Year |
Citation |
Score |
2024 |
Azu MA, Han GT, Wolf JM, Naples AJ, Chawarska K, Dawson G, Bernier RA, Jeste SS, Dziura JD, Webb SJ, Sugar CA, Shic F, McPartland JC. Clinician-caregiver informant discrepancy is associated with sex, diagnosis age, and intervention use among autistic children. Autism : the International Journal of Research and Practice. 13623613241279999. PMID 39344965 DOI: 10.1177/13623613241279999 |
0.531 |
|
2024 |
Griffin JW, Naples A, Bernier R, Chawarska K, Dawson G, Dziura J, Faja S, Jeste S, Kleinhans N, Sugar C, Webb SJ, Shic F, McPartland JC. Spatiotemporal Eye Movement Dynamics Reveal Altered Face Prioritization in Early Visual Processing Among Autistic Children. Biological Psychiatry. Cognitive Neuroscience and Neuroimaging. PMID 39237004 DOI: 10.1016/j.bpsc.2024.08.017 |
0.725 |
|
2024 |
Hudac CM, Dommer K, Mahony M, DesChamps TD, Cairney B, Earl R, Kurtz-Nelson EC, Bradshaw J, Bernier RA, Eichler EE, Neuhaus E, Webb SJ, Shic F. Visual and auditory attention in individuals with DYRK1A and SCN2A disruptive variants. Autism Research : Official Journal of the International Society For Autism Research. PMID 39080977 DOI: 10.1002/aur.3202 |
0.536 |
|
2024 |
Arutiunian V, Santhosh M, Neuhaus E, Sullivan CAW, Bernier RA, Bookheimer SY, Dapretto M, Geschwind DH, Jack A, McPartland JC, Van Horn JD, Pelphrey KA, Gupta AR, Webb SJ. A common genetic variant in the Neurexin family member CNTNAP2 is related to language but not communication skills in youth with Autism Spectrum Disorder. Autism Research : Official Journal of the International Society For Autism Research. PMID 38984666 DOI: 10.1002/aur.3193 |
0.692 |
|
2024 |
Dickinson A, Ryan D, McNaughton G, Levin A, Naples A, Borland H, Bernier R, Chawarska K, Dawson G, Dziura J, Faja S, Kleinhans N, Sugar C, Senturk D, Shic F, et al. Parsing evoked and induced gamma response differences in Autism: A visual evoked potential study. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. 165: 55-63. PMID 38959536 DOI: 10.1016/j.clinph.2024.05.015 |
0.682 |
|
2024 |
Arutiunian V, Santhosh M, Neuhaus E, Borland H, Tompkins C, Bernier RA, Bookheimer SY, Dapretto M, Gupta AR, Jack A, Jeste S, McPartland JC, Naples A, Van Horn JD, Pelphrey KA, et al. The relationship between gamma-band neural oscillations and language skills in youth with Autism Spectrum Disorder and their first-degree relatives. Molecular Autism. 15: 19. PMID 38711098 DOI: 10.1186/s13229-024-00598-1 |
0.692 |
|
2024 |
Neuhaus E, Rea H, Jones E, Benavidez H, Miles C, Whiting A, Johansson M, Eayrs C, Kurtz-Nelson EC, Earl R, Bernier RA, Eichler EE. Shared and divergent mental health characteristics of ADNP-, CHD8- and DYRK1A-related neurodevelopmental conditions. Journal of Neurodevelopmental Disorders. 16: 15. PMID 38622540 DOI: 10.1186/s11689-024-09532-1 |
0.334 |
|
2023 |
Neuhaus E, Bernier RA, Webb SJ. Social motivation by self- and caregiver-report: Reporter concordance and social correlates among autistic and neurotypical youth. Autism Research : Official Journal of the International Society For Autism Research. PMID 37987233 DOI: 10.1002/aur.3054 |
0.51 |
|
2023 |
Rea HM, Clawson A, Hudac CM, Santhosh M, Bernier RA, Earl RK, Pelphrey KA, Webb SJ, Neuhaus E. Pubertal maturation and timing effects on resting state electroencephalography in autistic and comparison youth. Developmental Psychobiology. 65: e22415. PMID 37860899 DOI: 10.1002/dev.22415 |
0.504 |
|
2023 |
Neuhaus E, Santhosh M, Kresse A, Aylward E, Bernier R, Bookheimer S, Jeste S, Jack A, McPartland JC, Naples A, Van Horn JD, Pelphrey K, Webb SJ. Frontal EEG alpha asymmetry in youth with autism: Sex differences and social-emotional correlates. Autism Research : Official Journal of the International Society For Autism Research. PMID 37776030 DOI: 10.1002/aur.3032 |
0.706 |
|
2023 |
Shic F, Barney EC, Naples AJ, Dommer KJ, Chang SA, Li B, McAllister T, Atyabi A, Wang Q, Bernier R, Dawson G, Dziura J, Faja S, Jeste SS, Murias M, et al. The Selective Social Attention task in children with autism spectrum disorder: Results from the Autism Biomarkers Consortium for Clinical Trials (ABC-CT) feasibility study. Autism Research : Official Journal of the International Society For Autism Research. PMID 37749934 DOI: 10.1002/aur.3026 |
0.764 |
|
2023 |
Kurtz-Nelson EC, Rea HM, Petriceks AC, Hudac CM, Wang T, Earl RK, Bernier RA, Eichler EE, Neuhaus E. Characterizing the autism spectrum phenotype in DYRK1A-related syndrome. Autism Research : Official Journal of the International Society For Autism Research. PMID 37497568 DOI: 10.1002/aur.2995 |
0.398 |
|
2023 |
Hudac CM, Friedman NR, Ward VR, Estreicher RE, Dorsey GC, Bernier RA, Kurtz-Nelson EC, Earl RK, Eichler EE, Neuhaus E. Characterizing Sensory Phenotypes of Subgroups with a Known Genetic Etiology Pertaining to Diagnoses of Autism Spectrum Disorder and Intellectual Disability. Journal of Autism and Developmental Disorders. PMID 37031308 DOI: 10.1007/s10803-023-05897-9 |
0.341 |
|
2023 |
Faja S, Sabatos-DeVito M, Sridhar A, Kuhn JL, Nikolaeva JI, Sugar CA, Webb SJ, Bernier RA, Sikich L, Hellemann G, Senturk D, Naples AJ, Shic F, Levin AR, Seow HA, et al. Evaluation of clinical assessments of social abilities for use in autism clinical trials by the autism biomarkers consortium for clinical trials. Autism Research : Official Journal of the International Society For Autism Research. PMID 36929131 DOI: 10.1002/aur.2905 |
0.749 |
|
2022 |
Jacokes Z, Jack A, Sullivan CAW, Aylward E, Bookheimer SY, Dapretto M, Bernier RA, Geschwind DH, Sukhodolsky DG, McPartland JC, Webb SJ, Torgerson CM, Eilbott J, Kenworthy L, Pelphrey KA, et al. Linear discriminant analysis of phenotypic data for classifying autism spectrum disorder by diagnosis and sex. Frontiers in Neuroscience. 16: 1040085. PMID 36466170 DOI: 10.3389/fnins.2022.1040085 |
0.732 |
|
2022 |
