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

Year Number of Results
1947 1
1957 3
1959 1
1961 2
1962 1
1964 1
1965 2
1967 1
1969 1
1972 1
1976 1
1980 1
1981 3
1983 1
1985 1
1986 4
1987 1
1988 1
1989 2
1990 3
1991 4
1992 4
1993 1
1994 3
1995 2
1996 2
1997 5
1999 6
2000 11
2001 5
2002 15
2003 17
2004 21
2005 18
2006 27
2007 39
2008 42
2009 51
2010 49
2011 70
2012 76
2013 68
2014 67
2015 98
2016 82
2017 68
2018 78
2019 91
2020 21
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956 results
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Page 1
Impact of Dietary Fats on Brain Functions
Chianese R, et al. Curr Neuropharmacol 2018 - Review. Among authors: Coppola G. PMID 29046155 Free PMC article.
De Novo Coding Variants Are Strongly Associated with Tourette Disorder
Willsey AJ, et al. Neuron 2017. Among authors: Coppola G. PMID 28472652 Free PMC article.
We identify four likely risk genes with multiple de novo damaging variants in unrelated probands: WWC1 (WW and C2 domain containing 1), CELSR3 (Cadherin EGF LAG seven-pass G-type receptor 3), NIPBL (Nipped-B-like), and FN1 (fibronectin 1). ...
We identify four likely risk genes with multiple de novo damaging variants in unrelated probands: WWC1 (WW and C2 domain containing 1), CELS …
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis
Wang S, et al. Cell Rep 2018. Among authors: Coppola G. PMID 30257206 Free PMC article.
We observe an overrepresentation of de novo damaging variants in simplex, but not multiplex, families; we identify a high-confidence TD risk gene, CELSR3 (cadherin EGF LAG seven-pass G-type receptor 3); we find that the genes mutated in TD patients are enriched for those related to cell polarity, suggesting a common pathway underlying pathobiology; and we confirm a statistically significant excess of de novo copy number variants in TD. ...
We observe an overrepresentation of de novo damaging variants in simplex, but not multiplex, families; we identify a high-confidence TD risk …
956 results
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