Michal Inbar‐Feigenberg

2.0k total citations
30 papers, 419 citations indexed

About

Michal Inbar‐Feigenberg is a scholar working on Physiology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Michal Inbar‐Feigenberg has authored 30 papers receiving a total of 419 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Physiology, 9 papers in Molecular Biology and 9 papers in Clinical Biochemistry. Recurrent topics in Michal Inbar‐Feigenberg's work include Lysosomal Storage Disorders Research (10 papers), Metabolism and Genetic Disorders (8 papers) and Glycogen Storage Diseases and Myoclonus (5 papers). Michal Inbar‐Feigenberg is often cited by papers focused on Lysosomal Storage Disorders Research (10 papers), Metabolism and Genetic Disorders (8 papers) and Glycogen Storage Diseases and Myoclonus (5 papers). Michal Inbar‐Feigenberg collaborates with scholars based in Canada, United States and France. Michal Inbar‐Feigenberg's co-authors include Sanaa Choufani, Rosanna Weksberg, Darci T. Butcher, Maian Roifman, Yi‐An Chen, Peter N. Ray, Leslie Steele, Cheryl Shuman, Cheryl Cytrynbaum and Shelly K. Weiss and has published in prestigious journals such as Fertility and Sterility, Clinica Chimica Acta and Quality of Life Research.

In The Last Decade

Michal Inbar‐Feigenberg

29 papers receiving 400 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michal Inbar‐Feigenberg Canada 10 191 113 111 81 77 30 419
Drago Bratkovic Australia 14 200 1.0× 87 0.8× 157 1.4× 40 0.5× 131 1.7× 48 419
Anke Schumann Germany 11 179 0.9× 64 0.6× 75 0.7× 37 0.5× 149 1.9× 32 379
Sunita Bijarnia‐Mahay India 13 257 1.3× 128 1.1× 75 0.7× 133 1.6× 241 3.1× 63 522
Sujatha Jagadeesh India 12 178 0.9× 165 1.5× 72 0.6× 61 0.8× 22 0.3× 39 456
Emma Glamuzina New Zealand 11 148 0.8× 62 0.5× 68 0.6× 61 0.8× 149 1.9× 30 323
Bushra Afroze Pakistan 11 228 1.2× 184 1.6× 44 0.4× 80 1.0× 105 1.4× 39 385
Mark Sharrard United Kingdom 10 212 1.1× 105 0.9× 73 0.7× 66 0.8× 178 2.3× 21 439
Zhuwen Gong China 13 237 1.2× 143 1.3× 41 0.4× 58 0.7× 176 2.3× 32 399
Ishwar C. Verma India 12 217 1.1× 162 1.4× 79 0.7× 111 1.4× 67 0.9× 47 558
Hanneke A. Haijes Netherlands 12 262 1.4× 75 0.7× 77 0.7× 40 0.5× 183 2.4× 18 409

Countries citing papers authored by Michal Inbar‐Feigenberg

Since Specialization
Citations

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

Fields of papers citing papers by Michal Inbar‐Feigenberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michal Inbar‐Feigenberg. 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 Michal Inbar‐Feigenberg. The network helps show where Michal Inbar‐Feigenberg may publish in the future.

