Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Venous Thrombosis and F5[original query] |
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| Candidate gene approach in association studies: would the factor V Leiden mutation have been found by this approach? European journal of human genetics : EJHG 2004 Jun 12 (6): 478-82. van Hylckama Vlieg Astrid, Sandkuijl Lodewijk A, Rosendaal Frits R, Bertina Rogier M, Vos Hans |
| Homozygosity for the C46T polymorphism of the F12 gene is a risk factor for venous thrombosis during the first pregnancy. Journal of thrombosis and haemostasis : JTH 2007 Apr 5 (4): 700-7. Cochery-Nouvellon E, Mercier E, Lissalde-Lavigne G, Daurès J-P, Quéré I, Dauzat M, Marès P, Gris J |
| Rapid triplex asymmetric real-time PCR hybridization probe assay for the joint genotyping of F2, F5 and F12. Clinical biochemistry 2009 Aug 42 (12): 1317-24. Martínez-Serra J, Gutierrez A, Amat J C, Galmés B, Vila A, Julia M, López H, Bautista A M, Truyols C, Ros T, Navarro M, Canaro M, Díaz M, Besalduch |
| Frequency of prothrombotic risk factors in patients with deep venous thrombosis and controls: their implications for thrombophilia screening in Chilean subjects. Genetic testing and molecular biomarkers 2010 Oct 14 (5): 599-602. Guzmán Neftalí, Salazar Luis |
| The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature disease. Journal of thrombosis and haemostasis : JTH 2010 Oct 8 (10): 2116-21. Mannucci P M, Asselta R, Duga S, Guella I, Spreafico M, Lotta L, Merlini P A, Peyvandi F, Kathiresan S, Ardissino |
| Resistance to activated protein C is a risk factor for pregnancy-related venous thrombosis in the absence of the F5 rs6025 (factor V Leiden) polymorphism. British journal of haematology 2011 Jul 154 (2): 241-7. Bergrem Astrid, Dahm Anders Erik Astrup, Jacobsen Anne Flem, Mowinckel Marie-Christine, Sandvik Leiv, Sandset Per Mort |
Genetics of venous thrombosis: insights from a new genome wide association study.
PloS one 2011 6 (9): e25581. Germain Marine, Saut Noémie, Greliche Nicolas, Dina Christian, Lambert Jean-Charles, Perret Claire, Cohen William, Oudot-Mellakh Tiphaine, Antoni Guillemette, Alessi Marie-Christine, Zelenika Diana, Cambien François, Tiret Laurence, Bertrand Marion, Dupuy Anne-Marie, Letenneur Luc, Lathrop Mark, Emmerich Joseph, Amouyel Philippe, Trégouët David-Alexandre, Morange Pierre-Emmanu |
| Candidate gene polymorphisms and the risk for pregnancy-related venous thrombosis. British journal of haematology 2012 Jun 157 (6): 753-61. Dahm Anders E A, Bezemer Irene D, Bergrem Astrid, Jacobsen Anne F, Jacobsen Eva M, Skretting Grethe, Rosendaal Frits R, Sandset Per Mort |
| Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.
British journal of haematology 2012 Apr 157 (2): 230-9. Oudot-Mellakh Tiphaine, Cohen William, Germain Marine, Saut Noémie, Kallel Choumous, Zelenika Diana, Lathrop Mark, Trégouët David-Alexandre, Morange Pierre-Emmanu |
| Haplotypes of TAFI gene and the risk of cerebral venous thrombosis--a case-control study. Thrombosis research 2013 Nov . Orikaza CM, Morelli VM, Matos MF, Lourenço DM |
| Three novel variants in the coagulation factor V gene associated with deep venous thrombosis in Chilean patients with Amerindian ethnic background. Clinica chimica acta; international journal of clinical chemistry 2015 Apr 444 24-8. Guzmán Neftalí, Larama Giovanni, Ávila Andrés, Salazar Luis |
| A Study on Hereditary Thrombophilia and Stroke in a Cohort from Sri Lanka. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2015 Oct . Kalpage Hasini A, Sumathipala Dulika S, Goonasekara Hemali W, Dissanayake Vajira |
| Genetic risk factors for venous thrombosis in women using combined oral contraceptives: update of the PILGRIM study. Clinical genetics 2016 Jul . Suchon Pierre, Frouh Fadi Al, Ibrahim Manal, Sarlon Gabrielle, Venton Geoffroy, Alessi Marie-Christine, Trégouët David-Alexandre, Morange Pierre-Emmanu |
| 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, |
| 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 |
| 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 |
| 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 |
| 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 |
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- Page last updated:Dec 04, 2023
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