Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: TBCA[original query] |
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A genome-wide study reveals copy number variants exclusive to childhood obesity cases. American journal of human genetics 2010 Nov 87 (5): 661-6. Glessner Joseph T, Bradfield Jonathan P, Wang Kai, Takahashi Nagahide, Zhang Haitao, Sleiman Patrick M, Mentch Frank D, Kim Cecilia E, Hou Cuiping, Thomas Kelly A, Garris Maria L, Deliard Sandra, Frackelton Edward C, Otieno F George, Zhao Jianhua, Chiavacci Rosetta M, Li Mingyao, Buxbaum Joseph D, Berkowitz Robert I, Hakonarson Hakon, Grant Struan F |
Genome-wide DNA methylation analysis in ankylosing spondylitis identifies HLA-B*27 dependent and independent DNA methylation changes in whole blood. Journal of autoimmunity 2019 May . Coit Patrick, Kaushik Prashant, Caplan Liron, Kerr Gail S, Walsh Jessica A, Dubreuil Maureen, Reimold Andreas, Sawalha Amr |
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors. Annals of neurology 2022 5 92 (2): 270-278. Liu Hui, Dehestani Mohammad, Blauwendraat Cornelis, Makarious Mary B, Leonard Hampton, Kim Jonggeol J, Schulte Claudia, Noyce Alastair, Jacobs Benjamin M, Foote Isabelle, Sharma Manu, , Nalls Mike, Singleton Andrew, Gasser Thomas, Bandres-Ciga Sa |
Interactions between nuclear and mitochondrial SNPs and Parkinson's disease risk. Mitochondrion 2022 2 63 85-88. Pickett Sarah J, Deen Dasha, Pyle Angela, Santibanez-Koref Mauro, Hudson Gav |
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