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Author Title Type [ Year(Asc)]
Filters: Keyword is Algorithms  [Clear All Filters]
2021
He Z, Liu L, Wang C, Le Guen Y, Lee J, Gogarten S, Lu F, Montgomery S, Tang H, Silverman EK et al..  2021.  Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.. Nat Commun. 12(1):3152.
2020
Du L, Liu F, Liu K, Yao X, Risacher SL, Han J, Saykin AJ, Shen L.  2020.  Associating Multi-Modal Brain Imaging Phenotypes and Genetic Risk Factors via a Dirty Multi-Task Learning Method.. IEEE Trans Med Imaging. 39(11):3416-3428.
Srinivasan D, Erus G, Doshi J, Wolk DA, Shou H, Habes M, Davatzikos C.  2020.  A comparison of Freesurfer and multi-atlas MUSE for brain anatomy segmentation: Findings about size and age bias, and inter-scanner stability in multi-site aging studies.. Neuroimage. 223:117248.
Lee J, Ganguli M, Weerman A, Chien S, Lee DYoung, Varghese M, Dey AB.  2020.  Online Clinical Consensus Diagnosis of Dementia: Development and Validation.. J Am Geriatr Soc. 68 Suppl 3:S54-S59.
Tang Z-Z, Sliwoski GR, Chen G, Jin B, Bush WS, Li B, Capra JA.  2020.  PSCAN: Spatial scan tests guided by protein structures improve complex disease gene discovery and signal variant detection.. Genome Biol. 21(1):217.
Zhao L, Zhang Z, Rodriguez SMBarral, Vardarajan BN, Renton AE, Goate AM, Mayeux R, Wang GT, Leal SM.  2020.  A quantitative trait rare variant nonparametric linkage method with application to age-at-onset of Alzheimer's disease.. Eur J Hum Genet. 28(12):1734-1742.
Kuksa PP, Lee C-Y, Amlie-Wolf A, Gangadharan P, Mlynarski EE, Chou Y-F, Lin H-J, Issen H, Greenfest-Allen E, Valladares O et al..  2020.  SparkINFERNO: a scalable high-throughput pipeline for inferring molecular mechanisms of non-coding genetic variants.. Bioinformatics. 36(12):3879-3881.
2018
Zhou Z, Wang W, San Wang L-, Zhang NRuonan.  2018.  Integrative DNA copy number detection and genotyping from sequencing and array-based platforms.. Bioinformatics. 34(14):2349-2355.

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