Jobst Meyer: Influence Statistics

Jobst Meyer

Jobst Meyer

Department of Neurobehavioral Genetics, Institute of Psychobiology, University of Trier, Trier, Germany | Department of Neurobehavioral Genetics, Institute of Psychobiology, ...

Jobst Meyer: Expert Impact

Concepts for which Jobst Meyer has direct influence: Catatonic schizophrenia , Periodic catatonia , Bipolar disorder , Panic disorder , Glucocorticoid receptor gene , Autistic symptoms , Psychiatric symptoms .

Jobst Meyer: KOL impact

Concepts related to the work of other authors for which for which Jobst Meyer has influence: Bipolar disorder , Attention deficit , Dna methylation , Serotonin transporter , Children adhd , Genetic variation , Glucocorticoid receptor .

KOL Resume for Jobst Meyer

Year
2020

Department of Neurobehavioral Genetics, Institute of Psychobiology, University of Trier, Trier, Germany

2019

Department of Neurobehavioral Genetics, Institute of Psychobiology, University of Trier, 54290, Trier, Germany

2018

Department of Neurobehavioral Genetics, Trier University, Trier, Germany

2017

Department of Neurobehavioral Genetics, Institute of Psychobiology, University of TrierJohanniterufer, Germany

2016

Department of Neurobehavioral Genetics University of Trier Trier Germany

2015

Department of Neurobehavioral Genetics, Institute of Psychobiology, University of Trier, Johanniterufer 15, 54290 Trier, Germany

Neurobehavioral Genetics, University of Trier

2014

Department of Neurobehavioral Genetics, University of Trier, Johanniterufer 15, 54290, Trier, Germany

2013

Department of Neurobehavioural Genetics, University of Trier, 54290, Trier, Germany

2012

Department of Neurobehavioral Genetics, Institute of Psychobiology, University of Trier, Trier, Germany.

2011

Department of Neurobehavioral Genetics, University of Trier, 54290 Trier, Germany

2010

Institute of Psychobiology, University of Trier, Trier, Germany

2009

Department of Neuro-Behavioral Genetics, Graduate School of Psychobiology, University of Trier, Trier, Germany

2008

Department of Neurobehavioural Genetics, University of Trier, 54290 Trier, Germany

2007

Abteilung für Verhaltensgenetik, Fachbereich I - Psychobiologie, Universität Trier, Trier

2005

Department of Neuro-Behavioral Genetics, University of Trier, D-54290 Trier, Germany

2004

Department of Neuro-Behavioral Genetics, University of Trier, Germany

2003

Department of Psychiatry and Psychotherapy, University of Würzburg, and, DE

2002

Department of Psychiatry and Psychotherapy, University of Wuerzburg, Fuechsleinstr. 15, D-97080 Würzburg, Germany

2001

Department of Psychiatry and Psychotherapy, University of Würzburg, D-97080, Würzburg, Germany

2000

Department of Psychiatry and Psychotherapy, University of Würzburg, Füchsleinstr. 15, D-97080 Würzburg, Germany, E-mail: DE

1999

Department of Psychiatry and Psychotherapy, University of Würzburg, Federal Republic of Germany, DE

1998

Department of Psychiatry, University of Würzburg, Füchsleinstrasse 15, 97080 Würzburg

