Biblio

Found 6 results
Filters: Author is L A Weiss  [Clear All Filters]
2017
Savova V, Vinogradova S, Pruss D, Gimelbrant AA, Weiss LA.  2017.  Risk alleles of genes with monoallelic expression are enriched in gain-of-function variants and depleted in loss-of-function variants for neurodevelopmental disorders.. Molecular psychiatry. 22:1785-1794.
2016
Zerbo O, Traglia M, Yoshida C, Heuer LS, Ashwood P, Delorenze GN, Hansen RL, Kharrazi M, Van de Water J, Yolken RH et al..  2016.  Maternal mid-pregnancy C-reactive protein and risk of autism spectrum disorders: the early markers for autism study.. Translational psychiatry. 6:e783.
2015
Desachy G, Croen LA, Torres AR, Kharrazi M, Delorenze GN, Windham GC, Yoshida CK, Weiss LA.  2015.  Increased female autosomal burden of rare copy number variants in human populations and in autism families.. Molecular psychiatry. 20:170-5.
2013
Martin P-M, Yang X, Robin N, Lam E, Rabinowitz JS, Erdman CA, Quinn J, Weiss LA, Hamilton SP, Kwok P-Y et al..  2013.  A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation.. Translational psychiatry. 3:e301.
2009
Miller DT, Shen Y, Weiss LA, Korn J, Anselm I, Bridgemohan C, Cox GF, Dickinson H, Gentile J, Harris DJ et al..  2009.  Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.. Journal of medical genetics. 46:242-8.
2003
Weiss LA, Escayg A, Kearney JA, Trudeau M, MacDonald BT, Mori M, Reichert J, Buxbaum JD, Meisler MH.  2003.  Sodium channels SCN1A, SCN2A and SCN3A in familial autism.. Molecular psychiatry. 8:186-94.