C9ORF72 expansion in a family with bipolar disorder (Q36864788)

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scientific article published on April 2013

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Language	Label	Description	Also known as
English	C9ORF72 expansion in a family with bipolar disorder	scientific article published on April 2013

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

3660726

retrieved

16 August 2017

title

C9ORF72 expansion in a family with bipolar disorder (English)

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Europe PubMed Central

PMC publication ID

3660726

retrieved

16 August 2017

main subject

bipolar disorder

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based on heuristic

inferred from title

author

Masoud Kamali

object named as

Masoud Kamali

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7

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Guy M. Lenk

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Guy M Lenk

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4

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Scott A. Langenecker

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Scott A Langenecker

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10

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author name string

Miriam H Meisler

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1

1 reference

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Europe PubMed Central

PMC publication ID

3660726

retrieved

16 August 2017

Adrienne E Grant

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2

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Europe PubMed Central

PMC publication ID

3660726

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16 August 2017

Julie M Jones

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3

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Europe PubMed Central

PMC publication ID

3660726

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16 August 2017

Fang He

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5

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Europe PubMed Central

PMC publication ID

3660726

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16 August 2017

Peter K Todd

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6

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Europe PubMed Central

PMC publication ID

3660726

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16 August 2017

Roger L Albin

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8

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Europe PubMed Central

PMC publication ID

3660726

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16 August 2017

Andrew P Lieberman

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9

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Europe PubMed Central

PMC publication ID

3660726

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16 August 2017

Melvin G McInnis

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11

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Europe PubMed Central

PMC publication ID

3660726

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16 August 2017

publication date

1 April 2013

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stated in

Europe PubMed Central

PMC publication ID

3660726

retrieved

16 August 2017

published in

Bipolar Disorders

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stated in

Europe PubMed Central

PMC publication ID

3660726

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16 August 2017

volume

15

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Europe PubMed Central

PMC publication ID

3660726

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16 August 2017

issue

3

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Europe PubMed Central

PMC publication ID

3660726

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16 August 2017

page(s)

326-332

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Europe PubMed Central

PMC publication ID

3660726

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16 August 2017

cites work

Frontotemporal dementia in a Brazilian kindred with the c9orf72 mutation

1 reference

stated in

PubMed Central

reference URL

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29 September 2017

Development of frontotemporal dementia in a case of bipolar affective disorder: is there a link?

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PubMed Central

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29 September 2017

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

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PubMed Central

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29 September 2017

Characterization of a family with c9FTD/ALS associated with the GGGGCC repeat expansion in C9ORF72.

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PubMed Central

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29 September 2017

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

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PubMed Central

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29 September 2017

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

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29 September 2017

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29 September 2017

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

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29 September 2017

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

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29 September 2017

Assessment of mild dementia with amyloid and dopamine terminal positron emission tomography

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PubMed Central

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29 September 2017

Smaller intracranial volume in prodromal Huntington's disease: evidence for abnormal neurodevelopment

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29 September 2017

Intermediate: cognitive phenotypes in bipolar disorder

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29 September 2017

RNA-mediated neuromuscular disorders

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29 September 2017

An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 gene

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29 September 2017

Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic dystrophy.

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29 September 2017

Anticipation in bipolar affective disorder

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660726

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29 September 2017

Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease

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PubMed Central

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4 September 2018

Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity

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4 September 2018

Early onset behavioral variant frontotemporal dementia due to the C9ORF72 hexanucleotide repeat expansion: psychiatric clinical presentations

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PubMed Central

reference URL

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4 September 2018

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

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PubMed Central

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4 September 2018

Secondary bipolar disorder and Diogenes syndrome in frontotemporal dementia: behavioral improvement with quetiapine and sodium valproate

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660726

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4 September 2018

Transmission of C9orf72 hexanucleotide repeat expansions in sporadic amyotrophic lateral sclerosis: an Australian trio study

2 references

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Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBDI.12063

retrieved

21 January 2018

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660726

retrieved

20 October 2018

Identifiers

DOI

10.1111/BDI.12063

1 reference

stated in

Europe PubMed Central

PMC publication ID

3660726

retrieved

16 August 2017

PMC publication ID

3660726

1 reference

stated in

Europe PubMed Central

PMC publication ID

3660726

retrieved

16 August 2017

PubMed publication ID

23551834

1 reference

stated in

Europe PubMed Central

PMC publication ID

3660726

retrieved

16 August 2017

ResearchGate publication ID

236102842

0 references

 

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