s office referrals to a multi-disciplinary cardiogenetics program T Siskind, N Williams, M Sebastin, R Marion, TV McDonald, C Walsh, ... Journal of community genetics 13 (6), 629-639, 2022 | 4 | 2022 |
| 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 |
| Future Frontiers: Exploration of practices, challenges, and educational needs of genetic counselors in emerging subspecialties P Ahimaz, M Ross, J Foltz, M Sebastin, K Naik, T Kramer, K Bogyo, ... Journal of Genetic Counseling 32 (6), 1238-1248, 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 |
| Exploring the role of genetic counselors in immunology: A study of immunologist and allergist perspectives P Ahimaz, JC Foltz, MJ Ross, ME Florido, M Sebastin, EY Joyce The journal of allergy and clinical immunology. In practice 11 (6), 1939 …, 2023 | | 2023 |
| P245: GUÍA application: Effectiveness in enhancing communication of genomic results in diverse, multilingual populations P Marathe, S Suckiel, J Odgis, K Gallagher, M Sebastin, K Bonini, ... Genetics in Medicine Open 1 (1), 2023 | | 2023 |
| P318: Impact of genetic counseling using GUÍA on diverse families’ understanding of genomic results: Finding from the NYCKidSeq randomized controlled trial S Suckiel, N Kelly, J Odgis, K Gallagher, M Sebastin, K Bonini, P Marathe, ... Genetics in Medicine Open 1 (1), 2023 | | 2023 |
| P217: Ectodermal dysplasia-A case report A Kruse, M Sebastin, D Lee, R Marion Genetics in Medicine Open 1 (1), 2023 | | 2023 |
| eP236: TeleKidSeq: Incorporating telehealth into clinical care of children from diverse backgrounds undergoing clinical genome sequencing M Sebastin, J Odgis, S Suckiel, K Bonini, M Di Biase, K Brown, P Marathe, ... Genetics in Medicine 24 (3), S150, 2022 | | 2022 |
| eP067: Diagnostic yield of genome sequencing versus targeted gene panel testing in diverse pediatric patients in the NYCKidSeq study N Abul-Husn, N Kelly, J Rodriguez, A Abhyankar, K Donohue, K Brown, ... Genetics in Medicine 24 (3), S45, 2022 | | 2022 |
| A novel pathogenic variant in FANCA uncovers a previously undiagnosed case of Fanconi Anemia (FA) in a 22-year-old woman H Zomer, A Rubinstein, R Eisenberg, R Marion, M Sebastin JOURNAL OF CLINICAL IMMUNOLOGY 41 (SUPPL 1), S72-S72, 2021 | | 2021 |
