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Artykuły w czasopismach na temat "Genetic risk factors"

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Tuma, Rabiya. "Genetic risk factors." Oncology Times 4, no. 6 (2007): 8. http://dx.doi.org/10.1097/01434893-200706000-00012.

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Sawikr, Yousef, Khlid G. ALqathafy, and Ibrahim S. Ibrahem. "Biochemical Markers and Genetic Risk Factors in Alzheimer's Disease." International Journal of Research Publication and Reviews 4, no. 12 (2023): 890–93. http://dx.doi.org/10.55248/gengpi.4.1223.123328.

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Pullicino, Patrick, Steven Greenberg, and Maurizio Trevisan. "Genetic stroke risk factors." Current Opinion in Neurology 10, no. 1 (1997): 58–63. http://dx.doi.org/10.1097/00019052-199702000-00012.

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Fung, Jenny N., Yadav Sapkota, Dale R. Nyholt, and Grant W. Montgomery. "Genetic Risk Factors for Endometriosis." Journal of Endometriosis and Pelvic Pain Disorders 9, no. 2 (2017): 69–76. http://dx.doi.org/10.5301/je.5000273.

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Advances in genetics and genomics are driving progress in understanding genetic risk factors for endometriosis. Genome-wide association scans (GWAS) in endometriosis have identified 11 genomic regions associated with increased risk of disease. Many of the regions contain interesting candidate genes, but the risk alleles may not always act through the obvious candidates. Functional evidence to identify the causal gene(s) will require multiple steps including better mapping precision, genetic studies on gene expression and epigenetic marks, chromatin looping and functional studies. Evidence from
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Roberts, Robert. "Molecular genetics: Cardiac disease and risk-related genes-Genetic risk factors." Clinical Cardiology 18, S4 (1995): IV13—IV19. http://dx.doi.org/10.1002/clc.4960181604.

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Cardno, A. G., M. C. O’Donovan, and M. J. Owen. "Genetic Risk Factors for Schizophrenia." International Journal of Mental Health 29, no. 3 (2000): 13–38. http://dx.doi.org/10.1080/00207411.2000.11449495.

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Yamada, Kazuo, and Masayasu Matsumoto. "Genetic Risk Factors of Stroke." Nosotchu 29, no. 6 (2007): 711. http://dx.doi.org/10.3995/jstroke.29.711.

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Montagnana, Martina, Elisa Danese, and Giuseppe Lippi. "Genetic risk factors of atherothrombosis." Polish Archives of Internal Medicine 124, no. 9 (2014): 474–82. http://dx.doi.org/10.20452/pamw.2409.

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Reitsma, Pieter H. "Genetic Risk Factors of Thrombosis." Blood 114, no. 22 (2009): SCI—43—SCI—43. http://dx.doi.org/10.1182/blood.v114.22.sci-43.sci-43.

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Abstract Abstract SCI-43 Venous thrombosis is a common episodic disease with a steep age gradient. Interactions between various risk factors determine the development of the disease, and the proportion of variance attributable to genetic factors may be as high as 50-60%. There are six (moderately) strong genetic risk factors. First there are heterozygous deficiencies of the natural anticoagulants protein C, protein S, and antithrombin. These deficiency states are quite rare in the general population (in all races) and their genetic architecture is complex with hundreds of documented mutations.
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Theile, M., H. Krause, L. Luebbe, M. Strauss, U. Kiessling, and E. Geissler. "Papovaviruses, possible genetic risk factors." Mutation Research/Environmental Mutagenesis and Related Subjects 147, no. 5 (1985): 324. http://dx.doi.org/10.1016/0165-1161(85)90216-x.

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Rozprawy doktorskie na temat "Genetic risk factors"

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Kelempisioti, A. (Anthi). "Genetic risk factors for intervertebral disc degeneration." Doctoral thesis, Oulun yliopisto, 2016. http://urn.fi/urn:isbn:9789526211350.

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Abstract Low back pain (LBP) is the leading cause of years lived with disabilities worldwide. Intervertebral disc (IVD) degeneration is a strong contributing factor to LBP. Recent studies have shown that genetic determinants contribute markedly to IVD degeneration but knowledge about the actual genes involved as well as their roles is still limited. The aim of this thesis work was to study genetic factors that may predispose to IVD degeneration. Using both family and case-control association study designs, variants in five genes showed association with IVD degeneration on magnetic resonance im
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Tilley, Louise. "Genetic risk factors in sporadic Alzheimer's disease." Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311748.

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Al-Chalabi, Ammar. "Genetic risk factors in amytrophic lateral sclerosis." Thesis, King's College London (University of London), 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321934.

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Burger, Marilize Cornelle. "Genetic risk factors for carpal tunnel syndrome." Doctoral thesis, University of Cape Town, 2014. http://hdl.handle.net/11427/12714.

