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Artykuły w czasopismach na temat „Genetic risk factors”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 25 lipca 2025

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1

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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5

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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10

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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11

Shubina, M. V., K. V. Kopylova, M. V. Smolnikova, N. N. Gorbacheva, and S. Yu Tereshchenko. "Genetic risk factors of headache." Russian Journal of Pain 21, no. 4 (2023): 11. http://dx.doi.org/10.17116/pain20232104111.

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Meyle, Kathrine Damm, and Per Guldberg. "Genetic risk factors for melanoma." Human Genetics 126, no. 4 (2009): 499–510. http://dx.doi.org/10.1007/s00439-009-0715-9.

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Isabel, Soto Angulo, Salvador Valdez García Jesús, and Francisco Balderrama Conde Jesús. "Genetic Variations and Risk Factors on Medulloblastoma." INTERNATIONAL JOURNAL OF MEDICAL SCIENCE AND CLINICAL RESEARCH STUDIES 03, no. 12 (2023): 3004–6. https://doi.org/10.5281/zenodo.10362277.

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Medulloblastoma, a highly aggressive brain tumor, presents a complex clinical landscape driven by intricate genetic variations and diverse risk factors. This review delves into the tumor's genetic origins, emphasizing molecular subgroups and their prognostic implications. Examining risk factors such as age, gender, genetics, and ethnicity provides a holistic perspective. Unraveling hereditary forms sheds light on familial predispositions. Racial disparities underscore the importance of tailored approaches. Decoding the complexities surrounding medulloblastoma informs refined diagnostics and pe

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14

Lucas, Sionne E. M., and Kathryn P. Burdon. "Genetic and Environmental Risk Factors for Keratoconus." Annual Review of Vision Science 6, no. 1 (2020): 25–46. http://dx.doi.org/10.1146/annurev-vision-121219-081723.

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Keratoconus, a progressive corneal ectasia, is a complex disease with both genetic and environmental risk factors. The exact etiology is not known and is likely variable between individuals. Conditions such as hay fever and allergy are associated with increased risk, while diabetes may be protective. Behaviors such as eye rubbing are also implicated, but direct causality has not been proven. Genetics plays a major role in risk for some individuals, with many large pedigrees showing autosomal inheritance patterns. Several genes have been implicated using linkage and follow-up sequencing in thes

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15

A., Lahari, Gnanankitha K., Poojitha V., Bhanuji Rao Paila., and Phani Satyavathi Nimmala. "The Impact of Environmental Factors on Schizophrenia Risk." International Journal of Innovative Science and Research Technology (IJISRT) 10, no. 2 (2025): 1145–53. https://doi.org/10.5281/zenodo.14959364.

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This journal explores the role of environmental influences in increasing the risk of developing schizophrenia, a complex mental health condition. While genetics play a significant role, research suggests that environmental elements such as prenatal infections, early life trauma, growing up in urban areas, and substance abuse significantly elevate the chances of schizophrenia, particularly in individuals with a genetic vulnerability. The interaction between these environmental triggers and genetic factors is complex, and gaining a deeper understanding of this relationship is essential for creat

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16

Arai, Hiroyuki. "Genetic Risk Factors in Senile Dementia." Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics 36, no. 4 (1999): 251–55. http://dx.doi.org/10.3143/geriatrics.36.251.

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Пивоварова, Д. Д., and Е. В. Машкина. "Genetic risk factors for hepatitis B." Nauchno-prakticheskii zhurnal «Medicinskaia genetika», no. 8(217) (August 31, 2020): 85–86. http://dx.doi.org/10.25557/2073-7998.2020.08.85-86.

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В работе в качестве материала для исследования были использованы образцы ДНК, выделенные из крови 99 людей в возрасте от 20 до 80 лет, из них 47 человек инфицированы вирусом гепатита В и 52 человека без вирусной нагрузки. По результатам исследования установлено, что аллель А полиморфизма rs1800450 гена MBL2 ассоциирован с высоким риском развития гепатита В, а наличие генотипа GG снижает такой риск; взаимодействие полиморфных вариантов гена STAT3 с генотипом GG гена MBL2 снижает риск развития гепатита В. DNA samples extracted from the blood of 99 people aged 20 to 80 years were used as the mate

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18

Skrzypa, Marzena, Natalia Potocka, Halina Bartosik-Psujek, and Izabela Zawlik. "Genetic risk factors of Alzheimer’s disease." European Journal of Clinical and Experimental Medicine 17, no. 1 (2019): 57–66. http://dx.doi.org/10.15584/ejcem.2019.1.10.

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19

Sahin-Tóth, Miklós, Péter Hegyi, and Miklós Tóth. "Genetic risk factors in chronic pancreatitis." Orvosi Hetilap 149, no. 36 (2008): 1683–88. http://dx.doi.org/10.1556/oh.2008.28441.

