Statistical analysis strategies for association studies involving rare variants

Cited by (452)

Items 401–452 of 452

1. Population Genetic Methods and Applications to Human Genomes
   Lucie M. Gattepaille · 2015 · KTH Publication Database DiVA (KTH Royal Institute of Technology)
2. A Biologically Informed Method for Detecting Associations with Rare Variants
   Carrie C Buchanan, John R. Wallace, Alex Frase, Eric S. Torstenson, Sarah A. Pendergrass, Marylyn DeRiggi Ritchie · 2012 · Lecture notes in computer science
3. Two Topics in Association Analysis of DNA Sequencing Data: Population Structure and Multivariate Traits
   Yiwei Zhang · 2013 · University of Minnesota Digital Conservancy (University of Minnesota)
4. Genome-wide association mapping of molecular and physiological component traits in maize
   Christian Riedelsheimer · 2014 · University writing server of the University of Hohenheim (Universität Hohenheim)
5. Variações de novo e raras no genoma de pacientes com transtornos do espectro do autismo verbais e não verbais
   Viviane Neri de Souza Reis · 2014 · Digital Library of Theses and Dissertations (Universidade de São Paulo)
6. Methods of association for genome data with rare variants and a multinomial response
   Janae Elizabeth Nicholson · 2013 · SHAREOK (University of Oklahoma; Oklahoma State University; Central Oklahoma University)
7. Techniques and Approaches to Genetic Analyses in Nephrological Disorders
   Laurel K. Willig · 2015 · Journal of Pediatric Genetics
8. Statistical Analysis of GWAS
   Florian Frommlet, Małgorzata Bogdan, David Ramsey · 2016 · Computational biology
9. Genetic etiology of sporadic ovarian cancer
   Ellen L. Goode, Mine S. Cicek, Catherine M. Phelan, Brooke L. Fridley · 2013 · Cambridge University Press eBooks
10. Human Genome Variation Discovery via Exome and Whole-Genome Sequencing
    Samuel Levy · 2012 · Elsevier eBooks
11. Introduction to statistical methods in genome-wide association studies
    Can Yang, Cong Li, Dongjun Chung, Mengjie Chen, Joel E. Gelernter, Hongyu Zhao · 2015 · Cambridge University Press eBooks
12. Introduction to Applications of Genomic Sequencing
    Stephan L. Zuchner · 2015 · Elsevier eBooks
13. Computational methods for the analysis of next generation sequencing data
    Wei Wang · 2014
14. Investigating Splicing Variants Uncovered by Next-Generation Sequencing the Alzheimer’s Disease Candidate Genes, CLU, PICALM, CR1, ABCA7, BIN1, the MS4A Locus, CD2AP, EPHA1 and CD33
    Naomi S. Clement, Anne Braae, James C. Turton, Jenny Lord, Tamar Guetta‐Baranes · 2016 · Journal of Alzheimer’s Disease & Parkinsonism
15. Genetic Studies of Endophenotypes From Spine CT Scans Provide Novel Insights Into the Contribution of Mechanosensory Pathways to Vertebral Fractures and Spinal Curvature
    Jonathan H. Tobias, Celia Louise Gregson · 2016 · Journal of Bone and Mineral Research
16. Methods for genome interpretation: causal gene discovery and personal phenotype prediction
    Yunching Chen · 2014
17. A model-free test for detecting disease association signals with multiple genetic variants and covariates
    JY Lee, Chiu‐Ying Chen, KF Cheng · 2016 · Statistical Methods in Medical Research
18. A new strategy of statistical analysis based on graphic analysis
    W.G. Duan Y. Yun H.L. Yan · 2015 · CRC Press eBooks