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Includes bibliographical references.<br>Carpal tunnel syndrome (CTS) is a common occupational injury that is caused by an increase in pressure within the carpal tunnel structure which, in turn, causes compression of the median nerve. Although several factors are believed to be associated with increased risk of CTS, the direct causes of this injury remain unknown and it is generally accepted that CTS, with the exception of acutely caused CTS, is a multifactorial condition. Although it is generally accepted that an increase in pressure within the carpal tunnel structure, which contains nine flex
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Abelson, Anna-Karin. "Genetic Risk Factors for Systemic Lupus Erythematosus : From Candidate Genes to Functional Variants." Doctoral thesis, Uppsala : Universitetsbiblioteket [distributör], 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-9367.

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Beskow, Anna. "Genetic Risk Factors for Cervical Carcinoma in situ." Doctoral thesis, Uppsala universitet, Institutionen för genetik och patologi, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3318.

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Oncogenic human papillomaviruses (HPVs) are implicated in 99.7 % of cervical cancer cases but require the co-operation of other factors. To investigate potential genetic risk factors we have typed the HLA class II DRB1 and DQB1 loci in 478 women diagnosed with cervical carcinoma in situ and in 608 age-matched controls. Quantitative measurements of HPV 16, HPV 18/45 and HPV 31 were obtained. The DRB1*1501 and DQB1*0602 alleles were found to increase the risk of HPV 16 infection. Carriers of DRB1*1501 and DQB1*0602 were also shown to have an increased risk of a higher viral load compared to non
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Mayosi, B. M. "Genetic determination of cardiovascular risk factors in families." Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249502.

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Maude, Sophia Karen. "An investigation of genetic risk factors for migraine." Thesis, University of Aberdeen, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248576.

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Migraine manifests itself episodically with incidence ranging from one attack in a lifetime to one almost every day. Most migraineurs suffer from typical migraine with or without aura, that is inherited in a complex manner. A small number of migraineurs suffer from FHM, a condition that exhibits Mendelian inheritance. BFNC is another rare episodic disorder that exhibits Mendelian inheritance. In a four generational family the BFNC phenotype was linked to the KCNQ2 gene on chromosome 20q13.3. Blood samples and epidemiological information were collected from 214 migraine probands in the Grampian
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Posthumus, Michael. "Genetic risk factors for anterior cruciate ligament ruptures." Doctoral thesis, University of Cape Town, 2009. http://hdl.handle.net/11427/3195.

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Includes abstract.<br>Includes bibliographical references (p. 197-215).<br>The primary aim of this thesis was to identify candidate genes that may be associated with ACL ruptures, and then use a genetic association approach following a case-control study design to identify specific sequence variants (single nucleotide polymorphisms, SNPs) within these candidate genes which may predispose individuals to ACL ruptures. Candidate genes (COL1A1, COL5A1 and COL12A1) were selected based on the biological function of their encoded proteins (type I, type V and type XII collagen respectively) within the
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Hughes, Katherine Carlson. "Dietary and Genetic Risk Factors for Parkinson's Disease." Thesis, Harvard University, 2016. http://nrs.harvard.edu/urn-3:HUL.InstRepos:27201728.

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Parkinson’s disease (PD) is the second most common neurodegenerative disease. Motor symptoms typically do not manifest until significant neuronal loss has already occurred, highlighting the need for early detection and prevention. In this dissertation, we sought to improve our understanding of PD epidemiology by studying associations between potential modifiable risk factors, including antioxidant vitamins, dairy products, and urate, and PD risk. We conducted prospective analyses within three large cohort studies: the Nurses’ Health Study, the Health Professionals Follow-up Study, and the Canc
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Książki na temat "Genetic risk factors"

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1946-, Choy Wai Nang, ed. Genetic toxicology and cancer risk assessment. Marcel Dekker, 2001.

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David, Brusick, ed. Methods for genetic risk assessment. Lewis Publishers, 1994.

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Kåre, Berg, ed. Genetic approaches of coronary heart disease and hypertension. Springer-Verlag, 1991.

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National Institute on Alcohol Abuse and Alcoholism (U.S.) and Editorial Experts Inc, eds. Alcoholism, an inherited disease. U.S. Department of Health and Human Services, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, National Institute on Alcohol Abuse and Alcoholism, 1985.

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Petrakis, Peter L. Alcoholism, and inherited disease. U.S. Dept. of Health and Human Services, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, National Institute on Alcohol Abuse and Alcoholism, 1985.

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Offit, Kenneth. Clinical cancer genetics: Risk counseling and management. Wiley-Liss, 1998.

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A, Levin Morris, and Strauss Harlee S, eds. Risk assessment in genetic engineering. McGraw-Hill, 1991.