Klaiman C, White S, Richardson S, McQueen E, Walum H, Aoki C, Smith C, Minjarez M, Bernier R, Pedapati E, Bishop S, Ence W, Wainer A, Moriuchi J, Tay SW, et al. Expert Clinician Certainty in Diagnosing Autism Spectrum Disorder in 16-30-Month-Olds: A Multi-site Trial Secondary Analysis. Journal of Autism and Developmental Disorders. PMID 36396807 DOI: 10.1007/s10803-022-05812-8 |
0.348 |
|
2022 |
Dingemans AJM, Truijen KMG, van de Ven S, Bernier R, Bongers EMHF, Bouman A, de Graaff-Herder L, Eichler EE, Gerkes EH, De Geus CM, van Hagen JM, Jansen PR, Kerkhof J, Kievit AJA, Kleefstra T, et al. The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8. Translational Psychiatry. 12: 421. PMID 36182950 DOI: 10.1038/s41398-022-02189-1 |
0.349 |
|
2022 |
Shurtz L, Schwartz C, DiStefano C, McPartland JC, Levin AR, Dawson G, Kleinhans NM, Faja S, Webb SJ, Shic F, Naples AJ, Seow H, Bernier RA, Chawarska K, Sugar CA, et al. Concomitant medication use in children with autism spectrum disorder: Data from the Autism Biomarkers Consortium for Clinical Trials. Autism : the International Journal of Research and Practice. 13623613221121425. PMID 36086805 DOI: 10.1177/13623613221121425 |
0.732 |
|
2022 |
Webb SJ, Naples AJ, Levin AR, Hellemann G, Borland H, Benton J, Carlos C, McAllister T, Santhosh M, Seow H, Atyabi A, Bernier R, Chawarska K, Dawson G, Dziura J, et al. The Autism Biomarkers Consortium for Clinical Trials: Initial Evaluation of a Battery of Candidate EEG Biomarkers. The American Journal of Psychiatry. appiajp21050485. PMID 36000217 DOI: 10.1176/appi.ajp.21050485 |
0.721 |
|
2022 |
Tsang T, Naples AJ, Barney EC, Xie M, Bernier R, Dawson G, Dziura J, Faja S, Jeste SS, McPartland JC, Nelson CA, Murias M, Seow H, Sugar C, Webb SJ, et al. Attention Allocation During Exploration of Visual Arrays in ASD: Results from the ABC-CT Feasibility Study. Journal of Autism and Developmental Disorders. PMID 35657448 DOI: 10.1007/s10803-022-05569-0 |
0.746 |
|
2022 |
Webb SJ, Emerman I, Sugar C, Senturk D, Naples AJ, Faja S, Benton J, Borland H, Carlos C, Levin AR, McAllister T, Santhosh M, Bernier RA, Chawarska K, Dawson G, et al. Identifying Age Based Maturation in the ERP Response to Faces in Children With Autism: Implications for Developing Biomarkers for Use in Clinical Trials. Frontiers in Psychiatry. 13: 841236. PMID 35615454 DOI: 10.3389/fpsyt.2022.841236 |
0.739 |
|
2022 |
Sridhar A, Kuhn J, Faja S, Sabatos-DeVito M, Nikolaeva JI, Dawson G, Nelson CA, Webb SJ, Bernier R, Jeste S, Chawarska K, Sugar CA, Shic F, Naples A, Dziura J, et al. Patterns of Intervention Utilization Among School-Aged Children with Autism Spectrum Disorder: Findings from a Multi-Site Research Consortium. Research in Autism Spectrum Disorders. 94. PMID 35444715 DOI: 10.1016/j.rasd.2022.101950 |
0.722 |
|
2022 |
Shic F, Naples AJ, Barney EC, Chang SA, Li B, McAllister T, Kim M, Dommer KJ, Hasselmo S, Atyabi A, Wang Q, Helleman G, Levin AR, Seow H, Bernier R, et al. The autism biomarkers consortium for clinical trials: evaluation of a battery of candidate eye-tracking biomarkers for use in autism clinical trials. Molecular Autism. 13: 15. PMID 35313957 DOI: 10.1186/s13229-021-00482-2 |
0.713 |
|
2021 |
Dillon EF, Kanne S, Landa RJ, Annett R, Bernier R, Bradley C, Carpenter L, Kim SH, Parish-Morris J, Schultz R, Wodka EL. Sex Differences in Autism: Examining Intrinsic and Extrinsic Factors in Children and Adolescents Enrolled in a National ASD Cohort. Journal of Autism and Developmental Disorders. PMID 34859339 DOI: 10.1007/s10803-021-05385-y |
0.354 |
|
2021 |
Neuhaus E, Lowry SJ, Santhosh M, Kresse A, Edwards LA, Keller J, Libsack EJ, Kang VY, Naples A, Jack A, Jeste S, McPartland JC, Aylward E, Bernier R, Bookheimer S, et al. Resting state EEG in youth with ASD: age, sex, and relation to phenotype. Journal of Neurodevelopmental Disorders. 13: 33. PMID 34517813 DOI: 10.1186/s11689-021-09390-1 |
0.717 |
|
2021 |
Aaronson B, Estes A, Rogers SJ, Dawson G, Bernier R. The Early Start Denver Model Intervention and Mu Rhythm Attenuation in Autism Spectrum Disorders. Journal of Autism and Developmental Disorders. PMID 34309743 DOI: 10.1007/s10803-021-05190-7 |
0.501 |
|
2021 |
Arnett AB, Wang T, Eichler EE, Bernier RA. Reflections on the genetics-first approach to advancements in molecular genetic and neurobiological research on neurodevelopmental disorders. Journal of Neurodevelopmental Disorders. 13: 24. PMID 34148555 DOI: 10.1186/s11689-021-09371-4 |
0.343 |
|
2021 |
Arnett AB, Wang T, Eichler EE, Bernier RA. Reflections on the genetics-first approach to advancements in molecular genetic and neurobiological research on neurodevelopmental disorders. Journal of Neurodevelopmental Disorders. 13: 24. PMID 34148555 DOI: 10.1186/s11689-021-09371-4 |
0.343 |
|
2021 |
Lawrence KE, Hernandez LM, Fuster E, Padgaonkar NT, Patterson G, Jung J, Okada NJ, Lowe JK, Hoekstra JN, Jack A, Aylward E, Gaab N, Van Horn JD, Bernier RA, McPartland JC, et al. Impact of autism genetic risk on brain connectivity: a mechanism for the female protective effect. Brain : a Journal of Neurology. PMID 34050743 DOI: 10.1093/brain/awab204 |
0.715 |
|
2021 |
Hudac CM, Naples A, DesChamps TD, Coffman MC, Kresse A, Ward T, Mukerji C, Aaronson B, Faja S, McPartland JC, Bernier R. Modeling temporal dynamics of face processing in youth and adults. Social Neuroscience. PMID 33882266 DOI: 10.1080/17470919.2021.1920050 |
0.508 |
|
2021 |
Jack A, Sullivan CAW, Aylward E, Bookheimer SY, Dapretto M, Gaab N, Van Horn JD, Eilbott J, Jacokes Z, Torgerson CM, Bernier RA, Geschwind DH, McPartland JC, Nelson CA, Webb SJ, et al. A neurogenetic analysis of female autism. Brain : a Journal of Neurology. PMID 33860292 DOI: 10.1093/brain/awab064 |
0.683 |
|
2021 |