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A hasnyálmirigy idült gyulladásos megbetegedését a mirigyszövet pusztulása, emésztési zavarok, krónikus fájdalom jellemzi, és cukorbetegség kísérheti. A betegséggel kapcsolatos genetikai tényezőket két csoportra oszthatjuk: 1. olyan génmutációk, amelyek önmagukban a betegség kialakulásához vezetnek, ezek elsősorban a kationos tripszinogén génjét érintik és igen ritkák, illetve 2. olyan génmutációk, amelyek hajlamosítanak a betegség kialakulására és egyéb kockázati tényezőkkel együtt okozzák a betegséget. Ezek tehát genetikai rizikófaktoroknak tekinthetők. Ilyen génmutációkat az utóbbi 10 évben

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20

Millichap, J. Gordon. "Genetic Risk Factors for Perinatal Stroke." Pediatric Neurology Briefs 27, no. 2 (2013): 10. http://dx.doi.org/10.15844/pedneurbriefs-27-2-2.

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Ye-Jee, Shim, and Lee Kun-Soo. "Genetic Risk Factors of Hemophilia A." Journal of Genetic Medicine 7, no. 1 (2010): 1–8. http://dx.doi.org/10.5734/jgm.2010.7.1.1.

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22

Vaikhanskaya, T. G., L. N. Sivitskaya, O. D. Levdansky, T. V. Kurushko, and N. G. Danilenko. "Genetic risk factors for dilated cardiomyopathy." Russian Journal of Cardiology 26, no. 10 (2021): 4628. http://dx.doi.org/10.15829/1560-4071-2021-4628.

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Aim. To study the diagnostic significance of genetic testing in patients with dilated cardiomyopathy (DCM), identify predictors of life-threatening ventricular tachyarrhythmias (VTAs) and assess adverse clinical outcomes in different genetic groups.Material and methods. The study included 126 unrelated patients with verified DCM as follows: 70 (55,6%) probands with criteria for familial DCM and 56 (44,4%) individuals with a probable hereditary component. All patients (age, 43,1±11,3 years; men, 92 (73%); left ventricular ejection fraction, 30,6±8,43%; left ventricular enddiastolic diameter, 68

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23

Sato, Naoyuki. "Non-genetic risk factors for dementia." Rinsho Shinkeigaku 52, no. 11 (2012): 968–70. http://dx.doi.org/10.5692/clinicalneurol.52.968.

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24

Krausz, Csilla, and Claudia Giachini. "Genetic Risk Factors in Male Infertility." Archives of Andrology 53, no. 3 (2007): 125–33. http://dx.doi.org/10.1080/01485010701271786.

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25

Stewart, L. L., L. L. Field, S. Ross, and R. G. MacArthur. "Genetic Risk Factors in Diabetic Retinopathy." Retina 14, no. 3 (1994): 289. http://dx.doi.org/10.1097/00006982-199414030-00030.

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26

Papakostas, Thanos D., Margaux A. Morrison, Anne Marie Lane, et al. "Genetic Risk Factors for Radiation Vasculopathy." Investigative Opthalmology & Visual Science 59, no. 3 (2018): 1547. http://dx.doi.org/10.1167/iovs.17-22791.

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27

Morgan, Laleh, Jackie Cooper, Hugh Montgomery, Steve Humphries, and Neil Kitchen. "Genetic Risk Factors for Subarachnoid Hemorrhage." Neurosurgery 61, no. 1 (2007): 197. http://dx.doi.org/10.1227/01.neu.0000279889.51914.3a.

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28

Friedman, D., S. Thompson, Y. Yasui, et al. "Genetic risk factors for second malignancy." Journal of Pediatric Hematology/Oncology 22, no. 4 (2000): 368. http://dx.doi.org/10.1097/00043426-200007000-00028.

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29

Jones, Nick. "Genetic risk factors for sporadic ALS." Nature Reviews Neurology 5, no. 11 (2009): 579. http://dx.doi.org/10.1038/nrneurol.2009.172.

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30

Wilson, WA, and AE Gharavi. "Genetic Risk Factors for aPL Syndrome." Lupus 5, no. 5 (1996): 398–403. http://dx.doi.org/10.1177/096120339600500513.

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MHC class II alleles and C4 deficiency alleles have been variably associated with aPL syndrome, but the extensive linkage disequilibrium among many of these alleles has made it difficult to assign a causal role for any of them. Interethnic studies of these and other alleles in large cohorts of subjects would help to clarify the roles of these alleles in aPL syndrome.

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31

Sato, Hideki, Norio Tanahashi, Daisuke Ito, Hidenori Hattori, Mitsuru Murata, and Norihiro Suzuki. "Genetic risk factors for cerebral infarction." Nosotchu 27, no. 4 (2005): 585–89. http://dx.doi.org/10.3995/jstroke.27.585.

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Zdoukopoulos, Nikos, and Elias Zintzaras. "Genetic Risk Factors for Placental Abruption." Epidemiology 19, no. 2 (2008): 309–23. http://dx.doi.org/10.1097/ede.0b013e3181635694.

