| 2020 |
Robinson M-E, Bardai G, Veilleux L-N, Glorieux FH, Rauch F. Musculoskeletal phenotype in two unrelated individuals with a recurrent nonsense variant in SGMS2. Bone. May 2020;134:115261. |
1 |
1 |
| 2021 |
Moffatt P, Boraschi-Diaz I, Bardai G, Rauch F. Muscle transcriptome in mouse models of osteogenesis imperfecta. Bone. July 2021;148:115940. |
0 |
0 |
| 2022 |
Ludwig K, Ward LM, Khan N, Robinson M-E, Miranda V, Bardai G, Moffatt P, Rauch F. Dominant osteogenesis imperfecta with low bone turnover caused by a heterozygous SP7 variant. Bone. July 2022;160:116400. |
1 |
1 |
| 2020 |
Manousaki D, Kämpe A, Forgetta V, Makitie RE, Bardai G, Belisle A, Li R, Andersson S, Makitie O, Rauch F, Richards JB. Increased burden of common risk alleles in children with a significant fracture history. J Bone Miner Res. May 2020;35(5):875-882. |
0 |
0 |
| 2023 |
Ludwig K, Wu Z, Bardai G, Mason P, Ward LM, Moffatt P, Rauch F. RNA sequencing of urine-derived cells for the characterization and diagnosis of osteogenesis imperfecta. J Bone Miner Res. August 2023;38(8):1125-1134. |
1 |
0 |