Researchers discover new gene variant causing inherited lung disease in Inuit
The newly discovered gene variant could contribute to high rates of Primary Ciliary Dyskinesia in Inuit populations
A genetic mutation found to cause chronic lung disease in indigenous children
A rare genetic mutation could explain why indigenous children have greatly increased rates of respiratory...
MUHC opens Quebec’s first multidisciplinary referral centre for endometriosis
EndoCARES offers state-of-the-art clinical care and will enhance basic, epidemiological and clinical research...
Giving children with brain-based developmental disabilities a voice in research
Creating real change for children and families: CIHR highlights the CHILD-BRIGHT Network
Too much pruning: A new study sheds light on how neurodegeneration occurs in the brain
A Montreal research team demonstrates how genetic mutations cause brain cell...
Endometriosis seems to increase the risk of preeclampsia
Findings of a new research study can help ensure that women with endometriosis who conceive spontaneously receive appropriate care
Picture a Scientist: the RI-MUHC marks International Women’s Day with film screening and discussion
A panel of RI-MUHC women scientists and allies discuss the roles of women in science
Loydie Jerome-Majewska receives the Anne McLaren Award
RI-MUHC researcher has shed light on genes responsible for human craniofacial syndromes and placental biology
Panel discussion at the RI-MUHC marks International Day of People Living with Disabilities
Experts and advocates joined the RI-MUHC community to discuss integrating people with disabilities into work...
RI-MUHC trainee wins best presentation award at the 2022 Congrès provincial de la recherche Mère-Enfant
Doctoral student Wajih Jawhar demonstrates that epigenetic...