Univ.-Prof. Dr. Jobst Meyer - Publikationen

Gassert, Franz; Schulte, Ulrich; Husemann, Martin et al.
From southern refugia to the northern range margin: genetic population structure of the common wall lizard, Podarcis muralis
JOURNAL OF BIOGEOGRAPHY. Bd. 40. H. 8. 2013 S. 1475 - 1489

Lee, S Hong; Ripke, Stephan; Neale, Benjamin M et al.
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
Nature genetics. Bd. 45. H. 9. 2013 S. 984 - 94

Lin, Michelle K.; Freitag, Christine M.; Schote, Andrea B. et al.
Haplotype Co-Segregation With Attention Deficit-Hyperactivity Disorder in Unrelated German Multi-Generation Families
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. Bd. 162. H. 8. 2013 S. 855 - 863

Hamshere, Marian L.; Langley, Kate; Martin, Joanna et al.
High Loading of Polygenic Risk for ADHD in Children With Comorbid Aggression
AMERICAN JOURNAL OF PSYCHIATRY. Bd. 170. H. 8. 2013 S. 909 - 916

Yang, Li; Neale, Benjamin M.; Liu, Lu et al.
Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: Genome-wide association study of both common and rare variants
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. Bd. 162B. H. 5. 2013 S. 419 - 430

Habel, Jan Christian; Cox, Siobhan; Gassert, Franz et al.
Population genetics of the East African White-eye species complex
CONSERVATION GENETICS. Bd. 14. H. 5. 2013 S. 1019 - 1028

Gruber, Oliver; Hasan, Alkomiet; Scherk, Harald et al.
Association of the brain-derived neurotrophic factor val66met polymorphism with magnetic resonance spectroscopic markers in the human hippocampus: in vivo evidence for effects on the glutamate system
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE. Bd. 262. H. 1. 2012 S. 23 - 31

Freitag, Christine M.; Haenig, Susann; Schneider, Anna et al.
Biological and psychosocial environmental risk factors influence symptom severity and psychiatric comorbidity in children with ADHD
JOURNAL OF NEURAL TRANSMISSION. Bd. 119. H. 1. 2012 S. 81 - 94

Ribases, Marta; Antoni Ramos-Quiroga, Josep; Hervas, Amaia et al.
Candidate system analysis in ADHD: Evaluation of nine genes involved in dopaminergic neurotransmission identifies association with DRD1
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY. Bd. 13. H. 4. 2012 S. 281 - 292

Reif, Andreas; Nguyen, T. Trang; Weissflog, Lena et al.
DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders (vol 36, pg 2318, 2011)
NEUROPSYCHOPHARMACOLOGY. Bd. 37. H. 4. 2012 S. 1076

Zilles, David; Meyer, Jobst; Schneider-Axmann, Thomas et al.
Genetic polymorphisms of 5-HTT and DAT but not COMT differentially affect verbal and visuospatial working memory functioning
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE. Bd. 262. H. 8. 2012 S. 667 - 676

Williams, Nigel M.; Franke, Barbara; Mick, Eric et al.
Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3
AMERICAN JOURNAL OF PSYCHIATRY. Bd. 169. H. 2. 2012 S. 195 - 204

Elia, Josephine; Glessner, Joseph T.; Wang, Kai et al.
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
NATURE GENETICS. Bd. 44. H. 1. 2012 S. 78 - U113

Stergiakouli, Evangelia; Hamshere, Marian; Holmans, Peter et al.
Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD
AMERICAN JOURNAL OF PSYCHIATRY. Bd. 169. H. 2. 2012 S. 186 - 194

Mertins, Vanessa; Schote, Andrea; Meyer, Jobst
Monoamine oxidase A gene (MAOA) is associated with free-riding in public goods experiments in females
BEHAVIOR GENETICS. Bd. 42. H. 6. 2012 S. 953

Kranz, Thorsten M.; Ekawardhani, Savira; Lin, Michelle K. et al.
The chromosome 15q14 locus for bipolar disorder and schizophrenia: Is C15orf53 a major candidate gene?
JOURNAL OF PSYCHIATRIC RESEARCH. Bd. 46. H. 11. 2012 S. 1414 - 1420

Reif, Andreas; Nguyen, T. Trang; Weissflog, Lena et al.
DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders
NEUROPSYCHOPHARMACOLOGY. Bd. 36. H. 11. 2011 S. 2318 - 2327

Mertins, Vanessa; Schote, Andrea B.; Hoffeld, Wolfgang et al.
Genetic Susceptibility for Individual Cooperation Preferences: The Role of Monoamine Oxidase A Gene (MAOA) in the Voluntary Provision of Public Goods
PLOS ONE. Bd. 6. H. 6. 2011

