Lista de obras - Christina M Lill - Dominio Público Uruguay

A Web-based database of genetic association studies in cutaneous melanoma enhanced with network-driven data exploration tools

artículo científico publicado en 2014

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

artículo científico publicado en 2012

Allosteric modulation of PS1/gamma-secretase conformation correlates with amyloid beta(42/40) ratio

artículo científico publicado en 2009

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients

artículo científico publicado en 2016

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

artículo científico publicado en 2013

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

scientific article published on 01 May 2019

Bilateral vertebral artery dissection, agenesis of both ICAs, and connective tissue aberrations

scientific article published on 01 April 2013

Class II HLA interactions modulate genetic risk for multiple sclerosis

artículo científico publicado en 2015

Closing the case ofAPOEin multiple sclerosis: no association with disease risk in over 29 000 subjects: Figure 1

Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma

artículo científico publicado en 2011

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

artículo científico publicado en 2012

Developing the "next generation" of genetic association databases for complex diseases

artículo científico publicado en 2012

Disentangling the genetics of lean mass

article

Distinguishing true from false positives in genomic studies: p values

artículo científico publicado en 2013

Genetisches Profil der Multiplen Sklerose: Risikogene und die „dunkle Materie“

artículo científico publicado en 2012

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

artículo científico publicado en 2019

Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk

artículo científico publicado en 2013

Genome-wide significant association with seven novel multiple sclerosis risk loci

artículo científico publicado en 2015

Impact of Parkinson's disease risk loci on age at onset

artículo científico publicado en 2015

Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sample.

artículo científico publicado en 2011

Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases

artículo científico publicado en 2011

Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease

artículo científico publicado en 2014

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

artículo científico publicado en 2014

Large-scale replication and heterogeneity in Parkinson disease genetic loci

artículo científico publicado en 2012

Launching the movement disorders society genetic mutation database (MDSGene).

artículo científico publicado en 2016

Low frequency and rare coding variation contributes to multiple sclerosis risk

MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

artículo científico publicado en 2013

MicroRNA-138 is a potential regulator of memory performance in humans

artículo científico publicado en 2014

Mutations in amyloid precursor protein affect its interactions with presenilin/gamma-secretase

artículo científico publicado en 2009

N-cadherin-based adhesion enhances Abeta release and decreases Abeta42/40 ratio

artículo científico publicado en 2008

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

artículo científico publicado en 2015

Neuronal activity and secreted amyloid β lead to altered amyloid β precursor protein and presenilin 1 interactions

artículo científico publicado en 2012

New candidates for CD4 T cell pathogenicity in experimental neuroinflammation and multiple sclerosis.

artículo científico publicado en 2015

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation

artículo científico publicado en 2016

PLD3 gene variants and Alzheimer's disease.

artículo científico publicado en 2015

Prediction of Melanoma Risk in a Southern European Population Based on a Weighted Genetic Risk Score

artículo científico publicado en 2015

Probing the epigenome by EWAS: a new era in brain disease research

artículo científico publicado en 2015

Recent advances and future challenges in the genetics of multiple sclerosis

artículo científico publicado en 2014

Risky behaviors and Parkinson disease: A mendelian randomization study

artículo científico publicado en 2019

Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study

artículo científico publicado en 2013

Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array

artículo científico publicado en 2015

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

scholarly article published 13 July 2017

The genetics of Alzheimer disease: back to the future

artículo científico publicado en 2010

The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease

artículo científico publicado en 2015

The role of clusterin, complement receptor 1, and phosphatidylinositol binding clathrin assembly protein in Alzheimer disease risk and cerebrospinal fluid biomarker levels

artículo científico publicado en 2011

Toward modernizing the systematic review pipeline in genetics: efficient updating via data mining

artículo científico publicado en 2012

Towards unveiling the genetics of neurodegenerative diseases

artículo científico publicado en 2011

Updated field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma: the MelGene database

artículo científico publicado en 2014

Lista de obras de Christina M Lill

A Web-based database of genetic association studies in cutaneous melanoma enhanced with network-driven data exploration tools

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

Allosteric modulation of PS1/gamma-secretase conformation correlates with amyloid beta(42/40) ratio

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

Bilateral vertebral artery dissection, agenesis of both ICAs, and connective tissue aberrations

Class II HLA interactions modulate genetic risk for multiple sclerosis

Closing the case ofAPOEin multiple sclerosis: no association with disease risk in over 29 000 subjects: Figure 1

Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

Developing the "next generation" of genetic association databases for complex diseases

Disentangling the genetics of lean mass

Distinguishing true from false positives in genomic studies: p values

Genetisches Profil der Multiplen Sklerose: Risikogene und die „dunkle Materie“

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk

Genome-wide significant association with seven novel multiple sclerosis risk loci

Impact of Parkinson's disease risk loci on age at onset

Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sample.

Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases

Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

Large-scale replication and heterogeneity in Parkinson disease genetic loci

Launching the movement disorders society genetic mutation database (MDSGene).

Low frequency and rare coding variation contributes to multiple sclerosis risk

MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

MicroRNA-138 is a potential regulator of memory performance in humans

Mutations in amyloid precursor protein affect its interactions with presenilin/gamma-secretase

N-cadherin-based adhesion enhances Abeta release and decreases Abeta42/40 ratio

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

Neuronal activity and secreted amyloid β lead to altered amyloid β precursor protein and presenilin 1 interactions

New candidates for CD4 T cell pathogenicity in experimental neuroinflammation and multiple sclerosis.

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation

PLD3 gene variants and Alzheimer's disease.

Prediction of Melanoma Risk in a Southern European Population Based on a Weighted Genetic Risk Score

Probing the epigenome by EWAS: a new era in brain disease research

Recent advances and future challenges in the genetics of multiple sclerosis

Risky behaviors and Parkinson disease: A mendelian randomization study

Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study

Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

The genetics of Alzheimer disease: back to the future

The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease

The role of clusterin, complement receptor 1, and phosphatidylinositol binding clathrin assembly protein in Alzheimer disease risk and cerebrospinal fluid biomarker levels

Toward modernizing the systematic review pipeline in genetics: efficient updating via data mining

Towards unveiling the genetics of neurodegenerative diseases

Updated field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma: the MelGene database