Annette Feigenbaum
Impact in
- Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
- Biochemistry top 2%
Papers in
-
- Metabolism and Genetic Disorders 36
-
- Mitochondrial Function and Pathology 18
- ATP Synthase and ATPases Research 5
- RNA regulation and disease 4
- Co-authors
- Susan Blasér (11 shared papers)B. H. Robinson (3 shared papers)John Christodoulou (3 shared papers)Joe T.R. Clarke (2 shared papers)Roumyana Petrova-Benedict (1 shared paper)Noreen L. Rudd (1 shared paper)Christina Smith (1 shared paper)Richard I. Kelley (2 shared papers)
- Journals
- Molecular Genetics and Metabolism (13 papers)Neurology (3 papers)Journal of Inherited Metabolic Disease (3 papers)Annals of Neurology (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Annette Feigenbaum
59 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 96
- Clinical Biochemistry 1.2k
- Biochemistry 200
- Molecular Biology 1.7k
- Rheumatology 247
- Neurology 134
Countries citing papers authored by Annette Feigenbaum
This map shows the geographic impact of Annette Feigenbaum'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 Annette Feigenbaum with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Annette Feigenbaum more than expected).
Fields of papers citing papers by Annette Feigenbaum
This network shows the impact of papers produced by Annette Feigenbaum. 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 Annette Feigenbaum. The network helps show where Annette Feigenbaum may publish in the future.
Co-authors
The 25 scholars most cited alongside Annette Feigenbaum, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 63 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high. | 1992 | 419 |
| 2 | 2003 | 181 | |
| 3 | 2002 | 146 | |
| 4 | 2002 | 135 | |
| 5 | 1997 | 123 | |
| 6 | 1999 | 90 | |
| 7 | 2014 | 84 | |
| 8 | 2013 | 74 | |
| 9 | 2006 | 69 | |
| 10 | 2008 | 64 | |
| 11 | 2001 | 61 | |
| 12 | 1996 | 59 | |
| 13 | 2011 | 56 | |
| 14 | 2010 | 54 | |
| 15 | 2016 | 53 | |
| 16 | 2011 | 48 | |
| 17 | 2014 | 45 | |
| 18 | 2007 | 42 | |
| 19 | 2005 | 41 | |
| 20 | 2007 | 40 |
About Annette Feigenbaum
Annette Feigenbaum is a scholar working on Clinical Biochemistry, Molecular Biology, Rheumatology, Genetics and Pediatrics, Perinatology and Child Health, having authored 63 papers that have together received 2.5k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (36 papers), Mitochondrial Function and Pathology (18 papers), Folate and B Vitamins Research (9 papers), Neonatal Health and Biochemistry (6 papers), Genomics and Rare Diseases (6 papers), ATP Synthase and ATPases Research (5 papers), RNA regulation and disease (4 papers) and Biochemical Acid Research Studies (4 papers). The work is most often cited by research in Clinical Biochemistry (1.2k citations), Biochemistry (200 citations), Molecular Biology (1.7k citations), Rheumatology (247 citations) and Neurology (134 citations). Annette Feigenbaum has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Susan Blasér, B. H. Robinson, John Christodoulou, Joe T.R. Clarke, Roumyana Petrova-Benedict, Noreen L. Rudd, Christina Smith, Richard I. Kelley, Salvatore DiMauro and Marjo S. van der Knaap. Their work appears in journals such as Molecular Genetics and Metabolism, Neurology, Journal of Inherited Metabolic Disease, Annals of Neurology and Genetics in Medicine.
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.