Tamam Bakchoul

ORCID: 0000-0002-6797-6812
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About
Contact & Profiles
Research Areas
  • Platelet Disorders and Treatments
  • Heparin-Induced Thrombocytopenia and Thrombosis
  • Blood groups and transfusion
  • Venous Thromboembolism Diagnosis and Management
  • Intramuscular injections and effects
  • COVID-19 Clinical Research Studies
  • Blood disorders and treatments
  • SARS-CoV-2 and COVID-19 Research
  • Blood properties and coagulation
  • Antiplatelet Therapy and Cardiovascular Diseases
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Cell Adhesion Molecules Research
  • Blood transfusion and management
  • Long-Term Effects of COVID-19
  • Blood donation and transfusion practices
  • Immunodeficiency and Autoimmune Disorders
  • Hematopoietic Stem Cell Transplantation
  • Hemophilia Treatment and Research
  • Monoclonal and Polyclonal Antibodies Research
  • Blood Coagulation and Thrombosis Mechanisms
  • Hemoglobinopathies and Related Disorders
  • SARS-CoV-2 detection and testing
  • Proteoglycans and glycosaminoglycans research
  • Renal Diseases and Glomerulopathies
  • Adipokines, Inflammation, and Metabolic Diseases

University of Tübingen
2016-2025

Bernstein Center for Computational Neuroscience Tübingen
2016-2025

University Children's Hospital Tübingen
2013-2025

Institute for Transfusion Medicine
2011-2024

Universitätsklinikum Tübingen
2016-2024

Universitätsmedizin Greifswald
2013-2019

Universität Greifswald
2012-2018

University of Giessen
2007-2016

Universitas Gadjah Mada
2016

Versiti Blood Center of Wisconsin
2008-2016

Ernest Turro William J. Astle Karyn Mégy Stefan Gräf Daniel Greene and 95 more Olga Shamardina Hana Lango Allen Alba Sanchis‐Juan Mattia Frontini Chantal Thys Jonathan Stephens Rutendo Mapeta Oliver S. Burren Kate Downes Matthias Haimel Salih Tuna Sri V. V. Deevi Timothy J. Aitman David Bennett Paul Calleja Keren Carss Mark J. Caulfield Patrick F. Chinnery Peter H. Dixon Daniel P. Gale Roger James Ania Koziell Michael Laffan Adam P. Levine Eamonn R. Maher Hugh S. Markus Joannella Morales Nicholas W. Morrell Andrew Mumford Elizabeth Ormondroyd Stuart Rankin Augusto Rendon Sylvia Richardson Irene Roberts Noémi Roy Moin A. Saleem Kenneth G. C. Smith Hannah Stark Rhea Tan Andreas C. Themistocleous Adrian J. Thrasher Hugh Watkins Andrew R. Webster Martin R. Wilkins Catherine Williamson James Whitworth Sean Humphray David Bentley Stephen Abbs Lara Abulhoul Julian Adlard Munaza Ahmed Timothy J. Aitman Hana Alachkar David Allsup J. P. Almeida Philip Ancliff Richard Antrobus Ruth Armstrong Gavin Arno Sofie Ashford William J. Astle Anthony Attwood Paul Aurora Christian Babbs Chiara Bacchelli Tamam Bakchoul Siddharth Banka Tadbir K. Bariana Julian Barwell Joana Batista Helen Baxendale Phil Beales David Bennett David Bentley Agnieszka Bierżyńska Tina Biss Maria Bitner‐Glindzicz Graeme Black Marta Bleda Iulia Blesneac Detlef Böckenhauer Harm Jan Bogaard Christian Bourne Sara Boyce John R. Bradley Eugene Bragin Gerome Breen Paul Brennan Carole Brewer Matthew A. Brown Andrew C. Browning Michael J. Browning Rachel Buchan Matthew Buckland

