Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Marieke C H De Visser"'
Autor:
Eleonora Porcu, Marco Medici, Giorgio Pistis, Claudia B Volpato, Scott G Wilson, Anne R Cappola, Steffan D Bos, Joris Deelen, Martin den Heijer, Rachel M Freathy, Jari Lahti, Chunyu Liu, Lorna M Lopez, Ilja M Nolte, Jeffrey R O'Connell, Toshiko Tanaka, Stella Trompet, Alice Arnold, Stefania Bandinelli, Marian Beekman, Stefan Böhringer, Suzanne J Brown, Brendan M Buckley, Clara Camaschella, Anton J M de Craen, Gail Davies, Marieke C H de Visser, Ian Ford, Tom Forsen, Timothy M Frayling, Laura Fugazzola, Martin Gögele, Andrew T Hattersley, Ad R Hermus, Albert Hofman, Jeanine J Houwing-Duistermaat, Richard A Jensen, Eero Kajantie, Margreet Kloppenburg, Ee M Lim, Corrado Masciullo, Stefano Mariotti, Cosetta Minelli, Braxton D Mitchell, Ramaiah Nagaraja, Romana T Netea-Maier, Aarno Palotie, Luca Persani, Maria G Piras, Bruce M Psaty, Katri Räikkönen, J Brent Richards, Fernando Rivadeneira, Cinzia Sala, Mona M Sabra, Naveed Sattar, Beverley M Shields, Nicole Soranzo, John M Starr, David J Stott, Fred C G J Sweep, Gianluca Usala, Melanie M van der Klauw, Diana van Heemst, Alies van Mullem, Sita H Vermeulen, W Edward Visser, John P Walsh, Rudi G J Westendorp, Elisabeth Widen, Guangju Zhai, Francesco Cucca, Ian J Deary, Johan G Eriksson, Luigi Ferrucci, Caroline S Fox, J Wouter Jukema, Lambertus A Kiemeney, Peter P Pramstaller, David Schlessinger, Alan R Shuldiner, Eline P Slagboom, André G Uitterlinden, Bijay Vaidya, Theo J Visser, Bruce H R Wolffenbuttel, Ingrid Meulenbelt, Jerome I Rotter, Tim D Spector, Andrew A Hicks, Daniela Toniolo, Serena Sanna, Robin P Peeters, Silvia Naitza
Publikováno v:
PLoS Genetics, Vol 9, Iss 2, p e1003266 (2013)
Thyroid hormone is essential for normal metabolism and development, and overt abnormalities in thyroid function lead to common endocrine disorders affecting approximately 10% of individuals over their life span. In addition, even mild alterations in
Externí odkaz:
https://doaj.org/article/e69c66d7aa444da8a3bac096f4be9764
Autor:
Christophe Tzourio, Lasse Folkersen, Marieke C H De Visser, Sara Lindström, Ramin Monajemi, Noémie Saut, David M. Smadja, Antonio Fabio Di Narzo, Jean-François Dartigues, Paul M. Ridker, Marine Germain, Mete Civelek, Nicholas L. Smith, François Cambien, Ares Rocanin-Arjo, Christopher Kabrhel, Alison H. Goodall, Aaron R. Folsom, Pieter H. Reitsma, Saonli Basu, Eline Slagboom, Lu-Chen Weng, Kent D. Taylor, Hugoline G. de Haan, Jeanine Houwing-Duitermaat, Peter Kraft, Panos Deloukas, Christopher P. Nelson, Claudine Berr, Lynda M. Rose, Ke Hao, Bruce M. Psaty, Nilesh J. Samani, Jennifer A. Brody, Pierre Suchon, Philippe Amouyel, Jean-François Deleuze, Kerri L. Wiggins, Grégoire Le Gal, Daniel I. Chasman, John A. Heit, Dylan Aïssi, Astrid van Hylckama Vlieg, Pierre-Emmanuel Morange, Mariza de Andrade, Weihong Tang, Frits R. Rosendaal, David-Alexandre Trégouët, Per Eriksson
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, 2015, 96 (4), pp.532-42. ⟨10.1016/j.ajhg.2015.01.019⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2015, 96 (4), pp.532-42. ⟨10.1016/j.ajhg.2015.01.019⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2015, 96 (4), pp.532-42. 〈10.1016/j.ajhg.2015.01.019〉
American Journal of Human Genetics, 96(4), 532-542
American Journal of Human Genetics, 2015, 96 (4), pp.532-42. ⟨10.1016/j.ajhg.2015.01.019⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2015, 96 (4), pp.532-42. ⟨10.1016/j.ajhg.2015.01.019⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2015, 96 (4), pp.532-42. 〈10.1016/j.ajhg.2015.01.019〉
American Journal of Human Genetics, 96(4), 532-542
International audience; Venous thromboembolism (VTE), the third leading cause of cardiovascular mortality, is a complex thrombotic disorder with environmental and genetic determinants. Although several genetic variants have been found associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d0698b5674becca37da8448174d2390
https://hal.univ-brest.fr/hal-01259946
https://hal.univ-brest.fr/hal-01259946
Autor:
Shirley, Uitte de Willige, Meridith E, Pyle, Hans L, Vos, Marieke C H, de Visser, Cathy, Lally, Nicole F, Dowling, W Craig, Hooper, Rogier M, Bertina, Harland, Austin
Publikováno v:
Thrombosis and haemostasis. 101(6)
Genetic determinants of venous thromboembolism (VTE) in the African-American population are poorly characterised. It was recently shown that fibrinogen gamma gene (FGG) polymorphisms 10034CT and 9340TC influence VTE risk in the Caucasian population.
Autor:
Vania M, Morelli, Marieke C H, de Visser, Nico H, van Tilburg, Hans L, Vos, Jeroen C J, Eikenboom, Frits R, Rosendaal, Rogier M, Bertina
Publikováno v:
Thrombosis and haemostasis. 97(4)
ABO blood group is a genetic determinant of von Willebrand factor (VWF) levels. We investigated the effect of ABO genotypes on VWF and factor VIII (FVIII) levels and on the degree to which VWF is loaded with A- and B-antigens, expressed as normalized
Publikováno v:
British journal of haematology. 118(3)
The effect of caeruloplasmin levels on the sensitivity for activated protein C (APC), measured by a clotting assay based on the activated partial thromboplastin time, was investigated in a large group of healthy individuals without factor V Leiden. A
Autor:
Sargurupremraj, Muralidharan, Suzuki, Hideaki, Jian, Xueqiu, Sarnowski, Chloé, Evans, Tavia E., Bis, Joshua C., Eiriksdottir, Gudny, Sakaue, Saori, Terzikhan, Natalie, Habes, Mohamad, Zhao, Wei, Armstrong, Nicola J., Hofer, Edith, Yanek, Lisa R., Hagenaars, Saskia P., Kumar, Rajan B., van den Akker, Erik B., McWhirter, Rebekah E., Trompet, Stella, Mishra, Aniket
Publikováno v:
Nature Communications; 12/8/2020, Vol. 11 Issue 1, p1-18, 18p
Publikováno v:
Biostatistics; Apr2013, Vol. 14 Issue 2, p220-231, 12p, 4 Charts
Publikováno v:
British Journal of Haematology; Sep2002, Vol. 118 Issue 3, p843-846, 4p