Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 40 Records) |
Query Trace: F13A1[original query] |
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Common variants in the haemostatic gene pathway contribute to risk of early-onset myocardial infarction in the Italian population. Thrombosis and haemostasis 2011 Oct 106 (4): 655-64. Guella Ilaria, Duga Stefano, Ardissino Diego, Merlini Pier Angelica, Peyvandi Flora, Mannucci Pier Mannuccio, Asselta Rosan |
Sequence variations in the FII, FV, F13A1, FGB and PAI-1 genes are associated with differences in myocardial perfusion. Pharmacogenomics 2011 Feb 12 (2): 195-203. Satra Maria, Samara Maria, Wozniak Greta, Tzavara Chara, Kontos Angelos, Valotassiou Varvara, Vamvakopoulos Nikolaos K, Tsougos Ioannis, Aleporou-Marinou Vassiliki, Patrinos George P, Kollia Panagoula, Georgoulias Panagiot |
Exploring the interaction between SNP genotype and postmenopausal hormone therapy effects on stroke risk. Genome medicine 2012 Jul 4 (7): 7. Huang Y, Ballinger DG, Stokowski R, Beilharz E, Robinson JG, Liu S, Robinson R, Henderson VW, Rossouw JE, Prentice RL |
Androgen levels and metabolic parameters are associated with a genetic variant of F13A1 in women with polycystic ovary syndrome. Gene 2012 Aug 504 (1): 133-9. Schweighofer N, Lerchbaum E, Trummer O, Schwetz V, Pilz S, Pieber T R, Obermayer-Pietsch |
Prevalence of thrombosis-related DNA polymorphisms in a healthy Greek population. In vivo (Athens, Greece) 0 26 (6): 1095-101. Yapijakis Christos, Serefoglou Zoe, Nixon Alexander M, Vylliotis Antonis, Ragos Vassilis, Vairaktaris Eleftheri |
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 |
Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population. PLoS genetics 2013 Mar 9 (3): e1003419. Haiman Christopher A, Han Ying, Feng Ye, Xia Lucy, Hsu Chris, Sheng Xin, Pooler Loreall C, Patel Yesha, Kolonel Laurence N, Carter Erin, Park Karen, Le Marchand Loic, Van Den Berg David, Henderson Brian E, Stram Daniel |
A common F13A1 intron 1 variant IVS1+12(A) is associated with mild FXIII deficiency in Caucasian population. Annals of hematology 2013 Jul 92 (7): 975-9. Ivaskevicius Vytautas, Biswas Arijit, Thomas Anne, Lyonga Sophie, Rott Hannelore, Halimeh Susan, Kappert Guenther, Klammroth Robert, Scholz Ute, Eberl Wolfgang, Harbrecht Ursula, Gnida Christine, Hertfelder Hans-Joerg, Marquardt Natascha, Oldenburg Johann |
Gastrointestinal stromal tumors: a case-only analysis of single nucleotide polymorphisms and somatic mutations. Clinical sarcoma research 2013 3 (1): 12. O'Brien Katie M, Orlow Irene, Antonescu Cristina R, Ballman Karla, McCall Linda, Dematteo Ronald, Engel Lawrence |
A genome-wide survey of CD4(+) lymphocyte regulatory genetic variants identifies novel asthma genes. The Journal of allergy and clinical immunology 2014 Nov 134 (5): 1153-62. Sharma Sunita, Zhou Xiaobo, Thibault Derek M, Himes Blanca E, Liu Andy, Szefler Stanley J, Strunk Robert, Castro Mario, Hansel Nadia N, Diette Gregory B, Vonakis Becky M, Adkinson N Franklin, Avila Lydiana, Soto-Quiros Manuel, Barraza-Villareal Albino, Lemanske Robert F, Solway Julian, Krishnan Jerry, White Steven R, Cheadle Chris, Berger Alan E, Fan Jinshui, Boorgula Meher Preethi, Nicolae Dan, Gilliland Frank, Barnes Kathleen, London Stephanie J, Martinez Fernando, Ober Carole, Celedón Juan C, Carey Vincent J, Weiss Scott T, Raby Benjamin |
