Avihu Boneh

7.4k total citations · 1 hit paper
111 papers, 5.3k citations indexed

About

Avihu Boneh is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Avihu Boneh has authored 111 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Molecular Biology, 64 papers in Clinical Biochemistry and 29 papers in Physiology. Recurrent topics in Avihu Boneh's work include Metabolism and Genetic Disorders (64 papers), Mitochondrial Function and Pathology (34 papers) and Diet and metabolism studies (18 papers). Avihu Boneh is often cited by papers focused on Metabolism and Genetic Disorders (64 papers), Mitochondrial Function and Pathology (34 papers) and Diet and metabolism studies (18 papers). Avihu Boneh collaborates with scholars based in Australia, Israel and Canada. Avihu Boneh's co-authors include David R. Thorburn, Canny Sugiana, Vamsi K. Mootha, David E. Hill, Sarah E. Calvo, James G. Evans, Betty Chang, Shao‐En Ong, Marc Vidal and David J. Pagliarini and has published in prestigious journals such as Cell, The Lancet and Journal of Clinical Investigation.

In The Last Decade

Avihu Boneh

109 papers receiving 5.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology

2008 1.6k citations Canny Sugiana, Avihu Boneh et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Avihu Boneh Australia	33	3.8k	2.7k	992	514	512	111	5.3k
Marinus Durán Netherlands	44	3.0k 0.8×	2.1k 0.8×	1.1k 1.1×	479 0.9×	657 1.3×	102	5.3k
Magdalena Ugarte Spain	38	3.3k 0.9×	2.9k 1.1×	753 0.8×	464 0.9×	479 0.9×	218	4.7k
Gregory M. Enns United States	36	2.5k 0.7×	2.0k 0.7×	687 0.7×	732 1.4×	621 1.2×	133	4.4k
Pinar T. Ozand Saudi Arabia	34	2.2k 0.6×	1.9k 0.7×	923 0.9×	496 1.0×	733 1.4×	163	4.4k
Nicola Longo United States	38	3.4k 0.9×	3.3k 1.2×	1.9k 1.9×	600 1.2×	715 1.4×	197	6.1k
Barbara Plecko Austria	37	2.3k 0.6×	1.9k 0.7×	984 1.0×	571 1.1×	747 1.5×	138	4.6k
Fumio Endo Japan	39	2.0k 0.5×	1.2k 0.4×	1.1k 1.1×	560 1.1×	553 1.1×	185	5.1k
Shamima Rahman United Kingdom	44	4.7k 1.2×	2.8k 1.0×	561 0.6×	641 1.2×	251 0.5×	160	6.3k
Hanna Mandel Israel	43	4.0k 1.0×	2.4k 0.9×	1.8k 1.8×	692 1.3×	449 0.9×	176	7.4k
Stefan Kölker Germany	44	3.9k 1.0×	4.2k 1.5×	955 1.0×	843 1.6×	895 1.7×	218	6.3k

Countries citing papers authored by Avihu Boneh

Since Specialization

Citations

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

Fields of papers citing papers by Avihu Boneh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Avihu Boneh

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Boneh, Avihu, et al.. (2018). Malignant brain tumors in patients with glutaric aciduria type I. Molecular Genetics and Metabolism. 125(3). 276–280. 10 indexed citations

Truby, Helen, et al.. (2017). The relationship between dietary intake, growth and body composition in Phenylketonuria. Molecular Genetics and Metabolism. 122(1-2). 36–42. 36 indexed citations

Truby, Helen, et al.. (2017). The Relationship between Dietary Intake, Growth, and Body Composition in Inborn Errors of Intermediary Protein Metabolism. The Journal of Pediatrics. 188. 163–172. 24 indexed citations

Tal, Galit, et al.. (2015). An audit of newborn screening procedure: Impact on infants presenting clinically before results are available. Molecular Genetics and Metabolism. 114(3). 403–408. 6 indexed citations

