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Raphael Bernier, Ph.D. - Publications

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Year Citation  Score
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  0.342
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  0.513
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  0.508
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  0.711
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  0.767
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  0.404
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  0.347
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  0.753
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  0.737
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  0.356
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  0.355
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  0.737
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  0.725
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  0.747
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  0.742
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  0.726
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  0.717
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  0.359
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  0.723
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  0.502
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  0.35
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  0.35
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  0.721
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  0.513
2021 Jansen NA, Braden RO, Srivastava S, Otness EF, Lesca G, Rossi M, Nizon M, Bernier RA, Quelin C, van Haeringen A, Kleefstra T, Wong MMK, Whalen S, Fisher SE, Morgan AT, et al. Clinical delineation of SETBP1 haploinsufficiency disorder. European Journal of Human Genetics : Ejhg. PMID 33867525 DOI: 10.1038/s41431-021-00888-9  0.303
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  0.689
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  0.696
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  0.722
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  0.687
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  0.581
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  0.492
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  0.372
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  0.743
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  0.686
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  0.362
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  0.74
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  0.435
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  0.694
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  0.737
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  0.346
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  0.687
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  0.363
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  0.459
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  0.729
2019 Guo H, Bettella E, Marcogliese PC, Zhao R, Andrews JC, Nowakowski TJ, Gillentine MA, Hoekzema K, Wang T, Wu H, Jangam S, Liu C, Ni H, Willemsen MH, van Bon BW, ... ... Bernier RA, et al. Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders. Nature Communications. 10: 4679. PMID 31616000 DOI: 10.1038/S41467-019-12435-8  0.305
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  0.724
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  0.788
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  0.566
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  0.325
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  0.439
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  0.448
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  0.594
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  0.753
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  0.386
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  0.389
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  0.411
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  0.725
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  0.321
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  0.432
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  0.505
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  0.68
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  0.313
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  0.741
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  0.334
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  0.721
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  0.422
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  0.427
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  0.741
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  0.804
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  0.37
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  0.76
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  0.383
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  0.371
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  0.463
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  0.509
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  0.362
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  0.553
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  0.337