McQuaid GA, Pelphrey KA, Bookheimer SY, Dapretto M, Webb SJ, Bernier RA, McPartland JC, Van Horn JD, Wallace GL. The gap between IQ and adaptive functioning in autism spectrum disorder: Disentangling diagnostic and sex differences. Autism : the International Journal of Research and Practice. 1362361321995620. PMID 33715473 DOI: 10.1177/1362361321995620 |
0.691 |
|
2021 |
Neuhaus E, Kang VY, Kresse A, Corrigan S, Aylward E, Bernier R, Bookheimer S, Dapretto M, Jack A, Jeste S, McPartland JC, Van Horn JD, Pelphrey K, Webb SJ. Language and Aggressive Behaviors in Male and Female Youth with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. PMID 33682042 DOI: 10.1007/s10803-020-04773-0 |
0.717 |
|
2020 |
Harrop C, Libsack E, Bernier R, Dapretto M, Jack A, McPartland JC, Van Horn JD, Webb SJ, Pelphrey K. Do Biological Sex and Early Developmental Milestones Predict the Age of First Concerns and Eventual Diagnosis in Autism Spectrum Disorder? Autism Research : Official Journal of the International Society For Autism Research. PMID 33274604 DOI: 10.1002/aur.2446 |
0.681 |
|
2020 |
Neuhaus E, Bernier RA, Webb SJ. Social Motivation Across Multiple Measures: Caregiver-Report of Children with Autism Spectrum Disorder. Autism Research : Official Journal of the International Society For Autism Research. PMID 32929890 DOI: 10.1002/Aur.2386 |
0.579 |
|
2020 |
Trinh S, Arnett A, Kurtz-Nelson E, Beighley J, Picoto M, Bernier R. Transcriptional subtyping explains phenotypic variability in genetic subtypes of autism spectrum disorder. Development and Psychopathology. 1-9. PMID 32912353 DOI: 10.1017/S0954579420000784 |
0.487 |
|
2020 |
Kim SH, Green-Snyder L, Lord C, Bishop S, Steinman KJ, Bernier R, Hanson E, Goin-Kochel RP, Chung WK. Language characterization in 16p11.2 deletion and duplication syndromes. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 32652891 DOI: 10.1002/Ajmg.B.32809 |
0.375 |
|
2020 |
Hudac CM, Bove J, Barber S, Duyzend M, Wallace A, Martin CL, Ledbetter DH, Hanson E, Goin-Kochel RP, Green-Snyder L, Chung WK, Eichler EE, Bernier RA. Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers. Autism Research : Official Journal of the International Society For Autism Research. PMID 32597026 DOI: 10.1002/Aur.2332 |
0.741 |
|
2020 |
Lawrence KE, Hernandez LM, Eilbott J, Jack A, Aylward E, Gaab N, Van Horn JD, Bernier RA, Geschwind DH, McPartland JC, Nelson CA, Webb SJ, Pelphrey KA, Bookheimer SY, Dapretto M, et al. Neural responsivity to social rewards in autistic female youth. Translational Psychiatry. 10: 178. PMID 32488083 DOI: 10.1038/S41398-020-0824-8 |
0.682 |
|
2020 |
Frasch MG, Shen C, Wu HT, Mueller A, Neuhaus E, Bernier RA, Kamara D, Beauchaine TP. Brief Report: Can a Composite Heart Rate Variability Biomarker Shed New Insights About Autism Spectrum Disorder in School-Aged Children? Journal of Autism and Developmental Disorders. PMID 32449059 DOI: 10.1007/S10803-020-04467-7 |
0.356 |
|
2020 |
Levin AR, Naples AJ, Scheffler AW, Webb SJ, Shic F, Sugar CA, Murias M, Bernier RA, Chawarska K, Dawson G, Faja S, Jeste S, Nelson CA, McPartland JC, Şentürk D. Day-to-Day Test-Retest Reliability of EEG Profiles in Children With Autism Spectrum Disorder and Typical Development. Frontiers in Integrative Neuroscience. 14: 21. PMID 32425762 DOI: 10.3389/Fnint.2020.00021 |
0.737 |
|
2020 |
Myers SM, Challman TD, Bernier R, Bourgeron T, Chung WK, Constantino JN, Eichler EE, Jacquemont S, Miller DT, Mitchell KJ, Zoghbi HY, Martin CL, Ledbetter DH. Insufficient Evidence for "Autism-Specific" Genes. American Journal of Human Genetics. PMID 32359473 DOI: 10.1016/J.Ajhg.2020.04.004 |
0.43 |
|
2020 |
Lawrence KE, Hernandez LM, Bowman HC, Padgaonkar NT, Fuster E, Jack A, Aylward E, Gaab N, Van Horn JD, Bernier RA, Geschwind DH, McPartland JC, Nelson CA, Webb SJ, Pelphrey KA, et al. Sex Differences in Functional Connectivity of the Salience, Default Mode, and Central Executive Networks in Youth with ASD. Cerebral Cortex (New York, N.Y. : 1991). PMID 32350530 DOI: 10.1093/Cercor/Bhaa105 |
0.689 |
|
2020 |
McPartland JC, Bernier RA, Jeste SS, Dawson G, Nelson CA, Chawarska K, Earl R, Faja S, Johnson SP, Sikich L, Brandt CA, Dziura JD, Rozenblit L, Hellemann G, Levin AR, et al. The Autism Biomarkers Consortium for Clinical Trials (ABC-CT): Scientific Context, Study Design, and Progress Toward Biomarker Qualification. Frontiers in Integrative Neuroscience. 14: 16. PMID 32346363 DOI: 10.3389/Fnint.2020.00016 |
0.732 |
|
2020 |
Schaaf CP, Betancur C, Yuen RKC, Parr JR, Skuse DH, Gallagher L, Bernier RA, Buchanan JA, Buxbaum JD, Chen CA, Dies KA, Elsabbagh M, Firth HV, Frazier T, Hoang N, et al. A framework for an evidence-based gene list relevant to autism spectrum disorder. Nature Reviews. Genetics. PMID 32317787 DOI: 10.1038/S41576-020-0231-2 |
0.339 |
|
2020 |
Hernandez LM, Lawrence KE, Padgaonkar NT, Inada M, Hoekstra JN, Lowe JK, Eilbott J, Jack A, Aylward E, Gaab N, Van Horn JD, Bernier RA, McPartland JC, Webb SJ, Pelphrey KA, et al. Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity. Translational Psychiatry. 10: 82. PMID 32127526 DOI: 10.1038/S41398-020-0750-9 |
0.681 |
|
2020 |
Cheng H, Gottlieb L, Marchi E, Kleyner R, Bhardwaj P, Rope AF, Rosenheck S, Moutton S, Philippe C, Eyaid W, Alkuraya FS, Toribio J, Mena R, Prada CE, Stessman H, ... Bernier R, et al. Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15. Human Molecular Genetics. PMID 32027362 DOI: 10.1093/Hmg/Ddz173 |
0.36 |
|
2020 |
Scott TM, Guo H, Eichler EE, Rosenfeld JA, Pang K, Liu Z, Lalani S, Weimin B, Yang Y, Bacino CA, Streff H, Lewis AM, Koenig MK, Thiffault I, Bellomo A, ... ... Bernier R, et al. BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability and autism spectrum disorder. Human Mutation. PMID 31999386 DOI: 10.1002/Humu.23992 |
0.454 |
|
2019 |
Webb SJ, Shic F, Murias M, Sugar CA, Naples AJ, Barney E, Borland H, Hellemann G, Johnson S, Kim M, Levin AR, Sabatos-DeVito M, Santhosh M, Senturk D, Dziura J, ... Bernier RA, et al. Biomarker Acquisition and Quality Control for Multi-Site Studies: The Autism Biomarkers Consortium for Clinical Trials. Frontiers in Integrative Neuroscience. 13: 71. PMID 32116579 DOI: 10.3389/Fnint.2019.00071 |
