Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 67 Records) |
| Query Trace: Thrombosis and F5[original query] |
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| A Prothrombotic Score Based on Genetic Polymorphisms of the Hemostatic System Differs in Patients with Ischemic Stroke, Myocardial Infarction, or Peripheral Arterial Occlusive Disease. Frontiers in cardiovascular medicine 2017 4 39. Herm Juliane, Hoppe Berthold, Siegerink Bob, Nolte Christian H, Koscielny Jürgen, Haeusler Karl Geo |
| Prevalence of F5 1691G>A, F2 20210G>A, and MTHFR 677C>T polymorphisms in Bosnian women with pregnancy loss. Bosnian journal of basic medical sciences 2017 May . Mahmutbegovic Emir, Marjanovic Damir, Medjedovic Edin, Mahmutbegovic Nevena, Dogan Serkan, Valjevac Amina, Czerska Ewa, Pawi?ska-Matecka Anna, Madlani Agnieszka, Adler Grazy |
| Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes. Journal of thrombosis and haemostasis : JTH 2018 Aug . de Haan H G, van Hylckama Vlieg A, Lotta L A, Gorski M M, Bucciarelli P, Martinelli I, Baglin T P, Peyvandi F, Rosendaal F R, |
| Subtype-specific clinical and prognostic relevance of tumor-expressed F5 and regulatory F5 variants in breast cancer: the CoCaV study. Journal of thrombosis and haemostasis : JTH 2018 5 16 (7): 1347-1356. Tinholt M, Garred Ø, Borgen E, Beraki E, Schlichting E, Kristensen V, Sahlberg K K, Iversen |
| [The association of hemostasis system genes with the development of ischemic stroke in patients under the age of 50 years]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 0 118 (9. Vyp. 2): 14-21. Kimelfeld E I, Koltsova E A, Petrova E A, Gudkova V V, Stahovskaya L V, Tupitsyna T V, Bondarenko E A, Slominsky P A, Limborska S |
A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process.
Journal of thrombosis and haemostasis : JTH 2019 Jul . Thibord Florian, Hardy Lise, Ibrahim-Kosta Manal, Saut Noémie, Pulcrano-Nicolas Anne-Sophie, Goumidi Louisa, Civelek Mete, Eriksson Per, Deleuze Jean-François, Le Goff Wilfried, Trégouët David-Alexandre, Morange Pierre-Emmanu |
| Genome-wide association study of peripheral artery disease in the Million Veteran Program.
Nature medicine 2019 Aug 25 (8): 1274-1279. Klarin Derek, Lynch Julie, Aragam Krishna, Chaffin Mark, Assimes Themistocles L, Huang Jie, Lee Kyung Min, Shao Qing, Huffman Jennifer E, Natarajan Pradeep, Arya Shipra, Small Aeron, Sun Yan V, Vujkovic Marijana, Freiberg Matthew S, Wang Lu, Chen Jinbo, Saleheen Danish, Lee Jennifer S, Miller Donald R, Reaven Peter, Alba Patrick R, Patterson Olga V, DuVall Scott L, Boden William E, Beckman Joshua A, Gaziano J Michael, Concato John, Rader Daniel J, Cho Kelly, Chang Kyong-Mi, Wilson Peter W F, O'Donnell Christopher J, Kathiresan Sekar, , Tsao Philip S, Damrauer Scott |
| Impact of prothrombotic genotypes on the association between family history of myocardial infarction and venous thromboembolism. Journal of thrombosis and haemostasis : JTH 2019 May . Småbrekke Birgit, Rinde Ludvig B, Evensen Line H, Morelli Vania M, Hveem Kristian, Gabrielsen Maiken E, Njølstad Inger, Mathiesen Ellisiv B, Rosendaal Frits R, Braekkan Sigrid K, Hansen John-Bjar |
| Genetic profiling revealed an increased risk of venous thrombosis in the Hungarian Roma population. Thrombosis research 2019 5 179 37-44. Fiatal Szilvia, Pikó Péter, Kósa Zsigmond, Sándor János, Ádány Ró |
| Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation. Scientific reports 2019 Mar 9 (1): 3750. Ibrahim-Kosta M, Suchon P, Couturaud F, Smadja D, Olaso R, Germain M, Saut N, Goumidi L, Derbois C, Thibord F, Debette S, Amouyel P, Deleuze J F, van Doorn P, Castoldi E, Patin E, Alessi M C, Trégouët D A, Morange P |
| Effect of prothrombotic genotypes on the risk of venous thromboembolism in patients with and without ischemic stroke. The Tromsø Study. Journal of thrombosis and haemostasis : JTH 2019 Feb . Rinde Ludvig B, Morelli Vania M, Småbrekke Birgit, Mathiesen Ellisiv B, Løchen Maja-Lisa, Njølstad Inger, Wilsgaard Tom, Smith Erin, Rosendaal Frits R, Frazer Kelly A, Braekkan Sigrid K, Hansen John-Bjar |
| [Hemostatic Gene Polymorphisms in Acute Coronary Syndrome with Nonobstructive Coronary Atherosclerosis]. Kardiologiia 2019 Oct 59 (10): 14-22. Fedorova S B, Kulagina I V, Ryabov V |
| 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 |
| 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 |
| The joint effect of genetic risk factors and different types of combined oral contraceptives on venous thrombosis risk. British journal of haematology 2020 4 191 (1): 90-97. Khialani Deeksha, le Cessie Saskia, Lijfering Willem M, Cannegieter Suzanne C, Rosendaal Frits R, van Hylckama Vlieg Astr |
| Novel exomic rare variants associated with venous thrombosis.
