Filtros de búsqueda

Lista de obras de Eva C. Schulte

"Malignant restless legs syndrome"--a curse or a blessing?

artículo científico publicado en 2013

A Longitudinal Approach to Biological Psychiatric Research: The PsyCourse Study

A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

artículo científico publicado en 2011

Acyclovir resistance in herpes simplex encephalitis.

artículo científico publicado en 2010

Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality

artículo científico publicado en 2021

Alterations in Lipid and Inositol Metabolisms in Two Dopaminergic Disorders

artículo científico publicado en 2016

Alterations in excitotoxicity and prostaglandin metabolism in a transgenic mouse model of Alzheimer's disease.

artículo científico publicado en 2009

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome

artículo científico publicado en 2014

Characterization of age-dependent and progressive cortical neuronal degeneration in presenilin conditional mutant mice.

artículo científico publicado en 2010

Clinical Phenotype and Genetics of Restless Legs Syndrome

article

Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity

artículo científico publicado en 2021

Comparative serum proteomic analysis of a selected protein panel in individuals with schizophrenia and bipolar disorder and the impact of genetic risk burden on serum proteomic profiles

artículo científico publicado en 2022

Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1

Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer's disease

artículo científico publicado en 2015

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative

artículo científico publicado en 2022

Family and genome-wide association studies of restless legs syndrome

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

artículo científico publicado en 2018

Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1

scientific journal article

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Interplay between the Genetics of Personality Traits, severe Psychiatric Disorders, and COVID-19 Host Genetics in the Susceptibility to SARS-CoV-2 Infection - ADDENDUM

artículo científico publicado en 2021

Interplay between the genetics of personality traits, severe psychiatric disorders and COVID-19 host genetics in the susceptibility to SARS-CoV-2 infection

artículo científico publicado en 2021

Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study

Mitochondrial membrane protein associated neurodegenration: a novel variant of neurodegeneration with brain iron accumulation

artículo científico publicado en 2012

Niemann-Pick C disease gene mutations and age-related neurodegenerative disorders

artículo científico publicado en 2013

Rare variants in LRRK1 and Parkinson's disease

artículo científico publicado en 2013

Rare variants in PLXNA4 and Parkinson's disease

artículo científico publicado en 2013

Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease

artículo científico publicado en 2015

Restless-legs-Syndrom und kardiovaskuläres Risiko

artículo científico publicado en 2011

Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome

artículo científico publicado en 2014

The Human Phenotype Ontology in 2024: phenotypes around the world

artículo científico publicado en 2023

The role ofSCARB2as susceptibility factor in Parkinson's disease

scholarly article by Franziska Hopfner et al published 13 February 2013 in Movement Disorders

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease

artículo científico publicado en 2012

When Parkinson’s disease patients go to sleep: specific sleep disturbances related to Parkinson’s disease ⬇️

artículo científico publicado el 1 de mayo de 2011

When restless legs syndrome turns malignant.

artículo científico publicado en 2013

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda