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  1. 1
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  2. 2
    Bin Yan, Shudong Wang, Huaqian Jia, Xing Liu, Xinzeng Wang, An efficient weighted tag SNP-set analytical method in genome-wide association studies, BMC Genetics, 2015, 16, 1

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  3. 3
    Lang Wu, Daniel J Schaid, Hugues Sicotte, Eric D Wieben, Hu Li, Gloria M Petersen, Case-only exome sequencing and complex disease susceptibility gene discovery: study design considerations, Journal of Medical Genetics, 2015, 52, 1, 10

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  4. 4
    Ananda S. Datta, Swati Biswas, Comparison of haplotype-based statistical tests for disease association with rare and common variants, Briefings in Bioinformatics, 2015, bbv072

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  5. 5
    Meng Wang, Shili Lin, Detecting associations of rare variants with common diseases: collapsing or haplotyping?, Briefings in Bioinformatics, 2015, 16, 5, 759

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  6. 6
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  7. 7
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  8. 8
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  9. 9
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  10. 10
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  11. 11
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  12. 12
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  13. 13
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  14. 14
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  15. 15
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  16. 16
    Peilin Jia, Zhongming Zhao, Network-assisted analysis to prioritize GWAS results: principles, methods and perspectives, Human Genetics, 2014, 133, 2, 125

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  17. 17
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  18. 18
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  19. 19
    Keli Liu, Shannon Fast, Matthew Zawistowski, Nathan L. Tintle, A Geometric Framework for Evaluating Rare Variant Tests of Association, Genetic Epidemiology, 2013, 37, 4
  20. 20
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  21. 21
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  22. 22
    Qianying Liu, Dan L. Nicolae, Lin S. Chen, Marbled Inflation From Population Structure in Gene-Based Association Studies With Rare Variants, Genetic Epidemiology, 2013, 37, 3
  23. 23
    Adam E Handel, Giulio Disanto, Sreeram V Ramagopalan, Next-generation sequencing in understanding complex neurological disease, Expert Review of Neurotherapeutics, 2013, 13, 2, 215

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  24. 24
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  25. 25
    Yan V. Sun, Integration of biological networks and pathways with genetic association studies, Human Genetics, 2012, 131, 10, 1677

    CrossRef

  26. 26
    Lucas D Ward, Manolis Kellis, Interpreting noncoding genetic variation in complex traits and human disease, Nature Biotechnology, 2012, 30, 11, 1095

    CrossRef

  27. 27
    Kai Wang, John H. Fingert, Statistical Tests for Detecting Rare Variants Using Variance-Stabilising Transformations, Annals of Human Genetics, 2012, 76, 5
  28. 28
    Junghyun Namkung, Paola Raska, Jia Kang, Yunlong Liu, Qing Lu, Xiaofeng Zhu, Analysis of exome sequences with and without incorporating prior biological knowledge, Genetic Epidemiology, 2011, 35, S1
  29. 29
    Heike Bickeböller, Jeanine J. Houwing-Duistermaat, Xuefeng Wang, Xiting Yan, Dealing with high dimensionality for the identification of common and rare variants as main effects and for gene-environment interaction, Genetic Epidemiology, 2011, 35, S1
  30. 30
    Yan V. Sun, Yun Ju Sung, Nathan Tintle, Andreas Ziegler, Identification of genetic association of multiple rare variants using collapsing methods, Genetic Epidemiology, 2011, 35, S1
  31. 31
    Inke R. König, Jeremie Nsengimana, Charalampos Papachristou, Matthew A. Simonson, Kai Wang, Jason A. Weisburd, Multiple testing in high-throughput sequence data: experiences from Group 8 of Genetic Analysis Workshop 17, Genetic Epidemiology, 2011, 35, S1
  32. 32
    Rémi Kazma, Julia N. Bailey, Population-based and family-based designs to analyze rare variants in complex diseases, Genetic Epidemiology, 2011, 35, S1
  33. 33
    Jack W. Kent, Rare variants, common markers: synthetic association and beyond, Genetic Epidemiology, 2011, 35, S1
  34. 34
    Joan E. Bailey-Wilson, Jennifer S. Brennan, Shelley B. Bull, Robert Culverhouse, Yoonhee Kim, Yuan Jiang, Jeesun Jung, Qing Li, Claudia Lamina, Ying Liu, Reedik Mägi, Yue S. Niu, Claire L. Simpson, Libo Wang, Yildiz E. Yilmaz, Heping Zhang, Zhaogong Zhang, Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data, Genetic Epidemiology, 2011, 35, S1
  35. 35
    Bingshan Li, Dajiang J. Liu, Suzanne M. Leal, Identifying Rare Variants Associated with Complex Traits via Sequencing, Current Protocols in Human Genetics,