10.1038/s41586-020-2434-2 article EN Nature 2020-06-24
Keren Carss Gavin Arno Marie Erwood Jonathan Stephens Alba Sanchis-Juan and 95 more Sarah Hull Karyn Mégy Detelina Grozeva Eleanor Dewhurst Samantha Malka Vincent Plagnol Christopher J. Penkett Kathleen Stirrups Roberta Rizzo Genevieve Wright Dragana Josifova Maria Bitner‐Glindzicz Richard H. Scott Emma Clement Louise Allen Ruth Armstrong Angela F. Brady Jenny Carmichael Manali Chitre Robert Henderson Jane A. Hurst Robert E. MacLaren Elaine Murphy Joan Paterson Elisabeth Rosser Dorothy Thompson Emma Wakeling Willem H. Ouwehand Michel Michaelides Anthony T. Moore Andrew R. Webster F. Lucy Raymond Timothy J. Aitman Hana Alachkar Sonia Ali Louise Allen David Allsup Gautum Ambegaonkar Julie Anderson Richard Antrobus Ruth Armstrong Gavin Arno Gururaj Arumugakani Sofie Ashford William F. Astle Antony Attwood Steve Austin Chiara Bacchelli Tamam Bakchoul Tadbir K. Bariana Helen Baxendale David Bennett Claire Bethune Shahnaz Bibi Maria Bitner‐Glindzicz Marta Bleda Harm Boggard Paula Bolton‐Maggs Claire Booth John R. Bradley Angie Brady Matthew A. Brown Michael J. Browning Christine Bryson Siobhan O. Burns Paul Calleja Natalie Canham Jenny Carmichael Keren Carss Mark J. Caulfield Elizabeth Chalmers Anita Chandra Patrick F. Chinnery Manali Chitre Colin Church Emma Clement Emma Clement Virginia Clowes Gerry Coghlan Peter Collins Nichola Cooper Amanda Creaser-Myers Rosa DaCosta Louise C. Daugherty Sophie Davies John S. Davis Minka De Vries Patrick Deegan Sri V. V. Deevi Charu Deshpande Lisa Devlin Eleanor Dewhurst Rainer Döffinger Natalie Dormand Elizabeth Drewe

10.1016/j.ajhg.2016.12.003 article EN publisher-specific-oa The American Journal of Human Genetics 2016-12-29
James Thaventhiran Hana Lango Allen Oliver S. Burren William Rae Daniel Greene and 95 more Emily Staples Zinan Zhang James H. R. Farmery Ilenia Simeoni Elizabeth Rivers Jesmeen Maimaris Christopher J. Penkett Jonathan Stephens Sri V. V. Deevi Alba Sanchis‐Juan Nicholas Gleadall Moira Thomas Ravishankar Sargur Pavels Gordins Helen Baxendale Matthew A. Brown Paul Tuijnenburg Austen Worth Steven Hanson Rachel Linger Matthew Buckland Paula Rayner-Matthews Kimberly Gilmour Crina Samarghitean Suranjith L. Seneviratne David M. Sansom Andy G. Lynch Karyn Mégy Eva Ellinghaus David Ellinghaus Silje F. Jørgensen Tom H. Karlsen Kathleen Stirrups Antony J. Cutler Dinakantha Kumararatne Anita Chandra David Edgar Archana Herwadkar Nichola Cooper Sofia Grigoriadou Aarnoud Huissoon Sarah Goddard Stephen Jolles Catharina Schuetz Felix Boschann Stephen Abbs Zoe Adhya Julian Adlard Maryam Afzal Irshad Ahmed Munaza Ahmed Saeed Ahmed Timothy J. Aitman Hana Alachkar Jayanthi Alamelu Raza Alikhan Carl E. Allen Louise Allen David Allsup Arif Alvi Gautam Ambegaonkar Ariharan Anantharachagan Philip Ancliff Julie A. Anderson Richard Antrobus Ruth Armstrong Gavin Arno Gururaj Arumugakani Rita Arya Sofie Ashford William J. Astle Anthony Attwood Steve Austin Yeşim Aydınok Waqar Ayub Christian Babbs Chiara Bacchelli Trevor Baglin Tamam Bakchoul Tadbir K. Bariana Jonathan Barratt Julian Barwell John Baski Rachel W. Bates Joana Batista Helen Baxendale Gareth Baynam David Bennett Claire Bethune Neha Bhatnagar Shahnaz Bibi Agnieszka Bierżyńska Tina Biss Maria Bitner‐Glindzicz Marta Bleda

