Biblio

Found 8 results
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H
Hwang Y-C, Lin C-F, Valladares O, Malamon J, Kuksa PP, Zheng Q, Gregory BD, San Wang L-.  2015.  HIPPIE: a high-throughput identification pipeline for promoter interacting enhancer elements.. Bioinformatics. 31(8):1290-2.
Hwang Y-C, Zheng Q, Gregory BD, San Wang L-.  2013.  High-throughput identification of long-range regulatory elements and their target promoters in the human genome.. Nucleic Acids Res. 41(9):4835-46.
Huang K-L, Marcora E, Pimenova AA, Di Narzo AF, Kapoor M, Jin SChih, Harari O, Bertelsen S, Fairfax BP, Czajkowski J et al..  2017.  A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.. Nat Neurosci. 20(8):1052-1061.
Hollingworth P, Harold D, Sims R, Gerrish A, Lambert J-C, Carrasquillo MM, Abraham R, Hamshere ML, Pahwa JSingh, Moskvina V et al..  2011.  Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.. Nat Genet. 43(5):429-35.
Höglinger GU, Melhem NM, Dickson DW, Sleiman PMA, San Wang L-, Klei L, Rademakers R, de Silva R, Litvan I, Riley DE et al..  2011.  Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.. Nat Genet. 43(7):699-705.
He L, Loika Y, Park Y, Bennett DA, Kellis M, Kulminski AM.  2021.  Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer's disease.. Transl Psychiatry. 11(1):146.
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JSingh, Moskvina V, Dowzell K, Williams A et al..  2009.  Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.. Nat Genet. 41(10):1088-93.
Han G, Sun J, Wang J, Bai Z, Song F, Lei H.  2014.  Genomics in neurological disorders.. Genomics Proteomics Bioinformatics. 12(4):156-63.