Jeroen Eikenboom received his MD degree in 1988 at the Erasmus University Rotterdam, the Netherlands. He obtained his PhD at the Leiden University in 1994; the subject of his thesis was “The inheritance of von Willebrand disease”. He was trained in internal medicine at the Leiden University Medical Center and registered as internist in 2001. Since then he sub-specialized in hematology and vascular medicine. He was appointed full professor of Internal Medicine/Hemostasis and Thrombosis in 2011.His clinical work is focused on bleeding disorders, thrombophilia and vascular medicine. His research is focused on the molecular genetics of von Willebrand disease, genotype-phenotype associations in von Willebrand disease, and the biochemical and cell biological aspects of synthesis, storage, secretion and clearance of von Willebrand factor. He has been (co)chairman of the Scientific Subcommittee on von Willebrand factor of the Scientific and Standardization Committee (SSC) of the International Society on Thrombosis and Haemostasis (ISTH) from 1999-2013. He is member of the editorial board of the Journal of Thrombosis and Haemostasis and the British Journal of Haematology and he is associate editor of HemaSphere. He is board member of the Dutch Society of Internists Vascular Medicine.
Manuel Monreal is Full Professor of Vascular Medicine at the Faculty of Medicine, Universidad Autónoma in Barcelona, and has also been Head of Internal Medicine at the Hospital Universitari Germans Trias i Pujol in Barcelona, Spain, since 1983 to 2018.
Professor Monreal undertook his medical training at the Faculty of Medicine, Universitat Autónoma de Barcelona, obtaining his degree in 1975, and then completed an internship and residency in internal medicine at the Hospital Universitari Vall d’Hebrón in Barcelona.
Professor Monreal has authored or co-authored more than 400 articles and has presented numerous lectures on the study and treatment of venous thromboembolism, peripheral artery disease and related topics. Professor Monreal has published articles in prominent journals including Journal of Thrombosis and Haemostasis, Chest, Circulation, Journal of the American College of Cardiology, The American Journal of Medicine, Archives of Internal Medicine and Thrombosis and Haemostasis. In addition, Professor Monreal is Coordinator of the Registro Informatizado de la Enfermedad Trombo Embólica (RIETE) registry.
Professor Monreal is a founding member and trustee of the Fundación para el Estudio de la Enfermedad Tromboembólica (FUENTE), president of the Spanish Society to study on Vascular Medicine, and member of several important societies, including the International Society on Thrombosis and Haemostasis and the Mediterranean League Against Thromboembolism.
GARCIA DE FRUTOS
PABLO GARCIA DE FRUTOS
Pablo joined the laboratory of Dr. Dahlbäck (Lund University, Sweden) in 1992. Since then, he have studied vitamin K-dependent proteins in plasma (VKDPs) as part of the global mechanisms of response to damage. VKDPs have a unique structure: they bind to phospholipid membranes negatively charged by their N-terminal GLA module, and with receptors or protein substrates from their C-terminal part. The inflammatory processes and haemostasis are interconnected, but the molecular mechanisms of this crosstalk are still being explored. Since 1998, my first line of work as a researcher of the MFR (Medical Research Council of Sweden) was to study of the biology of GAS6, a VKDP structurally similar to anticoagulant Protein S whose function was unknown. He continued this line of research after joining the Spanish Research Council (CSIC) in 2002 as a tenured scientist. The GAS6/ProS-TAM system is an essential component in the response to damage in adult tissues. Recently, we have determined the involvement of the GAS6/AXL axis in the fibrotic response of the liver and heart (i.e. heart failure).
Since June of 2009 he is the Head of the Department of Cell Death and Proliferation at the Institute of Biomedical Research of Barcelona (IIBB-CSIC). Also, I am the investigator in charge of the Associated Unit of “Tumoral mechanisms and cancer progression” of the IIBB-CSIC and the IMIM (Barcelona), since September 2018.
Member of the Editorial Board (Section Editor) of “Thrombosis and Haemostasis” (since 2003), and Associate Editor of “Plos One” (since 2014).
Dr Josefin Ahnström is a British Heart Foundation Research Fellow in the Centre for Haematology at Imperial College London. She has worked there on haemostasis and thrombosis since 2009, following her PhD at Lund University on apolipoprotein M in Björn Dahlbäck’s laboratory. Since 2017 she has been a Committee Member of the British Society for Haemostasis and Thrombosis.
