Random-Effects Model Aimed at Discovering Associations in Meta-Analysis of Genome-wide Association Studies von Han, Buhm, Eskin, Eleazar

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Interpreting meta-analyses of genome-wide association studies von Han, Buhm, Eskin, Eleazar

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Population structure in genetic studies: Confounding factors and mixed models von Sul, Jae Hoon, Martin, Lana S, Eskin, Eleazar

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Systematic benchmarking of omics computational tools von Mangul, Serghei, Martin, Lana S., Hill, Brian L., Lam, Angela Ka-Mei, Distler, Margaret G., Zelikovsky, Alex, Eskin, Eleazar, Flint, Jonathan

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Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma von Han, Yi, Jia, Qiong, Jahani, Pedram Shafiei, Hurrell, Benjamin P., Pan, Calvin, Huang, Pin, Gukasyan, Janet, Woodward, Nicholas C., Eskin, Eleazar, Gilliland, Frank D., Akbari, Omid, Hartiala, Jaana A., Allayee, Hooman

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Metalign: efficient alignment-based metagenomic profiling via containment min hash von LaPierre, Nathan, Alser, Mohammed, Eskin, Eleazar, Koslicki, David, Mangul, Serghei

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Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations von Taraszka, Kodi, Zaitlen, Noah, Eskin, Eleazar

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Robust Mendelian randomization in the presence of residual population stratification, batch effects and horizontal pleiotropy von Cinelli, Carlos, LaPierre, Nathan, Hill, Brian L., Sankararaman, Sriram, Eskin, Eleazar

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Colocalization of GWAS and eQTL Signals Detects Target Genes von Hormozdiari, Farhad, van de Bunt, Martijn, Segrè, Ayellet V., Li, Xiao, Joo, Jong Wha J., Bilow, Michael, Sul, Jae Hoon, Sankararaman, Sriram, Pasaniuc, Bogdan, Eskin, Eleazar

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Identifying causal variants by fine mapping across multiple studies von LaPierre, Nathan, Taraszka, Kodi, Huang, Helen, He, Rosemary, Hormozdiari, Farhad, Eskin, Eleazar

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Improving the usability and archival stability of bioinformatics software von Mangul, Serghei, Martin, Lana S, Eskin, Eleazar, Blekhman, Ran

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Integrating functional data to prioritize causal variants in statistical fine-mapping studies von Kichaev, Gleb, Yang, Wen-Yun, Lindstrom, Sara, Hormozdiari, Farhad, Eskin, Eleazar, Price, Alkes L, Kraft, Peter, Pasaniuc, Bogdan

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Chromosome conformation elucidates regulatory relationships in developing human brain von Won, Hyejung, de la Torre-Ubieta, Luis, Stein, Jason L., Parikshak, Neelroop N., Huang, Jerry, Opland, Carli K., Gandal, Michael J., Sutton, Gavin J., Hormozdiari, Farhad, Lu, Daning, Lee, Changhoon, Eskin, Eleazar, Voineagu, Irina, Ernst, Jason, Geschwind, Daniel H.

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Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing von Mandric, Igor, Rotman, Jeremy, Yang, Harry Taegyun, Strauli, Nicolas, Montoya, Dennis J., Van Der Wey, William, Ronas, Jiem R., Statz, Benjamin, Yao, Douglas, Petrova, Velislava, Zelikovsky, Alex, Spreafico, Roberto, Shifman, Sagiv, Zaitlen, Noah, Rossetti, Maura, Ansel, K. Mark, Eskin, Eleazar, Mangul, Serghei

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Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation von Gamazon, Eric R., Segrè, Ayellet V., van de Bunt, Martijn, Wen, Xiaoquan, Xi, Hualin S., Hormozdiari, Farhad, Ongen, Halit, Konkashbaev, Anuar, Derks, Eske M., Aguet, François, Quan, Jie, Nicolae, Dan L., Eskin, Eleazar, Kellis, Manolis, Getz, Gad, McCarthy, Mark I., Dermitzakis, Emmanouil T., Cox, Nancy J., Ardlie, Kristin G.

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Sparse PCA corrects for cell type heterogeneity in epigenome-wide association studies von Rahmani, Elior, Zaitlen, Noah, Baran, Yael, Eng, Celeste, Hu, Donglei, Galanter, Joshua, Oh, Sam, Burchard, Esteban G, Eskin, Eleazar, Zou, James, Halperin, Eran

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Variance component model to account for sample structure in genome-wide association studies von Kang, Hyun Min, Sul, Jae Hoon, Service, Susan K, Zaitlen, Noah A, Kong, Sit-yee, Freimer, Nelson B, Sabatti, Chiara, Eskin, Eleazar

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Efficient multiple-trait association and estimation of genetic correlation using the matrix-variate linear mixed model von Furlotte, Nicholas A, Eskin, Eleazar

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Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biology von Rahmani, Elior, Schweiger, Regev, Rhead, Brooke, Criswell, Lindsey A., Barcellos, Lisa F., Eskin, Eleazar, Rosset, Saharon, Sankararaman, Sriram, Halperin, Eran

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Improved methods for multi-trait fine mapping of pleiotropic risk loci von Kichaev, Gleb, Roytman, Megan, Johnson, Ruth, Eskin, Eleazar, Lindström, Sara, Kraft, Peter, Pasaniuc, Bogdan

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