Publications of S. Ripke

Weber, F.; Fontaine, B.; Cournu-Rebeix, I.; Kroner, A.; Knop, M.; Lutz, S.; Müller-Sarnowski, F.; Uhr, M.; Bettecken, T.; Kohli, M. et al.; Ripke, S.; Ising, M.; Rieckmann, P.; Brassat, D.; Semana, G.; Babron, M. C.; Mrejen, S.; Gout, C.; Lyon-Caen, O.; Yaouanq, J.; Edan, G.; Clanet, M.; Holsboer, F.; Clerget-Darpoux, F.; Müller-Myhsok, B.: IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations. Journal of Neurology 255 (Suppl. 2), pp. 52 - 53 (2008)

Menke, A.; Lucae, S.; Kloiber, S.; Horstmann, S.; Bettecken, T.; Uhr, M.; Ripke, S.; Ising, M.; Müller-Myhsok, B.; Holsboer, F. et al.; Binder, E. B.: Polymorphisms in metabotropic glutamate receptor 1 are associated with major depressive disorder. Biological Psychiatry 63 (7 Suppl. S), pp. 83S - 84S (2008)

Weber, F.; Fontaine, B.; Cournu-Rebeix, I.; Kroner, A.; Knop, M.; Lutz, S.; Müller-Sarnowski, F.; Uhr, M.; Bettecken, T.; Kohli, M. et al.; Ripke, S.; Ising, M.; Rieckmann, P.; Brassat, D.; Semana, G.; Babron, M. C.; Mrejen, S.; Gout, C.; Lyon-Caen, O.; Yaouanq, J.; Edan, G.; Clanet, M.; Holsboer, F.; Clerget-Darpoux, F.; Müller-Myhsok, B.: IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations. Genes and Immunity 9 (3), pp. 259 - 263 (2008)

Menke, A.; Lucae, S.; Kloiber, S.; Horstmann, S.; Uhr, M.; Pütz, B.; Ripke, S.; Müller-Myhsok, B.: Glutamate and interleukin receptor genes are associated with antidepressant treatment emergent suicidal ideation. European Neuropsychopharmacology 18 (Suppl. 1), pp. S70 - S71 (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)

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)

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)

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)

Aulchenko, Y. S.; Ripke, S.; Isaacs, A.; Van Duijn, C. M.: GenABEL: an R library for genorne-wide association analysis. Bioinformatics 23 (10), pp. 1294 - 1296 (2007)

Forstner, A. J.; Awasthi, S.; Wolf, C.; Maron, E.; Erhardt, A.; Eriksson, E.; Lavebratt, C.; Allgulander, C.; Woldbye, D. P. D.; Mors, O. et al.; Binder, E. B.; Ruck, C.; Ripke, S.; Deckert, J.; Schumacher, J.: Genome-wide association study of panic disorder. In European Neuropsychopharmacology, 29, p. S776 - S776. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, October 13, 2017 - October 17, 2017. Elsevier, Amsterdam (2019)