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Showing 25 to 36 of 87 entries
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Predicting diabetes: our relentless quest for genomic nuggets.

Diabetes care

Dagogo-Jack S.
PMID: 22275439
Diabetes Care. 2012 Feb;35(2):193-5. doi: 10.2337/dc11-2106.

No abstract available.

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Dagogo-Jack S. Predicting diabetes: our relentless quest for genomic nuggets. Diabetes Care. 2012;35(2):193-5doi: 10.2337/dc11-2106.
Dagogo-Jack, S. (2012). Predicting diabetes: our relentless quest for genomic nuggets. Diabetes care, 35(2), 193-5. https://doi.org/10.2337/dc11-2106
Dagogo-Jack, Samuel. "Predicting diabetes: our relentless quest for genomic nuggets." Diabetes care vol. 35,2 (2012): 193-5. doi: https://doi.org/10.2337/dc11-2106
Dagogo-Jack S. Predicting diabetes: our relentless quest for genomic nuggets. Diabetes Care. 2012 Feb;35(2):193-5. doi: 10.2337/dc11-2106. PMID: 22275439; PMCID: PMC3263887.
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5-HT1A gene variants and psychiatric disorders: a review of current literature and selection of SNPs for future studies.

The international journal of neuropsychopharmacology

Drago A, Ronchi DD, Serretti A.
PMID: 18047755
Int J Neuropsychopharmacol. 2008 Aug;11(5):701-21. doi: 10.1017/S1461145707008218. Epub 2007 Nov 30.

5-HT1A receptors are key components of the serotonin system, acting both pre- and post- synaptically in different brain areas. There is a growing amount of evidence showing the importance of 5-HT1A in different psychiatric disorders, from mood to anxiety...

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Drago A, Ronchi DD, Serretti A. 5-HT1A gene variants and psychiatric disorders: a review of current literature and selection of SNPs for future studies. Int J Neuropsychopharmacol. 2007;11(5):701-21doi: 10.1017/S1461145707008218.
Drago, A., Ronchi, D. D., & Serretti, A. (2008). 5-HT1A gene variants and psychiatric disorders: a review of current literature and selection of SNPs for future studies. The international journal of neuropsychopharmacology, 11(5), 701-21. https://doi.org/10.1017/S1461145707008218
Drago, Antonio, et al. "5-HT1A gene variants and psychiatric disorders: a review of current literature and selection of SNPs for future studies." The international journal of neuropsychopharmacology vol. 11,5 (2008): 701-21. doi: https://doi.org/10.1017/S1461145707008218
Drago A, Ronchi DD, Serretti A. 5-HT1A gene variants and psychiatric disorders: a review of current literature and selection of SNPs for future studies. Int J Neuropsychopharmacol. 2008 Aug;11(5):701-21. doi: 10.1017/S1461145707008218. Epub 2007 Nov 30. PMID: 18047755.
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Genetic aspects of intervertebral disc degeneration.

Reviews in the neurosciences

Hanaei S, Abdollahzade S, Khoshnevisan A, Kepler CK, Rezaei N.
PMID: 25996483
Rev Neurosci. 2015;26(5):581-606. doi: 10.1515/revneuro-2014-0077.

Intervertebral disc degeneration (IVDD) is one of the common causes of low back pain. Similar to many other multifactorial diseases, it is affected by environmental and genetic factors. Although not completely understood, genetic factors include a wide spectrum of...

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Hanaei S, Abdollahzade S, Khoshnevisan A, et al. Genetic aspects of intervertebral disc degeneration. Rev Neurosci. 2015;26(5):581-606doi: 10.1515/revneuro-2014-0077.
Hanaei, S., Abdollahzade, S., Khoshnevisan, A., Kepler, C. K., & Rezaei, N. (2015). Genetic aspects of intervertebral disc degeneration. Reviews in the neurosciences, 26(5), 581-606. https://doi.org/10.1515/revneuro-2014-0077
Hanaei, Sara, et al. "Genetic aspects of intervertebral disc degeneration." Reviews in the neurosciences vol. 26,5 (2015): 581-606. doi: https://doi.org/10.1515/revneuro-2014-0077
Hanaei S, Abdollahzade S, Khoshnevisan A, Kepler CK, Rezaei N. Genetic aspects of intervertebral disc degeneration. Rev Neurosci. 2015;26(5):581-606. doi: 10.1515/revneuro-2014-0077. PMID: 25996483.
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Associations of Polymorphisms in mir-196a2, mir-146a and mir-149 with Colorectal Cancer Risk: A Meta-Analysis.

