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Jennifer A. Gerdts, Ph.D. - Publications

Affiliations: 
2012 Psychology University of Washington, Seattle, Seattle, WA 
Area:
Clinical Psychology
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29 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 Neuhaus E, Osuna A, Tagavi DM, Shah-Hosseini S, Simmons S, Gerdts J, Thompson AD. Clinical Characteristics of Youth with Autism or Developmental Disability during Inpatient Psychiatric Admission. Journal of Clinical Medicine. 11. PMID 36362556 DOI: 10.3390/jcm11216328  0.549
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  0.358
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  0.319
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  0.345
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. 49: 361-384. DOI: 10.1080/02739615.2020.1741361  0.425
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  0.393
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  0.38
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  0.342
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  0.325
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  0.446
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  0.385
2018 Millin R, Kolodny T, Flevaris AV, Kale AM, Schallmo M, Gerdts J, Bernier RA, Murray S. Author response: Reduced auditory cortical adaptation in autism spectrum disorder Elife. DOI: 10.7554/Elife.36493.015  0.362
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  0.42
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  0.434
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  0.384
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  0.322
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  0.358
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, 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  0.385
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  0.4
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  0.45
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, ... ... Gerdts J, 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  0.456
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  0.426
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  0.361
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  0.378
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  0.373
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  0.461
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  0.425
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  0.354
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  0.434
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