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Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol.
Published in:
2018
By:
- Low-Kam, Cécile;
- Rhainds, David;
- Ken Sin Lo;
- Barhdadi, Amina;
- Boulé, Marie;
- Alem, Sonia;
- Pedneault-Gagnon, Valérie;
- Rhéaume, Eric;
- Dubé, Marie-Pierre;
- Busseuil, David;
- Hegele, Robert A.;
- Lettre, Guillaume;
- Tardif, Jean-Claude;
- Lo, Ken Sin
Publication type:
journal article
Discovery of anti-Formin-like 1 protein (FMNL1) antibodies in membranous nephropathy and other glomerular diseases.
Published in:
Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-17696-w
By:
- Bruschi, Maurizio;
- Cavalli, Andrea;
- Moll, Solange;
- Candiano, Giovanni;
- Scapozza, Leonardo;
- Patel, Jigar J.;
- Tan, John C.;
- Lo, Ken C.;
- Angeletti, Andrea;
- Ghiggeri, Gian Marco;
- Prunotto, Marco
Publication type:
Article
Proteome-wide identification of poly(ADP-ribose) binding proteins and poly(ADP-ribose)-associated protein complexes.
Published in:
Nucleic Acids Research, 2008, v. 36, n. 22, p. 6959, doi. 10.1093/nar/gkn771
By:
- Gagné, Jean-Philippe;
- Isabelle, Maxim;
- Lo, Ken Sin;
- Bourassa, Sylvie;
- Hendzel, Michael J.;
- Dawson, Valina L.;
- Dawson, Ted M.;
- Poirier, Guy G.
Publication type:
Article
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
Published in:
Nature Genetics, 2014, v. 46, n. 6, p. 629, doi. 10.1038/ng.2962
By:
- Auer, Paul L;
- Teumer, Alexander;
- Schick, Ursula;
- O'Shaughnessy, Andrew;
- Lo, Ken Sin;
- Chami, Nathalie;
- Carlson, Chris;
- de Denus, Simon;
- Dubé, Marie-Pierre;
- Haessler, Jeff;
- Jackson, Rebecca D;
- Kooperberg, Charles;
- Perreault, Louis-Philippe Lemieux;
- Nauck, Matthias;
- Peters, Ulrike;
- Rioux, John D;
- Schmidt, Frank;
- Turcot, Valérie;
- Völker, Uwe;
- Völzke, Henry
Publication type:
Article
<italic>PHACTR1</italic> splicing isoforms and eQTLs in atherosclerosis-relevant human cells.
Published in:
BMC Medical Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12881-018-0616-7
By:
- Codina-Fauteux, Valérie-Anne;
- Beaudoin, Mélissa;
- Lalonde, Simon;
- Lo, Ken Sin;
- Lettre, Guillaume
Publication type:
Article
Global Carbon Cycle and Climate Feedbacks in the NASA GISS ModelE2.1.
Published in:
Journal of Advances in Modeling Earth Systems, 2020, v. 12, n. 10, p. 1, doi. 10.1029/2019MS002030
By:
- Ito, Gen;
- Romanou, Anastasia;
- Kiang, Nancy Y.;
- Faluvegi, Gregory;
- Aleinov, Igor;
- Ruedy, Reto;
- Russell, Gary;
- Lerner, Paul;
- Kelley, Maxwell;
- Lo, Ken
Publication type:
Article
Historical (1850–2014) Aerosol Evolution and Role on Climate Forcing Using the GISS ModelE2.1 Contribution to CMIP6.
Published in:
Journal of Advances in Modeling Earth Systems, 2020, v. 12, n. 8, p. 1, doi. 10.1029/2019MS001978
By:
- Bauer, Susanne E.;
- Tsigaridis, Kostas;
- Faluvegi, Greg;
- Kelley, Maxwell;
- Lo, Ken K.;
- Miller, Ron L.;
- Nazarenko, Larissa;
- Schmidt, Gavin A.;
- Wu, Jingbo
Publication type:
Article
CMIP5 historical simulations (1850-2012) with GISS ModelE2.
Published in:
Journal of Advances in Modeling Earth Systems, 2014, v. 6, n. 2, p. 441, doi. 10.1002/2013MS000266
By:
- Miller, Ron L.;
- Schmidt, Gavin A.;
- Nazarenko, Larissa S.;
- Tausnev, Nick;
- Bauer, Susanne E.;
- DelGenio, Anthony D.;
- Kelley, Max;
- Lo, Ken K.;
- Ruedy, Reto;
- Shindell, Drew T.;
- Aleinov, Igor;
- Bauer, Mike;
- Bleck, Rainer;
- Canuto, Vittorio;
- Chen, Yonghua;
- Cheng, Ye;
- Clune, Thomas L.;
- Faluvegi, Greg;
- Hansen, James E.;
- Healy, Richard J.
Publication type:
Article
Whole-genome sequencing in French Canadians from Quebec.
Published in:
Human Genetics, 2016, v. 135, n. 11, p. 1213, doi. 10.1007/s00439-016-1702-6
By:
- Low-Kam, Cécile;
- Rhainds, David;
- Lo, Ken;
- Provost, Sylvie;
- Mongrain, Ian;
- Dubois, Anick;
- Perreault, Sylvie;
- Robinson, John;
- Hegele, Robert;
- Dubé, Marie-Pierre;
- Tardif, Jean-Claude;
- Lettre, Guillaume
Publication type:
Article
Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.
Published in:
Human Genetics, 2011, v. 129, n. 3, p. 307, doi. 10.1007/s00439-010-0925-1
By:
- Lo, Ken Sin;
- Wilson, James G.;
- Lange, Leslie A.;
- Folsom, Aaron R.;
- Galarneau, Geneviève;
- Ganesh, Santhi K.;
- Grant, Struan F. A.;
- Keating, Brendan J.;
- McCarroll, Steven A.;
- Mohler III, Emile R.;
- O'Donnell, Christopher J.;
- Palmas, Walter;
- Weihong Tang;
- Tracy, Russell P.;
- Reiner, Alexander P.;
- Lettre, Guillaume
Publication type:
Article
Optimus Primer: A PCR enrichment primer designprogram for next-generation sequencing ofhuman exonic regions.
