Crocq MA - Search Results

1

Isolation of a novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: a candidate for schizophrenia and bipolar disorder?

Chandy KG, Fantino E, Wittekindt O, Kalman K, Tong LL, Ho TH, Gutman GA, Crocq MA, Ganguli R, Nimgaonkar V, Morris-Rosendahl DJ, Gargus JJ. Chandy KG, et al. Among authors: crocq ma. Mol Psychiatry. 1998 Jan;3(1):32-7. doi: 10.1038/sj.mp.4000353. Mol Psychiatry. 1998. PMID: 9491810

2

Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents trios.

Wittekindt O, Schwab SG, Burgert E, Knapp M, Albus M, Lerer B, Hallmayer J, Rietschel M, Segman R, Borrmann M, Lichtermann D, Crocq MA, Maier W, Morris-Rosendahl DJ, Wildenauer DB. Wittekindt O, et al. Among authors: crocq ma. Mol Psychiatry. 1999 May;4(3):267-70. doi: 10.1038/sj.mp.4000495. Mol Psychiatry. 1999. PMID: 10395217

3

The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia.

Wittekindt O, Jauch A, Burgert E, Schärer L, Holtgreve-Grez H, Yvert G, Imbert G, Zimmer J, Hoehe MR, Macher JP, Chiaroni P, van Calker D, Crocq MA, Morris-Rosendahl DJ. Wittekindt O, et al. Among authors: crocq ma. Neurogenetics. 1998 Aug;1(4):259-65. doi: 10.1007/s100480050038. Neurogenetics. 1998. PMID: 10732800 Clinical Trial.

4

Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: tentative association between B37 and schizophrenia.

Morris-Rosendahl DJ, Burgert E, Uyanik G, Mayerova A, Duval F, Macher JP, Crocq MA. Morris-Rosendahl DJ, et al. Among authors: crocq ma. Am J Med Genet. 1997 May 31;74(3):324-30. doi: 10.1002/(sici)1096-8628(19970531)74:3<324::aid-ajmg15>3.0.co;2-q. Am J Med Genet. 1997. PMID: 9184318

5

No association between the tyrosine hydroxylase microsatellite marker HUMTH01 and schizophrenia or bipolar I disorder.

Burgert E, Crocq MA, Bausch E, Macher JP, Morris-Rosendahl DJ. Burgert E, et al. Among authors: crocq ma. Psychiatr Genet. 1998 Summer;8(2):45-8. doi: 10.1097/00041444-199800820-00002. Psychiatr Genet. 1998. PMID: 9686421

6

Neurodevelopmental disorders-the history and future of a diagnostic concept .

Morris-Rosendahl DJ, Crocq MA. Morris-Rosendahl DJ, et al. Among authors: crocq ma. Dialogues Clin Neurosci. 2020 Mar;22(1):65-72. doi: 10.31887/DCNS.2020.22.1/macrocq. Dialogues Clin Neurosci. 2020. PMID: 32699506 Free PMC article. Review.

7

Serotonin transporter (5-HTT) gene polymorphisms are not associated with susceptibility to mood disorders.

Hoehe MR, Wendel B, Grunewald I, Chiaroni P, Levy N, Morris-Rosendahl D, Macher JP, Sander T, Crocq MA. Hoehe MR, et al. Among authors: crocq ma. Am J Med Genet. 1998 Feb 7;81(1):1-3. doi: 10.1002/(sici)1096-8628(19980207)81:1<1::aid-ajmg1>3.0.co;2-2. Am J Med Genet. 1998. PMID: 9514579

8

Trend for an association between schizophrenia and D3S1310, a marker in proximity to the dopamine D3 receptor gene.

Jönsson EG, Nimgaonkar VL, Zhang XR, Shaw SH, Burgert E, Crocq MA, Chakravarti A, Sedvall GC. Jönsson EG, et al. Among authors: crocq ma. Am J Med Genet. 1999 Aug 20;88(4):352-7. Am J Med Genet. 1999. PMID: 10402502

9

Meta-analysis of the dopamine D3 receptor gene (DRD3) Ser9Gly variant and schizophrenia.

Jönsson EG, Kaiser R, Brockmöller J, Nimgaonkar VL, Crocq MA. Jönsson EG, et al. Among authors: crocq ma. Psychiatr Genet. 2004 Mar;14(1):9-12. doi: 10.1097/00041444-200403000-00002. Psychiatr Genet. 2004. PMID: 15091310 No abstract available.

10

A novel allelic variant of the human serotonin transporter gene regulatory polymorphism.

Delbrück SJ, Wendel B, Grunewald I, Sander T, Morris-Rosendahl D, Crocq MA, Berrettini WH, Hoehe MR. Delbrück SJ, et al. Among authors: crocq ma. Cytogenet Cell Genet. 1997;79(3-4):214-20. doi: 10.1159/000134726. Cytogenet Cell Genet. 1997. PMID: 9605856

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