Tova Naiman

577 total citations
20 papers, 469 citations indexed

About

Tova Naiman is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Tova Naiman has authored 20 papers receiving a total of 469 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Oncology. Recurrent topics in Tova Naiman's work include DNA Repair Mechanisms (5 papers), CRISPR and Genetic Engineering (5 papers) and Animal Genetics and Reproduction (5 papers). Tova Naiman is often cited by papers focused on DNA Repair Mechanisms (5 papers), CRISPR and Genetic Engineering (5 papers) and Animal Genetics and Reproduction (5 papers). Tova Naiman collaborates with scholars based in Israel, United States and Sweden. Tova Naiman's co-authors include Dan Canaani, Tal Teitz, Ruth Shomrat, Avi Orr‐Urtreger, Yuval Yaron, Paul Rozen, Cyril Legum, Idit Kopatz, Hana Strul and Paul Berg and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Gastroenterology.

In The Last Decade

Tova Naiman

20 papers receiving 455 citations

Peers

Countries citing papers authored by Tova Naiman

Since Specialization

Citations

This map shows the geographic impact of Tova Naiman'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 Tova Naiman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tova Naiman more than expected).

Fields of papers citing papers by Tova Naiman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tova Naiman. 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 Tova Naiman. The network helps show where Tova Naiman may publish in the future.

Co-authorship network of co-authors of Tova Naiman

This figure shows the co-authorship network connecting the top 25 collaborators of Tova Naiman. A scholar is included among the top collaborators of Tova Naiman 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 Tova Naiman. Tova Naiman 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	CD55-deficiency in Jews of Bukharan descent is caused by the Cromer blood type Dr(a−) variant 2022 ·Human Genetics ·Alina Kurolap, David Hagin, Tal Freund, Sigal Fishman, (unknown), Eli Brazowski, Josepha Yeshaya, Tova Naiman, Elon Pras, Jacob N. Ablin, Hagit Baris Feldman	5
2	Ethnic effect on FMR1 carrier rate and AGG repeat interruptions among Ashkenazi women 2014 ·Genetics in Medicine ·Karin Weiss, Avi Orr‐Urtreger, (unknown), Tova Naiman, Ruth Shomrat, (unknown), Yuval Yaron, Shay Ben‐Shachar	10
3	Preimplantation genetic diagnosis for fragile X syndrome using multiplex nested PCR 2007 ·Reproductive BioMedicine Online ·Mira Malcov, Tova Naiman, (unknown), (unknown), (unknown), Ami Amit, (unknown), Yuval Yaron	42
4	MECP2 Mutations in Israel: Implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome 2002 ·Human Mutation ·Yuval Yaron, Bruria Ben Zeev, Ruth Shomrat, Dani Bercovich, Tova Naiman, Avi Orr‐Urtreger	25
5	Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutations 2002 ·Human Mutation ·Nancy Gavert, Yuval Yaron, Tova Naiman, Dani Bercovich, Paul Rozen, Ruth Shomrat, Cyril Legum, Avi Orr‐Urtreger	33
6	Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia 2002 ·Cancer ·Paul Rozen, Tova Naiman, Hana Strul, Philipp Taussky, (unknown), Ruth Shomrat, (unknown), Yuval Yaron, Avi Orr‐Urtreger	30
7	The Risk of Fragile X Premutation Expansion Is Lower in Carriers Detected by General Prenatal Screening Than in Carriers from Known Fragile X Families 2000 ·Genetic Testing ·Eli Geva, Yuval Yaron, Ruth Shomrat, (unknown), (unknown), (unknown), Tova Naiman, (unknown), Avi Orr‐Urtreger	22
8	Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer 1999 ·Gastroenterology ·Paul Rozen, Ruth Shomrat, Hana Strul, Tova Naiman, (unknown), Cyril Legum, Avi Orr‐Urtreger	60
9	[Muir-Torre syndrome and HNPCC: importance of clinical diagnosis and genetic investigation in family members]. 1999 ·PubMed ·Hana Strul, Paul Rozen, Tova Naiman, Ruth Shomrat	1
10	Molecular Cloning of a Novel Human Gene Encoding a 63-kDa Protein and Its Sublocalization within the 11q13 Locus 1997 ·Genomics ·Boris Perelman, N. Dafni, Tova Naiman, (unknown), (unknown), (unknown), (unknown), Günther Weber, (unknown), Aziz Sancar, Iris Dotan, Dan Canaani	29
11	Establishment of an autocatalytic conditional mammalian system for expression of stringently regulated genes 1995 ·Nucleic Acids Research ·Iris Dotan, Idit Kopatz, Tova Naiman, Boris Perelman, N. Dafni, Dan Canaani	2
12	Assignment of the Human Casein Kinase II α′ Subunit Gene (CSNK2A1) to Chromosome 16p13.2-p13.3 1994 ·Genomics ·Teresa L. Yang‐Feng, Tova Naiman, Idit Kopatz, (unknown), N. Dafni, Dan Canaani	25
13	Mapping of the human caseis kinase II catalytic subunit genes: two loci carrying the homologues sewquences for the α subunit 1991 ·Nucleic Acids Research ·Teresa L. Yang‐Feng, (unknown), Idit Kopatz, Tova Naiman, Dan Canaani	20
14	Expression of the cDNA for the beta subunit of human casein kinase II confers partial UV resistance on xeroderma pigmentosum cells 1990 ·Mutation Research/DNA Repair ·Tal Teitz, (unknown), (unknown), Mary Bakhanashvili, Tova Naiman, Terry L. Timme, (unknown), Robb E. Moses, Dan Canaani	52
15	Isolation by polymerase chain reaction of a cDNA whose product partially complements the ultraviolet sensitivity of xeroderma pigmentosum group C cells 1990 ·Gene ·Tal Teitz, (unknown), (unknown), (unknown), Mary Bakhanashvili, Tova Naiman, Dan Canaani	20
16	The nucleotide sequence of the mouse cDNA encoding the beta subunit of casein kinase II 1990 ·Nucleic Acids Research ·Idit Kopatz, Tova Naiman, (unknown), Dan Canaani	16
17	Ultraviolet light-resistant primary transfectants of xeroderma pigmentosum cells are also DNA repair-proficient 1989 ·Biochemical and Biophysical Research Communications ·(unknown), Tova Naiman, Dan Canaani	5
18	A hypodiploid karyotype found in immortal human cells selected from a wide spectrum of posttransformation chromosomal complements 1989 ·Cancer Genetics and Cytogenetics ·Tova Naiman, Dan Canaani	3
19	Complementation of the UV-sensitive phenotype of a xeroderma pigmentosum human cell line by transfection with a cDNA clone library. 1987 ·Proceedings of the National Academy of Sciences ·Tal Teitz, Tova Naiman, Sofia Avissar, (unknown), Hiroto Okayama, Dan Canaani	24
20	Immortalization of xeroderma pigmentosum cells by simian virus 40 DNA having a defective origin of DNA replication 1986 ·Somatic Cell and Molecular Genetics ·Dan Canaani, Tova Naiman, Tal Teitz, Paul Berg	45

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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