1997

Department of Psychiatry, University of Würzburg, Würzburg

Prominent publications by Jobst Meyer

KOL-Index: 12575 . Attention-deficit/hyperactivity disorder (ADHD) is one of the most common child psychiatric disorders. Previous studies have reported a blunted cortisol response to challenging situations and a decreased cortisol awakening response (CAR) in children with ADHD. As ADHD often is comorbid with oppositional defiant disorder (ODD), conduct disorder (CD), or anxiety disorder (AnxD), and changes ...
Known for Children Adhd | Comorbid Disorders | Cortisol Awakening Response | Psychosocial Risk Factors
KOL-Index: 12464 . Attention-deficit/hyperactivity disorder (ADHD) is a common, highly heritable neurodevelopmental disorder. Genetic loci have not yet been identified by genome-wide association studies. Rare copy number variations (CNVs), such as chromosomal deletions or duplications, have been implicated in ADHD and other neurodevelopmental disorders. To identify rare (frequency ≤1%) CNVs that increase the ...
Known for Hyperactivity Disorder | Rare Copy | Adhd Patients | Cnvs Park2
KOL-Index: 11908 . Attention deficit/hyperactivity disorder (ADHD) is a highly heritable neurodevelopmental disorder of childhood onset. Clinical and biological evidence points to shared common central nervous system (CNS) pathology of ADHD and restless legs syndrome (RLS). It was hypothesized that variants previously found to be associated with RLS in two large genome-wide association studies (GWA), will ...
Known for Adhd Rls | Genetic Link | Restless Legs | Nominal Association
KOL-Index: 10644 . The nature of subtypes in schizophrenia and the meaning of heterogeneity in schizophrenia have been considered a principal controversy in psychiatric research. We addressed these issues in periodic catatonia, a clinical entity derived from Leonhard's classification of schizophrenias, in a genomewide linkage scan. Periodic catatonia is characterized by qualitative psychomotor disturbances ...
Known for Periodic Catatonia | Susceptibility Locus | Linkage Chromosome | Clinical Entity
KOL-Index: 10539 . Autism spectrum disorders (ASDs) are heterogeneous disorders presenting with increased rates of anxiety. The adenosine A2A receptor gene (ADORA2A) is associated with panic disorder and is located on chromosome 22q11.23. Its gene product, the adenosine A2A receptor, is strongly expressed in the caudate nucleus, which also is involved in ASD. As autistic symptoms are increased in individuals ...
Known for Adenosine A2a | Autistic Symptoms | Receptor Gene | Autism Spectrum Disorder
KOL-Index: 10214 . By conferring allele-specific transcriptional activity on the 5-HT transporter gene promoter in humans, the 5-HT transporter gene-linked polymorphic region (5-HTTLPR) influences a constellation of personality traits related to anxiety and increases the risk for neurodevelopmental, neurodegenerative, and psychiatric disorders. Here we have analyzed the presence and variability of the ...
Known for Rhesus Monkeys | Transporter Gene | Polymorphic Region | 5 Httlpr
KOL-Index: 10039 . The human MLC1 gene (also known as KIAA0027 and WKL1) and its murine orthologue (Mlc1) encode a putative transmembrane protein expressed primarily in brain. Recessive mutations within human MLC1 cause megalencephalic leukoencephalopathy with subcortical cysts (MLC), whereas a missense mutation resulting in a methionine substitution within a transmembrane leucine string of MLC has been ...
Known for Subcortical Cysts | Glial Cells | Mlc1 Expression | Bergmann Glia
KOL-Index: 9056 . Several linkage analyses implicated the chromosome 9q22 region in attention deficit/hyperactivity disorder (ADHD), a neurodevelopmental disease with remarkable persistence into adulthood. This locus contains the brain-expressed GTP-binding RAS-like 2 gene (DIRAS2) thought to regulate neurogenesis. As DIRAS2 is a positional and functional ADHD candidate gene, we conducted an association ...
Known for Adult Adhd | Personality Disorders | Bipolar Disorder | Promoter Region
KOL-Index: 8897 . Thermophilic species persisted in southern refugia during the cold phases of the Pleistocene, and expanded northwards during warming. These processes caused genetic imprints, such as a differentiation of genetic lineages and a loss of genetic diversity in the wake of (re)colonization. We used molecular markers and species distribution models (SDMs) to study the impact of range dynamics on ...
Known for Northern Range Margin | Common Wall Lizard | Podarcis Muralis | Genetic Diversity
KOL-Index: 8813 . Recessive mutations of the potassium chloride co-transporter 3 gene ( SLC12A6 , KCC3 ) cause severe peripheral neuropathy frequently associated with agenesis of the corpus callosum and psychoses (ACCPN). SLC12A6 is localized on chromosome 15q14, a region where linkage to schizophrenia and bipolar disorder has previously been shown. Mutation analysis of SLC12A6 was carried out by direct ...
Known for Bipolar Disorder | Rare Variants | Potassium Chloride | Transporter 3
KOL-Index: 8427 . The brain-derived neurotrophic factor (BDNF) is a key regulator of synaptic plasticity and has been suggested to be involved in the pathophysiology and pathogenesis of psychotic disorders, with particular emphasis on dysfunctions of the hippocampus. The aim of the present study was to replicate and to extend prior findings of BDNF val66met genotype effects on hippocampal volume and ...
Known for Val66met Polymorphism | Magnetic Resonance | Neurotrophic Factor | Bdnf Genotype
KOL-Index: 8361 . Several biochemical and pharmacological studies suggest that the catecholaminergic system involving the norepinephrine transporter (NET) is relevant for the pathogenesis of panic disorder. Three single nucleotide polymorphisms in the promoter or untranslated 5' region of the NET gene were investigated by means of RFLP analysis in a sample of 115 German patients with panic disorder and 115 ...
Known for Panic Disorder | Norepinephrine Transporter | Association Analysis | Net Gene
KOL-Index: 7964 . Abstract Autism spectrum disorders (ASD) are heterogeneous disorders with a high heritability and complex genetic architecture. Due to the central role of the fragile X mental retardation gene 1 protein (FMRP) pathway in ASD we investigated common functional variants of ASD risk genes regulating FMRP. We genotyped ten SNPs in two German patient sets (N = 192 and N = 254 families, ...
Known for Common Variants | Autism Spectrum Disorders | Asd Risk | Protein Fmrp
KOL-Index: 7955 . Attention deficit/hyperactivity disorder (ADHD) is a highly heritable common neurodevelopmental disorder with onset in childhood. A coding SNP (rs6265, Val66Met) of the brain-derived neurotrophic factor gene (BDNF) has recently been associated with ADHD. More specifically, paternal over-transmission of the common Val66 allele to affected children had been observed. We aimed to confirm ...
Known for Val66met Polymorphism | Neurotrophic Factor | Bdnf Adhd | Preferential Transmission
KOL-Index: 7815 . Working memory deficits are found in different psychiatric populations and are most pronounced in schizophrenia. There is preliminary evidence from pharmacological studies that the verbal and visuospatial subcomponents of working memory are subject to differential neurotransmitter modulation. Here, we investigated the impact of well-known polymorphisms of the dopamine transporter gene ...
Known for Genetic Polymorphisms | Schizophrenia Bipolar Disorder | Verbal Memory | Comt Genotype

Key People For Catatonic Schizophrenia

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#1
Max Fink
electroconvulsive therapy melancholic features major depression
#2
Georgios Petrides
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#3
George Bush
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Andrew Francis
electroconvulsive therapy catatonic signs prolonged catatonia
#5
Gabor Sandor Ungvari
hong kong electroconvulsive therapy bipolar disorder
#6
Georg Northoff
resting state neural activity spatiotemporal psychopathology

Department of Neurobehavioral Genetics, Institute of Psychobiology, University of Trier, Trier, Germany | Department of Neurobehavioral Genetics, Institute of Psychobiology, University of Trier, 54290, Trier, Germany | Department of Neurobehavioral G