Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 37 Records) |
Query Trace: KLKB1[original query] |
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Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1.
Hypertension 2013 Feb . Verweij N, Mahmud H, Leach IM, de Boer RA, Brouwers FP, Yu H, Asselbergs FW, Strück J, Bakker SJ, Gansevoort RT, Munroe PB, Hillege HL, van Veldhuisen DJ, van Gilst WH, Silljé HH, van der Harst P |
Genome-wide protein QTL mapping identifies human plasma kallikrein as a post-translational regulator of serum uPAR levels. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2014 Feb 28 (2): 923-34. Portelli Michael A, Siedlinski Mateusz, Stewart Ceri E, Postma Dirkje S, Nieuwenhuis Maartje A, Vonk Judith M, Nurnberg Peter, Altmuller Janine, Moffatt Miriam F, Wardlaw Andrew J, Parker Stuart G, Connolly Martin J, Koppelman Gerard H, Sayers I |
Genetic determinants influencing human serum metabolome among African Americans.
PLoS genetics 2014 Mar 10 (3): e1004212. Yu Bing, Zheng Yan, Alexander Danny, Morrison Alanna C, Coresh Josef, Boerwinkle Er |
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, , , |
Association between KLKB1 Polymorphisms and Pulmonary Thromboembolism. Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae 2015 Jun 37 (3): 274-8. Min-Ne Wang, Xiao-Mao X U, Zhen-Guo Zhai, Liang Sun, Bao-Min Fang, Fei Xiao, Jian G |
Genome-wide association analysis of plasma B-type natriuretic peptide in blacks: the Jackson Heart Study.
Circulation. Cardiovascular genetics 2015 Feb 8 (1): 122-30. Musani Solomon K, Fox Ervin R, Kraja Aldi, Bidulescu Aurelian, Lieb Wolfgang, Lin Honghuang, Beecham Ashley, Chen Ming-Huei, Felix Janine F, Fox Caroline S, Kao W H Linda, Kardia Sharon L R, Liu Ching-Ti, Nalls Mike A, Rundek Tatjana, Sacco Ralph L, Smith Jennifer, Sun Yan V, Wilson Gregory, Zhang Zhaogong, Mosley Thomas H, Taylor Herman A, Vasan Ramachandran |
Genome-wide association reveals that common genetic variation in the kallikrein-kinin system is associated with serum L-arginine levels.
Thrombosis and haemostasis 2016 Sep 116 (6): . Zhang Weihua, Jernerén Fredrik, Lehne Benjamin C, Chen Ming-Huei, Luben Robert N, Johnston Carole, Elshorbagy Amany, Eppinga Ruben N, Scott William R, Adeyeye Elizabeth, Scott James, Böger Rainer H, Khaw Kay-Tee, van der Harst Pim, Wareham Nicholas J, Vasan Ramachandran S, Chambers John C, Refsum Helga, Kooner Jaspal |
A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.
Human molecular genetics 2016 Aug 25 (16): 3635-3646. Lamina Claudia, Friedel Salome, Coassin Stefan, Rueedi Rico, Yousri Noha A, Seppälä Ilkka, Gieger Christian, Schönherr Sebastian, Forer Lukas, Erhart Gertraud, Kollerits Barbara, Marques-Vidal Pedro, Ried Janina, Waeber Gerard, Bergmann Sven, Dähnhardt Doreen, Stöckl Andrea, Kiechl Stefan, Raitakari Olli T, Kähönen Mika, Willeit Johann, Kedenko Ludmilla, Paulweber Bernhard, Peters Annette, Meitinger Thomas, Strauch Konstantin, Study Group Kora, Lehtimäki Terho, Hunt Steven C, Vollenweider Peter, Kronenberg Flori |
A Cross-sectional Study of KLKB1 and PRCP Polymorphisms in Patient Samples with Cardiovascular Disease. Frontiers in medicine 2016 3 17. Gittleman Haley R, Merkulova Alona, Alhalabi Omar, Stavrou Evi X, Veigl Martina L, Barnholtz-Sloan Jill S, Schmaier Alvin |
Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin system. BMC medical genetics 2016 17 (1): 21. Biswas Nilima, Maihofer Adam X, Mir Saiful Anam, Rao Fangwen, Zhang Kuixing, Khandrika Srikrishna, Mahata Manjula, Friese Ryan S, Hightower C Makena, Mahata Sushil K, Baker Dewleen G, Nievergelt Caroline M, Vaingankar Sucheta M, O'Connor Daniel |
Identification of novel loci affecting circulating chromogranins and related peptides.
