Glas, J.; Beynon, V.; Bachstein, B.; Steckenbiller, J.; Manolis, V.; Euba, A.; Müller-Myhsok, B.; Folwaczny, M.: Increased plasma concentration of surfactant protein D in chronic periodontitis independent of SFTPD genotype: potential role as a biomarker. Tissue Antigensr 72 (1), pp. 21 - 28 (2008)

Gschwendtner, A.; Ripke, S.; Freilinger, T.; Lichtner, P.; Müller-Myhsok, B.; Wichmann, H. E.; Meitinger, T.; Dichgans, M.: Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans. Stroke 39, pp. 1593 - 1596 (2008)

Ising, M.; Depping, A.-M.; Siebertz, A.; Lucae, S.; Unschuld, P. G.; Kloiber, S.; Horstmann, S.; Uhr, M.; Müller-Myhsok, B.; Holsboer, F.: Polymorphisms in the FKBP5 gene region modulates recovery from psychosocial stress in healthy controls. European Journal of Neuroscience 28, pp. 389 - 398 (2008)

Uhr, M.; Tontsch, A.; Namendorf, C.; Ripke, S.; Lucae, S.; Ising, M.; Dose, T.; Ebinger, M.; Rosenhagen, M.; Kohli, M. et al.; Kloiber, S.; Salyakina, D.; Bettecken, T.; Specht, M.; Pütz, B.; Binder, E. B.; Müller-Myhsok, B.; Holsboer, F.: Polymorphisms in the drug transporter Gene ABCB1 predict antidepressant treatment response in depression. Neuron 57, pp. 203 - 209 (2008)

Unschuld, P. G.; Ising, M.; Erhardt, A.; Lucae, S.; Kohli, M.; Kloiber, S.; Salyakina, D.; Thoeringer, C. K.; Kern, N.; Lieb, R. et al.; Uhr, M.; Binder, E. B.; Müller-Myhsok, B.; Holsboer, F.; Keck, M. E.: Polymorphisms in the galanin gene are associated with symptom-severity in female patients suffering from panic disorder. Journal of Affective Disorders 105, pp. 177 - 184 (2008)

Pfarr, K.; Fischer, P.; Arriens, S.; Douglas, J.; Mueller-Myhsok, B.; Fischer, K.; Timmann, C.; Supali, T.; Hoerauf, A.: Variant SNPs of the IL-10 promoter at positions-854 and -627 responsible for low IL-10 secretion are associated with lower levels of circulating Brugia timori microfilariae but not with filarial lymphedema. American Journal of Tropical Medicine and Hygiene 77 (5 Suppl. S), p. 226 - 226 (2007)

Heck, A.; Lieb, R.; Ellgas, A.; Pfister, H.; Lucae, S.; Erhardt, A.; Himmerich, H.; Horstmann, S.; Kloiber, S.; Ripke, S. et al.; Mueller-Myhsok, B.; Bettecken, T.; Uhr, M.; Holsboer, F.; Ising, M.: Polymorphisms in the angiotensin-converting enzyme gene region predict coping styles in healthy adults and depressed patients. Pharmacopsychiatry 40 (5), p. 209 - 209 (2007)

Kloiber, S.; Ripke, S.; Kohli, M.; Reppermund, S.; Salyakina, D.; Bettecken, T.; Ising, M.; Uhr, M.; Horstmann, S.; Dose, T. et al.; Unschuld, P. G.; Zihl, J.; Müller-Myhsok, B.; Holsboer, F.; Lucae, S.: Polymorphisms in the leptin gene are associated with resistance to antidepressant treatment and lower cognitive performance in depression. Pharmacopsychiatry 40 (5), pp. 210 - 211 (2007)

Kohli, M. A.; Salyakina, D.; Binder, E. B.; Lucae, S.; Ising, M.; Ripke, S.; Horstmann, S.; Kloiber, S.; Pütz, B.; Lieb, R. et al.; Uhr, M.; Müller, M. B.; Holsboer, F.; Müller-Myhsok, B.: SNPs in the NTRK2 gene are associated with depressive disorder. Pharmacopsychiatry 40 (5), p. 212 - 212 (2007)

Kohli, M. A.; Salyakina, D.; Lucae, S.; Ising, M.; Bettecken, T.; Ripke, S.; Uhr, M.; Kloiber, S.; Horstmann, S.; Pütz, B. et al.; Reppermund, S.; Heck, A.; Pfister, H.; Holsboer, F.; Müller-Myhsok, B.: Susceptibility gene hunting for recurrent unipolar depression using 400k genome-wide genotype data. Pharmacopsychiatry 40 (5), p. 212 - 212 (2007)

