Protein S Heerlen mutation heterozygosity is associated with venous thrombosis risk
Suchon, P, Germain, M, Delluc, A, Smadja, D, Jouven, X, Gyorgy, B, Saut, N, Ibrahim, M, Deleuze, J F, Alessi, M C, Morange, P E, Trégouët, D A
Published in Scientific reports (04.04.2017)
Published in Scientific reports (04.04.2017)
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Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation
Ibrahim-Kosta, M, Suchon, P, Couturaud, F, Smadja, D, Olaso, R, Germain, M, Saut, N, Goumidi, L, Derbois, C, Thibord, F, Debette, S, Amouyel, P, Deleuze, J F, van Doorn, P, Castoldi, E, Patin, E, Alessi, M C, Trégouët, D A, Morange, P E
Published in Scientific reports (06.03.2019)
Published in Scientific reports (06.03.2019)
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Polymorphisms of the tumor necrosis factor-alpha (TNF) and the TNF-alpha converting enzyme (TACE/ADAM17) genes in relation to cardiovascular mortality: the AtheroGene study
Morange, P. E., Tregouet, D. A., Godefroy, T., Saut, N., Bickel, C., Rupprecht, H. J., Lackner, K., Barbaux, S., Poirier, O., Peiretti, F., Nalbone, G., Juhan-Vague, I., Blankenberg, S., Tiret, L.
Published in Journal of molecular medicine (Berlin, Germany) (01.10.2008)
Published in Journal of molecular medicine (Berlin, Germany) (01.10.2008)
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Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility
Machev, N, Saut, N, Longepied, G, Terriou, P, Navarro, A, Levy, N, Guichaoua, M, Metzler-Guillemain, C, Collignon, P, Frances, A-M, Belougne, J, Clemente, E, Chiaroni, J, Chevillard, C, Durand, C, Ducourneau, A, Pech, N, McElreavey, K, Mattei, M-G, Mitchell, M J
Published in Journal of medical genetics (01.11.2004)
Published in Journal of medical genetics (01.11.2004)
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A multi‐stage multi‐design strategy provides strong evidence that the BAI3 locus is associated with early‐onset venous thromboembolism
ANTONI, G., MORANGE, P.‐E., LUO, Y., SAUT, N., BURGOS, G., HEATH, S., GERMAIN, M., BIRON‐ANDREANI, C., SCHVED, J.‐F., PERNOD, G., GALAN, P., ZELENIKA, D., ALESSI, M.‐C., DROUET, L., VISVIKIS‐SIEST, S., WELLS, P. S., LATHROP, M., EMMERICH, J., TREGOUET, D.‐A., GAGNON, F.
Published in Journal of thrombosis and haemostasis (01.12.2010)
Published in Journal of thrombosis and haemostasis (01.12.2010)
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Association of Plasminogen Activator Inhibitor (PAI)-1 (SERPINE1) SNPs With Myocardial Infarction, Plasma PAI-1, and Metabolic Parameters: The HIFMECH Study
Morange, P E, Saut, N, Alessi, M C, Yudkin, J S, Margaglione, M, Di Minno, G, Hamsten, A, Humphries, S E, Tregouet, D A, Juhan-Vague, I
Published in Arteriosclerosis, thrombosis, and vascular biology (01.10.2007)
Published in Arteriosclerosis, thrombosis, and vascular biology (01.10.2007)
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Biological and genetic factors influencing plasma factor VIII levels in a healthy family population: results from the Stanislas cohort
Morange, P. E., Tregouet, D. A., Frere, C., Saut, N., Pellegrina, L., Alessi, M. C., Visvikis, S., Tiret, L., Juhan‐Vague, I.
Published in British journal of haematology (01.01.2005)
Published in British journal of haematology (01.01.2005)
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TLR4 Asp299Gly, CD14 C-260T, plasma levels of the soluble receptor CD14 and the risk of coronary heart disease: The PRIME Study
MORANGE, P. E, TIRET, L, JUHAN-VAGUE, I, SAUT, N, LUC, G, ARVEILER, D, FERRIERES, J, AMOUYEL, P, EVANS, A, DUCIMETIERE, P, CAMBIEN, F
Published in European journal of human genetics : EJHG (01.12.2004)
Published in European journal of human genetics : EJHG (01.12.2004)
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Interaction between the C-260T polymorphism of the CD14 gene and the plasma IL-6 concentration on the risk of myocardial infarction: the HIFMECH study
Morange, P.E., Saut, N., Alessi, M.C., Frere, C., Hawe, E., Yudkin, J.S., Tremoli, E., Margaglione, M., Di Minno, G., Hamsten, A., Humphries, S.E., Juhan-Vague, I.
Published in Atherosclerosis (01.04.2005)
Published in Atherosclerosis (01.04.2005)
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RBMY evolved on the Y chromosome from a ubiquitously transcribed X-Y identical gene
Mattei, Marie-Geneviève, Mazeyrat, Sophie, Saut, Noëmie, Mitchell, Michael J
Published in Nature genetics (01.07.1999)
Published in Nature genetics (01.07.1999)
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The critical region of overlap defining the AZFa male infertility interval of proximal Yq contains three transcribed sequences
SARGENT, C. A, BOUCHER, C. A, TERRIOU, P, HARGREAVE, T, COOKE, H, MITCHELL, M, RAPPOLD, G. A, AFFARA, N. A, KIRSCH, S, BROWN, G, WEISS, B, TRUNDLEY, A, BURGOYNE, P, SAUT, N, DURAND, C, LEVY, N
Published in Journal of medical genetics (01.09.1999)
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Published in Journal of medical genetics (01.09.1999)
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The Mouse Y Chromosome Interval Necessary for Spermatogonial Proliferation is Gene Dense with Syntenic Homology to the Human AZFa Region
Mazeyrat, Sophie, Saut, Noëmie, Sargent, Carole A., Grimmond, Sean, Longepied, Guy, Ehrmann, Ingrid E., Ellis, Pamela S., Greenfield, Andy, Affara, Nabeel A., Mitchell, Michael J.
