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Environmental Health Perspectives|April 20, 2016
The Next Generation of Risk Assessment Multi-Year Study-Highlights of Findings, Applications to Risk Assessment, and Future DirectionsIla Cote, Melvin E Andersen, Gerald T Ankley, et al.Nature Genetics|August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autismJack M Fu, F Kyle Satterstrom, Minshi Peng, et al.American Journal of Human Genetics|September 22, 2005
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8qMatthew B McQueen, B Devlin, Stephen V Faraone, et al.Nature Genetics|February 27, 2019
Identification of common genetic risk variants for autism spectrum disorderJakob Grove, Stephan Ripke, Thomas D Als, et al.Neuron|June 11, 2011
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autismStephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, et al.Nature|November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autismSilvia De Rubeis, Xin He, Arthur P Goldberg, et al.Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.Proceedings of the National Academy of Sciences of the United States of America|April 8, 2022
Evaluation of individual and ensemble probabilistic forecasts of COVID-19 mortality in the United StatesEstee Y Cramer, Evan L Ray, Velma K Lopez, et al.Pageof 47