| Exome sequencing–based screening for BRCA1/2 expected pathogenic variants among adult biobank participants K Manickam, AH Buchanan, MLB Schwartz, MLG Hallquist, JL Williams, ... JAMA Network Open 1 (5), e182140-e182140, 2018 | 197 | 2018 |
| A model for genome-first care: returning secondary genomic findings to participants and their healthcare providers in a large research cohort MLB Schwartz, CZ McCormick, AL Lazzeri, ML D’Andra, MLG Hallquist, ... The American Journal of Human Genetics 103 (3), 328-337, 2018 | 147 | 2018 |
| Patient assessment of chatbots for the scalable delivery of genetic counseling T Schmidlen, M Schwartz, K DiLoreto, HL Kirchner, AC Sturm Journal of genetic counseling 28 (6), 1166-1177, 2019 | 111 | 2019 |
| Clinical outcomes of a genomic screening program for actionable genetic conditions AH Buchanan, HL Kirchner, MLB Schwartz, MA Kelly, T Schmidlen, ... Genetics in Medicine 22 (11), 1874-1882, 2020 | 101 | 2020 |
| Patient-centered precision health in a learning health care system: Geisinger’s genomic medicine experience MS Williams, AH Buchanan, FD Davis, WA Faucett, MLG Hallquist, ... Health Affairs 37 (5), 757-764, 2018 | 96 | 2018 |
| Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants AH Buchanan, K Manickam, MN Meyer, JK Wagner, MLG Hallquist, ... Genetics in Medicine 20 (5), 554-558, 2018 | 58 | 2018 |
| Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome … CM Haggerty, CA James, H Calkins, C Tichnell, JB Leader, DN Hartzel, ... Genetics in Medicine 19 (11), 1245-1252, 2017 | 52 | 2017 |
| Positive impact of genetic counseling assistants on genetic counseling efficiency, patient volume, and cost in a cancer genetics clinic MLG Hallquist, EP Tricou, MN Hallquist, JM Savatt, H Rocha, AE Evans, ... Genetics in Medicine 22 (8), 1348-1354, 2020 | 28 | 2020 |
| Clinical findings and diagnostic yield of arrhythmogenic cardiomyopathy through genomic screening of pathogenic or likely pathogenic desmosome gene variants ED Carruth, D Beer, A Alsaid, MLB Schwartz, M McMinn, MA Kelly, ... Circulation: Genomic and Precision Medicine 14 (2), e003302, 2021 | 17 | 2021 |
| Adding protective genetic variants to clinical reporting of genomic screening results: restoring balance MLB Schwartz, MS Williams, MF Murray Jama 317 (15), 1527-1528, 2017 | 15 | 2017 |
| Managing secondary genomic findings associated with arrhythmogenic right ventricular cardiomyopathy: case studies and proposal for clinical surveillance CM Haggerty, B Murray, C Tichnell, DP Judge, H Tandri, M Schwartz, ... Circulation: Genomic and Precision Medicine 11 (7), e002237, 2018 | 13 | 2018 |
| Generation and implementation of a patient-centered and patient-facing genomic test report in the EHR JM Goehringer, MA Bonhag, LK Jones, T Schmidlen, M Schwartz, ... eGEMs 6 (1), 2018 | 13 | 2018 |
| Exome sequencing-based screening for BRCA1/2 expected pathogenic variants among adult biobank participants. JAMA Netw Open. 2018; 1 (5): e182140 K Manickam, AH Buchanan, MLB Schwartz, MLG Hallquist, JL Williams, ... This reference emphasizes the potential role for expanded genetic testing in …, 2018 | 10 | 2018 |
| Genetic counseling for patients with positive genomic screening results: Considerations for when the genetic test comes first MLB Schwartz, AH Buchanan, MLG Hallquist, CM Haggerty, AC Sturm Journal of genetic counseling 30 (3), 634-644, 2021 | 9 | 2021 |
| Motivating cascade testing for familial hypercholesterolemia: applying the extended parallel process model for clinician communication G Campbell-Salome, NL Walters, IG Ladd, A Sheldon, CD Ahmed, ... Translational Behavioral Medicine 12 (7), 800-809, 2022 | 7 | 2022 |
| Testing and Management of Iron Overload After Genetic Screening–Identified Hemochromatosis JM Savatt, A Johns, MLB Schwartz, WS McDonald, ZM Salvati, NM Oritz, ... JAMA Network Open 6 (10), e2338995-e2338995, 2023 | 5 | 2023 |
| Adopted individuals’ interest in elective genomic testing J Edgar, A Bao, T Maga, M Schwartz, C Yates, S Spencer Journal of medical genetics 59 (2), 197-203, 2022 | 4 | 2022 |
| A model for genome-first care: returning secondary genomic findings to participants and their healthcare providers in a large research cohort MLB Schwartz, CZ McCormick, AL Lazzeri, DAM Lindbuchler, ... bioRxiv, 166975, 2017 | 4 | 2017 |
| Elective genomic testing: Practice resource of the National Society of Genetic Counselors CL Blout Zawatsky, D Bick, L Bier, B Funke, M Lebo, KL Lewis, E Orlova, ... Journal of Genetic Counseling 32 (2), 281-299, 2023 | 2 | 2023 |
| A Model for the Integration of Genome Sequencing Into a Pediatric Cardiology Clinic EJ Liston, KJ Kalbfleisch, KJ Stanley, RR Chaturvedi, I Cohn, ... The Canadian journal of cardiology 38 (9), 1454-1457, 2022 | 2 | 2022 |
