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Tamam Bakchoul
Tamam Bakchoul
Unknown affiliation
Verified email at med.uni-tuebingen.de
Title
Cited by
Cited by
Year
SARS-CoV-2-derived peptides define heterologous and COVID-19-induced T cell recognition
A Nelde, T Bilich, JS Heitmann, Y Maringer, HR Salih, M Roerden, ...
Nature immunology 22 (1), 74-85, 2021
6452021
Comprehensive rare variant analysis via whole-genome sequencing to determine the molecular pathology of inherited retinal disease
KJ Carss, G Arno, M Erwood, J Stephens, A Sanchis-Juan, S Hull, K Megy, ...
The American Journal of Human Genetics 100 (1), 75-90, 2017
4632017
Effects of liberal vs restrictive transfusion thresholds on survival and neurocognitive outcomes in extremely low-birth-weight infants: the ETTNO randomized clinical trial
AR Franz, C Engel, D Bassler, M Rüdiger, UH Thome, RF Maier, ...
Jama 324 (6), 560-570, 2020
2062020
Antibody-induced procoagulant platelets in severe COVID-19 infection
K Althaus, I Marini, J Zlamal, L Pelzl, A Singh, H Häberle, M Mehrländer, ...
Blood, The Journal of the American Society of Hematology 137 (8), 1061-1071, 2021
2042021
Autoantibody‐mediated complement activation on platelets is a common finding in patients with immune thrombocytopenic purpura (ITP)
A Najaoui, T Bakchoul, J Stoy, G Bein, MJ Rummel, S Santoso, UJ Sachs
European journal of haematology 88 (2), 167-174, 2012
1992012
A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss
S Stritt, P Nurden, E Turro, D Greene, SB Jansen, SK Westbury, ...
Blood, The Journal of the American Society of Hematology 127 (23), 2903-2914, 2016
1662016
Prospective evaluation of PF4/heparin immunoassays for the diagnosis of heparin-induced thrombocytopenia
T Bakchoul, A Giptner, A Najaoui, G Bein, S Santoso, UJH Sachs
Journal of Thrombosis and Haemostasis 7 (8), 1260-1265, 2009
1522009
Immune response to SARS-CoV-2 variants of concern in vaccinated individuals
M Becker, A Dulovic, D Junker, N Ruetalo, PD Kaiser, YT Pinilla, ...
Nature communications 12 (1), 3109, 2021
1512021
Recommendations for the clinical and laboratory diagnosis of VITT against COVID‐19: communication from the ISTH SSC Subcommittee on Platelet Immunology
I Nazy, UJ Sachs, DM Arnold, SE McKenzie, P Choi, K Althaus, MT Ahlen, ...
Journal of Thrombosis and Haemostasis 19 (6), 1585-1588, 2021
1502021
Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders
SK Westbury, E Turro, D Greene, C Lentaigne, AM Kelly, TK Bariana, ...
Genome medicine 7, 1-15, 2015
1452015
Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension
C Hadinnapola, M Bleda, M Haimel, N Screaton, A Swift, P Dorfmüller, ...
Circulation 136 (21), 2022-2033, 2017
1402017
Antenatal management in fetal and neonatal alloimmune thrombocytopenia: a systematic review
D Winkelhorst, MF Murphy, A Greinacher, N Shehata, T Bakchoul, ...
Blood, The Journal of the American Society of Hematology 129 (11), 1538-1547, 2017
1402017
Antibody-mediated procoagulant platelets in SARS-CoV-2-vaccination associated immune thrombotic thrombocytopenia
K Althaus, P Möller, G Uzun, A Singh, A Beck, M Bettag, H Bösmüller, ...
Haematologica 106 (8), 2170, 2021
1352021
Heparin-induced thrombocytopenia
A Greinacher, T Bakchoul, A Cuker, TE Warkentin
Platelets in Thrombotic and Non-Thrombotic Disorders: Pathophysiology …, 2017
1322017
Drug-associated thrombocytopenia
T Bakchoul, I Marini
Hematology 2014, the American Society of Hematology Education Program Book …, 2018
1222018
Antiendothelial αvβ3 antibodies are a major cause of intracranial bleeding in fetal/neonatal alloimmune thrombocytopenia
S Santoso, H Wihadmadyatami, T Bakchoul, S Werth, N Al-Fakhri, G Bein, ...
Arteriosclerosis, thrombosis, and vascular biology 36 (8), 1517-1524, 2016
1212016
A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies
E Turro, D Greene, A Wijgaerts, C Thys, C Lentaigne, TK Bariana, ...
Science translational medicine 8 (328), 328ra30-328ra30, 2016
1172016
Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders
A Greinacher, A Pecci, S Kunishima, K Althaus, P Nurden, CL Balduini, ...
Journal of Thrombosis and Haemostasis 15 (7), 1511-1521, 2017
962017
Fetal and neonatal alloimmune thrombocytopenia: recommendations for evidence‐based practice, an international approach
L Lieberman, A Greinacher, MF Murphy, J Bussel, T Bakchoul, S Corke, ...
British journal of haematology 185 (3), 549-562, 2019
942019
IGLV3-21*01 is an inherited risk factor for CLL through the acquisition of a single-point mutation enabling autonomous BCR signaling
PC Maity, M Bilal, MT Koning, M Young, CAM van Bergen, V Renna, ...
Proceedings of the National Academy of Sciences 117 (8), 4320-4327, 2020
852020
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