Allele-Specific Chromatin Remodeling in the ZPBP2/GSDMB/ORMDL3 Locus Associated with the Risk of Asthma and Autoimmune Disease
Verlaan, Dominique J., Berlivet, Soizik, Hunninghake, Gary M., Madore, Anne-Marie, Larivière, Mathieu, Moussette, Sanny, Grundberg, Elin, Kwan, Tony, Ouimet, Manon, Ge, Bing, Hoberman, Rose, Swiatek, Marcin, Dias, Joana, Lam, Kevin C.L., Koka, Vonda, Harmsen, Eef, Soto-Quiros, Manuel, Avila, Lydiana, Celedón, Juan C., Weiss, Scott T., Dewar, Ken, Sinnett, Daniel, Laprise, Catherine, Raby, Benjamin A., Pastinen, Tomi, Naumova, Anna K.
Published in American journal of human genetics (11.09.2009)
Published in American journal of human genetics (11.09.2009)
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Journal Article
Global patterns of cis variation in human cells revealed by high-density allelic expression analysis
Lam, Kevin C L, Dewar, Ken, Harmsen, Eef, Kwan, Tony, Gagné, Vincent, Joly, Marie-Michele, Beaulieu, Patrick, Göring, Harald H H, Naumova, Anna K, Koka, Vonda, Verlaan, Dominique J, Graziani, Alexandru, Le, Jennie, Pastinen, Tomi, Harvey, Edward J, Pokholok, Dmitry K, Morcos, Lisanne, Sinnett, Daniel, Ge, Bing, Montpetit, Alexandre, Majewski, Jacek, Blanchette, Mathieu, Hoberman, Rose, Grundberg, Elin, Hamon, Robert, Gunderson, Kevin L, Dias, Joana
Published in Nature Genetics (01.11.2009)
Published in Nature Genetics (01.11.2009)
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Journal Article
Genome-wide assessment of imprinted expression in human cells
Morcos, Lisanne, Ge, Bing, Koka, Vonda, Lam, Kevin C L, Pokholok, Dmitry K, Gunderson, Kevin L, Montpetit, Alexandre, Verlaan, Dominique J, Pastinen, Tomi
Published in Genome biology (21.03.2011)
Published in Genome biology (21.03.2011)
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Journal Article
Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines
Berlivet, Soizik, Moussette, Sanny, Ouimet, Manon, Verlaan, Dominique J., Koka, Vonda, Al Tuwaijri, Abeer, Kwan, Tony, Sinnett, Daniel, Pastinen, Tomi, Naumova, Anna K.
Published in Human genetics (01.07.2012)
Published in Human genetics (01.07.2012)
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Journal Article
Population genomics in a disease targeted primary cell model
Grundberg, Elin, Kwan, Tony, Ge, Bing, Lam, Kevin C L, Koka, Vonda, Kindmark, Andreas, Mallmin, Hans, Dias, Joana, Verlaan, Dominique J, Ouimet, Manon, Sinnett, Daniel, Rivadeneira, Fernando, Estrada, Karol, Hofman, Albert, van Meurs, Joyce M, Uitterlinden, André, Beaulieu, Patrick, Graziani, Alexandru, Harmsen, Eef, Ljunggren, Osten, Ohlsson, Claes, Mellström, Dan, Karlsson, Magnus K, Nilsson, Olle, Pastinen, Tomi
Published in Genome research (01.11.2009)
Published in Genome research (01.11.2009)
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Journal Article
Targeted screening of cis-regulatory variation in human haplotypes
Verlaan, Dominique J, Ge, Bing, Grundberg, Elin, Hoberman, Rose, Lam, Kevin C L, Koka, Vonda, Dias, Joana, Gurd, Scott, Martin, Nicolas W, Mallmin, Hans, Nilsson, Olof, Harmsen, Eef, Dewar, Ken, Kwan, Tony, Pastinen, Tomi
Published in Genome Research (01.01.2009)
Published in Genome Research (01.01.2009)
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Journal Article
Mutations in a Gene Encoding a Novel Protein Containing a Phosphotyrosine-Binding Domain Cause Type 2 Cerebral Cavernous Malformations
Liquori, Christina L., Berg, Michel J., Siegel, Adrian M., Huang, Elizabeth, Zawistowski, Jon S., Stoffer, T’Prien, Verlaan, Dominique, Balogun, Fiyinfolu, Hughes, Lori, Leedom, Tracey P., Plummer, Nicholas W., Cannella, Milena, Maglione, Vittorio, Squitieri, Ferdinando, Johnson, Eric W., Rouleau, Guy A., Ptacek, Louis, Marchuk, Douglas A.
