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

Year Number of Results
1992 2
1993 2
1994 1
1995 2
1996 4
1997 1
1998 4
1999 1
2000 3
2001 6
2002 5
2003 5
2004 3
2005 10
2006 2
2007 5
2008 4
2009 2
2010 6
2011 6
2012 2
2013 8
2014 11
2015 2
2016 1
2018 1
2020 2
2021 1
2023 2
2024 0

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100 results

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Page 1
Functional impact of global rare copy number variation in autism spectrum disorders.
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Bryson SE, Carson AR, Casallo G, Casey J, Chung BH, Cochrane L, Corsello C, Crawford EL, Crossett A, Cytrynbaum C, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green A, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Pilorge M, Piven J, Ponting CP, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Ri… See abstract for full author list ➔ Pinto D, et al. Among authors: vieland vj. Nature. 2010 Jul 15;466(7304):368-72. doi: 10.1038/nature09146. Epub 2010 Jun 9. Nature. 2010. PMID: 20531469 Free PMC article.
A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity.
Flanigan KM, Waldrop MA, Martin PT, Alles R, Dunn DM, Alfano LN, Simmons TR, Moore-Clingenpeel M, Burian J, Seok SC, Weiss RB, Vieland VJ. Flanigan KM, et al. Among authors: vieland vj. Eur J Hum Genet. 2023 Jun;31(6):663-673. doi: 10.1038/s41431-023-01329-5. Epub 2023 Mar 20. Eur J Hum Genet. 2023. PMID: 36935420
Next-generation linkage analysis.
Vieland VJ, Devoto M. Vieland VJ, et al. Hum Hered. 2011;72(4):227. doi: 10.1159/000334421. Epub 2011 Dec 23. Hum Hered. 2011. PMID: 22189464 Free article. No abstract available.
Where's the evidence?
Vieland VJ. Vieland VJ. Hum Hered. 2011;71(1):59-66. doi: 10.1159/000324838. Epub 2011 Mar 22. Hum Hered. 2011. PMID: 21422761 Free PMC article.
The emperor's new methods.
Spence MA, Greenberg DA, Hodge SE, Vieland VJ. Spence MA, et al. Among authors: vieland vj. Am J Hum Genet. 2003 May;72(5):1084-7. doi: 10.1086/374826. Epub 2003 Apr 18. Am J Hum Genet. 2003. PMID: 12704569 Free PMC article. No abstract available.
The replication requirement.
Vieland VJ. Vieland VJ. Nat Genet. 2001 Nov;29(3):244-5. doi: 10.1038/ng1101-244. Nat Genet. 2001. PMID: 11687787 No abstract available.
PEDSnet: a National Pediatric Learning Health System.
Forrest CB, Margolis PA, Bailey LC, Marsolo K, Del Beccaro MA, Finkelstein JA, Milov DE, Vieland VJ, Wolf BA, Yu FB, Kahn MG. Forrest CB, et al. Among authors: vieland vj. J Am Med Inform Assoc. 2014 Jul-Aug;21(4):602-6. doi: 10.1136/amiajnl-2014-002743. Epub 2014 May 12. J Am Med Inform Assoc. 2014. PMID: 24821737 Free PMC article.
100 results