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| JAK2V617F variant allele frequency, non-driver mutations, single-nucleotide variants and polycythemia vera outcome. Journal of cancer research and clinical oncology 2022 Oct . Kandu?a Zuzanna, Janowski Micha?, Wi?ckowska Barbara, Paczkowska Edyta, Lewandowski Krzyszt |
| Hematological relevance of JAK2 V617F and calreticulin mutations in Tunisian patients with essential thrombocythemia. Journal of clinical laboratory analysis 2022 Jun e24522. Abdelghani Maroua, Hammami Haifa, Zidi Wiem, Amouri Hassiba, Othmen Hind Ben Hadj, Farrah Ahlem, Menif Sam |
| Brain-Derived Neurotrophic Factor and Extracellular Vesicle-Derived miRNAs in an Italian Cohort of Individuals With Obesity: A Key to Explain the Link Between Depression and Atherothrombosis. Frontiers in cardiovascular medicine 2022 9 906483. Amadio Patrizia, Macchi Chiara, Favero Chiara, Zarà Marta, Solazzo Giulia, Dioni Laura, Sandrini Leonardo, Vigna Luisella, Greco Maria Francesca, Buoli Massimiliano, Sirtori Cesare R, Pesatori Angela Cecilia, Ieraci Alessandro, Ruscica Massimiliano, Barbieri Silvia Stella, Bollati Valenti |
| Association between CYP2C19 polymorphisms and clinical outcomes in patients undergoing stent procedure for cerebral artery stenosis. Scientific reports 2021 Mar 11 (1): 5974. Li Yan-Jiao, Chen Xuan, Tao Li-Na, Hu Xin-Yuan, Wang Xin-Lu, Song Yan-Qi |
| Impact of genetic variants on clinical outcome after percutaneous coronary intervention in elderly patients. Aging 2021 Mar 13 (5): 6506-6524. Cha Jung-Joon, Park Jae Hyoung, Joo Hyung Joon, Hong Soon Jun, Ahn Tae Hoon, Kim Byeong-Keuk, Shin WonYong, Ahn Sung Gyun, Yoon JungHan, Kim Yong Hoon, Cho Yun-Hyeong, Kang Woong Chol, Kim Weon, Lim Young-Hyo, Gwon Hyeon Cheol, Choi Woong Gil, Lim Do-S |
| Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation. Blood 2020 Dec . Goumidi Louisa, Thibord Florian, Wiggins Kerri L, Li-Gao Ruifang, Brown Michael R, van Hylckama Vlieg Astrid, Souto Juan Carlos, Soria Jose Manuel, Ibrahim-Kosta Manal, Saut Noémie, Daian-Bacq Delphine, Olaso Robert, Amouyel Philippe, Debette Stephanie, Boland Anne, Bailly Pascal, Morrison Alanna, Mook-Kanamori Dennis O, Deleuze Jean-François, Johnson Andrew D, de Vries Paul S, Sabater-Lleal Maria, Chiaroni Jacques, Smith Nicholas L, Rosendaal Frits R, Chasman Daniel I, Tregouet David, Morange Pierre-Emmanu |
| The risk of thrombosis in essential thrombocythemia is associated with the type of CALR mutation: A multicentre collaborative study. European journal of haematology 2020 Dec . Pérez Encinas Manuel M, Sobas Marta, Gómez-Casares María Teresa, Abuin Blanco Aitor, Noya Pereira María Soledad, Raya José María, Andrade-Campos Marcio Miguel, Álvarez Larrán Alberto, Lewandowki K, Lukasz Szukalski, Hernández Boluda Juan Carlos, Ferrer-Marín Francisca, Fox María Laura, Golos Aleksandra, Gasior Kabat Mercedes, Magro Mazo Elena, Czyz Anna, Martín Martín Alejandro, Bellosillo Paricio Beatriz, Quinteiro García Celsa, González Martín Jesús María, Stuckey Ru |
| Utilization of Whole Exome Sequencing Data to Identify Clinically Relevant Pharmacogenomic Variants in Pediatric Inflammatory Bowel Disease. Clinical and translational gastroenterology 2020 Dec 11 (12): e00263. Mulder Daniel J, Khalouei Sam, Warner Neil, Gonzaga-Jauregui Claudia, Church Peter C, Walters Thomas D, Ramani Arun K, Griffiths Anne M, Cohn Iris, Muise Aleixo |
| 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, E Gabrielsen Maiken, Brumpton Ben, Hindberg Kristian, Gran Olga V, Rosendaal Frits R, Braekkan Sigrid K, Hansen John-Bjar |
| 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 |
| CYP2C19 genotype and adverse cardiovascular outcomes after stent implantation in clopidogrel-treated Asian populations: A systematic review and meta-analysis. Platelets 2019 30 (2): 229-240. Xi Ziwei, Fang Fang, Wang Jiayang, AlHelal Jumana, Zhou Yujie, Liu W |
Genome-wide analysis of genetic determinants of circulating factor VII-activating protease (FSAP) activity.
