Human Genome Epidemiology Literature Finder
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Records 1 - 29 (of 29 Records) |
| Query Trace: Thrombophilia and F2[original query] |
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| Polymorphisms associated with thrombophilia and vascular homeostasis and the timing of menarche and menopause in 728 white women. Menopause (New York, N.Y.) 0 12 (3): 325-30. Tempfer Clemens B, Riener Eva-Katrin, Keck Christoph, Grimm Christoph, Heinze Georg, Huber Johannes C, Gitsch Gerald, Hefler Lukas |
| Multiplex assay for genetic testing of thrombophilia: a method for routine clinical care. Journal of clinical laboratory analysis 2007 21 (6): 349-55. López Mónica, Giraldo Pilar, Alvarez Patricia, Cornudella R, Pocoví Miguel, Martínez Antonio, Fontcuberta Jordi, Soria José Manu |
| Paternal endothelial protein C receptor 219Gly variant as a mild and limited risk factor for deep vein thrombosis during pregnancy. Journal of thrombosis and haemostasis : JTH 2010 Apr 8 (4): 707-13. Galanaud J P, Cochery-Nouvellon E, Alonso S, Chauleur C, Mercier E, Lissalde-Lavigne G, Fabbro-Peray P, Reny J L, Mares P, Dauzat M, Quere I, Gris J |
| Comparative incidence of a first thrombotic event in purely obstetric antiphospholipid syndrome with pregnancy loss: the NOH-APS observational study. Blood 2012 Mar 119 (11): 2624-32. Gris Jean-Christophe, Bouvier Sylvie, Molinari Nicolas, Galanaud Jean-Philippe, Cochery-Nouvellon Eva, Mercier Erik, Fabbro-Peray Pascale, Balducchi Jean-Pierre, Marès Pierre, Quéré Isabelle, Dauzat Mich |
| The association of inherited thrombophilia and intrauterine fetal death: a case-control study. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2011 Dec 22 (8): 8. Helgadottir LB, Skjeldestad FE, Jacobsen AF, Sandset PM, Jacobsen EM |
| Comparative incidence of pregnancy outcomes in thrombophilia-positive women from the NOH-APS observational study. Blood 2014 Jan 123 (3): 414-21. Bouvier Sylvie, Cochery-Nouvellon Eva, Lavigne-Lissalde Géraldine, Mercier Erick, Fabbro-Peray Pascale, Balducchi Jean-Pierre, Marès Pierre, Gris Jean-Christop |
| Risk assessment of venous thrombosis in families with known hereditary thrombophilia: the MARseilles-NImes prediction model. Journal of thrombosis and haemostasis : JTH 2014 Feb 12 (2): 138-146. Cohen W, Castelli C, Suchon P, Bouvet S, Aillaud M F, Brunet D, Barthet M C, Alessi M C, Trégouët D A, Morange P |
| Predicting venous thrombosis in women using a combination of genetic markers and clinical risk factors. Journal of thrombosis and haemostasis : JTH 2015 Feb 13 (2): 219-27. Bruzelius M, Bottai M, Sabater-Lleal M, Strawbridge R J, Bergendal A, Silveira A, Sundström A, Kieler H, Hamsten A, Odeberg |
| The Prevalence of the Prothrombin (F2) 20210G>A Mutation in a Cohort of Sri Lankan Patients with Thromboembolic Disorders. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2015 Sep 31 (3): 356-61. Gunathilake K M D, Sirisena U N D, Nisansala P K D, Goonasekera H W W, Jayasekara R W, Dissanayake V H |
| Hypercoagulability in adolescent girls on oral contraceptives-global coagulation profile and estrogen receptor polymorphisms. American journal of hematology 2015 Aug 90 (8): 725-31. Zia Ayesha, Callaghan Michael U, Callaghan Joseph H, Sawni Anju, Bartlett Heather, Backos Alcesa, Marshall Sharon, Chitlur Meera, Rajpurkar Madh |
| 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 Determinants of Thrombin Generation and Their Relation to Venous Thrombosis: Results from the GAIT-2 Project. PloS one 2016 11 (1): e0146922. Martin-Fernandez Laura, Ziyatdinov Andrey, Carrasco Marina, Millon Juan Antonio, Martinez-Perez Angel, Vilalta Noelia, Brunel Helena, Font Montserrat, Hamsten Anders, Souto Juan Carlos, Soria José Manu |