2016 Bernier R, Dawson G. 3 Autism Spectrum Disorders Development and Psychopathology. DOI: 10.1002/9781119125556.Devpsy303  0.656
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  0.382
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  0.34
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  0.378
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  0.362
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  0.623
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  0.56
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  0.365
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  0.726
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  0.417
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  0.409
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  0.334
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  0.335
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  0.386
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  0.685
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  0.53
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  0.561
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  0.708
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  0.551
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  0.423
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  0.4
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  0.382
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  0.489
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  0.462
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  0.596
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  0.402
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  0.311
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  0.505
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  0.62
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  0.437
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  0.578
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  0.327
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  0.689
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  0.412
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  0.5
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  0.362
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  0.32
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  0.391
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  0.475
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  0.555
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  0.417
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  0.439
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  0.481
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  0.485
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  0.562
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  0.403
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  0.499
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  0.354
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  0.411
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  0.633
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  0.391
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  0.577
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  0.594
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  0.536
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  0.691
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  0.576
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  0.698
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  0.605
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  0.588
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  0.676
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  0.599
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  0.314
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  0.433
Low-probability matches (unlikely to be authored by this person)
2018 al-Haddad B, Jacobsson B, Chabra S, Modzelewska D, Olson E, Bernier R, Enquobharie D, Östling S, Adams Waldorf K, Sengpiel V. Overlap in risk for psychiatric disorders after fetal exposure to infection: evidence from population-based swedish health registries American Journal of Obstetrics and Gynecology. 219: 641-642. DOI: 10.1016/J.Ajog.2018.10.084  0.297
2002 Heger A, Ticson L, Velasquez O, Bernier R. Children referred for possible sexual abuse: medical findings in 2384 children. Child Abuse & Neglect. 26: 645-59. PMID 12201160 DOI: 10.1016/S0145-2134(02)00339-3  0.297
2020 Guo H, Zhang Q, Dai R, Yu B, Hoekzema K, Tan J, Tan S, Jia X, Chung WK, Hernan R, Alkuraya FS, Alsulaiman A, Al-Muhaizea MA, Lesca G, Pons L, ... ... Bernier RA, et al. NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism. American Journal of Human Genetics. 107: 963-976. PMID 33157009 DOI: 10.1016/j.ajhg.2020.10.002  0.296
2019 Peterson JL, Earl R, Fox EA, Ma R, Haidar G, Pepper M, Berliner L, Wallace A, Bernier R. Trauma and Autism Spectrum Disorder: Review, Proposed Treatment Adaptations and Future Directions. Journal of Child & Adolescent Trauma. 12: 529-547. PMID 31819782 DOI: 10.1007/s40653-019-00253-5  0.294
2018 Cheng H, Dharmadhikari AV, Varland S, Ma N, Domingo D, Kleyner R, Rope AF, Yoon M, Stray-Pedersen A, Posey JE, Crews SR, Eldomery MK, Akdemir ZC, Lewis AM, Sutton VR, ... ... Bernier RA, et al. Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies. American Journal of Human Genetics. PMID 29656860 DOI: 10.1016/J.Ajhg.2018.03.004  0.293