0.724 |
|
2019 |
Beighley JS, Hudac CM, Arnett AB, Peterson JL, Gerdts J, Wallace AS, Mefford HC, Hoekzema K, Turner TN, O'Roak BJ, Eichler EE, Bernier RA. Clinical Phenotypes of Carriers of Mutations in CHD8 or Its Conserved Target Genes. Biological Psychiatry. PMID 31526516 DOI: 10.1016/J.Biopsych.2019.07.020 |
0.723 |
|
2019 |
Sabatos-DeVito M, Murias M, Dawson G, Howell T, Yuan A, Marsan S, Bernier RA, Brandt CA, Chawarska K, Dzuira JD, Faja S, Jeste SS, Naples A, Nelson CA, Shic F, et al. Methodological considerations in the use of Noldus EthoVision XT video tracking of children with autism in multi-site studies. Biological Psychology. PMID 31163191 DOI: 10.1016/J.Biopsycho.2019.05.012 |
0.789 |
|
2019 |
Neuhaus E, Webb SJ, Bernier RA. Linking social motivation with social skill: The role of emotion dysregulation in autism spectrum disorder. Development and Psychopathology. 1-13. PMID 30957732 DOI: 10.1017/S0954579419000361 |
0.564 |
|
2019 |
Niarchou M, Chawner SJRA, Doherty JL, Maillard AM, Jacquemont S, Chung WK, Green-Snyder L, Bernier RA, Goin-Kochel RP, Hanson E, Linden DEJ, Linden SC, Raymond FL, Skuse D, Hall J, et al. Psychiatric disorders in children with 16p11.2 deletion and duplication. Translational Psychiatry. 9: 8. PMID 30664628 DOI: 10.1038/S41398-018-0339-8 |
0.319 |
|
2019 |
Patowary A, Won SY, Oh SJ, Nesbitt RR, Archer M, Nickerson D, Raskind WH, Bernier R, Lee JE, Brkanac Z. Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene. Translational Psychiatry. 9: 4. PMID 30664616 DOI: 10.1038/S41398-018-0343-Z |
0.435 |
|
2018 |
Myers E, Stone WL, Bernier R, Lendvay T, Comstock B, Cowan C. The diagnosis conundrum: Comparison of crowdsourced and expert assessments of toddlers with high and low risk of autism spectrum disorder. Autism Research : Official Journal of the International Society For Autism Research. 11: 1629-1634. PMID 30475456 DOI: 10.1002/Aur.2030 |
0.446 |
|
2018 |
Neuhaus E, Bernier RA, Tham SW, Webb SJ. Gastrointestinal and Psychiatric Symptoms Among Children and Adolescents With Autism Spectrum Disorder. Frontiers in Psychiatry. 9: 515. PMID 30405456 DOI: 10.3389/Fpsyt.2018.00515 |
0.587 |
|
2018 |
Arnett AB, Hudac CM, DesChamps TD, Cairney BE, Gerdts J, Wallace AS, Bernier RA, Webb SJ. Auditory perception is associated with implicit language learning and receptive language ability in autism spectrum disorder. Brain and Language. 187: 1-8. PMID 30312833 DOI: 10.1016/J.Bandl.2018.09.007 |
0.756 |
|
2018 |
Arnett AB, Rhoads CL, Hoekzema K, Turner TN, Gerdts J, Wallace AS, Bedrosian-Sermone S, Eichler EE, Bernier RA. The autism spectrum phenotype in ADNP syndrome. Autism Research : Official Journal of the International Society For Autism Research. PMID 30107084 DOI: 10.1002/Aur.1980 |
0.38 |
|
2018 |
Arnett AB, Trinh S, Bernier RA. The state of research on the genetics of autism spectrum disorder: methodological, clinical and conceptual progress. Current Opinion in Psychology. 27: 1-5. PMID 30059871 DOI: 10.1016/j.copsyc.2018.07.004 |
0.382 |
|
2018 |
Van Dijck A, Vulto-van Silfhout AT, Cappuyns E, van der Werf IM, Mancini GM, Tzschach A, Bernier R, Gozes I, Eichler EE, Romano C, Lindstrand A, Nordgren A, Kvarnung M, Kleefstra T, et al. Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP. Biological Psychiatry. PMID 29724491 DOI: 10.1016/J.Biopsych.2018.02.1173 |
0.405 |
|
2018 |
Hudac CM, DesChamps TD, Arnett AB, Cairney BE, Ma R, Webb SJ, Bernier RA. Early enhanced processing and delayed habituation to deviance sounds in autism spectrum disorder. Brain and Cognition. 123: 110-119. PMID 29550506 DOI: 10.1016/J.Bandc.2018.03.004 |
0.773 |
|
2018 |
Wallace AS, Hudac CM, Steinman KJ, Peterson JL, DesChamps TD, Duyzend MH, Nuttle X, Eichler EE, Bernier RA. Longitudinal report of child with de novo 16p11.2 triplication. Clinical Case Reports. 6: 147-154. PMID 29375855 DOI: 10.1002/Ccr3.1236 |
0.723 |
|
2018 |
Gerdts J, Mancini J, Fox E, Rhoads C, Ward T, Easley E, Bernier RA. Interdisciplinary Team Evaluation: An Effective Method for the Diagnostic Assessment of Autism Spectrum Disorder. Journal of Developmental and Behavioral Pediatrics : Jdbp. PMID 29346136 DOI: 10.1097/Dbp.0000000000000549 |
0.315 |
|
2018 |
Schallmo M, Kale A, Kolodny T, Millin R, Bernier R, Murray S. Weaker neural suppression in autism spectrum disorder Journal of Vision. 18: 548. DOI: 10.1167/18.10.548 |
0.43 |
|
2018 |
Aaronson B, Estes AM, Rogers SJ, Dawson G, Bernier R. 5.15 The Impact of Comprehensive Behavioral Intervention on Mu Rhythm Attenuation in ASD Journal of the American Academy of Child & Adolescent Psychiatry. 57: S232. DOI: 10.1016/J.Jaac.2018.09.310 |
0.502 |
|
2017 |
Neuhaus E, Beauchaine TP, Bernier RA, Webb SJ. Child and family characteristics moderate agreement between caregiver and clinician report of autism symptoms. Autism Research : Official Journal of the International Society For Autism Research. PMID 29251835 DOI: 10.1002/Aur.1907 |
0.675 |
|
2017 |
Neuhaus E, Beauchaine TP, Bernier RA, Webb SJ. Child and family characteristics moderate agreement between caregiver and clinician report of autism symptoms. Autism Research : Official Journal of the International Society For Autism Research. PMID 29251835 DOI: 10.1002/aur.1907 |
0.308 |
|
2017 |
Luhrs K, Ward T, Hudac CM, Gerdts J, Stessman HAF, Eichler EE, Bernier RA. Associations between Familial Rates of Psychiatric Disorders and De Novo Genetic Mutations in Autism. Autism Research and Treatment. 2017: 9371964. PMID 29250444 DOI: 10.1155/2017/9371964 |
0.739 |
|
2017 |
Siper PM, De Rubeis S, Trelles MDP, Durkin A, Di Marino D, Muratet F, Frank Y, Lozano R, Eichler EE, Kelly M, Beighley J, Gerdts J, Wallace AS, Mefford HC, Bernier RA, et al. Prospective investigation of FOXP1 syndrome. Molecular Autism. 8: 57. PMID 29090079 DOI: 10.1186/S13229-017-0172-6 |
