Sebat, Jonathan

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism

Corominas, R., Yang, X., Lin, G. N., Kang, S., Shen, Y., Ghamsari, L., Broly, M., Rodriguez, M., Tam, S., Wanamaker, S. A., et al. (2014) · Nature Communications

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 140

Genomewide Association Study of Movement-Related Adverse Antipsychotic Effects

Åberg, K., Adkins, D. E., Bukszár, J., Webb, B. T., Caroff, S. N., Miller, D. D., Sebat, J., Stroup, S., Fanous, A. H., Vladimirov, V. I., et al. (2010) · Biological Psychiatry

Schizophrenia research and treatmentGenetic Associations and Epidemiology

Cited by 130

Frequency and complexity of de novo structural mutation in autism

Brandler, W. M., Antaki, D., Gujral, M., Noor, A., Rosanio, G., Chapman, T. R., Barrera, D. J., Lin, G. N., Malhotra, D., Watts, A. C., et al. (2016) · The American Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research

Cited by 104

Metal chelating properties of pyridine-2,6-bis(thiocarboxylic acid) produced by Pseudomonas spp. and the biological activities of the formed complexes

Cortese, M. S., Paszczynski, A., Lewis, T. A., Sebat, J. L., Borek, V., & Crawford, R. L. (2002) · Biometals

Inorganic and Organometallic ChemistryChromium effects and bioremediation

Cited by 68

SV2: accurate structural variation genotyping and de novo mutation detection from whole genomes

Antaki, D., Brandler, W. M., & Sebat, J. (2018) · Bioinformatics

Genomic variations and chromosomal abnormalitiesGenomics and Phylogenetic Studies

Cited by 45