2018 kolodny t, Millin R, Schallmo M, Kale A, Bernier R, Murray S. Hyper-upregulation of abnormally low neural response along the visual pathway in autism Journal of Vision. 18: 344. DOI: 10.1167/18.10.344  0.285
2015 Bernier R, Steinman KJ, Reilly B, Wallace AS, Sherr EH, Pojman N, Mefford HC, Gerdts J, Earl R, Hanson E, Goin-Kochel RP, Berry L, Kanne S, Snyder LG, Spence S, et al. Clinical phenotype of the recurrent 1q21.1 copy-number variant. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26066539 DOI: 10.1038/Gim.2015.78  0.284
2020 Kurtz-Nelson EC, Tham SW, Ahlers K, Cho D, Wallace AS, Eichler EE, Bernier RA, Earl RK. Brief Report: Associations Between Self-injurious Behaviors and Abdominal Pain Among Individuals with ASD-Associated Disruptive Mutations. Journal of Autism and Developmental Disorders. PMID 33175317 DOI: 10.1007/s10803-020-04774-z  0.282
2018 Schneider B, Reiss AL, Bernier R. Integrating Clinical Genetics Into Child Psychiatry: Lessons From Neurogenetics Clinics Journal of the American Academy of Child & Adolescent Psychiatry. 57: S15. DOI: 10.1016/J.Jaac.2018.07.063  0.281
2015 Hanson E, Bernier R, Porche K, Jackson FI, Goin-Kochel RP, Snyder LG, Snow AV, Wallace AS, Campe KL, Zhang Y, Chen Q, D'Angelo D, Moreno-De-Luca A, Orr PT, Boomer KB, et al. The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population. Biological Psychiatry. 77: 785-93. PMID 25064419 DOI: 10.1016/J.Biopsych.2014.04.021  0.28
2020 Kurtz-Nelson EC, Beighley JS, Hudac CM, Gerdts J, Wallace AS, Hoekzema K, Eichler EE, Bernier RA. Co-occurring medical conditions among individuals with ASD-associated disruptive mutations. Children's Health Care : Journal of the Association For the Care of Children's Health. 49: 361-384. PMID 33727758 DOI: 10.1080/02739615.2020.1741361  0.276
2020 Murray SO, Kolodny T, Schallmo MP, Gerdts J, Bernier RA. Late fMRI Response Components Are Altered in Autism Spectrum Disorder. Frontiers in Human Neuroscience. 14: 241. PMID 32694986 DOI: 10.3389/Fnhum.2020.00241  0.274
2021 Chawner SJRA, Doherty JL, Anney RJL, Antshel KM, Bearden CE, Bernier R, Chung WK, Clements CC, Curran SR, Cuturilo G, Fiksinski AM, Gallagher L, Goin-Kochel RP, Gur RE, Hanson E, et al. A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants. The American Journal of Psychiatry. 178: 77-86. PMID 33384013 DOI: 10.1176/appi.ajp.2020.20010015  0.273
2019 Al-Haddad BJS, Oler E, Armistead B, Elsayed NA, Weinberger DR, Bernier R, Burd I, Kapur R, Jacobsson B, Wang C, Mysorekar I, Rajagopal L, Adams Waldorf KM. The Fetal Origins of Mental Illness. American Journal of Obstetrics and Gynecology. PMID 31207234 DOI: 10.1016/J.Ajog.2019.06.013  0.272
2018 Guo H, Duyzend MH, Coe BP, Baker C, Hoekzema K, Gerdts J, Turner TN, Zody MC, Beighley JS, Murali SC, Nelson BJ, Bamshad MJ, Nickerson DA, Bernier RA, et al. Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30504930 DOI: 10.1038/S41436-018-0380-2  0.272
2020 Breen MS, Garg P, Tang L, Mendonca D, Levy T, Barbosa M, Arnett AB, Kurtz-Nelson E, Agolini E, Battaglia A, Chiocchetti AG, Freitag CM, Garcia-Alcon A, Grammatico P, Hertz-Picciotto I, ... ... Bernier RA, et al. Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype. American Journal of Human Genetics. PMID 32758449 DOI: 10.1016/J.Ajhg.2020.07.003  0.271
2016 Bramswig NC, Lüdecke HJ, Pettersson M, Albrecht B, Bernier RA, Cremer K, Eichler EE, Falkenstein D, Gerdts J, Jansen S, Kuechler A, Kvarnung M, Lindstrand A, Nilsson D, Nordgren A, et al. 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. PMID 27848077 DOI: 10.1007/S00439-016-1743-X  0.268
2018 Sanders SJ, Campbell AJ, Cottrell JR, Moller RS, Wagner FF, Auldridge AL, Bernier RA, Catterall WA, Chung WK, Empfield JR, George AL, Hipp JF, Khwaja O, Kiskinis E, Lal D, et al. Progress in Understanding and Treating SCN2A-Mediated Disorders. Trends in Neurosciences. PMID 29691040 DOI: 10.1016/J.Tins.2018.03.011  0.265
2020 Kolodny T, Schallmo MP, Gerdts J, Bernier RA, Murray SO. Response dissociation in hierarchical cortical circuits: a unique feature of autism spectrum disorder. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 32015023 DOI: 10.1523/Jneurosci.2376-19.2020  0.265
2017 Stessman HA, Xiong B, Coe BP, Wang T, Hoekzema K, Fenckova M, Kvarnung M, Gerdts J, Trinh S, Cosemans N, Vives L, Lin J, Turner TN, Santen G, Ruivenkamp C, ... ... Bernier RA, et al. Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. Nature Genetics. PMID 28191889 DOI: 10.1038/Ng.3792  0.258
2019 Al-Haddad BJS, Jacobsson B, Chabra S, Modzelewska D, Olson EM, Bernier R, Enquobahrie DA, Hagberg H, Östling S, Rajagopal L, Adams Waldorf KM, Sengpiel V. Long-term Risk of Neuropsychiatric Disease After Exposure to Infection In Utero. Jama Psychiatry. PMID 30840048 DOI: 10.1001/Jamapsychiatry.2019.0029  0.258
2019 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 31127942 DOI: 10.1093/hmg/ddz111  0.257
2022 Jia X, Zhang S, Tan S, Du B, He M, Qin H, Chen J, Duan X, Luo J, Chen F, Ouyang L, Wang J, Chen G, Yu B, Zhang G, ... ... Bernier RA, et al. De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders. Science Advances. 8: eabo7112. PMID 35977029 DOI: 10.1126/sciadv.abo7112  0.256
2023 Jones W, Klaiman C, Richardson S, Aoki C, Smith C, Minjarez M, Bernier R, Pedapati E, Bishop S, Ence W, Wainer A, Moriuchi J, Tay SW, Klin A. Eye-Tracking-Based Measurement of Social Visual Engagement Compared With Expert Clinical Diagnosis of Autism. Jama. 330: 854-865. PMID 37668621 DOI: 10.1001/jama.2023.13295  0.254
