Concepedia

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

Amélie Piton, J Gauthier, Fadi F. Hamdan, Ronald G. Lafrenière, Yanlian Yang, Édouard Henrion, S. B. Laurent, Anne Noreau, Patrick H. Thibodeau, Liliane Karemera,

Molecular Psychiatry · 2010 · 320 citations · 66 references

DOI

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References

66

SIFT: predicting amino acid changes that affect protein function

P.C. Ng · Nucleic Acids Research · 2003 · 6.9K citations · Full text

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

Manuel A. R. Ferreira · Nature · 2009 · 5K citations · Full text

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Ruthie E. Amir, Ignatia B. Van den Veyver, Mimi Wan et al. · Nature Genetics · 1999 · 5K citations

, , +9

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Annemieke J.M.H. Verkerk, Maura Pieretti, James S. Sutcliffe et al. · Cell · 1991 · 3.5K citations

, , +12

Autism as a strongly genetic disorder: evidence from a British twin study

Anthony Bailey, Ann Le Couteur, Irving I. Gottesman et al. · Psychological Medicine · 1995 · 2.5K citations

, , +14