Merry Passage
Impact in
- Physiology top 2%
- Lysosomal Storage Disorders Research
- Rheumatology top 5%
- Glycogen Storage Diseases and Myoclonus
Papers in
- Physiology 16
- Lysosomal Storage Disorders Research 16
- Co-authors
- Emil Kakkis (9 shared papers)Patricia Dickson (15 shared papers)Larry J. Shapiro (8 shared papers)P. H. Yen (6 shared papers)Michael F. McEntee (6 shared papers)Steven Q. Le (9 shared papers)Stephen R. Hanson (4 shared papers)Carole Vogler (4 shared papers)
- Journals
- Molecular Genetics and Metabolism (8 papers)Human Genetics (2 papers)Biochemical Journal (2 papers)Apmis (1 paper)Proceedings of the National Academy of Sciences (1 paper)
- Partner nations
- United StatesFinlandTaiwan
In The Last Decade
Merry Passage
33 papers receiving 1.4k citations
Merry Passage's Hit Papers
Peers
Comparison fields: 5 of 71
- Physiology 959
- Rheumatology 235
- Physiology 62
- Genetics 356
- Epidemiology 339
Countries citing papers authored by Merry Passage
This map shows the geographic impact of Merry Passage'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 Merry Passage with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Merry Passage more than expected).
Fields of papers citing papers by Merry Passage
This network shows the impact of papers produced by Merry Passage. 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 Merry Passage. The network helps show where Merry Passage may publish in the future.
Co-authors
The 25 scholars most cited alongside Merry Passage, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Enzyme-Replacement Therapy in Mucopolysaccharidosis I Hit paper breakdown → | 2001 | 526 |
| 2 | 2007 | 141 | |
| 3 | 2004 | 135 | |
| 4 | Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 Robertsonian translocation carrier. | 1991 | 125 |
| 5 | 2008 | 90 | |
| 6 | Role of the pseudoautosomal region in sex-chromosome pairing during male meiosis: meiotic studies in a man with a deletion of distal Xp. | 1992 | 90 |
| 7 | 2004 | 53 | |
| 8 | 2010 | 48 | |
| 9 | 1992 | 30 | |
| 10 | 2015 | 30 | |
| 11 | 2012 | 24 | |
| 12 | 1989 | 21 | |
| 13 | 2011 | 18 | |
| 14 | 2005 | 17 | |
| 15 | 1985 | 15 | |
| 16 | 2011 | 13 | |
| 17 | 1992 | 9 | |
| 18 | 1994 | 9 | |
| 19 | Steroid sulfatase gene in XX males. | 1990 | 9 |
| 20 | 1998 | 8 |
About Merry Passage
Merry Passage is a scholar working on Physiology, Molecular Biology, Genetics, Rheumatology and Pediatrics, Perinatology and Child Health, having authored 33 papers that have together received 1.5k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (16 papers), Glycogen Storage Diseases and Myoclonus (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Animal Genetics and Reproduction (4 papers), Chromosomal and Genetic Variations (4 papers), Spinal Dysraphism and Malformations (3 papers), Biomedical Research and Pathophysiology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Physiology (959 citations), Rheumatology (235 citations), Physiology (62 citations), Genetics (356 citations) and Epidemiology (339 citations). Merry Passage has collaborated with scholars based in United States, Finland and Taiwan. Frequent co-authors include Emil Kakkis, Patricia Dickson, Larry J. Shapiro, P. H. Yen, Michael F. McEntee, Steven Q. Le, Stephen R. Hanson, Carole Vogler, T. Mohandas and Robin Winkler Doroshow. Their work appears in journals such as Molecular Genetics and Metabolism, Human Genetics, Biochemical Journal, Apmis and Proceedings of the National Academy of Sciences.
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.