Year |
Citation |
Score |
2023 |
Fernandez TV, Williams ZP, Kline T, Rajendran S, Augustine F, Wright N, Sullivan CAW, Olfson E, Abdallah SB, Liu W, Hoffman EJ, Gupta AR, Singer HS. Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene. Plos One. 18: e0291978. PMID 37788244 DOI: 10.1371/journal.pone.0291978 |
0.704 |
|
2023 |
Weinschutz Mendes H, Neelakantan U, Liu Y, Fitzpatrick SE, Chen T, Wu W, Pruitt A, Jin DS, Jamadagni P, Carlson M, Lacadie CM, Enriquez KD, Li N, Zhao D, Ijaz S, ... ... Hoffman EJ, et al. High-throughput functional analysis of autism genes in zebrafish identifies convergence in dopaminergic and neuroimmune pathways. Cell Reports. 42: 112243. PMID 36933215 DOI: 10.1016/j.celrep.2023.112243 |
0.421 |
|
2021 |
Enriquez KD, Gupta AR, Hoffman EJ. Signaling Pathways and Sex Differential Processes in Autism Spectrum Disorder. Frontiers in Psychiatry. 12: 716673. PMID 34690830 DOI: 10.3389/fpsyt.2021.716673 |
0.657 |
|
2021 |
DeSpenza T, Carlson M, Panchagnula S, Robert S, Duy PQ, Mermin-Bunnell N, Reeves BC, Kundishora A, Elsamadicy AA, Smith H, Ocken J, Alper SL, Jin SC, Hoffman EJ, Kahle KT. PTEN mutations in autism spectrum disorder and congenital hydrocephalus: developmental pleiotropy and therapeutic targets. Trends in Neurosciences. PMID 34625286 DOI: 10.1016/j.tins.2021.08.007 |
0.372 |
|
2020 |
Jin SC, Dong W, Kundishora AJ, Panchagnula S, Moreno-De-Luca A, Furey CG, Allocco AA, Walker RL, Nelson-Williams C, Smith H, Dunbar A, Conine S, Lu Q, Zeng X, Sierant MC, ... ... Hoffman EJ, et al. Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus. Nature Medicine. PMID 33077954 DOI: 10.1038/s41591-020-1090-2 |
0.45 |
|
2019 |
Cappi C, Oliphant ME, Péter Z, Zai G, Conceição do Rosário M, Sullivan CAW, Gupta AR, Hoffman EJ, Virdee M, Olfson E, Abdallah SB, Willsey AJ, Shavitt RG, Miguel EC, Kennedy JL, et al. De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. Biological Psychiatry. PMID 31771860 DOI: 10.1016/J.Biopsych.2019.09.029 |
0.722 |
|
2019 |
Hoffman EJ. 42.2 WHOLE-BRAIN ACTIVITY MAPPING AND HIGH-THROUGHPUT DRUG SCREENING IN ZEBRAFISH MODELS OF ASD RISK GENES Journal of the American Academy of Child & Adolescent Psychiatry. 58: S363. DOI: 10.1016/J.Jaac.2019.07.886 |
0.357 |
|
2019 |
Hoffman EJ, Cochran D. RESEARCH SYMPOSIUM: ADVANCES IN THE GENETICS OF NEURODEVELOPMENTAL DISORDERS: TRANSLATING FINDINGS TO THE CLINIC Journal of the American Academy of Child & Adolescent Psychiatry. 58: S315. DOI: 10.1016/J.Jaac.2019.07.727 |
0.432 |
|
2018 |
Sakai C, Ijaz S, Hoffman EJ. Zebrafish Models of Neurodevelopmental Disorders: Past, Present, and Future. Frontiers in Molecular Neuroscience. 11: 294. PMID 30210288 DOI: 10.3389/Fnmol.2018.00294 |
0.544 |
|
2018 |
Hoffman EJ, Manoli D, State M. From Bench to Bedside: Molecular and Genetic Mechanisms in Neurodevelopmental Disorders Journal of the American Academy of Child & Adolescent Psychiatry. 57: S275-S276. DOI: 10.1016/J.Jaac.2018.07.640 |
0.653 |
|
2017 |
Hoffman EJ. 18.2 Identifying Novel Neurochemical Mechanisms With Relevance to Autism Using Zebrafish Models of Risk Genes Journal of the American Academy of Child & Adolescent Psychiatry. 56: S329. DOI: 10.1016/J.Jaac.2017.07.681 |
0.469 |
|
2017 |
Hoffman EJ, State M. 18.0 Molecular and Genetic Mechanisms in Autism: From Bench to Bedside Journal of the American Academy of Child & Adolescent Psychiatry. 56: S329. DOI: 10.1016/J.Jaac.2017.07.679 |
0.601 |
|
2017 |
Palumbo ML, McDougle CJ, Hoffman EJ. 13.0 Neurogenetic Syndromes Associated With Autism Spectrum Disorder: Three Syndromes That Include Atypical Social Interaction Journal of the American Academy of Child and Adolescent Psychiatry. 56. DOI: 10.1016/J.Jaac.2017.07.075 |
0.405 |
|
2016 |
Ijaz S, Hoffman EJ. Zebrafish: A Translational Model System for Studying Neuropsychiatric Disorders. Journal of the American Academy of Child and Adolescent Psychiatry. 55: 746-8. PMID 27566113 DOI: 10.1016/J.Jaac.2016.06.008 |
0.443 |
|
2016 |
Hoffman EJ, Turner KJ, Fernandez JM, Cifuentes D, Ghosh M, Ijaz S, Jain RA, Kubo F, Bill BR, Baier H, Granato M, Barresi MJ, Wilson SW, Rihel J, State MW, et al. Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2. Neuron. PMID 26833134 DOI: 10.1016/J.Neuron.2015.12.039 |
0.642 |
|
2016 |
Ijaz S, Ghosh M, Wilson S, Rihel J, Giraldez AJ, State M, Hoffman EJ. 5.32 A ZEBRAFISH MODEL FOR IDENTIFYING COMMON BIOLOGICAL MECHANISMS AND PHARMACOLOGICAL PATHWAYS IN AUTISM SPECTRUM DISORDERS Journal of the American Academy of Child & Adolescent Psychiatry. 55: S194. DOI: 10.1016/J.Jaac.2016.09.291 |
0.665 |
|
2016 |
Hoffman EJ. 20.3 ZEBRAFISH MODELS OF AUTISM-RISK GENES AS A PATH TOWARD DRUG DISCOVERY Journal of the American Academy of Child & Adolescent Psychiatry. 55: S289. DOI: 10.1016/J.Jaac.2016.07.234 |
0.389 |
|
2016 |
Hoffman EJ, State M. 20.0 Molecular and Genetic Mechanisms in Autism Spectrum Disorder: From Bench to Bedside Journal of the American Academy of Child & Adolescent Psychiatry. 55: S288. DOI: 10.1016/J.Jaac.2016.07.231 |
0.672 |
|
2013 |
Willsey AJ, Sanders SJ, Li M, Dong S, Tebbenkamp AT, Muhle RA, Reilly SK, Lin L, Fertuzinhos S, Miller JA, Murtha MT, Bichsel C, Niu W, Cotney J, Ercan-Sencicek AG, ... ... Hoffman EJ, et al. Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell. 155: 997-1007. PMID 24267886 DOI: 10.1016/J.Cell.2013.10.020 |
0.65 |
|
2010 |
Hoffman EJ, State MW. Progress in cytogenetics: implications for child psychopathology. Journal of the American Academy of Child and Adolescent Psychiatry. 49: 736-51; quiz 856-7. PMID 20643309 DOI: 10.1016/J.Jaac.2010.03.016 |
0.629 |
|
2009 |
Hoffman EJ. Clinical features and diagnosis of autism and other pervasive developmental disorders Primary Psychiatry. 16: 36-44. |
0.386 |
|
2008 |
Sakurai T, Reichert J, Hoffman EJ, Cai G, Jones HB, Faham M, Buxbaum JD. A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders. Autism Research : Official Journal of the International Society For Autism Research. 1: 251-7. PMID 19360675 DOI: 10.1002/Aur.30 |
0.48 |
|
2008 |
Cai G, Edelmann L, Goldsmith JE, Cohen N, Nakamine A, Reichert JG, Hoffman EJ, Zurawiecki DM, Silverman JM, Hollander E, Soorya L, Anagnostou E, Betancur C, Buxbaum JD. Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT. Bmc Medical Genomics. 1: 50. PMID 18925931 DOI: 10.1186/1755-8794-1-50 |
0.458 |
|
2008 |
Hoffman EJ, Mathew SJ. Anxiety disorders: a comprehensive review of pharmacotherapies. The Mount Sinai Journal of Medicine, New York. 75: 248-62. PMID 18704983 DOI: 10.1002/Msj.20041 |
0.384 |
|
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