CENTER ON HUMAN DEVELOPMENT AND DISABILITYdepts.washington.edu/chdd/iddrc/iddrc_currentpubs2017.pdf · CENTER ON HUMAN DEVELOPMENT AND DISABILITY . E. UNICE . K. ENNEDY . S. HRIVER

January – December 2016

CENTER ON HUMAN DEVELOPMENT AND DISABILITY

EUNICE KENNEDY SHRIVER INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER

SELECTED PUBLICATIONS BY CHDD RESEARCH AFFILIATES

Contributions to Intellectual and Developmental Disabilities

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January - December 2017

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Kristina Adams Waldorf Harrell, M. I., Burnside, K., Whidbey, C., Vornhagen, J., Adams Waldorf, K. M., &

Rajagopal, L. (2017). Exploring the Pregnant Guinea Pig as a Model for Group B Streptococcus Intrauterine Infection. Journal of infectious diseases and medicine, 2 PMCID: PMC5635843 Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/29034376

Li, J., Baird, M. A., Davis, M. A., Tai, W., Zweifel, L. S., Adams Waldorf, K. M.,…Gao, X. (2017). Dramatic enhancement of the detection limits of bioassays via ultrafast deposition of polydopamine. Nature Biomedical Engineering, 1 PMCID: PMC5654575 10.1038/s41551-017-0082

Susan Astley Ali, S., Kerns, K. A., Mulligan, B. P., Olson, H. C., & Astley, S. J. (2017). An

investigation of intra-individual variability in children with Fetal Alcohol Spectrum Disorder (FASD). Child Neuropsychology, 10.1080/09297049.2017.1302579, 1-21.

Elizabeth Aylward Aldridge, K., Collett, B. R., Wallace, E. R., Birgfeld, C., Austin, J. R., Yeh, R., Aylward,

E.,…Speltz, M. L. (2017). Structural brain differences in school-age children with and without single-suture craniosynostosis. Journal of Neurosurgery Pediatrics, 19, 479-489. PMCID: PMC5642047 10.3171/2016.9.PEDS16107

Frost, C., Mulick, A., Scahill, R. I., Owen, G., Aylward, E., Leavitt, B. R.,…Investigators, T.-H. (2017). Design optimization for clinical trials in early-stage manifest Huntington's disease. Movement Disorders, 10.1002/mds.27122

Scahill, R. I., Andre, R., Tabrizi, S. J., & Aylward, E. H. (2017). Structural imaging in premanifest and manifest Huntington disease. Handbook of Clinical Neurology, 144, 247-261. 10.1016/B978-0-12-801893-4.00020-1

Velasquez, F., Qin, X. A., Reilly, M. A., Neuhaus, E., Estes, A., Aylward, E., & Kleinhans, N. M. (2017). Neural correlates of emotional inhibitory control in autism spectrum disorders. Research in Developmental Disabilities, 64, 64-77. 10.1016/j.ridd.2017.03.008

Raphael Bernier Ackerman, S., Schoenbrun, S., Hudac, C., & Bernier, R. (2017). Erratum to: Interactive

Effects of Prenatal Antidepressant Exposure and Likely Gene Disrupting Mutations on the Severity of Autism Spectrum Disorder. Journal of Autism and Developmental Disorders, 47, 3497. 10.1007/s10803-017-3301-3

Ackerman, S., Schoenbrun, S., Hudac, C., & Bernier, R. (2017). Interactive effects of prenatal antidepressant exposure and likely gene disrupting mutations on the severity of autism spectrum disorder. Journal of Autism and Developmental Disorders, 47, 3489-3496. 10.1007/s10803-017-3246-6

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Arnett, A. B., Cairney, B. E., Wallace, A. S., Gerdts, J., Turner, T. N., Eichler, E. E., & Bernier, R. A. (2017). Comorbid symptoms of inattention, autism, and executive cognition in youth with putative genetic risk. Journal of Child Psychology and Psychiatry and Allied Disciplines, 59, 268-276. PMCID: PMC5812799 10.1111/jcpp.12815

