Hava Peretz

2.2k total citations
67 papers, 1.7k citations indexed

About

Hava Peretz is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Hava Peretz has authored 67 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Hematology, 15 papers in Molecular Biology and 15 papers in Genetics. Recurrent topics in Hava Peretz's work include Platelet Disorders and Treatments (15 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (12 papers) and Blood Coagulation and Thrombosis Mechanisms (9 papers). Hava Peretz is often cited by papers focused on Platelet Disorders and Treatments (15 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (12 papers) and Blood Coagulation and Thrombosis Mechanisms (9 papers). Hava Peretz collaborates with scholars based in Israel, United States and United Kingdom. Hava Peretz's co-authors include Uri Seligsohn, Ariella Zivelin, Nurit Rosenberg, Nurit Kornbrot, Rivka Yatuv, Sali Usher, Abraham Loyter, Z. Toister, Barry S. Coller and Ayala Lagziel and has published in prestigious journals such as The Journal of Cell Biology, Blood and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Hava Peretz

65 papers receiving 1.6k citations

Peers

Countries citing papers authored by Hava Peretz

Since Specialization

Citations

This map shows the geographic impact of Hava Peretz's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hava Peretz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hava Peretz more than expected).

Fields of papers citing papers by Hava Peretz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hava Peretz. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hava Peretz. The network helps show where Hava Peretz may publish in the future.

