FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Jobst Meyer

Research Profile

Disorders

Concepts & Ideas

Physiology

Genes & Molecular Sequences

Anatomy

Chemicals & Drugs

Procedures

Co-author Network

Publications

TOP 3
Anne Kröger; Jobst Meyer; Haukur Palmason; Christiane Seitz; Susann Hänig; Christine M Freitag
Risk factors of autistic symptoms in children with ADHD.
Christine M Freitag; Konstantin Agelopoulos; Ellen Huy; Matthias Rothermundt; Petra Krakowitzky; Jobst Meyer; Jürgen Deckert; Alexander Von Gontard; Carsten Hohoff
Adenosine A(2A) receptor gene (ADORA2A) variants may increase autistic symptoms and anxiety in autism spectrum disorder.
Benno Graf Schimmelmann; Susann Friedel; Thuy Trang Nguyen; S Sauer; C I Ganz Vogel; Kerstin Konrad; C Wilhelm; J Sinzig; Tobias Renner; Marcel Romanos; H Palmason; Astrid Dempfle; Susanne Walitza; Christine M Freitag; Jobst Meyer; Martin Linder; Helmut Schäfer; Andreas Warnke; Klaus-Peter Lesch; B Herpertz-Dahlman; Anke Hinney; Johannes Hebebrand
Exploring the genetic link between RLS and ADHD.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Jobst Meyer (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2011: Anne Kröger; Jobst Meyer; Haukur Palmason; Christiane Seitz; Susann Hänig; Christine M Freitag
Risk factors of autistic symptoms in children with ADHD.
European child & adolescent psychiatry 2011;20(11-12):561-70.
2010: Christine M Freitag; Konstantin Agelopoulos; Ellen Huy; Matthias Rothermundt; Petra Krakowitzky; Jobst Meyer; Jürgen Deckert; Alexander Von Gontard; Carsten Hohoff
Adenosine A(2A) receptor gene (ADORA2A) variants may increase autistic symptoms and anxiety in autism spectrum disorder.
European child & adolescent psychiatry 2010;19(1):67-74.
2009: Benno Graf Schimmelmann; Susann Friedel; Thuy Trang Nguyen; S Sauer; C I Ganz Vogel; Kerstin Konrad; C Wilhelm; J Sinzig; Tobias Renner; Marcel Romanos; H Palmason; Astrid Dempfle; Susanne Walitza; Christine M Freitag; Jobst Meyer; Martin Linder; Helmut Schäfer; Andreas Warnke; Klaus-Peter Lesch; B Herpertz-Dahlman; Anke Hinney; Johannes Hebebrand
Exploring the genetic link between RLS and ADHD.
Journal of psychiatric research 2009;43(10):941-5.
2008: Klaus-Peter Lesch; Nina Timmesfeld; Tobias Renner; Rebecca Halperin; Christoph Röser; T Trang Nguyen; David Craig; Jasmin Romanos; Monika Heine; Jobst Meyer; Christine M Freitag; Andreas Warnke; Marcel Romanos; Helmut Schäfer; Susanne Walitza; Andreas Reif; Dietrich A Stephan; Christian Jacob
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.
Journal of neural transmission (Vienna, Austria : 1996) 2008;115(11):1573-85.
2008: Marcel Romanos; Christine M Freitag; Christian Jacob; David Craig; Astrid Dempfle; T T Nguyen; R Halperin; Susanne Walitza; Tobias Renner; C Seitz; J Romanos; H Palmason; Andreas Reif; M Heine; C Windemuth-Kieselbach; C Vogler; J Sigmund; Andreas Warnke; Helmut Schäfer; Jobst Meyer; Dietrich A Stephan; Klaus-Peter Lesch
Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12.
Molecular psychiatry 2008;13(5):522-30.
2007: Sandra Selch; Alexander Strobel; Julia Haderlein; Jobst Meyer; Christian P Jacob; Angelika Schmitt; Klaus-Peter Lesch; Andreas Reif
