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364 results
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Genetic heterogeneity in catatonic schizophrenia: a family study.
Beckmann H, Franzek E, Stöber G. Beckmann H, et al. Am J Med Genet. 1996 May 31;67(3):289-300. doi: 10.1002/(SICI)1096-8628(19960531)67:3<289::AID-AJMG5>3.0.CO;2-I. Am J Med Genet. 1996. PMID: 8725746
Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13.
Stöber G, Meyer J, Nanda I, Wienker TF, Saar K, Knapp M, Jatzke S, Schmid M, Lesch KP, Beckmann H. Stöber G, et al. Among authors: beckmann h. Am J Med Genet. 2000 Jun 12;96(3):392-7. doi: 10.1002/1096-8628(20000612)96:3<392::aid-ajmg29>3.0.co;2-r. Am J Med Genet. 2000. PMID: 10898920
Exonic variants of the GABA(B) receptor gene and panic disorder.
Sand PG, Godau C, Riederer P, Peters C, Franke P, Nöthen MM, Stöber G, Fritze J, Maier W, Propping P, Lesch KP, Riess O, Sander T, Beckmann H, Deckert J. Sand PG, et al. Among authors: beckmann h. Psychiatr Genet. 2000 Dec;10(4):191-4. doi: 10.1097/00041444-200010040-00007. Psychiatr Genet. 2000. PMID: 11324945
Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.
Stöber G, Saar K, Rüschendorf F, Meyer J, Nürnberg G, Jatzke S, Franzek E, Reis A, Lesch KP, Wienker TF, Beckmann H. Stöber G, et al. Among authors: beckmann h. Am J Hum Genet. 2000 Nov;67(5):1201-7. doi: 10.1016/S0002-9297(07)62950-4. Epub 2000 Sep 19. Am J Hum Genet. 2000. PMID: 11001582 Free PMC article.
Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder.
Deckert J, Catalano M, Syagailo YV, Bosi M, Okladnova O, Di Bella D, Nöthen MM, Maffei P, Franke P, Fritze J, Maier W, Propping P, Beckmann H, Bellodi L, Lesch KP. Deckert J, et al. Among authors: beckmann h. Hum Mol Genet. 1999 Apr;8(4):621-4. doi: 10.1093/hmg/8.4.621. Hum Mol Genet. 1999. PMID: 10072430
Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies.
Deckert J, Nöthen MM, Albus M, Franzek E, Rietschel M, Ren H, Stiles GL, Knapp M, Weigelt B, Maier W, Beckmann H, Propping P. Deckert J, et al. Among authors: beckmann h. Am J Med Genet. 1998 Feb 7;81(1):18-23. doi: 10.1002/(sici)1096-8628(19980207)81:1<18::aid-ajmg4>3.0.co;2-j. Am J Med Genet. 1998. PMID: 9514582
Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disorders.
Stöber G, Nöthen MM, Pörzgen P, Brüss M, Bönisch H, Knapp M, Beckmann H, Propping P. Stöber G, et al. Among authors: beckmann h. Am J Med Genet. 1996 Nov 22;67(6):523-32. doi: 10.1002/(SICI)1096-8628(19961122)67:6<523::AID-AJMG3>3.0.CO;2-I. Am J Med Genet. 1996. PMID: 8950409
Neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) and panic disorder: an association study.
Steinlein OK, Deckert J, Nöthen MM, Franke P, Maier W, Beckmann H, Propping P. Steinlein OK, et al. Among authors: beckmann h. Am J Med Genet. 1997 Apr 18;74(2):199-201. doi: 10.1002/(sici)1096-8628(19970418)74:2<199::aid-ajmg17>3.0.co;2-d. Am J Med Genet. 1997. PMID: 9129724
[Cycloid psychoses as atypical manic-depressive disorders. Results of a family study].
Jabs B, Althaus G, Bartsch A, Schmidtke A, Stöber G, Beckmann H, Pfuhlmann B. Jabs B, et al. Among authors: beckmann h. Nervenarzt. 2006 Sep;77(9):1096-100, 1102-4. doi: 10.1007/s00115-006-2077-z. Nervenarzt. 2006. PMID: 16502008 German.
Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity.
Stöber G, Seelow D, Rüschendorf F, Ekici A, Beckmann H, Reis A. Stöber G, et al. Among authors: beckmann h. Hum Genet. 2002 Oct;111(4-5):323-30. doi: 10.1007/s00439-002-0805-4. Epub 2002 Aug 29. Hum Genet. 2002. PMID: 12384773
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