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Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD).
Bergmann C, Senderek J, Windelen E, Küpper F, Middeldorf I, Schneider F, Dornia C, Rudnik-Schöneborn S, Konrad M, Schmitt CP, Seeman T, Neuhaus TJ, Vester U, Kirfel J, Büttner R, Zerres K; APN (Arbeitsgemeinschaft für Pädiatrische Nephrologie). Bergmann C, et al. Among authors: schneider f. Kidney Int. 2005 Mar;67(3):829-48. doi: 10.1111/j.1523-1755.2005.00148.x. Kidney Int. 2005. PMID: 15698423 Free article.
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD).
Bergmann C, Senderek J, Küpper F, Schneider F, Dornia C, Windelen E, Eggermann T, Rudnik-Schöneborn S, Kirfel J, Furu L, Onuchic LF, Rossetti S, Harris PC, Somlo S, Guay-Woodford L, Germino GG, Moser M, Büttner R, Zerres K. Bergmann C, et al. Among authors: schneider f. Hum Mutat. 2004 May;23(5):453-63. doi: 10.1002/humu.20029. Hum Mutat. 2004. PMID: 15108277 Review.
Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with differences in frontal brain activation in a working memory task in healthy individuals.
Krug A, Markov V, Eggermann T, Krach S, Zerres K, Stöcker T, Shah NJ, Schneider F, Nöthen MM, Treutlein J, Rietschel M, Kircher T. Krug A, et al. Among authors: schneider f. Neuroimage. 2008 Oct 1;42(4):1569-76. doi: 10.1016/j.neuroimage.2008.05.058. Epub 2008 Jun 12. Neuroimage. 2008. PMID: 18606232
The impact of a Dysbindin schizophrenia susceptibility variant on fiber tract integrity in healthy individuals: a TBSS-based diffusion tensor imaging study.
Nickl-Jockschat T, Stöcker T, Markov V, Krug A, Huang R, Schneider F, Habel U, Zerres K, Nöthen MM, Treutlein J, Rietschel M, Shah NJ, Kircher T. Nickl-Jockschat T, et al. Among authors: schneider f. Neuroimage. 2012 Apr 2;60(2):847-53. doi: 10.1016/j.neuroimage.2011.10.012. Epub 2011 Oct 14. Neuroimage. 2012. PMID: 22019876
A Neuregulin-1 schizophrenia susceptibility variant causes perihippocampal fiber tract anomalies in healthy young subjects.
Nickl-Jockschat T, Stöcker T, Krug A, Markov V, Huang R, Schneider F, Habel U, Eickhoff SB, Zerres K, Nöthen MM, Treutlein J, Rietschel M, Shah NJ, Kircher T. Nickl-Jockschat T, et al. Among authors: schneider f. Brain Behav. 2014 Mar;4(2):215-26. doi: 10.1002/brb3.203. Epub 2014 Jan 19. Brain Behav. 2014. PMID: 24683514 Free PMC article.
Genetic variation in the G72 gene is associated with increased frontotemporal fiber tract integrity.
Nickl-Jockschat T, Stöcker T, Krug A, Markov V, Maximov II, Huang R, Schneider F, Habel U, Eickhoff SB, Zerres K, Nöthen MM, Rietschel M, Jon Shah N, Treutlein J, Kircher T. Nickl-Jockschat T, et al. Among authors: schneider f. Eur Arch Psychiatry Clin Neurosci. 2015 Jun;265(4):291-301. doi: 10.1007/s00406-014-0516-6. Epub 2014 Jul 17. Eur Arch Psychiatry Clin Neurosci. 2015. PMID: 25031104
Neuregulin 1 ICE-single nucleotide polymorphism in first episode schizophrenia correlates with cerebral activation in fronto-temporal areas.
Kircher T, Thienel R, Wagner M, Reske M, Habel U, Kellermann T, Frommann I, Schwab S, Wölwer W, von Wilmsdorf M, Braus DF, Schmitt A, Rapp A, Stöcker T, Shah NJ, Henn FA, Sauer H, Gaebel W, Maier W, Schneider F. Kircher T, et al. Among authors: schneider f. Eur Arch Psychiatry Clin Neurosci. 2009 Mar;259(2):72-9. doi: 10.1007/s00406-008-0837-4. Epub 2008 Sep 19. Eur Arch Psychiatry Clin Neurosci. 2009. PMID: 18806920
Adherence to guidelines for treatment of depression in in-patients.
Schneider F, Härter M, Brand S, Sitta P, Menke R, Hammer-Filipiak U, Kudling R, Heindl A, Herold K, Frommberger U, Elmer O, Hetzel G, Witt G, Wolfersdorf M, Berger M, Gaebel W. Schneider F, et al. Br J Psychiatry. 2005 Nov;187:462-9. doi: 10.1192/bjp.187.5.462. Br J Psychiatry. 2005. PMID: 16260823
1,999 results