Human molecular genetics 2017 Jan 26 (1): 233-242. Benyamin Beben, Maihofer Adam X, Schork Andrew J, Hamilton Bruce A, Rao Fangwen, Schmid-Schönbein Geert W, Zhang Kuixing, Mahata Manjula, Stridsberg Mats, Schork Nicholas J, Biswas Nilima, Hook Vivian Y, Wei Zhiyun, Montgomery Grant W, Martin Nicholas G, Nievergelt Caroline M, Whitfield John B, O'Connor Daniel |
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 |
Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of Onset. International archives of allergy and immunology 2017 11 174 (3-4): 200-204. Gianni Panagiota, Loules Gedeon, Zamanakou Maria, Kompoti Maria, Csuka Dorottya, Psarros Fotis, Magerl Markus, Moldovan Dimitru, Maurer Marcus, Speletas Matthaios G, Farkas Henriette, Germenis Anastasios |
Genetic predisposition to bevacizumab-induced hypertension. Gynecologic oncology 2017 Sep . Frey Melissa K, Dao Fanny, Olvera Narciso, Konner Jason A, Dickler Maura N, Levine Douglas |
Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes. Journal of thrombosis and haemostasis : JTH 2018 Aug . de Haan H G, van Hylckama Vlieg A, Lotta L A, Gorski M M, Bucciarelli P, Martinelli I, Baglin T P, Peyvandi F, Rosendaal F R, |
Heritability and Genome-Wide Association Study of Plasma Cholesterol in Chinese Adult Twins.
Frontiers in endocrinology 2018 9 677. Liu Hui, Wang Weijing, Zhang Caixia, Xu Chunsheng, Duan Haiping, Tian Xiaocao, Zhang Dongfe |
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 |
Genetic profiling revealed an increased risk of venous thrombosis in the Hungarian Roma population. Thrombosis research 2019 5 179 37-44. Fiatal Szilvia, Pikó Péter, Kósa Zsigmond, Sándor János, Ádány Ró |
COVID-19-Related Coagulopathy-Is Transferrin a Missing Link? Diagnostics (Basel, Switzerland) 2020 8 10 (8): . McLaughlin Katie-May, Bechtel Marco, Bojkova Denisa, Münch Christian, Ciesek Sandra, Wass Mark N, Michaelis Martin, Cinatl Jindri |
Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence. Journal of thrombosis and haemostasis : JTH 2020 3 18 (7): 1598-1617. Barco Stefano, Sollfrank Stefanie, Trinchero Alice, Adenaeuer Anke, Abolghasemi Hassan, Conti Laura, Häuser Friederike, Kremer Hovinga Johanna A, Lackner Karl J, Loewecke Felicia, Miloni Erwin, Vazifeh Shiran Nader, Tomao Luigi, Wuillemin Walter A, Zieger Barbara, Lämmle Bernhard, Rossmann Hei |
c.451dupT in KLKB1 is common in Nigerians, confirming a higher prevalence of severe prekallikrein deficiency in Africans compared to Europeans. Journal of thrombosis and haemostasis : JTH 2020 10 19 (1): 147-152. Adenaeuer Anke, Ezigbo Eyiuche D, Fawzy Nazir Hanan, Barco Stefano, Trinchero Alice, Laubert-Reh Dagmar, Strauch Konstantin, Wild Philipp S, Lackner Karl J, Lämmle Bernhard, Rossmann Hei |
Kallikrein augments the anticoagulant function of the protein C system in thrombin generation.