10.1038/s41586-020-2265-1 article EN Nature 2020-05-06

SARS-CoV-2 is evolving with mutations in the receptor binding domain (RBD) being of particular concern. It important to know how much cross-protection offered between strains following vaccination or infection. Here, we obtain serum and saliva samples from groups vaccinated (Pfizer BNT-162b2), infected uninfected individuals characterize antibody response RBD mutant strains. Vaccinated have a robust humoral after second dose high IgG titers saliva. Antibody responses however show...

10.1038/s41467-021-23473-6 article EN cc-by Nature Communications 2021-05-25

The COVID-19 pandemic has resulted in significant morbidity and mortality worldwide. To prevent severe infection, mass vaccination campaigns with several vaccine types are currently underway. We report pathological immunological findings 8 patients who developed vaccine-induced immune thrombotic thrombocytopenia (VITT) after administration of SARS-CoV-2 ChAdOx1 nCoV-19. analyzed patient material using enzyme assays, flow cytometry heparin-induced platelet aggregation assay performed...

10.3324/haematol.2021.279000 article EN cc-by-nc Haematologica 2021-05-20

It is commonly accepted that antibody-mediated removal of platelets represents a major mechanism platelet destruction in immune thrombocytopenic purpura (ITP). Although complement activation may participate clearance, frequency and specificity have not yet been studied systematically ITP.We examined blood samples from 240 patients with ITP. Samples were assessed for the presence free bound autoantibodies by standard glycoprotein-specific assay (monoclonal antibody-specific immobilization...

10.1111/j.1600-0609.2011.01718.x article EN European Journal Of Haematology 2011-10-10
Charaka Hadinnapola Marta Bleda Matthias Haimel Nicholas Screaton Andrew J. Swift and 95 more Peter Dorfmüller Stephen Preston Mark Southwood Jules Hernández‐Sánchez Jennifer M. Martin Carmen Treacy Katherine Yates Harm Jan Bogaard Colin Church Gerry Coghlan Robin Condliffe Paul A. Corris Simon Gibbs Barbara Girerd Simon Holden Marc Humbert David G. Kiely Allan Lawrie Rajiv D. Machado Robert Ross Shahin Moledina David Montani Michael Newnham Andrew J. Peacock Joanna Pepke‐Żaba Paula Rayner-Matthews Olga Shamardina Florent Soubrier Laura Southgate Jay Suntharalingam Mark Toshner Richard C. Trembath Anton Vonk Noordegraaf Martin R. Wilkins Stephen J. Wort John Wharton Stefan Gräf Nicholas W. Morrell Timothy J. Aitman David Bennett Mark J. Caulfield Patrick F. Chinnery Daniel P. Gale Ania Koziell Taco W. Kuijpers Michael Laffan Eamonn R. Maher Hugh S. Markus Willem H. Ouwehand David J. Perry F. Lucy Raymond Irene Roberts Kenneth G. C. Smith Adrian J. Thrasher Hugh Watkins Catherine Williamson Geoffrey Woods Sofie Ashford John R. Bradley Debra Fletcher Tracey Hammerton Roger James Nathalie Kingston Willem H. Ouwehand Christopher J. Penkett F. Lucy Raymond Kathleen Stirrups Marijke Veltman Timothy M. Young Sofie Ashford Matthew A. Brown Emma Clement John Davis Eleanor Dewhurst Marie Erwood Amy Frary Rachel Linger Sofia Papadia Karola Rehnström Hannah Stark David Allsup Steve Austin Tamam Bakchoul Tadbir K. Bariana Paula Bolton‐Maggs Elizabeth Chalmers Peter Collins Wendy N. Erber Tamara Everington Rémi Favier Kathleen Freson Bruce Furie Michael Gattens Keith Gomez Daniel Greene

Background: Pulmonary arterial hypertension (PAH) is a rare disease with an emerging genetic basis. Heterozygous mutations in the gene encoding bone morphogenetic protein receptor type 2 ( BMPR2 ) are commonest cause of PAH, whereas biallelic eukaryotic translation initiation factor alpha kinase 4 EIF2AK4 described pulmonary veno-occlusive disease/pulmonary capillary hemangiomatosis. Here, we determine frequency these and define genotype-phenotype characteristics large cohort patients...