Journal of thrombosis and haemostasis : JTH 2018 Aug . Olsson M, Stanne T M, Pedersen A, Lorentzen E, Kara E, Martinez-Palacian A, Rønnow Sand N P, Jacobsen A F, Sandset P M, Sidelmann J J, Engström G, Melander O, Kanse S M, Jern |
| Non-genetic and genetic risk factors for adult cerebral venous thrombosis. Thrombosis research 2018 Jul 169 15-22. Green Mackenzie, Styles Toby, Russell Timothy, Sada Charif, Jallow Ebrima, Stewart Jack, Lazariashvili Otar, Lubomirova Irina, Cotlarciuc Ioana, Sharma Sapna, Han Thang S, Sharma Pank |
| Impact of interleukin 6 promoter polymorphisms (-174 G?>?C, -572 G?>?C and -597 G?>?A) on plasma IL-6 levels and their influence on the development of DVT: a study from India. Hematology (Amsterdam, Netherlands) 2018 Jun 1-6. Sharma Amit, Singh Kanwaljeet, Biswas Arijit, Ranjan Ravi, Kishor Kamal, Pandey Hareram, Kumar Ravi, Mahapatra Manoranjan, Oldenburg Johannes, Saxena Re |
| Influence of tissue factor polymorphisms (603A>G and 5466A>G) on plasma tissue factor levels and their impact on deep vein thrombosis risk in young Indian population. Journal of thrombosis and thrombolysis 2018 May . Kishor Kamal, Sharma Amit, Singh Kanwaljeet, Ranjan Ravi, Pandey Hareram, Kumar Ravi, Kamal Vineet Kumar, Mishra Pravas, Mahapatra Manoranjan, Saxena Re |
| Impact of baseline clinical and laboratory features on the risk of thrombosis in children with acute lymphoblastic leukemia: A prospective evaluation. Pediatric blood & cancer 2018 Jan . Athale Uma H, Mizrahi T, Laverdière C, Nayiager T, Delva Y-L, Foster G, Thabane L, David M, Leclerc J-M, Chan A K |
| Risk of venous thromboembolism in association with factor V leiden in cancer patients - The EDITH case-control study. PloS one 2018 13 (5): e0194973. Heraudeau Adeline, Delluc Aurélien, Le Henaff Mickaël, Lacut Karine, Leroyer Christophe, Desrues Benoit, Couturaud Francis, Tromeur Céci |
| The association between P selectin glycoprotein ligand 1 gene variable number of tandem repeats polymorphism and risk of thrombosis in Behçet's disease. International journal of rheumatic diseases 2017 Aug . Cosan Fulya, Oku Basar, Gedar Totuk Ozgun M, Abaci Neslihan, Ustek Duran, Diz Kucukkaya Reyhan, Gul Ahm |
| The Role of Protein Z and Protein Z-Dependent Protease Inhibitor Polymorphisms in the Development of Prosthetic Heart Valve Thrombosis. The Journal of heart valve disease 2017 Jul 26 (4): 460-466. Karakoyun Süleyman, Ozan Gürsoy Mustafa, Kalç?k Macit, Yesin Mahmut, Gündüz Sabahattin, Ali Astarc?o?lu Mehmet, Bayram Zübeyde, Çakal Beytullah, Bayam Emrah, Özkan Mehm |
| C-reactive protein gene polymorphism predicts the risk of thromboembolic stroke in patients with atrial fibrillation: a more than 10-year prospective follow-up study. Journal of thrombosis and haemostasis : JTH 2017 May . Chang Sheng-Nan, Lai Ling-Ping, Chiang Fu-Tien, Lin Jiunn-Lee, Hwang Juey-Jen, Tsai Chia- |
