Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 202 Records) |
| Query Trace: Thrombosis and IMPACT[original query] |
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| Essential Thrombocythemia: One-Center Data in a Changing Disease. Medicina (Kaunas, Lithuania) 2022 12 58 (12): . Pirciulescu Nicoleta, Gaman Mihnea-Alexandru, Mihailescu Marina, Constantin Cristina, Dragomir Mihaela, Dobrea Camelia, Costache Simona, Ursuleac Iulia, Coriu Daniel, Crisan Ana Manue |
| Implication of diabetic status on platelet reactivity and clinical outcomes after drug-eluting stent implantation: results from the PTRG-DES consortium. Cardiovascular diabetology 2023 9 22 (1): 245. Ki-Hyun Jeon, Young-Hoon Jeong, In-Ho Chae, Byeong-Keuk Kim, Hyung Joon Joo, Kiyuk Chang, Yongwhi Park, Young Bin Song, Sung Gyun Ahn, Sang Yeub Lee, Jung Rae Cho, Ae-Young Her, Hyo-Soo Kim, Moo Hyun Kim, Do-Sun Lim, Eun-Seok Shin, Jung-Won Suh, |
| Seizures in cerebral venous thrombosis - A retrospective analysis of a tertiary centre cohort. Clinical neurology and neurosurgery 2023 7 232 107840. Leonor Dias, Marta Carval |
| The impact of PROS1 mutation position on thrombotic risk in protein S-deficient patients. Research and practice in thrombosis and haemostasis 2023 6 7 (4): 100194. Tereza Fenclova, Miloslava Matyskova, Dana Provaznikova, Frantisek Marecek, Vera Geierova, Zuzana Kovarova-Kudrnova, Ingrid Hrachovino |
| Polygenic risk scores and risk stratification in deep vein thrombosis. Thrombosis research 2023 6 228 151-162. Valeria Lo Faro, Therese Johansson, Julia Höglund, Fatemeh Hadizadeh, Åsa Johanss |
| 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 |
| Platelet function studies in myeloproliferative neoplasms patients with Calreticulin or JAK2 mutation. Research and practice in thrombosis and haemostasis 2023 3 7 (2): 100060. Guy Alexandre, Helzy Khalil, Mansier Olivier, Bordet Jean-Claude, Rivière Etienne, Fiore Mathieu, James Chl |
| [Hereditary Spherocytosis and Pregnancy: A Case Report]. Acta medica portuguesa 2023 2 . Miguel Andreia, Alves Maria José, Massa Ana Catari |
| Impact of Toll-Like Receptor 2 and 9 Gene Polymorphisms on COVID-19: Susceptibility, Severity, and Thrombosis. Journal of inflammation research 2023 2 16 665-675. Alhabibi Alshaymaa M, Hassan Asmaa S, Abd Elbaky Nashwa Mohamed, Eid Hoda Asaad, Khalifa Mohie Aldeen Abd Alzaher, Wahab Maisa A, Althoqapy Azza Ali, Abdou Aml E, Zakaria Doaa Mohammed, Nassef Eman Mostafa, Kasim Sammar Ahmed, Saleh Ola I, Elsheikh Asmaa Abdelghany, Lotfy Mahmoud, Sayed Al |
| Impact of SERPINC1 mutation on thrombotic phenotype in children with congenital antithrombin deficiency-first analysis of the International Society on Thrombosis and Haemostasis pediatric antithrombin deficiency database and biorepository. Journal of thrombosis and haemostasis : JTH 2023 2 . Kumar Riten, Bakeer Nihal, Dawson Jennifer, Al-Mughairy Alyaa, Stanek Joseph, Dunn Amy, Male Christoph, Chan Anthony, Williams Suz |
| The association between EPCR gene p.Ser219Gly polymorphism and venous thromboembolism risk: a case-control study, meta-analysis, and a reproducibility study. Frontiers in cardiovascular medicine 2023 12 10 1270093. Dóra Pituk, Tünde Miklós, Ágota Schlammadinger, Katalin Rázsó, Zsuzsanna Berecz |
| Whole F9 gene sequencing identified deep intronic variations in genetically unresolved hemophilia B patients. Journal of thrombosis and haemostasis : JTH 2023 1 . Dericquebourg Amy, Fretigny Mathilde, Chatron Nicolas, Tardy Brigitte, Zawadzki Christophe, Chambost Hervé, Vinciguerra Christine, Jourdy Yoha |
| Impact of CYP2C19 Genotype Status on Clinical Outcomes in Patients with Symptomatic Coronary Artery Disease, Stroke, and Peripheral Arterial Disease: A Systematic Review and Meta-Analysis. Drugs 2024 9 . Dominique P M S M Maas, Loes H Willems, Josephine Kranendonk, Cornelis Kramers, Michiel C War |