0.327 |
|
2017 |
Earl RK, Turner TN, Mefford HC, Hudac CM, Gerdts J, Eichler EE, Bernier RA. Clinical phenotype of ASD-associated DYRK1A haploinsufficiency. Molecular Autism. 8: 54. PMID 29034068 DOI: 10.1186/S13229-017-0173-5 |
0.727 |
|
2017 |
Ackerman S, Schoenbrun S, Hudac C, Bernier R. 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. PMID 28887608 DOI: 10.1007/s10803-017-3301-3 |
0.72 |
|
2017 |
Krupp DR, Barnard RA, Duffourd Y, Evans SA, Mulqueen RM, Bernier R, Rivière JB, Fombonne E, O'Roak BJ. Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder. American Journal of Human Genetics. PMID 28867142 DOI: 10.1016/J.Ajhg.2017.07.016 |
0.415 |
|
2017 |
Goin-Kochel RP, Trinh S, Barber S, Bernier R. Gene Disrupting Mutations Associated with Regression in Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. PMID 28856484 DOI: 10.1007/S10803-017-3256-4 |
0.423 |
|
2017 |
Ackerman S, Schoenrbun S, Hudac C, Bernier R. Interactive Effects of Prenatal Antidepressant Exposure and Likely Gene Disrupting Mutations on the Severity of Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. PMID 28770524 DOI: 10.1007/S10803-017-3246-6 |
0.74 |
|
2017 |
Hudac CM, Stessman HAF, DesChamps TD, Kresse A, Faja S, Neuhaus E, Webb SJ, Eichler EE, Bernier RA. Exploring the heterogeneity of neural social indices for genetically distinct etiologies of autism. Journal of Neurodevelopmental Disorders. 9: 24. PMID 28559932 DOI: 10.1186/S11689-017-9199-4 |
0.803 |
|
2017 |
Patowary A, Nesbitt R, Archer M, Bernier R, Brkanac Z. Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder. Autism Research : Official Journal of the International Society For Autism Research. PMID 28419775 DOI: 10.1002/Aur.1792 |
0.367 |
|
2017 |
Bernier R, Hudac CM, Chen Q, Zeng C, Wallace AS, Gerdts J, Earl R, Peterson J, Wolken A, Peters A, Hanson E, Goin-Kochel RP, Kanne S, Snyder LG, Chung WK, et al. Developmental trajectories for young children with 16p11.2 copy number variation. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 28349640 DOI: 10.1002/Ajmg.B.32525 |
0.759 |
|
2017 |
Jansen S, Geuer S, Pfundt R, Brough R, Ghongane P, Herkert JC, Marco EJ, Willemsen MH, Kleefstra T, Hannibal M, Shieh JT, Lynch SA, Flinter F, FitzPatrick DR, Gardham A, ... ... Bernier R, et al. De Novo Truncating Mutations in the Last and Penultimate Exons of PPM1D Cause an Intellectual Disability Syndrome. American Journal of Human Genetics. PMID 28343630 DOI: 10.1016/J.Ajhg.2017.02.005 |
0.377 |
|
2016 |
Rubinstein M, Patowary A, Stanaway IB, McCord E, Nesbitt RR, Archer M, Scheuer T, Nickerson D, Raskind WH, Wijsman EM, Bernier R, Catterall WA, Brkanac Z. Association of rare missense variants in the second intracellular loop of Na1.7 sodium channels with familial autism. Molecular Psychiatry. 23: 231-239. PMID 27956748 DOI: 10.1038/Mp.2016.222 |
0.369 |
|
2016 |
Jane Webb S, Garrison MM, Bernier R, McClintic AM, King BH, Mourad PD. Severity of ASD symptoms and their correlation with the presence of copy number variations and exposure to first trimester ultrasound. Autism Research : Official Journal of the International Society For Autism Research. PMID 27582229 DOI: 10.1002/Aur.1690 |
0.457 |
|
2016 |
Green Snyder L, D'Angelo D, Chen Q, Bernier R, Goin-Kochel RP, Wallace AS, Gerdts J, Kanne S, Berry L, Blaskey L, Kuschner E, Roberts T, Sherr E, Martin CL, Ledbetter DH, et al. Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication. Journal of Autism and Developmental Disorders. PMID 27207092 DOI: 10.1007/S10803-016-2807-4 |
0.504 |
|
2016 |
Stessman HA, Willemsen MH, Fenckova M, Penn O, Hoischen A, Xiong B, Wang T, Hoekzema K, Vives L, Vogel I, Brunner HG, van der Burgt I, Ockeloen CW, Schuurs-Hoeijmakers JH, Klein Wassink-Ruiter JS, ... ... Bernier RA, et al. Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders. American Journal of Human Genetics. 98: 541-552. PMID 26942287 DOI: 10.1016/J.Ajhg.2016.02.004 |
0.357 |
|
2016 |
Faja S, Dawson G, Sullivan K, Meltzoff AN, Estes A, Bernier R. Executive function predicts the development of play skills for verbal preschoolers with autism spectrum disorders. Autism Research : Official Journal of the International Society For Autism Research. PMID 26890821 DOI: 10.1002/Aur.1608 |
0.554 |
|
2016 |
Lugtenberg D, Reijnders MR, Fenckova M, Bijlsma EK, Bernier R, van Bon BW, Smeets E, Vulto-van Silfhout AT, Bosch D, Eichler EE, Mefford HC, Carvill GL, Bongers EM, Schuurs-Hoeijmakers JH, Ruivenkamp CA, et al. De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila. European Journal of Human Genetics : Ejhg. PMID 26757981 DOI: 10.1038/Ejhg.2015.282 |
0.332 |
|
2016 |
Bernier R, Dawson G. 3 Autism Spectrum Disorders Development and Psychopathology. DOI: 10.1002/9781119125556.Devpsy303 |
0.653 |
|
2015 |
Duyzend MH, Nuttle X, Coe BP, Baker C, Nickerson DA, Bernier R, Eichler EE. Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV. American Journal of Human Genetics. PMID 26749307 DOI: 10.1016/J.Ajhg.2015.11.017 |
0.378 |
|
2015 |
Hippolyte L, Maillard AM, Rodriguez-Herreros B, Pain A, Martin-Brevet S, Ferrari C, Conus P, Macé A, Hadjikhani N, Metspalu A, Reigo A, Kolk A, Männik K, Barker M, Isidor B, ... ... Bernier R, et al. The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition. Biological Psychiatry. PMID 26742926 DOI: 10.1016/J.Biopsych.2015.10.021 |
0.341 |
|
2015 |
D'Angelo D, Lebon S, Chen Q, Martin-Brevet S, Snyder LG, Hippolyte L, Hanson E, Maillard AM, Faucett WA, Macé A, Pain A, Bernier R, Chawner SJ, David A, Andrieux J, et al. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. Jama Psychiatry. 1-11. PMID 26629640 DOI: 10.1001/Jamapsychiatry.2015.2123 |
0.374 |
|
2015 |
