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Auswahl der wissenschaftlichen Literatur zum Thema „Risk variants“
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Zeitschriftenartikel zum Thema "Risk variants"
Han, Shengtong. „Bayesian Rare Variant Analysis Identifies Novel Schizophrenia Putative Risk Genes“. Journal of Personalized Medicine 14, Nr. 8 (02.08.2024): 822. http://dx.doi.org/10.3390/jpm14080822.
Der volle Inhalt der QuelleShah, Shrijal S., Herbert Lannon, Leny Dias, Jia-Yue Zhang, Seth L. Alper, Martin R. Pollak und David J. Friedman. „APOL1 Kidney Risk Variants Induce Cell Death via Mitochondrial Translocation and Opening of the Mitochondrial Permeability Transition Pore“. Journal of the American Society of Nephrology 30, Nr. 12 (26.09.2019): 2355–68. http://dx.doi.org/10.1681/asn.2019020114.
Der volle Inhalt der QuelleBayley, Jean Pierre, Birke Bausch, Johannes Adriaan Rijken, Leonie Theresia van Hulsteijn, Jeroen C. Jansen, David Ascher, Douglas Eduardo Valente Pires et al. „Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma–paraganglioma“. Journal of Medical Genetics 57, Nr. 2 (06.09.2019): 96–103. http://dx.doi.org/10.1136/jmedgenet-2019-106214.
Der volle Inhalt der QuellePark, Jihye, Soo Youn Lee, Su Youn Baik, Chan Hee Park, Jun Hee Yoon, Brian Y. Ryu und Ju Han Kim. „Gene-Wise Burden of Coding Variants Correlates to Noncoding Pharmacogenetic Risk Variants“. International Journal of Molecular Sciences 21, Nr. 9 (27.04.2020): 3091. http://dx.doi.org/10.3390/ijms21093091.
Der volle Inhalt der QuelleBarbirou, Mouadh, Amanda A. Miller, Amel Mezlini, Balkiss Bouhaouala-Zahar und Peter J. Tonellato. „Variant Characterization of a Representative Large Pedigree Suggests “Variant Risk Clusters” Convey Varying Predisposition of Risk to Lynch Syndrome“. Cancers 15, Nr. 16 (12.08.2023): 4074. http://dx.doi.org/10.3390/cancers15164074.
Der volle Inhalt der QuelleCannon-Albright, Lisa Anne, Craig Carl Teerlink, Jeff Stevens, Franklin W. Huang, Csilla Sipeky, Johanna Schleutker, Rolando Hernandez, Julio Facelli, Neeraj Agarwal und Donald L. Trump. „A Rare Variant in ERF (rs144812092) Predisposes to Prostate and Bladder Cancers in an Extended Pedigree“. Cancers 13, Nr. 10 (15.05.2021): 2399. http://dx.doi.org/10.3390/cancers13102399.
Der volle Inhalt der QuelleBoddicker, Nicholas J., Raphael Mwangi, Dennis P. Robinson, Allison C. Rosenthal, Thomas M. Habermann, Andrew L. Feldman, Lisa M. Rimsza et al. „Abstract 5233: Germline CHEK2 variants and risk of lymphoma“. Cancer Research 83, Nr. 7_Supplement (04.04.2023): 5233. http://dx.doi.org/10.1158/1538-7445.am2023-5233.
Der volle Inhalt der QuelleAment, Seth A., Szabolcs Szelinger, Gustavo Glusman, Justin Ashworth, Liping Hou, Nirmala Akula, Tatyana Shekhtman et al. „Rare variants in neuronal excitability genes influence risk for bipolar disorder“. Proceedings of the National Academy of Sciences 112, Nr. 11 (17.02.2015): 3576–81. http://dx.doi.org/10.1073/pnas.1424958112.
Der volle Inhalt der QuelleTu, J. J., L. Kuhn, L. Denny, K. J. Beattie, A. Lorincz und T. C. Wright. „Molecular variants of human papillomavirus type 16 and risk for cervical neoplasia in South Africa“. International Journal of Gynecologic Cancer 16, Nr. 2 (März 2006): 736–42. http://dx.doi.org/10.1136/ijgc-00009577-200603000-00043.