An Islet-Targeted Genome-Wide Association Scan Identifies Novel Genes Implicated in Cytokine-Mediated Islet Stress in Type 2 Diabetes. Endocrinology 2015 Sep 156 (9): 3147-56. Sharma Poonam R, Mackey Aaron J, Dejene Eden A, Ramadan James W, Langefeld Carl D, Palmer Nicholette D, Taylor Kent D, Wagenknecht Lynne E, Watanabe Richard M, Rich Stephen S, Nunemaker Craig |
The APOE E4 Allele Confers Increased Risk of Ischemic Stroke Among Greek Carriers. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 0 25 (3): 471-8. Konialis Christopher, Spengos Konstantinos, Iliopoulos Panagiotis, Karapanou Sophia, Gialafos Elias, Hagnefelt Birgitta, Vemmos Konstantinos, Zakopoulos Nikolaos, Pangalos Constantin |
Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: Identification of fourteen novel mutations. Blood cells, molecules & diseases 2016 Mar 57 81-4. Shanbhag Sharda, Ghosh Kanjaksha, Shetty Shrima |
Candidate gene analysis of the fibrinogen phenotype reveals the importance of polygenic co-regulation. Matrix biology : journal of the International Society for Matrix Biology 2016 Oct . Cronjé H Toinét, Nienaber-Rousseau Cornelie, Zandberg Lizelle, Chikowore Tinashe, de Lange Zelda, van Zyl Tertia, Pieters Marli |
Association of the F13A1 Val34Leu polymorphism and recurrent pregnancy loss: A meta-analysis. European journal of obstetrics, gynecology, and reproductive biology 2017 Jun 215 234-240. Jung Jae Hyun, Kim Jae-Hoon, Song Gwan Gyu, Choi Sung J |
Genetic determinants of circulating GIP and GLP-1 concentrations.
JCI insight 2017 Nov 2 (21): . Almgren Peter, Lindqvist Andreas, Krus Ulrika, Hakaste Liisa, Ottosson-Laakso Emilia, Asplund Olof, Sonestedt Emily, Prasad Rashmi B, Laurila Esa, Orho-Melander Marju, Melander Olle, Tuomi Tiinamaija, Holst Jens Juul, Nilsson Peter M, Wierup Nils, Groop Leif, Ahlqvist Em |
Coagulation F13A1 V34L, fibrinogen and homocysteine versus conventional risk factors in the pathogenesis of MI in young persons. Acta cardiologica 2017 Oct 1-7. Vishwajeet Vikarn, Jamwal Manu, Sharma Prashant, Das Reena, Ahluwalia Jasmina, Dogra Rupinder Kaur, Rohit Manoj Kum |
F13A1 Gene Variant (V34L) and Residual Circulating FXIIIA Levels Predict Short- and Long-Term Mortality in Acute Myocardial Infarction after Coronary Angioplasty. International journal of molecular sciences 2018 Sep 19 (9): . Ansani Lucia, Marchesini Jlenia, Pestelli Gabriele, Luisi Giovanni Andrea, Scillitani Giulia, Longo Giovanna, Milani Daniela, Serino Maria Luisa, Tisato Veronica, Gemmati Dona |
Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis. Haemophilia : the official journal of the World Federation of Hemophilia 2018 11 25 (1): 127-135. Saes Joline L, Simons Annet, de Munnik Sonja A, Nijziel Marten R, Blijlevens Nicole M A, Jongmans Marjolijn C, van der Reijden Bert A, Smit Yolba, Brons Paul P, van Heerde Waander L, Schols Saskia E |
