Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Methylenetetrahydrofolate Reductase (NADPH2)/genetics"'
Autor:
Betina H. Thuesen, Allan Linneberg, Mogens Fenger, Camilla H. Sandholt, Tea Skaaby, Torben Hansen, Niels Grarup, Lise Lotte N. Husemoen, Torben Jørgensen, Oluf Pedersen
Publikováno v:
Husemoen, L L N, Skaaby, T, Jorgensen, T, Thuesen, B H, Fenger, M, Grarup, N, Sandholt, C H, Hansen, T, Pedersen, O & Linneberg, A 2014, ' MTHFR C677T genotype and cardiovascular risk in a general population without mandatory folic acid fortification ', European Journal of Nutrition, vol. 53, no. 7, pp. 1549-1559 . https://doi.org/10.1007/s00394-014-0659-2
Meta-analyses have suggested an effect of MTHFR C677T genotype (rs1801133), a proxy for blood total homocysteine, on cardiovascular disease (CVD) in populations with low population dietary folate. The aim was to examine the association and effect mod
Publikováno v:
Ophthalmologica, Vol. 232, No 1 (2014) pp. 46-52
Background: To assess the prevalence of thrombophilia in patients with central (CRVO) and branch retinal vein occlusion (BRVO). Methods: In 139 patients with CRVO (n = 88) and BRVO (n = 51) and in 40 healthy controls factor VIII, fibrinogen, antithro
Autor:
Peter Holmans, Udo Seedorf, Beverley M. Shields, Peter McGruffin, Arne Pfeufer, Steve Eyre, Nathalie J. Prescott, Michael Boehnke, Valentina Moskovina, Abiodun Onipinla, Leena Peltonen, Nadira Yuldasheva, Peter M. Nilsson, Valeria Romanazzi, Vincent Mooser, Göran Berglund, Alistair S. Hall, Dominic P. Kwiatkowski, Barry Widmer, Benjamin F. Voight, Stefania Bandinelli, Mark M. Iles, Sven Bergmann, Thomas Meitinger, James P. Boorman, Simonetta Guarrera, Nazneen Rahman, Murielle Bochud, Graham A. Hitman, Emma Keniry, Nelson B. Freimer, Richard Dobson, Francis S. Collins, Gerjan Navis, Jennifer L. Pointon, Richard N. Bergman, Ruth J. F. Loos, Roberto Lorbeer, Carolina A. Braga Marcano, Christian Gieger, Florian Ernst, Xin Yuan, Catherine Potter, Hazel E. Drummond, Allan H. Young, George Kirov, John F. Peden, Helen Stevens, David Clayton, Mattijs E. Numans, Katherine Gordon-Smith, Anne Farmer, Alastair Forbes, M. Khalid Mohiuddin, John A. Todd, Christopher G. Mathew, David A. Collier, Mark I. McCarthy, Francesca Bredin, Clive M. Onnie, Dan Davidson, Markus Perola, Pamela Whittaker, Yvonne T. van der Schouw, Rathi Ravindrarajan, I. C.A. Spencer, Teresa Ferreira, Nilesh J. Samani, Serge Hercberg, Gonçalo R. Abecasis, Christopher J. Groves, Nicholas John Craddock, Angela Döring, Edward G. Lakatta, Muminatou Jallow, Wendy L. McArdle, David Bentley, Susana Eyheramendy, Uwe Völker, Christopher Newton-Cheh, Jaspal S. Kooner, Hugh Watkins, Gavin Lucas, H. T. Leung, Marjo Ritta Jarvelin, Johanna Kuusisto, Wiek H. van Gilst, Wendy Thomson, Lou R. Cardon, Harold Snieder, Marju Orho-Melander, Patricia B. Munroe, Toshiko Tanaka, Jeffrey C. Barrett, Azhar Maqbool, Henry Völzke, John M. C. Connell, Elaine R. Nimmo, John R. B. Perry, Michael R. Stratton, Ralph McGinnis, Pekka Jousilahti, Michiel L. Bots, Ian Jones, Elizabeth Meech, Matthew A. Brown, Johannie Gungadoo, Jian'an Luan, Jilur Ghori, Richard J. Dixon, N. Charlotte Onland-Moret, Fulvio