Co-authorship network of co-authors of Hava Peretz

This figure shows the co-authorship network connecting the top 25 collaborators of Hava Peretz. A scholar is included among the top collaborators of Hava Peretz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hava Peretz. Hava Peretz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews 2013 ·Journal of Thrombosis and Haemostasis ·Hava Peretz, Ophira Salomon, Ronit Mor-Cohen, Sali Usher, M. Zucker, Ariella Zivelin, Uri Seligsohn	6
2	Association of the -757T>C polymorphism in the CRP gene with circulating C-reactive protein levels and carotid atherosclerosis 2009 ·Thrombosis Research ·Einor Ben Assayag, Shani Shenhar‐Tsarfaty, Irena Bova, Shlomo Berliner, Sali Usher, Hava Peretz, Itzhak Shapira, Natan M. Bornstein	15
3	Glycohaemoglobin as a determinant of increased fibrinogen concentrations and low‐grade inflammation in apparently healthy nondiabetic individuals 2007 ·Clinical Endocrinology ·Ori Rogowski, Itzhak Shapira, Hava Peretz, Shlomo Berliner	16
4	Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria 2007 ·Molecular Genetics and Metabolism ·Hava Peretz, (unknown), David Levartovsky, Ayala Lagziel, (unknown), (unknown), Hanna Shalev, Daniel Landau	35
5	Polymorphic Markers in the XDH Gene as Diagnostic Tools for Typing Classical Xanthinuria 2006 ·Kluwer Academic Publishers eBooks ·Ayala Lagziel, David Levartovsky, Oded Sperling, Kimiyoshi Ichida, Hava Peretz	2
6	Role of CYP2D6 polymorphism in predicting liver fibrosis progression rate in Caucasian patients with chronic hepatitis C 2006 ·Liver International ·Sigal Fishman, Yoav Lurie, Hava Peretz, (unknown), (unknown), Laurie Blendis, Moshe Leshno, Eli Brazowski, Guy Rosner, Zamir Halpern, Ran Oren	6
7	Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patients 2006 ·Journal of Thrombosis and Haemostasis ·Everette Jacob Remington Nelson, Sukesh C. Nair, Hava Peretz, Barry S. Coller, Uri Seligsohn, Mammen Chandy, Alok Srivastava	22
8	A 13-bp deletion in αIIb gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia 2005 ·Journal of Thrombosis and Haemostasis ·Nurit Rosenberg, Hagit Hauschner, Hava Peretz, (unknown), Meytal Landau, Elizabeth Shenkman, Gili Kenet, Barry S. Coller, (unknown), Uri Seligsohn	31
9	A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families 2003 ·European Journal of Human Genetics ·Emanuel Yakobson, Shlomit Eisenberg, (unknown), David Halle, Ephrat Levy‐Lahad, Raphael Catane, Mark Safro, V. M. Sobolev, (unknown), Gordon Peters, Anna Ruiz, Josep Malvehy, Susana Puig, Agnès Chompret, (unknown), Raphael Shafir, Hava Peretz, Brigitte Bressac–de Paillerets	19
10	Cytokine network in nonresponding chronic hepatitis C patients with genotype 1: role of triple therapy with interferon alpha, ribavirin, and ursodeoxycholate 2001 ·Clinical Biochemistry ·Manuela G. Neuman, Laurence M. Blendis, Neil H. Shear, Izabella M. Malkiewicz, (unknown), Gady G Katz, (unknown), Zamir Halpern, Shlomo Brill, Hava Peretz, (unknown), Fred M. Konikoff	13
11	Two p16 (CDKN2A) germline mutations in 30 Israeli melanoma families 2000 ·European Journal of Human Genetics ·Emanuel Yakobson, (unknown), Esther Azizi, Eyal Winkler, Norman J. Lassam, David Hogg, Sharon Brookes, Gordon Peters, Michal Lotem, Abraham Zlotogorski, Marina Landau, Mark Safro, Raphael Shafir, Eitan Friedman, Hava Peretz	21
12	Molecular characterization of four novel mutations causing factor VII deficiency 2000 ·The Hematology Journal ·Hannah Tamary, (unknown), Lea Shalmon, Rina Zaizov, (unknown), Aharon Klar, Hava Peretz, Benjamin Brenner, Naomi Lanir, Ariela Zivelin, Uri Seligsohn	10
13	Age Estimates of Two Common Mutations Causing Factor XI Deficiency: Recent Genetic Drift Is Not Necessary for Elevated Disease Incidence among Ashkenazi Jews 1999 ·The American Journal of Human Genetics ·David B. Goldstein, David Reich, Neil Bradman, Sali Usher, Uri Seligsohn, Hava Peretz	50
14	Mendelian Diseases among Roman Jews: Implications for the Origins of Disease Alleles 1999 ·The Journal of Clinical Endocrinology & Metabolism ·Carole Oddoux, Encarna Guillén‐Navarro, (unknown), (unknown), (unknown), (unknown), Kyriakie Sarafoglou, (unknown), Hava Peretz, Uri Seligsohn, Lucio Luzzatto, (unknown), Michael Nardi, Margaret Karpatkin, Ivona Aksentijevich, Daniel L. Kastner, Felicia B. Axelrod, Harry Ostrer	12
15	Screening for Tumour Suppressor p16(CDKN2A) Germline Mutations in Israeli Melanoma Families 1998 ·Clinical Chemistry and Laboratory Medicine (CCLM) ·Emanuel Yakobson, (unknown), (unknown), (unknown), (unknown), Marina Landau, Sarah Brenner, Sali Usher, Hava Peretz	7
16	Pheochromocytoma due to unilateral adrenal medullary hyperplasia 1997 ·Clinical Endocrinology ·(unknown), Avraham Ishay, Hava Peretz, (unknown), Nathan Kaufman, Rafael Luboshitzky	15
17	Cys 618 Arg mutation in the RET proto-oncogene associated with familial medullary thyroid carcinoma and maternally transmitted Hirschsprung's disease suggesting a role for imprinting 1997 ·Human Mutation ·Hava Peretz, (unknown), E. Baron, A. Biton, Ruth Gershoni, (unknown), (unknown), Emanuel Yakobson, E. Graff, Mordechai Lapidot	33
18	Differential Proliferative Characteristics of Alveolar Fibroblastsin Interstitial Lung Diseases: Regulative Role of IL‐1 and PGE₂ 1994 ·Mediators of Inflammation ·Elizabeth Fireman, (unknown), Joel Greif, Hava Peretz, Shmuel Kivity, M Topilsky, (unknown), Alon Yellin, Ron N. Apte	4
19	Molecular Genetics Aspects of Factor XI Deficiency and Glanzmann Thrombasthenia 1994 ·Pathophysiology of Haemostasis and Thrombosis ·Uri Seligsohn, Hava Peretz	7
20	SYNOVIAL AND SERUM LEVELS OF METHOTREXATE DURING METHOTREXATE THERAPY OF RHEUMATOID ARTHRITIS 1989 ·Lara D. Veeken ·Moshe Tishler, Dan Caspi, E. Graff, R Segal, Hava Peretz, Michal Yaron	33

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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