Neuhaus E, Bernier RA, Beauchaine TP. Children with Autism Show Altered Autonomic Adaptation to Novel and Familiar Social Partners. Autism Research : Official Journal of the International Society For Autism Research. PMID 26305051 DOI: 10.1002/Aur.1543 |
0.361 |
|
2015 |
Hudac CM, Kresse A, Aaronson B, DesChamps TD, Webb SJ, Bernier RA. Modulation of mu attenuation to social stimuli in children and adults with 16p11.2 deletions and duplications. Journal of Neurodevelopmental Disorders. 7: 25. PMID 26213586 DOI: 10.1186/S11689-015-9118-5 |
0.782 |
|
2015 |
Chapman NH, Nato AQ, Bernier R, Ankenman K, Sohi H, Munson J, Patowary A, Archer M, Blue EM, Webb SJ, Coon H, Raskind WH, Brkanac Z, Wijsman EM. Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes. Human Genetics. 134: 1055-68. PMID 26204995 DOI: 10.1007/S00439-015-1585-Y |
0.618 |
|
2015 |
Neuhaus E, Kresse A, Faja S, Bernier RA, Webb SJ. Face processing among twins with and without autism: social correlates and twin concordance. Social Cognitive and Affective Neuroscience. PMID 26137974 DOI: 10.1093/Scan/Nsv085 |
0.557 |
|
2015 |
Krumm N, Turner TN, Baker C, Vives L, Mohajeri K, Witherspoon K, Raja A, Coe BP, Stessman HA, He ZX, Leal SM, Bernier R, Eichler EE. Excess of rare, inherited truncating mutations in autism. Nature Genetics. 47: 582-8. PMID 25961944 DOI: 10.1038/Ng.3303 |
0.36 |
|
2015 |
Higdon R, Earl RK, Stanberry L, Hudac CM, Montague E, Stewart E, Janko I, Choiniere J, Broomall W, Kolker N, Bernier RA, Kolker E. The promise of multi-omics and clinical data integration to identify and target personalized healthcare approaches in autism spectrum disorders. Omics : a Journal of Integrative Biology. 19: 197-208. PMID 25831060 DOI: 10.1089/Omi.2015.0020 |
0.725 |
|
2015 |
van Bon BW, Coe BP, Bernier R, Green C, Gerdts J, Witherspoon K, Kleefstra T, Willemsen MH, Kumar R, Bosco P, Fichera M, Li D, Amaral D, Cristofoli F, Peeters H, et al. Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. Molecular Psychiatry. PMID 25707398 DOI: 10.1038/Mp.2015.5 |
0.411 |
|
2015 |
Mazina V, Gerdts J, Trinh S, Ankenman K, Ward T, Dennis MY, Girirajan S, Eichler EE, Bernier R. Epigenetics of autism-related impairment: copy number variation and maternal infection. Journal of Developmental and Behavioral Pediatrics : Jdbp. 36: 61-7. PMID 25629966 DOI: 10.1097/Dbp.0000000000000126 |
0.405 |
|
2015 |
Neuhaus E, Bernier RA, Beauchaine TP. Electrodermal Response to Reward and Non-Reward Among Children With Autism. Autism Research : Official Journal of the International Society For Autism Research. PMID 25599655 DOI: 10.1002/Aur.1451 |
0.333 |
|
2015 |
Moreno-De-Luca A, Evans DW, Boomer KB, Hanson E, Bernier R, Goin-Kochel RP, Myers SM, Challman TD, Moreno-De-Luca D, Slane MM, Hare AE, Chung WK, Spiro JE, Faucett WA, Martin CL, et al. The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions. Jama Psychiatry. 72: 119-26. PMID 25493922 DOI: 10.1001/Jamapsychiatry.2014.2147 |
0.329 |
|
2015 |
Nelson TM, Sheller B, Friedman CS, Bernier R. Educational and therapeutic behavioral approaches to providing dental care for patients with Autism Spectrum Disorder. Special Care in Dentistry : Official Publication of the American Association of Hospital Dentists, the Academy of Dentistry For the Handicapped, and the American Society For Geriatric Dentistry. 35: 105-13. PMID 25470557 DOI: 10.1111/Scd.12101 |
0.381 |
|
2015 |
McPartland JC, Bernier R, South M. Realizing the translational promise of psychophysiological research in ASD. Journal of Autism and Developmental Disorders. 45: 277-82. PMID 25429873 DOI: 10.1007/S10803-014-2325-1 |
0.682 |
|
2015 |
Naples A, Nguyen-Phuc A, Coffman M, Kresse A, Faja S, Bernier R, McPartland JC. Erratum to: A computer-generated animated face stimulus set for psychophysiological research. Behavior Research Methods. 47: 571. PMID 25304732 DOI: 10.3758/S13428-014-0518-3 |
0.525 |
|
2015 |
Naples A, Nguyen-Phuc A, Coffman M, Kresse A, Faja S, Bernier R, McPartland JC. A computer-generated animated face stimulus set for psychophysiological research. Behavior Research Methods. 47: 562-70. PMID 25028164 DOI: 10.3758/S13428-014-0491-X |
0.558 |
|
2015 |
Webb SJ, Bernier R, Henderson HA, Johnson MH, Jones EJ, Lerner MD, McPartland JC, Nelson CA, Rojas DC, Townsend J, Westerfield M. Guidelines and best practices for electrophysiological data collection, analysis and reporting in autism. Journal of Autism and Developmental Disorders. 45: 425-43. PMID 23975145 DOI: 10.1007/S10803-013-1916-6 |
0.704 |
|
2015 |
Chapman NH, Nato AQ, Bernier R, Ankenman K, Sohi H, Munson J, Patowary A, Archer M, Blue EM, Webb SJ, Coon H, Raskind WH, Brkanac Z, Wijsman EM. Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes Human Genetics. DOI: 10.1007/s00439-015-1585-y |
0.545 |
|
2014 |
O'Roak BJ, Stessman HA, Boyle EA, Witherspoon KT, Martin B, Lee C, Vives L, Baker C, Hiatt JB, Nickerson DA, Bernier R, Shendure J, Eichler EE. Recurrent de novo mutations implicate novel genes underlying simplex autism risk. Nature Communications. 5: 5595. PMID 25418537 DOI: 10.1038/Ncomms6595 |
0.417 |
|
2014 |
Buxbaum JD, Bolshakova N, Brownfeld JM, Anney RJ, Bender P, Bernier R, Cook EH, Coon H, Cuccaro M, Freitag CM, Hallmayer J, Geschwind D, Klauck SM, Nurnberger JI, Oliveira G, et al. The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses. Molecular Autism. 5: 34. PMID 25392729 DOI: 10.1186/2040-2392-5-34 |
0.397 |
|
2014 |
Vandeweyer G, Helsmoortel C, Van Dijck A, Vulto-van Silfhout AT, Coe BP, Bernier R, Gerdts J, Rooms L, van den Ende J, Bakshi M, Wilson M, Nordgren A, Hendon LG, Abdulrahman OA, Romano C, et al. The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 166: 315-26. PMID 25169753 DOI: 10.1002/Ajmg.C.31413 |
0.377 |
|
2014 |
Bernier R, Golzio C, Xiong B, Stessman HA, Coe BP, Penn O, Witherspoon K, Gerdts J, Baker C, Vulto-van Silfhout AT, Schuurs-Hoeijmakers JH, Fichera M, Bosco P, Buono S, Alberti A, et al. Disruptive CHD8 mutations define a subtype of autism early in development. Cell. 158: 263-76. PMID 24998929 DOI: 10.1016/J.Cell.2014.06.017 |
