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FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants.
Mitter D, Pringsheim M, Kaulisch M, Plümacher KS, Schröder S, Warthemann R, Abou Jamra R, Baethmann M, Bast T, Büttel HM, Cohen JS, Conover E, Courage C, Eger A, Fatemi A, Grebe TA, Hauser NS, Heinritz W, Helbig KL, Heruth M, Huhle D, Höft K, Karch S, Kluger G, Korenke GC, Lemke JR, Lutz RE, Patzer S, Prehl I, Hoertnagel K, Ramsey K, Rating T, Rieß A, Rohena L, Schimmel M, Westman R, Zech FM, Zoll B, Malzahn D, Zirn B, Brockmann K. Mitter D, et al. Among authors: malzahn d. Genet Med. 2018 Jan;20(1):98-108. doi: 10.1038/gim.2017.75. Epub 2017 Jun 29. Genet Med. 2018. PMID: 28661489 Free article.
Issues in association mapping with high-density SNP data and diverse family structures.
Bickeböller H, Goddard KA, Igo RP Jr, Kraft P, Lozano JP, Pankratz N, Balavarca Y, Bardel C, Charoen P, Croiseau P, Guo CY, Joo J, Köhler K, Madsen A, Malzahn D, Monsees G, Sohns M, Ye Z. Bickeböller H, et al. Among authors: malzahn d. Genet Epidemiol. 2007;31 Suppl 1:S22-33. doi: 10.1002/gepi.20277. Genet Epidemiol. 2007. PMID: 18046763
Modification of cognitive performance in schizophrenia by complexin 2 gene polymorphisms.
Begemann M, Grube S, Papiol S, Malzahn D, Krampe H, Ribbe K, Friedrichs H, Radyushkin KA, El-Kordi A, Benseler F, Hannke K, Sperling S, Schwerdtfeger D, Thanhäuser I, Gerchen MF, Ghorbani M, Gutwinski S, Hilmes C, Leppert R, Ronnenberg A, Sowislo J, Stawicki S, Stödtke M, Szuszies C, Reim K, Riggert J, Eckstein F, Falkai P, Bickeböller H, Nave KA, Brose N, Ehrenreich H. Begemann M, et al. Among authors: malzahn d. Arch Gen Psychiatry. 2010 Sep;67(9):879-88. doi: 10.1001/archgenpsychiatry.2010.107. Arch Gen Psychiatry. 2010. PMID: 20819981
Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.
Budde M, Friedrichs S, Alliey-Rodriguez N, Ament S, Badner JA, Berrettini WH, Bloss CS, Byerley W, Cichon S, Comes AL, Coryell W, Craig DW, Degenhardt F, Edenberg HJ, Foroud T, Forstner AJ, Frank J, Gershon ES, Goes FS, Greenwood TA, Guo Y, Hipolito M, Hood L, Keating BJ, Koller DL, Lawson WB, Liu C, Mahon PB, McInnis MG, McMahon FJ, Meier SM, Mühleisen TW, Murray SS, Nievergelt CM, Nurnberger JI Jr, Nwulia EA, Potash JB, Quarless D, Rice J, Roach JC, Scheftner WA, Schork NJ, Shekhtman T, Shilling PD, Smith EN, Streit F, Strohmaier J, Szelinger S, Treutlein J, Witt SH, Zandi PP, Zhang P, Zöllner S, Bickeböller H, Falkai PG, Kelsoe JR, Nöthen MM, Rietschel M, Schulze TG, Malzahn D. Budde M, et al. Among authors: malzahn d. Eur Neuropsychopharmacol. 2019 Jan;29(1):156-170. doi: 10.1016/j.euroneuro.2018.10.005. Epub 2018 Nov 29. Eur Neuropsychopharmacol. 2019. PMID: 30503783 Free article.
Quantifying the contribution of genetic variants for survival phenotypes.
Müller M, Döring A, Küchenhoff H, Lamina C, Malzahn D, Bickeböller H, Vollmert C, Klopp N, Meisinger C, Heinrich J, Kronenberg F, Wichmann HE, Heid IM. Müller M, et al. Among authors: malzahn d. Genet Epidemiol. 2008 Sep;32(6):574-85. doi: 10.1002/gepi.20333. Genet Epidemiol. 2008. PMID: 18428429
A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder.
Heilbronner U, Malzahn D, Strohmaier J, Maier S, Frank J, Treutlein J, Mühleisen TW, Forstner AJ, Witt SH, Cichon S, Falkai P, Nöthen MM, Rietschel M, Schulze TG. Heilbronner U, et al. Among authors: malzahn d. Eur Neuropsychopharmacol. 2015 Dec;25(12):2262-70. doi: 10.1016/j.euroneuro.2015.09.012. Epub 2015 Oct 9. Eur Neuropsychopharmacol. 2015. PMID: 26475575 Free article.
41 results