The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease.

Dermaut B; Cruts M; Slooter AJ; Van Gestel S; De Jonghe C; Vanderstichele H; Vanmechelen E; Breteler MM; Hofman A; van Duijn CM; Van Broeckhoven C

doi:10.1086/302200

The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease.

ORCIDs linked to this article

American Journal of Human Genetics, 01 Jan 1999, 64(1):290-292
https://doi.org/10.1086/302200 PMID: 9915968 PMCID: PMC1377727

Free full text in Europe PMC

A comment on this article appears in "Genetic testing should not be advocated as a diagnostic tool in familial forms of dementia." Am J Hum Genet. 2000 Oct;67(4):1033-5.

Abstract

No abstract provided.

Free full text

Am J Hum Genet. 1999 Jan; 64(1): 290–292.

https://doi.org/10.1086/302200

PMCID: PMC1377727

PMID: 9915968

The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease.

B Dermaut, M Cruts, A J Slooter, S Van Gestel, C De Jonghe, H Vanderstichele, E Vanmechelen, M M Breteler, A Hofman, C M van Duijn, and C Van Broeckhoven

This article has been cited by other articles in PMC.

Full Text

The Full Text of this article is available as a PDF (1.4M).

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

Full text links

Read article at publisher's site: https://doi.org/10.1086/302200

Read article for free, from open access legal sources, via Unpaywall: http://www.cell.com/article/S0002929707616826/pdf

Citations & impact

Impact metrics

Citations

Jump to Citations

Data citations

Jump to Data

Citations of article over time

Alternative metrics

Altmetric item for https://www.altmetric.com/details/7648623

Altmetric
Discover the attention surrounding your research
https://www.altmetric.com/details/7648623

Smart citations by scite.ai
Explore citation contexts and check if this article has been supported or disputed.
https://scite.ai/reports/10.1086/302200

Supporting

Mentioning

Contrasting

Article citations

Patient with PSEN1 Glu318Gly and Other Possible Disease Risk Mutations, Diagnosed with Early Onset Alzheimer's Disease.
Yang Y, Bagyinszky E, An SSA
Int J Mol Sci, 24(20):15461, 23 Oct 2023
Cited by: 2 articles | PMID: 37895139 | PMCID: PMC10607718
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC
Semantic and right temporal variant of FTD: Next generation sequencing genetic analysis on a single-center cohort.
Rossi G, Salvi E, Mehmeti E, Ricci M, Villa C, Prioni S, Moda F, Di Fede G, Tiraboschi P, Redaelli V, Coppola C, Koch G, Canu E, Filippi M, Agosta F, Giaccone G, Caroppo P
Front Aging Neurosci, 14:1085406, 08 Dec 2022
Cited by: 2 articles | PMID: 36570531 | PMCID: PMC9773257
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC
Singular cases of Alzheimer's disease disclose new and old genetic "acquaintances".
Coppola C, Saracino D, Oliva M, Cipriano L, Puoti G, Pappatà S, Di Fede G, Catania M, Ricci M, Cimini S, Giaccone G, Bonavita S, Rossi G
Neurol Sci, 42(5):2021-2029, 02 Oct 2020
Cited by: 1 article | PMID: 33006056 | PMCID: PMC8043869
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC
Influence of low frequency PSEN1 variants on familial Alzheimer's disease risk in Brazil.
Abdala BB, Dos Santos JM, Gonçalves AP, da Motta LB, Laks J, de Borges MB, Gonçalves Pimentel MM, Santos-Rebouças CB
Neurosci Lett, 653:341-345, 26 May 2017
Cited by: 5 articles | PMID: 28554858
Atypical Huntington's disease with the clinical presentation of behavioural variant of frontotemporal dementia.
Sutovsky S, Smolek T, Alafuzoff I, Blaho A, Parrak V, Turcani P, Palkovic M, Petrovic R, Novak M, Zilka N
J Neural Transm (Vienna), 123(12):1423-1433, 10 Jun 2016
Cited by: 2 articles | PMID: 27287334

Go to all (28) article citations

Data

Data that cites the article

This data has been provided by curated databases and other sources that have cited the article.

Diseases in OMIM

PRESENILIN 1; PSEN1(OMIM - 104311)

Proteins in UniProt

Presenilin-1(UniProt - P49768)

GlyGen is an international glycobioinformatics knowledgebase funded by The National Institutes of Health to facilitate glycoscience research by integrating diverse kinds of information, including glycomics, genomics, proteomics (and glycoproteomics), cell biology, developmental biology and biochemistry.

https://www.glygen.org/publication/MED/9915968

Search life-sciences literature (45,103,589 articles, preprints and more)