Pathology oncology research : POR

Xu L, Tang W.
PMID: 26208586
Pathol Oncol Res. 2016 Apr;22(2):261-7. doi: 10.1007/s12253-014-9843-1. Epub 2015 Jul 26.

MicroRNAs (miRNAs) are non-coding RNAs which act as tumor suppressors or oncogenes. And single nucleotide polymorphism (SNP) in miRNA regions is one type of genetic variations in human genome. Various studies have investigated the associations of miRNAs SNP and...

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Xu L, Tang W. Associations of Polymorphisms in mir-196a2, mir-146a and mir-149 with Colorectal Cancer Risk: A Meta-Analysis. Pathol Oncol Res. 2015;22(2):261-7doi: 10.1007/s12253-014-9843-1.
Xu, L., & Tang, W. (2016). Associations of Polymorphisms in mir-196a2, mir-146a and mir-149 with Colorectal Cancer Risk: A Meta-Analysis. Pathology oncology research : POR, 22(2), 261-7. https://doi.org/10.1007/s12253-014-9843-1
Xu, Liping, and Tang, Wenru. "Associations of Polymorphisms in mir-196a2, mir-146a and mir-149 with Colorectal Cancer Risk: A Meta-Analysis." Pathology oncology research : POR vol. 22,2 (2016): 261-7. doi: https://doi.org/10.1007/s12253-014-9843-1
Xu L, Tang W. Associations of Polymorphisms in mir-196a2, mir-146a and mir-149 with Colorectal Cancer Risk: A Meta-Analysis. Pathol Oncol Res. 2016 Apr;22(2):261-7. doi: 10.1007/s12253-014-9843-1. Epub 2015 Jul 26. PMID: 26208586.
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Clinical uncertainty of prostate cancer genetic risk panels.

Science translational medicine

Pomerantz M, Freedman ML.
PMID: 23616119
Sci Transl Med. 2013 Apr 24;5(182):182ed6. doi: 10.1126/scitranslmed.3004696.

No abstract available.

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Pomerantz M, Freedman ML. Clinical uncertainty of prostate cancer genetic risk panels. Sci Transl Med. 2013;5(182):182ed6doi: 10.1126/scitranslmed.3004696.
Pomerantz, M., & Freedman, M. L. (2013). Clinical uncertainty of prostate cancer genetic risk panels. Science translational medicine, 5(182), 182ed6. https://doi.org/10.1126/scitranslmed.3004696
Pomerantz, Mark, and Freedman, Matthew L. "Clinical uncertainty of prostate cancer genetic risk panels." Science translational medicine vol. 5,182 (2013): 182ed6. doi: https://doi.org/10.1126/scitranslmed.3004696
Pomerantz M, Freedman ML. Clinical uncertainty of prostate cancer genetic risk panels. Sci Transl Med. 2013 Apr 24;5(182):182ed6. doi: 10.1126/scitranslmed.3004696. PMID: 23616119.
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Genome-Wide Association Study Identifies Genetic Risk Factors for Spastic Cerebral Palsy.

Neurosurgery

Hale AT, Akinnusotu O, He J, Wang J, Hibshman N, Shannon CN, Naftel RP.
PMID: 34098570
Neurosurgery. 2021 Aug 16;89(3):435-442. doi: 10.1093/neuros/nyab184.

BACKGROUND: Although many clinical risk factors of spastic cerebral palsy (CP) have been identified, the genetic basis of spastic CP is largely unknown. Here, using whole-genome genetic information linked to a deidentified electronic health record (BioVU) with replication in...

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Hale AT, Akinnusotu O, He J, et al. Genome-Wide Association Study Identifies Genetic Risk Factors for Spastic Cerebral Palsy. Neurosurgery. 2021;89(3):435-442doi: 10.1093/neuros/nyab184.
Hale, A. T., Akinnusotu, O., He, J., Wang, J., Hibshman, N., Shannon, C. N., & Naftel, R. P. (2021). Genome-Wide Association Study Identifies Genetic Risk Factors for Spastic Cerebral Palsy. Neurosurgery, 89(3), 435-442. https://doi.org/10.1093/neuros/nyab184
Hale, Andrew T, et al. "Genome-Wide Association Study Identifies Genetic Risk Factors for Spastic Cerebral Palsy." Neurosurgery vol. 89,3 (2021): 435-442. doi: https://doi.org/10.1093/neuros/nyab184
Hale AT, Akinnusotu O, He J, Wang J, Hibshman N, Shannon CN, Naftel RP. Genome-Wide Association Study Identifies Genetic Risk Factors for Spastic Cerebral Palsy. Neurosurgery. 2021 Aug 16;89(3):435-442. doi: 10.1093/neuros/nyab184. PMID: 34098570; PMCID: PMC8364821.
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Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank.

