Search

Your search keyword '"Montpetit, Alexandre"' showing total 391 results

Search Constraints

Start Over You searched for: Author "Montpetit, Alexandre" Remove constraint Author: "Montpetit, Alexandre"
391 results on '"Montpetit, Alexandre"'

Search Results

1. Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors

2. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

3. Deciphering a novel complex inversion affecting F8 in a family with severe haemophilia A by optical genome mapping

4. A second update on mapping the human genetic architecture of COVID-19

5. Publisher Correction: Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer

6. H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis

7. Molecular subgroups of atypical teratoid rhabdoid tumours in children: an integrated genomic and clinicopathological analysis

9. Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer

12. Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas

14. The Biobanque québécoise de la COVID-19 (BQC19)—A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectories

15. K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas

16. Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

18. Analyses of associations with asthma in four asthma population samples from Canada and Australia

21. HLA class I alleles tag HLA-DRBI*1501 haplotypes for differential risk in multiple sclerosis susceptibility

23. Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between Endothelin-1 and high density lipoprotein cholesterol

24. Genetic variants of FTO influence adiposity, insulin sensitivity, leptin levels, and resting metabolic rate in the Quebec family study

25. A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients

27. Susceptibility to leprosy is associated with PARK2 and PACRG

28. Genetic Information and the Prediction of Incident Type 2 Diabetes in a High-Risk Multiethnic Population: The EpiDREAM genetic study

30. The International HapMap Project

41. A genome-wide association study identifies novel risk loci for type 2 diabetes

46. Integrative genomic analysis of matched primary and metastatic pediatric osteosarcoma

47. Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation

48. The Biobanque québécoise de la COVID-19 (BQC19)—A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectories.

49. Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation

50. Analysis of the conservation of synteny between Fugu and human chromosome 12

Catalog

Books, media, physical & digital resources