Bernier, R., Hudac, C. M., Chen, Q., Zeng, C., Wallace, A. S., Gerdts, J.,…Simons V. I. P. Consortium. (2017). Developmental trajectories for young children with 16p11.2 copy number variation. American Journal of Medical Genetics B: Neuropsychiatric Genetics, 174, 367-380. 10.1002/ajmg.b.32525

Bramswig, N. C., Ludecke, H. J., Pettersson, M., Albrecht, B., Bernier, R. A., Cremer, K.,…Eichler, E. E.,…Wieczorek, D. (2017). Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism. Human Genetics, 136, 179-192. PMCID: PMC5821420 10.1007/s00439-016-1743-x

Carvalho, J. O., Springate, B., Bernier, R. A., & Davis, J. (2017). Psychometrics of the AAN Caregiver Driving Safety Questionnaire and contributors to caregiver concern about driving safety in older adults. International Psychogeriatrics, 10.1017/S1041610217001727, 1-10.

Earl, R. K., Turner, T. N., Mefford, H. C., Hudac, C. M., Gerdts, J., Eichler, E. E., & Bernier, R. A. (2017). Clinical phenotype of ASD-associated DYRK1A haploinsufficiency. Molecular Autism, 8, 54. PMCID: PMC5629761 10.1186/s13229-017-0173-5

Geisheker, M. R., Heymann, G., Wang, T., Coe, B. P., Turner, T. N., Stessman, H. A. F., Bernier, R.,…Eichler, E. E. (2017). Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains. Nature Neuroscience, 20, 1043-1051. PMCID: PMC5539915 10.1038/nn.4589

Goin-Kochel, R. P., Trinh, S., Barber, S., & Bernier, R. (2017). Gene Disrupting Mutations Associated with Regression in Autism Spectrum Disorder. Journal of Autism and Developmental Disorders, 47, 3600-3607. PMCID: PMC5693665 10.1007/s10803-017-3256-4

Hudac, C. M., Stessman, H. A. F., DesChamps, T. D., Kresse, A., Faja, S., Neuhaus, E., Webb, S. J., Eichler, E. E., Bernier, R. A. (2017). Exploring the heterogeneity of neural social indices for genetically distinct etiologies of autism. Journal of Neurodevelopmental Disorders, 9, 24. PMCID: PMC5446693 10.1186/s11689-017-9199-4

Jansen, S., Geuer, S., Pfundt, R., Brough, R., Ghongane, P., Herkert, J. C., Bernier, R. A.,…de Vries, B. B. (2017). De Novo Truncating Mutations in the Last and Penultimate Exons of PPM1D Cause an Intellectual Disability Syndrome. American Journal of Human Genetics, 100, 650-658. PMCID: PMC5384016 10.1016/j.ajhg.2017.02.005

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Jansen, S., Hoischen, A., Coe, B. P., Carvill, G. L., Van Esch, H., Bosch, D. G. M., Bernier, R. A., Eichler, E. E.,…de Vries, B. B. A. (2017). A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency. European Journal of Human Genetics, 10.1038/s41431-017-0039-5

Krupp, D. R., Barnard, R. A., Duffourd, Y., Evans, S. A., Mulqueen, R. M., Bernier, R.,…O'Roak, B. J. (2017). Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder. American Journal of Human Genetics, 101, 369-390. PMCID: PMC5590950 10.1016/j.ajhg.2017.07.016

Patowary, A., Nesbitt, R., Archer, M., Bernier, R., & Brkanac, Z. (2017). Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder. Autism Research, 10, 1338-1343. PMCID: PMC5573912 10.1002/aur.1792

Siper, P. M., De Rubeis, S., Trelles, M. D. P., Durkin, A., Di Marino, D., Muratet, F., Eichler, E. E., Mefford, H. C., Bernier, R. A.,…Buxbaum, J. D. (2017). Prospective investigation of FOXP1 syndrome. Molecular Autism, 8, 57. PMCID: PMC5655854 10.1186/s13229-017-0172-6

