Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: Neoplasms and F2[original query] |
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Genetic susceptibility, smoking, obesity and risk of venous thromboembolism. British journal of haematology 2010 Apr 149 (2): 273-9. Severinsen Marianne T, Overvad Kim, Johnsen Søren P, Dethlefsen Claus, Madsen Poul H, Tjønneland Anne, Kristensen Søren |
Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family. Journal of the American Academy of Dermatology 2012 Jul . Maubec E, Chaudru V, Mohamdi H, Blondel C, Margaritte-Jeannin P, Forget S, Corda E, Boitier F, Dalle S, Vabres P, Perrot JL, Lyonnet DS, Zattara H, Mansard S, Grange F, Leccia MT, Vincent-Fetita L, Martin L, Crickx B, Joly P, Thomas L, Bressac-de Paillerets B, Avril MF, Demenais F |
High prevalence of the c.1227_1228dup (p.Glu410GlyfsX43) mutation in Tunisian families affected with MUTYH-associated-polyposis. Familial cancer 2012 Sep 11 (3): 503-8. Abdelmaksoud-Dammak Rania, Miladi-Abdennadher Imen, Amouri Ali, Tahri Nabil, Ayadi Lobna, Khabir Abdelmajid, Frikha Foued, Gargouri Ali, Mokdad-Gargouri Ra |
Effect of thrombosis-related gene polymorphisms upon oral cancer: a regression analysis. Anticancer research 2013 Sep 33 (9): 4033-9. Vylliotis Antonis, Yapijakis Christos, Nkenke Emeka, Nisyrios Themistoklis, Avgoustidis Dimitrios, Adamopoulou Maria, Ragos Vasilios, Vassiliou Stavros, Koronellos Nikolas, Vairaktaris Eleftheri |
Increased coagulation activity and genetic polymorphisms in the F5, F10 and EPCR genes are associated with breast cancer: a case-control study. BMC cancer 2014 14 845. Tinholt Mari, Viken Marte Kathrine, Dahm Anders Erik, Vollan Hans Kristian Moen, Sahlberg Kristine Kleivi, Garred Oystein, Børresen-Dale Anne-Lise, Jacobsen Anne Flem, Kristensen Vessela, Bukholm Ida, Kåresen Rolf, Schlichting Ellen, Skretting Grethe, Lie Benedicte Alexandra, Sandset Per Morten, Iversen Ni |
No association between mitochondrial DNA copy number and colorectal adenomas. Molecular carcinogenesis 2015 Aug . Thyagarajan Bharat, Guan Weihua, Fedirko Veronika, Barcelo Helene, Tu Huakang, Gross Myron, Goodman Michael, Bostick Roberd |
Genetic diversity of hepatitis B virus and mutations associated to hepatocellular carcinoma in patients from Venezuela, with different stages of liver disease. Investigacio?n cli?nica 2016 Mar 57 (1): 38-46. Puche Mary L, Kay-Valero Sharon, Michelli Pedro, Oropeza Maria D, Loureiro Carmen L, Devesa Marisol, Dagher Lucy, Puol Flor |
Phenotypic and clinical implications of variants in the dihydropyrimidine dehydrogenase gene. Biochimica et biophysica acta 2016 04 1862 (4): 754-762. Kuilenburg André B P van, Meijer Judith, Tanck Michael W T, Dobritzsch Doreen, Zoetekouw Lida, Dekkers Lois-Lee, Roelofsen Jeroen, Meinsma Rutger, Wymenga Machteld, Kulik Wim, Büchel Barbara, Hennekam Raoul C M, Largiadèr Carlo |
Maternal genetic backgrounds contribute to the genetic susceptibility of tongue cancer patients in Hunan, central of China. Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2017 Feb 1-6. Zhou Hai-Yan, Shu Hong-Ying, Dai Jie, Li Hong-Chao, Tang Li, Wang Hua-Wei, Ni B |
Increased incidence of cancer in the follow-up of obstetric antiphospholipid syndrome within the NOH-APS cohort. Haematologica 2019 5 105 (2): 490-497. Gris Jean-Christophe, Mousty Éve, Bouvier Sylvie, Ripart Sylvie, Cochery-Nouvellon Éva, Fabbro-Peray Pascale, Broner Jonathan, Letouzey Vincent, Pérez-Martin Anton |
Combined effects of five prothrombotic genotypes and cancer on the risk of a first venous thromboembolic event. Journal of thrombosis and haemostasis : JTH 2020 Jul . Skille Hanne, Paulsen Benedikte, Hveem Kristian, Gabrielsen Maiken E, Brumpton Ben, Hindberg Kristian, Gran Olga V, Rosendaal Frits R, Braekkan Sigrid K, Hansen John-Bjar |
