E-LIB Suche - Ergebnisse für: Lo, Ken Sin

1

Multimodal CRISPR perturbations of GWAS loci associated wit..:

Wünnemann, Florian ; Fotsing Tadjo, Thierry ; Beaudoin, Mélissa...
PLOS Genetics. 19 (2023) 3 - p. e1010680 , 2023

2

Variation and impact of polygenic hematologic traits in mon..:

Pincez, Thomas ; Lo, Ken Sin ; D'Orengiani, Anne-Laure Pham Hung d'Alexandry...
Haematologica. 108 (2022) 3 - p. 870-881 , 2022

Link: https://doi.org/10.3324/..

3

Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 7..:

Chen, Ming-Huei ; Raffield, Laura M. ; Mousas, Abdou...
Cell. 182 (2020) 5 - p. 1198-1213.e14 , 2020

Link: https://doi.org/10.1016/..

4

The Polygenic and Monogenic Basis of Blood Traits and Disea..:

Vuckovic, Dragana ; Bao, Erik L. ; Akbari, Parsa...
Cell. 182 (2020) 5 - p. 1214-1231.e11 , 2020

Link: https://doi.org/10.1016/..

5

Integrative analysis of vascular endothelial cell genomic f..:

Lalonde, Simon ; Codina-Fauteux, Valérie-Anne ; de Bellefon, Sébastian Méric...
Genome Biology. 20 (2019) 1 - p. , 2019

Link: https://doi.org/10.1186/..

6

Protein-coding variants implicate novel genes related to li..:

Justice, Anne E. ; Karaderi, Tugce ; Highland, Heather M....
Nature Genetics. 51 (2019) 3 - p. 452-469 , 2019

Link: https://doi.org/10.1038/..

7

Variants at theAPOE/C1/C2/C4Locus Modulate Cholesterol Effl..:

Low‐Kam, Cécile ; Rhainds, David ; Lo, Ken Sin...
Journal of the American Heart Association. 7 (2018) 16 - p. , 2018

Link: https://doi.org/10.1161/..

8

PHACTR1 splicing isoforms and eQTLs in atherosclerosis-rele..:

Codina-Fauteux, Valérie-Anne ; Beaudoin, Mélissa ; Lalonde, Simon..
BMC Medical Genetics. 19 (2018) 1 - p. , 2018

Link: https://doi.org/10.1186/..

9

Rare and low-frequency coding variants alter human adult he..:

Marouli, Eirini ; Graff, Mariaelisa ; Medina-Gomez, Carolina...
Nature. 542 (2017) 7640 - p. 186-190 , 2017

Link: https://doi.org/10.1038/..

10

Whole-genome sequencing in French Canadians from Quebec:

Low-Kam, Cécile ; Rhainds, David ; Lo, Ken Sin...
Human Genetics. 135 (2016) 11 - p. 1213-1221 , 2016

Link: https://doi.org/10.1007/..

11

Defining the role of common variation in the genomic and bi..:

The Electronic Medical Records and Genomics (eMERGE) Consortium ; Wood, Andrew R ; Esko, Tonu...
Nature Genetics. 46 (2014) 11 - p. 1173-1186 , 2014

Link: https://doi.org/10.1038/..

12

Rare and low-frequency coding variants in CXCR2 and other g..:

Auer, Paul L ; Teumer, Alexander ; Schick, Ursula...
Nature Genetics. 46 (2014) 6 - p. 629-634 , 2014

Link: https://doi.org/10.1038/..

13

Nonsense Mutations in BAG3 are Associated With Early-Onset ..:

Chami, Nathalie ; Tadros, Rafik ; Lemarbre, François...
Canadian Journal of Cardiology. 30 (2014) 12 - p. 1655-1661 , 2014

Link: https://doi.org/10.1016/..

14

Strategies to fine-map genetic associations with lipid leve..:

Lo, Ken Sin ; Vadlamudi, Swarooparani ; Fogarty, Marie P...
Genomics. 104 (2014) 2 - p. 105-112 , 2014

Link: https://doi.org/10.1016/..

15

Deep Resequencing of GWAS Loci Identifies Rare Variants in ..:

Beaudoin, Mélissa ; Goyette, Philippe ; Boucher, Gabrielle...
PLoS Genetics. 9 (2013) 9 - p. e1003723 , 2013

Link: https://doi.org/10.1371/..