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Ariella Zivelin

Observed names: A ZIVELIN, A Zivelin, A. ZIVELIN, A. Zivelin, ARIELLA ZIVELIN, Zivelin Ariella
Observed institutions: Goethe University Frankfurt, University of Southern California, Scripps Research Institute, Cincinnati Children's Hospital Medical Center, University of Vienna, Inserm, Tel Aviv University, Technion – Israel Institute of Technology, University of Milan, Tel Aviv Sourasky Medical Center, Sheba Medical Center, Leiden University Medical Center, Rabin Medical Center, Rambam Health Care Campus, Royal Hallamshire Hospital, Maccabi Healthcare Services, University of California San Diego, Carmel Medical Center, Carmel (Israel), Centre Hospitalier de la Côte Basque, Hôtel-Dieu de Paris, Université Paris Descartes, Weizmann Institute of Science, All India Institute of Medical Sciences
OpenAlex ID: A5058228103
Geographic Distribution of the 20210 G to A Prothrombin Variant
1998 · C. J. M. Doggen, A. Zivelin, et al. · Thrombosis and Haemostasis · 696
Mutations in the ER–Golgi Intermediate Compartment Protein ERGIC-53 Cause Combined Deficiency of Coagulation Factors V and VIII
1998 · William C Nichols, Uri Seligsohn, et al. · Cell · 458
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Single and Combined Prothrombotic Factors in Patients With Idiopathic Venous Thromboembolism
1999 · Ophira Salomon, David M. Steinberg, et al. · Arteriosclerosis Thrombosis and Vascular Biology · 245
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Patients with severe factor XI deficiency have a reduced incidence of deep-vein thrombosis
2010 · Ophira Salomon, David Steinberg, et al. · Thrombosis and Haemostasis · 239
The Frequent 5,10-Methylenetetrahydrofolate Reductase C677T Polymorphism Is Associated with a Common Haplotype in Whites, Japanese, and Africans
2002 · Nurit Rosenberg, Mitsuru Murata, et al. · The American Journal of Human Genetics · 239
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A Single Genetic Origin for a Common Caucasian Risk Factor for Venous Thrombosis
1997 · Ariella Zivelin, John H. Griffin, et al. · Blood · 234
Thrombophilia as a Multigenic Disorder
1997 · Uri Seligsohn, Ariella Zivelin · Thrombosis and Haemostasis · 189
Inhibition of tissue factor/factor VIIa activity in plasma requires factor X and an additional plasma component
1985 · NL Sanders, SP Bajaj, et al. · Blood · 158
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Improved Method for Genotyping Apolipoprotein E Polymorphisms by a PCR-Based Assay Simultaneously Utilizing Two Distinct Restriction Enzymes
1997 · Ariella Zivelin, Nurit Rosenberg, et al. · Clinical Chemistry · 157
A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene
1998 · Ariella Zivelin, Nurit Rosenberg, et al. · Blood · 152
One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews [see comments]
1995 · O Shpilberg, H Peretz, et al. · Blood · 146
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Inherited factor XI deficiency confers no protection against acute myocardial infarction
2003 · O. Salomon, D.M. Steinberg, et al. · Journal of Thrombosis and Haemostasis · 134
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Mechanism of the anticoagulant effect of warfarin as evaluated in rabbits by selective depression of individual procoagulant vitamin K-dependent clotting factors.
1993 · A Zivelin, L V Rao, et al. · Journal of Clinical Investigation · 134
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Clinical Significance of Antibodies to Bovine and Human Thrombin and Factor V After Surgical Use of Bovine Thrombin
1992 · Samuel I. Rapaport, Ariella Zivelin, et al. · American Journal of Clinical Pathology · 130
Identification and Functional Analysis of Two Novel Mutations in the Multidrug Resistance Protein 2 Gene in Israeli Patients with Dubin-Johnson Syndrome
2001 · Ronit Mor-Cohen, Ariella Zivelin, et al. · Journal of Biological Chemistry · 114
Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene
2002 · Ariella Zivelin, Frederic Bauduer, et al. · Blood · 113
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The Two Common Mutations Causing Factor XI Deficiency in Jews Stem From Distinct Founders: One of Ancient Middle Eastern Origin and Another of More Recent European Origin
1997 · Hava Peretz, Avital Mulai, et al. · Blood · 108
The Relative Frequency of Hereditary Thrombotic Disorders Among 107 Patients with Thrombophilia in Israel
1989 · O Ben-Tal, A Zivelin, et al. · Thrombosis and Haemostasis · 100
Plasma replacement therapy during labor is not mandatory for women with severe factor XI deficiency
2005 · Ophira Salomon, David M Steinberg, et al. · Blood Coagulation & Fibrinolysis · 98
The Role of Factor XI in Thrombin Generation Induced by Low Concentrations of Tissue Factor
2001 · Irene Keularts, Ariella Zivelin, et al. · Thrombosis and Haemostasis · 97
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Homocysteine and oxidized low density lipoprotein enhanced platelet adhesion to endothelial cells under flow conditions: distinct mechanisms of thrombogenic modulation.
2000 · R Dardik, D Varon, et al. · PubMed · 95
ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families.
1999 · W C Nichols, V H Terry, et al. · PubMed · 90
Homocysteine and Oxidized Low Density Lipoprotein Enhance Platelet Adhesion to Endothelial Cells under Flow Conditions: Distinct Mechanisms of Thrombogenic Modulation
2000 · D. Varon, I. Tamarin, et al. · Thrombosis and Haemostasis · 82
A common ancestral mutation (C128X) occurring in 11 non‐Jewish families from the UK with factor XI deficiency
2004 · P.H.B. Bolton‐Maggs, H. Peretz, et al. · Journal of Thrombosis and Haemostasis · 76
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Cerebrovascular Events in Patients With Significant Stenosis of the Carotid Artery Are Associated With Hyperhomocysteinemia and Platelet Antigen-1 (Leu33Pro) Polymorphism
2001 · J.Y. Streifler, N. Rosenberg, et al. · Stroke · 61
Works count: 96
Citation count: 5,679
H-index: 38
I10-index: 70
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