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Page 1
A Systematic Evaluation of Machine Learning-Based Biomarkers for Major Depressive Disorder.
Winter NR, Blanke J, Leenings R, Ernsting J, Fisch L, Sarink K, Barkhau C, Emden D, Thiel K, Flinkenflügel K, Winter A, Goltermann J, Meinert S, Dohm K, Repple J, Gruber M, Leehr EJ, Opel N, Grotegerd D, Redlich R, Nitsch R, Bauer J, Heindel W, Gross J, Risse B, Andlauer TFM, Forstner AJ, Nöthen MM, Rietschel M, Hofmann SG, Pfarr JK, Teutenberg L, Usemann P, Thomas-Odenthal F, Wroblewski A, Brosch K, Stein F, Jansen A, Jamalabadi H, Alexander N, Straube B, Nenadic I, Kircher T, Dannlowski U, Hahn T. Winter NR, et al. Among authors: nenadic i. JAMA Psychiatry. 2024 Apr 1;81(4):386-395. doi: 10.1001/jamapsychiatry.2023.5083. JAMA Psychiatry. 2024. PMID: 38198165
Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter.
Treutlein J, Mühleisen TW, Frank J, Mattheisen M, Herms S, Ludwig KU, Treutlein T, Schmael C, Strohmaier J, Bösshenz KV, Breuer R, Paul T, Witt SH, Schulze TG, Schlösser RG, Nenadic I, Sauer H, Becker T, Maier W, Cichon S, Nöthen MM, Rietschel M. Treutlein J, et al. Among authors: nenadic i. Schizophr Res. 2009 Jun;111(1-3):123-30. doi: 10.1016/j.schres.2009.03.011. Epub 2009 Apr 5. Schizophr Res. 2009. PMID: 19346103
Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients.
Mühleisen TW, Basmanav FB, Forstner AJ, Mattheisen M, Priebe L, Herms S, Breuer R, Moebus S, Nenadic I, Sauer H, Mössner R, Maier W, Rujescu D, Ludwig M, Rietschel M, Nöthen MM, Cichon S. Mühleisen TW, et al. Among authors: nenadic i. Schizophr Res. 2011 Apr;127(1-3):35-40. doi: 10.1016/j.schres.2011.01.001. Epub 2011 Feb 1. Schizophr Res. 2011. PMID: 21288692
Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophrenia.
Schultz CC, Nenadic I, Koch K, Wagner G, Roebel M, Schachtzabel C, Mühleisen TW, Nöthen MM, Cichon S, Deufel T, Kiehntopf M, Rietschel M, Reichenbach JR, Sauer H, Schlösser RG. Schultz CC, et al. Among authors: nenadic i. Neuropsychopharmacology. 2011 Jul;36(8):1747-53. doi: 10.1038/npp.2011.56. Epub 2011 Apr 20. Neuropsychopharmacology. 2011. PMID: 21508934 Free PMC article.
Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophrenia.
Nenadic I, Maitra R, Scherpiet S, Gaser C, Schultz CC, Schachtzabel C, Smesny S, Reichenbach JR, Treutlein J, Mühleisen TW, Deufel T, Cichon S, Rietschel M, Nöthen MM, Sauer H, Schlösser RG. Nenadic I, et al. J Psychiatr Res. 2012 Dec;46(12):1531-9. doi: 10.1016/j.jpsychires.2012.08.026. Epub 2012 Sep 25. J Psychiatr Res. 2012. PMID: 23017809
Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia.
Mattheisen M, Mühleisen TW, Strohmaier J, Treutlein J, Nenadic I, Alblas M, Meier S, Degenhardt F, Herms S, Hoffmann P, Witt SH, Giegling I, Sauer H, Schulze TG, Rujescu D, Nöthen MM, Rietschel M, Cichon S. Mattheisen M, et al. Among authors: nenadic i. Schizophr Res. 2012 Nov;141(2-3):262-5. doi: 10.1016/j.schres.2012.08.027. Epub 2012 Sep 24. Schizophr Res. 2012. PMID: 23017826
No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder.
Degenhardt F, Priebe L, Strohmaier J, Herms S, Hoffmann P, Mattheisen M, Mössner R, Nenadic I, Sauer H, Rujescu D, Maier W, Schulze TG, Rietschel M, Nöthen MM, Cichon S. Degenhardt F, et al. Among authors: nenadic i. Psychiatr Genet. 2013 Feb;23(1):45-6. doi: 10.1097/YPG.0b013e328358645b. Psychiatr Genet. 2013. PMID: 23250005 No abstract available.
Common variation in NCAN, a risk factor for bipolar disorder and schizophrenia, influences local cortical folding in schizophrenia.
Schultz CC, Mühleisen TW, Nenadic I, Koch K, Wagner G, Schachtzabel C, Siedek F, Nöthen MM, Rietschel M, Deufel T, Kiehntopf M, Cichon S, Reichenbach JR, Sauer H, Schlösser RG. Schultz CC, et al. Among authors: nenadic i. Psychol Med. 2014 Mar;44(4):811-20. doi: 10.1017/S0033291713001414. Psychol Med. 2014. PMID: 23795679
Copy number variants in German patients with schizophrenia.
Priebe L, Degenhardt F, Strohmaier J, Breuer R, Herms S, Witt SH, Hoffmann P, Kulbida R, Mattheisen M, Moebus S, Meyer-Lindenberg A, Walter H, Mössner R, Nenadic I, Sauer H, Rujescu D, Maier W, Rietschel M, Nöthen MM, Cichon S. Priebe L, et al. Among authors: nenadic i. PLoS One. 2013 Jul 2;8(7):e64035. doi: 10.1371/journal.pone.0064035. Print 2013. PLoS One. 2013. PMID: 23843933 Free PMC article.
Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene.
Luo XJ, Li M, Huang L, Steinberg S, Mattheisen M, Liang G, Donohoe G, Shi Y, Chen C, Yue W, Alkelai A, Lerer B, Li Z, Yi Q, Rietschel M, Cichon S, Collier DA, Tosato S, Suvisaari J, Rujescu D, Golimbet V, Silagadze T, Durmishi N, Milovancevic MP, Stefansson H, Schulze TG, Nöthen MM, Chen C, Lyne R, Morris DW, Gill M, Corvin A, Zhang D, Dong Q, Moyzis RK, Stefansson K, Sigurdsson E, Hu F; MooDS SCZ Consortium; Su B, Gan L. Luo XJ, et al. Mol Psychiatry. 2014 Jul;19(7):774-83. doi: 10.1038/mp.2013.103. Epub 2013 Aug 20. Mol Psychiatry. 2014. PMID: 23958956
317 results