(Q45291909)

11 December 2017

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title

Dynamic mutations and psychiatric genetics (English)

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11 December 2017

M C O'Donovan

1

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11 December 2017

M J Owen

series ordinal

2

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11 December 2017

language of work or name

English

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publication date

1 January 1996

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11 December 2017

published in

Psychological Medicine

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11 December 2017

volume

26

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11 December 2017

issue

1

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11 December 2017

page(s)

1-6

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Trinucleotide repeat length instability and age of onset in Huntington's disease

11 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS0033291700033663

7 January 2021

Direct detection of novel expanded trinucleotide repeats in the human genome

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https://api.crossref.org/works/10.1017%2FS0033291700033663

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Detection of expanded CAG repeats in bipolar affective disorder using the repeat expansion detection (RED) method

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https://api.crossref.org/works/10.1017%2FS0033291700033663

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Expanded CAG repeats in schizophrenia and bipolar disorder

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https://api.crossref.org/works/10.1017%2FS0033291700033663

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The 1993-94 Généthon human genetic linkage map

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Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

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Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)

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https://api.crossref.org/works/10.1017%2FS0033291700033663

7 January 2021

The problem of anticipation in pedigrees of dystrophia myotonica

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https://api.crossref.org/works/10.1017%2FS0033291700033663

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The molecular genetics of schizophrenia

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https://api.crossref.org/works/10.1017%2FS0033291700033663

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

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https://api.crossref.org/works/10.1017%2FS0033291700033663

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Imprinting and anticipation. Are they relevant to genetic studies of schizophrenia?

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https://api.crossref.org/works/10.1017%2FS0033291700033663

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

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https://api.crossref.org/works/10.1017%2FS0033291700033663

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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

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https://api.crossref.org/works/10.1017%2FS0033291700033663

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Dynamic mutations hit double figures

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https://api.crossref.org/works/10.1017%2FS0033291700033663

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Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

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Anticipation in Swedish families with bipolar affective disorder.

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Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

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CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

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Further segregation analysis of the fragile X syndrome with special reference to transmitting males

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Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

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The Huxley Lecture ON HEREDITARY ASPECTS OF NERVOUS AND MENTAL DISEASES

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Anticipation in Huntington's disease is inherited through the male line but may originate in the female

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Absence of expression of the FMR-1 gene in fragile X syndrome

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The strength of the genetic effect. Is there room for an environmental influence in the aetiology of schizophrenia?

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Familial myoclonic dementia masquerading as Creutzfeldt-Jakob disease

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Fragile X genotype characterized by an unstable region of DNA.

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10.1017/S0033291700033663

Identifiers

DOI

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