Journal of thrombosis and haemostasis : JTH 2021 9 . Wan Jun, Vadaq Nadira, Konings Joke, Jaeger Martin, Kumar Vinod, de Laat Bas, Joosten Leo, Netea Mihai G, van der Ven Andre J, de Groot Philip G, de Mast Quirijn, Roest Ma |
Genome-wide association study of cardiac troponin I in the general population.
Human molecular genetics 2021 . Moksnes Marta R, Røsjø Helge, Richmond Anne, Lyngbakken Magnus N, Graham Sarah E, Hansen Ailin Falkmo, Wolford Brooke N, Gagliano Taliun Sarah A, LeFaive Jonathon, Rasheed Humaira, Thomas Laurent F, Zhou Wei, Aung Nay, Surakka Ida, Douville Nicholas J, Campbell Archie, Porteous David J, Petersen Steffen E, Munroe Patricia B, Welsh Paul, Sattar Naveed, Smith George Davey, Fritsche Lars G, Nielsen Jonas B, Åsvold Bjørn Olav, Hveem Kristian, Hayward Caroline, Willer Cristen J, Brumpton Ben M, Omland Torbjø |
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 |
Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE). Frontiers in allergy 2022 7 3 868185. Parsopoulou Faidra, Loules Gedeon, Zamanakou Maria, Csuka Dorottya, Szilagyi Agnes, Kompoti Maria, Porebski Grzegorz, Psarros Fotis, Magerl Markus, Valerieva Anna, Staevska Maria, Obtulowicz Krystyna, Maurer Marcus, Speletas Matthaios, Farkas Henriette, Germenis Anastasios |
Genetics of osteopontin in patients with chronic kidney disease: The German Chronic Kidney Disease study. PLoS genetics 2022 4 18 (4): e1010139. Cheng Yurong, Li Yong, Scherer Nora, Grundner-Culemann Franziska, Lehtimäki Terho, Mishra Binisha H, Raitakari Olli T, Nauck Matthias, Eckardt Kai-Uwe, Sekula Peggy, Schultheiss Ulla T, |
Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature 2022 10 611 (7934): 115-123. Mishra Aniket, Malik Rainer, Hachiya Tsuyoshi, Jürgenson Tuuli, Namba Shinichi, Posner Daniel C, Kamanu Frederick K, Koido Masaru, Le Grand Quentin, Shi Mingyang, He Yunye, Georgakis Marios K, Caro Ilana, Krebs Kristi, Liaw Yi-Ching, Vaura Felix C, Lin Kuang, Winsvold Bendik Slagsvold, Srinivasasainagendra Vinodh, Parodi Livia, Bae Hee-Joon, Chauhan Ganesh, Chong Michael R, Tomppo Liisa, Akinyemi Rufus, Roshchupkin Gennady V, Habib Naomi, Jee Yon Ho, Thomassen Jesper Qvist, Abedi Vida, Cárcel-Márquez Jara, Nygaard Marianne, Leonard Hampton L, Yang Chaojie, Yonova-Doing Ekaterina, Knol Maria J, Lewis Adam J, Judy Renae L, Ago Tetsuro, Amouyel Philippe, Armstrong Nicole D, Bakker Mark K, Bartz Traci M, Bennett David A, Bis Joshua C, Bordes Constance, Børte Sigrid, Cain Anael, Ridker Paul M, Cho Kelly, Chen Zhengming, Cruchaga Carlos, Cole John W, de Jager Phil L, de Cid Rafael, Endres Matthias, Ferreira Leslie E, Geerlings Mirjam I, Gasca Natalie C, Gudnason Vilmundur, Hata Jun, He Jing, Heath Alicia K, Ho Yuk-Lam, Havulinna Aki S, Hopewell Jemma C, Hyacinth