Tsvia Frumkin

702 total citations
16 papers, 505 citations indexed

About

Tsvia Frumkin is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Tsvia Frumkin has authored 16 papers receiving a total of 505 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pediatrics, Perinatology and Child Health, 8 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Tsvia Frumkin's work include Prenatal Screening and Diagnostics (11 papers), Renal and related cancers (7 papers) and Pluripotent Stem Cells Research (4 papers). Tsvia Frumkin is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Renal and related cancers (7 papers) and Pluripotent Stem Cells Research (4 papers). Tsvia Frumkin collaborates with scholars based in Israel, Denmark and United States. Tsvia Frumkin's co-authors include Mira Malcov, Dalit Ben‐Yosef, Yuval Yaron, Ami Amit, Foad Azem, Tamar Schwartz, Rachel Eiges, Achia Urbach, Amir Eden and Nissim Benvenisty and has published in prestigious journals such as Cell stem cell, Fertility and Sterility and Molecular and Cellular Endocrinology.

In The Last Decade

Tsvia Frumkin

16 papers receiving 495 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Tsvia Frumkin Israel 9 294 209 198 121 64 16 505
Tamar Schwartz Israel 11 273 0.9× 103 0.5× 136 0.7× 118 1.0× 61 1.0× 18 481
Robert Prosser United States 10 585 2.0× 136 0.7× 121 0.6× 201 1.7× 21 0.3× 14 777
Teija Peura Australia 14 490 1.7× 73 0.3× 245 1.2× 289 2.4× 12 0.2× 35 651
Valérie Nalesso France 9 368 1.3× 68 0.3× 253 1.3× 241 2.0× 45 0.7× 13 612
Luciano Calzari Italy 14 338 1.1× 166 0.8× 230 1.2× 78 0.6× 18 0.3× 38 519
Shoukhrat Mitalipov United States 10 501 1.7× 95 0.5× 113 0.6× 260 2.1× 8 0.1× 16 697
Crista Martinovich United States 8 391 1.3× 96 0.5× 271 1.4× 379 3.1× 18 0.3× 12 666
Mélanie Steffens Germany 11 84 0.3× 97 0.5× 17 0.1× 104 0.9× 85 1.3× 20 355
Stephen C. Collins United States 9 160 0.5× 72 0.3× 130 0.7× 64 0.5× 52 0.8× 12 333
B Delobel France 11 170 0.6× 117 0.6× 313 1.6× 61 0.5× 21 0.3× 18 451

Countries citing papers authored by Tsvia Frumkin

Since Specialization
Citations

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

Fields of papers citing papers by Tsvia Frumkin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tsvia Frumkin

This figure shows the co-authorship network connecting the top 25 collaborators of Tsvia Frumkin. A scholar is included among the top collaborators of Tsvia Frumkin 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 Tsvia Frumkin. Tsvia Frumkin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Gershoni, Moran, Ron Hauser, Ofer Lehavi, et al.. (2023). A pathogenic variant in the uncharacterized RNF212B gene results in severe aneuploidy male infertility and repeated IVF failure. Human Genetics and Genomics Advances. 4(3). 100189–100189. 6 indexed citations
2.
Samara, Nivin, Sagit Peleg, Tsvia Frumkin, et al.. (2022). New insights regarding origin of monosomy occurrence in early developing embryos as demonstrated in preimplantation genetic testing. Molecular Cytogenetics. 15(1). 11–11. 3 indexed citations
3.
Amir, Hadar, Shiri Barbash‐Hazan, Yael Kalma, et al.. (2018). Time-lapse imaging reveals delayed development of embryos carrying unbalanced chromosomal translocations. Journal of Assisted Reproduction and Genetics. 36(2). 315–324. 24 indexed citations
4.
Frumkin, Tsvia, Sagit Peleg, Adi Reches, et al.. (2017). Complex chromosomal rearrangement—a lesson learned from PGS. Journal of Assisted Reproduction and Genetics. 34(8). 1095–1100. 8 indexed citations
5.
Amir, Hadar, Yael Kalma, Tal Cohen, et al.. (2017). Time-lapse imaging reveals delayed development of embryos carrying unbalanced chromosomal translocations. Fertility and Sterility. 108(3). e149–e149. 3 indexed citations
6.
Malcov, Mira, Sagit Peleg, Tsvia Frumkin, et al.. (2017). Improving preimplantation genetic diagnosis (PGD) reliability by selection of sperm donor with the most informative haplotype. Reproductive Biology and Endocrinology. 15(1). 31–31. 3 indexed citations
7.
Hasson, Joseph, Mira Malcov, Tsvia Frumkin, et al.. (2017). Obstetric and neonatal outcomes of pregnancies conceived after preimplantation genetic diagnosis: cohort study and meta-analysis. Reproductive BioMedicine Online. 35(2). 208–218. 22 indexed citations
8.
9.
Ben‐Yehudah, Ahmi, Mira Malcov, Tsvia Frumkin, & Dalit Ben‐Yosef. (2012). Mutated Human Embryonic Stem Cells for the Study of Human Genetic Disorders. Methods in molecular biology. 873. 179–207. 2 indexed citations
10.
Ben‐Yosef, Dalit, Ami Amit, Mira Malcov, et al.. (2011). Female Sex Bias in Human Embryonic Stem Cell Lines. Stem Cells and Development. 21(3). 363–372. 21 indexed citations
11.
Frumkin, Tsvia, Mira Malcov, Michael Telias, et al.. (2010). Human embryonic stem cells carrying mutations for severe genetic disorders. In Vitro Cellular & Developmental Biology - Animal. 46(3-4). 327–336. 21 indexed citations
12.
Malcov, Mira, Tsvia Frumkin, Tamar Shwartz, et al.. (2008). Elucidation of abnormal fertilization by single-cell analysis with fluorescence in situ hybridization and polymorphic marker analysis. Fertility and Sterility. 91(3). 932.e3–932.e6. 4 indexed citations
13.
Barbash‐Hazan, Shiri, Tsvia Frumkin, Mira Malcov, et al.. (2008). Preimplantation aneuploid embryos undergo self-correction in correlation with their developmental potential. Fertility and Sterility. 92(3). 890–896. 129 indexed citations
14.
Frumkin, Tsvia, Mira Malcov, Yuval Yaron, & Dalit Ben‐Yosef. (2007). Elucidating the origin of chromosomal aberrations in IVF embryos by preimplantation genetic analysis. Molecular and Cellular Endocrinology. 282(1-2). 112–119. 28 indexed citations
15.
Eiges, Rachel, Achia Urbach, Mira Malcov, et al.. (2007). Developmental Study of Fragile X Syndrome Using Human Embryonic Stem Cells Derived from Preimplantation Genetically Diagnosed Embryos. Cell stem cell. 1(5). 568–577. 222 indexed citations
16.

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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