2021 Padhi EM, Hayeck TJ, Cheng Z, Chatterjee S, Mannion BJ, Byrska-Bishop M, Willems M, Pinson L, Redon S, Benech C, Uguen K, Audebert-Bellanger S, Le Marechal C, Férec C, Efthymiou S, ... ... Bernier RA, et al. Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism. Human Genomics. 15: 44. PMID 34256850 DOI: 10.1186/s40246-021-00342-3  0.253
2021 Padhi EM, Hayeck TJ, Cheng Z, Chatterjee S, Mannion BJ, Byrska-Bishop M, Willems M, Pinson L, Redon S, Benech C, Uguen K, Audebert-Bellanger S, Le Marechal C, Férec C, Efthymiou S, ... ... Bernier RA, et al. Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism. Human Genomics. 15: 44. PMID 34256850 DOI: 10.1186/s40246-021-00342-3  0.253
2022 Chen G, Yu B, Tan S, Tan J, Jia X, Zhang Q, Zhang X, Jiang Q, Hua Y, Han Y, Luo S, Hoekzema K, Bernier RA, Earl RK, Kurtz-Nelson EC, et al. GIGYF1 disruption associates with autism and impaired IGF-1R signaling. The Journal of Clinical Investigation. PMID 35917186 DOI: 10.1172/JCI159806  0.253
2017 Jansen S, Hoischen A, Coe BP, Carvill GL, Van Esch H, Bosch DGM, Andersen UA, Baker C, Bauters M, Bernier RA, van Bon BW, Claahsen-van der Grinten HL, Gecz J, Gilissen C, Grillo L, et al. A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency. European Journal of Human Genetics : Ejhg. PMID 29209020 DOI: 10.1038/S41431-017-0039-5  0.252
2021 Wilfert AB, Turner TN, Murali SC, Hsieh P, Sulovari A, Wang T, Coe BP, Guo H, Hoekzema K, Bakken TE, Winterkorn LH, Evani US, Byrska-Bishop M, Earl RK, Bernier RA, et al. Recent ultra-rare inherited variants implicate new autism candidate risk genes. Nature Genetics. PMID 34312540 DOI: 10.1038/s41588-021-00899-8  0.251
2020 Schallmo MP, Kolodny T, Kale AM, Millin R, Flevaris AV, Edden RAE, Gerdts J, Bernier RA, Murray SO. Weaker neural suppression in autism. Nature Communications. 11: 2675. PMID 32472088 DOI: 10.1038/S41467-020-16495-Z  0.249
2019 Salpietro V, Dixon CL, Guo H, Bello OD, Vandrovcova J, Efthymiou S, Maroofian R, Heimer G, Burglen L, Valence S, Torti E, Hacke M, Rankin J, Tariq H, Colin E, ... ... Bernier RA, et al. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. Nature Communications. 10: 3094. PMID 31300657 DOI: 10.1038/S41467-019-10910-W  0.248
2014 Deriziotis P, O'Roak BJ, Graham SA, Estruch SB, Dimitropoulou D, Bernier RA, Gerdts J, Shendure J, Eichler EE, Fisher SE. De novo TBR1 mutations in sporadic autism disrupt protein functions. Nature Communications. 5: 4954. PMID 25232744 DOI: 10.1038/Ncomms5954  0.244
2018 Guo H, Wang T, Wu H, Long M, Coe BP, Li H, Xun G, Ou J, Chen B, Duan G, Bai T, Zhao N, Shen Y, Li Y, Wang Y, ... ... Bernier RA, et al. Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model. Molecular Autism. 9: 64. PMID 30564305 DOI: 10.1186/s13229-018-0247-z  0.242
2018 Millin R, Kolodny T, Flevaris AV, Kale AM, Schallmo MP, Gerdts J, Bernier RA, Murray S. Reduced auditory cortical adaptation in autism spectrum disorder. Elife. 7. PMID 30362457 DOI: 10.7554/Elife.36493  0.242
2017 Arnett AB, Cairney BE, Wallace AS, Gerdts J, Turner TN, Eichler EE, Bernier RA. Comorbid symptoms of inattention, autism, and executive cognition in youth with putative genetic risk. Journal of Child Psychology and Psychiatry, and Allied Disciplines. PMID 28921525 DOI: 10.1111/Jcpp.12815  0.237
2021 Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, Kvarnung M, Lindstrand A, Nordgren A, Gecz J, Iascone M, ... ... Bernier RA, et al. Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders. Genome Medicine. 13: 63. PMID 33874999 DOI: 10.1186/s13073-021-00870-6  0.232
2021 Cousin MA, Creighton BA, Breau KA, Spillmann RC, Torti E, Dontu S, Tripathi S, Ajit D, Edwards RJ, Afriyie S, Bay JC, Harper KM, Beltran AA, Munoz LJ, Falcon Rodriguez L, ... ... Bernier RA, et al. Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome. Nature Genetics. PMID 34211179 DOI: 10.1038/s41588-021-00886-z  0.223
2021 Cousin MA, Creighton BA, Breau KA, Spillmann RC, Torti E, Dontu S, Tripathi S, Ajit D, Edwards RJ, Afriyie S, Bay JC, Harper KM, Beltran AA, Munoz LJ, Falcon Rodriguez L, ... ... Bernier RA, et al. Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome. Nature Genetics. PMID 34211179 DOI: 10.1038/s41588-021-00886-z  0.223
2018 Murray SO, Schallmo MP, Kolodny T, Millin R, Kale A, Thomas P, Rammsayer TH, Troche SJ, Bernier RA, Tadin D. Sex Differences in Visual Motion Processing. Current Biology : Cb. PMID 30122530 DOI: 10.1016/J.Cub.2018.06.014  0.203
2019 Fenckova M, Blok LER, Asztalos L, Goodman DP, Cizek P, Singgih EL, Glennon JC, IntHout J, Zweier C, Eichler EE, von Reyn CR, Bernier RA, Asztalos Z, Schenck A. Habituation Learning Is a Widely Affected Mechanism in Drosophila Models of Intellectual Disability and Autism Spectrum Disorders. Biological Psychiatry. PMID 31272685 DOI: 10.1016/j.biopsych.2019.04.029  0.201
2019 Guo H, Li Y, Shen L, Wang T, Jia X, Liu L, Xu T, Ou M, Hoekzema K, Wu H, Gillentine MA, Liu C, Ni H, Peng P, Zhao R, ... ... Bernier RA, et al. Disruptive variants of associate with autism and interfere with neuronal development and synaptic transmission. Science Advances. 5: eaax2166. PMID 31579823 DOI: 10.1126/Sciadv.Aax2166  0.2
2017 Schallmo M, Flevaris A, Kale A, Millin R, Bernier R, Murray S. Divisive normalization versus inhibition during visual motion integration in humans Journal of Vision. 17: 795. DOI: 10.1167/17.10.795  0.191
