Genetic or epigenetic difference causing discordance between monozygotic twins as a clue to molecular basis of mental disorders (Q34556925)

3 August 2017

1 reference

title

Genetic or epigenetic difference causing discordance between monozygotic twins as a clue to molecular basis of mental disorders (English)

1 reference

3 August 2017

Kato T

1

1 reference

3 August 2017

Iwamoto K

2

1 reference

3 August 2017

Kakiuchi C

3

1 reference

3 August 2017

Kuratomi G

4

1 reference

3 August 2017

Okazaki Y

5

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 July 2005

1 reference

3 August 2017

1 reference

3 August 2017

10

1 reference

3 August 2017

7

1 reference

3 August 2017

622-630

1 reference

https://scigraph.springernature.com/pub.10.1038/sj.mp.4001662

3 August 2017

0 references

cites work

Prenatal origin of schizophrenia in a subgroup of discordant monozygotic twins.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Prenatal underdevelopment and schizophrenia: a case report of monozygotic twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Anatomical abnormalities in the brains of monozygotic twins discordant for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Pathogenesis of schizophrenia: Part I. Symptomatology, cognitive characteristics and brain morphology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Search for a genetic event in monozygotic twins discordant for schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Monozygotic twins exhibit numerous epigenetic differences: clues to twin discordance?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Appraisal of genetic and epigenetic congruity of a monozygotic twin pair discordant for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Psychiatric epigenetics: a new focus for the new century

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Epigenetic inheritance at the agouti locus in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Transgenerational inheritance of epigenetic states at the murine Axin(Fu) allele occurs after maternal and paternal transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Epigenetic contributors to the discordance of monozygotic twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Epigenetic programming by maternal behavior

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Some causes of genotypic and phenotypic discordance in monozygotic twin pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Monozygotic twins with discordant sexual phenotypes due to different ratios of mosaicism of 47,X,idic(Y),idic(Y)/46,X, idic(Y)/45,X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Monozygotic twins with chromosome 22q11 deletion and discordant phenotypes: updates with an epigenetic hypothesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Mitochondrial DNA deletion in "identical" twin brothers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Uneven distribution of mitochondrial DNA mutation in MERRF dizygotic twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Unstable genes--unstable mind?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Beckwith-Wiedemann syndrome and IVF: a case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Epigenetics and assisted reproductive technology: a call for investigation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

A de novo Alu insertion results in neurofibromatosis type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Retroviral RNA identified in the cerebrospinal fluids and brains of individuals with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Molecular characterization of a 2.7-kb, 12q13-specific, retroviral-related sequence isolated by RDA from monozygotic twin pairs discordant for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Molecular characterization of a MSRV-like sequence identified by RDA from monozygotic twin pairs discordant for schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Epigenetics and bipolar disorder: New opportunities and challenges

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Evaluating the parent-of-origin effect in bipolar affective disorder. Is a more penetrant subtype transmitted paternally?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Valproic acid inhibits histone deacetylase activity and suppresses excitotoxicity-induced GAPDH nuclear accumulation and apoptotic death in neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

The methyl donor S-Adenosylmethionine inhibits active demethylation of DNA: a candidate novel mechanism for the pharmacological effects of S-Adenosylmethionine

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Confirming unexpressed genotypes for schizophrenia. Risks in the offspring of Fischer's Danish identical and fraternal discordant twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Schizophrenia: an epigenetic puzzle?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Increased occurrence of schizophrenia and other psychiatric illnesses among twins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

An epigenetic mouse model for molecular and behavioral neuropathologies related to schizophrenia vulnerability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

A genomic scanning method for higher organisms using restriction sites as landmarks

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

A Danish Twin Study of Manic-Depressive Disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Impaired feedback regulation of XBP1 as a genetic risk factor for bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Focus on protein kinase A and protein kinase C, critical components of signal transduction system, in mood disorders and suicide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

A case-control study provides evidence of association for a functional polymorphism -197C/G in XBP1 to schizophrenia and suggests a sex-dependent effect

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Association of the XBP1-116C/G polymorphism with schizophrenia in the Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Chronobiological approach for treatment-resistant rapid cycling affective disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

DNA methylation and chromosome instability in lymphoblastoid cell lines.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Retrotransposable L1 elements expressed in rheumatoid arthritis synovial tissue: association with genomic DNA hypomethylation and influence on gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Integrated genomic and epigenomic analyses pinpoint biallelic gene inactivation in tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

A microarray-based method for detecting methylated loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Establishment of methylation-sensitive-representational difference analysis and isolation of hypo- and hypermethylated genomic fragments in mouse liver tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

A genomic screen for genes upregulated by demethylation and histone deacetylase inhibition in human colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

DNA stability and schizophrenia in twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Evaluation of parent-of-origin effect in bipolar affective disorder relating to susceptibility loci on chromosome 18

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

Genomic discordance between monozygotic twins discordant for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Monozygotic twin girls with diploid/triploid chromosome mosaicism and cutaneous pigmentary dysplasia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Mosaic trisomy 11p in monozygotic twins with discordant clinical phenotypes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Myoblast transplantation between monozygotic twin girl carriers of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Parent-of-origin effect in transmission of bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Switch mechanism in affective illness and oral S-adenosylmethionine (SAM)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Parent-of-origin effect and evidence for differential transmission in periodic catatonia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

No evidence for a parent-of-origin effect detected in the pattern of inheritance of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Search for retroviral related DNA polymorphisms using RAPD PCR in schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Analysis of the DRPLA triplet repeat in brain tissue and leukocytes from schizophrenics.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

A subtracted probe derived from lymphocytes of twins discordant for schizophrenia hybridizes to selective areas of rat brain

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Expression in normals and in subjects with schizophrenia of a novel gene fragment originally isolated from monozygotic twins discordant for schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001662

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001662

1 reference

Dimensions Publication ID

3 August 2017

0 references

1 reference