Publikationen von Bertram Müller-Myhsok
Alle Typen
Zeitschriftenartikel (376)
2006
Zeitschriftenartikel
15 (16), S. 2438 - 2445 (2006)
P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder. Human Molecular Genetics
Zeitschriftenartikel
21 (1), S. 28 - 33 (2006)
Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome. Movement Disorders 2005
Zeitschriftenartikel
11 (12), S. 1031 - 1037 (2005)
Association of polymorphisms in the interleukin-18 gene in patients with Crohn's disease depending on the CARD15/NOD2 genotype. Inflammatory Bowel Diseases
Zeitschriftenartikel
69, S. 771 - 771 (2005)
SimPed: A simulation program to generate haplotype and genotype data for pedigree structures. Annals of Human Genetics
Zeitschriftenartikel
69, S. 772 - 773 (2005)
Rapid simulation of p-values for product methods and multiple-testing adjustment in association studies. Annals of Human Genetics
Zeitschriftenartikel
54 (10), S. 1421 - 1427 (2005)
Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease. Gut
Zeitschriftenartikel
138B (1), S. 82 - 82 (2005)
A glutamine to arginine mutation in the C-terminal domain of P2RX7 determines the risk for mood disorders. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics
Zeitschriftenartikel
138B (1), S. 44 - 44 (2005)
Genetic implications of the endocannabinoid system in anxiety disorders versus depressive disorders: Is there any evidence for the continuum hypothesis? American Journal of Medical Genetics Part B-Neuropsychiatric Genetics
Zeitschriftenartikel
138B (1), S. 48 - 48 (2005)
The cortisol and ACTH response in the combined Dex/CRH test of acutely depressed patients varies significantly between 5-HT2A receptor genotypes. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics
Zeitschriftenartikel
138B (1), S. 45 - 45 (2005)
Syndromal panic attacks are possibly associated with polymorphisms in the angiotensin converting enzyme (ACE) gene. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics
Zeitschriftenartikel
38 (5), S. 240 - 240 (2005)
Genetic implications of the endocannabinoid system in anxiety disorders versus depressive disorders: is there any evidence for the continuum hypothesis? Pharmacopsychiatry
Zeitschriftenartikel
38 (5), S. 274 - 274 (2005)
Within- and Inter-gene interactions in FKBP5 and GR genes and its association with early response. Pharmacopsychiatry
Zeitschriftenartikel
77 (3), S. 514 - 515 (2005)
On rapid simulation of P values in association studies - Reply to Lin. American Journal of Human Genetics
Zeitschriftenartikel
38 (5), S. 282 - 282 (2005)
Polymorphisms in the serotonin receptor gene HTR2A modulate disease severity and susceptibility for anxiety disorders but not depression and are associated with specific personality traits. Pharmacopsychiatry
Zeitschriftenartikel
29 (6), S. 1017 - 1020 (2005)
The usefulness of single nucleotide polymorphisms (SNPs) for genetic epidemiological investigation of complex psychiatric diseases. Progress in Neuro-Psychopharmacology & Biological Psychiatry
Zeitschriftenartikel
379 (3), S. 195 - 198 (2005)
Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease. Neuroscience Letters
Zeitschriftenartikel
76 (3), S. 399 - 408 (2005)
Rapid simulation of P values for product methods and multiple-testing adjustment in association studies. American Journal of Human Genetics
Zeitschriftenartikel
6 (1), S. 55 - 56 (2005)
Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome. Neurogenetics
Zeitschriftenartikel
13 (2), S. 193 - 197 (2005)
PARK11 is not linked with Parkinson's disease in European families. European Journal of Human Genetics
Zeitschriftenartikel
60 (2), S. 119 - 122 (2005)
SimPed: A simulation program to generate haplotype and genotype data for pedigree structures. Human Heredity