Lista de obras - John S. K. Kauwe - Dominio Público Uruguay

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.

artículo científico publicado en 2017

A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin

artículo científico publicado en 2015

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease

artículo científico publicado en 2005

Alzheimer's disease risk variants show association with cerebrospinal fluid amyloid beta

artículo científico publicado en 2008

Apolipoprotein E levels in cerebrospinal fluid and the effects of ABCA1 polymorphisms

artículo científico publicado en 2007

Association and expression analyses with single-nucleotide polymorphisms in TOMM40 in Alzheimer disease

artículo científico publicado en 2011

Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family

artículo científico publicado en 2004

Association studies between common variants in prolyl isomerase Pin1 and the risk for late-onset Alzheimer's disease

artículo científico publicado en 2007

Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme

artículo científico publicado en 2005

Association studies testing for risk for late-onset Alzheimer's disease with common variants in the beta-amyloid precursor protein (APP).

artículo científico publicado en 2007

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Cerebrospinal fluid APOE levels: an endophenotype for genetic studies for Alzheimer's disease

artículo científico publicado en 2012

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

artículo científico publicado en 2011

DAPK1 variants are associated with Alzheimer's disease and allele-specific expression

artículo científico publicado en 2006

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study

artículo científico publicado en 2014

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

scholarly article published in Nature Genetics

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

article

Extreme cerebrospinal fluid amyloid beta levels identify family with late-onset Alzheimer's disease presenilin 1 mutation

artículo científico publicado en 2007

Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease

artículo científico publicado en 2011

GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease

artículo científico publicado en 2013

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

Genes for a 'Wellderly' Life

artículo científico publicado en 2016

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

artículo científico publicado en 2010

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genome-wide association study for variants that modulate relationships between cerebrospinal fluid amyloid-beta 42, tau, and p-tau levels

artículo científico publicado en 2018

Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers

artículo científico publicado en 2017

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

artículo científico publicado en 2009

Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation

artículo científico publicado en 2014

Genome-wide association study of prolactin levels in blood plasma and cerebrospinal fluid

artículo científico publicado en 2016

Genome-wide, high-content siRNA screening identifies the Alzheimer's genetic risk factor FERMT2 as a major modulator of APP metabolism

artículo científico publicado en 2016

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

artículo científico publicado en 2006

Haplotype-based association analysis of the MAPT locus in late onset Alzheimer's disease

scientific article published on 31 January 2007

Missense variant in TREML2 protects against Alzheimer's disease

scientific article published on 21 December 2013

Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia

artículo científico publicado en 2008

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

artículo científico publicado en 2012

Novel presenilin 1 variant (P117A) causing Alzheimer's disease in the fourth decade of life.

artículo científico publicado en 2008

Phosphorylated tau-Aβ42 ratio as a continuous trait for biomarker discovery for early-stage Alzheimer's disease in multiplex immunoassay panels of cerebrospinal fluid

artículo científico publicado en 2014

Popular solunar tables fail to predict fishing success in North American recreational freshwater trout fisheries

artículo científico publicado en 2023

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease

artículo científico publicado en 2014

Rarity of the Alzheimer disease-protective APP A673T variant in the United States

artículo científico publicado en 2015

Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease

artículo científico publicado en 2009

SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease

artículo científico publicado en 2010

TREM2 Variants in Alzheimer's Disease ⬇️

artículo científico publicado el 14 de noviembre de 2012

The Ramp Atlas: facilitating tissue and cell-specific ramp sequence analyses through an intuitive web interface

scientific article published on 30 May 2022

The genome of a giant (trevally): Caranx ignobilis

The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease

artículo científico publicado en 2012

Transethnic genome-wide scan identifies novel Alzheimer's disease loci

artículo científico publicado en 2017

Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease

artículo científico publicado en 2006

Validating predicted biological effects of Alzheimer's disease associated SNPs using CSF biomarker levels

artículo científico publicado en 2010

Variants in ACPP are associated with cerebrospinal fluid Prostatic Acid Phosphatase levels

artículo científico publicado en 2016

Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels

artículo científico publicado en 2016

Variants in PPP3R1 and MAPT are associated with more rapid functional decline in Alzheimer's disease: the Cache County Dementia Progression Study

artículo científico publicado en 2013

Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition

artículo científico publicado en 2008

Lista de obras de John S. K. Kauwe

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.

A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease

Alzheimer's disease risk variants show association with cerebrospinal fluid amyloid beta

Apolipoprotein E levels in cerebrospinal fluid and the effects of ABCA1 polymorphisms

Association and expression analyses with single-nucleotide polymorphisms in TOMM40 in Alzheimer disease

Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family

Association studies between common variants in prolyl isomerase Pin1 and the risk for late-onset Alzheimer's disease

Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme

Association studies testing for risk for late-onset Alzheimer's disease with common variants in the beta-amyloid precursor protein (APP).

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Cerebrospinal fluid APOE levels: an endophenotype for genetic studies for Alzheimer's disease

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

DAPK1 variants are associated with Alzheimer's disease and allele-specific expression

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Extreme cerebrospinal fluid amyloid beta levels identify family with late-onset Alzheimer's disease presenilin 1 mutation

Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease

GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

Genes for a 'Wellderly' Life

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Genome-wide association study for variants that modulate relationships between cerebrospinal fluid amyloid-beta 42, tau, and p-tau levels

Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation

Genome-wide association study of prolactin levels in blood plasma and cerebrospinal fluid

Genome-wide, high-content siRNA screening identifies the Alzheimer's genetic risk factor FERMT2 as a major modulator of APP metabolism

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

Haplotype-based association analysis of the MAPT locus in late onset Alzheimer's disease

Missense variant in TREML2 protects against Alzheimer's disease

Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

Novel presenilin 1 variant (P117A) causing Alzheimer's disease in the fourth decade of life.

Phosphorylated tau-Aβ42 ratio as a continuous trait for biomarker discovery for early-stage Alzheimer's disease in multiplex immunoassay panels of cerebrospinal fluid

Popular solunar tables fail to predict fishing success in North American recreational freshwater trout fisheries

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease

Rarity of the Alzheimer disease-protective APP A673T variant in the United States

Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease

SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease

TREM2 Variants in Alzheimer's Disease ⬇️

The Ramp Atlas: facilitating tissue and cell-specific ramp sequence analyses through an intuitive web interface

The genome of a giant (trevally): Caranx ignobilis

The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease

Transethnic genome-wide scan identifies novel Alzheimer's disease loci

Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease

Validating predicted biological effects of Alzheimer's disease associated SNPs using CSF biomarker levels

Variants in ACPP are associated with cerebrospinal fluid Prostatic Acid Phosphatase levels

Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels

Variants in PPP3R1 and MAPT are associated with more rapid functional decline in Alzheimer's disease: the Cache County Dementia Progression Study

Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition