Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 72 Records) |
Query Trace: F7[original query] |
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Association of seven thrombotic pathway gene CpG-SNPs with coronary heart disease. Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie 2015 May 72 98-102. Ye Huadan, Zhou Annan, Hong Qingxiao, Chen Xiaoying, Xin Yanfei, Tang Linlin, Dai Dongjun, Ji Huihui, Xu Mingqing, Wang Dao Wen, Duan Shiw |
Modulation of the COMT Val(158)Met polymorphism on resting-state EEG power. Frontiers in human neuroscience 2015 9 136. Solís-Ortiz Silvia, Pérez-Luque Elva, Gutiérrez-Muñoz May |
Can Genetic Analysis of Putative Blood Alzheimer's Disease Biomarkers Lead to Identification of Susceptibility Loci? PloS one 2015 10 (12): e0142360. Barber Robert C, Phillips Nicole R, Tilson Jeffrey L, Huebinger Ryan M, Shewale Shantanu J, Koenig Jessica L, Mitchel Jeffrey S, O'Bryant Sid E, Waring Stephen C, Diaz-Arrastia Ramon, Chasse Scott, Wilhelmsen Kirk C, |
Large deletions play a minor but essential role in congenital coagulation factor VII and X deficiencies. Ha?mostaseologie 2015 35 Suppl 1 S36-42. Rath M, Najm J, Sirb H, Kentouche K, Dufke A, Pauli S, Hackmann K, Liehr T, Hübner C A, Felbor U, |
[Polymorphism (353)R>Q of Gene of Blood Clotting Factor FVII and Plasma Hemostasis]. Genetika 2016 Feb 52 (2): 242-8. Bairova T A, Gommellya M V, Dolgich V V, Philippov E S, Kolesnikova L |
Isotypic analysis of antibodies against activated Factor VII in patients with Factor VII deficiency using the x-MAP technology. Thrombosis research 2016 Feb 141 22-27. Pfeiffer Caroline, Mathieu-Dupas Eve, Logghe Pauline, Lissalde-Lavigne Géraldine, Balicchi Julien, Caliskan Umran, Valentin Thomas, Laune Daniel, Molina Franck, Schved Jean François, Giansily-Blaizot Muri |
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 |
F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study. Thrombosis and haemostasis 2017 Apr . Quintavalle Gabriele, Riccardi Federica, Rivolta Gianna Franca, Martorana Davide, Di Perna Caterina, Percesepe Antonio, Tagliaferri Annarita, |
Associations of activated coagulation factor VII and factor VIIa-antithrombin levels with genome-wide polymorphisms and cardiovascular disease risk. Journal of thrombosis and haemostasis : JTH 2017 Nov . Olson N C, Raffield L M, Lange L A, Lange E M, Longstreth W T, Chauhan G, Debette S, Seshadri S, Reiner A P, Tracy R |
[Analysis of Phenotype and L12R Mutation in Signal Peptide and 3' Non-translation Region c11814-insAA Mutation of F7 Gene in a Family with Hereditary Coagulation Factor VII Deficiency]. Zhongguo shi yan xue ye xue za zhi 2018 4 26 (2): 508-515. Liu Shan, Zhang Jing-Yu, Li Zheng-Rong, Wang Yan, Niu Zhi-Yun, Lin Feng- |
Reproductive response to male joining with ewes with different allelic variants of the MTNR1A gene. Animal reproduction science 2018 12 200 67-74. Mura Maria Consuelo, Luridiana Sebastiano, Pulinas Luisa, Di Stefano Maria Veronica, Carcangiu Vincen |
Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis. Haemophilia : the official journal of the World Federation of Hemophilia 2018 11 25 (1): 127-135. Saes Joline L, Simons Annet, de Munnik Sonja A, Nijziel Marten R, Blijlevens Nicole M A, Jongmans Marjolijn C, van der Reijden Bert A, Smit Yolba, Brons Paul P, van Heerde Waander L, Schols Saskia E |
The impact of R353Q genetic polymorphism in coagulation factor VII on the initial anticoagulant effect exerted by warfarin. European journal of clinical pharmacology 2019 Mar 75 (3): 343-350. Shaul Chanan, Blotnick Simcha, Deutsch Liat, Rosenberg Gilad, Caraco Yose |
Next-generation sequencing and recombinant expression characterized aberrant splicing mechanisms and provided correction strategies in factor VII deficiency. Haematologica 2019 7 105 (3): 829-837. Ferraresi Paolo, Balestra Dario, Guittard Caroline, Buthiau Delphine, Pan-Petesh Brigitte, Maestri Iva, Farah Roula, Pinotti Mirko, Giansily-Blaizot Muri |
[A clinical and genetic analysis of risk factors for the development of acute and chronic cerebral ischemia]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2019 119 (3. Vyp. 2): 62-67. Anisimova A V, Gunchenko A S, Ikonnikova A Yu, Galkin S S, Avdonina M A, Nasedkina T |
[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 |
A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology.