Der volle Inhalt der QuelleVogan, Kyle. „Bladder exstrophy risk variants“. Nature Genetics 47, Nr. 5 (28.04.2015): 429. http://dx.doi.org/10.1038/ng.3298.
Der volle Inhalt der QuelleDissertationen zum Thema "Risk variants"
Dubois, Patrick Charles Alexander. „Genetic risk variants in intestinal inflammatory disorders“. Thesis, Queen Mary, University of London, 2010. http://qmro.qmul.ac.uk/xmlui/handle/123456789/704.
Der volle Inhalt der QuelleWinton, Helen Louise. „Inflammation related genetic variants in high risk corneal transplantation“. Thesis, University of Bristol, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617796.
Der volle Inhalt der QuelleCameli, Cinzia <1988>. „Investigation of genetic risk variants for nicotine dependence and cluster headache“. Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2016. http://amsdottorato.unibo.it/8583/1/Cinzia_Cameli_PhD_Thesis.pdf.
Der volle Inhalt der QuelleZhao, Jing. „Rare and common genetic variant associations with quantitative human phenotypes“. Diss., Georgia Institute of Technology, 2015. http://hdl.handle.net/1853/53923.
Der volle Inhalt der QuelleSong, Ci, Nancy L. Pedersen, Chandra A. Reynolds, Maria Sabater-Lleal, Stavroula Kanoni, Christina Willenborg, Ann-Christine Syvänen et al. „Genetic Variants from Lipid-Related Pathways and Risk for Incident Myocardial Infarction“. Uppsala universitet, Molekylär medicin, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-200108.
Der volle Inhalt der QuelleEggert, Stacey Lynn. „Identification and Characterization of Genetic Variants Conveying Risk to Develop Uterine Leiomyomata“. Thesis, Harvard University, 2011. http://dissertations.umi.com/gsas.harvard:10005.
Der volle Inhalt der QuelleWest, S. L. „The search for genetic variants that influence the risk of colorectal cancer“. Thesis, University College London (University of London), 2011. http://discovery.ucl.ac.uk/1302552/.
Der volle Inhalt der QuelleHamdi, Yosr. „Evaluation of the association between common genetic variants and breast cancer risk“. Doctoral thesis, Université Laval, 2017. http://hdl.handle.net/20.500.11794/28384.
Der volle Inhalt der QuelleBreast cancer is the most common malignancy in women. A set of environmental and genetic factors are involved in this complex disease. This project focused on the genetic components of breast cancer susceptibility and breast cancer risk modification in BRCA1 and BRCA2 mutation carriers. Currently, about half of the inherited susceptibility to breast cancer can be imputed to a combination of high-, intermediate-, and low-risk alleles. Thus, many as yet unknown susceptibility loci remain to be identified. Moreover, recent studies have provided evidence for the involvement of genetic risk factors that might considerably modify the risk of developing breast cancer in BRCA1 and BRCA2 mutation carriers. Furthermore, genome-wide association studies have shown that several genetic variants within non-coding gene regions are associated with breast cancer risk. In this project, we focused on regulatory gene variants and their association with breast cancer risk. The project was divided in two parts. In the first section, we evaluated the direct association between single-nucleotide polymorphisms associated with differential allelic expression and breast cancer risk in order to identify new loci of breast cancer susceptibility. In the second part, we evaluated the functional impact on gene expression of variants identified within the promoter regions of selected candidate genes and then, characterize the functional impact of these variants. In summary, the first part of this project has led to the identification of a new low-penetrance locus associated with breast cancer risk on the 4q21 locus (rs11099601; odds ratio=1.05, p= 6.4 x 10-6), and two new modifiers of breast cancer risk in BRCA1 mutations carriers (11q22.3 locus and the wild type allele of BRCA1). The second part of the project allowed us to describe new functional variants within the promoters of the selected breast cancer gene candidates. Other association studies in larger cohorts and further functional analysis will be required to confirm these results, which will allow their inclusion in breast cancer risk prediction tools and thus ensure a more accurate estimation of breast cancer risk.
