Gerdts, Jennifer
University of Washington
10 papers on CoChatORCID 0000-0002-8170-3052
Most cited papers
- Verified
Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development
Bernier, R., Golzio, C., Xiong, B., Stessman, H. A., Coe, B. P., Penn, O., Witherspoon, K., Gerdts, J., Baker, C., Vulto-van Silfhout, A. T., et al. (2014) · Cell
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 798
- Verified
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Stessman, H. A. F., Xiong, B., Coe, B. P., Wang, T., Hoekzema, K., Fenckova, M., Kvarnung, M., Gerdts, J., Trinh, S., Cosemans, N., et al. (2017) · Nature Genetics
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 559
- Verified
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Zhou, X., Feliciano, P., Shu, C., Wang, T., Astrovskaya, I., Hall, J. B., Obiajulu, J. U., Wright, J. R., Murali, S. C., Xu, S. X., et al. (2022) · Nature Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 453
- Verified
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes
Feliciano, P., Zhou, X., Astrovskaya, I., Turner, T. N., Wang, T., Brueggeman, L., Barnard, R., Hsieh, A., Snyder, L. G., Muzny, D. M., et al. (2019) · npj Genomic Medicine
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 247
- Verified
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID
van Bon, B. W. M., Coe, B. P., Bernier, R., Green, C., Gerdts, J., Witherspoon, K., Kleefstra, T., Willemsen, M. H., Kumar, R., Bosco, P., et al. (2016) · Molecular Psychiatry
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 204
- Verified
The broader autism phenotype and its implications on the etiology and treatment of autism spectrum disorders
Gerdts, J., & Bernier, R. (2011) · Autism Research and Treatment
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 146
- Verified
Epigenetics of Autism-related Impairment: Copy Number Variation and Maternal Infection
Mazina, V., Gerdts, J., Trinh, S., Ankenman, K., Ward, T., Dennis, M. Y., Girirajan, S., Eichler, E. E., & Bernier, R. (2015) · Journal of Developmental & Behavioral Pediatrics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 101
- Verified
Reduced auditory cortical adaptation in autism spectrum disorder
Millin, R., Kolodny, T., Flevaris, A. V., Kale, A. M., Schallmo, M.-P., Gerdts, J., Bernier, R. A., & Murray, S. (2018) · eLife
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 64
- Verified
Auditory perception is associated with implicit language learning and receptive language ability in autism spectrum disorder
Arnett, A. B., Hudac, C. M., DesChamps, T. D., Cairney, B. E., Gerdts, J., Wallace, A. S., Bernier, R. A., & Webb, S. J. (2018) · Brain and Language
Autism Spectrum Disorder ResearchLanguage Development and Disorders
Cited by 26
- Verified
Late fMRI Response Components Are Altered in Autism Spectrum Disorder
Murray, S. O., Kolodny, T., Schallmo, M.-P., Gerdts, J., & Bernier, R. A. (2020) · Frontiers in Human Neuroscience
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 7
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