Walker, Michael F.
University of California, San Francisco
6 papers on CoChat
Most cited papers
- Verified
The contribution of de novo coding mutations to autism spectrum disorder
Iossifov, I., O’Roak, B. J., Sanders, S. J., Ronemus, M., Krumm, N., Levy, D., Stessman, H. A., Witherspoon, K. T., Vives, L., Patterson, K. E., et al. (2014) · Nature
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 2,585
- Verified
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
- Verified
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci
Sanders, S. J., He, X., Willsey, A. J., Ercan-Sencicek, A. G., Samocha, K. E., Cicek, A. E., Murtha, M. T., Bal, V. H., Bishop, S. L., Dong, S., et al. (2015) · Neuron
Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities
Cited by 1,430
- Verified
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Werling, D. M., Brand, H., An, J.-Y., Stone, M. R., Zhu, L., Glessner, J. T., Collins, R. L., Dong, S., Layer, R. M., Markenscoff-Papadimitriou, E., et al. (2018) · Nature Genetics
Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology
Cited by 293
- Verified
Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons
Griesi-Oliveira, K., Acab, A., Gupta, A. R., Sunaga, D. Y., Chailangkarn, T., Nicol, X., Nunez, Y., Walker, M. F., Murdoch, J. D., Sanders, S. J., et al. (2015) · Molecular Psychiatry
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 236
- Verified
De Novo Coding Variants Are Strongly Associated with Tourette Disorder
Willsey, A. J., Fernandez, T. V., Yu, D., King, R. A., Dietrich, A., Xing, J., Sanders, S. J., Mandell, J. D., Huang, A. Y., Richer, P., et al. (2017) · Neuron
Obsessive-Compulsive Spectrum DisordersGenomics and Rare Diseases
Cited by 187
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