Výsledky vyhledávání - "C. H. de Visser"

Akademický článek

A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.

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

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Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism

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

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

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The HR2 Haplotype of Factor V: Effects on Factor V Levels, Normalized Activated Protein C Sensitivity Ratios and the Risk of Venous Thrombosis

Autor: Joan F. Guasch, Rogier M. Bertina, Pieter Willem Kamphuisen, Hans L. Vos, C. H. de Visser, Frits R. Rosendaal

Publikováno v: Thrombosis and Haemostasis. 83:577-582

SummaryWe studied the HR2 haplotype of the factor V gene in a case-control study for venous thrombosis including 474 patients with a first deep-vein thrombosis and 474 age- and sex-matched healthy controls (Leiden Thrombophilia Study, LETS). We inves

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::23ab3b4a1bceada2aa9760141770f5c9
https://doi.org/10.1055/s-0037-1613866

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Fibrinogen gamma gene 3'-end polymorphisms and risk of venous thromboembolism in the African-American and Caucasian population

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.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f881ce704e66784ef6aee0b637fc8207
https://pubmed.ncbi.nlm.nih.gov/19492150

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ABO blood group genotypes, plasma von Willebrand factor levels and loading of von Willebrand factor with A and B antigens

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::94b7fd989378f6d1711b3473c8425c33
https://pubmed.ncbi.nlm.nih.gov/17393014

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The effect of plasma caeruloplasmin levels on the sensitivity for activated protein C

Autor: Marieke C H, de Visser, John H M, Souverijn, Frits R, Rosendaal, Rogier M, Bertina

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dab23f83a0790c01490fcda2aaa5f9aa
https://pubmed.ncbi.nlm.nih.gov/12181057

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