(Q36645949)

15 August 2017

C9ORF72 repeat expansions not detected in a group of patients with schizophrenia (English)

1 reference

15 August 2017

1 reference

8

Richard Mayeux

1 reference

15 August 2017

6

Jeffrey Lieberman

1 reference

15 August 2017

1

Edward D Huey

1 reference

15 August 2017

Peter L Nagy

2

1 reference

15 August 2017

Laura Rodriguez-Murillo

3

1 reference

15 August 2017

Masood Manoochehri

4

1 reference

15 August 2017

Jill Goldman

5

1 reference

15 August 2017

Maria Karayiorgou

7

1 reference

15 August 2017

language of work or name

1 reference

1 October 2012

1 reference

15 August 2017

Neurobiology of Aging

1 reference

15 August 2017

34

1 reference

15 August 2017

4

1 reference

15 August 2017

1309.e9-10

1 reference

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

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3584690

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3584690

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3584690

Progranulin (GRN) in two siblings of a Latino family and in other patients with schizophrenia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3584690

Frontotemporal dementia presenting as schizophrenia-like psychosis in young people: clinicopathological series and review of cases.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3584690

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3584690

C9orf72 repeat expansions in patients with ALS and FTD.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3584690

Negative schizophrenic symptoms and the frontal lobe syndrome: one and the same?

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3584690

Detecting polymorphisms and mutations in candidate genes

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3584690

Morbid risk for schizophrenia in first-degree relatives of people with frontotemporal dementia

20 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23036583

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.NEUROBIOLAGING.2012.08.011

1 reference

15 August 2017

1 reference

15 August 2017

PubMed publication ID

23036583

1 reference