| The role of inflammatory proteins in regulating the impact of lipid specifications on deep venous thrombosis: a two sample and mediated Mendelian randomization study. Frontiers in cardiovascular medicine 2024 9 11 1434600. Fan Dong, Jiahao Sun, Yudong Zha |
| The Impact of Cardiovascular Disease Gene Polymorphism and Interaction with Homocysteine on Deep Vein Thrombosis. ACS omega 2024 9 9 (38): 39836-39845. Lei-Lei Niu, Hao-Liang Fan, Jie Cao, Qiu-Xiang Du, Qian-Qian Jin, Ying-Yuan Wang, Jun-Hong S |
| Impaired arterial dilation and increased NOX2 generated oxidative stress in subjects with ataxia-telangiectasia mutated (ATM) kinase. Redox biology 2024 9 77 103347. Lorenzo Loffredo, Annarosa Soresina, Bianca Laura Cinicola, Martina Capponi, Francesca Salvatori, Simona Bartimoccia, Vittorio Picchio, Maurizio Forte, Caterina Caputi, Roberto Poscia, Vincenzo Leuzzi, Alberto Spalice, Pasquale Pignatelli, Raffaele Badolato, Marzia Duse, Francesco Violi, Roberto Carnevale, Anna Maria Zicari, |
| Causal Relationships of Circulating Inflammatory Proteins and Portal Vein Thrombosis: A Mendelian Randomization Study. Seminars in thrombosis and hemostasis 2024 9 . Bihui Zhang, Ziping Yao, Pengyu Li, Guochen Niu, Ziguang Yan, Kang She, Gong Cheng, Min Ya |
| The influence of 4G/5G polymorphism in the plasminogen-activator-inhibitor-1 promoter on COVID-19 severity and endothelial dysfunction. Frontiers in immunology 2024 9 15 1445294. Tetiana Yatsenko, Ricardo Rios, Tatiane Nogueira, Yousef Salama, Satoshi Takahashi, Eisuke Adachi, Yoko Tabe, Nobutaka Hattori, Taro Osada, Toshio Naito, Kazuhisa Takahashi, Koichi Hattori, Beate Heiss |
| Secondary Solid Cancers Among Patients with Philadelphia Chromosome-Negative Myeloproliferative Neoplasms: A Multicenter Study. Turkish journal of haematology : official journal of Turkish Society of Haematology 2024 8 . Fehmi Hindilerden, Özge Nuran Akay, Elif Aksoy, Aynur Da?lar-Aday, Emine Gültürk, Meliha Nalçac?, ?pek Yönal Hindilerd |
| Impact of somatic gene mutations on the risk of thrombosis in myelofibrosis. Leukemia 2024 8 . Irene Pastor-Galán, Arturo Pereira, Eduardo Arellano-Rodrigo, Iván Martín, Adrián Mosquera-Orgueira, María-Teresa Gómez-Casares, Alberto Hernández-Sánchez, Francisca Ferrer-Marín, Elvira Mora, Patricia Velez, Rosa Ayala, Anna Angona, Natalia de Las Heras, Elena Magro, María-Isabel Mata-Vázquez, María-Laura Fox, Sonia González de Villambrosía, María-José Ramírez, Ana García, Valentín García-Gutiérrez, Amparo Cáceres, María-Antonia Durán, María-Alicia Senín, José-María Raya, José Antonio González, Beatriz Cuevas, Blanca Xicoy, Marta Garrote, Blanca Ferrer, Manuel Pérez-Encinas, Jesús María Hernández-Rivas, Beatriz Bellosillo, Alberto Álvarez-Larrán, Juan Carlos Hernández-Bolu |
| Impact of proton pump inhibitor use on clinical outcomes in East Asian patients receiving clopidogrel following drug-eluting stent implantation. BMC medicine 2024 8 22 (1): 335. Ju Hyeon Kim, Soon Jun Hong, Jung-Joon Cha, Subin Lim, Hyung Joon Joo, Jae Hyoung Park, Cheol Woong Yu, Tae Hoon Ahn, Young-Hoon Jeong, Byeong-Keuk Kim, Kiyuk Chang, Yongwhi Park, Young Bin Song, Sung Gyun Ahn, Jung-Won Suh, Sang Yeub Lee, Jung Rae Cho, Ae-Young Her, Hyo-Soo Kim, Moo Hyun Kim, Eun-Seok Shin, Do-Sun L |
| Type 2N von Willebrand disease: Genotype drives different bleeding phenotypes and treatment needs. Journal of thrombosis and haemostasis : JTH 2024 7 . Mélanie Daniel, Catherine Ternisien, Sabine Castet, Céline Falaise, Roseline D'Oiron, Fabienne Volot, Nathalie Itzhar, Brigitte Pan-Petesch, Emmanuelle Jeanpierre, Camille Paris, Christophe Zawadzki, Maximilien Desvages, Annabelle Dupont, Agnès Veyradier, Yohann Repessé, Antoine Babuty, Marc Trossaërt, Pierre Boisseau, Cécile V Denis, Peter J Lenting, Jenny Goudemand, Antoine Rauch, Sophie Sus |