Diabetologia

Fall T, Gustafsson S, Orho-Melander M, Ingelsson E.
PMID: 30003307
Diabetologia. 2018 Oct;61(10):2174-2179. doi: 10.1007/s00125-018-4686-z. Epub 2018 Jul 12.

AIMS/HYPOTHESIS: Coronary artery disease (CAD) is a common complication among individuals with diabetes. A better understanding of the genetic background of CAD in this population has the potential to suggest novel molecular targets for screening, risk assessment and drug...

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Fall T, Gustafsson S, Orho-Melander M, et al. Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank. Diabetologia. 2018;61(10):2174-2179doi: 10.1007/s00125-018-4686-z.
Fall, T., Gustafsson, S., Orho-Melander, M., & Ingelsson, E. (2018). Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank. Diabetologia, 61(10), 2174-2179. https://doi.org/10.1007/s00125-018-4686-z
Fall, Tove, et al. "Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank." Diabetologia vol. 61,10 (2018): 2174-2179. doi: https://doi.org/10.1007/s00125-018-4686-z
Fall T, Gustafsson S, Orho-Melander M, Ingelsson E. Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank. Diabetologia. 2018 Oct;61(10):2174-2179. doi: 10.1007/s00125-018-4686-z. Epub 2018 Jul 12. PMID: 30003307; PMCID: PMC6133153.
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Genetically proxied morning chronotype was associated with a reduced risk of prostate cancer.

Sleep

Sun X, Ye D, Jiang M, Qian Y, Mao Y.
PMID: 33878190
Sleep. 2021 Oct 11;44(10). doi: 10.1093/sleep/zsab104.

STUDY OBJECTIVES: Observational epidemiological studies have suggested that chronotype may play a role in the pathogenesis and progression of prostate cancer. However, whether there is a causal association remains unknown. The aim of the present study was to examine...

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Sun X, Ye D, Jiang M, et al. Genetically proxied morning chronotype was associated with a reduced risk of prostate cancer. Sleep. 2021;44(10)doi: 10.1093/sleep/zsab104.
Sun, X., Ye, D., Jiang, M., Qian, Y., & Mao, Y. (2021). Genetically proxied morning chronotype was associated with a reduced risk of prostate cancer. Sleep, 44(10), . https://doi.org/10.1093/sleep/zsab104
Sun, Xiaohui, et al. "Genetically proxied morning chronotype was associated with a reduced risk of prostate cancer." Sleep vol. 44,10 (2021). doi: https://doi.org/10.1093/sleep/zsab104
Sun X, Ye D, Jiang M, Qian Y, Mao Y. Genetically proxied morning chronotype was associated with a reduced risk of prostate cancer. Sleep. 2021 Oct 11;44(10). doi: 10.1093/sleep/zsab104. PMID: 33878190.
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Next steps in the identification of gene targets for type 1 diabetes.

Diabetologia

Grant SFA, Wells AD, Rich SS.
PMID: 32797243
Diabetologia. 2020 Nov;63(11):2260-2269. doi: 10.1007/s00125-020-05248-8. Epub 2020 Aug 14.

The purpose of this review is to provide a view of the future of genomics and other omics approaches in defining the genetic contribution to all stages of risk of type 1 diabetes and the functional impact and clinical...

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Grant SFA, Wells AD, Rich SS. Next steps in the identification of gene targets for type 1 diabetes. Diabetologia. 2020;63(11):2260-2269doi: 10.1007/s00125-020-05248-8.
Grant, S. F. A., Wells, A. D., & Rich, S. S. (2020). Next steps in the identification of gene targets for type 1 diabetes. Diabetologia, 63(11), 2260-2269. https://doi.org/10.1007/s00125-020-05248-8
Grant, Struan F A, et al. "Next steps in the identification of gene targets for type 1 diabetes." Diabetologia vol. 63,11 (2020): 2260-2269. doi: https://doi.org/10.1007/s00125-020-05248-8
Grant SFA, Wells AD, Rich SS. Next steps in the identification of gene targets for type 1 diabetes. Diabetologia. 2020 Nov;63(11):2260-2269. doi: 10.1007/s00125-020-05248-8. Epub 2020 Aug 14. PMID: 32797243; PMCID: PMC7527360.
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A comprehensive in Silico analysis of the functional and structural impact of single nucleotide polymorphisms (SNPs) in the human IL-33 gene.

