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Hamideh Yadegari

Observed names: H Yadegari, H. YADEGARI, H. Yadegari
ORCID: 0000-0002-2006-8497
Observed ORCID: 0000-0002-2006-8497
OpenAlex ID: A5033589468
Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients
2012 · Hamideh Yadegari, Julia Driesen, et al. · Thrombosis and Haemostasis · 62
Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5′ splice site
2016 · Hamideh Yadegari, Arijit Biswas, et al. · Blood · 41
Large deletions identified in patients with von Willebrand disease using multiple ligation‐dependent probe amplification
2011 · H. YADEGARI, J. DRIESEN, et al. · Journal of Thrombosis and Haemostasis · 25
von Willebrand factor neutralizing and non-neutralizing alloantibodies in 213 subjects with type 3 von Willebrand disease enrolled in 3WINTERS-IPS
2023 · Maria Teresa Pagliari, Ulrich Budde, et al. · Journal of Thrombosis and Haemostasis · 20
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Insights into pathological mechanisms of missense mutations in C-terminal domains of von Willebrand factor causing qualitative or quantitative von Willebrand disease
2013 · H. Yadegari, J. Driesen, et al. · Haematologica · 15
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Unravelling the spectrum of von Willebrand factor variants in quantitative von Willebrand disease: results from a German cohort study
2024 · Alexander Krahforst, Hamideh Yadegari, et al. · Journal of Thrombosis and Haemostasis · 14
The Current Understanding of Molecular Pathogenesis of Quantitative von Willebrand Disease, Types 1 and 3
2020 · Hamideh Yadegari, Johannes Oldenburg · Hämostaseologie · 14
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Potentials of Endothelial Colony-Forming Cells: Applications in Hemostasis and Thrombosis Disorders, from Unveiling Disease Pathophysiology to Cell Therapy
2023 · Nadine Schwarz, Hamideh Yadegari · Hämostaseologie · 13
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Multifaceted pathomolecular mechanism of a VWF large deletion involved in the pathogenesis of severe VWD
2021 · Hamideh Yadegari, Muhammad Ahmer Jamil, et al. · Blood Advances · 13
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Disruption of Structural Disulfides of Coagulation FXIII-B Subunit; Functional Implications for a Rare Bleeding Disorder
2019 · Sneha Singh, Mohammad Suhail Akhter, et al. · International Journal of Molecular Sciences · 12
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Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand disease
2019 · Shariq Ahmed, Hamideh Yadegari, et al. · Haemophilia · 10
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Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS‐IPS study
2022 · Maria Teresa Pagliari, Frits R. Rosendaal, et al. · Journal of Thrombosis and Haemostasis · 9
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Landscape and Spectrum of VWF Variants in Type 2 Von Willebrand Disease: Insights from a German Patient Cohort
2025 · Hamideh Yadegari, Susan Halimeh, et al. · Thrombosis and Haemostasis · 8
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A Homozygous Deep Intronic Variant Causes Von Willebrand Factor Deficiency and Lack of Endothelial-Specific Secretory Organelles, Weibel–Palade Bodies
2022 · Hamideh Yadegari, Muhammad Ahmer Jamil, et al. · International Journal of Molecular Sciences · 8
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von Willebrand factor propeptide missense variants affect anterograde transport to Golgi resulting in ER retention
2021 · Hamideh Yadegari, Arijit Biswas, et al. · Human Mutation · 8
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Ex Vivo Modeling of the PC (Protein C) Pathway Using Endothelial Cells and Plasma: A Personalized Approach
2022 · Nadine Schwarz, Jens Müller, et al. · Arteriosclerosis Thrombosis and Vascular Biology · 7
Exploring the structural similarity yet functional distinction between coagulation factor XIII-B and complement factor H sushi domains
2019 · Mohammad Suhail Akhter, Sneha Singh, et al. · Journal of Thrombosis and Thrombolysis · 7
Von Willebrand Factor at the Crossroads of Hemostasis and Inflammation
2026 · Hamideh Yadegari · Hämostaseologie · 6
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Effect of daclizumab (Zenapax) on prevention of acute rejection of renal transplantation
2003 · F Poorrezagholi, B Einollahi, et al. · Transplantation Proceedings · 5
Interplay between circulating von Willebrand factor and neutrophils: implications for inflammation, neutrophil function, and von Willebrand factor clearance
2025 · Alua Kuanyshbek, Hamideh Yadegari, et al. · Haematologica · 4
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ATZ11 Recognizes Not Only Z-α1-Antitrypsin-Polymers and Complexed Forms of Non-Z-α1-Antitrypsin but Also the von Willebrand Factor
2014 · Diane Goltz, Kanishka Hittetiya, et al. · PLoS ONE · 2
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OC 07.2 Investigating the Dominant Negative Effect of Heterozygous F13B Gene Mutations Detected from Mild FXIII Deficiency Patients
2023 · H. Javed, S. Singh, et al. · Research and Practice in Thrombosis and Haemostasis · 1
Molecular Genetics Analysis of Von Williebrand Disease: Studies in Cohort Pakistani Patients
2015 · Shariq Ahmed, Arshi Naz, et al. · Blood · 1
Diagnostic and Treatment Availability of von Willebrand Disease Within Europe: Insights From a European Association for Hemophilia and Allied Disorders (EAHAD) Survey
2026 · Omid Seidizadeh, Ana Boban, et al. · Haemophilia
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PB1143 Disrupted Weibel–Palade Body Scaffolding Drives Nuclear Redirection of Angiopoietin-2 in Endothelial Cells
2026 · Emmanuel Mmorosah, Johannes Oldenburg, et al. · Research and Practice in Thrombosis and Haemostasis
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Works count: 33
Citation count: 305
H-index: 10
I10-index: 11
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