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634 results
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Periodic catatonia: a schizophrenic subtype with major gene effect and anticipation.
Stöber G, Franzek E, Lesch KP, Beckmann H. Stöber G, et al. Among authors: lesch kp. Eur Arch Psychiatry Clin Neurosci. 1995;245(3):135-41. doi: 10.1007/BF02193085. Eur Arch Psychiatry Clin Neurosci. 1995. PMID: 7669819
The corticotropin-releasing factor (CRF)-system and monoaminergic afferents in the central amygdala: investigations in different mouse strains and comparison with the rat.
Asan E, Yilmazer-Hanke DM, Eliava M, Hantsch M, Lesch KP, Schmitt A. Asan E, et al. Among authors: lesch kp. Neuroscience. 2005;131(4):953-67. doi: 10.1016/j.neuroscience.2004.11.040. Neuroscience. 2005. PMID: 15749348
Norepinephrine transporter gene (NET) variants in patients with panic disorder.
Sand PG, Mori T, Godau C, Stöber G, Flachenecker P, Franke P, Nöthen MM, Fritze J, Maier W, Lesch KP, Riederer P, Beckmann H, Deckert J. Sand PG, et al. Among authors: lesch kp. Neurosci Lett. 2002 Nov 15;333(1):41-4. doi: 10.1016/s0304-3940(02)00984-9. Neurosci Lett. 2002. PMID: 12401556
OCD-like behavior is caused by dysfunction of thalamo-amygdala circuits and upregulated TrkB/ERK-MAPK signaling as a result of SPRED2 deficiency.
Ullrich M, Weber M, Post AM, Popp S, Grein J, Zechner M, Guerrero González H, Kreis A, Schmitt AG, Üçeyler N, Lesch KP, Schuh K. Ullrich M, et al. Among authors: lesch kp. Mol Psychiatry. 2018 Feb;23(2):444-458. doi: 10.1038/mp.2016.232. Epub 2017 Jan 10. Mol Psychiatry. 2018. PMID: 28070119 Free PMC article.
Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.
Jarick I, Volckmar AL, Pütter C, Pechlivanis S, Nguyen TT, Dauvermann MR, Beck S, Albayrak Ö, Scherag S, Gilsbach S, Cichon S, Hoffmann P, Degenhardt F, Nöthen MM, Schreiber S, Wichmann HE, Jöckel KH, Heinrich J, Tiesler CM, Faraone SV, Walitza S, Sinzig J, Freitag C, Meyer J, Herpertz-Dahlmann B, Lehmkuhl G, Renner TJ, Warnke A, Romanos M, Lesch KP, Reif A, Schimmelmann BG, Hebebrand J, Scherag A, Hinney A. Jarick I, et al. Among authors: lesch kp. Mol Psychiatry. 2014 Jan;19(1):115-21. doi: 10.1038/mp.2012.161. Epub 2012 Nov 20. Mol Psychiatry. 2014. PMID: 23164820 Free PMC article.
Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.
Lesch KP, Selch S, Renner TJ, Jacob C, Nguyen TT, Hahn T, Romanos M, Walitza S, Shoichet S, Dempfle A, Heine M, Boreatti-Hümmer A, Romanos J, Gross-Lesch S, Zerlaut H, Wultsch T, Heinzel S, Fassnacht M, Fallgatter A, Allolio B, Schäfer H, Warnke A, Reif A, Ropers HH, Ullmann R. Lesch KP, et al. Mol Psychiatry. 2011 May;16(5):491-503. doi: 10.1038/mp.2010.29. Epub 2010 Mar 23. Mol Psychiatry. 2011. PMID: 20308990
Tph2 gene variants modulate response control processes in adult ADHD patients and healthy individuals.
Baehne CG, Ehlis AC, Plichta MM, Conzelmann A, Pauli P, Jacob C, Gutknecht L, Lesch KP, Fallgatter AJ. Baehne CG, et al. Among authors: lesch kp. Mol Psychiatry. 2009 Nov;14(11):1032-9. doi: 10.1038/mp.2008.39. Epub 2008 Apr 22. Mol Psychiatry. 2009. PMID: 18427560
Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12.
Romanos M, Freitag C, Jacob C, Craig DW, Dempfle A, Nguyen TT, Halperin R, Walitza S, Renner TJ, Seitz C, Romanos J, Palmason H, Reif A, Heine M, Windemuth-Kieselbach C, Vogler C, Sigmund J, Warnke A, Schäfer H, Meyer J, Stephan DA, Lesch KP. Romanos M, et al. Among authors: lesch kp. Mol Psychiatry. 2008 May;13(5):522-30. doi: 10.1038/mp.2008.12. Epub 2008 Feb 26. Mol Psychiatry. 2008. PMID: 18301393
No missense mutation of WKL1 in a subgroup of probands with schizophrenia.
Devaney JM, Donarum EA, Brown KM, Meyer J, Stöber G, Lesch KP, Nestadt G, Stephan DA, Pulver AE. Devaney JM, et al. Among authors: lesch kp. Mol Psychiatry. 2002;7(4):419-23. doi: 10.1038/sj.mp.4001022. Mol Psychiatry. 2002. PMID: 11986987
Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus.
Meyer J, Ortega G, Schraut K, Nürnberg G, Rüschendorf F, Saar K, Mössner R, Wienker TF, Reis A, Stöber G, Lesch KP. Meyer J, et al. Among authors: lesch kp. Mol Psychiatry. 2002;7(2):220-3. doi: 10.1038/sj.mp.4000970. Mol Psychiatry. 2002. PMID: 11840317
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