2024 Küry S, Stanton JE, van Woerden G, Hsieh TC, Rosenfelt C, Scott-Boyer MP, Most V, Wang T, Papendorf JJ, de Konink C, Deb W, Vignard V, Studencka-Turski M, Besnard T, Hajdukowicz AM, ... ... Bernier RA, et al. Unveiling the crucial neuronal role of the proteasomal ATPase subunit gene in neurodevelopmental proteasomopathies. Medrxiv : the Preprint Server For Health Sciences. PMID 38293138 DOI: 10.1101/2024.01.13.24301174  0.188
2019 Turner TN, Wilfert AB, Bakken TE, Bernier RA, Pepper MR, Zhang Z, Torene RI, Retterer K, Eichler EE. Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders. American Journal of Human Genetics. PMID 31785789 DOI: 10.1016/j.ajhg.2019.11.003  0.185
2019 Coe BP, Stessman HAF, Sulovari A, Geisheker MR, Bakken TE, Lake AM, Dougherty JD, Lein ES, Hormozdiari F, Bernier RA, Eichler EE. Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity. Nature Genetics. 51: 106-116. PMID 30559488 DOI: 10.1038/S41588-018-0288-4  0.185
2020 Kolodny T, Schallmo MP, Gerdts J, Edden RAE, Bernier RA, Murray SO. Concentrations of Cortical GABA and Glutamate in Young Adults With Autism Spectrum Disorder. Autism Research : Official Journal of the International Society For Autism Research. PMID 32297709 DOI: 10.1002/Aur.2300  0.184
2020 Wang T, Hoekzema K, Vecchio D, Wu H, Sulovari A, Coe BP, Gillentine MA, Wilfert AB, Perez-Jurado LA, Kvarnung M, Sleyp Y, Earl RK, Rosenfeld JA, Geisheker MR, Han L, ... ... Bernier RA, et al. Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders. Nature Communications. 11: 5398. PMID 33087701 DOI: 10.1038/s41467-020-19289-5  0.179
2020 Wang T, Hoekzema K, Vecchio D, Wu H, Sulovari A, Coe BP, Gillentine MA, Wilfert AB, Perez-Jurado LA, Kvarnung M, Sleyp Y, Earl RK, Rosenfeld JA, Geisheker MR, Han L, ... ... Bernier RA, et al. Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders. Nature Communications. 11: 4932. PMID 33004838 DOI: 10.1038/s41467-020-18723-y  0.179
2016 Turner TN, Yi Q, Krumm N, Huddleston J, Hoekzema K, F Stessman HA, Doebley AL, Bernier RA, Nickerson DA, Eichler EE. denovo-db: a compendium of human de novo variants. Nucleic Acids Research. PMID 27907889 DOI: 10.1093/Nar/Gkw865  0.174
2017 Geisheker MR, Heymann G, Wang T, Coe BP, Turner TN, Stessman HAF, Hoekzema K, Kvarnung M, Shaw M, Friend K, Liebelt J, Barnett C, Thompson EM, Haan E, Guo H, ... ... Bernier RA, et al. Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains. Nature Neuroscience. PMID 28628100 DOI: 10.1038/Nn.4589  0.164
2021 Goldmann JM, Hampstead JE, Wong WSW, Wilfert AB, Turner TN, Jonker MA, Bernier R, Huynen MA, Eichler EE, Veltman JA, Maxwell GL, Gilissen C. Differences in the number of de novo mutations between individuals are due to small family-specific effects and stochasticity. Genome Research. PMID 34301630 DOI: 10.1101/gr.271809.120  0.163
2019 Nellåker C, Alkuraya FS, Baynam G, Bernier RA, Bernier FPJ, Boulanger V, Brudno M, Brunner HG, Clayton-Smith J, Cogné B, Dawkins HJS, deVries BBA, Douzgou S, Dudding-Byth T, Eichler EE, et al. Enabling Global Clinical Collaborations on Identifiable Patient Data: The Minerva Initiative. Frontiers in Genetics. 10: 611. PMID 31417602 DOI: 10.3389/Fgene.2019.00611  0.163
2021 Earl RK, Ward T, Gerdts J, Eichler EE, Bernier RA, Hudac CM. Sleep Problems in Children with ASD and Gene Disrupting Mutations. The Journal of Genetic Psychology. 1-18. PMID 33998396 DOI: 10.1080/00221325.2021.1922869  0.156
2004 Hutchins SS, Jiles R, Bernier R. Elimination of measles and of disparities in measles childhood vaccine coverage among racial and ethnic minority populations in the United States. The Journal of Infectious Diseases. 189: S146-52. PMID 15106103 DOI: 10.1086/379651  0.15
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. Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication. Translational Psychiatry. 9: 107. PMID 30837452 DOI: 10.1038/S41398-019-0441-6  0.148
2019 Giannuzzi G, Schmidt PJ, Porcu E, Willemin G, Munson KM, Nuttle X, Earl R, Chrast J, Hoekzema K, Risso D, Männik K, De Nittis P, Baratz ED, Herault Y, ... ... Bernier RA, et al. The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals. American Journal of Human Genetics. PMID 31668704 DOI: 10.1016/J.Ajhg.2019.09.023  0.126
1991 Pirlot P, Bernier R. Brain growth and differentiation in two fetal bats: qualitative and quantitative aspects. The American Journal of Anatomy. 190: 167-81. PMID 2012004 DOI: 10.1002/aja.1001900206  0.121
2024 Bouvarel H, Agard E, Billant J, Levron A, Chudzinski R, Plas H, Bernier R, Sejournet L, Chaperon M, Dot C. Correction: Long-term real-life outcomes of the Clareon® hydrophobic intraocular lens: the Clarte study in 191 eyes : 3-years real-life outcomes of the Clareon® intraocular lens. Bmc Ophthalmology. 24: 178. PMID 38641586 DOI: 10.1186/s12886-024-03451-4  0.12
2021 Coll-Tané M, Gong NN, Belfer SJ, van Renssen LV, Kurtz-Nelson EC, Szuperak M, Eidhof I, van Reijmersdal B, Terwindt I, Durkin J, Verheij MMM, Kim CN, Hudac CM, Nowakowski TJ, Bernier RA, et al. The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defects. Science Advances. 7. PMID 34088660 DOI: 10.1126/sciadv.abe2626  0.12
2018 Schallmo MP, Millin R, Kale AM, Kolodny T, Edden RAE, Bernier RA, Murray SO. Glutamatergic facilitation of neural responses in MT enhances motion perception in humans. Neuroimage. PMID 30312807 DOI: 10.1016/J.Neuroimage.2018.10.001  0.117
1990 Modlin JF, Onorato IM, McBean AM, Albrecht P, Thoms ML, Nerhood L, Bernier R. The humoral immune response to type 1 oral poliovirus vaccine in children previously immunized with enhanced potency inactivated poliovirus vaccine or live oral poliovirus vaccine. American Journal of Diseases of Children (1960). 144: 480-4. PMID 2157337  0.107
