Jatzke S - Search Results

1

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: jatzke s. 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.

2

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: jatzke s. 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

3

hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia.

Stöber G, Meyer J, Nanda I, Wienker TF, Saar K, Jatzke S, Schmid M, Lesch KP, Beckmann H. Stöber G, et al. Among authors: jatzke s. Eur Arch Psychiatry Clin Neurosci. 2000;250(4):163-8. doi: 10.1007/s004060070020. Eur Arch Psychiatry Clin Neurosci. 2000. PMID: 11009068

4

Susceptibility for schizophrenia is not influenced by a functional insertion/deletion variant in the promoter of the serotonin transporter gene.

Stöber G, Jatzke S, Heils A, Jungkunz G, Fuchs E, Knapp M, Riederer P, Lesch KP. Stöber G, et al. Among authors: jatzke s. Eur Arch Psychiatry Clin Neurosci. 1998;248(2):82-6. doi: 10.1007/s004060050022. Eur Arch Psychiatry Clin Neurosci. 1998. PMID: 9684917

5

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: jatzke s. Neuroreport. 1998 Nov 16;9(16):3595-9. doi: 10.1097/00001756-199811160-00010. Neuroreport. 1998. PMID: 9858366

6

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. Among authors: jatzke s. Mol Psychiatry. 2001 May;6(3):302-6. doi: 10.1038/sj.mp.4000869. Mol Psychiatry. 2001. PMID: 11326298

7

Insertion/deletion variant (-141C Ins/Del) in the 5' regulatory region of the dopamine D2 receptor gene: lack of association with schizophrenia and bipolar affective disorder. Short communication.

Stöber G, Jatzke S, Heils A, Jungkunz G, Knapp M, Mössner R, Riederer P, Lesch KP. Stöber G, et al. Among authors: jatzke s. J Neural Transm (Vienna). 1998;105(1):101-9. doi: 10.1007/s007020050041. J Neural Transm (Vienna). 1998. PMID: 9588764

8

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: jatzke s. J Neural Transm (Vienna). 1999;106(11-12):1223-30. doi: 10.1007/s007020050236. J Neural Transm (Vienna). 1999. PMID: 10651116

9

Serotonin transporter promoter polymorphism influences topography of inhibitory motor control.

Fallgatter AJ, Jatzke S, Bartsch AJ, Hamelbeck B, Lesch KP. Fallgatter AJ, et al. Among authors: jatzke s. Int J Neuropsychopharmacol. 1999 Jun;2(2):115-120. doi: 10.1017/S1461145799001455. Int J Neuropsychopharmacol. 1999. PMID: 11281979 Free article.

10

High ethanol tolerance in young adults is associated with the low-activity variant of the promoter of the human serotonin transporter gene.

Türker T, Sodmann R, Goebel U, Jatzke S, Knapp M, Lesch KP, Schuster R, Schütz H, Weiler G, Stöber G. Türker T, et al. Among authors: jatzke s. Neurosci Lett. 1998 Jun 5;248(3):147-50. doi: 10.1016/s0304-3940(98)00347-4. Neurosci Lett. 1998. PMID: 9654330

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