| Evidence-based assessment of congenital heart disease genes to enable returning results in a genomic study EL Griffin, SN Nees, SU Morton, J Wynn, N Patel, V Jobanputra, ... Circulation: Genomic and Precision Medicine 16 (2), e003791, 2023 | 10 | 2023 |
| LHX2 haploinsufficiency causes a variable neurodevelopmental disorder CM Schmid, A Gregor, G Costain, CF Morel, L Massingham, J Schwab, ... Genetics in Medicine 25 (7), 100839, 2023 | 4 | 2023 |
| Impact of preheart transplant spirometry and DLCO measurement on post-transplant pulmonary outcomes A Tao, J Raikhelkar, L Benvenuto, VK Topkara, K Brenner, J Fried, ... The Journal of Heart and Lung Transplantation 42 (6), 819-827, 2023 | 1 | 2023 |
| De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features X Pan, AM Tao, S Lu, M Ma, SB Hannan, R Slaugh, SD Williams, ... The American Journal of Human Genetics 111 (4), 742-760, 2024 | | 2024 |
| LHX2 haploinsufficiency causes a variable neurodevelopmental disorder C Schmid, A Gregor, G Costain, C Morel, L Massingham, J Schwab, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 48-49, 2024 | | 2024 |
| Impact of Pre-Heart Transplant Pulmonary Function Tests on Post-Transplant Pulmonary Outcomes A Tao, J Raikhelkar, J Griffin, L Benvenuto, J Fried, V Topkara, K Takeda, ... The Journal of Heart and Lung Transplantation 41 (4), S323, 2022 | | 2022 |