2018 Schallmo MP, Kale AM, Millin R, Flevaris AV, Brkanac Z, Edden RA, Bernier RA, Murray S. Suppression and facilitation of human neural responses. Elife. 7. PMID 29376822 DOI: 10.7554/Elife.30334  0.099
2000 Briss PA, Rodewald LE, Hinman AR, Shefer AM, Strikas RA, Bernier RR, Carande-Kulis VG, Yusuf HR, Ndiaye SM, Williams SM. Reviews of evidence regarding interventions to improve vaccination coverage in children, adolescents, and adults. The Task Force on Community Preventive Services. American Journal of Preventive Medicine. 18: 97-140. PMID 10806982  0.09
1992 Cutts FT, Zell ER, Mason D, Bernier RH, Dini EF, Orenstein WA. Monitoring progress toward US preschool immunization goals. Jama. 267: 1952-5. PMID 1548828 DOI: 10.1001/jama.1992.03480140078037  0.089
1990 Orenstein WA, Atkinson W, Mason D, Bernier RH. Barriers to vaccinating preschool children. Journal of Health Care For the Poor and Underserved. 1: 315-30. PMID 2130911  0.086
2015 Upshaw MB, Bernier RA, Sommerville JA. Infants' grip strength predicts mu rhythm attenuation during observation of lifting actions with weighted blocks. Developmental Science. PMID 25939632 DOI: 10.1111/Desc.12308  0.082
1990 Orenstein WA, Bernier RH. Surveillance. Information for action. Pediatric Clinics of North America. 37: 709-34. PMID 2190144  0.08
2019 Cao M, MacDonald JW, Liu HL, Weaver M, Cortes M, Durosier LD, Burns P, Fecteau G, Desrochers A, Schulkin J, Antonelli MC, Bernier RA, Dorschner M, Bammler TK, Frasch MG. α7 Nicotinic Acetylcholine Receptor Signaling Modulates Ovine Fetal Brain Astrocytes Transcriptome in Response to Endotoxin. Frontiers in Immunology. 10: 1063. PMID 31143190 DOI: 10.3389/fimmu.2019.01063  0.072
1995 Grant A, Delisle E, Dubois S, Niyonsenga T, Bernier R. Implementation of a province-wide computerized network in Quebec: the FAMUS Project. M.D. Computing : Computers in Medical Practice. 12: 45-9. PMID 7854078  0.067
2000 Hutchins SS, Sherrod J, Bernier R. Assessing immunization coverage in private practice. Journal of the National Medical Association. 92: 163-8. PMID 10976172  0.065
2008 Fleischman A, Shoelson SE, Bernier R, Goldfine AB. Salsalate improves glycemia and inflammatory parameters in obese young adults. Diabetes Care. 31: 289-94. PMID 17959861 DOI: 10.2337/Dc07-1338  0.063
2013 Seo BJ, Nissly C, Troy M, Angeli G, Bernier R, Stepp L, Williams E. Estimation of normalized point-source sensitivity of segment surface specifications for extremely large telescopes. Applied Optics. 52: 4111-22. PMID 23842151 DOI: 10.1364/Ao.52.004111  0.062
1992 Grant A, Lussier Y, Delisle E, Dubois S, Bernier R. The TEAM evaluation approach to Project FAMUS, a pan-Canadian risk register for primary care. Proceedings / the ... Annual Symposium On Computer Application [Sic] in Medical Care. Symposium On Computer Applications in Medical Care. 734-8. PMID 1482968  0.061
2007 Goldfine AB, Mun EC, Devine E, Bernier R, Baz-Hecht M, Jones DB, Schneider BE, Holst JJ, Patti ME. Patients with neuroglycopenia after gastric bypass surgery have exaggerated incretin and insulin secretory responses to a mixed meal. The Journal of Clinical Endocrinology and Metabolism. 92: 4678-85. PMID 17895322 DOI: 10.1210/jc.2007-0918  0.059
2013 Bernier R. In the person of Christ, in the person of the church | In persona Christi, in persona Ecclesiae Revue Thomiste. 113: 443-451.  0.059
2009 Patti ME, Houten SM, Bianco AC, Bernier R, Larsen PR, Holst JJ, Badman MK, Maratos-Flier E, Mun EC, Pihlajamaki J, Auwerx J, Goldfine AB. Serum bile acids are higher in humans with prior gastric bypass: potential contribution to improved glucose and lipid metabolism. Obesity (Silver Spring, Md.). 17: 1671-7. PMID 19360006 DOI: 10.1038/Oby.2009.102  0.056
1988 Paice MG, Bernier R, Jurasek L. Viscosity-enhancing bleaching of hardwood kraft pulp with xylanase from a cloned gene. Biotechnology and Bioengineering. 32: 235-9. PMID 18584740 DOI: 10.1002/bit.260320214  0.053
1995 Bernier R, Tremblay M. Homologous interference resulting from the presence of defective particles of human immunodeficiency virus type 1. Journal of Virology. 69: 291-300. PMID 7983721 DOI: 10.1128/Jvi.69.1.291-300.1995  0.051
1994 Orenstein WA, Bernier RH. Toward immunizing every child on time. Pediatrics. 94: 545-7. PMID 7936869  0.05
1996 Tremblay M, Olivier M, Bernier R. Leishmania and the pathogenesis of HIV infection. Parasitology Today (Personal Ed.). 12: 257-61. PMID 15275189 DOI: 10.1016/0169-4758(96)10021-1  0.049
2015 DiFazio M, Silverberg ND, Kirkwood MW, Bernier R, Iverson GL. Prolonged Activity Restriction After Concussion: Are We Worsening Outcomes? Clinical Pediatrics. PMID 26130391 DOI: 10.1177/0009922815589914  0.047
1991 Bernier R, Arsenault HH. Deconvolution of two-dimensional images with zeros in the transfer function. Applied Optics. 30: 5163-8. PMID 20717338 DOI: 10.1364/Ao.30.005163  0.043
1998 Bernier R, Barbeau B, Olivier M, Tremblay MJ. Mycobacterium tuberculosis mannose-capped lipoarabinomannan can induce NF-kappaB-dependent activation of human immunodeficiency virus type 1 long terminal repeat in T cells. The Journal of General Virology. 79: 1353-61. PMID 9634075 DOI: 10.1099/0022-1317-79-6-1353  0.043
1996 Orenstein WA, Hadler S, Kuritsky JN, Bernier RH. Rotavirus vaccines--from licensure to disease reduction. The Journal of Infectious Diseases. 174: S118-24. PMID 8752301  0.043