| 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 |
| 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 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 |
| [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 |
| 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 |
| Investigation of the influence of thrombophilic genes polymorphism, including serpin 1 (pai-i), fii, prothrombin and itgb3-? integrin, on the frequency of stroke in association with controllable risk factors for its occurrence. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2020 4 73 (3): 471-477. Oros Mikhail M, Lutz Vitaly V, Pavlo Andrukh H, Sitkar Andrii |
| 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 |
| PlA2 Polymorphism of Platelet Glycoprotein IIb/IIIa and C677T Polymorphism of Methylenetetrahydrofolate Reductase (MTHFR), but Not Factor V Leiden and Prothrombin G20210A Polymorphisms, Are Associated with More Severe Forms of Legg-Calvé-Perthes Disease. Children (Basel, Switzerland) 2021 Jul 8 (7): . García-Alfaro María Dolores, Pérez-Nuñez María Isabel, Amigo María Teresa, Arbona Carmelo, Ballesteros María Ángeles, González-Lamuño Domin |
| Predictive Ability of a Clinical-Genetic Risk Score for Venous Thromboembolism in Northern and Southern European Populations. TH open : companion journal to thrombosis and haemostasis 2021 7 5 (3): e303-e311. Salas Eduardo, Farm Maria, Pich Sara, Onelöv Liselotte, Guillen Kevin, Ortega Israel, Antovic Jovan P, Soria Jose Manu |
| Prevalence of thrombophilia-associated genetic risk factors in blood donors of a regional hospital in southern Brazil. Hematology, transfusion and cell therapy 2021 Mar . Dick-Guareschi Jéssica, Fontana Juliana Cristine, Sanseverino Maria Teresa Vieira, Kubaski Francyne, Sekine Leo, Mesquita Nanci Félix, Onsten Tor Gunnar Hugo, Leistner-Segal Sand |
| PROS1 variant in sudden death case of pulmonary embolism caused by calcification in the inferior vena cava: The importance of postmortem genetic analysis. Legal medicine (Tokyo, Japan) 2022 2 55 102029. Miura Aya, Funayama Kazuhisa, Nyuzuki Hiromi, Takahashi Naoya, Yamamoto Takuma, Koyama Akihide, Ikeuchi Takeshi, Takatsuka Hisakazu, Nishio Haji |
| 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 |
Whole exome sequencing identifies genetic variants in Chinese Han pregnant women with venous thromboembolism.
Thrombosis research 2022 Mar 211 49-55. Shen Yupei, Zhang Yan, Xiong Ying, Zhang Zhiping, Zhang Baohua, Li Aihong, Zhang Zhaofeng, Ding Jing, Du Jing, Che Y |
| To Test or Not to Test: Routine Thrombophilia Diagnostic Screening of Women with Reproductive Failures. Journal of clinical medicine 2023 12 12 (24): . Urszula Wysocka, Kinga Sa?aci?ska, Iwona Pinkier, ?ukasz K?pczy?ski, Wojciech A?aszewski, Lech Dudarewicz, Agnieszka Ga |
| Polymorphisms of ACE and thrombophilic genes: risk for recurrent pregnancy loss. Journal of clinical pathology 2023 11 76 (12): 832-838. Olivera Miljanovi?, Vesna Ili?, Sla?ana Teofilov, Bojana Cikota-Aleksi?, Zvonko Mag |
| Prothrombin G20210A Mutation is Rare but not Absent Among North Indian Patients with Thromboembolic Events. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2024 7 40 (3): 522-526. Priti Satyarthi, Debadrita Ray, Vasant Kumar, Chander Hans, Hari Kishan Senee, Jasmina Ahluwalia, Reena Das, Arihant Jain, Kartik Vinay Mahesh, Narender Kum |
| Factor V Leiden (R506Q), Prothrombin G20210A, and MTHFR C677T Variants and Thrombophilia in Qatar Biobank Participants: A Case Control Study. Pathophysiology : the official journal of the International Society for Pathophysiology 2024 10 31 (4): 608-620. Sapha Shibeeb, Nada Al-Rayashi, Nehal Shams, Tameem Hadvan, Ejaife O Agbani, Atiyeh M Abdall |
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