19. An Ant-Colony Based Approach for Identifying a Minimal Set of Rare Variants Underlying Complex Traits
    Xuanping Zhang, Zhongmeng Zhao, Yan Chang, Aiyuan Yang, Yixuan Wang, Ruoyu Liu, Maomao, Xiao Xiao, Jiayin Wang · 2017 · Lecture notes in computer science
20. From Hype to Hope: Genome-Wide Association Studies in Soybean
    Chengsong Zhu, Babu Valliyodan, Yan Li, Junyi Gai, Henry T. Nguyen · 2017 · Compendium of plant genomes
21. Use of Genotypes of Common Variants for Genome-Wide Regional Association Analysis
    A. V. Kirichenko, Irina V. Zorkoltseva, Nadezhda M. Belonogova, Tatiana I. Axenovich · 2018 · Russian Journal of Genetics
22. Methods and results from the genome-wide association group at GAW20
    Xuexia Wang, Felix Boekstegers, Regina Brinster · 2018 · BMC Genetics
23. A BAYESIAN APPROACH TO LEARNING DECISION TREES FOR PATIENT-SPECIFIC MODELS
    Joyeeta Dutta‐Moscato · 2018 · D-Scholarship@Pitt (University of Pittsburgh)
24. Épidémiologie, environnement et génétique dans la sclérose en plaques
    Gilles Louis Defer, Marc Debouverie, Isabelle Bardou, Mehdi Benamar, Raphaël Bernard‐Valnet, Pierre Branger, David Brassat, Naïl Benallegue, Floriane Calocer, Vincent Damotte et al. · 2019 · Elsevier eBooks
25. Whole-exome capture and next-generation sequencing to discover rare variants predisposing to congenital heart disease
    Matthieu J. Miossec · 2016
26. A rigorous method for integrating multiple heterogeneous databases in genetic studies
    József Bukszár, Edwin J. C. G. van den Oord · 2020 · bioRxiv (Cold Spring Harbor Laboratory)
27. Exome sequence analysis of siblings affected with Niemann-Pick type C disease
    Shaun Carswell · 2017
28. A New Strategy using Date Integration for Identifying Interactions between Genes and Environment
    Jiabin Zhou, Sucai Tian, Jiaqi Wang, Yixing Guo · 2021 · Journal of Physics Conference Series
29. Simulation Research on the Methods of Multi-Gene Region Association Analysis Based on a Functional Linear Model
    Shijing Li, Fujie Zhou, Jiayu Shen, Hui Zhang, Yongxian Wen · 2022 · Genes
30. Bayesian Penalized Methods for High-Dimensional Data
    Zakaria Khondker · 2019 · Carolina Digital Repository (University of North Carolina at Chapel Hill)
31. Genetic Inheritance and Population Genetics
    Tatiana Foroud, Daniel L. Koller · 2012 · Springer eBooks
32. Faculty Opinions recommendation of Rediscovering the value of families for psychiatric genetics research.
    John I. Nürnberger · 2019 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
33. Rare Variant Analysis in Unrelated Individuals
    Tao Feng, Xiaofeng Zhu · 2018 · Translational bioinformatics
34. Exome sequencing reveals aggregates of rare variants in glycosyltransferase and other genes influencing immunoglobulin G and transferrin glycosylation
    Arianna Landini, Paul R. H. J. Timmers, Azra Frkatović-Hodžić, Irena Trbojević‐Akmačić, Frano Vučković, Tea Pribić, Gannie Tzoneva, Alan R. Shuldiner, Ozren Polašek, Caroline Hayward et al. · 2022 · medRxiv
35. A fast and efficient approach for gene-based association studies of ordinal phenotypes
    Nanxing Li, Lili Chen, Yajing Zhou, Qianran Wei · 2023 · Statistical Applications in Genetics and Molecular Biology
36. Genetics of Inflammatory Bowel Diseases
    Christopher J. Cardinale, Hakon H. Hakonarson · 2023 · Springer eBooks
37. Statistical Methods in Genetic Epidemiology
