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

Year Number of Results
1993 1
1998 1
2002 2
2004 2
2005 3
2006 4
2007 6
2008 2
2009 5
2010 1
2011 7
2012 4
2013 4
2014 6
2015 8
2016 7
2017 4
2018 2
2019 4
2020 1
2021 3
2022 0
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Search Results

60 results
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Page 1
Prader-Willi syndrome.
Cassidy SB, Schwartz S, Miller JL, Driscoll DJ. Cassidy SB, et al. Among authors: driscoll dj. Genet Med. 2012 Jan;14(1):10-26. doi: 10.1038/gim.0b013e31822bead0. Epub 2011 Sep 26. Genet Med. 2012. PMID: 22237428 Review.
Prader-Willi Syndrome.
Driscoll DJ, Miller JL, Schwartz S, Cassidy SB. Driscoll DJ, et al. 1998 Oct 6 [updated 2017 Dec 14]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 1998 Oct 6 [updated 2017 Dec 14]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301505 Free Books & Documents. Review.
Prader-Willi syndrome.
Cassidy SB, Driscoll DJ. Cassidy SB, et al. Among authors: driscoll dj. Eur J Hum Genet. 2009 Jan;17(1):3-13. doi: 10.1038/ejhg.2008.165. Epub 2008 Sep 10. Eur J Hum Genet. 2009. PMID: 18781185 Free PMC article.
Clinical and genetic aspects of Angelman syndrome.
Williams CA, Driscoll DJ, Dagli AI. Williams CA, et al. Among authors: driscoll dj. Genet Med. 2010 Jul;12(7):385-95. doi: 10.1097/GIM.0b013e3181def138. Genet Med. 2010. PMID: 20445456 Review.
Birth seasonality studies in a large Prader-Willi syndrome cohort.
Butler MG, Kimonis V, Dykens E, Gold JA, Tamura R, Miller JL, Driscoll DJ. Butler MG, et al. Among authors: driscoll dj. Am J Med Genet A. 2019 Aug;179(8):1531-1534. doi: 10.1002/ajmg.a.61263. Epub 2019 Jun 21. Am J Med Genet A. 2019. PMID: 31225937 Free PMC article.
Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study.
Butler MG, Hartin SN, Hossain WA, Manzardo AM, Kimonis V, Dykens E, Gold JA, Kim SJ, Weisensel N, Tamura R, Miller JL, Driscoll DJ. Butler MG, et al. Among authors: driscoll dj. J Med Genet. 2019 Mar;56(3):149-153. doi: 10.1136/jmedgenet-2018-105301. Epub 2018 May 5. J Med Genet. 2019. PMID: 29730598 Free PMC article.
Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental Syndromes.
Veatch OJ, Malow BA, Lee HS, Knight A, Barrish JO, Neul JL, Lane JB, Skinner SA, Kaufmann WE, Miller JL, Driscoll DJ, Bird LM, Butler MG, Dykens EM, Gold JA, Kimonis V, Bacino CA, Tan WH, Kothare SV, Peters SU, Percy AK, Glaze DG. Veatch OJ, et al. Among authors: driscoll dj. Pediatr Neurol. 2021 Oct;123:30-37. doi: 10.1016/j.pediatrneurol.2021.07.009. Epub 2021 Jul 24. Pediatr Neurol. 2021. PMID: 34388423
60 results