Her current research interests include structural and functional studies of coagulation proteins, as well as regulation of proteoglycans in the extracellular matrix. Her major focus has been determining the molecular mechanisms involved in the anticoagulant pathways. She uses biochemical and kinetic approaches to study formation of various pro- and anticoagulant protein complexes. A recent research interest has been the cofactor roles of protein S and factor V in the TFPI and APC anticoagulant pathways.
Cécile Denis is director of research at INSERM (Institut National de la Santé et de la Recherche Médicale) in Kremlin-Bicêtre Hospital next to Paris, France. After completing her PhD in 1993 at University of Paris, she spent the next seven years working at Harvard Medical School in Boston. Back in France, she obtained a permanent position at INSERM and developed her own research team.
Since 2010, she is the director of Inserm Unit 1176, an Inserm laboratory covering a large aspect of hemostasis research from platelet function to coagulation proteins and involved in the developement of new therapeutics for bleeding disorders. Her long-standing personal interest has been on von Willebrand factor and von Willebrand disease and development of animal models.
She received prizes from the French Academy of Sciences in 2006 and from the International Society of Thrombosis and Haemostasis in 2017. She has also received the French Légion d’Honneur in 2012. She has published more than 125 papers in the field of Thrombosis and Haemostasis and is inventor on 11 related patents.
Gordon Lowe graduated MB,ChB with honours and gold medal from the University of St Andrews in 1972. He trained in general medicine with an interest in haemostasis, thrombosis and vascular diseases in the University Department of Medicine, Glasgow Royal Infirmary from 1974; and graduated MD (Dundee) with commendation in 1984. He was appointed Senior Lecturer, University of Glasgow and Consultant Physician in 1985; and from 1987 was Co-Director of the West of Scotland Haemophilia and Thrombosis Centre, and Director of the University’s Haemostasis and Thrombosis Research Laboratory, with a focus on epidemiology and clinical trials. In 1993 he was appointed Professor of Vascular Medicine. He was President, BSHT 1990-1; Co-Chair of the ISTH Subcommittee on Predictive and Diagnostic Variables in Thrombotic Diseases; Vice-President, ISTH 2001-3; and Chair, Scottish Intercollegiate Guidelines Network (SIGN) 2002-7. He graduated DSc (Glasgow) in 2007; and received an ISTH Investigator Recognition Award in 2009. Retiring that year, he developed his interests in medical history, music and railways.
Kimberly Martinod is an assistant professor in the Department of Cardiovascular Sciences, Faculty of Medicine, at KU Leuven in Belgium. She performed her doctoral studies in Denisa Wagner’s lab and received her PhD degree in Immunology from Harvard Medical School for her thesis titled “Neutrophil extracellular traps in thrombosis and inflammation.” As a Transfusion Biology Research Fellow at Boston Children’s Hospital, she investigated the role of peptidylarginine deiminase 4 (PAD4) and NETs in fibrotic tissue remodeling during aging. In 2016, she joined Simon De Meyer’s group in the Laboratory for Thrombosis Research at the KU Leuven Kulak Kortrijk campus, where as a Marie Skłodowska-Curie Postdoctoral Fellow she has studied the interaction between the blood protein von Willebrand factor and neutrophils in their activation leading to NETosis.
Her (growing) research group, located at the Center for Molecular and Vascular Biology in Leuven, focuses on the interplay between thrombosis and inflammation in cardiac disease, specifically in the development of heart failure. She is, since 2018, a co-chair of the Scientific Subcommittee on Vascular Biology of the International Society on Thrombosis and Haemostasis.
Leon Schurgers is professor of vascular calcification and vice chair of the department of biochemistry, which is part of the Cardiovascular Research Institute CARIM, the largest research institute of the University of Maastricht. His work includes molecular biology, biochemistry, animal and human nutrition, pharmacology, and clinical studies in the fields of vascular disease. He is leading the scientific part on vitamin K-research, vascular smooth muscle cells and iPSCs and supervising technical engineers, post docs and PhD students.
His project line tries to elucidate the molecular mechanisms of vitamin K-dependent proteins (VKDP) by which (vascular) calcification is initiated and propagated: key cellular events include phenotypic switching of vascular smooth muscle cells (VSMC) and the formation of extracellular vesicles and apoptotic bodies contributing to the initiation and progression of calcification. The regulation of VKDP biosynthesis, its sites of action and its putative relationship with apoptosis is insufficient to understand the pathogenesis of ectopic calcification at a level that allows the development of novel diagnostic tools and therapeutic strategies for VKDP.
