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Mitochondrial mutations and polymorphisms in psychiatric disorders.

Frontiers in genetics

Sequeira A, Martin MV, Rollins B, Moon EA, Bunney WE, Macciardi F, Lupoli S, Smith EN, Kelsoe J, Magnan CN, van Oven M, Baldi P, Wallace DC, Vawter MP.
PMID: 22723804
Front Genet. 2012 Jun 20;3:103. doi: 10.3389/fgene.2012.00103. eCollection 2012.

Mitochondrial deficiencies with unknown causes have been observed in schizophrenia (SZ) and bipolar disorder (BD) in imaging and postmortem studies. Polymorphisms and somatic mutations in mitochondrial DNA (mtDNA) were investigated as potential causes with next generation sequencing of mtDNA...

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Sequeira A, Martin MV, Rollins B, et al. Mitochondrial mutations and polymorphisms in psychiatric disorders. Front Genet. 2012;3:103doi: 10.3389/fgene.2012.00103.
Sequeira, A., Martin, M. V., Rollins, B., Moon, E. A., Bunney, W. E., Macciardi, F., Lupoli, S., Smith, E. N., Kelsoe, J., Magnan, C. N., van Oven, M., Baldi, P., Wallace, D. C., & Vawter, M. P. (2012). Mitochondrial mutations and polymorphisms in psychiatric disorders. Frontiers in genetics, 3103. https://doi.org/10.3389/fgene.2012.00103
Sequeira, Adolfo, et al. "Mitochondrial mutations and polymorphisms in psychiatric disorders." Frontiers in genetics vol. 3 (2012): 103. doi: https://doi.org/10.3389/fgene.2012.00103
Sequeira A, Martin MV, Rollins B, Moon EA, Bunney WE, Macciardi F, Lupoli S, Smith EN, Kelsoe J, Magnan CN, van Oven M, Baldi P, Wallace DC, Vawter MP. Mitochondrial mutations and polymorphisms in psychiatric disorders. Front Genet. 2012 Jun 20;3:103. doi: 10.3389/fgene.2012.00103. eCollection 2012. PMID: 22723804; PMCID: PMC3379031.
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Circadian polymorphisms associated with affective disorders.

Journal of circadian rhythms

Kripke DF, Nievergelt CM, Joo E, Shekhtman T, Kelsoe JR.
PMID: 19166596
J Circadian Rhythms. 2009 Jan 23;7:2. doi: 10.1186/1740-3391-7-2.

BACKGROUND: Clinical symptoms of affective disorders, their response to light treatment, and sensitivity to other circadian interventions indicate that the circadian system has a role in mood disorders. Possibly the mechanisms involve circadian seasonal and photoperiodic mechanisms. Since genetic...

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Kripke DF, Nievergelt CM, Joo E, et al. Circadian polymorphisms associated with affective disorders. J Circadian Rhythms. 2009;7:2doi: 10.1186/1740-3391-7-2.
Kripke, D. F., Nievergelt, C. M., Joo, E., Shekhtman, T., & Kelsoe, J. R. (2009). Circadian polymorphisms associated with affective disorders. Journal of circadian rhythms, 72. https://doi.org/10.1186/1740-3391-7-2
Kripke, Daniel F, et al. "Circadian polymorphisms associated with affective disorders." Journal of circadian rhythms vol. 7 (2009): 2. doi: https://doi.org/10.1186/1740-3391-7-2
Kripke DF, Nievergelt CM, Joo E, Shekhtman T, Kelsoe JR. Circadian polymorphisms associated with affective disorders. J Circadian Rhythms. 2009 Jan 23;7:2. doi: 10.1186/1740-3391-7-2. PMID: 19166596; PMCID: PMC2661876.
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Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder.

Frontiers in genetics

Judy JT, Seifuddin F, Pirooznia M, Mahon PB, Jancic D, Goes FS, Schulze T, Cichon S, Noethen M, Rietschel M, Depaulo JR, Potash JB, Zandi PP.
PMID: 23730306
Front Genet. 2013 May 17;4:87. doi: 10.3389/fgene.2013.00087. eCollection 2013.

Genome-wide association studies (GWAS) have implicated ANK3 as a susceptibility gene for bipolar disorder (BP). We examined whether epistasis with ANK3 may contribute to the "missing heritability" in BP. We first identified via the STRING database 14 genes encoding...

