Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 34 Records) |
Query Trace: KNG1[original query] |
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Population-specific coding variant underlies genome-wide association with adiponectin level. Human molecular genetics 2012 Jan 21 (2): 463-71. Croteau-Chonka Damien C, Wu Ying, Li Yun, Fogarty Marie P, Lange Leslie A, Kuzawa Christopher W, McDade Thomas W, Borja Judith B, Luo Jingchun, AbdelBaky Omar, Combs Terry P, Adair Linda S, Lange Ethan M, Mohlke Karen |
KNG1 Ile581Thr and susceptibility to venous thrombosis. Blood 2011 Mar 117 (13): 3692-4. Morange Pierre-Emmanuel, Oudot-Mellakh Tiphaine, Cohen William, Germain Marine, Saut Noémie, Antoni Guillemette, Alessi Marie-Christine, Bertrand Marion, Dupuy Anne-Marie, Letenneur Luc, Lathrop Mark, Lopez Lorna M, Lambert Jean-Charles, Emmerich Joseph, Amouyel Philippe, Trégouët David-Alexand |
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.
American journal of human genetics 2012 Jul 91 (1): 152-62. Tang Weihong, Schwienbacher Christine, Lopez Lorna M, Ben-Shlomo Yoav, Oudot-Mellakh Tiphaine, Johnson Andrew D, Samani Nilesh J, Basu Saonli, Gögele Martin, Davies Gail, Lowe Gordon D O, Tregouet David-Alexandre, Tan Adrian, Pankow James S, Tenesa Albert, Levy Daniel, Volpato Claudia B, Rumley Ann, Gow Alan J, Minelli Cosetta, Yarnell John W G, Porteous David J, Starr John M, Gallacher John, Boerwinkle Eric, Visscher Peter M, Pramstaller Peter P, Cushman Mary, Emilsson Valur, Plump Andrew S, Matijevic Nena, Morange Pierre-Emmanuel, Deary Ian J, Hicks Andrew A, Folsom Aaron |
A genome-wide association study identifies KNG1 as a genetic determinant of plasma factor XI Level and activated partial thromboplastin time. Arteriosclerosis, thrombosis, and vascular biology 2012 Aug 32 (8): 2008-16. Sabater-Lleal Maria, Martinez-Perez Angel, Buil Alfonso, Folkersen Lasse, Souto Juan Carlos, Bruzelius Maria, Borrell Montserrat, Odeberg Jacob, Silveira Angela, Eriksson Per, Almasy Laura, Hamsten Anders, Soria José Manu |
A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array. European journal of human genetics : EJHG 2013 Jul 21 (7): 779-83. Gaunt Tom R, Lowe Gordon D O, Lawlor Debbie A, Casas Juan-Pablo, Day Ian N |
Variants in adiponectin signaling pathway genes show little association with subclinical CVD in the diabetes heart study. Obesity (Silver Spring, Md.) 2013 Sep 21 (9): E456-62. Cox Amanda J, Lambird John E, An S Sandy, Register Thomas C, Langefeld Carl D, Carr J Jeffrey, Freedman Barry I, Bowden Donald |
Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes.