Co-authorship network of co-authors of Michal Inbar‐Feigenberg

This figure shows the co-authorship network connecting the top 25 collaborators of Michal Inbar‐Feigenberg. A scholar is included among the top collaborators of Michal Inbar‐Feigenberg 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 Michal Inbar‐Feigenberg. Michal Inbar‐Feigenberg 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.
Muenzer, Joseph, Barbara K. Burton, Paul Harmatz, et al.. (2024). Evaluation of early treatment with intravenous idursulfase and intrathecal idursulfase‐ IT on cognitive function in siblings with neuronopathic mucopolysaccharidosis II. Journal of Inherited Metabolic Disease. 48(3). e12790–e12790. 1 indexed citations
2.
Vanderhout, Shelley, Beth K. Potter, Maureen Smith, et al.. (2023). Ethical and practical considerations related to data sharing when collecting patient-reported outcomes in care-based child health research. Quality of Life Research. 32(8). 2319–2328. 1 indexed citations
3.
Blasér, Susan, et al.. (2023). An unusually mild case of biotin-thiamine-responsive basal ganglia disease. Molecular Genetics and Metabolism Reports. 37. 101004–101004. 1 indexed citations
4.
Chimienti, Guglielmina, Alessia De Nisco, Tiziana Latronico, et al.. (2022). Retrograde response to mitochondrial dysfunctions associated to LOF variations in FLAD1 exon 2: unraveling the importance of RFVT2. Free Radical Research. 56(7-8). 511–525. 6 indexed citations
5.
Muenzer, Joseph, Barbara K. Burton, Paul Harmatz, et al.. (2022). Intrathecal idursulfase-IT in patients with neuronopathic mucopolysaccharidosis II: Results from a phase 2/3 randomized study. Molecular Genetics and Metabolism. 137(1-2). 127–139. 23 indexed citations
6.
Muenzer, Joseph, Barbara K. Burton, Paul Harmatz, et al.. (2022). Long-term open-label extension study of the safety and efficacy of intrathecal idursulfase-IT in patients with neuronopathic mucopolysaccharidosis II. Molecular Genetics and Metabolism. 137(1-2). 92–103. 8 indexed citations
7.
Tingley, Kylie, Michal Inbar‐Feigenberg, John J. Mitchell, et al.. (2021). Establishing a core outcome set for mucopolysaccharidoses (MPS) in children: study protocol for a rapid literature review, candidate outcomes survey, and Delphi surveys. Trials. 22(1). 816–816. 2 indexed citations
8.
Roth, Johannes, Michal Inbar‐Feigenberg, Julian Raiman, et al.. (2021). Ultrasound findings of finger, wrist and knee joints in Mucopolysaccharidosis Type I. Molecular Genetics and Metabolism. 133(3). 289–296. 3 indexed citations
9.
Siddiqui, Iram, Andrea Guerin, Neal Sondheimer, et al.. (2020). Liver transplantation for Gaucher disease presenting as neonatal cholestasis: Case report and literature review. Pediatric Transplantation. 24(4). e13718–e13718. 3 indexed citations
10.
Costain, Gregory, Susan Blasér, Susan Walker, et al.. (2020). Genome sequencing identifies a rare case of moderate Zellweger spectrum disorder caused by a PEX3 defect: Case report and literature review. Molecular Genetics and Metabolism Reports. 25. 100664–100664. 3 indexed citations
11.
Longo, Nicola, George A. Díaz, Uta Lichter‐Konecki, et al.. (2020). Glycerol phenylbutyrate efficacy and safety from an open label study in pediatric patients under 2 months of age with urea cycle disorders. Molecular Genetics and Metabolism. 132(1). 19–26. 10 indexed citations
12.
Schulze, Andreas, et al.. (2019). The utility of dried blood spot monitoring of branched-chain amino acids for maple syrup urine disease: A retrospective chart review study. Clinica Chimica Acta. 500. 195–201. 2 indexed citations
13.
Inbar‐Feigenberg, Michal, et al.. (2019). Use of waxy maize heat modified starch in the treatment of children between 2 and 5 years with glycogen storage disease type I: A retrospective study. Molecular Genetics and Metabolism Reports. 21. 100536–100536. 9 indexed citations
14.
Hannah‐Shmouni, Fady, Lauren MacNeil, Murray Potter, et al.. (2018). Severe cystic degeneration and intractable seizures in a newborn with molybdenum cofactor deficiency type B. Molecular Genetics and Metabolism Reports. 18. 11–13. 8 indexed citations
15.
Costain, Gregory, Maha Saleh, Greg Ryan, et al.. (2018). Challenges in Diagnosing Rare Genetic Causes of Common In Utero Presentations: Report of Two Patients with Mucolipidosis Type II (I-Cell Disease). Journal of Pediatric Genetics. 7(3). 134–137. 3 indexed citations
16.
Inbar‐Feigenberg, Michal, Susan Blasér, Cynthia Hawkins, et al.. (2018). Mitochondrial POLG related disorder presenting prenatally with fetal cerebellar growth arrest. Metabolic Brain Disease. 33(4). 1369–1373. 6 indexed citations
17.
Nochi, Zahra, et al.. (2018). A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy. JIMD Reports. 45. 37–44. 30 indexed citations
18.
Bruun, Theodora U. J., Dawn Cordeiro, Jaina Patel, et al.. (2016). Phenotype, biochemical features, genotype and treatment outcome of pyridoxine-dependent epilepsy. Metabolic Brain Disease. 32(2). 443–451. 37 indexed citations
19.
Inbar‐Feigenberg, Michal, Sanaa Choufani, Darci T. Butcher, Maian Roifman, & Rosanna Weksberg. (2013). Basic concepts of epigenetics. Fertility and Sterility. 99(3). 607–615. 117 indexed citations
20.
Inbar‐Feigenberg, Michal, Sanaa Choufani, Cheryl Cytrynbaum, et al.. (2012). Mosaicism for genome‐wide paternal uniparental disomy with features of multiple imprinting disorders: Diagnostic and management issues. American Journal of Medical Genetics Part A. 161(1). 13–20. 46 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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