Published in:
BMC Research Notes, 2010, v. 3, p. 185, doi. 10.1186/1756-0500-3-185
By:
- Brown, Andrew M. K.;
- Ken Sin Lo;
- Guelpa, Paul;
- Beaudoin, Mélissa;
- Rioux, John D.;
- Tardif, Jean-Claude;
- Phillips, Michael S.;
- Lettre, Guillaume
Publication type:
Article
Genome Wide Copy Number Abnormalities in Pediatric Medulloblastomas as Assessed by Array Comparative Genome Hybridization.
Published in:
Brain Pathology, 2007, v. 17, n. 3, p. 282, doi. 10.1111/j.1750-3639.2007.00072.x
By:
- Lo, Ken C.;
- Rossi, Michael R.;
- Eberhart, Charles G.;
- Cowell, John K.
Publication type:
Article
Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization.
Published in:
Genes, Chromosomes & Cancer, 2008, v. 47, n. 3, p. 221, doi. 10.1002/gcc.20524
By:
- Lo, Ken C.;
- Bailey, Dione;
- Burkhardt, Tania;
- Gardina, Paul;
- Turpaz, Yaron;
- Cowell, John K.
Publication type:
Article
Candidate glioblastoma development gene identification using concordance between copy number abnormalities and gene expression level changes.
Published in:
Genes, Chromosomes & Cancer, 2007, v. 46, n. 10, p. 875, doi. 10.1002/gcc.20474
By:
- Lo, Ken C.;
- Rossi, Michael R.;
- LaDuca, Jeffrey;
- Hicks, David G.;
- Turpaz, Yaron;
- Hawthorn, Lesleyann;
- Cowell, John K.
Publication type:
Article
Overlay analysis of the oligonucleotide array gene expression profiles and copy number abnormalities as determined by array comparative genomic hybridization in medulloblastomas.
Published in:
Genes, Chromosomes & Cancer, 2007, v. 46, n. 1, p. 53, doi. 10.1002/gcc.20388
By:
- Ken C. Lo;
- Michael R. Rossi;
- Tania Burkhardt;
- Scott L. Pomeroy;
- John K. Cowell
Publication type:
Article
Epigenetic mechanisms underlying arsenic-associated lung carcinogenesis.
Published in:
Archives of Toxicology, 2015, v. 89, n. 11, p. 1959, doi. 10.1007/s00204-014-1351-2
By:
- Breda, Simone;
- Claessen, Sandra;
- Lo, Ken;
- Herwijnen, Marcel;
- Brauers, Karen;
- Lisanti, Sofia;
- Theunissen, Daniël;
- Jennen, Danyel;
- Gaj, Stan;
- Kok, Theo;
- Kleinjans, Jos
Publication type:
Article
Comprehensive Profiling of the Rheumatoid Arthritis Antibody Repertoire.
Published in:
Arthritis & Rheumatology, 2020, v. 72, n. 2, p. 242, doi. 10.1002/art.41089
By:
- Lo, Ken C.;
- Sullivan, Eric;
- Bannen, Ryan M.;
- Jin, Huiyan;
- Rowe, Mark;
- Li, Hanying;
- Pinapati, Richard S.;
- Cartwright, Adam J.;
- Tan, John C.;
- Patel, Jigar;
- Keystone, Edward C.;
- Siminovitch, Katherine A.
Publication type:
Article
Array comparative genome hybridization analysis of acute lymphoblastic leukaemia and acute megakaryoblastic leukaemia in patients with Down syndrome.
Published in:
British Journal of Haematology, 2008, v. 142, n. 6, p. 934, doi. 10.1111/j.1365-2141.2008.07280.x
By:
- Lo, Ken C.;
- Chalker, Jane;
- Strehl, Sabine;
- Neat, Michael;
- Smith, Owen;
- Dastugue, Nicole;
- Kearney, Lyndal;
- Izraeli, Shai;
- Kempski, Helena;
- Cowell, John K.
Publication type:
Article
Deep Resequencing of GWAS Loci Identifies Rare Variants in CARD9, IL23R and RNF186 That Are Associated with Ulcerative Colitis.
Published in:
PLoS Genetics, 2013, v. 9, n. 9, p. 1, doi. 10.1371/journal.pgen.1003723
By:
- Beaudoin, Mélissa;
- Goyette, Philippe;
- Boucher, Gabrielle;
- Lo, Ken Sin;
- Rivas, Manuel A.;
- Stevens, Christine;
- Alikashani, Azadeh;
- Ladouceur, Martin;
- Ellinghaus, David;
- Törkvist, Leif;
- Goel, Gautam;
- Lagacé, Caroline;
- Annese, Vito;
- Bitton, Alain;
- Begun, Jakob;
- Brant, Steve R.;
- Bresso, Francesca;
- Cho, Judy H.;
- Duerr, Richard H.;
- Halfvarson, Jonas
Publication type:
Article
Integrative analysis of vascular endothelial cell genomic features identifies AIDA as a coronary artery disease candidate gene.
Published in:
Genome Biology, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s13059-019-1749-5
By:
- Lalonde, Simon;
- Codina-Fauteux, Valérie-Anne;
- de Bellefon, Sébastian Méric;
- Leblanc, Francis;
- Beaudoin, Mélissa;
- Simon, Marie-Michelle;
- Dali, Rola;
- Kwan, Tony;
- Lo, Ken Sin;
- Pastinen, Tomi;
- Lettre, Guillaume
Publication type:
Article
Multimodal CRISPR perturbations of GWAS loci associated with coronary artery disease in vascular endothelial cells.
Published in:
PLoS Genetics, 2023, v. 18, n. 3, p. 1, doi. 10.1371/journal.pgen.1010680
By:
- Wünnemann, Florian;
- Fotsing Tadjo, Thierry;
- Beaudoin, Mélissa;
- Lalonde, Simon;
- Lo, Ken Sin;
- Kleinstiver, Benjamin P.;
- Lettre, Guillaume
Publication type:
Article