Stessman, H. A., Xiong, B., Coe, B. P., Wang, T., Hoekzema, K., Fenckova, M.,…Bernier, R. A., Eichler, E. E. (2017). Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. Nature Genetics 49, 515-526. PMCID: PMC5374041 10.1038/ng.3792

Turner, T. N., Yi, Q., Krumm, N., Huddleston, J., Hoekzema, K., HA, F. S., Bernier, R. A.,…Eichler, E. E. (2017). denovo-db: a compendium of human de novo variants. Nucleic Acids Research, 45, D804-D811. PMCID: PMC5210614 10.1093/nar/gkw865

Wallace, A. S., Hudac, C. M., Steinman, K., Peterson, J., DesChamps, T. D., Duyzend, M. H.,…Eichler, E.E., Bernier, R.A. (in press). Longitudinal report of child with de novo 16p11.2 triplication. Clinical Case Reports

Webb, S. J., Garrison, M. M., Bernier, R., McClintic, A. M., King, B. H., & Mourad, P. D. (2017). Severity of ASD symptoms and their correlation with the presence of copy number variations and exposure to first trimester ultrasound. Autism Research, 10, 472-484. PMCID: PMC5332517 10.1002/aur.1690

Virginia Berninger Berninger, V., Abbott, R., & Cook, C. R. (2017). Relationships of attention and

executive functions to oral language, reading, and writing skills and systems in middle childhood and early adolescence. Journal of Learning Disabilities, 50, 434-449. PMCID: PMC4938801 10.1177/0022219415617167

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Longcamp, M., Richards, T. L., Velay, J. L., & Berninger, V. W. (2016). Neuroanatomy of Handwriting and Related Reading and Writing Skills in Adults and Children with and without Learning Disabilities: French-American Connections. Pratiques, 171-172 PMCID: PMC5297261 Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/28190914

Richards, T. L., Berninger, V. W., Yagle, K. J., Abbott, R. D., & Peterson, D. J. (2017). Changes in DTI Diffusivity and fMRI Connectivity Cluster Coefficients for Students with and without Specific Learning Disabilities In Written Language: Brain's Response to Writing Instruction. Journal of Nature and Science, 3 PMCID: PMC5488805 Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/28670621

Wolf, B., Abbott, R. D., & Berninger, V. W. (2017). Effective beginning handwriting instruction: Multi-modal, consistent format for 2 years, and linked to spelling and composing. Reading and Writing: An Interdisciplinary Journal, 30, 299-317. 10.1007/s11145-016-9674-4

Kristie Bjornson Bjornson, K. (2017). Response to "Developing a Clinical Protocol for Habitual Physical

Activity Monitoring in Youth With Cerebral Palsy".29, 187-188. 10.1097/PEP.0000000000000391

Gannotti, M. E., Bailes, A., Bjornson, K., O'Neil, M., Grant-Buettler, M., & Dusing, S. (2017). Pediatric Rehabilitation Services for Children With Cerebral Palsy: What Can Existing Data Sources Tell Us? Pediatric Physical Therapy, 29, 179-186. 10.1097/PEP.0000000000000377

Cathryn Booth-LaForce Barstead, M. G., Smith, K. A., Laursen, B., Booth-LaForce, C., King, S., & Rubin, K. H.

(2017). Shyness, Preference for Solitude, and Adolescent Internalizing: The Roles of Maternal, Paternal, and Best-Friend Support. Journal of Research on Adolescence, 10.1111/jora.12350

Zoran Brkanac Patowary, A., Nesbitt, R., Archer, M., Bernier, R., & Brkanac, Z. (2017). Next

Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder. Autism Research, 10, 1338-1343. PMCID: PMC5573912 10.1002/aur.1792

Thomas Burbacher Grant, K. S., Petroff, R., Isoherranen, N., Stella, N., & Burbacher, T. M. (2017).