Published in Human molecular genetics (01.10.1998)
Published in Human molecular genetics (01.10.1998)
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O1 Facteurs prédictifs de la résistance au clopidogrel à 1 mois du syndrome coronarien aigu chez le patient diabétique
Gaborit, B, Grosdidier, C, Saut, N, Loundou, A, Bonnet, J.L, Alessi, M.-C, Morange, P.E, Dutour, A, Cuisset, T
Published in Diabetes & metabolism (01.03.2012)
Published in Diabetes & metabolism (01.03.2012)
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B013 Genetic polymorphisms of the lamina maturation pathway and their association with the metabolic syndrome: the desir prospective study
Fontaine-Bisson, B, Alessi, M.-C, Saut, N, Fumeron, F, Marre, M, Dutour, A, Badens, C, Levy, N, Tichet, J, Juhan-Vague, I, Tregouet, D.-A, Balkau, B, Morange, P.-E
Published in Archives of cardiovascular diseases (2009)
Published in Archives of cardiovascular diseases (2009)
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Factor V Leiden G1691A and prothrombin G20210A mutations are common in Tunisia
Frere, C., Saut, N., Boukef, M. K., Zili, M., Toumi, N. E. H.
Published in Journal of thrombosis and haemostasis (01.11.2003)
Published in Journal of thrombosis and haemostasis (01.11.2003)
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Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism
Germain, Marine, Chasman, Daniel I., de Haan, Hugoline, Tang, Weihong, Lindström, Sara, Weng, Lu-Chen, de Andrade, Mariza, de Visser, Marieke C.H., Wiggins, Kerri L., Suchon, Pierre, Saut, Noémie, Smadja, David M., Le Gal, Grégoire, van Hylckama Vlieg, Astrid, Di Narzo, Antonio, Hao, Ke, Nelson, Christopher P., Rocanin-Arjo, Ares, Folkersen, Lasse, Monajemi, Ramin, Rose, Lynda M., Brody, Jennifer A., Slagboom, Eline, Aïssi, Dylan, Gagnon, France, Deleuze, Jean-Francois, Deloukas, Panos, Tzourio, Christophe, Dartigues, Jean-Francois, Berr, Claudine, Taylor, Kent D., Civelek, Mete, Eriksson, Per, Psaty, Bruce M., Houwing-Duitermaat, Jeanine, Goodall, Alison H., Cambien, François, Kraft, Peter, Amouyel, Philippe, Samani, Nilesh J., Basu, Saonli, Ridker, Paul M., Rosendaal, Frits R., Kabrhel, Christopher, Folsom, Aaron R., Heit, John, Reitsma, Pieter H., Trégouët, David-Alexandre, Smith, Nicholas L., Morange, Pierre-Emmanuel
Published in American journal of human genetics (02.04.2015)
Published in American journal of human genetics (02.04.2015)
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Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Thibord, Florian, Klarin, Derek, Brody, Jennifer A, Chen, Ming-Huei, Levin, Michael G, Chasman, Daniel I, Goode, Ellen L, Hveem, Kristian, Teder-Laving, Maris, Martinez-Perez, Angel, Aïssi, Dylan, Daian-Bacq, Delphine, Ito, Kaoru, Natarajan, Pradeep, Lutsey, Pamela L, Nadkarni, Girish N, de Vries, Paul S, Cuellar-Partida, Gabriel, Wolford, Brooke N, Pattee, Jack W, Kooperberg, Charles, Braekkan, Sigrid K, Li-Gao, Ruifang, Saut, Noemie, Sept, Corriene, Germain, Marine, Judy, Renae L, Wiggins, Kerri L, Ko, Darae, O'Donnell, Christopher J, Taylor, Kent D, Giulianini, Franco, De Andrade, Mariza, Nøst, Therese H, Boland, Anne, Empana, Jean-Philippe, Koyama, Satoshi, Gilliland, Thomas, Do, Ron, Huffman, Jennifer E, Wang, Xin, Zhou, Wei, Manuel Soria, Jose, Carlos Souto, Juan, Pankratz, Nathan, Haessler, Jeffery, Hindberg, Kristian, Rosendaal, Frits R, Turman, Constance, Olaso, Robert, Kember, Rachel L, Bartz, Traci M, Lynch, Julie A, Heckbert, Susan R, Armasu, Sebastian M, Brumpton, Ben, Smadja, David M, Jouven, Xavier, Komuro, Issei, Clapham, Katharine R, Loos, Ruth J F, Willer, Cristen J, Sabater-Lleal, Maria, Pankow, James S, Reiner, Alexander P, Morelli, Vania M, Ridker, Paul M, Vlieg, Astrid van Hylckama, Deleuze, Jean-François, Kraft, Peter, Rader, Daniel J, Min Lee, Kyung, Psaty, Bruce M, Heidi Skogholt, Anne, Emmerich, Joseph, Suchon, Pierre, Rich, Stephen S, Vy, Ha My T, Tang, Weihong, Jackson, Rebecca D, Hansen, John-Bjarne, Morange, Pierre-Emmanuel, Kabrhel, Christopher, Trégouët, David-Alexandre, Damrauer, Scott M, Johnson, Andrew D, Smith, Nicholas L
Published in Circulation (New York, N.Y.) (18.10.2022)
Published in Circulation (New York, N.Y.) (18.10.2022)
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