British journal of haematology 2020 Mar . Deguchi Hiroshi, Shukla Meenal, Hayat Mohammed, Torkamani Ali, Elias Darlene J, Griffin John |
| Myocardial infarction, prothrombotic genotypes, and venous thrombosis risk: The Tromsø Study. Research and practice in thrombosis and haemostasis 2020 Feb 4 (2): 247-254. Sejrup Joakim K, Morelli Vania M, Løchen Maja-Lisa, Njølstad Inger, Mathiesen Ellisiv B, Wilsgaard Tom, Hansen John-Bjarne, Brækkan Sigrid |
| Polymorphisms of F2 (G20210A), F5 (G1691A), F 7 (G10976A), F 13(G13T), FGB, ITGA2, ITGB3, PAI-I genes and its association with thrombotic complications in patients suffering from Takayasu aortoarteritis of Urals population. Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2021 Sep 49 (6): 448-455. Borodina Irina, Salavatova Gezel, Shardina Lub |
| 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 |
| Joint Effect of Multiple Prothrombotic Genotypes and Obesity on the Risk of Incident Venous Thromboembolism. Thrombosis and haemostasis 2021 5 122 (2): 267-276. Frischmuth Tobias, Hindberg Kristian, Gabrielsen Maiken E, Brumpton Ben, Hveem Kristian, Brækkan Sigrid K, Hansen John-Bjarne, Morelli Vânia |
| Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism. Clinica chimica acta; international journal of clinical chemistry 2021 5 519 247-254. Athar Mohammad, Ghita Ibrahim S, Albagenny Amani A, Abduljaleel Zainularifeen, Shadab Ghulam, Elsendiony Ahmed, Halawani Saeed H, Alkazmi Mohammad M, Alquthami Khalid, Alkhuzae Mohammad M, Althebyani Abdulaziz A, Bogari Neda M, Dannoun Anas, Al-Allaf Faisal |
| Prevalence of the Factor V Leiden Mutation Arg534Gln in Western Region of Saudi Arabia: Functional Alteration and Association Study With Different Populations. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2021 1 27 1076029620978532. Athar Mohammad, Abduljaleel Zainularifeen, Ghita Ibrahim S, Albagenny Amani A, Halawani Saeed H, Alkazmi Mohammad M, Elbjeirami Wafa M, Alquthami Khalid, Alkhuzae Mohammad M, Ragab Fadel M, Al-Allaf Faisal |
| Genetic markers for inherited thrombophilia related pregnancy loss and implantation failure in Indian population - implications for diagnosis and clinical management. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2022 2 35 (25): 9406-9414. Udumudi Anuradha, Lava Chait |
| Clinical impact of the PAI-1 4G/5G polymorphism in Chinese patients with venous thromboembolism. Thrombosis journal 2022 11 20 (1): 68. Wang Ziran, Kong Lingjun, Luo Guoju, Zhang Han, Sun Fengchun, Liang Wenjuan, Wu Wei, Guo Zijian, Zhang Rui, Dou Yali |
| A combination of strongly associated prothrombotic single nucleotide polymorphisms could efficiently predict venous thrombosis risk. Frontiers in cardiovascular medicine 2023 9 10 1224462. Shewaye Fituma Natae, Mohammed Abdulridha Merzah, János Sándor, Róza Ádány, Zsuzsanna Bereczky, Szilvia Fiat |
| 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 |
| Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism. Nature genetics 2023 1 55 (3): 399-409. Ghouse Jonas, Tragante Vinicius, Ahlberg Gustav, Rand Søren A, Jespersen Jakob B, Leinøe Eva Birgitte, Vissing Christoffer Rasmus, Trudsø Linea, Jonsdottir Ingileif, Banasik Karina, Brunak Søren, Ostrowski Sisse R, Pedersen Ole B, Sørensen Erik, Erikstrup Christian, Bruun Mie Topholm, Nielsen Kaspar Rene, Køber Lars, Christensen Alex H, Iversen Kasper, Jones David, Knowlton Kirk U, Nadauld Lincoln, Halldorsson Gisli H, Ferkingstad Egil, Olafsson Isleifur, Gretarsdottir Solveig, Onundarson Pall T, Sulem Patrick, Thorsteinsdottir Unnur, Thorgeirsson Gudmundur, Gudbjartsson Daniel F, Stefansson Kari, Holm Hilma, Olesen Morten Salling, Bundgaard Henni |
| The incidence of the thrombophilic SNPs rs6025, rs1799963, rs2066865, rs2289252, and rs8176719 in chronic thromboembolic pulmonary hypertension. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2024 8 30 10760296241271369. Kvasni?ka Jan, Jansa Pavel, Cífková Renata, Dušková Daniela, Bob?íková Petra, Šev?ík Martin, Zenáhlíková Zuzana, Kvasni?ka Tom |
| Comparison of an Unlabeled Probe High-Resolution Melting Analysis Assay (HRMA) for Factor V Leiden 1691 G/A Mutation to a Fluorogenic 5' Nuclease PCR Hydrolysis Assay. The journal of applied laboratory medicine 2024 5 . Heping Han, Sally Lew |
| Genome-Wide Search for Nonadditive Allele Effects Identifies PSKH2 as Involved in the Variability of Factor V Activity. Journal of the American Heart Association 2024 10 e034943. Blandine Gendre, Angel Martinez-Perez, Marcus E Kleber, Astrid van Hylckama Vlieg, Anne Boland, Robert Olaso, Marine Germain, Gaëlle Munsch, Angela Patricia Moissl, Pierre Suchon, Juan Carlos Souto, José Manuel Soria, Jean-François Deleuze, Winfried März, Frits R Rosendaal, Maria Sabater-Lleal, Pierre-Emmanuel Morange, David-Alexandre Trégouët, |
- Page last reviewed:Feb 1, 2024
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