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Camille Tremblay‐Laganière

Observed names: Camille Tremblay-Laganiere, Camille Tremblay-Laganière, Tremblay-Laganière, Camille
Observed institutions: University of Ottawa, Centre Hospitalier Universitaire Sainte-Justine, Hôpital Maisonneuve-Rosemont, Institut du Savoir Montfort, CHU Sainte-Justine Research Center, Université de Montréal
ORCID: 0009-0000-8337-2122
Observed ORCID: 0009-0000-8337-2122
OpenAlex ID: A5006752387
Efficient and Robust NK-Cell Transduction With Baboon Envelope Pseudotyped Lentivector
2019 · Aurelien B.L. Colamartino, William Lemieux, et al. · Frontiers in Immunology · 187
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Polychlorinated biphenyl 126 exposure in rats alters skeletal muscle mitochondrial function
2018 · Camille Tremblay-Laganière, Léa Garneau, et al. · Environmental Science and Pollution Research · 20
PIGG variant pathogenicity assessment reveals characteristic features within 19 families
2021 · Camille Tremblay-Laganière, Reza Maroofian, et al. · Genetics in Medicine · 13
PIGH deficiency can be associated with severe neurodevelopmental and skeletal manifestations
2020 · Camille Tremblay‐Laganière, Rauan Kaiyrzhanov, et al. · Clinical Genetics · 10
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Generation of functional human T cell development in NOD/SCID/IL2rγnull humanized mice without using fetal tissue: Application as a model of HIV infection and persistence
2023 · Chloé Colas, Olga Volodina, et al. · Stem Cell Reports · 8
A New Specific Promoter Allow Hematopoietic Stem Cell Immunotherapy Approach Against Acute Lymphoblastic Leukemia Using Chimeric Antigen Receptor
2019 · Aurelien Colamartino, Panojot Bifsha, et al. · Transplantation and Cellular Therapy · 4
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Homozygous variant in TKFC abolishing triokinase activities is associated with isolated immunodeficiency
2024 · Camille Tremblay-Laganière, Coralie Michaud, et al. · Journal of Medical Genetics · 3
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A Complex Arrhythmic Phenotype in a Pediatric Patient with Variants in SCN5A and KCNH2
2026 · David Bienjonetti-Boudreau, Camille Tremblay-Laganiere, et al. · Genes
Rapidly Expanded EBV-Specific T Cells for the Treatment of Refractory EBV Reactivation and EBV-Related Lymphoproliferative Disorders
2025 · Lorne Schweitzer, Stéphanie Thiant, et al. · Open Forum Infectious Diseases
P332: A homozygous POU3F2 polyproline tract expansion is associated with severe psychomotor delay, developmental and epileptic encephalopathy, and ichthyosis
2023 · Camille Tremblay-Laganière, Sophie Ehresmann, et al. · Genetics in Medicine Open
Author response for " PIGH deficiency can be associated with severe neurodevelopmental and skeletal manifestations"
2020 · Camille Tremblay‐Laganière, Rauan Kaiyrzhanov, et al.
Thérapie génique ciblant CD33 dans les cellules souches hématopoïétiques, une approche innovatrice pour le traitement de la leucémie myéloïde aiguë
2018 · Tremblay-Laganière, Camille
Works count: 13
Citation count: 245
H-index: 5
I10-index: 4
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