Circulation. Cardiovascular genetics 2015 Feb 8 (1): 131-40. Lieb Wolfgang, Chen Ming-Huei, Teumer Alexander, de Boer Rudolf A, Lin Honghuang, Fox Ervin R, Musani Solomon K, Wilson James G, Wang Thomas J, Völzke Henry, Petersen Ann-Kristin, Meisinger Christine, Nauck Matthias, Schlesinger Sabrina, Li Yong, Menard Jöel, Hercberg Serge, Wichmann H-Erich, Völker Uwe, Rawal Rajesh, Bidlingmaier Martin, Hannemann Anke, Dörr Marcus, Rettig Rainer, van Gilst Wiek H, van Veldhuisen Dirk J, Bakker Stephan J L, Navis Gerjan, Wallaschofski Henri, Meneton Pierre, van der Harst Pim, Reincke Martin, Vasan Ramachandran S, , , |
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 |
Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans. American journal of hematology 2015 Jun 90 (6): 534-40. Tang Weihong, Cushman Mary, Green David, Rich Stephen S, Lange Leslie A, Yang Qiong, Tracy Russell P, Tofler Geoffrey H, Basu Saonli, Wilson James G, Keating Brendan J, Weng Lu-Chen, Taylor Herman A, Jacobs David R, Delaney Joseph A, Palmer Cameron D, Young Taylor, Pankow James S, O'Donnell Christopher J, Smith Nicholas L, Reiner Alexander P, Folsom Aaron |
F11 is associated with recurrent VTE in women. A prospective cohort study. Thrombosis and haemostasis 2015 Oct 115 (2): . Bruzelius M, Ljungqvist M, Bottai M, Bergendal A, Strawbridge R J, Holmström M, Silveira A, Kieler H, Hamsten A, Lärfars G, Odeberg |
A genetic association study of activated partial thromboplastin time in European Americans and African Americans: the ARIC Study. Human molecular genetics 2015 Apr 24 (8): 2401-8. Weng Lu-Chen, Cushman Mary, Pankow James S, Basu Saonli, Boerwinkle Eric, Folsom Aaron R, Tang Weiho |
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 |
Relationship between the gene polymorphisms of kallikrein-kinin system and Alzheimer's disease in a Hunan Han Chinese population. International journal of clinical and experimental pathology 2015 8 (12): 15550-62. Deng Yanyao, Hou Deren, Tian Mi, Li Wei, Feng Xialu, Yu Zhuli |
Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study. Human molecular genetics 2017 9 26 (17): 3442-3450. de Vries Paul S, Yu Bing, Feofanova Elena V, Metcalf Ginger A, Brown Michael R, Zeighami Atefeh L, Liu Xiaoming, Muzny Donna M, Gibbs Richard A, Boerwinkle Eric, Morrison Alanna |
Next generation sequencing to dissect the genetic architecture of KNG1 and F11 loci using factor XI levels as an intermediate phenotype of thrombosis. PloS one 2017 12 (4): e0176301. Martin-Fernandez Laura, Gavidia-Bovadilla Giovana, Corrales Irene, Brunel Helena, Ramírez Lorena, López Sonia, Souto Juan Carlos, Vidal Francisco, Soria José Manu |
Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels.
Human molecular genetics 2017 Feb 26 (3): 637-649. Sennblad Bengt, Basu Saonli, Mazur Johanna, Suchon Pierre, Martinez-Perez Angel, van Hylckama Vlieg Astrid, Truong Vinh, Li Yuhuang, Gådin Jesper R, Tang Weihong, Grossman Vera, de Haan Hugoline G, Handin Niklas, Silveira Angela, Souto Juan Carlos, Franco-Cereceda Anders, Morange Pierre-Emmanuel, Gagnon France, Soria Jose Manuel, Eriksson Per, Hamsten Anders, Maegdefessel Lars, Rosendaal Frits R, Wild Philipp, Folsom Aaron R, Trégouët David-Alexandre, Sabater-Lleal Mar |
Genome-wide association study identifies genes associated with neuropathy in patients with head and neck cancer.
Scientific reports 2018 Jun 8 (1): 8789. Reyes-Gibby Cielito C, Wang Jian, Yeung Sai-Ching J, Chaftari Patrick, Yu Robert K, Hanna Ehab Y, Shete Sanj |
Genetic effects of BDKRB2 and KNG1 on deep venous thrombosis after orthopedic surgery and the potential mediator. Scientific reports 2018 Nov 8 (1): 17332. Wang Qingfeng, Cheng Guoping, Wang Xiaohui, Wang Dandan, Yang Yanmei, Chen Ke, Ye Jiumin, Qing Zho |
Genetic determinants of activity and antigen levels of contact system factors. Journal of thrombosis and haemostasis : JTH 2018 Oct . Rohmann J L, de Haan H G, Algra A, Vossen C Y, Rosendaal F R, Siegerink |
A gender-specific association of the polymorphism Ile197Met in the kininogen 1 gene with plasma irbesartan concentrations in Chinese patients with essential hypertension. Journal of human hypertension 2018 Oct . Hu Shengnan, Cheng Jun, Weinstock Justin, Fan Xiu, Venners Scott A, Hsu Yi-Hsiang, Suwen Wu , Pan Faming, Zha Xiangdong, Sun Jinlu, Jiang Shanqun, Xu Xipi |
Decreased plasma kallikrein activity is associated with reduced kidney function in individuals with type 1 diabetes. Diabetologia 2020 4 63 (7): 1349-1354. Härma Mari-Anne, Dahlström Emma H, Sandholm Niina, Forsblom Carol, Groop Per-Henrik, Lehto Markku, |
Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor. Journal of clinical medicine 2020 10 9 (11): . Loules Gedeon, Parsopoulou Faidra, Zamanakou Maria, Csuka Dorottya, Bova Maria, González-Quevedo Teresa, Psarros Fotis, Porebski Gregor, Speletas Matthaios, Firinu Davide, Del Giacco Stefano, Suffritti Chiara, Makris Michael, Vatsiou Sofia, Zanichelli Andrea, Farkas Henriette, Germenis Anastasios |
Next Generation Sequencing of 502 Lifestyle and Nutrition related Genetic Polymorphisms reveals Independent Loci for Low Serum 25-hydroxyvitamin D Levels among Adult Respondents of the 2013 Philippine National Nutrition Survey. Journal of the ASEAN Federation of Endocrine Societies 2021 36 (1): 56-63. Zumaraga Mark Pretzel, Concepcion Mae Anne, Duante Charmaine, Rodriguez Mariet |
Common genetic variants associated with obesity in an African-American and Hispanic/Latino population. PloS one 2021 16 (5): e0250697. Chalazan Brandon, Palm Denada, Sridhar Arvind, Lee Christina, Argos Maria, Daviglus Martha, Rehman Jalees, Konda Sreenivas, Darbar Dawo |
Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.