Lucae, S.; Marcus, I.; Saemann, P.; Bettecken, T.; Uhr, M.; Ripke, S.; Kohli, M.; Kloiber, S.; Bondy, B.; Rupprecht, R. et al.; Domschke, K.; Arolt, V.; Lichtner, P.; Holsboer, F.; Müller-Myhsok, B.: Whole genome analysis reveals new potential drug targets as predictors of antidepressant treatment response. Pharmacopsychiatry 40 (5), p. 213 - 213 (2007)

Ohli, M. A.; Salyakina, D.; Binder, E. B.; Lucae, S.; Ising, M.; Ripke, S.; Horstmann, S.; Kloiber, S.; Pütz, B.; Fey, K. et al.; Uhr, M.; Müller, M. B.; Holsboer, F.; Müller-Myhsok, B.: SNPs in the NTRK2 gene are associated with age-at-onset of depressive disorder and attempted suicide. Pharmacopsychiatry 40 (5), pp. 211 - 212 (2007)

Unschuld, P. G.; Ising, M.; Erhardt, A.; Lucae, S.; Kohli, M.; Kloiber, S.; Salyakina, D.; Thoeringer, C. K.; Lieb, R.; Uhr, M. et al.; Binder, E. B.; Müller-Myhsok, B.; Holsboer, F.; Keck, M. E.: Polymorphisms in the galanin gene are associated with symptom-severity in female patients suffering from panic disorder. Pharmacopsychiatry 40 (5), p. 217 - 217 (2007)

Erhardt, A.; Lucae, S.; Unschuld, P. G.; Ising, M.; Kern, N.; Salyakina, D.; Lieb, R.; Uhr, M.; Binder, E. B.; Keck, M. E. et al.; Müller-Myhsok, B.; Holsboer, F.: Association of polymorphisms in P2RX7 and CaMKKb with anxiety disorders. Journal of Affective Disorders 101 (1-3), pp. 159 - 168 (2007)

Winkelmann, J.; Schormair, B.; Lichtner, P.; Ripke, S.; Xiong, L.; Jalilzadeh, S.; Fulda, S.; Pütz, B.; Eckstein, G.; Hauk, S. et al.; Trenkwalder, C.; Zimprich, A.; Stiasny-Kolster, K.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Peglau, I.; Eisensehr, I.; Montplaisir, J.; Turecki, G.; Rouleau, G.; Gieger, C.; Illig, T.; Wichmann, E.; Holsboer, F.; Müller-Myhsok, B.; Meitinger, T.: Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nature Genetics 39 (8), pp. 1000 - 1006 (2007)

Rosenberger, A.; Sharma, M.; Müller-Myhsok, B.; Gasser, T.; Bickeböller, H.: Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease. BMC Genetics 8, doi: 10.1186/1471-2156-8-44 (2007)

Unschuld, P. G.; Ising, M.; Erhardt, A.; Lucae, S.; Kloiber, S.; Kohli, M.; Salyakina, D.; Welt, T.; Kern, N.; Lieb, R. et al.; Uhr, M.; Binder, E. B.; Müller-Myhsok, B.; Holsboer, F.; Keck, M. E.: Polymorphisms in the serotonin receptor gene HTR2A are associated with quantitative traits in panic disorder. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 144B (4), pp. 424 - 429 (2007)

Anthoni, H.; Zucchelli, M.; Matsson, H.; Müller-Myhsok, B.; Fransson, I.; Schumacher, J.; Massinen, S.; Onkamo, P.; Warnke, A.; Griesemann, H. et al.; Hoffmann, P.; Nopola-Hemmi, J.; Lyytinen, H.; Schulte-Koerne, G.; Kere, J.; Nothen, M. M.; Peyrard-Janvid, M.: A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Human Molecular Genetics 16 (6), pp. 667 - 677 (2007)

Opherk, C.; Peters, N.; O'Sullivan, M.; Holtmannspötter, M.; Gschwendtner, A.; Müller-Myhsok, B.; Dichgans, M.: Heritability of MRI lesion volume in CADASIL: Evidence for genetic modifiers. Stroke 38 (2), pp. 583 - 584 (2007)

Kemlink, D.; Polo, O.; Montagna, P.; Provini, F.; Stiasny-Kolster, K.; Oertel, W.; de Weerd, A.; Nevsimalova, S.; Sonka, K.; Högl, B. et al.; Frauscher, B.; Poewe, W.; Trenkwalder, C.; Pramstaller, P. P.; Ferini-Strambi, L.; Zucconi, M.; Konofal, E.; Arnulf, I.; Hadjigeorgiou, G. M.; Happe, S.; Klein, C.; Hiller, A.; Lichtner, P.; Meitinger, T.; Müller-Myhsok, B.; Winkelmann, J.: Family-based association study of the loci 2 and 3 in a European restless legs syndrome population. Movement Disorders 22 (2), pp. 207 - 212 (2007)