Ricceri, Anthony J. Balmforth, Catherine E. Todhunter, Inês Barroso, Sheila Bingham, Timo T. Valle, Fredrik O. Vannberg, Diana Zelenika, Stephen Sawcer, Anneli Pouta, David M. Evans, Cuno S. P. M. Uiterwaal, Pilar Galan, Georg Homuth, Hannah Donovan, David J. Conway, Paul Elliott, Alessandra Allione, Paul E. de Jong, Miles Parkes, Amy Chaney, John C. Chambers, Toby Johnson, Isaac Subirana, Vesela Gateva, Cathryn M. Lewis, Christopher J. O'Donnell, Hana Lango, David Schlessinger, Mark J. Caulfield, Thorsten Reffelmann, Jamie Barbour, Karen L. Mohlke, Sarah E. Hunt, Thilo Winzer, Frances M K Williams, Christopher Mathew, I. Wallace, Anuj Goel, Jaakko Tuomilehto, Louise V. Wain, Gabriel Crawford, Samantha L. Hider, Detelinea Grozeva, Elaine K. Green, Paul D. Gilbert, Peter S. Braund, Jaume Marrugat, Rainer Rettig, Pim van der Harst, Yik Ying Teo, Andrew P. Morris, Guiseppe Matullo, Serena Sanna, Cristen J. Willer, Suzannah Bumpstead, Niall C. Taylor, Jacques S. Beckmann, Pierre Meneton, Elin Org, Luigi Ferrucci, Doug Easton, Sheila Seal, Joanne M. Heward, Anne U. Jackson, Eleftheria Zeggini, Rachel M. Freathy, Maris Laan, Paul Wordsworth, Sarah Nutland, Kerstin Koch, Sian Ceasar, Anders Hamsten, Judith M. Hussey, Tariq Ahmad, Derek P. Jewell, Paul Scheet, Charlie W. Lees, C Farrar, Christopher Prowse, Markku Laakso, David St Clair, Kate Downes, Diederick E. Grobbee, Paul Burton, Simon C. Potter, Ian N. Bruce, Tim D. Spector, Anne Barton, H.-Erich Wichmann, Matthew J. Simmonds, David Hadley, Cecilia M. Lindgren, Gérard Waeber, Nigel W. Rayner, Melanie J. Newport, Manjinder S. Sandhu, Audrey Duncanson, Guangju Zhai, Simon Heath, Susan M. Ring, Alessandra Di Gregorio, Richard Williamson, Nicholas J. Wareham, Zhan Su, Olle Melander, John R. Thompson, Alexander Teumer, Sheila A. Fisher, Lachlan J. M. Coin, Leif Groop, Giovanni Tognoni, Amanda Elkin, Alan J. Silman, Jack Satsangi, Jane Worthington, Martin Farrall, John Webster, Niall Cardin, Neil Walker, Anna F. Dominiczak, Jeremy D. Sanderson, Damjan Vukcevic, Bryan Howie, Silvia Polidoro, Stephen G. Ball, Mark Tremelling, Stephen Newhouse, Stephen M. Schwartz, Lori L. Bonnycastle, Chris Wallace, Kijoung Song, Mario A. Morken, I. Nicol Ferrier, Beverley Barke, Paolo Vineis, Manuela Uda, Deborah P M Symmons, Emily J. Lyons, Mingzhan Xue, Timothy M. Frayling, Stephen C.L. Cough, David Withers, Adrian V. S. Hill, Suzanne Stevens, Jennifer Jolley, Marcus Dörr, Kirk A. Rockett, David B. Dunger, Mark Walker, Jayne A. Franklyn, Lisa Jones, David S. Siscovick, Ann-Christine Syvänen, Laura J. Scott, Morris J. Brown, Barbera Cant, Michael Inouye, Feng Zhang, Carlotta Sacerdote, Katherine S. Elliott, Jonathan Marchini, Peter Donnely, Michael John Owen, An Goris, Marcus Prembey, Andrew T. Hattersley, Gerome Breen, Marian L. Hamshere, Thomas Illig, Samer S. Najjar, Nicole Soranzo, Kay-Tee Khaw, Graham R. Walters, Willem H. Ouwehand, David P. Strachan, Martin D. Tobin, Alastair Compston, John C. Mansfield, David Altshuler, Salvatore Panico, Sekar Kathiresan, Dawn M. Waterworth, Michael N. Weedon, D. Timothy Bishop, Claire Bryan, Alexandra S. Knight, Kate L. Lee, Paul F. O'Reilly, Massimo Mangino, Michael