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Judy JT, Seifuddin F, Pirooznia M, et al. Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder. Front Genet. 2013;4:87doi: 10.3389/fgene.2013.00087.
Judy, J. T., Seifuddin, F., Pirooznia, M., Mahon, P. B., Jancic, D., Goes, F. S., Schulze, T., Cichon, S., Noethen, M., Rietschel, M., Depaulo, J. R., Potash, J. B., & Zandi, P. P. (2013). Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder. Frontiers in genetics, 487. https://doi.org/10.3389/fgene.2013.00087
Judy, Jennifer Toolan, et al. "Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder." Frontiers in genetics vol. 4 (2013): 87. doi: https://doi.org/10.3389/fgene.2013.00087
Judy JT, Seifuddin F, Pirooznia M, Mahon PB, Jancic D, Goes FS, Schulze T, Cichon S, Noethen M, Rietschel M, Depaulo JR, Potash JB, Zandi PP. Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder. Front Genet. 2013 May 17;4:87. doi: 10.3389/fgene.2013.00087. eCollection 2013. PMID: 23730306; PMCID: PMC3656345.
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Symptom profiles and illness course among Anabaptist and Non-Anabaptist adults with major mood disorders.

International journal of bipolar disorders

Gill KE, Cardenas SA, Kassem L, Schulze TG, McMahon FJ.
PMID: 27734417
Int J Bipolar Disord. 2016 Dec;4(1):21. doi: 10.1186/s40345-016-0062-4. Epub 2016 Oct 12.

BACKGROUND: Anabaptists comprise large and growing Amish and Mennonite populations with a unique genetic heritage and cultural background. Little is known about the symptoms and course of major mood disorders in Anabaptists. Even less is known about the impact...

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Gill KE, Cardenas SA, Kassem L, et al. Symptom profiles and illness course among Anabaptist and Non-Anabaptist adults with major mood disorders. Int J Bipolar Disord. 2016;4(1):21doi: 10.1186/s40345-016-0062-4.
Gill, K. E., Cardenas, S. A., Kassem, L., Schulze, T. G., & McMahon, F. J. (2016). Symptom profiles and illness course among Anabaptist and Non-Anabaptist adults with major mood disorders. International journal of bipolar disorders, 4(1), 21. https://doi.org/10.1186/s40345-016-0062-4
Gill, Kelly E, et al. "Symptom profiles and illness course among Anabaptist and Non-Anabaptist adults with major mood disorders." International journal of bipolar disorders vol. 4,1 (2016): 21. doi: https://doi.org/10.1186/s40345-016-0062-4
Gill KE, Cardenas SA, Kassem L, Schulze TG, McMahon FJ. Symptom profiles and illness course among Anabaptist and Non-Anabaptist adults with major mood disorders. Int J Bipolar Disord. 2016 Dec;4(1):21. doi: 10.1186/s40345-016-0062-4. Epub 2016 Oct 12. PMID: 27734417; PMCID: PMC5061680.
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CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis.

Psychiatry investigation

Cho CH, Lee HJ, Woo HG, Choi JH, Greenwood TA, Kelsoe JR.
PMID: 26207136
Psychiatry Investig. 2015 Jul;12(3):402-7. doi: 10.4306/pi.2015.12.3.402. Epub 2015 Jul 06.

Although bipolar disorder is highly heritable, the identification of specific genetic variations is limited because of the complex traits underlying the disorder. We performed a genome-wide association study of bipolar disorder using a subphenotype that shows hypersomnia symptom during...

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Cho CH, Lee HJ, Woo HG, et al. CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis. Psychiatry Investig. 2015;12(3):402-7doi: 10.4306/pi.2015.12.3.402.
Cho, C. H., Lee, H. J., Woo, H. G., Choi, J. H., Greenwood, T. A., & Kelsoe, J. R. (2015). CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis. Psychiatry investigation, 12(3), 402-7. https://doi.org/10.4306/pi.2015.12.3.402
Cho, Chul-Hyun, et al. "CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis." Psychiatry investigation vol. 12,3 (2015): 402-7. doi: https://doi.org/10.4306/pi.2015.12.3.402
Cho CH, Lee HJ, Woo HG, Choi JH, Greenwood TA, Kelsoe JR. CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis. Psychiatry Investig. 2015 Jul;12(3):402-7. doi: 10.4306/pi.2015.12.3.402. Epub 2015 Jul 06. PMID: 26207136; PMCID: PMC4504925.
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A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis.

BioData mining

Lekman M, Karlsson R, Graae L, Hössjer O, Kockum I.
PMID: 26692414
BioData Min. 2015 Dec 18;8:42. doi: 10.1186/s13040-015-0076-y. eCollection 2015.

BACKGROUND: The genetic background to bipolar disorder (BPD) has been attributed to different genetic and genomic risk factors. In the present study we hypothesized that inherited copy number variations (CNVs) contribute to susceptibility of BPD. We screened 637 BP-pedigrees...