0.483 |
|
2014 |
Ackerman S, Wenegrat J, Rettew D, Althoff R, Bernier R. No increase in autism-associated genetic events in children conceived by assisted reproduction. Fertility and Sterility. 102: 388-93. PMID 24842673 DOI: 10.1016/J.Fertnstert.2014.04.020 |
0.456 |
|
2014 |
Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, ... ... Bernier R, et al. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics. 94: 677-94. PMID 24768552 DOI: 10.1016/J.Ajhg.2014.03.018 |
0.591 |
|
2014 |
Bernier R, Aaronson B, Kresse A. EEG mu rhythm in typical and atypical development. Journal of Visualized Experiments : Jove. PMID 24747917 DOI: 10.3791/51412 |
0.401 |
|
2014 |
Stessman HA, Bernier R, Eichler EE. A genotype-first approach to defining the subtypes of a complex disease. Cell. 156: 872-7. PMID 24581488 DOI: 10.1016/J.Cell.2014.02.002 |
0.308 |
|
2014 |
Ankenman K, Elgin J, Sullivan K, Vincent L, Bernier R. Nonverbal and verbal cognitive discrepancy profiles in autism spectrum disorders: influence of age and gender. American Journal On Intellectual and Developmental Disabilities. 119: 84-99. PMID 24450323 DOI: 10.1352/1944-7558-119.1.84 |
0.501 |
|
2014 |
King BH, Navot N, Bernier R, Webb SJ. Update on diagnostic classification in autism. Current Opinion in Psychiatry. 27: 105-9. PMID 24441420 DOI: 10.1097/Yco.0000000000000040 |
0.615 |
|
2014 |
Neuhaus E, Bernier R, Beauchaine TP. Brief report: social skills, internalizing and externalizing symptoms, and respiratory sinus arrhythmia in autism. Journal of Autism and Developmental Disorders. 44: 730-7. PMID 23982488 DOI: 10.1007/S10803-013-1923-7 |
0.436 |
|
2013 |
Dawson G, Bernier R. A quarter century of progress on the early detection and treatment of autism spectrum disorder. Development and Psychopathology. 25: 1455-72. PMID 24342850 DOI: 10.1017/S0954579413000710 |
0.574 |
|
2013 |
Krumm N, O'Roak BJ, Karakoc E, Mohajeri K, Nelson B, Vives L, Jacquemont S, Munson J, Bernier R, Eichler EE. Transmission disequilibrium of small CNVs in simplex autism. American Journal of Human Genetics. 93: 595-606. PMID 24035194 DOI: 10.1016/J.Ajhg.2013.07.024 |
0.321 |
|
2013 |
Bernier R, Aaronson B, McPartland J. The role of imitation in the observed heterogeneity in EEG mu rhythm in autism and typical development. Brain and Cognition. 82: 69-75. PMID 23511847 DOI: 10.1016/J.Bandc.2013.02.008 |
0.684 |
|
2013 |
Girirajan S, Dennis MY, Baker C, Malig M, Coe BP, Campbell CD, Mark K, Vu TH, Alkan C, Cheng Z, Biesecker LG, Bernier R, Eichler EE. Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder. American Journal of Human Genetics. 92: 221-37. PMID 23375656 DOI: 10.1016/J.Ajhg.2012.12.016 |
0.407 |
|
2013 |
Gerdts JA, Bernier R, Dawson G, Estes A. The broader autism phenotype in simplex and multiplex families. Journal of Autism and Developmental Disorders. 43: 1597-605. PMID 23117424 DOI: 10.1007/S10803-012-1706-6 |
0.497 |
|
2013 |
Oberman LM, McCleery JP, Hubbard EM, Bernier R, Wiersema JR, Raymaekers R, Pineda JA. Developmental changes in mu suppression to observed and executed actions in autism spectrum disorders. Social Cognitive and Affective Neuroscience. 8: 300-4. PMID 22302843 DOI: 10.1093/scan/nsr097 |
0.358 |
|
2012 |
Marchani EE, Chapman NH, Cheung CY, Ankenman K, Stanaway IB, Coon HH, Nickerson D, Bernier R, Brkanac Z, Wijsman EM. Identification of rare variants from exome sequence in a large pedigree with autism. Human Heredity. 74: 153-64. PMID 23594493 DOI: 10.1159/000346560 |
0.316 |
|
2012 |
O'Roak BJ, Vives L, Fu W, Egertson JD, Stanaway IB, Phelps IG, Carvill G, Kumar A, Lee C, Ankenman K, Munson J, Hiatt JB, Turner EH, Levy R, O'Day DR, ... ... Bernier R, et al. Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. Science (New York, N.Y.). 338: 1619-22. PMID 23160955 DOI: 10.1126/Science.1227764 |
0.387 |
|
2012 |
Zufferey F, Sherr EH, Beckmann ND, Hanson E, Maillard AM, Hippolyte L, Macé A, Ferrari C, Kutalik Z, Andrieux J, Aylward E, Barker M, Bernier R, Bouquillon S, Conus P, et al. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders. Journal of Medical Genetics. 49: 660-8. PMID 23054248 DOI: 10.1136/Jmedgenet-2012-101203 |
0.469 |
|
2012 |
Dawson G, Bernier R, Ring RH. Social attention: a possible early indicator of efficacy in autism clinical trials. Journal of Neurodevelopmental Disorders. 4: 11. PMID 22958480 DOI: 10.1186/1866-1955-4-11 |
0.557 |
|
2012 |
O'Roak BJ, Vives L, Girirajan S, Karakoc E, Krumm N, Coe BP, Levy R, Ko A, Lee C, Smith JD, Turner EH, Stanaway IB, Vernot B, Malig M, Baker C, ... ... Bernier R, et al. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature. 485: 246-50. PMID 22495309 DOI: 10.1038/Nature10989 |
0.412 |
|
2012 |
Ackerman S, Reilly B, Bernier R. Tympanostomy tube placement in children with autism. Journal of Developmental and Behavioral Pediatrics : Jdbp. 33: 252-8. PMID 22343482 DOI: 10.1097/Dbp.0B013E31824B9F57 |
0.435 |
|
2012 |
Chen YZ, Matsushita M, Girirajan S, Lisowski M, Sun E, Sul Y, Bernier R, Estes A, Dawson G, Minshew N, Shellenberg GD, Eichler EE, Rieder MJ, Nickerson DA, Tsuang DW, et al. Evidence for involvement of GNB1L in autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 61-71. PMID 22095694 DOI: 10.1002/Ajmg.B.32002 |
0.476 |
|
2012 |
Lord C, Petkova E, Hus V, Gan W, Lu F, Martin DM, Ousley O, Guy L, Bernier R, Gerdts J, Algermissen M, Whitaker A, Sutcliffe JS, Warren Z, Klin A, et al. A multisite study of the clinical diagnosis of different autism spectrum disorders. Archives of General Psychiatry. 69: 306-13. PMID 22065253 DOI: 10.1001/Archgenpsychiatry.2011.148 |
0.479 |
|
2012 |
Bernier R, Gerdts J, Munson J, Dawson G, Estes A. Evidence for broader autism phenotype characteristics in parents from multiple-incidence autism families. Autism Research : Official Journal of the International Society For Autism Research. 5: 13-20. PMID 21905246 DOI: 10.1002/Aur.226 |