Soemedi, Rachel. „Contribution of copy number variants to the risk of sporadic congenital heart disease“. Thesis, University of Newcastle Upon Tyne, 2012. http://hdl.handle.net/10443/1740.
Der volle Inhalt der QuelleKvaskoff, Marina. „Endometriosis and naevus-associated gene variants in relation to risk of cutaneous melanoma“. Paris 11, 2009. http://www.theses.fr/2009PA11T090.
Der volle Inhalt der QuelleBücher zum Thema "Risk variants"
Popkin, Ronna. Variants of Significance? The Production and Management of Genetic Risk for Breast and Ovarian Cancer in the Era of Multi-Gene Panel Testing. [New York, N.Y.?]: [publisher not identified], 2019.
Den vollen Inhalt der Quelle findenLajeri, Fatma. Risk aversion and prudence: The case of mean-variance preferences. Fontainebleau: INSEAD, 1993.
Den vollen Inhalt der Quelle findenMartin, Jolie Mae. Variance-seeking for positive (and variance-aversion for negative) experiences: Risk-seeking in the domain of gains? Boston]: Harvard Business School, 2008.
Den vollen Inhalt der Quelle findenCopeland, Laurence S. Inflation, interest rate risk and the variance of common stock prices. Manchester: Manchester Business School, 1986.
Den vollen Inhalt der Quelle findenO'Gorman, Aongus J. Mean-risk analysis: An examination of semivariance as an alternative to the traditional risk measure of variance. Dublin: University College Dublin, 1994.
Den vollen Inhalt der Quelle findenJohnson, D. G. The robustness of mean and variance approximations in pert and risk analysis. Loughborough, Leics: Loughborough University Business School, 1997.
Den vollen Inhalt der Quelle findenGeyer, Alois. Information, Erwartung und Risiko: Aspekte der Verteilung, Abhängigkeit und Varianz von finanzwirtschaftlichen Zeitreihen. München: VVF, 1992.
Den vollen Inhalt der Quelle findenHoldt, Lesca M., und Daniel Teupser. Genetic background of atherosclerosis and its risk factors. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656653.003.0002.
Der volle Inhalt der QuellePenney, Kathryn L., Kyriaki Michailidou, Deanna Alexis Carere, Chenan Zhang, Brandon Pierce, Sara Lindström und Peter Kraft. Genetic Epidemiology of Cancer. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0005.
Der volle Inhalt der QuelleMerriman, Tony R. The genetic basis of gout. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199668847.003.0040.
Der volle Inhalt der QuelleBuchteile zum Thema "Risk variants"
Pfeiffer, Ruth M., und Mitchell H. Gail. „Risk estimates based on genetic variants and family studies“. In Absolute Risk, 135–49. Boca Raton : Taylor & Francis, a CRC title, part of the Taylor & Francis imprint, a member of the Taylor & Francis Group, the academic division of T&F Informa plc, 2017. |: Chapman and Hall/CRC, 2017. http://dx.doi.org/10.1201/9781315117539-9.
Der volle Inhalt der QuelleSong, Yiqing, Cuilin Zhang, Lu Wang, Qi Dai und Simin Liu. „Magnesium Intake, Genetic Variants, and Diabetes Risk“. In Magnesium in Human Health and Disease, 103–18. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-044-1_6.
Der volle Inhalt der QuelleVelaga, Ravi, Masakazu Toi, Nobuko Kawaguchi-Sakita, John R. Benson und Noriko Senda. „Hereditary Breast Cancer and Pathogenic Germline Variants“. In Screening and Risk Reduction Strategies for Breast Cancer, 45–59. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-19-7630-8_3.
Der volle Inhalt der QuelleNegi, Archita, und Farshid Hajati. „Analysis of Variants of KNN for Disease Risk Prediction“. In Advanced Information Networking and Applications, 531–45. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-99619-2_50.