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Symposium on Phenotypic Variation in Populations: Relevance to Risk Assessment (1986 Brookhaven National Laboratory). Phenotypic variation in populations: Relevance to risk assessment. Plenum Press, 1988.

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1960-, Foulkes William D., and Hodgson S. V, eds. Inherited susceptibility to cancer: Clinical, predictive, and ethical perspectives. Cambridge University Press, 1998.

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Teichler-Zallen, Doris. To test or not to test: A guide to genetic screening and risk. Thorndike Press, 2009.

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Części książek na temat "Genetic risk factors"

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Thiriet, Marc. "Genetic Risk Factors." In Biomathematical and Biomechanical Modeling of the Circulatory and Ventilatory Systems. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-89315-0_7.

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Hetherington, J. "Genetic Risk Factors for Glaucoma." In Pathogenesis and Risk Factors of Glaucoma. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-60203-0_8.

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Hollingworth, Paul, and Julie Williams. "Genetic Risk Factors for Dementia." In The Handbook of Alzheimer's Disease and Other Dementias. Wiley-Blackwell, 2011. http://dx.doi.org/10.1002/9781444344110.ch6.

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Li, Donghui. "Risk Factors and Genetic Predisposition." In Pancreatic Cancer: A Multidisciplinary Approach. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05724-3_2.

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Spitz, Margaret R. "Risk factors and genetic susceptibility." In Head and Neck Cancer. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-2023-8_4.

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Waldinger, Marcel D. "Risks Factors in Premature Ejaculation: The Genetic Risk Factor." In Premature Ejaculation. Springer Milan, 2012. http://dx.doi.org/10.1007/978-88-470-2646-9_9.

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Berg, K. "Genetic Risk Factors for Atherosclerotic Disease." In Human Genetics. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71635-5_40.

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Combarros, Onofre. "Genetic Risk Factors for Alzheimer’s Disease." In Neurodegenerative Diseases. Springer London, 2014. http://dx.doi.org/10.1007/978-1-4471-6380-0_4.

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Tsang, Kin-Lun, Zhe-Hui Feng, Hong Jiang, Shu-Leong Ho, and David B. Ramsden. "Genetic Risk Factors in Parkinson’s Disease." In Mapping the Progress of Alzheimer’s and Parkinson’s Disease. Springer US, 2002. http://dx.doi.org/10.1007/978-0-306-47593-1_42.

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Baker, Jessica H., Lauren Janson, Sara E. Trace, and Cynthia M. Bulik. "Genetic Risk Factors for Eating Disorders." In The Wiley Handbook of Eating Disorders. John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118574089.ch28.

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Streszczenia konferencji na temat "Genetic risk factors"

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Petersen, Gloria M. "Abstract IA03: Genetic and non-genetic risk factors of pancreatic cancer." In Abstracts: AACR Special Conference on Pancreatic Cancer: Advances in Science and Clinical Care; May 12-15, 2016; Orlando, FL. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.panca16-ia03.

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Gamara, Rex Paolo C., Antipas T. Teologo, King Harold A. Recto, Romano Q. Neyra, and Argel A. Bandala. "Genetic Neural Network for Diabetes Likelihood Prediction Using Risk Factors." In 2023 IEEE 15th International Conference on Humanoid, Nanotechnology, Information Technology, Communication and Control, Environment, and Management (HNICEM). IEEE, 2023. http://dx.doi.org/10.1109/hnicem60674.2023.10589131.

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Francis-Lyon, Patricia, Shashank Belvadi, and Fu-Yuan Cheng. "Detection and characterization of interactions of genetic risk factors in disease." In Python in Science Conference. SciPy, 2013. http://dx.doi.org/10.25080/majora-8b375195-007.

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Cimino, Silvia. "Genetic Factors In Families: Parental Psychopathological Risk And Offspring’s Develompmental Oucomes." In 11th International Conference on Education and Educational Psychology. European Publisher, 2020. http://dx.doi.org/10.15405/epiceepsy.20111.35.

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Hernandez Cordero, A. I., X. Li, S. Milne, et al. "Integrative Genomic Analysis Highlights Potential Genetic Risk Factors for Covid-19." In American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a3765.

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Fialkovska, Anastasiia, and Svetlana Ilchenko. "The genetic risk factors for developing chronic bronchitis in adolescent smokers." In ERS International Congress 2019 abstracts. European Respiratory Society, 2019. http://dx.doi.org/10.1183/13993003.congress-2019.pa5387.

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Gunther, Max L., James C. Jackson, Pratik Pandharipande, et al. "Genetic Risk Factors For Long-Term Cognitive Impairment After Critical Illness." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a6718.

