Yujun Han

Affiliations: 
2005-2010 Plant Biology University of Georgia, Athens, Athens, GA, United States 
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"Yujun Han"
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Oz-Levi D, Olender T, Bar-Joseph I, et al. (2019) Noncoding deletions reveal a gene that is critical for intestinal function. Nature
Liu X, Bi B, Xu X, et al. (2019) Rapid identification of a candidate nicosulfuron sensitivity gene (Nss) in maize (Zea mays L.) via combining bulked segregant analysis and RNA-seq. Tag. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
Appenzeller S, Balling R, Barisic N, et al. (2017) Erratum: De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies (American Journal of Human Genetics (2014) 95(4) (360–370)(S0002929714003838)(10.1016/j.ajhg.2014.08.013)) American Journal of Human Genetics. 100: 179
Petrovski S, Gussow AB, Wang Q, et al. (2015) The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity. Plos Genetics. 11: e1005492
Jiang Y, Han Y, Petrovski S, et al. (2015) Incorporating Functional Information in Tests of Excess De Novo Mutational Load. American Journal of Human Genetics
Cirulli ET, Lasseigne BN, Petrovski S, et al. (2015) Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways. Science (New York, N.Y.). 347: 1436-41
Zhu X, Petrovski S, Xie P, et al. (2015) Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Wei Q, Zhan X, Zhong X, et al. (2015) A Bayesian framework for de novo mutation calling in parents-offspring trios. Bioinformatics (Oxford, England). 31: 1375-81
Liu Q, Cirulli ET, Han Y, et al. (2015) Systematic assessment of imputation performance using the 1000 Genomes reference panels. Briefings in Bioinformatics. 16: 549-62
Jiang Y, Satten GA, Han Y, et al. (2014) Utilizing population controls in rare-variant case-parent association tests. American Journal of Human Genetics. 94: 845-53
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