Yefim Anbinder

1.5k total citations
9 papers, 1.1k citations indexed

About

Yefim Anbinder is a scholar working on Cell Biology, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yefim Anbinder has authored 9 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cell Biology, 5 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yefim Anbinder's work include Hemoglobin structure and function (5 papers), Neonatal Health and Biochemistry (4 papers) and Folate and B Vitamins Research (3 papers). Yefim Anbinder is often cited by papers focused on Hemoglobin structure and function (5 papers), Neonatal Health and Biochemistry (4 papers) and Folate and B Vitamins Research (3 papers). Yefim Anbinder collaborates with scholars based in Israel, United States and Germany. Yefim Anbinder's co-authors include Nadine Cohen, Raymonde Szargel, Adel Shalata, Hanna Mandel, Valentina Labay, Ann Saada, Drora Berkowitz, Staffan Eriksson, Orly Elpeleg and Corina Hartman and has published in prestigious journals such as Nature Genetics, Diabetes Care and Diabetes.

In The Last Decade

Yefim Anbinder

9 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yefim Anbinder Israel	8	621	344	252	145	125	9	1.1k
Beverly Gibson United States	7	502 0.8×	311 0.9×	161 0.6×	142 1.0×	372 3.0×	10	1.3k
Eduardo López Spain	13	682 1.1×	137 0.4×	111 0.4×	25 0.2×	240 1.9×	17	1.2k
Francesca Mercuri Australia	16	329 0.5×	171 0.5×	83 0.3×	25 0.2×	215 1.7×	25	1.1k
Maciej Pronicki Poland	21	795 1.3×	360 1.0×	57 0.2×	57 0.4×	115 0.9×	95	1.3k
M Hermier France	11	325 0.5×	69 0.2×	85 0.3×	50 0.3×	100 0.8×	63	1.1k
Nobuhiro Ban Japan	19	727 1.2×	65 0.2×	73 0.3×	124 0.9×	149 1.2×	24	1.7k
Shiri Kalet-Litman Israel	7	195 0.3×	31 0.1×	353 1.4×	181 1.2×	157 1.3×	7	668
Takaya Ishihara Japan	17	1.1k 1.8×	379 1.1×	128 0.5×	54 0.4×	192 1.5×	25	1.4k
France Demaugre France	24	1.1k 1.7×	1.1k 3.2×	122 0.5×	270 1.9×	293 2.3×	51	1.7k
Shanti Balasubramaniam Australia	17	487 0.8×	248 0.7×	24 0.1×	77 0.5×	87 0.7×	39	926

Countries citing papers authored by Yefim Anbinder

Since Specialization

Citations

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

Fields of papers citing papers by Yefim Anbinder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yefim Anbinder

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

All Works

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9 of 9 papers shown

1.

Orchard, Trevor J., Wanjie Sun, Patricia A. Cleary, et al.. (2013). Haptoglobin Genotype and the Rate of Renal Function Decline in the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Study. Diabetes. 62(9). 3218–3223. 33 indexed citations

2.

Orchard, Trevor J., Wanjie Sun, Patricia A. Cleary, et al.. (2013). Haptoglobin Genotype and the Rate of Renal Function Decline in the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Study. Diabetes Care. 3 indexed citations

3.

Simpson, Melissa, Janet K. Snell‐Bergeon, Gregory L. Kinney, et al.. (2011). Haptoglobin genotype predicts development of coronary artery calcification in a prospective cohort of patients with type 1 diabetes. Cardiovascular Diabetology. 10(1). 99–99. 36 indexed citations

4.

Levy, Andrew P., Rabea Asleh, Shany Blum, et al.. (2009). Haptoglobin: Basic and Clinical Aspects. Antioxidants and Redox Signaling. 12(2). 293–304. 222 indexed citations

5.

Milman, Uzi, Shany Blum, Chen Shapira, et al.. (2007). Vitamin E Supplementation Reduces Cardiovascular Events in a Subgroup of Middle-Aged Individuals With Both Type 2 Diabetes Mellitus and the Haptoglobin 2-2 Genotype. Arteriosclerosis Thrombosis and Vascular Biology. 28(2). 341–347. 209 indexed citations

6.

Sprecher, Eli, Richard N. Bergman, Gabriele Richard, et al.. (2001). Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin. Nature Genetics. 29(2). 134–136. 120 indexed citations

7.

Mandel, Hanna, Raymonde Szargel, Valentina Labay, et al.. (2001). The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA. Nature Genetics. 29(3). 337–341. 430 indexed citations

8.

Raz, Tal, Valentina Labay, Raymonde Szargel, et al.. (2000). The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia geneSLC19A2 of eight families. Human Mutation. 16(1). 37–42. 48 indexed citations

9.

Shalata, Adel, Hanna Mandel, C. Dorche, et al.. (2000). Prenatal diagnosis and carrier detection for molybdenum cofactor deficiency type A in Northern Israel using polymorphic DNA markers. Prenatal Diagnosis. 20(1). 7–11. 11 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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