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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Disease and RASA2[original query]
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. GWAS Catalog
Human molecular genetics 2012 Apr 21 (8): 1897-906.
Mead Simon, Uphill James, Beck John, Poulter Mark, Campbell Tracy, Lowe Jessica, Adamson Gary, Hummerich Holger, Klopp Norman, Rückert Ina-Maria, Wichmann H-Erich, Azazi Dhoyazan, Plagnol Vincent, Pako Wandagi H, Whitfield Jerome, Alpers Michael P, Whittaker John, Balding David J, Zerr Inga, Kretzschmar Hans, Collinge Jo
Next-generation sequencing identifies rare variants associated with Noonan syndrome.
Proceedings of the National Academy of Sciences of the United States of America 2014 Aug 111 (31): 11473-8.
Chen Peng-Chieh, Yin Jiani, Yu Hui-Wen, Yuan Tao, Fernandez Minerva, Yung Christina K, Trinh Quang M, Peltekova Vanya D, Reid Jeffrey G, Tworog-Dube Erica, Morgan Margaret B, Muzny Donna M, Stein Lincoln, McPherson John D, Roberts Amy E, Gibbs Richard A, Neel Benjamin G, Kucherlapati Ra
The associations of two SNPs in miRNA-146a and one SNP in ZBTB38-RASA2 with the disease susceptibility and the clinical features of the Chinese patients of sCJD and FFI.
Prion 2017 12 12 (1): 34-41.
Gao Chen, Shi Qiang, Wei Jing, Zhou Wei, Xiao Kang, Wang Jing, Shi Qi, Dong Xiao-Pi
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