Journal of the American Heart Association 2021 Oct e022482. Leskelä Jaakko, Toppila Iiro, Härma Mari-Anne, Palviainen Teemu, Salminen Aino, Sandholm Niina, Pietiäinen Milla, Kopra Elisa, Pais de Barros Jean-Paul, , Lassenius Mariann I, Kumar Anmol, Harjutsalo Valma, Roslund Kajsa, Forsblom Carol, Loukola Anu, Havulinna Aki S, Lagrost Laurent, Salomaa Veikko, Groop Per-Henrik, Perola Markus, Kaprio Jaakko, Lehto Markku, Pussinen Pirkko |
Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes. Frontiers in genetics 2022 8 13 914376. Mathey Carina M, Maj Carlo, Scheer Annika B, Fazaal Julia, Wedi Bettina, Wieczorek Dorothea, Amann Philipp M, Löffler Harald, Koch Lukas, Schöffl Clemens, Dickel Heinrich, Ganjuur Nomun, Hornung Thorsten, Forkel Susann, Greve Jens, Wurpts Gerda, Hallberg Pär, Bygum Anette, Von Buchwald Christian, Karawajczyk Malgorzata, Steffens Michael, Stingl Julia, Hoffmann Per, Heilmann-Heimbach Stefanie, Mangold Elisabeth, Ludwig Kerstin U, Rasmussen Eva R, Wadelius Mia, Sachs Bernhardt, Nöthen Markus M, Forstner Andreas |
Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations.
Journal of thrombosis and haemostasis : JTH 2022 3 20 (6): 1331-1349. Temprano-Sagrera Gerard, Sitlani Colleen M, Bone William P, Martin-Bornez Miguel, Voight Benjamin F, Morrison Alanna C, Damrauer Scott M, de Vries Paul S, Smith Nicholas L, Sabater-Lleal Mar |
Cryptogenic Stroke in the Young: Role of Candidate Gene Polymorphisms in Indian Patients with Ischemic Etiology. Neurology India 2022 1 69 (6): 1655-1662. Salomi Bodda S B, Solomon Raja, Turaka Vijay Prakash, Aaron Sanjith, Christudass Christhunesa |
Identification of tumor antigens and immune subtypes of hepatocellular carcinoma for mRNA vaccine development. World journal of gastrointestinal oncology 2023 11 15 (10): 1717-1738. Tai-Liang Lu, Cheng-Long Li, Yong-Qiang Gong, Fu-Tao Hou, Chao-Wu Ch |
Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency-causing KNG1 variants, and estimated prevalence. Journal of thrombosis and haemostasis : JTH 2023 1 21 (2): 237-254. Adenaeuer Anke, Barco Stefano, Trinchero Alice, Krutmann Sarah, Nazir Hanan Fawzy, Ambaglio Chiara, Rocco Vincenzo, Pancione Ylenia, Tomao Luigi, Ruiz-Sáez Arlette, Echenagucia Marion, Alesci Sonja, Sollfrank Stefanie, Ezigbo Eyiuche D, Häuser Friederike, Lackner Karl J, Lämmle Bernhard, Rossmann Hei |
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- Page last updated:Apr 22, 2024
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