| Genetics of congenital heart disease K Williams, J Carson, C Lo Biomolecules 9 (12), 879, 2019 | 166 | 2019 |
| Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease P Teekakirikul, W Zhu, GC Gabriel, CB Young, K Williams, LJ Martin, ... Human Genetics and Genomics Advances 2 (3), 2021 | 15 | 2021 |
| Rare and Common Variants Uncover the Role of the Atria in Coarctation of the Aorta W Zhu, K Williams, C Young, JH Lin, P Teekakirikul, CW Lo Genes 13 (4), 636, 2022 | 6 | 2022 |
| Contribution of LRP1 in Human Congenital Heart Disease Correlates with Its Roles in the Outflow Tract and Atrioventricular Cushion Development AB Arrigo, W Zhu, KA Williams, C Guzman-Moreno, C Lo, JHI Lin Genes 14 (4), 947, 2023 | | 2023 |
| Ciliary genes contribute to a complex genetic model of congenital heart disease KA Williams University of Pittsburgh, 2021 | | 2021 |
| A Rare MEGF8 Variant is Involved in the Genetic Risk for Transposition of the Great Arteries A Moreau de Bellaing, K Williams, S Li, AS Bais, CB Young, CW Lo Circulation 138 (Suppl_1), A16615-A16615, 2018 | | 2018 |