Conlon O'Donovan, Jing Hua Zhao, Konstantinos A. Papadakis, Jennifer H. Barrett, Joanne Pereira-Gale, N J Timpson, Stephan B. Felix, Panos Deloukas, Nicholas A. Watkins, Anna-Liisa Hartikainen, Peter Vollenweider, Richard Jones, Anne Hinks, Fraser Cummings, Noha Lim, Linda A. Bradbury, Rhian G. William, Nita G. Forouhi, Roberto Eluosa, Ingeleif B. Hallgrimsdottir, Giorgio Sirugo, Robert Luben, Veikko Salomaa, Robert Clarke, Sally John, Ursula Everson, Emma King, Ivan Nikolov, Heather M. Stringham, Antony P. Attwood, Angelo Scuteri
Publikováno v:
Nature Genetics, vol. 41, no. 6, pp. 666-676
Nature Genetics; Vol 41
Nature Genetics, 41(6), 666-676. Nature Publishing Group
Nature Genetics, 41, 666. Nature Publishing Group
Newton-Cheh, C, Johnson, T, Gateva, V, Tobin, M D, Bochud, M, Coin, L, Najjar, S S, Zhao, J H, Heath, S C, Eyheramendy, S, Papadakis, K, Voight, B F, Scott, L J, Zhang, F, Farrall, M, Tanaka, T, Wallace, C, Chambers, J C, Khaw, K-T, Nilsson, P, van der Harst, P, Polidoro, S, Grobbee, D E, Onland-Moret, N C, Bots, M L, Wain, L V, Elliott, K S, Teumer, A, Luan, J, Lucas, G, Kuusisto, J, Burton, P R, Hadley, D, McArdle, W L, Brown, M, Dominiczak, A, Newhouse, S J, Samani, N J, Webster, J, Zeggini, E, Beckmann, J S, Bergmann, S, Lim, N, Song, K, Vollenweider, P, Waeber, G, Waterworth, D M, Yuan, X & Groop, L & Orho-Melander, M 2009, ' Genome-wide association study identifies eight loci associated with blood pressure ', Nature Genetics, vol. 41, no. 6, pp. 666-76 . https://doi.org/10.1038/ng.361
Nature genetics
Nature Genetics
Nature Genetics; Vol 41
Nature Genetics, 41(6), 666-676. Nature Publishing Group
Nature Genetics, 41, 666. Nature Publishing Group
Newton-Cheh, C, Johnson, T, Gateva, V, Tobin, M D, Bochud, M, Coin, L, Najjar, S S, Zhao, J H, Heath, S C, Eyheramendy, S, Papadakis, K, Voight, B F, Scott, L J, Zhang, F, Farrall, M, Tanaka, T, Wallace, C, Chambers, J C, Khaw, K-T, Nilsson, P, van der Harst, P, Polidoro, S, Grobbee, D E, Onland-Moret, N C, Bots, M L, Wain, L V, Elliott, K S, Teumer, A, Luan, J, Lucas, G, Kuusisto, J, Burton, P R, Hadley, D, McArdle, W L, Brown, M, Dominiczak, A, Newhouse, S J, Samani, N J, Webster, J, Zeggini, E, Beckmann, J S, Bergmann, S, Lim, N, Song, K, Vollenweider, P, Waeber, G, Waterworth, D M, Yuan, X & Groop, L & Orho-Melander, M 2009, ' Genome-wide association study identifies eight loci associated with blood pressure ', Nature Genetics, vol. 41, no. 6, pp. 666-76 . https://doi.org/10.1038/ng.361
Nature genetics
Nature Genetics
Elevated blood pressure is a common, heritable cause of cardiovascular disease worldwide. To date, identification of common genetic variants influencing blood pressure has proven challenging. We tested 2.5 million genotyped and imputed SNPs for assoc
Autor:
Küçüktaşçi K, Semiz S, Balci YI, Özsari T, Gürses D, Önem G, Saçar M, Düzcan F, Yüksel D, Semiz E
Wolfram syndrome-1 is a rare and severe autosomal recessive neurodegenerative disease characterized by diabetes mellitus (DM), optic atrophy, diabetes insipidus, and deafness. Poorly controlled type 1 DM increases the risk for thrombosis. However, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::71892b7e9bc76aae570542a580b0d6f0
