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Analyzing pathways from childhood maltreatment to internalizing symptoms and disorders in children and adolescents (AMIS): a study protocol.
White LO, Klein AM, Kirschbaum C, Kurz-Adam M, Uhr M, Müller-Myhsok B, Hoffmann K, Sierau S, Michel A, Stalder T, Horlich J, Keil J, Andreas A, Resch L, Binser MJ, Costa A, Giourges E, Neudecker E, Wolf C, Scheuer S, Ising M, von Klitzing K. White LO, et al. Among authors: wolf c. BMC Psychiatry. 2015 Jun 10;15:126. doi: 10.1186/s12888-015-0512-z. BMC Psychiatry. 2015. PMID: 26058452 Free PMC article.
Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis.
Nischwitz S, Cepok S, Kroner A, Wolf C, Knop M, Müller-Sarnowski F, Pfister H, Roeske D, Rieckmann P, Hemmer B, Ising M, Uhr M, Bettecken T, Holsboer F, Müller-Myhsok B, Weber F. Nischwitz S, et al. Among authors: wolf c. J Neuroimmunol. 2010 Oct 8;227(1-2):162-6. doi: 10.1016/j.jneuroim.2010.06.003. Epub 2010 Jul 2. J Neuroimmunol. 2010. PMID: 20598377
Possible associations of NTRK2 polymorphisms with antidepressant treatment outcome: findings from an extended tag SNP approach.
Hennings JM, Kohli MA, Czamara D, Giese M, Eckert A, Wolf C, Heck A, Domschke K, Arolt V, Baune BT, Horstmann S, Brückl T, Klengel T, Menke A, Müller-Myhsok B, Ising M, Uhr M, Lucae S. Hennings JM, et al. Among authors: wolf c. PLoS One. 2013 Jun 4;8(6):e64947. doi: 10.1371/journal.pone.0064947. Print 2013. PLoS One. 2013. PMID: 23750220 Free PMC article.
The neuronal transporter gene SLC6A15 confers risk to major depression.
Kohli MA, Lucae S, Saemann PG, Schmidt MV, Demirkan A, Hek K, Czamara D, Alexander M, Salyakina D, Ripke S, Hoehn D, Specht M, Menke A, Hennings J, Heck A, Wolf C, Ising M, Schreiber S, Czisch M, Müller MB, Uhr M, Bettecken T, Becker A, Schramm J, Rietschel M, Maier W, Bradley B, Ressler KJ, Nöthen MM, Cichon S, Craig IW, Breen G, Lewis CM, Hofman A, Tiemeier H, van Duijn CM, Holsboer F, Müller-Myhsok B, Binder EB. Kohli MA, et al. Among authors: wolf c. Neuron. 2011 Apr 28;70(2):252-65. doi: 10.1016/j.neuron.2011.04.005. Neuron. 2011. PMID: 21521612 Free PMC article.
More CLEC16A gene variants associated with multiple sclerosis.
Nischwitz S, Cepok S, Kroner A, Wolf C, Knop M, Müller-Sarnowski F, Pfister H, Rieckmann P, Hemmer B, Ising M, Uhr M, Bettecken T, Holsboer F, Müller-Myhsok B, Weber F. Nischwitz S, et al. Among authors: wolf c. Acta Neurol Scand. 2011 Jun;123(6):400-6. doi: 10.1111/j.1600-0404.2010.01421.x. Epub 2010 Sep 16. Acta Neurol Scand. 2011. PMID: 20849399
Imaging genetics of FOXP2 in dyslexia.
Wilcke A, Ligges C, Burkhardt J, Alexander M, Wolf C, Quente E, Ahnert P, Hoffmann P, Becker A, Müller-Myhsok B, Cichon S, Boltze J, Kirsten H. Wilcke A, et al. Among authors: wolf c. Eur J Hum Genet. 2012 Feb;20(2):224-9. doi: 10.1038/ejhg.2011.160. Epub 2011 Sep 7. Eur J Hum Genet. 2012. PMID: 21897444 Free PMC article.
PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites.
Glas J, Seiderer J, Czamara D, Pasciuto G, Diegelmann J, Wetzke M, Olszak T, Wolf C, Müller-Myhsok B, Balschun T, Achkar JP, Kamboh MI, Franke A, Duerr RH, Brand S. Glas J, et al. Among authors: wolf c. PLoS One. 2012;7(12):e52873. doi: 10.1371/journal.pone.0052873. Epub 2012 Dec 27. PLoS One. 2012. PMID: 23300802 Free PMC article.
2,041 results