Sandra E. Kleiman

1.7k total citations
67 papers, 1.3k citations indexed

About

Sandra E. Kleiman is a scholar working on Reproductive Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Sandra E. Kleiman has authored 67 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Reproductive Medicine, 41 papers in Genetics and 35 papers in Molecular Biology. Recurrent topics in Sandra E. Kleiman's work include Sperm and Testicular Function (47 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (35 papers) and Sexual Differentiation and Disorders (21 papers). Sandra E. Kleiman is often cited by papers focused on Sperm and Testicular Function (47 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (35 papers) and Sexual Differentiation and Disorders (21 papers). Sandra E. Kleiman collaborates with scholars based in Israel, United States and United Kingdom. Sandra E. Kleiman's co-authors include Leah Yogev, Ron Hauser, Amnon Botchan, Haim Yavetz, Gedalia Paz, Ofer Lehavi, Batia Bar‐Shira Maymon, H. Yavetz, G. Paz and Ronni Gamzu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Human Molecular Genetics.

In The Last Decade

Sandra E. Kleiman

67 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandra E. Kleiman Israel 22 869 796 769 362 101 67 1.3k
Lanlan Meng China 18 471 0.5× 472 0.6× 393 0.5× 415 1.1× 35 0.3× 56 938
C. Carolan France 17 765 0.9× 561 0.7× 748 1.0× 1.4k 3.8× 47 0.5× 28 1.8k
Masaki Iwamoto Japan 19 326 0.4× 747 0.9× 1.1k 1.4× 1.0k 2.9× 44 0.4× 33 1.7k
Antoni Riera‐Escamilla Spain 13 742 0.9× 612 0.8× 565 0.7× 449 1.2× 56 0.6× 24 1.2k
Indira Hinduja India 20 639 0.7× 220 0.3× 378 0.5× 552 1.5× 32 0.3× 52 1.1k
Sylviane Hennebicq France 20 1.0k 1.2× 578 0.7× 814 1.1× 840 2.3× 60 0.6× 54 1.8k
Raoudha Zouari France 17 829 1.0× 540 0.7× 437 0.6× 695 1.9× 28 0.3× 23 1.2k
Debbie Montjean France 17 614 0.7× 300 0.4× 436 0.6× 529 1.5× 24 0.2× 41 1.1k
Ester Margarit Spain 17 183 0.2× 489 0.6× 313 0.4× 92 0.3× 130 1.3× 32 800
DM de Kretser Australia 9 372 0.4× 239 0.3× 359 0.5× 214 0.6× 27 0.3× 13 772

Countries citing papers authored by Sandra E. Kleiman

Since Specialization
Citations

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

Fields of papers citing papers by Sandra E. Kleiman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra E. Kleiman. 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 Sandra E. Kleiman. The network helps show where Sandra E. Kleiman may publish in the future.

Co-authorship network of co-authors of Sandra E. Kleiman

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

All Works

20 of 20 papers shown
1.
Lehavi, Ofer, et al.. (2023). MicroRNAs expression in semen and testis of azoospermic men. Andrology. 11(4). 687–697. 6 indexed citations
2.
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
3.
Kleiman, Sandra E., Atif Zeadna, Eliahu Levitas, et al.. (2021). Pathogenic variations in Germ Cell Nuclear Acidic Peptidase (GCNA) are associated with human male infertility. European Journal of Human Genetics. 29(12). 1781–1788. 11 indexed citations
4.
Gershoni, Moran, Ron Hauser, Leah Yogev, et al.. (2017). A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes. Genetics in Medicine. 19(9). 998–1006. 108 indexed citations
5.
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
6.
Yogev, Leah, Gedalia Paz, Haim Yavetz, et al.. (2016). New insights into the role of the Brdt protein in the regulation of development and spermatogenesis in the mouse. Gene Expression Patterns. 20(2). 130–137. 5 indexed citations
7.
Botchan, Amnon, Ofer Lehavi, Gedalia Paz, et al.. (2013). Preservation of sperm of cancer patients: extent of use and pregnancy outcome in a tertiary infertility center. Asian Journal of Andrology. 15(3). 382–386. 30 indexed citations
8.
Kleiman, Sandra E., Ronit Almog, Leah Yogev, et al.. (2012). Screening for partial AZFa microdeletions in the Y chromosome of infertile men: is it of clinical relevance?. Fertility and Sterility. 98(1). 43–47.e2. 41 indexed citations
9.
Paz, Gedalia, Haim Yavetz, Leah Yogev, et al.. (2012). Genetic and physiological study of morphologically abnormal human zona pellucida. European Journal of Obstetrics & Gynecology and Reproductive Biology. 165(1). 70–76. 20 indexed citations
10.
Paz, Gedalia, Leah Yogev, Haim Yavetz, et al.. (2011). Expression of BET genes in testis of men with different spermatogenic impairments. Fertility and Sterility. 97(1). 46–52.e5. 17 indexed citations
11.
Kleiman, Sandra E., Ofer Lehavi, Ron Hauser, et al.. (2011). CDY1 and BOULE transcripts assessed in the same biopsy as predictive markers for successful testicular sperm retrieval. Fertility and Sterility. 95(7). 2297–2302.e1. 17 indexed citations
12.
Yogev, Leah, Sandra E. Kleiman, Ron Hauser, et al.. (2008). Assessing the predictive value of hyaluronan binding ability for the freezability potential of human sperm. Fertility and Sterility. 93(1). 154–158. 11 indexed citations
13.
Lehavi, Ofer, Leah Yogev, Ron Hauser, et al.. (2008). USP26 gene variations in fertile and infertile men. Human Reproduction. 24(2). 477–484. 30 indexed citations
14.
Yogev, Leah, et al.. (2005). Differentiating between primary and secondary Sertoli-cell-only syndrome by histologic and hormonal parameters. Fertility and Sterility. 83(6). 1856–1858. 6 indexed citations
15.
Carvalho, Cláudia, Jorge Rocha, Fabrício R. Santos, et al.. (2004). Y-Chromosome Haplotypes in Azoospermic Israeli Men. Human Biology. 76(3). 469–478. 6 indexed citations
16.
Kleiman, Sandra E., Leah Yogev, Einav Nili Gal‐Yam, et al.. (2003). Reduced Human Germ Cell‐Less (HGCL) Expression in Azoospermic Men With Severe Germinal Cell Impairment. Journal of Andrology. 24(5). 670–675. 15 indexed citations
17.
Kirsch, Stefan, Sandra E. Kleiman, Kenneth P. Roberts, et al.. (2002). Localisation of the Y chromosome stature gene to a 700 kb interval in close proximity to the centromere. Journal of Medical Genetics. 39(7). 507–513. 13 indexed citations
18.
Maymon, Batia Bar‐Shira, Leah Yogev, Gedalia Paz, et al.. (2002). Sertoli cell maturation in men with azoospermia of different etiologies. Fertility and Sterility. 77(5). 904–909. 40 indexed citations
19.
Yogev, Leah, Ronni Gamzu, Gedalia Paz, et al.. (2001). Rate of homologous chromosome bivalents in spermatocytes may predict completion of spermatogenesis in azoospermic men. Human Genetics. 110(1). 30–35. 12 indexed citations
20.
Avigad, Smadar, Sandra E. Kleiman, B. E. Cohen, et al.. (1991). Compound heterozygosity in nonphenylketonuria hyperphenylalanemia: the contribution of mutations for classical phenylketonuria.. PubMed. 49(2). 393–9. 26 indexed citations

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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