Cannabis use during pregnancy: Pharmacokinetics and effects on child development. Pharmacology and Therapeutics, 10.1016/j.pharmthera.2017.08.014

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Jing, J., Petroff, R., Shum, S., Crouthamel, B., Topletz, A. R., Grant, K. S., Burbacher, T. M.,…Isoherranen, N. (2017). Toxicokinetics and physiologically based pharmacokinetic modeling of the shellfish toxin Domoic Acid in nonhuman primates. Drug Metabolism and Disposition, 46, 155-165. PMCID: PMC5776359 10.1124/dmd.117.078485

Shiotani, M., Cole, T. B., Hong, S., Park, J. J. Y., Griffith, W. C., Burbacher, T. M., Costa, L. G.,…Faustman, E. M. (2017). Neurobehavioral assessment of mice following repeated oral exposures to Domoic acid during prenatal development. Neurotoxicology and Teratology 64, 8-19. 10.1016/j.ntt.2017.09.002

Tigges, B. B., Kaar, J. L., Erbstein, N., Silberman, P., Winseck, K., Lopez-Class, M., & Burbacher, T. M. (2017). Effectiveness of community outreach and engagement in recruitment success for a prebirth cohort. Journal of Clinical and Translational Science, 1, 184-191. PMCID: PMC5647659 10.1017/cts.2017.7

Heather Carmichael Olson Hanlon-Dearman, A., Chen, M. L., & Carmichael Olson, H. (2017). Understanding and

Managing Sleep Disruption in Children with FASD. Biochemistry and Cell Biology, 10.1139/bcb-2017-0064

Petrenko, C. L. M., Pandolfino, M. E., Quamma, J., & Carmichael Olson, H. (2017). Emotional understanding in school-aged children with Fetal Alcohol Spectrum Disorders: A promising target for intervention. Journal of Population Therapeutics and Clinical Pharmacology, 24, e21-e31. PMCID: PMC5627645 10.22374/1710-6222.24.2.5

Tsang, T. W., Carmichael Olson, H., Latimer, J., Fitzpatrick, J., Hand, M., Oscar, J.,…Elliott, E. J. (2017). Behavior in children with Fetal Alcohol Spectrum Disorders in remote Australia: A population-based study. Journal of Development and Behavioral Pediatrics, 38, 528-537. 10.1097/DBP.0000000000000463

William Catterall Catterall, W. A. (2017). Forty Years of Sodium Channels: Structure, Function,

Pharmacology, and Epilepsy. Neurochemical Research, 42, 2495-2504. PMCID: PMC5693772 10.1007/s11064-017-2314-9

Catterall, W. A., Wisedchaisri, G., & Zheng, N. (2017). The chemical basis for electrical signaling. Nature Chemical Biology , 13, 455-463. PMCID: PMC5464002 10.1038/nchembio.2353

Gamal El-Din, T. M., Lenaeus, M. J., & Catterall, W. A. (2017). Structural and Functional Analysis of Sodium Channels Viewed from an Evolutionary Perspective. Handbook of Experimental Pharmacology, 10.1007/164_2017_61

Kaplan, J. S., Stella, N., Catterall, W. A., & Westenbroek, R. E. (2017). Cannabidiol attenuates seizures and social deficits in a mouse model of Dravet syndrome. Proceedings of the National Academy of Science of the United States of America, 114, 11229-11234. PMCID: PMC5651774 10.1073/pnas.1711351114

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Lenaeus, M. J., Gamal El-Din, T. M., Ing, C., Ramanadane, K., Pomes, R., Zheng, N., & Catterall, W. A. (2017). Structures of closed and open states of a voltage-gated sodium channel. Proceedings of the National Academy of Science of the United States of America, 114, E3051-E3060. PMCID: PMC5393245 10.1073/pnas.1700761114

Jeffrey Chamberlain Bengtsson, N. E., Hall, J. K., Odom, G. L., Phelps, M. P., Andrus, C. R., Hawkins, R.