Brown, Ruth M., et al.. (2014). Thiamine-Responsive and Non-responsive Patients with PDHC-E1 Deficiency: A Retrospective Assessment. JIMD Reports. 15. 13–27. 30 indexed citations

Pitt, James, et al.. (2014). Biochemical and molecular characteristics of patients with organic acidaemias and urea cycle disorders identified through newborn screening. Molecular Genetics and Metabolism. 113(1-2). 46–52. 13 indexed citations

Brown, Amy, Louise Crowe, Miriam H. Beauchamp, Vicki Anderson, & Avihu Boneh. (2014). Neurodevelopmental Profiles of Children with Glutaric Aciduria Type I Diagnosed by Newborn Screening: A Follow-Up Case Series. JIMD Reports. 18. 125–134. 10 indexed citations

Truby, Helen, et al.. (2014). New ways of defining protein and energy relationships in inborn errors of metabolism. Molecular Genetics and Metabolism. 112(4). 247–258. 7 indexed citations

Lim, Sze Chern, Justine E. Marum, Elena J. Tucker, et al.. (2013). Mutations in LYRM4, encoding iron–sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes. Human Molecular Genetics. 22(22). 4460–4473. 81 indexed citations

10.

Rötig, Agnès, Avihu Boneh, Pascale de Lonlay, et al.. (2013). Beneficial effects of resveratrol on respiratory chain defects in patients' fibroblasts involve estrogen receptor and estrogen-related receptor alpha signaling. Human Molecular Genetics. 23(8). 2106–2119. 54 indexed citations

11.

Wilcken, Bridget, Pamela Joy, Veronica Wiley, et al.. (2009). NEWBORN SCREENING BY TANDEM MASS SPECTROMETRY: A COHORT STUDY COMPARING OUTCOME IN SCREENED AND CLINICALLY DIAGNOSED PATIENTS AT SIX YEARS OF AGE. Molecular Genetics and Metabolism. 98. 3–3. 1 indexed citations

12.

Caciotti, Anna, Maria Alice Donati, Avihu Boneh, et al.. (2005). Role of ?-galactosidase and elastin binding protein in lysosomal and nonlysosomal complexes of patients with GM1-gangliosidosis. Human Mutation. 25(3). 285–292. 35 indexed citations

13.

Kirby, Denise M., Renato Salemi, Canny Sugiana, et al.. (2004). NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency. Journal of Clinical Investigation. 114(6). 837–845. 14 indexed citations

14.

Braverman, Nancy, Li Chen, Paul Lin, et al.. (2002). Mutation analysis ofPEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype. Human Mutation. 20(4). 284–297. 95 indexed citations

15.

Morrone, Amelia, Sabrina Malvagia, Maria Alice Donati, et al.. (2002). Clinical findings and biochemical and molecular analysis of four patients with holocarboxylase synthetase deficiency. American Journal of Medical Genetics. 111(1). 10–18. 21 indexed citations

16.

Boneh, Avihu, et al.. (2001). Splenectomy in two siblings with G‐CSF‐dependent glycogen storage disease type Ib. Journal of Inherited Metabolic Disease. 24(3). 419–422. 1 indexed citations

17.

Dasvarma, Ayan, et al.. (2000). The clinical spectrum of cytochrome c deficiency in Leigh syndrome patients with and without mutations in the SURF1 gene. The American Journal of Human Genetics. 67(4). 64–64. 2 indexed citations

18.

Boneh, Avihu. (1995). Possible role for protein kinase C in the pathogenesis of inborn errors of metabolism. Journal of Cellular Biochemistry. 59(1). 27–32. 11 indexed citations

19.

Boneh, Avihu, et al.. (1994). Effect of fatty acids and their acyl-CoA esters on protein kinase C activity in fibroblasts: Possible implications in fatty acid oxidation defects. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1221(1). 66–72. 26 indexed citations

20.

Boneh, Avihu, et al.. (1987). Audiometric evidence for two forms of X‐linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouse. American Journal of Medical Genetics. 27(4). 997–1003. 33 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.

Explore authors with similar magnitude of impact