ASSOCIATION BETWEEN DIABETICS AND INTESTINAL CANCER WITH THE RISK OF MUTATION IN CD38 GENE IN IRANIAN POPULATION. Arquivos de gastroenterologia 2020 6 57 (2): 137-143. Shokrzadeh Mohammad, Goleij Pouya, Behravan Elmira, Ghassemi-Barghi Nasrin, Salehabadi Yaser, Rezaei Abolhas |
Prothrombotic genotypes and risk of major bleeding in patients with incident venous thromboembolism. Thrombosis research 2020 Apr 191 82-89. Johnsen Håkon S, Bjøri Esben, Hindberg Kristian, Brækkan Sigrid K, Morelli Vânia M, Hansen John-Bjar |
Differences in erythrocyte phospholipid membrane long-chain polyunsaturated fatty acids and the prevalence of fatty acid desaturase genotype among African Americans and European Americans. Prostaglandins, leukotrienes, and essential fatty acids 2020 Nov 164 102216. Rifkin S B, Shrubsole M J, Cai Q, Smalley W E, Ness R M, Swift L L, Milne G, Zheng W, Murff H |
Prothrombotic genotypes and risk of venous thromboembolism in occult cancer. Thrombosis research 2021 Jul 205 17-23. Skille Hanne, Paulsen Benedikte, Hveem Kristian, Severinsen Marianne T, Gabrielsen Maiken E, Kristensen Søren R, Næss Inger Anne, Hindberg Kristian, Tjønneland Anne, Brækkan Sigrid K, Hansen John-Bjar |
The Higher Prevalence of Venous Thromboembolism in the Hungarian Roma Population Could Be Due to Elevated Genetic Risk and Stronger Gene-Environmental Interactions. Frontiers in cardiovascular medicine 2021 11 8 647416. Natae Shewaye Fituma, Kósa Zsigmond, Sándor János, Merzah Mohammed Abdulridha, Bereczky Zsuzsanna, Pikó Péter, Ádány Róza, Fiatal Szilv |
Genome-wide association study meta-analysis identifies three novel loci for circulating anti-Müllerian hormone levels in women.
Human reproduction (Oxford, England) 2022 3 37 (5): 1069-1082. Verdiesen Renée M G, van der Schouw Yvonne T, van Gils Carla H, Verschuren W M Monique, Broekmans Frank J M, Borges Maria C, Gonçalves Soares Ana L, Lawlor Deborah A, Eliassen A Heather, Kraft Peter, Sandler Dale P, Harlow Siobán D, Smith Jennifer A, Santoro Nanette, Schoemaker Minouk J, Swerdlow Anthony J, Murray Anna, Ruth Katherine S, Onland-Moret N Charlot |
Cancer-associated thrombosis by cancer sites and inherited factors in a prospective population-based cohort. Thrombosis research 2023 7 229 69-72. Zhuqing Shi, Jun Wei, Andrew S Rifkin, Chi-Hsiung Wang, Liana K Billings, Jonathan S H Woo, Mark S Talamonti, Tilley Jenkins Vogel, Elena Moore, Bruce E Brockstein, Janardan D Khandekar, Henry M Dunnenberger, Peter J Hulick, David Duggan, S Lilly Zheng, Cheong Jun Lee, Brian T Helfand, Alfonso J Tafur, Jianfeng |
Missense variant interaction scanning reveals a critical role of the FERM domain for tumor suppressor protein NF2 conformation and function. Life science alliance 2023 6 6 (8): . Christina S Moesslacher, Elisabeth Auernig, Jonathan Woodsmith, Andreas Feichtner, Evelyne Jany-Luig, Stefanie Jehle, Josephine M Worseck, Christian L Heine, Eduard Stefan, Ulrich Stel |
Risk assessment of venous thromboembolism in inflammatory bowel disease by inherited risk in a population-based incident cohort. World journal of gastroenterology 2023 10 29 (39): 5494-5502. Andrew S Rifkin, Zhuqing Shi, Jun Wei, Siqun Lilly Zheng, Brian T Helfand, Jonathan S Cordova, Vincent F Biank, Alfonso J Tafur, Omar Khan, Jianfeng |
Haemostatic gene variations in cervical cancer-associated venous thrombosis: considerations for clinical strategies. Journal of thrombosis and thrombolysis 2024 4 . Beatriz Vieira Neto, Valéria Tavares, José Brito da Silva, Joana Liz-Pimenta, Inês Soares Marques, Lurdes Salgado, Luísa Carvalho, Deolinda Pereira, Rui Medeir |
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