User profiles for B. Muller-Myhsok
Bertram Müller-MyhsokVerified email at psych.mpg.de Cited by 68639 |
Analysis of shared heritability in common disorders of the brain
…, J Huang, C Sandor, C Webber, B Muller-Myhsok… - Science, 2018 - science.org
INTRODUCTION Brain disorders may exhibit shared symptoms and substantial epidemiological
comorbidity, inciting debate about their etiologic overlap. However, detailed study of …
comorbidity, inciting debate about their etiologic overlap. However, detailed study of …
[HTML][HTML] Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
…, IC Carbajal, P Vieregge, F Asmus, B Müller-Myhsok… - Neuron, 2004 - cell.com
We have previously linked families with autosomal-dominant, late-onset parkinsonism to
chromosome 12p11.2-q13.1 (PARK8). By high-resolution recombination mapping and …
chromosome 12p11.2-q13.1 (PARK8). By high-resolution recombination mapping and …
Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment
…, M Uhr, T Rein, F Holsboer, B Muller-Myhsok - Nature …, 2004 - nature.com
The stress hormone–regulating hypothalamic-pituitary-adrenal (HPA) axis has been
implicated in the causality 1 as well as the treatment of depression 2 . To investigate a possible …
implicated in the causality 1 as well as the treatment of depression 2 . To investigate a possible …
[HTML][HTML] Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Background Restless legs syndrome is a prevalent chronic neurological disorder with
potentially severe mental and physical health consequences. Clearer understanding of the …
potentially severe mental and physical health consequences. Clearer understanding of the …
Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome
…, P Kern, J Winkelmann, B Müller-Myhsok… - Nature …, 2001 - nature.com
The dystonias are a common clinically and genetically heterogeneous group of movement
disorders. More than ten loci for inherited forms of dystonia have been mapped, but only three …
disorders. More than ten loci for inherited forms of dystonia have been mapped, but only three …
A beginners guide to SNP calling from high-throughput DNA-sequencing data
High-throughput DNA sequencing (HTS) is of increasing importance in the life sciences. One
of its most prominent applications is the sequencing of whole genomes or targeted regions …
of its most prominent applications is the sequencing of whole genomes or targeted regions …
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
Migraine is a debilitating neurological disorder affecting around one in seven people worldwide,
but its molecular mechanisms remain poorly understood. There is some debate about …
but its molecular mechanisms remain poorly understood. There is some debate about …
P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder
…, R Lieb, F Holsboer, B Müller-Myhsok - Human molecular …, 2006 - academic.oup.com
The P2RX7 gene is located within a region on chromosome 12q24.31 that has been identified
as a susceptibility locus for affective disorders by linkage and association studies. P2RX7 …
as a susceptibility locus for affective disorders by linkage and association studies. P2RX7 …
[PDF][PDF] The neuronal transporter gene SLC6A15 confers risk to major depression
…, CM van Duijn, F Holsboer, B Müller-Myhsok… - Neuron, 2011 - cell.com
Major depression (MD) is one of the most prevalent psychiatric disorders and a leading
cause of loss in work productivity. A combination of genetic and environmental risk factors …
cause of loss in work productivity. A combination of genetic and environmental risk factors …
Genome-wide meta-analysis identifies new susceptibility loci for migraine
…, JM Vink, K Heikkilä, M Alexander, B Muller-Myhsok… - Nature …, 2013 - nature.com
Migraine is the most common brain disorder, affecting approximately 14% of the adult
population, but its molecular mechanisms are poorly understood. We report the results of a meta-…
population, but its molecular mechanisms are poorly understood. We report the results of a meta-…