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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 1
1986 1
1993 1
2004 1
2005 3
2006 2
2008 2
2010 2
2011 1
2013 2
2014 3
2015 2
2016 1
2017 3
2018 4
2019 7
2020 11
2021 10
2022 4
2024 0

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49 results

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Page 1
Reduced sleep pressure in young children with autism.
Arazi A, Meiri G, Danan D, Michaelovski A, Flusser H, Menashe I, Tarasiuk A, Dinstein I. Arazi A, et al. Among authors: flusser h. Sleep. 2020 Jun 15;43(6):zsz309. doi: 10.1093/sleep/zsz309. Sleep. 2020. PMID: 31848619
Ethnic Disparities in the Diagnosis of Autism in Southern Israel.
Kerub O, Haas EJ, Meiri G, Bilenko N, Flusser H, Michaelovski A, Dinstein I, Davidovitch N, Menashe I. Kerub O, et al. Among authors: flusser h. Autism Res. 2021 Jan;14(1):193-201. doi: 10.1002/aur.2421. Epub 2020 Oct 20. Autism Res. 2021. PMID: 33078561 Clinical Trial.
Association Between Abnormal Fetal Head Growth and Autism Spectrum Disorder.
Regev O, Cohen G, Hadar A, Schuster J, Flusser H, Michaelovski A, Meiri G, Dinstein I, Hershkovitch R, Menashe I. Regev O, et al. Among authors: flusser h. J Am Acad Child Adolesc Psychiatry. 2021 Aug;60(8):986-997. doi: 10.1016/j.jaac.2020.11.019. Epub 2020 Dec 27. J Am Acad Child Adolesc Psychiatry. 2021. PMID: 33378701
Brief Report: The Negev Hospital-University-Based (HUB) Autism Database.
Meiri G, Dinstein I, Michaelowski A, Flusser H, Ilan M, Faroy M, Bar-Sinai A, Manelis L, Stolowicz D, Yosef LL, Davidovitch N, Golan H, Arbelle S, Menashe I. Meiri G, et al. Among authors: flusser h. J Autism Dev Disord. 2017 Sep;47(9):2918-2926. doi: 10.1007/s10803-017-3207-0. J Autism Dev Disord. 2017. PMID: 28631035
Quantifying the social symptoms of autism using motion capture.
Budman I, Meiri G, Ilan M, Faroy M, Langer A, Reboh D, Michaelovski A, Flusser H, Menashe I, Donchin O, Dinstein I. Budman I, et al. Among authors: flusser h. Sci Rep. 2019 May 22;9(1):7712. doi: 10.1038/s41598-019-44180-9. Sci Rep. 2019. PMID: 31118483 Free PMC article.
SEC31A mutation affects ER homeostasis, causing a neurological syndrome.
Halperin D, Kadir R, Perez Y, Drabkin M, Yogev Y, Wormser O, Berman EM, Eremenko E, Rotblat B, Shorer Z, Gradstein L, Shelef I, Birk R, Abdu U, Flusser H, Birk OS. Halperin D, et al. Among authors: flusser h. J Med Genet. 2019 Mar;56(3):139-148. doi: 10.1136/jmedgenet-2018-105503. Epub 2018 Nov 21. J Med Genet. 2019. PMID: 30464055
Phenotypic variability and mutation hotspot in COX15-related Leigh syndrome.
Halperin D, Drabkin M, Wormser O, Yogev Y, Dolgin V, Shorer Z, Gradstein L, Shelef I, Flusser H, Birk OS. Halperin D, et al. Among authors: flusser h. Am J Med Genet A. 2020 Jun;182(6):1506-1512. doi: 10.1002/ajmg.a.61577. Epub 2020 Mar 31. Am J Med Genet A. 2020. PMID: 32232962
49 results