MLC1 polymorphisms are specifically associated with periodic catatonia, a subgroup of chronic schizophrenia.
Biological psychiatry 2007;61(10):1211-4.
2006: Rainald Mössner; Christine M Freitag; Martin Marziniak; Dirk Moser; Claudia Sommer; Jobst Meyer
The functional Val158Met variant of the COMT gene is not associated with migraine with or without aura.
The journal of headache and pain 2006;7(3):165-6.
2006: Jens R Wendland; M Hampe; Timothy K Newman; Yana V Syagailo; Jobst Meyer; W Schempp; A Timme; Stephen J Suomi; Klaus-Peter Lesch
Structural variation of the monoamine oxidase A gene promoter repeat polymorphism in nonhuman primates.
Genes, brain, and behavior 2006;5(1):40-5.
2005: Jobst Meyer; Kirsten Johannssen; Christine M Freitag; Kerstin Schraut; Isabel Teuber; Astrid Hahner; Christian Mainhardt; Rainald Mössner; Hans-Peter Volz; Thomas F Wienker; Darleen McKeane; Dietrich A Stephan; Guy Rouleau; Andreas Reif; Klaus-Peter Lesch
Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2005;8(4):495-504.
2005: Rainald Mössner; Annette Weichselbaum; Martin Marziniak; Christine M Freitag; Klaus-Peter Lesch; Claudia Sommer; Jobst Meyer
A highly polymorphic poly-glutamine stretch in the potassium channel KCNN3 in migraine.
Headache 2005;45(2):132-6.
2003: Angelika Schmitt; Viktor Gofferje; Melanie Weber; Jobst Meyer; Rainald Mössner; Klaus-Peter Lesch
The brain-specific protein MLC1 implicated in megalencephalic leukoencephalopathy with subcortical cysts is expressed in glial cells in the murine brain.
Glia 2003;44(3):283-95.
2003: V Steinke; Jobst Meyer; Yana V Syagailo; Gabriela Ortega; H Hameister; Rainald Mössner; Angelika Schmitt; Klaus-Peter Lesch
The genomic organization of the murine Mlc1 (Wkl1, KIAA0027) gene.
Journal of neural transmission (Vienna, Austria : 1996) 2003;110(4):333-43.
2002: Jobst Meyer; Marion Mai; Gabriela Ortega; Rainald Mössner; Klaus-Peter Lesch
Mutational analysis of the connexin 36 gene (CX36) and exclusion of the coding sequence as a candidate region for catatonic schizophrenia in a large pedigree.
Schizophrenia research 2002;58(1):87-91.
2002: Yana V Syagailo; Olga Okladnova; Ella Reimer; Marcus Grässle; Rainald Mössner; Stefan Gattenlöhner; Alexander Marx; Jobst Meyer; Klaus-Peter Lesch
Structural and functional characterization of the human PAX7 5'-flanking regulatory region.
Gene 2002;294(1-2):259-68.
2002: Jobst Meyer; W Saam; Rainald Mössner; O Cangir; Gabriela Ortega; Thomas Tatschner; Peter Riederer; Thomas F Wienker; Klaus-Peter Lesch
Evolutionary conserved microsatellites in the promoter region of the 5-hydroxytryptamine receptor 2C gene (HTR2C) are not associated with bipolar disorder in females.
Journal of neural transmission (Vienna, Austria : 1996) 2002;109(5-6):939-46.
2002: Jobst Meyer; Gabriela Ortega; K Schraut; G Nürnberg; Franz Rüschendorf; Kathrin Saar; Rainald Mössner; Thomas F Wienker; André Reis; Gerald Stöber; Klaus-Peter Lesch
Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus.
Molecular psychiatry 2002;7(2):220-3.
2001: J Gross; O Grimm; Gabriela Ortega; Isabel Teuber; Klaus-Peter Lesch; Jobst Meyer