Published in American journal of human genetics (01.12.2003)
Published in American journal of human genetics (01.12.2003)
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Journal Article
Promoter polymorphisms in CHI3L1 are associated with asthma
Verlaan, Dominique J., PhD, Ouimet, Manon, MSc, Adoue, Veronique, MSc, Sirois-Gagnon, Dave, MSc, Larivière, Mathieu, MSc, Ge, Bing, MSc, Beaulieu, Patrick, MSc, Dias, Joana, MEng, Lam, Kevin C.L., MSc, Koka, Vonda, MSc, Laprise, Catherine, PhD, Pastinen, Tomi, MD, PhD, Sinnett, Daniel, PhD
Published in Journal of allergy and clinical immunology (01.08.2012)
Published in Journal of allergy and clinical immunology (01.08.2012)
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Journal Article
A probabilistic approach for SNP discovery in high-throughput human resequencing data
Hoberman, Rose, Dias, Joana, Ge, Bing, Harmsen, Eef, Mayhew, Michael, Verlaan, Dominique J, Kwan, Tony, Dewar, Ken, Blanchette, Mathieu, Pastinen, Tomi
Published in Genome Research (01.09.2009)
Published in Genome Research (01.09.2009)
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Journal Article
A cis-Acting Regulatory Variant in the IL2RA Locus
Qu, Hui-Qi, Verlaan, Dominique J, Ge, Bing, Lu, Yang, Lam, Kevin C. L, Grabs, Rosemarie, Harmsen, Eef, Hudson, Thomas J, Hakonarson, Hakon, Pastinen, Tomi, Polychronakos, Constantin
Published in The Journal of immunology (1950) (15.10.2009)
Published in The Journal of immunology (1950) (15.10.2009)
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Journal Article
The 14q restless legs syndrome locus in the French Canadian population
Levchenko, Anastasia, Montplaisir, Jacques-Yves, Dubé, Marie-Pierre, Riviere, Jean-Baptiste, St-Onge, Judith, Turecki, Gustavo, Xiong, Lan, Thibodeau, Pascale, Desautels, Alex, Verlaan, Dominique J., Rouleau, Guy A.
Published in Annals of neurology (01.06.2004)
Published in Annals of neurology (01.06.2004)
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Journal Article
A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family
Rivière, Jean-Baptiste, Verlaan, Dominique J., Shekarabi, Masoud, Lafrenière, Ronald G., Bénard, Mélanie, Der Kaloustian, Vazken M., Shbaklo, Zuhayr, Rouleau, Guy A.
Published in Annals of neurology (01.10.2004)
Published in Annals of neurology (01.10.2004)
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Journal Article
Krit1 Missense Mutations Lead to Splicing Errors in Cerebral Cavernous Malformation
Verlaan, Dominique J., Siegel, Adrian M., Rouleau, Guy A.
Published in American journal of human genetics (01.06.2002)
Published in American journal of human genetics (01.06.2002)
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Journal Article
CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations
Verlaan, Dominique J., Laurent, Sandra B., Rochefort, Daniel L., Liquori, Christina L., Marchuk, Douglas A., Siegel, Adrian M., Rouleau, Guy A.
Published in Annals of neurology (01.05.2004)
Published in Annals of neurology (01.05.2004)
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Journal Article
A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11
Kinirons, Peter, Verlaan, Dominique J., Dubé, Marie-Pierre, Poirier, Josée, Deacon, Charles, Lortie, Anne, Clément, Jean-François, Desbiens, Richard, Carmant, Lionel, Cieuta-Walti, Cecile, Shevell, Michael, Rouleau, Guy A., Cossette, Patrick
Published in American journal of medical genetics. Part A (01.03.2008)
Published in American journal of medical genetics. Part A (01.03.2008)
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Journal Article
A Novel Duplication Confirms the Involvement of 5q23.2 in Autosomal Dominant Leukodystrophy
Meijer, Inge A, Simoes-Lopes, Ana A, Laurent, Sandra, Katz, Tanya, St-Onge, Judith, Verlaan, Dominique J, Dupré, Nicolas, Thibault, Manon, Mathurin, Johanne, Bouchard, Jean-Pierre, Rouleau, Guy A
Published in Archives of neurology (Chicago) (01.11.2008)
Published in Archives of neurology (Chicago) (01.11.2008)
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Journal Article
Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation
Dupré, Nicolas, Verlaan, Dominique J, Hand, Collette K, Laurent, Sandra B, Turecki, Gustavo, Davenport, W Jeptha, Acciarri, Nicola, Dichgans, Johannes, Ohkuma, Akio, Siegel, Adrian M, Rouleau, Guy A
Published in Canadian journal of neurological sciences (01.05.2003)
Published in Canadian journal of neurological sciences (01.05.2003)
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