0.56 |
|
2012 |
Bernier R, Webb SJ, Dawson G. Understanding Impairments in Social Engagement in Autism The Development of Social Engagement: Neurobiological Perspectives. DOI: 10.1093/acprof:oso/9780195168716.003.0011 |
0.635 |
|
2012 |
O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S, Karakoc E, MacKenzie AP, Ng SB, Baker C, Rieder MJ, Nickerson DA, Bernier R, Fisher SE, Shendure J, et al. Corrigendum: Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (Nature Genetics (2011) 43, (585-589)) Nature Genetics. 44: 471. DOI: 10.1038/Ng0412-471 |
0.398 |
|
2011 |
Gerdts J, Bernier R. The broader autism phenotype and its implications on the etiology and treatment of autism spectrum disorders. Autism Research and Treatment. 2011: 545901. PMID 22937250 DOI: 10.1155/2011/545901 |
0.496 |
|
2011 |
Girirajan S, Brkanac Z, Coe BP, Baker C, Vives L, Vu TH, Shafer N, Bernier R, Ferrero GB, Silengo M, Warren ST, Moreno CS, Fichera M, Romano C, Raskind WH, et al. Relative burden of large CNVs on a range of neurodevelopmental phenotypes. Plos Genetics. 7: e1002334. PMID 22102821 DOI: 10.1371/Journal.Pgen.1002334 |
0.35 |
|
2011 |
O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S, Karakoc E, Mackenzie AP, Ng SB, Baker C, Rieder MJ, Nickerson DA, Bernier R, Fisher SE, Shendure J, et al. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nature Genetics. 43: 585-9. PMID 21572417 DOI: 10.1038/Ng.835 |
0.405 |
|
2011 |
Chapman NH, Estes A, Munson J, Bernier R, Webb SJ, Rothstein JH, Minshew NJ, Dawson G, Schellenberg GD, Wijsman EM. Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16. Human Genetics. 129: 59-70. PMID 20963441 DOI: 10.1007/S00439-010-0899-Z |
0.63 |
|
2010 |
Bernier R, Mao A, Yen J. Psychopathology, families, and culture: autism. Child and Adolescent Psychiatric Clinics of North America. 19: 855-67. PMID 21056350 DOI: 10.1016/J.Chc.2010.07.005 |
0.388 |
|
2010 |
Neuhaus E, Beauchaine TP, Bernier R. Neurobiological correlates of social functioning in autism. Clinical Psychology Review. 30: 733-48. PMID 20570622 DOI: 10.1016/J.Cpr.2010.05.007 |
0.414 |
|
2009 |
Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, ... ... Bernier R, et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature. 459: 569-73. PMID 19404257 DOI: 10.1038/Nature07953 |
0.573 |
|
2009 |
Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, ... ... Bernier R, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 459: 528-33. PMID 19404256 DOI: 10.1038/Nature07999 |
0.59 |
|
2008 |
Faja S, Aylward E, Bernier R, Dawson G. Becoming a face expert: a computerized face-training program for high-functioning individuals with autism spectrum disorders. Developmental Neuropsychology. 33: 1-24. PMID 18443967 DOI: 10.1080/87565640701729573 |
0.534 |
|
2007 |
Bernier R, Dawson G, Webb S, Murias M. EEG mu rhythm and imitation impairments in individuals with autism spectrum disorder. Brain and Cognition. 64: 228-37. PMID 17451856 DOI: 10.1016/J.Bandc.2007.03.004 |
0.688 |
|
2007 |
Dawson G, Estes A, Munson J, Schellenberg G, Bernier R, Abbott R. Quantitative assessment of autism symptom-related traits in probands and parents: Broader Phenotype Autism Symptom Scale. Journal of Autism and Developmental Disorders. 37: 523-36. PMID 16868845 DOI: 10.1007/S10803-006-0182-2 |
0.573 |
|
2006 |
Webb SJ, Dawson G, Bernier R, Panagiotides H. ERP evidence of atypical face processing in young children with autism. Journal of Autism and Developmental Disorders. 36: 881-90. PMID 16897400 DOI: 10.1007/S10803-006-0126-X |
0.695 |
|
2006 |
Richler J, Luyster R, Risi S, Hsu WL, Dawson G, Bernier R, Dunn M, Hepburn S, Hyman SL, McMahon WM, Goudie-Nice J, Minshew N, Rogers S, Sigman M, Spence MA, et al. Is there a 'regressive phenotype' of Autism Spectrum Disorder associated with the measles-mumps-rubella vaccine? A CPEA Study. Journal of Autism and Developmental Disorders. 36: 299-316. PMID 16729252 DOI: 10.1007/S10803-005-0070-1 |
0.602 |
|
2006 |
Molloy CA, Morrow AL, Meinzen-Derr J, Dawson G, Bernier R, Dunn M, Hyman SL, McMahon WM, Goudie-Nice J, Hepburn S, Minshew N, Rogers S, Sigman M, Spence MA, Tager-Flusberg H, et al. Familial autoimmune thyroid disease as a risk factor for regression in children with Autism Spectrum Disorder: a CPEA Study. Journal of Autism and Developmental Disorders. 36: 317-24. PMID 16598435 DOI: 10.1007/S10803-005-0071-0 |
0.584 |
|
2005 |
Bernier R, Dawson G, Panagiotides H, Webb S. Individuals with autism spectrum disorder show normal responses to a fear potential startle paradigm. Journal of Autism and Developmental Disorders. 35: 575-83. PMID 16167091 DOI: 10.1007/S10803-005-0002-0 |
0.673 |
|
2005 |
Luyster R, Richler J, Risi S, Hsu WL, Dawson G, Bernier R, Dunn M, Hepburn S, Hyman SL, McMahon WM, Goudie-Nice J, Minshew N, Rogers S, Sigman M, Spence MA, et al. Early regression in social communication in autism spectrum disorders: a CPEA Study. Developmental Neuropsychology. 27: 311-36. PMID 15843100 DOI: 10.1207/S15326942Dn2703_2 |
0.598 |
|
2003 |
Brown WA, Cammuso K, Sachs H, Winklosky B, Mullane J, Bernier R, Svenson S, Arin D, Rosen-Sheidley B, Folstein SE. Autism-related language, personality, and cognition in people with absolute pitch: results of a preliminary study. Journal of Autism and Developmental Disorders. 33: 163-7; discussion 16. PMID 12757355 DOI: 10.1023/A:1022987309913 |
0.317 |
|
1999 |
Barrett S, Beck JC, Bernier R, Bisson E, Braun TA, Casavant TL, Childress D, Folstein SE, Garcia M, Gardiner MB, Gilman S, Haines JL, Hopkins K, Landa R, Meyer NH, et al. An autosomal genomic screen for autism. Collaborative linkage study of autism. American Journal of Medical Genetics. 88: 609-15. PMID 10581478 DOI: 10.1002/(SICI)1096-8628(19991215)88:6<609::AID-AJMG7>3.0.CO;2-L |
0.429 |
|
Show low-probability matches. |