Here is a list of publications by RARE.Qc members over the past few weeks.
Articles:
- Daniela Buhas & Geneviève Bernard: Long-read sequencing & TANGO2 deficiency
- Krista L Best: Manual wheelchair training & Knowledge translation
- Anne-Laure Lapeyraque & Alexandra Cambier: Immunoglobulin Profiling in Complement-mediated diseases
- François Dragon & Laurent Cappadocia: SLY1 expression in E. coli
- Michel Cayouette: Cone plasticity
- Noémi Dahan-Oliel: Arthrogryposis multiplex congenita
- Frank Rauch & Noémi Dahan-Oliel : Arthrogryposis multiplex congenita
- Simon Décary: Musculoskeletal disorders & Self-Management
- Thomas M. Durcan: α-Synuclein aggregates screening
- Maria Helena Fernandes: Osseointegration & Implant biomaterials
- Stéphanie Forté: Transcranial Doppler in Sickle Cell Disease
- Anne-Marie Laberge : Utility in Health Technology Assessments
- Ian M. MacDonald: Choroideremia & Novel mutations
- Jean-Paul Makhzoum: Guselkumab trial in Giant cell arteritis
- Kenneth A. Myers: 2q24.3 duplications & Epilepsy
- Kenneth A Myers: Ring chromosome 20 syndrome
- Elena Netchiporouk: Systemic sclerosis
- Thomas Pincez : Sickle cell disease
- Constantin Polychronakos: Machine learning & Type 1 diabetes classification
- Marc Pouliot: Neutrophil FcγRI & oxidative responses
- Guy A. Rouleau: Dentists & Recognition of neurodegenerative conditions
- Guy A. Rouleau : Essential tremors
- François Routhier: Universal accessibility
- Adam J. Shapiro : Primary Ciliary Dyskinesia in children
- Daniel Charouf, David S Rosenblatt & Myriam Srour: Posterior fossa malformations
- Jacques P. Tremblay : Mouse model for dysferlinopathy
- Sasha Bernatsky & Évelyne Vinet: Intrahepatic Cholestasis of Pregnancy & Systemic Lupus Erythematosus
- Hugo Wurtele: AI tool for DNA fiber analysis