2008 Buchanan J, Chen L, Gingrich DM, Liu S, Chen H, Farrell J, Kierstead J, Lanni F, Lissauer D, Ma H, Makowiecki D, Radeka V, Rescia S, Takai H, Ghazlane H, ... ... Bernier R, et al. Design and implementation of the front end board for the readout of the ATLAS liquid argon calorimeters Journal of Instrumentation. 3. DOI: 10.1088/1748-0221/3/03/P03004  0.041
1999 Shefer A, Briss P, Rodewald L, Bernier R, Strikas R, Yusuf H, Ndiaye S, Wiliams S, Pappaioanou M, Hinman AR. Improving immunization coverage rates: an evidence-based review of the literature. Epidemiologic Reviews. 21: 96-142. PMID 10520476  0.04
1997 Barbeau B, Bernier R, Dumais N, Briand G, Olivier M, Faure R, Posner BI, Tremblay M. Activation of HIV-1 long terminal repeat transcription and virus replication via NF-kappaB-dependent and -independent pathways by potent phosphotyrosine phosphatase inhibitors, the peroxovanadium compounds. The Journal of Biological Chemistry. 272: 12968-77. PMID 9148903 DOI: 10.1074/Jbc.272.20.12968  0.039
2003 Davidson RA, Travis MT, Bernier RM. Bruns-Garland syndrome (diabetic amyotrophy). Orthopedics. 26: 87-8. PMID 12555842  0.039
2010 Stahl HP, Alongi C, Arneson A, Bernier R, Brown B, Chaney D, Cole G, Daniel J, Dettmann L, Eng R, Gallagher B, Garfield R, Hadaway J, Johnson P, Lee A, et al. Survey of interferometric techniques used to test JWST optical components Proceedings of Spie - the International Society For Optical Engineering. 7790. DOI: 10.1117/12.862234  0.037
1997 Bernier R, Tremblay M, Tsoukas C, Bergeron MG. Drug sensitivity of human immunodeficiency virus type 1 isolates after ribavirin therapy. The Journal of Infectious Diseases. 175: 176-8. PMID 8985215 DOI: 10.1093/Infdis/175.1.176  0.036
1997 LeBaron CW, Chaney M, Baughman AL, Dini EF, Maes E, Dietz V, Bernier R. Impact of measurement and feedback on vaccination coverage in public clinics, 1988-1994. Jama. 277: 631-5. PMID 9039880  0.036
1999 Xhignesse M, Laplante P, Grant AM, Niyonsenga T, Delisle E, Vanasse N, Bernier R. Antiplatelet and lipid-lowering therapies for the secondary prevention of cardiovascular disease: are we doing enough? The Canadian Journal of Cardiology. 15: 185-9. PMID 10079778  0.036
2010 Abreu H, Aharrouche M, Aleksa M, Aperio-Bella JL, Archambault P, Arfaoui S, Arnaez O, Auge E, Aurousseau M, Bahinipati S, Ban J, Banfi D, Barajas A, Barillari T, Bazan A, ... ... Bernier R, et al. Performance of the electronic readout of the ATLAS liquid argon calorimeters Journal of Instrumentation. 5. DOI: 10.1088/1748-0221/5/09/P09003  0.036
1990 Markowitz LE, Sepulveda J, Diaz-Ortega JL, Valdespino JL, Albrecht P, Zell ER, Stewart J, Zarate ML, Bernier RH. Immunization of six-month-old infants with different doses of Edmonston-Zagreb and Schwarz measles vaccines. The New England Journal of Medicine. 322: 580-7. PMID 2304505 DOI: 10.1056/NEJM199003013220903  0.035
1995 Bernier R, Turco SJ, Olivier M, Tremblay M. Activation of human immunodeficiency virus type 1 in monocytoid cells by the protozoan parasite Leishmania donovani. Journal of Virology. 69: 7282-5. PMID 7474154 DOI: 10.1128/Jvi.69.11.7282-7285.1995  0.034
2015 Zhong WZ, Rusinek A, Jankowiak T, Abed F, Bernier R, Sutter G. Influence of interfacial friction and specimen configuration in Split Hopkinson Pressure Bar system Tribology International. 90: 1-14. DOI: 10.1016/J.Triboint.2015.04.002  0.032
1991 Onorato IM, Modlin JF, McBean AM, Thoms ML, Losonsky GA, Bernier RH. Mucosal immunity induced by enhance-potency inactivated and oral polio vaccines. The Journal of Infectious Diseases. 163: 1-6. PMID 1845806  0.031
2011 Chetouane F, Bernier Ré, Fadil A. Modelling and discrete-event simulation for ski lifts service operations design International Journal of Services, Economics and Management. 3: 393-410. DOI: 10.1504/IJSEM.2011.042784  0.031
2016 Bernier RA, Hillary FG. Trends in alcohol use during moderate and severe traumatic brain injury: 18 years of neurotrauma in Pennsylvania Brain Injury. 1-8. DOI: 10.3109/02699052.2015.1127998  0.03
2016 Zhong WZ, Mbarek IA, Rusinek A, Bernier R, Jankowiak T, Sutter G. Development of an experimental set-up for dynamic force measurements during impact and perforation, coupling to numerical simulations International Journal of Impact Engineering. 91: 102-115. DOI: 10.1016/j.ijimpeng.2016.01.006  0.029
2009 Bernier RY, Locke A, Hanson JM. Lobsters and crabs as potential vectors for tunicate dispersal in the southern Gulf of St. Lawrence, Canada Aquatic Invasions. 4: 105-110. DOI: 10.3391/ai.2009.4.1.11  0.029
1992 Cutts FT, Orenstein WA, Bernier RH. Causes of low preschool immunization coverage in the United States. Annual Review of Public Health. 13: 385-98. PMID 1599595 DOI: 10.1146/annurev.pu.13.050192.002125  0.029
2008 Barrett DH, Bernier RH, Sowell AL. Strengthening public health ethics at the centers for disease control and prevention. Journal of Public Health Management and Practice : Jphmp. 14: 348-53. PMID 18552645 DOI: 10.1097/01.PHH.0000324562.80157.ef  0.028
2009 Cao X, Roy G, Roy N, Bernier R. Comparison of the relationships between lidar integrated backscattered light and accumulated depolarization ratios for linear and circular polarization for water droplets, fog oil, and dust. Applied Optics. 48: 4130-41. PMID 19623227 DOI: 10.1364/AO.48.004130  0.027
2015 Wang S, Lipa JA, Gwo DH, Triebes K, Turneaure JP, Farley RP, Davidson D, Bower KA, Acworth EB, Bernier RJ, Huff LW, Schweiger PF, Goebel JH. The design and performance of the Gravity Probe B telescope Classical and Quantum Gravity. 32. DOI: 10.1088/0264-9381/32/22/224008  0.027