| Prognostic Impact of CYP2C19 Genotypes on Long-Term Clinical Outcomes in Older Patients After Percutaneous Coronary Intervention. Journal of the American Heart Association 2024 5 13 (10): e032248. Ju Hyeon Kim, Seung-Jun Lee, Jung-Joon Cha, Jae Hyoung Park, Soon Jun Hong, Tae Hoon Ahn, Byeong-Keuk Kim, Kiyuk Chang, Yongwhi Park, Young Bin Song, Sung Gyun Ahn, Jung-Won Suh, Sang Yeub Lee, Jung Rae Cho, Ae-Young Her, Young-Hoon Jeong, Hyo-Soo Kim, Moo Hyun Kim, Eun-Seok Shin, Do-Sun Lim, |
| ADAMTS13, von Willebrand Factor, Platelet Microparticles, Factor VIII, and Impact of Somatic Mutations in the Pathogenesis of Splanchnic Vein Thrombosis Associated with BCR-ABL-Negative Myeloproliferative Neoplasms. Life (Basel, Switzerland) 2024 4 14 (4): . Roberto Castelli, Alessandra Berzuini, Roberto Manetti, Alessandro Palmerio Delitala, Dante Castro, Giuseppe Sanna, Marta Chiara Sircana, Nicia Isabella Profili, Arianna Bartoli, Leyla La Cava, Giorgio Lambertenghi Deliliers, Mattia Donadoni, Antonio Gida |
| The effect of hereditary thrombophilia on recurrent pregnancy loss: a retrospective cohort study. BMC pregnancy and childbirth 2024 11 24 (1): 719. Hasan Berkan Sayal, Mehmet Sinan Beks |
| Clinical and Genetic Markers of Vascular Toxicity in Glioblastoma Patients: Insights from NRG Oncology RTOG-0825. Neuro-oncology 2024 11 . Joshua D Strauss, Mark R Gilbert, Minesh Mehta, Ang Li, Renke Zhou Ms, Melissa L Bondy, Erik P Sulman, Ying Yuan, Yanhong Liu, Elizabeth Vera, Merideth M Wendland, Volker W Stieber, Vinaykumar K Puduvalli, Serah Choi, Nina L Martinez, H Ian Robins, Grant K Hunter, Chi-Fan Lin, Vivian A Guedes, Melissa A Richard, Stephanie L Pugh, Terri S Armstrong, Michael E Scheur |
| Features and allele frequency of JAK2 Exon 12-mutated polycythemia vera in comparison with JAK2V617F-mutated disease. Archives of medical research 2024 10 56 (2): 103109. Chin-Hsuan Chuang, Ming-Chung Kuo, Jin-Hou Wu, Tung-Liang Lin, Po-Nan Wang, Yueh-Shih Chang, Tung-Hui Lin, Ting-Yu Huang, Yu-Shin Hung, Hsiao-Wen Kao, Che-Wei Ou, Hung Chang, Lee-Yung Sh |
| Rivaroxaban for Thromboembolism Prophylaxis in Patients with Nephrotic Syndrome: A Single-Arm, Prospective Study. Kidney diseases (Basel, Switzerland) 2024 10 10 (5): 346-358. Meng Wei, Xue Wu, Liteng Wang, Zhichun Gu, Yuanmao Tu, Lihua Zhang, Jiong Zhang, Honglang Xie, Qing Zhou, Yanan Chu, Zhen Cheng, Guohua Zhou, Qinxin So |
| DNMT3A/TET2/ASXL1 mutations are an age-independent thrombotic risk factor in polycythemia vera patients: an observational study. Thrombosis and haemostasis 2024 1 . Adrián Segura-Díaz, Ruth Stuckey, Yanira Florido, Marta Sobas, Alberto Alvarez-Larran, Francisca Ferrer, Manuel M Pérez-Encinas, Gonzalo Carreño-Tarragona, María Laura Fox, Barbara Tazón Vega, Barbara Cuevas, Juan Francisco López Rodríguez, Nuria Farías-Sánchez, Jesús M González-Martín, María Teresa Gómez-Casares, Cristina Bilbao-Siey |
| Prognostic Implication of Platelet Reactivity According to Left Ventricular Systolic Dysfunction Status in Patients Treated With Drug-Eluting Stent Implantation: Analysis of the PTRG-DES Consortium. Journal of Korean medical science 2024 1 39 (3): e27. Donghoon Han, Sun-Hwa Kim, Dong Geum Shin, Min-Kyung Kang, Seonghoon Choi, Namho Lee, Byeong-Keuk Kim, Hyung Joon Joo, Kiyuk Chang, Yongwhi Park, Young Bin Song, Sung Gyun Ahn, Jung-Won Suh, Sang Yeub Lee, Ae-Young Her, Young-Hoon Jeong, Hyo-Soo Kim, Moo Hyun Kim, Do-Sun Lim, Eun-Seok Shin, Jung Rae Cho, |
- Page last reviewed:Feb 1, 2024
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