Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Disease and KLKB1[original query] |
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| 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 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 |
| 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 |
| 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 |
| 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 |
| 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 |
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