    André Scherag, Duncan Thomas, Heike Bickeböller · 2024 · Springer eBooks
38. TRIO RVEMVS: A Bayesian framework for rare variant association analysis with expectation-maximization variable selection using family trio data
    Duo Yu, Matthew D. Koslovsky, Margaret C. Steiner, Kusha A Mohammadi, Chenguang Zhang, Michael D. Swartz · 2024 · PLoS ONE
39. Exome Analysis Points APOE4 Haplotype as Major Risk to Develop Mesoamerican Nephropathy
    Iván Landires, Karen Courville, Gumercindo Pimentel-Peralta, Raúl Cumbrera, Norman Bustamante, Mauricio Arcos‐Burgos, Virginia Núñez-Samudio · 2024 · medRxiv
40. An APOE ε4–Uric Acid Axis Underpins Mesoamerican Nephropathy
    Iván Landires, Karen Courville, Raúl Cumbrera, Norman Bustamante, Gumercindo Pimentel-Peralta, Jorge Ivan Velez, Richard J. Johnson, Mauricio Arcos‐Burgos, Virginia Núñez-Samudio · 2025 · Research Square
41. Association Studies to Map Genes for Disease-Related Traits in Humans
    Robert L. Hanson, Alka Malhotra · 2015 · Springer eBooks
42. Revisiting Mutagenesis in the Age of High-Throughput Sequencing
    Subhajyoti De, R. Matthew Ward · 2013 · Springer eBooks
43. Strategies and statistical methods for linkage disequilibrium-based mapping of complex traits
    Tianye Jia · 2012 · UPT. Syiah Kuala University Library (Syiah Kuala University)
44. Additional file 1 of Genomic analysis reveals the association of KIT and MITF variants with the white spotting in swamp buffaloes
    Dongmei Dai, Eka Meutia Sari, Si, Jingfang, Hidayat Ashari, Muhammad Ihsan Andi Dagong, Alfredo Pauciullo, Johannes Arjen Lenstra, Han, Jianlin, Zhang, Yi · 2024 · Figshare
45. Additional file 2 of Genomic analysis reveals the association of KIT and MITF variants with the white spotting in swamp buffaloes
    Dongmei Dai, Eka Meutia Sari, Si, Jingfang, Hidayat Ashari, Muhammad Ihsan Andi Dagong, Alfredo Pauciullo, Johannes Arjen Lenstra, Jianlin Han, Zhang, Yi · 2024 · Figshare
46. Scalable and accurate rare-variant association tests for whole genome sequencing time-to-event analysis in large biobanks
    Shuang Song, Xihao Li, Hufeng Zhou, Zilin Li, Xihong Lin · 2026 · Proceedings of the National Academy of Sciences
47. Analyses ‘genome entier’ de la cohorte griv de patients à profil extrême du sida
    Sigrid Le Clerc · 2010 · theses.fr (ABES)
48. Rôle des effets épistatiques dans l’évolution d’une population à régime de reproduction mixte, et dans la régulation de l’expression des gènes homéologues chez une espèce autogame allotétraploïde, le blé dur (Triticum turgidum).
    Constance Vagne · 2014 · theses.fr (ABES)
49. The transgenic Drosophila HLA-B27 : a new model for the study of spondyloarthritis
    Benjamin Grandon · 2018 · theses.fr (ABES)
50. Genome‐Wide Homozygosity Predicts Inbreeding Depression in the Hihi/Stitchbird ( Notiomystis cincta ) Better Than Realised Load
    Hui Zhen Tan, Katarina C. Stuart, Joseph G. Guhlin, Tram Vi, Selina Patel, Laura Duntsch, John G. Ewen, Patricia Brekke, Anna W. Santure · 2026 · Evolutionary Applications
51. Genome-Wide Association Study in Plant Breeding: Principles, Applications, Limitations, and Future Perspectives
    Jenifer Camila Godoy dos Santos, Boris M.E. Alladassi, Alexander Edward Lipka · 2026 · Elsevier eBooks
52. Statistical Methods for High Dimensional Networked Data Analysis.
    Yan Zhou · 2015 · Deep Blue (University of Michigan)