| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S00439-016-1702-6 |
| P698 | PubMed publication ID | 27376640 |
| P50 | author | Jean-Claude Tardif | Q16244673 |
| Marie-Pierre Dubé | Q30002184 | ||
| Robert A. Hegele | Q58046422 | ||
| P2093 | author name string | Guillaume Lettre | |
| Ken Sin Lo | |||
| Sylvie Perreault | |||
| Cécile Low-Kam | |||
| David Rhainds | |||
| Ian Mongrain | |||
| Sylvie Provost | |||
| John F Robinson | |||
| Anick Dubois | |||
| Marie-Pierre Dubé | |||
| P2860 | cites work | An integrated map of genetic variation from 1,092 human genomes | Q22122153 |
| The NHGRI GWAS Catalog, a curated resource of SNP-trait associations | Q24568334 | ||
| A map of human genome variation from population-scale sequencing | Q24617794 | ||
| Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants | Q24645076 | ||
| A second generation human haplotype map of over 3.1 million SNPs | Q24651939 | ||
| Fast and accurate short read alignment with Burrows-Wheeler transform | Q24653853 | ||
| Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering | Q24655574 | ||
| PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
| The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data | Q27860742 | ||
| Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers | Q28267312 | ||
| Whole-genome sequence-based analysis of high-density lipoprotein cholesterol | Q28659476 | ||
| Discovery and refinement of loci associated with lipid levels | Q28661470 | ||
| Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease | Q29417023 | ||
| A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease | Q29417111 | ||
| Integrating common and rare genetic variation in diverse human populations | Q29547220 | ||
| A framework for variation discovery and genotyping using next-generation DNA sequencing data | Q29547262 | ||
| Admixed ancestry and stratification of Quebec regional populations | Q34163262 | ||
| A linear complexity phasing method for thousands of genomes | Q34237936 | ||
| Whole-genome sequence variation, population structure and demographic history of the Dutch population | Q34426935 | ||
| Human genetics: lessons from Quebec populations | Q34433453 | ||
| Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel | Q34461378 | ||
| Myocardial Infarction-Associated SNP at 6p24 Interferes With MEF2 Binding and Associates With PHACTR1 Expression Levels in Human Coronary Arteries | Q35637464 | ||
| Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs | Q35722160 | ||
| Height-reducing variants and selection for short stature in Sardinia | Q36232888 | ||
| Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels | Q36232895 | ||
| Large-scale association analysis identifies new risk loci for coronary artery disease | Q36921066 | ||
| Genome-wide patterns of identity-by-descent sharing in the French Canadian founder population | Q39670054 | ||
| Low-coverage sequencing: implications for design of complex trait association studies | Q42596059 | ||
| Genomic and genealogical investigation of the French Canadian founder population structure. | Q45985294 | ||
| Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm | Q47073320 | ||
| When Genetics and Genealogies Tell Different Stories-Maternal Lineages in Gaspesia | Q48766862 | ||
| Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians. | Q50606987 | ||
| Deep Human Genealogies Reveal a Selective Advantage to Be on an Expanding Wave Front | Q57197865 | ||
| Pooled DNA Resequencing of 68 Myocardial Infarction Candidate Genes in French Canadians | Q57239659 | ||
| The Saguenay-Lac-Saint-Jean asthma familial collection: the genetics of asthma in a young founder population | Q87473612 | ||
| P433 | issue | 11 | |
| P921 | main subject | whole genome sequencing | Q2068526 |
| P304 | page(s) | 1213-1221 | |
| P577 | publication date | 2016-07-04 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Whole-genome sequencing in French Canadians from Quebec | |
| P478 | volume | 135 |
| Q94581252 | Estimating Lactase Nonpersistence Distributions in the Multi-Ethnic Canadian Demographic: A Population-Based Study |
| Q56022528 | Genetic-Driven Druggable Target Identification and Validation |
| Q47327388 | Human genetic variation alters CRISPR-Cas9 on- and off-targeting specificity at therapeutically implicated loci |
| Q40061670 | Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels. |
| Q47121697 | Polygenic determinants in extremes of high-density lipoprotein cholesterol |
| Q50087966 | Population Stratification in Genetic Association Studies |
| Q92652358 | Validation of Genome-Wide Polygenic Risk Scores for Coronary Artery Disease in French Canadians |
| Q58129761 | Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol |
| Q64039959 | Whole-Exome Sequencing in the Isolated Populations of Cilento from South Italy |
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