Mutational analysis of the neuronal cadherin gene CELSR1 and exclusion as a candidate for catatonic schizophrenia in a large family.
Psychiatric genetics 2001;11(4):197-200.
2001: Jobst Meyer; A Huberth; Gabriela Ortega; Yana V Syagailo; Susanne Jatzke; Rainald Mössner; Tim M Strom; I Ulzheimer-Teuber; Gerald Stöber; Angelika Schmitt; Klaus-Peter Lesch
A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree.
Molecular psychiatry 2001;6(3):302-6.
2001: Yana V Syagailo; Gerald Stöber; Marcus Grässle; E Reimer; Michael Knapp; G Jungkunz; Olga Okladnova; Jobst Meyer; Klaus-Peter Lesch
Association analysis of the functional monoamine oxidase A gene promoter polymorphism in psychiatric disorders.
American journal of medical genetics 2001;105(2):168-71.
2001: Claudia Rubie; F Schmidt; Michael Knapp; Julia Sprandel; C Wiegand; Jobst Meyer; G Jungkunz; Peter Riederer; Gerald Stöber
The human dopamine transporter gene: the 5'-flanking region reveals five diallelic polymorphic sites in a Caucasian population sample.
Neuroscience letters 2001;297(2):125-8.
2000: Gerald Stöber; Kathrin Saar; Franz Rüschendorf; Jobst Meyer; G Nürnberg; Susanne Jatzke; E Franzek; André Reis; Klaus-Peter Lesch; Thomas F Wienker; Helmut Beckmann
Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.
American journal of human genetics 2000;67(5):1201-7.
2000: Gerald Stöber; Jobst Meyer; Indrajit Nanda; Thomas F Wienker; Kathrin Saar; Michael Knapp; Susanne Jatzke; Michael Schmid; Klaus-Peter Lesch; Helmut Beckmann
Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13.
American journal of medical genetics 2000;96(3):392-7.
2000: Gerald Stöber; Jobst Meyer; Indrajit Nanda; Thomas F Wienker; Kathrin Saar; Susanne Jatzke; Michael Schmid; Klaus-Peter Lesch; Helmut Beckmann
hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia.
European archives of psychiatry and clinical neuroscience 2000;250(4):163-8.
1999: Klaus-Peter Lesch; Susanne Jatzke; Jobst Meyer; Gerald Stöber; Olga Okladnova; Rainald Mössner; Peter Riederer
Mosaicism for a serotonin transporter gene promoter-associated deletion: decreased recombination in depression.
Journal of neural transmission (Vienna, Austria : 1996) 1999;106(11-12):1223-30.
1998: Gerald Stöber; Susanne Jatzke; Jobst Meyer; Olga Okladnova; Michael Knapp; Helmut Beckmann; Klaus-Peter Lesch
Short CAG repeats within the hSKCa3 gene associated with schizophrenia: results of a family-based study.
Neuroreport 1998;9(16):3595-9.
1998: Jobst Meyer; P Wiedemann; Olga Okladnova; Michael Brüss; T Staab; Gerald Stöber; Peter Riederer; Heinz Bönisch; Klaus-Peter Lesch
Cloning and functional characterization of the human norepinephrine transporter gene promoter.
Journal of neural transmission (Vienna, Austria : 1996) 1998;105(10-12):1341-50.
1997: Klaus-Peter Lesch; Jobst Meyer; K Glatz; G Flügge; Anke Hinney; Johannes Hebebrand; Sabine M Klauck; Annemarie Poustka; Fritz Poustka; Dominik Bengel; Rainald Mössner; Peter Riederer; A Heils
The 5-HT transporter gene-linked polymorphic region (5-HTTLPR) in evolutionary perspective: alternative biallelic variation in rhesus monkeys. Rapid communication.
Journal of neural transmission (Vienna, Austria : 1996) 1997;104(11-12):1259-66.