Blood 2019 Feb 133 (9): 967-977. de Vries Paul S, Sabater-Lleal Maria, Huffman Jennifer E, Marten Jonathan, Song Ci, Pankratz Nathan, Bartz Traci M, de Haan Hugoline G, Delgado Graciela E, Eicher John D, Martinez-Perez Angel, Ward-Caviness Cavin K, Brody Jennifer A, Chen Ming-Huei, de Maat Moniek P M, Frånberg Mattias, Gill Dipender, Kleber Marcus E, Rivadeneira Fernando, Soria José Manuel, Tang Weihong, Tofler Geoffrey H, Uitterlinden André G, van Hylckama Vlieg Astrid, Seshadri Sudha, Boerwinkle Eric, Davies Neil M, Giese Anne-Katrin, Ikram M Kamran, Kittner Steven J, McKnight Barbara, Psaty Bruce M, Reiner Alex P, Sargurupremraj Muralidharan, Taylor Kent D, , , Fornage Myriam, Hamsten Anders, März Winfried, Rosendaal Frits R, Souto Juan Carlos, Dehghan Abbas, Johnson Andrew D, Morrison Alanna C, O'Donnell Christopher J, Smith Nicholas |
Determining the association of thrombophilic gene polymorphisms with recurrent pregnancy loss in Iranian women. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2020 6 36 (12): 1082-1085. Khorshidi Fatemeh, Hajizadeh Sonia, Choobineh Hamid, Alizadeh Shaban, Sharifi Mohammad Jafar, Kavosh Zeinab, Omidkhoda Azad |
Aptamer-modified FXa generation assays to investigate hypercoagulability in plasma from patients with ischemic heart disease. Thrombosis research 2020 4 189 140-146. Baroni Marcello, Martinelli Nicola, Lunghi Barbara, Marchetti Giovanna, Castagna Annalisa, Stefanoni Filippo, Pinotti Mirko, Woodhams Barry, Olivieri Oliviero, Bernardi Frances |
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 |
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 |
Monogenic Causes of Apparently Idiopathic Perinatal Intracranial Hemorrhage. Annals of neurology 2021 2 89 (4): 813-822. Hausman-Kedem Moran, Malinger Gustavo, Modai Shira, Kushner Steven A, Shiran Shelly I, Ben-Sira Liat, Roth Jonathan, Constantini Shlomi, Fattal-Valevski Aviva, Ben-Shachar Sh |
Risk of Recurrent Pregnancy Loss in the Ukrainian Population Using a Combined Effect of Genetic Variants: A Case-Control Study. Genes 2021 Jan 12 (1): . Loizidou Eleni M, Kucherenko Anastasia, Tatarskyy Pavlo, Chernushyn Sergey, Livshyts Ganna, Gulkovskyi Roman, Vorobiova Iryna, Antipkin Yurii, Gorodna Oleksandra, Kaakinen Marika A, Prokopenko Inga, Livshits Ludmi |
Clinical phenotype and F7 gene genotype in 40 Tunisian patients with congenital factor VII deficiency. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2022 7 33 (5): 280-284. Ouardani Cherifa, Elmahmoudi Hejer, ELborgi Wejden, Gharbi Maroua, Meriem Achour, Gouider Em |
Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes.
American journal of human genetics 2022 5 109 (6): 1117-1139. Nieves-Colón Maria A, Badillo Rivera Keyla M, Sandoval Karla, Villanueva Dávalos Vanessa, Enriquez Lencinas Luis E, Mendoza-Revilla Javier, Adhikari Kaustubh, González-Buenfil Ram, Chen Jessica W, Zhang Elisa T, Sockell Alexandra, Ortiz-Tello Patricia, Hurtado Gloria Malena, Condori Salas Ramiro, Cebrecos Ricardo, Manzaneda Choque José C, Manzaneda Choque Franz P, Yábar Pilco Germán P, Rawls Erin, Eng Celeste, Huntsman Scott, Burchard Esteban, Ruiz-Linares Andrés, González-José Rolando, Bedoya Gabriel, Rothhammer Francisco, Bortolini Maria Cátira, Poletti Giovanni, Gallo Carla, Bustamante Carlos D, Baker Julie C, Gignoux Christopher R, Wojcik Genevieve L, Moreno-Estrada Andr |
Whole-exome sequencing of 14?389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Human molecular genetics 2022 May . Pankratz Nathan, Wei Peng, Brody Jennifer A, Chen Ming-Huei, de Vries Paul S, Huffman Jennifer E, Stimson Mary Rachel, Auer Paul L, Boerwinkle Eric, Cushman Mary, de Maat Moniek P M, Folsom Aaron R, Franco Oscar H, Gibbs Richard A, Haagenson Kelly K, Hofman Albert, Johnsen Jill M, Kovar Christie L, Kraaij Robert, McKnight Barbara, Metcalf Ginger A, Muzny Donna, Psaty Bruce M, Tang Weihong, Uitterlinden André G, van Rooij Jeroen G J, Dehghan Abbas, O'Donnell Christopher J, Reiner Alex P, Morrison Alanna C, Smith Nicholas |
Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effect. Haemophilia : the official journal of the World Federation of Hemophilia 2022 12 . Sharma Ritika, Jamwal Manu, Senee Hari Kishan, Singh Namrata, Kumar Narender, Hans Chander, Kler Anita, Bansal Deepak, Trehan Amita, Malhotra Pankaj, Ahluwalia Jasmina, Das Ree |
The prevalence and linkage disequilibrium of 21 genetic variations related to thrombophilia, folate cycle, and hypertension in reproductive age women of Rostov region (Russia). Annals of human genetics 2023 11 . Oksana Yurievna Bordaeva, Ekaterina Grigorievna Derevyanchuk, Dema Alset, Maria Aleksandrovna Amelina, Tatiana Pavlovna Shkur |
The Association of Different Genetic Variants with the Development of Hypoxic-Ischemic Encephalopathy. Biomedicines 2023 10 11 (10): . Vesna Pavlov, Anet Papazovska Cherepnalkovski, Marino Marcic, Ljiljana Marcic, Radenka Kuzmanic Sami |
Genotype-Phenotype Relationship among 785 Unrelated White Women with Inherited Congenital Factor VII Deficiency: A Three-Center Database Study. Journal of clinical medicine 2024 1 13 (1): . Susan Halimeh, Lydia Koch, Gili Kenet, Piotr Kuta, Tess Rahmfeld, Monika Stoll, Ulrike Nowak-Göt |
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- Page last updated:Apr 22, 2024
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