2010 Bernier R. Using LibGuides as a Web 2.0 content management system and a collaboration tool for engineering librarians Asee Annual Conference and Exposition, Conference Proceedings.  0.026
1988 McBean AM, Thoms ML, Albrecht P, Cuthie JC, Bernier R. Serologic response to oral polio vaccine and enhanced-potency inactivated polio vaccines. American Journal of Epidemiology. 128: 615-28. PMID 2843039  0.026
2015 Everitt CWF, Muhlfelder B, Debra DB, Parkinson BW, Turneaure JP, Silbergleit AS, Acworth EB, Adams M, Adler R, Bencze WJ, Berberian JE, Bernier RJ, Bower KA, Brumley RW, Buchman S, et al. The Gravity Probe B test of general relativity Classical and Quantum Gravity. 32. DOI: 10.1088/0264-9381/32/22/224001  0.026
1998 Bernier R, Barbeau B, Tremblay MJ, Olivier M. The lipophosphoglycan of Leishmania donovani up-regulates HIV-1 transcription in T cells through the nuclear factor-kappaB elements. Journal of Immunology (Baltimore, Md. : 1950). 160: 2881-8. PMID 9510191  0.025
1995 Sahn D, Bernier R. Have structural adjustments led to health sector reform in Africa? Health Policy (Amsterdam, Netherlands). 32: 193-214. PMID 10156639 DOI: 10.1016/0168-8510(95)00736-C  0.022
2010 Chetouane F, Bernier R, Collart-Dutilleul S. Simulation and optimisation of lift networks in a provincial skiing resort Ifac Proceedings Volumes (Ifac-Papersonline). 22-27. DOI: 10.3182/20100908-3-PT-3007.00006  0.021
2008 Buchanan NJ, Chen L, Gingrich DM, Liu S, Chen H, Damazio D, Densing F, Duffin S, Farrell J, Kandasamy S, Kierstead J, Lanni F, Lissauer D, Ma H, Makowiecki D, ... ... Bernier R, et al. ATLAS liquid argon calorimeter front end electronics Journal of Instrumentation. 3. DOI: 10.1088/1748-0221/3/09/P09003  0.02
2011 Roy G, Cao X, Bernier R. On the information content of linear and circular depolarization signatures of bioaerosols Proceedings of Spie - the International Society For Optical Engineering. 8018. DOI: 10.1117/12.883713  0.019
2010 Arneson A, Alongi C, Bernier R, Boese E, Daniel J, Dettmann L, Garfield R, Glatzel H, Kincade J, Johnson P, Lee A, Magruder A, Patel A, Seilonen M, Surges G, et al. Successful production of the Engineering Development Unit (EDU) primary mirror segment and flight unit tertiary mirror for JWST Proceedings of Spie - the International Society For Optical Engineering. 7731. DOI: 10.1117/12.858049  0.018
2014 Fras T, Rusinek A, Pȩcherski RB, Bernier R, Jankowiak T. Analysis of friction influence on material deformation under biaxial compression state Tribology International. 80: 14-24. DOI: 10.1016/j.triboint.2014.06.019  0.017
2010 Hoffmann R, Bernier R, Smith S, McMillen S. A four-step biotreatability protocol for crude oil impacted soil Society of Petroleum Engineers - Spe International Conference On Health, Safety and Environment in Oil and Gas Exploration and Production 2010. 3: 1955-1969.  0.013
1994 Orenstein WA, Bernier RH. Crossing the divide from vaccine technology to vaccine delivery. The critical role of providers. Jama. 272: 1138-9. PMID 7933328  0.013
1994 Bernier RH. Toward a more population-based approach to immunization: fostering private- and public-sector collaboration. American Journal of Public Health. 84: 1567-8. PMID 7943471  0.012
2011 Cao X, Roy G, Bernier R, Tremblay G, Roy S, Laflamme C. Lidar signal depolarization by solid targets and application of polarimetric lidar to Terrain Mapping and 3D imagery Proceedings of Spie - the International Society For Optical Engineering. 8040. DOI: 10.1117/12.883883  0.011
2010 Cao X, Roy G, Bernier R. Lidar polarization discrimination of bioaerosols Proceedings of Spie - the International Society For Optical Engineering. 7672. DOI: 10.1117/12.849649  0.01
2010 Rodríguez-Martínez JA, Rusinek A, Chevrier P, Bernier R, Arias A. Temperature measurements on ES steel sheets subjected to perforation by hemispherical projectiles International Journal of Impact Engineering. 37: 828-841. DOI: 10.1016/j.ijimpeng.2009.12.005  0.01
2009 Cao X, Roy G, Roy N, Bernier R. On mathematical relationships between lidae integrated backscattered light and integrated depolarization ratios for linear and circular polarization for water droplets Proceedings of Spie - the International Society For Optical Engineering. 7475. DOI: 10.1117/12.830109  0.01
2004 Bernier R, Midthun K. Getting the science right and doing the right science in vaccine safety. American Journal of Public Health. 94: 914-7. PMID 15249288  0.01
1998 Grant AM, Niyonsenga T, Dion I, Delisle E, Xhignesse M, Bernier R. Cardiovascular disease. Physician attitudes toward prevention and treatment. Canadian Family Physician Mã©Decin De Famille Canadien. 44: 780-7. PMID 9585851  0.01
1996 Demers P, Thompson P, Bernier RG, Lemire J, Laflamme P. Effect of occlusive pressure patching on the rate of epithelial wound healing after photorefractive keratectomy. Journal of Cataract and Refractive Surgery. 22: 59-62. PMID 8656364  0.01
1995 Ackermann HW, Azizbekyan RR, Bernier RL, de Barjac H, Saindoux S, Valéro JR, Yu MX. Phage typing of Bacillus subtilis and B. thuringiensis. Research in Microbiology. 146: 643-57. PMID 8584788  0.01
1994 Dietz V, Zell E, Eddins D, Bernier R, Orenstein W. Vaccination coverage in the USA. Lancet. 344: 1439-40. PMID 7968103 DOI: 10.1016/S0140-6736(94)90610-6  0.01
1989 Orenstein WA, Bernier RH, Chen RT. Pertussis--a disease and a vaccine that are not going away. The Western Journal of Medicine. 150: 339-41. PMID 2735038  0.01
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