Hinney, Anke; Scherag, Andre; Jarick, Ivonne et al.
Genome-Wide Association Study in German Patients With Attention Deficit/Hyperactivity Disorder
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. Bd. 156B. H. 8. 2011 S. 888 - 897

Kroeger, Anne; Haenig, Susann; Seitz, Christiane et al.
Risk factors of autistic symptoms in children with ADHD
EUROPEAN CHILD & ADOLESCENT PSYCHIATRY. Bd. 20. H. 11-12. 2011 S. 561 - 570

Cao-Lei, Lei; Leija, Salomon Carlos; Kumsta, Robert et al.
Transcriptional control of the human glucocorticoid receptor: identification and analysis of alternative promoter regions
HUMAN GENETICS. Bd. 129. H. 5. 2011 S. 533 - 543

Freitag, Christine M.; Agelopoulos, Konstantin; Huy, Ellen et al.
Adenosine A(2A) receptor gene (ADORA2A) variants may increase autistic symptoms and anxiety in autism spectrum disorder
EUROPEAN CHILD & ADOLESCENT PSYCHIATRY. Bd. 19. H. 1. 2010 S. 67 - 74

Gruber, Oliver; Trost, Sarah; Wobrock, Thomas et al.
Association of DISC1 Genetic Variation with Intermediate Phenotypes in Neuroimaging: Replication and Further Extension
BIOLOGICAL PSYCHIATRY. Bd. 67. H. 9. 2010 S. 163S

Gruber, Oliver; Trost, Sarah; Wobrock, Thomas et al.
ASSOCIATION OF SCHIZOPHRENIA SUSCEPTIBILITY GENES WITH INTERMEDIATE PHENOTYPES: NEW FINDINGS FROM GENOMIC IMAGING
SCHIZOPHRENIA RESEARCH. Bd. 117. H. 2-3. 2010 S. 335 - 336

Palmason, Haukur; Moser, Dirk; Sigmund, Jessica et al.
Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant
JOURNAL OF NEURAL TRANSMISSION. Bd. 117. H. 2. 2010 S. 259 - 267

Neale, Benjamin M.; Medland, Sarah; Ripke, Stephan et al.
Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY. Bd. 49. H. 9. 2010 S. 906 - 920

Neale, Benjamin M.; Medland, Sarah E.; Ripke, Stephan et al.
Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY. Bd. 49. H. 9. 2010 S. 884 - 897

Scherk, Harald; Gruber, Oliver; Menzel, Patrick et al.
5-HTTLPR genotype influences amygdala volume
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE. Bd. 259. H. 4. 2009 S. 212 - 217

Kumsta, Robert; Moser, Dirk; Streit, Fabian et al.
Characterization of a Glucocorticoid Receptor Gene (GR, NR3C1) Promoter Polymorphism Reveals Functionality and Extends a Haplotype With Putative Clinical Relevance
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. Bd. 150B. H. 4. 2009 S. 476 - 482

Freitag, Christine M.; Haenig, Susann; Palmason, Haukur et al.
Cortisol awakening response in healthy children and children with ADHD: Impact of comorbid disorders and psychosocial risk factors
PSYCHONEUROENDOCRINOLOGY. Bd. 34. H. 7. 2009 S. 1019 - 1028

Scherk, Harald; Backens, Martin; Schneider-Axmann, Thomas et al.
Dopamine transporter genotype influences N-acetyl-aspartate in the left putamen
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY. Bd. 10. H. 4. 2009 S. 524 - 530

Moser, Dirk; Ekawardhani, Savira; Kumsta, Robert et al.
Functional Analysis of a Potassium-Chloride Co-Transporter 3 (SLC12A6) Promoter Polymorphism Leading to an Additional DNA Methylation Site
NEUROPSYCHOPHARMACOLOGY. Bd. 34. H. 2. 2009 S. 458 - 467

Meyer, Jobst
An extensive multi-centre study on genetics and gene x environment interaction of ADHD
INTERNATIONAL JOURNAL OF PSYCHOLOGY. Bd. 43. H. 3-4. 2008 S. 717

Freitag, Christine M.; Meyer, Jobst; Reif, Andreas et al.
Environmental risk factors and attention-deficit/hyperactivity disorder symptoms
ARCHIVES OF GENERAL PSYCHIATRY. Bd. 65. H. 3. 2008 S. 356 - 357

Macedo, Joana A.; Hesse, Judith; Turner, Jonathan D. et al.
Glucocorticoid sensitivity in fibromyalgia patients: Decreased expression of corticosteroid receptors and glucocorticoid-induced leucine zipper
PSYCHONEUROENDOCRINOLOGY. Bd. 33. H. 6. 2008 S. 799 - 809

