Bjornson, Robert D.

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

Sanders, S. J., Murtha, M. T., Gupta, A. R., Murdoch, J. D., Raubeson, M. J., Willsey, A. J., Ercan-Sencicek, A. G., DiLullo, N. M., Parikshak, N. N., Stein, J. L., et al. (2012) · Nature

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 2,084

De novo mutations in histone-modifying genes in congenital heart disease

Zaidi, S., Choi, M., Wakimoto, H., Ma, L., Jiang, J., Overton, J. D., Romano-Adesman, A., Bjornson, R. D., Breitbart, R. E., Brown, K. K., et al. (2013) · Nature

Congenital heart defects researchGenomics and Rare Diseases

Cited by 934

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

Jin, S. C., Homsy, J., Zaidi, S., Lu, Q., Morton, S., DePalma, S. R., Zeng, X., Qi, H., Chang, W., Sierant, M. C., et al. (2017) · Nature Genetics

Congenital heart defects researchGenomics and Rare Diseases

Cited by 875

AlleleSeq: analysis of allele-specific expression and binding in a network framework.

Rozowsky, J., Abyzov, A., Wang, J., Alves, P., Raha, D., Harmanci, A., Leng, J., Bjornson, R., Kong, Y., Kitabayashi, N., et al. (2011) · Molecular Systems Biology

Genomics and Phylogenetic StudiesGenomics and Chromatin Dynamics

Cited by 316

X!!Tandem, an Improved Method for Running X!Tandem in Parallel on Collections of Commodity Computers

Bjornson, R. D., Carriero, N. J., Colangelo, C., Shifman, M., Cheung, K.-H., Miller, P. L., & Williams, K. (2008) · Journal of Proteome Research

Advanced Proteomics Techniques and ApplicationsParallel Computing and Optimization Techniques

Cited by 152

Little’s Law

Dongarra, J., Luszczek, P., Feautrier, P., Zee, F. G., Chan, E., Geijn, R. A., Bjornson, R., Dongarra, J., Luszczek, P., Philippe, B., et al. (2011) · Encyclopedia of Parallel Computing

Advanced Queuing Theory AnalysisManagement and Optimization Techniques

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