Polymorphisms of F2, PROC, PROZ, and F13A1 Genes are Associated With Recurrent Spontaneous Abortion in Chinese Han Women. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2018 Jan 1076029617750487. Xu Zuying, Zhang Ying, Liu Wei, Liu Yunyun, Su Yezhou, Xing Qiong, He Xiaojin, Wei Zhaolian, Cao Yunxia, Xiang Huif |
Genetic and lifestyle predictors of ischemic stroke severity and outcome. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2019 7 40 (12): 2565-2572. Celap Ivana, Nikolac Gabaj Nora, Demarin Vida, Basic Kes Vanja, Simundic Ana-Mar |
Population study of thrombophilic markers and pharmacogenetic markers of warfarin prevalence in Bosnia and Herzegovina. Croatian medical journal 2019 Jun 60 (3): 212-220. Ašic Adna, Salazar Ramona, Storm Niels, Dogan Serkan, Höppner Wolfgang, Marjanovic Damir, Primorac Drag |
Increased coagulation factor XIII activity but not genetic variants of coagulation factors is associated with myocardial infarction in young patients. Journal of thrombosis and thrombolysis 2019 Apr . Ambroziak M, Kurylowicz A, Budaj |
Inflammatory and immune response genes: A genetic analysis of inhibitor development in Iranian hemophilia A patients. Pediatric hematology and oncology 2019 Mar 1-12. Naderi Niloofar, Yousefi Hossein, Mollazadeh Sahar, Seyed Mikaeili Afsaneh, Keshavarz Norouzpour Masoumeh, Jazebi Mohammad, Moazezi Nekooi Asl Seyedeh Somayeh, Namvar Ali, Azizi Saraji Alireza, Agi Elnaz, Bolhassani Az |
Genetic polymorphisms associated with upper gastrointestinal bleeding: a systematic review. The pharmacogenomics journal 2020 Sep . Forgerini Marcela, Lucchetta Rosa Camila, Urbano Gustavo, de Nadai Tales Rubens, de Carvalho Mastroianni Patríc |
Mining TCGA database for tumor mutation burden and their clinical significance in bladder cancer. Bioscience reports 2020 4 40 (4): . Lv Jia, Zhu Yongze, Ji Alin, Zhang Qi, Liao Guodo |
Exome-Sequencing Identifies Novel Genes Associated with Recurrent Pregnancy Loss in a Chinese Cohort. Frontiers in genetics 2021 12 12 746082. Xiang Huifen, Wang Chunyan, Pan Hong, Hu Qian, Wang Ruyi, Xu Zuying, Li Tengyan, Su Yezhou, Ma Xu, Cao Yunxia, Wang Binb |
Maternal Thrombophilic and Hypofibrinolytic Genetic Variants in Idiopathic Recurrent Pregnancy Loss: a Continuing Mystery. Reproductive sciences (Thousand Oaks, Calif.) 2022 Aug . Younis Mahmoud, Ali Mohamed A M, Ghareeb Doaa A, Youssef Rehab, Fathy Shadia |
An Exploratory Study Using Next-Generation Sequencing to Identify Prothrombotic Variants in Patients with Cerebral Vein Thrombosis. International journal of molecular sciences 2023 5 24 (9): . Robert Anton Kramer, Robert Zimmermann, Julian Strobel, Susanne Achenbach, Armin Michael Ströbel, Holger Hackstein, David Alexander Christian Messerer, Sabine Schneid |
Identification of genetic biomarkers associated with pharmacokinetics and pharmacodynamics of apixaban in Chinese healthy volunteers. Expert opinion on drug metabolism & toxicology 2023 3 1-9. Mu Guangyan, Xie Qiufen, Liu Zhiyan, Zhang Hanxu, Meng Xianmin, Song Jinfang, Zhou Shuang, Wang Zhe, Wang Zining, Zhao Xia, Jiang Jie, Liao Maoxing, Bao Jiachun, Zhang Fan, Xiang Qian, Cui Yim |
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