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Xu, Yu, Chonghao Wang, Zeming Li, et al. "A machine learning model for disease risk prediction by integrating genetic and non-genetic factors." In 2022 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2022. http://dx.doi.org/10.1109/bibm55620.2022.9994925.

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Guy, Attia, Levinberg Roee, Arad Erez, Ilan Davidov, and Ludmila Sidorenko. "New Biotechnological Opportunities to Assess the Influence of Lifestyle Factors in Obesity." In 12th International Conference on Electronics, Communications and Computing. Technical University of Moldova, 2022. http://dx.doi.org/10.52326/ic-ecco.2022/bme.05.

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Background. Obesity results from a malfunction of the body's weight-control mechanisms, which may be influenced by environmental changes. Essentially, the obesity risk relies on two significant interdependent factors: genetic variations (single-nucleotide polymorphisms, haplotypes) and environmental risk exposure. Due to new biotechnologies over 127 potential genes for obesity have been identified, and evidence supports the function of 22 genes in at least five distinct groups. Gene and environment interactions mean that the synergy between genotype and environment is neither additive or multi
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Zhang, Zhu, Zhaoman Wan, Mingming Su, Haobo Li, and Zhenguo Zhai. "Genetic Insights through Chinese VTE Pedigree Interpretation Using the ACMG Method: Unraveling Potencial Genetic Risk Factors." In ERS Congress 2024 abstracts. European Respiratory Society, 2024. http://dx.doi.org/10.1183/13993003.congress-2024.oa5557.

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Raporty organizacyjne na temat "Genetic risk factors"

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Sarma, Aruna. Genetic and Hormonal Risk Factors for Cancer in African American Men. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada455088.

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Mack, Thomas M. Genetic Abnormalities in Breast Cancer Tumors and Relationships to Environmental and Genetic Risk Factors Using Twins. Defense Technical Information Center, 1995. http://dx.doi.org/10.21236/ada303152.

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Mack, Thomas M. Genetic Abnormalities in Breast Cancer Tumors and Relationships to environmental and Genetic Risk Factors Using Twins. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada393066.

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Sarma, Aruna V. Genetic and Hormonal Risk Factors for Prostate Cancer in African American Men. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada442683.

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Cao, Xianling, Xuanyou Zhou, Naixin Xu, Songchang Chang, and Chenming Xu. Association of IL-4 and IL-10 Polymorphisms with Preterm Birth Susceptibility: A Systematic Review and Meta-Analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.4.0044.

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Review question / Objective: The aim of our systematic review and meta-analysis was to summarize the effects of IL-4 and IL-10 gene polymorphism and clarify their possible association with PTB. Condition being studied: World Health Organization (WHO) defines preterm birth (PTB) as babies born alive before 37 weeks of pregnancy are completed. The new estimates show that the prevalence of PTB during 2014 ranged from 8.7% to13.4% of all live births, about 15 million preterm babies born each year. Besides, PTB is the leading cause of death worldwide for children below 5 years of age. Babies born p
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Gelmann, Edward P. Genetic Risk Factor for Prostate Cancer. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada434784.

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Gelmann, Edward P. Genetic Risk Factor for Prostate Cancer. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada414867.

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Seale, Maria, Natàlia Garcia-Reyero, R. Salter, and Alicia Ruvinsky. An epigenetic modeling approach for adaptive prognostics of engineered systems. Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/11681/41282.

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Prognostics and health management (PHM) frameworks are widely used in engineered systems, such as manufacturing equipment, aircraft, and vehicles, to improve reliability, maintainability, and safety. Prognostic information for impending failures and remaining useful life is essential to inform decision-making by enabling cost versus risk estimates of maintenance actions. These estimates are generally provided by physics-based or data-driven models developed on historical information. Although current models provide some predictive capabilities, the ability to represent individualized dynamic f
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Gelmann, Edward P. Genetics Risk Factor for Prostate Cancer. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada422932.

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Wongpiyabovorn, Jongkonnee, Nattiya Hirankarn, Yingyos Avihingsanon, Tewin Tencomnao, Yong Poovorawan, and Kriangsak Ruchusatsawat. The association between immunogenetics and genetic susceptibility of psoriasis in Thai population. Chulalongkorn University, 2006. https://doi.org/10.58837/chula.res.2006.27.

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Psoriasis is T-cell-mediated skin autoimmunity, required environmental triggers and genetic susceptibility factors to become manifested. Psoriasis is a chronic skin disease characterized by the abnormal hyperproliferation and differentiation of the epidermis, elongated and prominent blood vessels and a thick perivascular lymphocytic infiltrate. Vascular endothelial growth factor (VEGF) gene play important role in pathogenesis of various diseases with angiogenic basis such as breast cancer and autoimmune disease including psoriasis. Many studies analyzed the association of VEGF gene polymorphis
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