D.,…Chamberlain, J. S. (2017). Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy. Nature Communications, 8, 16007. PMCID: PMC5489999 10.1038/ncomms16007

Bengtsson, N. E., Hall, J. K., Odom, G. L., Phelps, M. P., Andrus, C. R., Hawkins, R. D.,…Chamberlain, J. S. (2017). Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy. Nature Communications, 8, 14454. PMCID: PMC5316861 10.1038/ncomms14454

Chamberlain, J. R., & Chamberlain, J. S. (2017). Progress toward Gene Therapy for Duchenne Muscular Dystrophy. Molecular Therapy, 25, 1125-1131. PMCID: PMC5417844 10.1016/j.ymthe.2017.02.019

Dimitri Christakis Anderson, C. A., Bushman, B. J., Bartholow, B. D., Cantor, J., Christakis, D., Coyne, S.

M.,…Ybarra, M. (2017). Screen Violence and Youth Behavior. Pediatrics, 140, S142-S147. 10.1542/peds.2016-1758T

Christakis, D. A., & Rivara, F. P. (2017). Guns and Violent Media-A Toxic Mix With an Available Antidote. JAMA Pediatrics, 171, 1040-1041. 10.1001/jamapediatrics.2017.2383

Lucio Costa Chang, Y. C., Cole, T. B., & Costa, L. G. (2017). Behavioral Phenotyping for Autism

Spectrum Disorders in Mice. Current Protocols in Toxicology, 72, 11 22 11-11 22 21. PMCID: PMC5494990 10.1002/cptx.19

Costa, L. G. (2017). Organophosphorus compounds at 80: some old and new issues. Toxicological Sciences, 10.1093/toxsci/kfx266

Costa, L. G. (2017). Overview of Neurotoxicology. Current Protocols in Toxicology, 74, 11 11 11-11 11 11. 10.1002/cptx.36

Costa, L. G., Chang, Y. C., & Cole, T. B. (2017). Developmental Neurotoxicity of Traffic-Related Air Pollution: Focus on Autism. Current Environmental Health Reports, 4, 156-165. 10.1007/s40572-017-0135-2

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Costa, L. G., Cole, T. B., Coburn, J., Chang, Y. C., Dao, K., & Roque, P. J. (2017). Neurotoxicity of traffic-related air pollution. Neurotoxicology, 59, 133-139. PMCID: PMC4875879 10.1016/j.neuro.2015.11.008

Costa, L. G., Cole, T. B., Garrick, J. M., Marsillach, J., & Furlong, C. E. (2017). Metals and Paraoxonases. Advances in Neurobiology, 18, 85-111. 10.1007/978-3-319-60189-2_5

Roque, P. J., & Costa, L. G. (2017). Co-Culture of Neurons and Microglia. Current Protocols in Toxicology, 74, 11 24 11-11 24 17. 10.1002/cptx.32


Timothy Cox Gallagher, E. R., Siebold, B., Collett, B. R., Cox, T. C., Aziz, V., & Cunningham, M. L.

(2017). Associations between laterality of orofacial clefts and medical and academic outcomes. American Journal of Medical Genetics, A, 10.1002/ajmg.a.38567

Lee, E., Le, T., Zhu, Y., Elakis, G., Turner, A., Lo, W., Cox, T.,…Roscioli, T. (2017). A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations. Genetics in Medicine, 10.1038/gim.2017.214

Parada-Sanchez, M. T., Chu, E. Y., Cox, L. L., Undurty, S. S., Standley, J. M., Murray, J. C., & Cox, T. C. (2017). Disrupted IRF6-NME1/2 Complexes as a Cause of Cleft Lip/Palate. Journal of Dental Research, 96, 1330-1338. PMCID: PMC5613882 10.1177/0022034517723615

Tamasas, B., & Cox, T. C. (2017). Massively Increased Caries Susceptibility in an Irf6 Cleft Lip/Palate Model. Journal of Dental Research, 96, 315-322. 10.1177/0022034516679376