Importantly, these findings will help to understand the paradoxal observation that patients with low vitamin K-status during oral anticoagulant treatment develop massive ectopic calcification and our results might provide new insights in prognostic and preventive measures.
Marina Noris has an in-depth expertise in rare genetic renal diseases particularly in rare complement related kidney diseases. In this field Dr Noris greatly contributed to discover the genetic causes of atypical hemolytic uremic syndrome (aHUS), describing the mutations in genes encoding complement regulatory proteins, factor H, membrane cofactor protein and thrombomodulin and their functional consequences. Her discoveries have been described in a number of publications in high impact journals, including the Lancet, Blood, the Journal of the American Society of Nephrology and the New England Journal of Medicine. Her research also clarified that the specific genetic defect has a great impact on the clinical course of this disease and on the risk of disease recurrence after kidney transplantation and contributed to the recent achievement of a specific cure with the anti-C5 antibody Eculizumab (approved by EMEA and FDA).
In 2010 her laboratory was accredited by Regione Lombardia and the Italian National Health Service as a reference centre for biochemical and genetic diagnostic tests in patients with aHUS and TTP and in 2015 the accreditation was extended to C3G/MPGN, steroid resistant nephrotic syndrome and PKD. On July 2017 the laboratory received the ISO 9001/2008 certification for biochemical and genetic analysis in patients with rare diseases.
Her group also discovered the genetic cause of very rare renal disease, the glomerulopathy with fibronectin deposits and a new genetic form of childhood onset familial FSGS associated with mutation in the myosin 1E gene. Using next generation sequencing technology her group has identified a new genetic form of recessive steroid resistant nephrotic syndrome (SRNS) associated with mutations in the myosin 1 E gene. Dr. Noris has been invited to hold lectures at a number of National and International congresses and is author and co-author of more than 200 scientific articles, reviews and monographs.
Dr. Weitz is Professor of Medicine and Biochemistry and Biomedical Sciences at McMaster University and Executive Director of the Thrombosis and Atherosclerosis Research Institute. Board Certified in Internal Medicine, Hematology and Medical Oncology, Dr. Weitz focuses his clinical practice on patients with thrombotic disorders. His research spans the spectrum from basic studies in the biochemistry of blood coagulation and fibrinolysis to animal models of thrombosis and on to clinical trials of antithrombotic therapy. The breadth of his work is highlighted by his over 530 publications in journals as diverse as the Journal of Clinical Investigation, Journal of Biological Chemistry, Biochemistry, Circulation, Blood, Annals of Internal Medicine, New England Journal of Medicine and Lancet, and 65 book chapters. The recipient of numerous awards, Dr. Weitz is a Fellow of the American Heart Association, the Royal Society of Canada and the Canadian Academy of Health Sciences.
Dr Yotis Senis was awarded a BScH in Life Sciences in 1993, an MSc in 1996 and a PhD in 2002 in Pathology, Queen’s University, Canada. His MSc was under the supervision of Professor Alan Giles on the clearance and biosynthesis of VWF during disseminated intravascular coagulation, and his PhD was under the supervision of Professor Peter Greer on the regulation of haematopoiesis by the tyrosine kinases Fps and Fer. In 2002 he joined the laboratory of Professor Steve Watson in Pharmacology, University of Oxford, UK as a postdoctoral researcher, characterizing novel receptors and signalling pathways regulating platelet function. In 2003 he was appointed to a 5 year research position in the Birmingham Platelet Group, Physiology, University of Birmingham, UK, which allowed him to start developing his research interests on platelet tyrosine phosphatases. He was awarded a BHF Intermediate Basic Science Research Fellowship in 2009 and a Senior Fellowship in 2013 investigating the inhibitory receptor G6b-B and tyrosine phosphatases Shp1 and Shp2. He was promoted to Chair in Cellular Haemostasis in the College of Medical and Dental Sciences, University of Birmingham in 2013. In 2019 he was appointed Director of Research at Etablissement Français du Sang / Inserm UMR S1255 Strasbourg, France under the Directorship of Dr Christian Gachet. In his research, Dr Senis takes a multidisciplinary approach investigating how tyrosine phosphatases work in conjunction with tyrosine kinases to regulate platelet activation, with the overall objective of identifying novel anti-thrombotic drug targets.