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 13:166-171
Factor V Leiden causing activated protein C resistance is the most common inherited form of thrombophilia leading to thrombosis. Its frequency shows great ethnic and geographic variations. The aim of this study was to determine the frequency of FV Le
Autor:
Sophia N. Kalantaridou, Alexandros Sotiriadis, Leucothea Dova, Evangelos Paraskevaidis, George Vartholomatos, Theodor Stefos, Matthaios Pavlou, Nicolaos Kolaitis
Publikováno v:
American Journal of Reproductive Immunology. 57:133-141
PROBLEM: To compare the prevalence of five common thrombophilic polymorphisms and their combination in women with recurrent miscarriage and a control group. METHOD OF STUDY: Genomic analysis using polymerase chain reaction (PCR) was carried out in pa
Autor:
Meena Kumari, Claire E. Hastie, Jonathan Stephens, Patricia B. Munroe, Christopher P. Nelson, John M. C. Connell, Martin D. Tobin, Hani Neuvrith, Jean Tichet, Paul Burton, Gudrun Veldre, Daniele Cusi, Anna Levinsson, Paul Elliott, Elin Org, Erika Salvi, Tina Shah, Nabila Devos, Harm-Jan Westra, Juan-Pablo Casas, Olle Melander, Jan A. Staessen, Nilesh J. Samani, Jackie A. Cooper, Peter S. Braund, Neil R Poulter, Alive V. Stanton, Abiodun Onipinla, Marcel G. M. Wolfs, Steve E. Humphries, Philippa J. Talmud, Rebecca Hardy, Fotios Drenos, Maris Laan, Mark J. Caulfield, Richard Dobson, Willem H. Ouwehand, Yun Zhang, Li Chen, SG Wannamethee, Sue Shaw-Hawkins, Christopher Newton-Cheh, Eoin O'Brien, Simon A. McG. Thom, Maria Grazia Franzosi, Charles A. Mein, Mika Kivimäki, Tom R. Gaunt, Jennifer G. Sambrook, Andrea Stucchi, Annika Rosengren, Sonia Shah, Thomas Hedner, George A. Wells, Dag S. Thelle, Debbie A Lawlor, Pierre-François Plouin, Fredrik Nyberg, Richard W Morris, Ian N M Day, Vesela Gateva, Lude Franke, Peter S. Sever, Morris J. Brown, Margus Putku, Sandosh Padmanabhan, John F. Peden, Pim van der Harst, Jutta Palmen, Ioanna Tzoulaki, Alexandre F.R. Stewart, Andrew Wong, Peeter Juhanson, Marciej Tomaszewski, Alison H. Goodall, Martin Farrall, Wai K. Lee, Nicola Glorioso, Hugh Watkins, Xavier Jeunemaitre, Anders Hamsten, Robert Clarke, Anna F. Dominiczak, Mark Lathrop, Stephen Newhouse, Margus Viigimaa, George Davey Smith, Robert Roberts, John C. Whittaker, Michael V. Holmes, Toby Johnson, F. Gerald R. Fowkes, Aroon D. Hingorani, Udo Seedorf, Siim Sõber, Denis C. Shields, Diana Kuh, Chris Wallace, Philip Howard, Peter H. Whincup, Gonçalo R. Abecasis, Anuj Goel, Christian Delles, Björn Wahlstrand
Publikováno v:
American Journal of Human Genetics, 89(6), 688-700. CELL PRESS
American journal of human genetics, vol. 89, no. 6, pp. 688-700
The American Journal of Human Genetics; Vol 89
Johnson, T, Gaunt, T R, Newhouse, S J, Padmanabhan, S, Tomaszewski, M, Kumari, M, Morris, R W, Tzoulaki, I, O'Brien, E T, Poulter, N R, Sever, P, Shields, D C, Thom, S, Wannamethee, S G, Whincup, P H, Brown, M J, Connell, J M, Dobson, R J, Howard, P J, Mein, C A, Onipinla, A, Shaw-Hawkins, S, Zhang, Y, Smith, G D, Day, I N M, Lawlor, D A, Goodall, A H, Fowkes, F G, Abecasis, G R, Elliott, P, Gateva, V, Braund, P S, Burton, P R, Nelson, C P, Tobin, M D, van der Harst, P, Glorioso, N, Neuvrith, H, Salvi, E, Staessen, J A, Stucchi, A, Devos, N, Jeunemaitre, X, Plouin, P-F, Tichet, J, Juhanson, P, Org, E, Putku, M, Sober, S, Veldre, G 2011, ' Blood Pressure Loci Identified with a Gene-Centric Array ', American Journal of Human Genetics, vol. 89, no. 6, pp. 688-700 . https://doi.org/10.1016/j.ajhg.2011.10.013
