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

Year Number of Results
2002 1
2003 1
2005 2
2007 1
2008 1
2009 2
2010 1
2011 2
2012 2
2013 7
2014 11
2015 7
2016 5
2017 8
2018 13
2019 10
2020 13
2021 12
2022 13
2023 23
2024 8

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119 results

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Page 1
A multidisciplinary approach and consensus statement to establish standards of care for Angelman syndrome.
Duis J, Nespeca M, Summers J, Bird L, Bindels-de Heus KGCB, Valstar MJ, de Wit MY, Navis C, Ten Hooven-Radstaake M, van Iperen-Kolk BM, Ernst S, Dendrinos M, Katz T, Diaz-Medina G, Katyayan A, Nangia S, Thibert R, Glaze D, Keary C, Pelc K, Simon N, Sadhwani A, Heussler H, Wheeler A, Woeber C, DeRamus M, Thomas A, Kertcher E, DeValk L, Kalemeris K, Arps K, Baym C, Harris N, Gorham JP, Bohnsack BL, Chambers RC, Harris S, Chambers HG, Okoniewski K, Jalazo ER, Berent A, Bacino CA, Williams C, Anderson A. Duis J, et al. Among authors: wheeler a. Mol Genet Genomic Med. 2022 Mar;10(3):e1843. doi: 10.1002/mgg3.1843. Epub 2022 Feb 11. Mol Genet Genomic Med. 2022. PMID: 35150089 Free PMC article. Review.
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
Tassone F, Protic D, Allen EG, Archibald AD, Baud A, Brown TW, Budimirovic DB, Cohen J, Dufour B, Eiges R, Elvassore N, Gabis LV, Grudzien SJ, Hall DA, Hessl D, Hogan A, Hunter JE, Jin P, Jiraanont P, Klusek J, Kooy RF, Kraan CM, Laterza C, Lee A, Lipworth K, Losh M, Loesch D, Lozano R, Mailick MR, Manolopoulos A, Martinez-Cerdeno V, McLennan Y, Miller RM, Montanaro FAM, Mosconi MW, Potter SN, Raspa M, Rivera SM, Shelly K, Todd PK, Tutak K, Wang JY, Wheeler A, Winarni TI, Zafarullah M, Hagerman RJ. Tassone F, et al. Among authors: wheeler a. Cells. 2023 Sep 21;12(18):2330. doi: 10.3390/cells12182330. Cells. 2023. PMID: 37759552 Free PMC article. Review.
Age of diagnosis for children with chromosome 15q syndromes.
Wheeler AC, Gantz MG, Cope H, Strong TV, Bohonowych JE, Moore A, Vogel-Farley V. Wheeler AC, et al. J Neurodev Disord. 2023 Nov 7;15(1):37. doi: 10.1186/s11689-023-09504-x. J Neurodev Disord. 2023. PMID: 37936142 Free PMC article.
Public Health Literature Review of Fragile X Syndrome.
Raspa M, Wheeler AC, Riley C. Raspa M, et al. Among authors: wheeler ac. Pediatrics. 2017 Jun;139(Suppl 3):S153-S171. doi: 10.1542/peds.2016-1159C. Pediatrics. 2017. PMID: 28814537 Free PMC article. Review.
Associated features in females with an FMR1 premutation.
Wheeler AC, Bailey DB Jr, Berry-Kravis E, Greenberg J, Losh M, Mailick M, Milà M, Olichney JM, Rodriguez-Revenga L, Sherman S, Smith L, Summers S, Yang JC, Hagerman R. Wheeler AC, et al. J Neurodev Disord. 2014;6(1):30. doi: 10.1186/1866-1955-6-30. Epub 2014 Jul 30. J Neurodev Disord. 2014. PMID: 25097672 Free PMC article. Review.
Multi-tract multi-symptom relationships in pediatric concussion.
Guberman GI, Stojanovski S, Nishat E, Ptito A, Bzdok D, Wheeler AL, Descoteaux M. Guberman GI, et al. Among authors: wheeler al. Elife. 2022 May 17;11:e70450. doi: 10.7554/eLife.70450. Elife. 2022. PMID: 35579325 Free PMC article.
119 results