Der volle Inhalt der QuellePack, Allan I. „Evolving Approaches to Identifying Genetic Risk Variants for Sleep Disorders“. In Translational Medicine Research, 3–20. Dordrecht: Springer Netherlands, 2022. http://dx.doi.org/10.1007/978-94-024-2168-2_1.
Der volle Inhalt der QuelleMoustafa, Julia Sarah El-Sayed, und Philippe Froguel. „Copy Number Variants and Their Contribution to the Risk of Obesity“. In The Genetics of Obesity, 55–70. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-8642-8_4.
Der volle Inhalt der QuelleWortsman, Ximena, und Camila Ferreira-Wortsman. „Relevant Topographic Anatomy of the Head, Anatomical Variants, and Risk Zones“. In Textbook of Dermatologic Ultrasound, 101–29. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-08736-3_6.
Der volle Inhalt der QuelleSakr, Rita A., und Hassan Ghazal. „Genetic Testing for Cancer Risk in the UAE“. In Cancer Care in the United Arab Emirates, 235–43. Singapore: Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-99-6794-0_15.
Der volle Inhalt der QuelleDe Timmerman, Romeo, Anne-Sophie Bafort, Sofie Van de Geuchte, Mieke Vandenbroucke und Stef Slembrouck. „Chapter 5. Formulations of risk and responsibility in COVID-19 contact tracing telephone interactions in Flanders, Belgium“. In Risk Discourse and Responsibility, 118–41. Amsterdam: John Benjamins Publishing Company, 2023. http://dx.doi.org/10.1075/pbns.336.05det.
Der volle Inhalt der QuelleAnumba, Dilly OC, und Shamanthi M. Jayasooriya. „Prenatal Risk Assessment for Preterm Birth in Low-Resource Settings: Demographics and Obstetric History“. In Evidence Based Global Health Manual for Preterm Birth Risk Assessment, 15–23. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04462-5_3.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Risk variants"
Leung, Hareton K. N. „Variants of Risk and Opportunity“. In 2010 17th Asia Pacific Software Engineering Conference (APSEC). IEEE, 2010. http://dx.doi.org/10.1109/apsec.2010.52.
Der volle Inhalt der QuelleHunter, David J. „Prediction of disease risk using common genetic variants“. In AACR International Conference: Molecular Diagnostics in Cancer Therapeutic Development– Sep 27-30, 2010; Denver, CO. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/diag-10-pl5-2.
Der volle Inhalt der QuellePermuth-Wey, Jennifer, Ya-Yu Tsai, Y. Ann Chen, Zhihua Chen, Johnathan M. Lancaster, Edwin Iverson, Harvey Risch et al. „Abstract 2835: Mitochondrial genetic variants influence ovarian cancer risk“. In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-2835.
Der volle Inhalt der QuelleSchmitt, Robert, Bjorn Falk, Maximilian Russmann, Christian Brecher, Werner Herfs und Adam Malik. „Risk management across variants requirements and outlook for an efficient risk assessment of machines“. In 2015 First IEEE International Symposium on Systems Engineering (ISSE). IEEE, 2015. http://dx.doi.org/10.1109/syseng.2015.7302758.
Der volle Inhalt der QuelleDu, Mengmeng, Shuo Jiao, Stephanie A. Rosse, Manish Gala, Goncalo Abecasis, Stephane Bezieau, Hermann Brenner et al. „Abstract 2190: Fine-mapping of common genetic variants associated with colorectal tumor risk identified potential functional variants“. In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-2190.
Der volle Inhalt der QuelleKelemen, Linda E., Jonathan Tyrer, Catherine M. Phelan, Susan J. Ramus, Andrew Berchuck, Simon A. Gayther, Ellen L. Goode et al. „Abstract 3283: GWAS identifies risk variants for mucinous ovarian carcinoma“. In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-3283.
Der volle Inhalt der QuelleAndavolu, Radhika G., Jean-Luc Cardenas, Ross Shore, Zach Rubin, James MacMurray, Krishna Kanth Chiravuri, Murthy VS Andavolu und Svetlana Rubakovic. „Abstract 1932: Association of genetic variants with prostate cancer risk.“ In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-1932.