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Lekman M, Karlsson R, Graae L, et al. A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis. BioData Min. 2015;8:42doi: 10.1186/s13040-015-0076-y.
Lekman, M., Karlsson, R., Graae, L., Hössjer, O., & Kockum, I. (2015). A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis. BioData mining, 842. https://doi.org/10.1186/s13040-015-0076-y
Lekman, Magnus, et al. "A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis." BioData mining vol. 8 (2015): 42. doi: https://doi.org/10.1186/s13040-015-0076-y
Lekman M, Karlsson R, Graae L, Hössjer O, Kockum I. A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis. BioData Min. 2015 Dec 18;8:42. doi: 10.1186/s13040-015-0076-y. eCollection 2015. PMID: 26692414; PMCID: PMC4683747.
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Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles.

Psychiatry investigation

Kripke DF, Klimecki WT, Nievergelt CM, Rex KM, Murray SS, Shekhtman T, Tranah GJ, Loving RT, Lee HJ, Rhee MK, Shadan FF, Poceta JS, Jamil SM, Kline LE, Kelsoe JR.
PMID: 25395965
Psychiatry Investig. 2014 Oct;11(4):345-62. doi: 10.4306/pi.2014.11.4.345. Epub 2014 Oct 20.

People called night owls habitually have late bedtimes and late times of arising, sometimes suffering a heritable circadian disturbance called delayed sleep phase syndrome (DSPS). Those with DSPS, those with more severe progressively-late non-24-hour sleep-wake cycles, and those with...

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Kripke DF, Klimecki WT, Nievergelt CM, et al. Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles. Psychiatry Investig. 2014;11(4):345-62doi: 10.4306/pi.2014.11.4.345.
Kripke, D. F., Klimecki, W. T., Nievergelt, C. M., Rex, K. M., Murray, S. S., Shekhtman, T., Tranah, G. J., Loving, R. T., Lee, H. J., Rhee, M. K., Shadan, F. F., Poceta, J. S., Jamil, S. M., Kline, L. E., & Kelsoe, J. R. (2014). Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles. Psychiatry investigation, 11(4), 345-62. https://doi.org/10.4306/pi.2014.11.4.345
Kripke, Daniel F, et al. "Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles." Psychiatry investigation vol. 11,4 (2014): 345-62. doi: https://doi.org/10.4306/pi.2014.11.4.345
Kripke DF, Klimecki WT, Nievergelt CM, Rex KM, Murray SS, Shekhtman T, Tranah GJ, Loving RT, Lee HJ, Rhee MK, Shadan FF, Poceta JS, Jamil SM, Kline LE, Kelsoe JR. Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles. Psychiatry Investig. 2014 Oct;11(4):345-62. doi: 10.4306/pi.2014.11.4.345. Epub 2014 Oct 20. PMID: 25395965; PMCID: PMC4225198.
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Evaluation of potential novel variations and their interactions related to bipolar disorders: analysis of genome-wide association study data.

Neuropsychiatric disease and treatment

Acikel C, Aydin Son Y, Celik C, Gul H.
PMID: 27920536
Neuropsychiatr Dis Treat. 2016 Nov 24;12:2997-3004. doi: 10.2147/NDT.S112558. eCollection 2016.

BACKGROUND: Multifactor dimensionality reduction (MDR) is a nonparametric approach that can be used to detect relevant interactions between single-nucleotide polymorphisms (SNPs). The aim of this study was to build the best genomic model based on SNP associations and to...

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Acikel C, Aydin Son Y, Celik C, et al. Evaluation of potential novel variations and their interactions related to bipolar disorders: analysis of genome-wide association study data. Neuropsychiatr Dis Treat. 2016;12:2997-3004doi: 10.2147/NDT.S112558.
Acikel, C., Aydin Son, Y., Celik, C., & Gul, H. (2016). Evaluation of potential novel variations and their interactions related to bipolar disorders: analysis of genome-wide association study data. Neuropsychiatric disease and treatment, 122997-3004. https://doi.org/10.2147/NDT.S112558
Acikel, Cengizhan, et al. "Evaluation of potential novel variations and their interactions related to bipolar disorders: analysis of genome-wide association study data." Neuropsychiatric disease and treatment vol. 12 (2016): 2997-3004. doi: https://doi.org/10.2147/NDT.S112558
Acikel C, Aydin Son Y, Celik C, Gul H. Evaluation of potential novel variations and their interactions related to bipolar disorders: analysis of genome-wide association study data. Neuropsychiatr Dis Treat. 2016 Nov 24;12:2997-3004. doi: 10.2147/NDT.S112558. eCollection 2016. PMID: 27920536; PMCID: PMC5127431.
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Showing 1 to 8 of 8 entries