Mark D. Ludman
Impact in
- Physiology top 5%
- Lysosomal Storage Disorders Research
- Genetics top 5%
- Connective tissue disorders research
- Genetic and Kidney Cyst Diseases
Papers in
- Genetics 16
- Genetic and Kidney Cyst Diseases 5
- Connective tissue disorders research 4
- BRCA gene mutations in cancer 3
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- Glycosylation and Glycoproteins Research 3
- Co-authors
- Christopher Naugler (2 shared papers)Andrew Orr (6 shared papers)Duane L. Guernsey (5 shared papers)Makoto Matsuoka (5 shared papers)Haiyan Jiang (5 shared papers)Mathew Nightingale (5 shared papers)Susan C. Evans (4 shared papers)Meghan Ferguson (4 shared papers)
- Journals
- Journal of Medical Genetics (2 papers)Genetics in Medicine (2 papers)Metabolism (1 paper)Pediatric Research (1 paper)Prenatal Diagnosis (1 paper)
- Partner nations
- CanadaUnited StatesIsrael
In The Last Decade
Mark D. Ludman
41 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 92
- Physiology 323
- Genetics 359
- Clinical Biochemistry 73
- Genetics 89
- Cell Biology 145
Countries citing papers authored by Mark D. Ludman
This map shows the geographic impact of Mark D. Ludman'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 Mark D. Ludman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark D. Ludman more than expected).
Fields of papers citing papers by Mark D. Ludman
This network shows the impact of papers produced by Mark D. Ludman. 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 Mark D. Ludman. The network helps show where Mark D. Ludman may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark D. Ludman, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 182 | |
| 2 | 1994 | 102 | |
| 3 | 1997 | 82 | |
| 4 | 2009 | 61 | |
| 5 | 2013 | 58 | |
| 6 | 1997 | 54 | |
| 7 | 2010 | 52 | |
| 8 | 1996 | 48 | |
| 9 | 1992 | 46 | |
| 10 | Mutations in a novel serine protease PRSS56 in families with nanophthalmos. | 2011 | 43 |
| 11 | 1985 | 42 | |
| 12 | 2015 | 34 | |
| 13 | 1989 | 32 | |
| 14 | 1996 | 28 | |
| 15 | Bone marrow transplantation in Maroteaux-Lamy syndrome (MPS type 6): status 40 months after BMT. | 1986 | 27 |
| 16 | 1993 | 26 | |
| 17 | 2009 | 26 | |
| 18 | 1993 | 23 | |
| 19 | 1995 | 19 | |
| 20 | Prevalence of breast and colorectal cancer in Ashkenazi Jewish carriers of Fanconi anemia and Bloom syndrome. | 2007 | 19 |
About Mark D. Ludman
Mark D. Ludman is a scholar working on Genetics, Molecular Biology, Physiology, Genetics and Pediatrics, Perinatology and Child Health, having authored 41 papers that have together received 1.2k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (8 papers), Genetic and Kidney Cyst Diseases (5 papers), Connective tissue disorders research (4 papers), Glycosylation and Glycoproteins Research (3 papers), Carbohydrate Chemistry and Synthesis (3 papers), Prenatal Screening and Diagnostics (3 papers), BRCA gene mutations in cancer (3 papers) and Cancer, Hypoxia, and Metabolism (3 papers). The work is most often cited by research in Physiology (323 citations), Genetics (359 citations), Clinical Biochemistry (73 citations), Genetics (89 citations) and Cell Biology (145 citations). Mark D. Ludman has collaborated with scholars based in Canada, United States and Israel. Frequent co-authors include Christopher Naugler, Andrew Orr, Duane L. Guernsey, Makoto Matsuoka, Haiyan Jiang, Mathew Nightingale, Susan C. Evans, Meghan Ferguson, Andrea L. Rideout and Tania S. Burgert. Their work appears in journals such as Journal of Medical Genetics, Genetics in Medicine, Metabolism, Pediatric Research and Prenatal Diagnosis.
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.