Der volle Inhalt der QuelleTingle, Sharna, Danielle Carrick, Sheri Schully, Mindy Clyne und Stefanie A. Nelson. „Abstract 5572: Tracking the functional analysis of cancer risk variants“. In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-5572.
Der volle Inhalt der QuelleCraig, Daniel J., Mazzin Elsamaloty, Thomas M. Blomquist, Erin L. Crawford und James C. Willey. „Abstract 2222: Using rare variants to characterize lung cancer risk“. In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-2222.
Der volle Inhalt der QuelleChiu, Kuo-Liang, Wen-Shin Chang, Chia-Wen Tsai, Mei-Chin Mong, Te-Chun Hsia und Da-Tian Bau. „MEG3 SNP variants are associated with the risk of asthma“. In ERS International Congress 2023 abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/13993003.congress-2023.pa2320.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Risk variants"
Chang, Bao-Li. Sequence Variants in Estrogen Receptors and Risk for Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, März 2004. http://dx.doi.org/10.21236/ada425852.
Der volle Inhalt der QuelleMurph, Leigh. The Estrogen Receptor and Its Variants as Risk Factors in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, November 2001. http://dx.doi.org/10.21236/ada405667.
Der volle Inhalt der QuelleTuite, Ashleigh R., David N. Fisman, Ayodele Odutayo, Pavlos Bobos, Vanessa Allen, Isaac I. Bogoch, Adalsteinn D. Brown et al. COVID-19 Hospitalizations, ICU Admissions and Deaths Associated with the New Variants of Concern. Ontario COVID-19 Science Advisory Table, März 2021. http://dx.doi.org/10.47326/ocsat.2021.02.18.1.0.
Der volle Inhalt der QuelleLehman, Donna, und Robin Leach. Assessing the Role of Copy Number Variants in Prostate Cancer Risk and Progression Using a Novel Genomewide Screening Method. Fort Belvoir, VA: Defense Technical Information Center, Dezember 2014. http://dx.doi.org/10.21236/ada615419.
Der volle Inhalt der QuelleLehman, Donna, Robin Leach und August Blackburn. Assessing the Role of Copy Number Variants in Prostate Cancer Risk and Progression Using a Novel Genome-Wide Screening Method. Fort Belvoir, VA: Defense Technical Information Center, Oktober 2010. http://dx.doi.org/10.21236/ada542445.
Der volle Inhalt der QuelleLehman, Donna, August Blackburn und Robin Leach. Assessing the Role of Copy Number Variants in Prostate Cancer Risk and Progression using a Novel Genome-Wide Screening Method. Fort Belvoir, VA: Defense Technical Information Center, Oktober 2012. http://dx.doi.org/10.21236/ada568305.
Der volle Inhalt der QuelleLehman, Donna, und Robin Leach. Assessing the Role of Copy Number Variants in Prostate Cancer Risk and Progression Using a Novel Genome-Wide Screening Method. Fort Belvoir, VA: Defense Technical Information Center, Oktober 2013. http://dx.doi.org/10.21236/ada594060.
Der volle Inhalt der QuelleLehman, Donna. Assessing the Role of Copy Number Variants in Prostate Cancer Risk and Progression Using a Novel Genome-Wide Screening Method. Fort Belvoir, VA: Defense Technical Information Center, Oktober 2011. http://dx.doi.org/10.21236/ada554128.
Der volle Inhalt der QuelleJia, Ziqi, Jiang Wu, Jiaxin Li, Jiaqi Liu und Xiang Wang. Meta-analysis of breast cancer risk associated with established germline pathogenic variants in breast cancer-predisposition genes in population-based studies. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, Februar 2021. http://dx.doi.org/10.37766/inplasy2021.2.0017.
Der volle Inhalt der QuelleWelch, David, und Gregory Deierlein. Technical Background Report for Structural Analysis and Performance Assessment (PEER-CEA Project). Pacific Earthquake Engineering Research Center, University of California, Berkeley, CA, November 2020. http://dx.doi.org/10.55461/yyqh3072.
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