Found: 21

Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol.

Discovery of anti-Formin-like 1 protein (FMNL1) antibodies in membranous nephropathy and other glomerular diseases.

Proteome-wide identification of poly(ADP-ribose) binding proteins and poly(ADP-ribose)-associated protein complexes.

Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.

<italic>PHACTR1</italic> splicing isoforms and eQTLs in atherosclerosis-relevant human cells.

Global Carbon Cycle and Climate Feedbacks in the NASA GISS ModelE2.1.

Historical (1850–2014) Aerosol Evolution and Role on Climate Forcing Using the GISS ModelE2.1 Contribution to CMIP6.

CMIP5 historical simulations (1850-2012) with GISS ModelE2.

Whole-genome sequencing in French Canadians from Quebec.

Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.

Optimus Primer: A PCR enrichment primer designprogram for next-generation sequencing ofhuman exonic regions.

Genome Wide Copy Number Abnormalities in Pediatric Medulloblastomas as Assessed by Array Comparative Genome Hybridization.

Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization.

Candidate glioblastoma development gene identification using concordance between copy number abnormalities and gene expression level changes.

Overlay analysis of the oligonucleotide array gene expression profiles and copy number abnormalities as determined by array comparative genomic hybridization in medulloblastomas.

Epigenetic mechanisms underlying arsenic-associated lung carcinogenesis.

Comprehensive Profiling of the Rheumatoid Arthritis Antibody Repertoire.

Array comparative genome hybridization analysis of acute lymphoblastic leukaemia and acute megakaryoblastic leukaemia in patients with Down syndrome.

Deep Resequencing of GWAS Loci Identifies Rare Variants in <i>CARD9</i>, <i>IL23R</i> and <i>RNF186</i> That Are Associated with Ulcerative Colitis.

Integrative analysis of vascular endothelial cell genomic features identifies AIDA as a coronary artery disease candidate gene.

Multimodal CRISPR perturbations of GWAS loci associated with coronary artery disease in vascular endothelial cells.