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Results by year

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

Year Number of Results
1975 1
1978 1
1980 1
1981 5
1982 2
1984 2
1985 2
1987 1
1988 3
1989 1
1990 3
1991 7
1992 9
1993 9
1994 5
1995 10
1996 8
1997 10
1998 5
1999 5
2000 9
2001 6
2002 5
2003 5
2004 6
2005 4
2006 3
2007 11
2008 8
2009 2
2010 8
2011 5
2012 9
2013 7
2014 8
2015 6
2016 4
2017 4
2018 2
2019 2
2020 3
2021 5
2022 4
2023 2
2024 0

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Search Results

208 results

Results by year

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Page 1
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. Among authors: warren st. Genet Med. 2011 Sep;13(9):777-84. doi: 10.1097/GIM.0b013e31822c79f9. Genet Med. 2011. PMID: 21844811 Free PMC article.
A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies.
Kang Y, Zhou Y, Li Y, Han Y, Xu J, Niu W, Li Z, Liu S, Feng H, Huang W, Duan R, Xu T, Raj N, Zhang F, Dou J, Xu C, Wu H, Bassell GJ, Warren ST, Allen EG, Jin P, Wen Z. Kang Y, et al. Among authors: warren st. Nat Neurosci. 2021 Oct;24(10):1377-1391. doi: 10.1038/s41593-021-00913-6. Epub 2021 Aug 19. Nat Neurosci. 2021. PMID: 34413513 Free PMC article.
Fragile X syndrome.
Garber KB, Visootsak J, Warren ST. Garber KB, et al. Among authors: warren st. Eur J Hum Genet. 2008 Jun;16(6):666-72. doi: 10.1038/ejhg.2008.61. Epub 2008 Apr 9. Eur J Hum Genet. 2008. PMID: 18398441 Free PMC article. Review.
Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion.
Purcell RH, Sefik E, Werner E, King AT, Mosley TJ, Merritt-Garza ME, Chopra P, McEachin ZT, Karne S, Raj N, Vaglio BJ, Sullivan D, Firestein BL, Tilahun K, Robinette MI, Warren ST, Wen Z, Faundez V, Sloan SA, Bassell GJ, Mulle JG. Purcell RH, et al. Among authors: warren st. Sci Adv. 2023 Aug 18;9(33):eadh0558. doi: 10.1126/sciadv.adh0558. Epub 2023 Aug 16. Sci Adv. 2023. PMID: 37585521 Free PMC article.
Neuroscience: fragile dopamine.
Weinshenker D, Warren ST. Weinshenker D, et al. Among authors: warren st. Nature. 2008 Oct 2;455(7213):607-8. doi: 10.1038/455607a. Nature. 2008. PMID: 18833269 No abstract available.
Emery-Dreifuss muscular dystrophy.
Zacharias AS, Wagener ME, Warren ST, Hopkins LC. Zacharias AS, et al. Among authors: warren st. Semin Neurol. 1999;19(1):67-79. doi: 10.1055/s-2008-1040827. Semin Neurol. 1999. PMID: 10711990 Review.
The human genome: a diamond in the rough.
Emanuel BS, Warren ST, Garber KB. Emanuel BS, et al. Among authors: warren st. Curr Opin Genet Dev. 2012 Jun;22(3):189-90. doi: 10.1016/j.gde.2012.04.005. Epub 2012 May 18. Curr Opin Genet Dev. 2012. PMID: 22608825 No abstract available.
Local RNA translation at the synapse and in disease.
Liu-Yesucevitz L, Bassell GJ, Gitler AD, Hart AC, Klann E, Richter JD, Warren ST, Wolozin B. Liu-Yesucevitz L, et al. Among authors: warren st. J Neurosci. 2011 Nov 9;31(45):16086-93. doi: 10.1523/JNEUROSCI.4105-11.2011. J Neurosci. 2011. PMID: 22072660 Free PMC article. Review.
208 results