Hyacinth I, Inouye Michael, Jacob Mina A, Jeon Christina E, Jern Christina, Kamouchi Masahiro, Keene Keith L, Kitazono Takanari, Kittner Steven J, Konuma Takahiro, Kumar Amit, Lacaze Paul, Launer Lenore J, Lee Keon-Joo, Lepik Kaido, Li Jiang, Li Liming, Manichaikul Ani, Markus Hugh S, Marston Nicholas A, Meitinger Thomas, Mitchell Braxton D, Montellano Felipe A, Morisaki Takayuki, Mosley Thomas H, Nalls Mike A, Nordestgaard Børge G, O'Donnell Martin J, Okada Yukinori, Onland-Moret N Charlotte, Ovbiagele Bruce, Peters Annette, Psaty Bruce M, Rich Stephen S, Rosand Jonathan, Sabatine Marc S, Sacco Ralph L, Saleheen Danish, Sandset Else Charlotte, Salomaa Veikko, Sargurupremraj Muralidharan, Sasaki Makoto, Satizabal Claudia L, Schmidt Carsten O, Shimizu Atsushi, Smith Nicholas L, Sloane Kelly L, Sutoh Yoichi, Sun Yan V, Tanno Kozo, Tiedt Steffen, Tatlisumak Turgut, Torres-Aguila Nuria P, Tiwari Hemant K, Trégouët David-Alexandre, Trompet Stella, Tuladhar Anil Man, Tybjærg-Hansen Anne, van Vugt Marion, Vibo Riina, Verma Shefali S, Wiggins Kerri L, Wennberg Patrik, Woo Daniel, Wilson Peter W F, Xu Huichun, Yang Qiong, Yoon Kyungheon, , , , , , , , , , , , , , , , Millwood Iona Y, Gieger Christian, Ninomiya Toshiharu, Grabe Hans J, Jukema J Wouter, Rissanen Ina L, Strbian Daniel, Kim Young Jin, Chen Pei-Hsin, Mayerhofer Ernst, Howson Joanna M M, Irvin Marguerite R, Adams Hieab, Wassertheil-Smoller Sylvia, Christensen Kaare, Ikram Mohammad A, Rundek Tatjana, Worrall Bradford B, Lathrop G Mark, Riaz Moeen, Simonsick Eleanor M, Kõrv Janika, França Paulo H C, Zand Ramin, Prasad Kameshwar, Frikke-Schmidt Ruth, de Leeuw Frank-Erik, Liman Thomas, Haeusler Karl Georg, Ruigrok Ynte M, Heuschmann Peter Ulrich, Longstreth W T, Jung Keum Ji, Bastarache Lisa, Paré Guillaume, Damrauer Scott M, Chasman Daniel I, Rotter Jerome I, Anderson Christopher D, Zwart John-Anker, Niiranen Teemu J, Fornage Myriam, Liaw Yung-Po, Seshadri Sudha, Fernández-Cadenas Israel, Walters Robin G, Ruff Christian T, Owolabi Mayowa O, Huffman Jennifer E, Milani Lili, Kamatani Yoichiro, Dichgans Martin, Debette Stephan |
KLKB1 and CLSTN2 are associated with HDL-mediated cholesterol efflux capacity in a genome-wide association study. Atherosclerosis 2023 2 368 1-11. Schachtl-Riess Johanna F, Schönherr Sebastian, Lamina Claudia, Forer Lukas, Coassin Stefan, Streiter Gertraud, Kheirkhah Azin, Li Yong, Meiselbach Heike, Di Maio Silvia, Eckardt Kai-Uwe, Köttgen Anna, Kronenberg Florian, |
Prion Mutations in Republic of Republic of Korea, China, and Japan. International journal of molecular sciences 2023 1 24 (1): . Kim Dan Yeong, Shim Kyu Hwan, Bagyinszky Eva, An Seong Soo |
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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