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Patrick Danoy

Showing results (1-10 of 27) with videos related to

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Biochemical and Biophysical Research Communications|December 5, 2006
A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damagePatrick Danoy, Eiichiro Sonoda, Mark Lathrop, et al.
G3 (Bethesda, Md.)|January 15, 2013
Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samplesLei Jiang, Dana Willner, Patrick Danoy, et al.
American Journal of Medical Genetics|July 13, 2002
SNPs in the CpG island of NAP1L2: a possible link between DNA methylation and neural tube defects?Ute Christine Rogner, Patrick Danoy, Fumihiko Matsuda, et al.
Carcinogenesis|May 12, 2007
Polymorphism discovery in 62 DNA repair genes and haplotype associations with risks for lung and head and neck cancersStefan Michiels, Patrick Danoy, Philippe Dessen, et al.
International Journal of Cancer|May 2, 2008
Variants in DNA double-strand break repair and DNA damage-response genes and susceptibility to lung and head and neck cancersPatrick Danoy, Stefan Michiels, Philippe Dessen, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 5, 2010
Saliva-derived DNA performs well in large-scale, high-density single-nucleotide polymorphism microarray studiesMelanie Bahlo, Jim Stankovich, Patrick Danoy, et al.
Annals of the Rheumatic Diseases|July 26, 2011
Association of variants in MMEL1 and CTLA4 with rheumatoid arthritis in the Han Chinese populationPatrick Danoy, Meng Wei, Hadler Johanna, et al.
Ophthalmology|April 24, 2012
Glaucoma risk alleles at CDKN2B-AS1 are associated with lower intraocular pressure, normal-tension glaucoma, and advanced glaucomaKathryn P Burdon, April Crawford, Robert J Casson, et al.
Human Genetics|October 27, 2010
Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21Sian E Piret, Patrick Danoy, Karin Dahan, et al.
Plos Genetics|December 15, 2010
Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's diseasePatrick Danoy, Karena Pryce, Johanna Hadler, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Biochemical and Biophysical Research Communications|December 5, 2006
A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damagePatrick Danoy, Eiichiro Sonoda, Mark Lathrop, et al.
G3 (Bethesda, Md.)|January 15, 2013
Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samplesLei Jiang, Dana Willner, Patrick Danoy, et al.
American Journal of Medical Genetics|July 13, 2002
SNPs in the CpG island of NAP1L2: a possible link between DNA methylation and neural tube defects?Ute Christine Rogner, Patrick Danoy, Fumihiko Matsuda, et al.
Carcinogenesis|May 12, 2007
Polymorphism discovery in 62 DNA repair genes and haplotype associations with risks for lung and head and neck cancersStefan Michiels, Patrick Danoy, Philippe Dessen, et al.
International Journal of Cancer|May 2, 2008
Variants in DNA double-strand break repair and DNA damage-response genes and susceptibility to lung and head and neck cancersPatrick Danoy, Stefan Michiels, Philippe Dessen, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 5, 2010
Saliva-derived DNA performs well in large-scale, high-density single-nucleotide polymorphism microarray studiesMelanie Bahlo, Jim Stankovich, Patrick Danoy, et al.
Annals of the Rheumatic Diseases|July 26, 2011
Association of variants in MMEL1 and CTLA4 with rheumatoid arthritis in the Han Chinese populationPatrick Danoy, Meng Wei, Hadler Johanna, et al.
Ophthalmology|April 24, 2012
Glaucoma risk alleles at CDKN2B-AS1 are associated with lower intraocular pressure, normal-tension glaucoma, and advanced glaucomaKathryn P Burdon, April Crawford, Robert J Casson, et al.
Human Genetics|October 27, 2010
Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21Sian E Piret, Patrick Danoy, Karin Dahan, et al.
Plos Genetics|December 15, 2010
Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's diseasePatrick Danoy, Karena Pryce, Johanna Hadler, et al.
Pageof 3