| IVIg for Treatment of Severe Refractory Heparin-Induced Thrombocytopenia. Chest 2017 Apr . Padmanabhan Anand, Jones Curtis G, Pechauer Shannon M, Curtis Brian R, Bougie Daniel W, Irani Mehraboon S, Bryant Barbara J, Alperin Jack B, Deloughery Thomas G, Mulvey Kevin P, Dhakal Binod, Wen Renren, Wang Demin, Aster Richard |
| Prevalence of Factor V Leiden-G1691A and MTHFR-C677T Thrombosis Gene Modifier in Iron Deficiency Anemia: A Pathophysiological Effect in Indian Isolates. Indian journal of clinical biochemistry : IJCB 2017 Mar 32 (1): 103-105. Pandey S K, Pandey S, Mishra R M, Indurkar |
| Towards the genetic basis of cerebral venous thrombosis-the BEAST Consortium: a study protocol. BMJ open 2016 Nov 6 (11): e012351. Cotlarciuc Ioana, Marjot Thomas, Khan Muhammad S, Hiltunen Sini, Haapaniemi Elena, Metso Tiina M, Putaala Jukka, Zuurbier Susanna M, Brouwer Matthijs C, Passamonti Serena M, Bucciarelli Paolo, Pappalardo Emanuela, Patel Tasmin, Costa Paolo, Colombi Marina, Canhão Patrícia, Tkach Aleksander, Santacroce Rosa, Margaglione Maurizio, Favuzzi Giovanni, Grandone Elvira, Colaizzo Donatella, Spengos Kostas, Arauz Antonio, Hodge Amanda, Ditta Reina, Debette Stephanie, Zedde Marialuisa, Pare Guillaume, Ferro José M, Thijs Vincent, Pezzini Alessandro, Majersik Jennifer J, Martinelli Ida, Coutinho Jonathan M, Tatlisumak Turgut, Sharma Pankaj, |
| Gene polymorphism of CYP2C19*2, *3 and CYP3A4*1B and early stent thrombosis: case reports and literature review. Personalized medicine 2016 Sep 13 (5): 423-428. Kulmyrzaeva Nazgul, Tatarunas Vacis, Skipskis Vilius, Smagulova Gaziza, Seitmaganbetova Nazgul, Veikutiene Audrone, Lesauskaite Vai |
| Genetic Risk Factors in Venous Thromboembolism. Advances in experimental medicine and biology 2016 Sep . Hotoleanu Cristi |
| The efficacy of tissue factor -603A/G and +5466A>G polimorphisms at the development of venous thromboembolism in cancer patients. Experimental oncology 2016 Sep 38 (3): 187-90. Ero?lu A, Ceylan G G, Ozturk E, Yalcin A, Yalcin B, Karasoy |
| 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 |
| Next-Generation Sequencing and In Vitro Expression Study of ADAMTS13 Single Nucleotide Variants in Deep Vein Thrombosis. PloS one 2016 11 (11): e0165665. Pagliari Maria Teresa, Lotta Luca A, de Haan Hugoline G, Valsecchi Carla, Casoli Gloria, Pontiggia Silvia, Martinelli Ida, Passamonti Serena M, Rosendaal Frits R, Peyvandi Flo |
| Impact of ABCB1 and CYP2D6 polymorphisms on tamoxifen treatment outcomes and adverse events in breast cancer patients. Journal of B.U.ON. : official journal of the Balkan Union of Oncology 0 22 (5): 1217-1226. Argalacsova Sona, Slanar Ondrej, Bakhouche Hana, Pertuzelka Lub |
| Impact of Angiotensin-converting Enzyme and Matrix Metalloproteinase-3 Gene Polymorphisms on Risk for Developing Vascular Access Failure in Hemodialysis Patients - A Pilot Study. Indian journal of nephrology 0 29 (5): 329-333. Jankovic Aleksandar, Tosic Jelena, Buzadzic Ivana, Djuric Petar, Bulatovic Ana, Markovic Dragana, Popovic Jovan, Dimkovic Na |
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- Page last updated:Nov 22, 2022
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