10.1161/circulationaha.117.028351 article EN cc-by Circulation 2017-10-03

Abstract The humoral immune response to SARS-CoV-2 is a benchmark for immunity and detailed analysis required understand the manifestation progression of COVID-19, monitor seroconversion within general population, support vaccine development. majority currently available commercial serological assays only quantify antibody against individual antigens, limiting our understanding response. To overcome this, we have developed multiplex immunoassay (MultiCoV-Ab) including spike nucleocapsid...

10.1038/s41467-021-20973-3 article EN cc-by Nature Communications 2021-02-19

Objective— Fetal/neonatal alloimmune thrombocytopenia is a severe bleeding disorder, which can result in intracranial hemorrhage (ICH), leading to death or neurological sequelae. In whites, maternal anti–human platelet antigen-1a (HPA-1a) antibodies are responsible for the majority of cases. No predictive factors ICH available guide prophylactic treatment during pregnancy. this study, we investigated from mothers with ICH-positive fetal/neonatal and ICH-negative identify serological...

10.1161/atvbaha.116.307281 article EN Arteriosclerosis Thrombosis and Vascular Biology 2016-06-10

Significance CLL is characterized by autonomous B cell receptor (BCR) signaling. subsets are empirically defined sequence similarities of the BCR heavy chain. However, in unfavorable subset 2, an acquired mutation (termed R110) light chain stimulates This study demonstrates that oncogenic R110 dictates prognosis and not restricted to conventional 2. Interestingly, carriers a particular light-chain allele ( IGLV3-21 * 01 ) predisposed develop because this enables signaling as single-point...

10.1073/pnas.1913810117 article EN cc-by Proceedings of the National Academy of Sciences 2020-02-11

Uterus transplantation (UTx) can provide a route to motherhood for women with Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS), congenital disorder characterized by uterovaginal aplasia, but functional ovaries. Based on our four successful living-donor transplantations and two resulting births, this analysis presents parameters relevant standardizing recipient/donor selection, UTx surgery, postoperative treatment, their implementation in routine settings. We descriptively analyzed...

10.3390/jcm9082485 article EN Journal of Clinical Medicine 2020-08-03

Myocardial ischemia is one of the leading health problems worldwide. Therapy consists restitution coronary perfusion which followed by myocardial inflammation. Platelet-neutrophil interaction a crucial process during inflammation, yet its consequences are not fully understood. Here, we show that platelet-neutrophil complexes (PNCs) increased in patients with acute infarction and this associated levels neuronal guidance protein semaphorin 7A (SEMA7A). To investigate further, injected WT...

10.1038/s41467-020-14958-x article EN cc-by Nature Communications 2020-03-11

The prognostic value of preformed donor-specific HLA antibodies (DSA), which are only detectable by sensitive methods, remains controversial for kidney transplantation.The outcome 4233 consecutive transplants performed between 2012 and 2015 in 18 German transplant centers was evaluated. Most used a stepwise pretransplant antibody screening with bead array tests differentiation positive samples single antigen assays. Using these results, DSA against HLA-A, -B, -C, -DRB1 -DQB1 were determined....

10.2215/cjn.13401118 article EN Clinical Journal of the American Society of Nephrology 2019-06-18

Anemia is a common complication of chronic kidney disease, affecting the quality life patients. Among various factors, such as iron and erythropoietin deficiency, reduced red blood cell (RBC) lifespan has been implicated in pathogenesis anemia. However, mechanistic data on vivo RBC dysfunction disease are lacking. Herein, we describe development disease-associated anemia mice with proteinuric resulting from either administration doxorubicin or an inducible podocin deficiency. In both...

10.1016/j.kint.2021.08.024 article EN cc-by-nc-nd Kidney International 2021-09-16
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