| Motivations, concerns and preferences of personal genome sequencing research participants: baseline findings from the HealthSeq project SC Sanderson, MD Linderman, SA Suckiel, GA Diaz, RE Zinberg, ... European Journal of Human Genetics 24 (1), 14-20, 2016 | 138 | 2016 |
| 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 | 104 | 2020 |
| Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public SC Sanderson, SA Suckiel, M Zweig, EP Bottinger, EW Jabs, ... Genetics in Medicine 18 (5), 501-512, 2016 | 70 | 2016 |
| Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project SC Sanderson, MD Linderman, SA Suckiel, R Zinberg, M Wasserstein, ... European Journal of Human Genetics 25 (3), 280-292, 2017 | 69 | 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 | 65 | 2023 |
| Implementing genomic screening in diverse populations NS Abul-Husn, ER Soper, GT Braganza, JE Rodriguez, N Zeid, S Cullina, ... Genome medicine 13, 1-11, 2021 | 62 | 2021 |
| How do students react to analyzing their own genomes in a whole-genome sequencing course?: outcomes of a longitudinal cohort study SC Sanderson, MD Linderman, R Zinberg, A Bashir, A Kasarskis, ... Genetics in Medicine 17 (11), 866-874, 2015 | 32 | 2015 |
| 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 | 29 | 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 | 29 | 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 | 25 | 2021 |
| Preparing the next generation of genomicists: a laboratory-style course in medical genomics MD Linderman, A Bashir, GA Diaz, A Kasarskis, SC Sanderson, ... BMC Medical Genomics 8, 1-3, 2015 | 24 | 2015 |
| Impact of genomic counseling on informed decision-making among ostensibly healthy individuals seeking personal genome sequencing: the HealthSeq project SA Suckiel, MD Linderman, SC Sanderson, GA Diaz, M Wasserstein, ... Journal of genetic counseling 25, 1044-1053, 2016 | 23 | 2016 |
| Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years MD Linderman, SC Sanderson, A Bashir, GA Diaz, A Kasarskis, R Zinberg, ... BMC medical genomics 11 (1), 1-12, 2018 | 22 | 2018 |
| 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 | 21 | 2021 |
| 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 | 20 | 2021 |
| Clinical genetic counseling and translation considerations for polygenic scores in personalized risk assessments: a practice resource from the national society of genetic … H Wand, SS Kalia, BM Helm, SA Suckiel, D Brockman, N Vriesen, ... Journal of genetic counseling 32 (3), 558-575, 2023 | 17 | 2023 |
| Lynch Syndrome–Associated variants and Cancer Rates in an Ancestrally Diverse Biobank RE Rosenblum, C Ang, SA Suckiel, ER Soper, MR Sigireddi, S Cullina, ... JCO Precision Oncology 1, 1429-1444, 2020 | 15 | 2020 |
| 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 | 14 | 2021 |
| Genomic screening identifies individuals at high risk for hereditary transthyretin amyloidosis ER Soper, SA Suckiel, GT Braganza, AR Kontorovich, EE Kenny, ... Journal of Personalized Medicine 11 (1), 49, 2021 | 14 | 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 | 13 | 2022 |
