Meyer J - Search Results

1

Mutational analysis of the neuronal cadherin gene CELSR1 and exclusion as a candidate for catatonic schizophrenia in a large family.

Gross J, Grimm O, Ortega G, Teuber I, Lesch KP, Meyer J. Gross J, et al. Among authors: meyer j. Psychiatr Genet. 2001 Dec;11(4):197-200. doi: 10.1097/00041444-200112000-00003. Psychiatr Genet. 2001. PMID: 11807409

2

Mutational analysis of the connexin 36 gene (CX36) and exclusion of the coding sequence as a candidate region for catatonic schizophrenia in a large pedigree.

Meyer J, Mai M, Ortega G, Mössner R, Lesch KP. Meyer J, et al. Schizophr Res. 2002 Nov 1;58(1):87-91. doi: 10.1016/s0920-9964(02)00206-2. Schizophr Res. 2002. PMID: 12363395

3

A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree.

Meyer J, Huberth A, Ortega G, Syagailo YV, Jatzke S, Mössner R, Strom TM, Ulzheimer-Teuber I, Stöber G, Schmitt A, Lesch KP. Meyer J, et al. Mol Psychiatry. 2001 May;6(3):302-6. doi: 10.1038/sj.mp.4000869. Mol Psychiatry. 2001. PMID: 11326298

4

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. Mol Psychiatry. 2002;7(2):220-3. doi: 10.1038/sj.mp.4000970. Mol Psychiatry. 2002. PMID: 11840317

5

Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder.

Meyer J, Johannssen K, Freitag CM, Schraut K, Teuber I, Hahner A, Mainhardt C, Mössner R, Volz HP, Wienker TF, McKeane D, Stephan DA, Rouleau G, Reif A, Lesch KP. Meyer J, et al. Int J Neuropsychopharmacol. 2005 Dec;8(4):495-504. doi: 10.1017/S1461145705005821. Epub 2005 Aug 5. Int J Neuropsychopharmacol. 2005. PMID: 16098236 Free article.

6

MLC1 polymorphisms are specifically associated with periodic catatonia, a subgroup of chronic schizophrenia.

Selch S, Strobel A, Haderlein J, Meyer J, Jacob CP, Schmitt A, Lesch KP, Reif A. Selch S, et al. Among authors: meyer j. Biol Psychiatry. 2007 May 15;61(10):1211-4. doi: 10.1016/j.biopsych.2006.08.030. Epub 2007 Jan 8. Biol Psychiatry. 2007. PMID: 17210142

7

The genomic organization of the murine Mlc1 (Wkl1, KIAA0027) gene.

Steinke V, Meyer J, Syagailo YV, Ortega G, Hameister H, Mössner R, Schmitt A, Lesch KP. Steinke V, et al. Among authors: meyer j. J Neural Transm (Vienna). 2003 Apr;110(4):333-43. doi: 10.1007/s00702-002-0788-2. J Neural Transm (Vienna). 2003. PMID: 12658361

8

Short CAG repeats within the hSKCa3 gene associated with schizophrenia: results of a family-based study.

Stöber G, Jatzke S, Meyer J, Okladnova O, Knapp M, Beckmann H, Lesch KP. Stöber G, et al. Among authors: meyer j. Neuroreport. 1998 Nov 16;9(16):3595-9. doi: 10.1097/00001756-199811160-00010. Neuroreport. 1998. PMID: 9858366

9

Mosaicism for a serotonin transporter gene promoter-associated deletion: decreased recombination in depression.

Lesch KP, Jatzke S, Meyer J, Stöber G, Okladnova O, Mössner R, Riederer P. Lesch KP, et al. Among authors: meyer j. J Neural Transm (Vienna). 1999;106(11-12):1223-30. doi: 10.1007/s007020050236. J Neural Transm (Vienna). 1999. PMID: 10651116

10

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: meyer j. 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

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