Computational biology and chemistry

Falahi S, Karaji AG, Koohyanizadeh F, Rezaiemanesh A, Salari F.
PMID: 34455166
Comput Biol Chem. 2021 Oct;94:107560. doi: 10.1016/j.compbiolchem.2021.107560. Epub 2021 Aug 16.

Interleukin 33 (IL-33) is the latest member of the IL-1 cytokine family, which plays both pro - and anti-inflammatory functions. Numerous Single-nucleotide polymorphisms (SNPs) in the IL-33 gene have been recognized to be associated with a vast variety of...

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Falahi S, Karaji AG, Koohyanizadeh F, et al. A comprehensive in Silico analysis of the functional and structural impact of single nucleotide polymorphisms (SNPs) in the human IL-33 gene. Comput Biol Chem. 2021;94:107560doi: 10.1016/j.compbiolchem.2021.107560.
Falahi, S., Karaji, A. G., Koohyanizadeh, F., Rezaiemanesh, A., & Salari, F. (2021). A comprehensive in Silico analysis of the functional and structural impact of single nucleotide polymorphisms (SNPs) in the human IL-33 gene. Computational biology and chemistry, 94107560. https://doi.org/10.1016/j.compbiolchem.2021.107560
Falahi, Sara, et al. "A comprehensive in Silico analysis of the functional and structural impact of single nucleotide polymorphisms (SNPs) in the human IL-33 gene." Computational biology and chemistry vol. 94 (2021): 107560. doi: https://doi.org/10.1016/j.compbiolchem.2021.107560
Falahi S, Karaji AG, Koohyanizadeh F, Rezaiemanesh A, Salari F. A comprehensive in Silico analysis of the functional and structural impact of single nucleotide polymorphisms (SNPs) in the human IL-33 gene. Comput Biol Chem. 2021 Oct;94:107560. doi: 10.1016/j.compbiolchem.2021.107560. Epub 2021 Aug 16. PMID: 34455166.
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Sample size in pilot genetic studies.

Clinical and translational science

Hyslop T.
PMID: 20443841
Clin Transl Sci. 2008 Sep;1(2):162. doi: 10.1111/j.1752-8062.2008.00042.x.

No abstract available.

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Hyslop T. Sample size in pilot genetic studies. Clin Transl Sci. 2008;1(2):162doi: 10.1111/j.1752-8062.2008.00042.x.
Hyslop, T. (2008). Sample size in pilot genetic studies. Clinical and translational science, 1(2), 162. https://doi.org/10.1111/j.1752-8062.2008.00042.x
Hyslop, Terry. "Sample size in pilot genetic studies." Clinical and translational science vol. 1,2 (2008): 162. doi: https://doi.org/10.1111/j.1752-8062.2008.00042.x
Hyslop T. Sample size in pilot genetic studies. Clin Transl Sci. 2008 Sep;1(2):162. doi: 10.1111/j.1752-8062.2008.00042.x. PMID: 20443841; PMCID: PMC5439550.
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Chronic kidney disease: the "perfect storm" of cardiometabolic risk illuminates genetic diathesis in cardiovascular disease.

Journal of the American College of Cardiology

Towler DA.
PMID: 23727212
J Am Coll Cardiol. 2013 Aug 27;62(9):799-801. doi: 10.1016/j.jacc.2013.04.063. Epub 2013 May 29.

No abstract available.

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Towler DA. Chronic kidney disease: the "perfect storm" of cardiometabolic risk illuminates genetic diathesis in cardiovascular disease. J Am Coll Cardiol. 2013;62(9):799-801doi: 10.1016/j.jacc.2013.04.063.
Towler, D. A. (2013). Chronic kidney disease: the "perfect storm" of cardiometabolic risk illuminates genetic diathesis in cardiovascular disease. Journal of the American College of Cardiology, 62(9), 799-801. https://doi.org/10.1016/j.jacc.2013.04.063
Towler, Dwight A. "Chronic kidney disease: the "perfect storm" of cardiometabolic risk illuminates genetic diathesis in cardiovascular disease." Journal of the American College of Cardiology vol. 62,9 (2013): 799-801. doi: https://doi.org/10.1016/j.jacc.2013.04.063
Towler DA. Chronic kidney disease: the "perfect storm" of cardiometabolic risk illuminates genetic diathesis in cardiovascular disease. J Am Coll Cardiol. 2013 Aug 27;62(9):799-801. doi: 10.1016/j.jacc.2013.04.063. Epub 2013 May 29. PMID: 23727212; PMCID: PMC3837500.
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Showing 25 to 36 of 87 entries