| Incidence of venous thromboembolism in families with inherited thrombophilia P Simioni, BJ Sanson, P Prandoni, D Tormene, PW Friederich, B Girolami, ... Thrombosis and haemostasis 81 (02), 198-202, 1999 | 449 | 1999 |
| Inflammation, innate immunity and blood coagulation J Xu, F Lupu, CT Esmon Hämostaseologie 30 (01), 5-9, 2010 | 250 | 2010 |
| Malignant cells fuel tumor growth by educating infiltrating leukocytes to produce the mitogen Gas6 S Loges, T Schmidt, M Tjwa, K Van Geyte, D Lievens, E Lutgens, ... Blood, The Journal of the American Society of Hematology 115 (11), 2264-2273, 2010 | 191 | 2010 |
| Protein S deficiency: a database of mutations–summary of the first update S Gandrille, D Borgel, N Sala, Y Espinosa-Parrilla, R Simmonds, ... Thrombosis and haemostasis 84 (11), 918-918, 2000 | 172 | 2000 |
| Decreased ADAMTS-13 (A disintegrin-like and metalloprotease with thrombospondin type 1 repeats) is associated with a poor prognosis in sepsis-induced organ failure K Martin, D Borgel, N Lerolle, HB Feys, L Trinquart, K Vanhoorelbeke, ... Critical care medicine 35 (10), 2375-2382, 2007 | 166 | 2007 |
| Protein S deficiency: a database of mutations S Gandrille, D Borgel, H Ireland, DA Lane, R Simmonds, PH Reitsma, ... Thrombosis and haemostasis 77 (06), 1201-1214, 1997 | 138 | 1997 |
| Protein C and protein S deficiencies. M Aiach, D Borgel, P Gaussem, J Emmerich, M Alhenc-Gelas, S Gandrille Seminars in hematology 34 (3), 205-216, 1997 | 127 | 1997 |
| Elevated growth-arrest-specific protein 6 plasma levels in patients with severe sepsis D Borgel, S Clauser, C Bornstain, I Bièche, A Bissery, V Remones, ... Critical care medicine 34 (1), 219-222, 2006 | 126 | 2006 |
| Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the … S Gandrille, D Borgel, V Eschwege-Gufflet, MF Aillaud, M Dreyfus, ... | 120 | 1995 |
| International clinical guidelines for the management of phosphomannomutase 2‐congenital disorders of glycosylation: diagnosis, treatment and follow up R Altassan, R Péanne, J Jaeken, R Barone, M Bidet, D Borgel, S Brasil, ... Journal of inherited metabolic disease 42 (1), 5-28, 2019 | 111 | 2019 |
| Clinical, laboratory and molecular findings and long-term follow-up data in 96 French patients with PMM2-CDG (phosphomannomutase 2-congenital disorder of glycosylation) and … M Schiff, C Roda, ML Monin, A Arion, M Barth, N Bednarek, M Bidet, ... Journal of medical genetics 54 (12), 843-851, 2017 | 106 | 2017 |
| Protein S deficiency D Borgel, S Gandrille, M Aiach Thrombosis and haemostasis 78 (07), 351-356, 1997 | 93 | 1997 |
| Inefficacy of ultrasound-guided local injections of autologous conditioned plasma for recent epicondylitis: results of a double-blind placebo-controlled randomized clinical … B Montalvan, P Le Goux, S Klouche, D Borgel, P Hardy, M Breban Rheumatology 55 (2), 279-285, 2016 | 87 | 2016 |
| A comparative study of the protein C pathway in septic and nonseptic patients with organ failure D Borgel, C Bornstain, PH Reitsma, N Lerolle, S Gandrille, F Dali-Ali, ... American journal of respiratory and critical care medicine 176 (9), 878-885, 2007 | 87 | 2007 |
| The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency J Duchemin, S Gandrille, D Borgel, P Feurgard, M Alhenc-Gelas, ... | 87 | 1995 |
| Vitamin K–dependent protein S: beyond the protein C pathway B Dahlbäck Seminars in thrombosis and hemostasis 44 (02), 176-184, 2018 | 84 | 2018 |
| Association of specific haplotypes of GAS6 gene with stroke X Muñoz, V Obach, B Hurtado, PG de Frutos, Á Chamorro, N Sala Thrombosis and haemostasis 98 (08), 406-412, 2007 | 77 | 2007 |
| Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies D Borgel, J Duchemin, M Alhenc-Gelas, C Matheron, M Aiach, S Gandrille Journal of Laboratory and Clinical Medicine 128 (2), 218-227, 1996 | 69 | 1996 |
| Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott–Aldrich syndrome A Magnani, M Semeraro, F Adam, C Booth, L Dupré, EC Morris, ... Nature Medicine 28 (1), 71-80, 2022 | 67 | 2022 |
| Acquired protein S deficiency leads to obliterative portal venopathy and to compensatory nodular regenerative hyperplasia in HIV-infected patients VO Mallet, A Varthaman, D Lasne, JP Viard, H Gouya, D Borgel, ... Aids 23 (12), 1511-1518, 2009 | 67 | 2009 |
