Hadas Ityel

1.2k total citations
4 papers, 111 citations indexed

About

Hadas Ityel is a scholar working on Surgery, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Hadas Ityel has authored 4 papers receiving a total of 111 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Surgery, 2 papers in Molecular Biology and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Hadas Ityel's work include Muscle and Compartmental Disorders (1 paper), Congenital Anomalies and Fetal Surgery (1 paper) and Cardiomyopathy and Myosin Studies (1 paper). Hadas Ityel is often cited by papers focused on Muscle and Compartmental Disorders (1 paper), Congenital Anomalies and Fetal Surgery (1 paper) and Cardiomyopathy and Myosin Studies (1 paper). Hadas Ityel collaborates with scholars based in Israel, United States and Norway. Hadas Ityel's co-authors include Ben Pode‐Shakked, Yair Anikster, Jacob Levy, Young Ah Seo, Nechama Shalva, Bluma Berman, Shannon L. Kelleher, Alexander Goncearenco, Yehuda G. Assaraf and Aharon Klar and has published in prestigious journals such as Journal of Biological Chemistry, Pediatric Nephrology and Molecular Syndromology.

In The Last Decade

Hadas Ityel

4 papers receiving 107 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hadas Ityel Israel	4	65	43	29	28	19	4	111
Hélène Morel France	5	47 0.7×	21 0.5×	35 1.2×	25 0.9×	2 0.1×	11	107
Erik Waldenström Sweden	6	167 2.6×	34 0.8×	118 4.1×	93 3.3×	12 0.6×	6	222
Koki Matsuo Japan	8	9 0.1×	42 1.0×	6 0.2×	4 0.1×	35 1.8×	17	198
Rongqing Yang China	5	28 0.4×	81 1.9×	20 0.7×		19 1.0×	8	140
Iskren Kotzev Bulgaria	7	8 0.1×	24 0.6×	8 0.3×	6 0.2×	12 0.6×	18	135
Stina Bodén Sweden	6	27 0.4×	23 0.5×	2 0.1×	3 0.1×	18 0.9×	14	192
Liliana R. Santos Portugal	5	62 1.0×	51 1.2×	12 0.4×	3 0.1×	3 0.2×	9	168
M Tsukada Japan	6	11 0.2×	24 0.6×	6 0.2×	13 0.5×	5 0.3×	17	76
Anthony Cabrera United States	3	82 1.3×	15 0.3×	52 1.8×	34 1.2×	1 0.1×	3	100
J. E. Davis United States	5	11 0.2×	17 0.4×	8 0.3×	8 0.3×	16 0.8×	8	75

Countries citing papers authored by Hadas Ityel

Since Specialization

Citations

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

Fields of papers citing papers by Hadas Ityel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hadas Ityel

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

All Works

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4 of 4 papers shown

1.

Vivante, Asaf, Hadas Ityel, Ben Pode‐Shakked, et al.. (2017). Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases. Pediatric Nephrology. 32(12). 2273–2282. 27 indexed citations

2.

Ven, Amelie T. van der, Shirlee Shril, Hadas Ityel, et al.. (2017). Whole-Exome Sequencing Reveals FAT4 Mutations in a Clinically Unrecognizable Patient with Syndromic CAKUT: A Case Report. Molecular Syndromology. 8(5). 272–277. 5 indexed citations

3.

Seo, Young Ah, Hadas Ityel, Nechama Shalva, et al.. (2012). A Dominant Negative Heterozygous G87R Mutation in the Zinc Transporter, ZnT-2 (SLC30A2), Results in Transient Neonatal Zinc Deficiency. Journal of Biological Chemistry. 287(35). 29348–29361. 74 indexed citations

4.

Ityel, Hadas, et al.. (2011). Splenic torsion of a wandering spleen.. PubMed. 13(2). 119–20. 5 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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