American journal of human genetics, vol. 89, no. 6, pp. 688-700
The American Journal of Human Genetics; Vol 89
Johnson, T, Gaunt, T R, Newhouse, S J, Padmanabhan, S, Tomaszewski, M, Kumari, M, Morris, R W, Tzoulaki, I, O'Brien, E T, Poulter, N R, Sever, P, Shields, D C, Thom, S, Wannamethee, S G, Whincup, P H, Brown, M J, Connell, J M, Dobson, R J, Howard, P J, Mein, C A, Onipinla, A, Shaw-Hawkins, S, Zhang, Y, Smith, G D, Day, I N M, Lawlor, D A, Goodall, A H, Fowkes, F G, Abecasis, G R, Elliott, P, Gateva, V, Braund, P S, Burton, P R, Nelson, C P, Tobin, M D, van der Harst, P, Glorioso, N, Neuvrith, H, Salvi, E, Staessen, J A, Stucchi, A, Devos, N, Jeunemaitre, X, Plouin, P-F, Tichet, J, Juhanson, P, Org, E, Putku, M, Sober, S, Veldre, G 2011, ' Blood Pressure Loci Identified with a Gene-Centric Array ', American Journal of Human Genetics, vol. 89, no. 6, pp. 688-700 . https://doi.org/10.1016/j.ajhg.2011.10.013
Raised blood pressure (BP) is a major risk factor for cardiovascular disease. Previous studies have identified 47 distinct genetic variants robustly associated with BP, but collectively these explain only a few percent of the heritability for BP phen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a055dcda09bbb36bdfdb963307732402
https://lirias.kuleuven.be/handle/123456789/341626
https://lirias.kuleuven.be/handle/123456789/341626
Autor:
E.V. Tsianos, K.H. Katsanos, C.D. Zois, Nikolaos Kolaitis, Ioannis Asproudis, Taxiarchis Felekis, Georgios Vartholomatos
Publikováno v:
Journal of Crohn'scolitis. 4(4)
Large spectrums of ophthalmic manifestations from the anterior to the posterior segment have been so far reported in patients with inflammatory bowel disease. Anterior ischemic optic neuropathy is caused by acute ischemic infarction of the optic nerv
Autor:
Vekris, M. D., Ovrenovits, M., Dova, L., Beris, A. E., Soucacos, P. N., Kolaitis, N., Vartholomatos, G.
The evolution of microsurgery popularized the free functioning muscle transfers as secondary procedures to reanimate paralyzed extremities after severance of the brachial plexus, especially when the surgeon deals with late cases. Studies considering
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::68fa4584d063d94cee377f0a9cb05ede
http://olympias.lib.uoi.gr/jspui/handle/123456789/21503
http://olympias.lib.uoi.gr/jspui/handle/123456789/21503
OBJECTIVE: To evaluate whether the C677T polymorphism of the methylenetetrahydofolate reductase (MTHFR) gene is consistently associated with hypertension in pregnancy. DESIGN: Meta-analysis of studies comparing women with and without hypertension in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::a30ccdc6590a53c059ac0d928461bbd7
http://olympias.lib.uoi.gr/jspui/handle/123456789/23666
http://olympias.lib.uoi.gr/jspui/handle/123456789/23666