Yamada, S., Wallingford, M. C., Borgeia, S., Cox, T. C., & Giachelli, C. M. (2017). Loss of PiT-2 results in abnormal bone development and decreased bone mineral density and length in mice. Biochemical and Biophysical Research Communications, 10.1016/j.bbrc.2017.11.071

Yu, K., Deng, M., Naluai-Cecchini, T., Glass, I. A., & Cox, T. C. (2017). Differences in Oral Structure and Tissue Interactions during Mouse vs. Human Palatogenesis: Implications for the Translation of Findings from Mice. Frontiers in Physiology, 8, 154. PMCID: PMC5350148 10.3389/fphys.2017.00154

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Michael Cunningham Clarke, C. M., Fok, V. T., Gustafson, J. A., Smyth, M. D., Timms, A. E., Frazar, C.

D.,…Cunningham, M. L. (2017). Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. American Journal of Medical Genetics, A, 10.1002/ajmg.a.38540

Gallagher, E. R., Siebold, B., Collett, B. R., Cox, T. C., Aziz, V., & Cunningham, M. L. (2017). Associations between laterality of orofacial clefts and medical and academic outcomes. American Journal of Medical Genetics, A, 10.1002/ajmg.a.38567

Gordon, C. T., Xue, S., Yigit, G., Filali, H., Chen, K., Rosin, N., Cunningham, M. L.,…Reversade, B. (2017). De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. Nature Genetics 49, 249-255. 10.1038/ng.3765

Hakim, C. H., Wasala, N. B., Pan, X., Kodippili, K., Yue, Y., Zhang, K., Cunningham, M. L.,…Duan, D. (2017). A Five-Repeat Micro-Dystrophin Gene Ameliorated Dystrophic Phenotype in the Severe DBA/2J-mdx Model of Duchenne Muscular Dystrophy. Molecular Therapy. Methods and Clinical Development, 6, 216-230. PMCID: PMC5596503 10.1016/j.omtm.2017.06.006

Wenger, T. L., Dahl, J., Bhoj, E. J., Rosen, A., McDonald-McGinn, D., Zackai, E.,…Cunningham, M. L.,…Perkins, J. (2017). Tracheal cartilaginous sleeves in children with syndromic craniosynostosis. Genetics in Medicine, 19, 62-68. 10.1038/gim.2016.60

Raimondo D’Ambrosio Kadam, S. D., D'Ambrosio, R., Duveau, V., Roucard, C., Garcia-Cairasco, N., Ikeda,

A.,…Kelly, K. M. (2017). Methodological standards and interpretation of video-electroencephalography in adult control rodents. A TASK1-WG1 report of the AES/ILAE Translational Task Force of the ILAE. Epilepsia, 58 Suppl 4, 10-27. PMCID: PMC5679281 10.1111/epi.13903

Stephen Dager Dimian, A. F., Botteron, K. N., Dager, S. R., Elison, J. T., Estes, A. M., Pruett, J. R.,

Jr.,…IBIS Network. (2017). Potential Risk Factors for the Development of Self-Injurious Behavior among Infants at Risk for Autism Spectrum Disorder. Journal of Autism and Developmental Disorders, 47, 1403-1415. PMCID: PMC5385192 10.1007/s10803-017-3057-9

Eggebrecht, A. T., Elison, J. T., Feczko, E., Todorov, A., Wolff, J. J., Kandala, S., Estes, A. M.,.Dager, S. R.,…Pruett, J. R., Jr. (2017). Joint Attention and Brain Functional Connectivity in Infants and Toddlers. Cerebral Cortex, 27, 1709-1720. PMCID: PMC5452276 10.1093/cercor/bhw403

