Robin Lachmann
Impact in
- Physiology top 0.2%
- Lysosomal Storage Disorders Research
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Papers in
- Physiology 83
- Lysosomal Storage Disorders Research 76
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- Metabolism and Genetic Disorders 31
- Co-authors
- Elaine Murphy (34 shared papers)Frances M. Platt (11 shared papers)Derralynn A. Hughes (19 shared papers)Timothy Martin Cox (11 shared papers)Stacey Efstathiou (11 shared papers)Raymond Allen Dwek (5 shared papers)Terry D. Butters (5 shared papers)Carla E. M. Hollak (11 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (26 papers)Molecular Genetics and Metabolism (14 papers)Orphanet Journal of Rare Diseases (12 papers)Journal of General Virology (3 papers)The Lancet (3 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Robin Lachmann
164 papers receiving 8.7k citations
Robin Lachmann's Hit Papers
Peers
Comparison fields: 5 of 126
- Physiology 4.1k
- Clinical Biochemistry 931
- Nephrology 678
- Cell Biology 1.2k
- Rheumatology 867
Countries citing papers authored by Robin Lachmann
This map shows the geographic impact of Robin Lachmann'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 Robin Lachmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robin Lachmann more than expected).
Fields of papers citing papers by Robin Lachmann
This network shows the impact of papers produced by Robin Lachmann. 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 Robin Lachmann. The network helps show where Robin Lachmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Robin Lachmann, 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 172 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mipomersen, an apolipoprotein B synthesis inhibitor, for lowering of LDL cholesterol concentrations in patients with homozygous familial hypercholesterolaemia: a randomised, double-blind, placebo-controlled trial Hit paper breakdown → | 2010 | 779 |
| 2 | 2000 | 634 | |
| 3 | Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease Hit paper breakdown → | 2009 | 591 |
| 4 | Identification and Assessment of Anderson-Fabry Disease by Cardiovascular Magnetic Resonance Noncontrast Myocardial T1 Mapping Hit paper breakdown → | 2013 | 408 |
| 5 | 2016 | 305 | |
| 6 | 2015 | 294 | |
| 7 | 2012 | 285 | |
| 8 | 2018 | 279 | |
| 9 | 2004 | 206 | |
| 10 | 2015 | 196 | |
| 11 | 2014 | 159 | |
| 12 | 2004 | 132 | |
| 13 | 2016 | 132 | |
| 14 | 2019 | 132 | |
| 15 | 2017 | 131 | |
| 16 | 2004 | 127 | |
| 17 | 2018 | 124 | |
| 18 | 2011 | 116 | |
| 19 | 2018 | 113 | |
| 20 | 2012 | 104 |
About Robin Lachmann
Robin Lachmann is a scholar working on Physiology, Clinical Biochemistry, Rheumatology, Epidemiology and Molecular Biology, having authored 172 papers that have together received 9.0k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (76 papers), Metabolism and Genetic Disorders (31 papers), Glycogen Storage Diseases and Myoclonus (15 papers), Mitochondrial Function and Pathology (14 papers), Trypanosoma species research and implications (14 papers), Herpesvirus Infections and Treatments (11 papers), Cellular transport and secretion (10 papers) and Carbohydrate Chemistry and Synthesis (10 papers). The work is most often cited by research in Physiology (4.1k citations), Clinical Biochemistry (931 citations), Nephrology (678 citations), Cell Biology (1.2k citations) and Rheumatology (867 citations). Robin Lachmann has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Elaine Murphy, Frances M. Platt, Derralynn A. Hughes, Timothy Martin Cox, Stacey Efstathiou, Raymond Allen Dwek, Terry D. Butters, Carla E. M. Hollak, Atul B Mehta and Perry Mark Elliott. Their work appears in journals such as Journal of Inherited Metabolic Disease, Molecular Genetics and Metabolism, Orphanet Journal of Rare Diseases, Journal of General Virology and The Lancet.
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.