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Corral, J., JA Iniesta, R. Gonza-Conejero, ML Lozano, J. Rivera, and V. Vicente. "Migraine and prothrombotic genetic risk factors." Cephalalgia 18, no. 5 (1998): 257–60. http://dx.doi.org/10.1046/j.1468-2982.1998.1805257.x.

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Bonaïti-Pellié, C. "Genetic risk factors in colorectal cancer." European Journal of Cancer Prevention 8 (December 1999): S33. http://dx.doi.org/10.1097/00008469-199912001-00005.

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Hamsten, A. "Genetic determination of haemostatic risk factors." Atherosclerosis 144 (May 1999): 14–15. http://dx.doi.org/10.1016/s0021-9150(99)80050-1.

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Feltkamp, T. E. W., Lucien A. Aarden, Cees J. Lucas, Cor L. Verweij, and René R. P. de Vries. "Genetic risk factors for autoimmune diseases." Immunology Today 20, no. 1 (1999): 10–12. http://dx.doi.org/10.1016/s0167-5699(98)01347-4.

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Gyllensten, U., A. Beskow, M. Moberg, and J. Rønnholm. "Genetic risk factors for cervical cancer." European Journal of Cancer 37 (April 2001): S140. http://dx.doi.org/10.1016/s0959-8049(01)81012-1.

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Altukhova, OB, MI Churnosov, and OP Lebedeva. "Genetic Risk Factors of Large Myomas." Journal of Minimally Invasive Gynecology 22, no. 6 (2015): S157. http://dx.doi.org/10.1016/j.jmig.2015.08.593.

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Billingsley, K. J., S. Bandres-Ciga, S. Saez-Atienzar, and A. B. Singleton. "Genetic risk factors in Parkinson’s disease." Cell and Tissue Research 373, no. 1 (2018): 9–20. http://dx.doi.org/10.1007/s00441-018-2817-y.

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Franco, Rendrik F., and Pieter H. Reitsma. "Genetic risk factors of venous thrombosis." Human Genetics 109, no. 4 (2001): 369–84. http://dx.doi.org/10.1007/s004390100593.

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Burlingame, Janet, Hyeong Jun Ahn, John Chen, and Johann Urschitz. "579: Genetic risk factors for preeclampsia." American Journal of Obstetrics and Gynecology 208, no. 1 (2013): S247. http://dx.doi.org/10.1016/j.ajog.2012.10.745.

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Hinney, Anke, Susann Friedel, Helmut Remschmidt, and Johannes Hebebrand. "Genetic Risk Factors in Eating Disorders." American Journal of PharmacoGenomics 4, no. 4 (2004): 209–23. http://dx.doi.org/10.2165/00129785-200404040-00001.

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Tilley, L., K. Morgan, and N. Kalsheker. "Genetic risk factors in Alzheimer's disease." Molecular Pathology 51, no. 6 (1998): 293–304. http://dx.doi.org/10.1136/mp.51.6.293.

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Sharabitdinova, Gulshad Gafurkhanovna. "GENETIC RISK FACTORS FOR CARDIOVASCULAR DISEASE." Theoretical & Applied Science 59, no. 03 (2018): 240–43. http://dx.doi.org/10.15863/tas.2018.03.59.41.

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Zöller, Bengt, Peter J. Svensson, Björn Dahlbäck, Christina Lind-Hallden, Christer Hallden, and Johan Elf. "Genetic risk factors for venous thromboembolism." Expert Review of Hematology 13, no. 9 (2020): 971–81. http://dx.doi.org/10.1080/17474086.2020.1804354.

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Kwinta, Przemko, Mirosław Bik-Multanowski, Zofia Mitkowska, Tomasz Tomasik, Magdalena Legutko, and Jacek Józef Pietrzyk. "Genetic Risk Factors of Bronchopulmonary Dysplasia." Pediatric Research 64, no. 6 (2008): 682–88. http://dx.doi.org/10.1203/pdr.0b013e318184edeb.

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Djordjevic, Valentina, Marija Stankovic, Vesna Brankovic-Sreckovic, et al. "Prothrombotic Genetic Risk Factors in Stroke." Clinical and Applied Thrombosis/Hemostasis 18, no. 6 (2012): 658–61. http://dx.doi.org/10.1177/1076029611432136.

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Whitcomb, David C. "Genetic Risk Factors for Pancreatic Disorders." Gastroenterology 144, no. 6 (2013): 1292–302. http://dx.doi.org/10.1053/j.gastro.2013.01.069.

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Opal, S., S. Garg, J. Jain, and I. Walia. "Genetic factors affecting dental caries risk." Australian Dental Journal 60, no. 1 (2015): 2–11. http://dx.doi.org/10.1111/adj.12262.

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KOHARA, K., Y. TABARA, T. NAGAI, J. NAKURA, and T. MIKI. "Genetic risk factors for arterial stiffness." American Journal of Hypertension 18, no. 5 (2005): A82. http://dx.doi.org/10.1016/j.amjhyper.2005.03.228.

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