Raphael Bernier, Ph.D. - Publications

Affiliations: 
 

131 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.656
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  0.731
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  0.366
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  0.366
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  0.737
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  0.534
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  0.703
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  0.707
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  0.732
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  0.695
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  0.307
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  0.503
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  0.374
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  0.745
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  0.696
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  0.349
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  0.745
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  0.446
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  0.707
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  0.739
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  0.35
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  0.704
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  0.369
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  0.472
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  0.732
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  0.321
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  0.727
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  0.779
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  0.568
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  0.33
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  0.452
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  0.441
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  0.599
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  0.755
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  0.389
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  0.4
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  0.413
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  0.304
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  0.771
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  0.727
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  0.324
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  0.442
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  0.508
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  0.304
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  0.683
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  0.743
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  0.341
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  0.725
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  0.724
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  0.432
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  0.434
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  0.742
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  0.806
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  0.379
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  0.756
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  0.397
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  0.383
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  0.461
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  0.513
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  0.374
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  0.557
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  0.343
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  0.391
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  0.349
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  0.384
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  0.353
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  0.78
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  0.636
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  0.565
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  0.376
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  0.428
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  0.415
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  0.328
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  0.389
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  0.696
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  0.547
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  0.574
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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  0.576
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