| GATA 5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient K Kassab, H Hariri, L Gharibeh, AC Fahed, M Zein, I El‐Rassy, M Nemer, ... Molecular Genetics & Genomic Medicine 4 (2), 160-171, 2016 | 31 | 2016 |
| Lrp6 is a target of the PTH-activated αNAC transcriptional coregulator M Pellicelli, H Hariri, JA Miller, R St-Arnaud Biochimica et Biophysica Acta (BBA)-Gene Regulatory Mechanisms 1861 (2), 61-71, 2018 | 18 | 2018 |
| A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the … A Khalil, C Al-Haddad, H Hariri, K Shibbani, F Bitar, M Kurban, G Nemer, ... Frontiers in Cardiovascular Medicine 4, 58, 2017 | 16 | 2017 |
| Ubiquitin specific peptidase Usp53 regulates osteoblast versus adipocyte lineage commitment H Hariri, WN Addison, R St-Arnaud Scientific reports 11 (1), 8418, 2021 | 13 | 2021 |
| Expression and role of ubiquitin-specific peptidases in osteoblasts H Hariri, R St-Arnaud International Journal of Molecular Sciences 22 (14), 7746, 2021 | 10 | 2021 |
| Nfil3, a target of the NACA transcriptional coregulator, affects osteoblast and osteocyte gene expression differentially H Hariri, M Pellicelli, R St-Arnaud Bone 141, 115624, 2020 | 10 | 2020 |
| USP53 regulates bone homeostasis by controlling rankl expression in osteoblasts and bone marrow adipocytes H Hariri, O Kose, A Bezdjian, SJ Daniel, R St‐Arnaud Journal of Bone and Mineral Research 38 (4), 578-596, 2020 | 9 | 2020 |
| New PTH signals mediating bone anabolism H Hariri, M Pellicelli, R St-Arnaud Current Molecular Biology Reports 3, 133-141, 2017 | 9 | 2017 |
| Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis H Hariri, M Kurban, C Al-Haddad, AC Fahed, S Poladian, A Khalil, ... Journal of Dermatological Science 92 (3), 237-244, 2018 | 5 | 2018 |
| P329 GATA5: a key player in congenital heart diseases. K Kassab, H Hariri, A Fahed, I El-Rassi, F Bitar, G Nemer Cardiovascular Research 103, 2014 | 1 | 2014 |
| Deficiency of glucocorticoid receptor in bone marrow adipocytes has mild effects on bone and hematopoiesis but does not influence expansion of marrow adiposity with caloric … RL Schill, J Visser, ML Ashby, Z Li, KT Lewis, A Morales-Hernandez, ... Frontiers in Endocrinology 15, 1397081, 2024 | | 2024 |
| Identification of novel target genes of the parathyroid hormone-activated NACA transcriptional coregulator in bone H Hariri McGill University, 2020 | | 2020 |
| Identification of Novel Target Genes of the PTH-Activated NACA Transcriptional Coregulator in Bone HM Hariri McGill University (Canada), 2020 | | 2020 |
| Usp53, a PTH target regulating cell lineage fate and bone turnover H Hariri, M Pellicelli, R St-Arnaud JOURNAL OF BONE AND MINERAL RESEARCH 34, 85-85, 2019 | | 2019 |
| Usp53, a novel target gene of the PTH-activated alpha NAC transcriptional coregulator. H Hariri, W Addison, M Pellicelli, R St-Arnaud JOURNAL OF BONE AND MINERAL RESEARCH 32, S340-S341, 2017 | | 2017 |
| P569 A novel role for NFATC1 in patients with both congenital heart disease and glaucoma. H Hariri, T Farhat, R Khalaf, A Fahed, C Al-Haddad, M Arabi, F Bitar, ... Cardiovascular Research 103, 2014 | | 2014 |
| A novel role for NFATC1 gene in patients with both congenital heart diseases and eye defects HM Hariri Theses, Dissertations, and Projects, 2014 | | 2014 |