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Emerson, R. W., Adams, C., Nishino, T., Hazlett, H. C., Wolff, J. J., Zwaigenbaum, L., Estes, A. M., Dager, S. R.,…Piven, J. (2017). Functional neuroimaging of high-risk 6-month-old infants predicts a diagnosis of autism at 24 months of age. Science Translational Medicine, 9 PMCID: PMC5819345 10.1126/scitranslmed.aag2882

Estes, A., Munson, J., John, T. S., Dager, S. R., Rodda, A., Botteron, K., …,Guralnick, M.J., IBIS Network. (2017). Parent Support of Preschool Peer Relationships in Younger Siblings of Children with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders, 10.1007/s10803-017-3202-5 PMCID: PMC5738288

Hazlett, H. C., Gu, H., Munsell, B. C., Kim, S. H., Styner, M., Wolff, J. J., Dager, S. R., Estes, A. M., Shaw, D.,…IBIS Network. (2017). Early brain development in infants at high risk for autism spectrum disorder. Nature, 542, 348-351. PMCID: PMC5336143 10.1038/nature21369

Lewis, J. D., Evans, A. C., Pruett, J. R., Jr., Botteron, K. N., McKinstry, R. C., Zwaigenbaum, L., Estes, A. M., Dager, S. R.,…Infant Brain Imaging Study Network. (2017). The Emergence of Network Inefficiencies in Infants With Autism Spectrum Disorder. Biological Psychiatry, 82, 176-185. PMCID: PMC5524449 10.1016/j.biopsych.2017.03.006

Marrus, N., Eggebrecht, A. T., Todorov, A., Elison, J. T., Wolff, J. J., Cole, L., Estes, A. M., Dager, S. R.,…Pruett, J. R., Jr. (2017). Walking, Gross Motor Development, and Brain Functional Connectivity in Infants and Toddlers. Cerebral Cortex, 10.1093/cercor/bhx313, 1-14

Mitra, A., Snyder, A. Z., Tagliazucchi, E., Laufs, H., Elison, J., Emerson, R. W., Dager, S. R., Estes, A. M.,…Raichle, M. (2017). Resting-state fMRI in sleeping infants more closely resembles adult sleep than adult wakefulness. PLoS One, 12, e0188122. PMCID: PMC5693436 10.1371/journal.pone.0188122

Shen, M. D., Kim, S. H., McKinstry, R. C., Gu, H., Hazlett, H. C., Nordahl, C. W., Estes, A. M., Dager, S. R.,…Gu, H. (2017). Increased Extra-axial Cerebrospinal Fluid in High-Risk Infants Who Later Develop Autism. Biological Psychiatry, 82, 186-193. PMCID: PMC5531051 10.1016/j.biopsych.2017.02.1095

Swanson, M. R., Shen, M. D., Wolff, J. J., Boyd, B., Clements, M., Rehg, J., Dager, S. R., Ester, A. M.,…IBIS Network. (2017). Naturalistic Language Recordings Reveal "Hypervocal" Infants at High Familial Risk for Autism. Child Development, 10.1111/cdev.12777 PMCID: PMC5592123

Swanson, M. R., Wolff, J. J., Elison, J. T., Gu, H., Hazlett, H., Botteron, K., Dager, S. R., Estes, A. M.,…Piven, J. (2017). Splenium developmentand early spoken language in human infants. Developmental Science, 20, e12360. PMCID: PMC4840090 10.1111/desc.12360

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Wolff, J. J., Swanson, M. R., Elison, J. T., Gerig, G., Pruett, J. R., Jr., Styner, M. A., Dager, S. R., Estes, A. M.,…IBIS Network. (2017). Neural circuitry at age 6 months associated with later repetitive behavior and sensory responsiveness in autism. Molecular Autism, 8, 8. PMCID: PMC5351210 10.1186/s13229-017-0126-z

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CENTER ON HUMAN DEVELOPMENT AND DISABILITYdepts.washington.edu/chdd/iddrc/iddrc_currentpubs2017.pdf · CENTER ON HUMAN DEVELOPMENT AND DISABILITY . E. UNICE . K. ENNEDY . S. HRIVER