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Results by year

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

Year Number of Results
1952 1
1959 1
1961 1
1962 1
1963 2
1964 1
1966 1
1969 1
1974 1
1975 1
1977 1
1979 1
1980 6
1982 1
1984 3
1985 4
1986 2
1987 4
1988 2
1989 2
1990 6
1991 3
1992 5
1993 8
1994 4
1995 8
1996 13
1997 3
1998 7
1999 8
2000 1
2001 8
2002 4
2003 6
2004 3
2005 7
2006 5
2007 3
2008 2
2009 2
2010 3
2011 1
2012 2
2014 1
2015 1
2016 1
2017 1
2024 0

Text availability

Article attribute

Article type

Publication date

PubMed (cited) for id: 194050

152 results

Results by year

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Page 1
A human neurodevelopmental model for Williams syndrome.
Chailangkarn T, Trujillo CA, Freitas BC, Hrvoj-Mihic B, Herai RH, Yu DX, Brown TT, Marchetto MC, Bardy C, McHenry L, Stefanacci L, Järvinen A, Searcy YM, DeWitt M, Wong W, Lai P, Ard MC, Hanson KL, Romero S, Jacobs B, Dale AM, Dai L, Korenberg JR, Gage FH, Bellugi U, Halgren E, Semendeferi K, Muotri AR. Chailangkarn T, et al. Nature. 2016 Aug 18;536(7616):338-43. doi: 10.1038/nature19067. Epub 2016 Aug 10. Nature. 2016. PMID: 27509850 Free PMC article.
Skin findings in Williams syndrome.
Kozel BA, Bayliss SJ, Berk DR, Waxler JL, Knutsen RH, Danback JR, Pober BR. Kozel BA, et al. Am J Med Genet A. 2014 Sep;164A(9):2217-25. doi: 10.1002/ajmg.a.36628. Epub 2014 Jun 11. Am J Med Genet A. 2014. PMID: 24920525 Free PMC article.
Duplication of GTF2I results in separation anxiety in mice and humans.
Mervis CB, Dida J, Lam E, Crawford-Zelli NA, Young EJ, Henderson DR, Onay T, Morris CA, Woodruff-Borden J, Yeomans J, Osborne LR. Mervis CB, et al. Am J Hum Genet. 2012 Jun 8;90(6):1064-70. doi: 10.1016/j.ajhg.2012.04.012. Epub 2012 May 10. Am J Hum Genet. 2012. PMID: 22578324 Free PMC article.
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, Moreno-De-Luca D, Moreno-De-Luca A, Mulle JG, Warren ST, Richard G, Compton JG, Fuller AE, Gliem TJ, Huang S, Collinson MN, Beal SJ, Ackley T, Pickering DL, Golden DM, Aston E, Whitby H, Shetty S, Rossi MR, Rudd MK, South ST, Brothman AR, Sanger WG, Iyer RK, Crolla JA, Thorland EC, Aradhya S, Ledbetter DH, Martin CL. Kaminsky EB, et al. Genet Med. 2011 Sep;13(9):777-84. doi: 10.1097/GIM.0b013e31822c79f9. Genet Med. 2011. PMID: 21844811 Free PMC article.
Williams-Beuren syndrome.
Game X, Panicker J, Fowler CJ. Game X, et al. N Engl J Med. 2010 Apr 15;362(15):1449; author reply 1450. doi: 10.1056/NEJMc1001965. N Engl J Med. 2010. PMID: 20393184 No abstract available.
Williams-Beuren syndrome.
Pober BR. Pober BR. N Engl J Med. 2010 Jan 21;362(3):239-52. doi: 10.1056/NEJMra0903074. N Engl J Med. 2010. PMID: 20089974 Review. No abstract available.
152 results