Zhou, Kaixin; Dempfle, Astrid; Arcos-Burgos, Mauricio et al.
Meta-Analysis of Genome-Wide Linkage Scans of Attention Deficit Hyperactivity Disorder
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. Bd. 147B. H. 8. 2008 S. 1392 - 1398

Lesch, Klaus-Peter; Timmesfeld, Nina; Renner, Tobias J. et al.
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
JOURNAL OF NEURAL TRANSMISSION. Bd. 115. H. 11. 2008 S. 1573 - 1585

Freitag, Christine M.; Retz-Junginger, Petra; Retz, Wolfgang et al.
German adaptation of the autism-spectrum quotient (AQ): Evaluation and short version AQ-k
ZEITSCHRIFT FUR KLINISCHE PSYCHOLOGIE UND PSYCHOTHERAPIE. Bd. 36. H. 4. 2007 S. 280 - 289

Selch, Sandra; Strobel, Alexander; Haderlein, Julia et al.
MLC1 polymorphisms are specifically associated with periodic catatonia, a subgroup of chronic schizophrenia
BIOLOGICAL PSYCHIATRY. Bd. 61. H. 10. 2007 S. 1211 - 1214

Moser, Dirk; Molitor, Anne; Kumsta, Robert et al.
The glucocorticoid receptor gene exon 1-F promoter is not methylated at the NGFI-A binding site in human hippocampus
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY. Bd. 8. H. 4. 2007 S. 262 - 268

Meyer, Jobst; Walitza, Susanne; Palmason, Haukur et al.
Exclusion of major candidate loci in multiplex ADHD families
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. Bd. 141B. H. 7. 2006 S. 757

Ekawardhani, Savira; Moser, Dirk; Schuelter, Ulrike et al.
Genetic heterogeneity at the chromosome 15q14 candidate schizophrenia locus
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. Bd. 141B. H. 7. 2006 S. 795 - 796

Mossner, Rainald; Freitag, Christine M; Marziniak, Martin et al.
The functional Val158Met variant of the COMT gene is not associated with migraine with or without aura.
The journal of headache and pain. Bd. 7. H. 3. 2006 S. 165 - 6

Mossner, R; Weichselbaum, A; Marziniak, M et al.
A highly polymorphic poly-glutamine stretch in the potassium channel KCNN3 in migraine
HEADACHE. Bd. 45. H. 2. 2005 S. 132 - 136

Lee, YJ; Hohoff, C; Domschke, K et al.
Norepinephrine transporter (NET) promoter and 5 '-UTR polymorphisms: association analysis in panic disorder
NEUROSCIENCE LETTERS. Bd. 377. H. 1. 2005 S. 40 - 43

Meyer, J; Johannssen, K; Freitag, CM et al.
Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY. Bd. 8. H. 4. 2005 S. 495 - 504

Schmitt, A; Gofferje, V; Weber, M et al.
The brain-specific protein MLC1 implicated in megalencephalic leukoencephalopathy with subcortical cysts is expressed in glial cells in the murine brain
GLIA. Bd. 44. H. 3. 2003 S. 283 - 295

Meyer, J; Mai, M; Ortega, G et al.
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. Bd. 58. H. 1. 2002 S. 87 - 91

Syagailo, YV; Okladnova, O; Reimer, E et al.
Structural and functional characterization of the human PAX7 5 '-flanking regulatory region
GENE. Bd. 294. H. 1-2. 2002 S. 259 - 268

Meyer, J; Sudbeck, P; Held, M et al.
Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations.
Human molecular genetics. Bd. 6. H. 1. 1997 S. 91 - 8

Wirth, J; Wagner, T; Meyer, J et al.
Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9.
Human genetics. Bd. 97. H. 2. 1996 S. 186 - 93

Wagner, T; Wirth, J; Meyer, J et al.
Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9.
Cell. Bd. 79. H. 6. 1994 S. 1111 - 20

Weber, S; Schmid, M; Meyer, J et al.
A linear vector carrying human telomeres is replicated in unfertilized eggs of Xenopus laevis.
Cell biology international. Bd. 17. H. 6. 1993 S. 623 - 4

Meyer, J; Nick, S; Stamminger, T et al.
Inhibition of HIV-1 replication by a high-copy-number vector expressing antisense RNA for reverse transcriptase.
Gene. Bd. 129. H. 2. 1993 S. 263 - 8

Eder, C; Maercker, C; Meyer, J et al.
The processing of macronuclear DNA sequences during macronuclear development of the hypotrichous ciliate Stylonychia lemnae.
The International journal of developmental biology. Bd. 37. H. 3. 1993 S. 473 - 7