Mark Leppert
Impact in
- Pathology and Forensic Medicine top 0.5%
- Genetic factors in colorectal cancer
- Genetics top 2%
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 51
- Genomic variations and chromosomal abnormalities 33
- Genomics and Rare Diseases 8
- Neurogenetic and Muscular Disorders Research 6
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- DNA and Nucleic Acid Chemistry 48
- DNA Repair Mechanisms 29
- Genomics and Chromatin Dynamics 10
- CRISPR and Genetic Engineering 7
- Co-authors
- Peter O'Connell (107 shared papers)Gregory Mark Lathrop (112 shared papers)Ray L. White (75 shared papers)J.-M. Lalouel (56 shared papers)Yusuke Nakamura (95 shared papers)Lisa N. Spirio (5 shared papers)Yusuke Nakamura (14 shared papers)Mary L. Carlson (21 shared papers)
- Journals
- Nucleic Acids Research (109 papers)Neurology (6 papers)The American Journal of Human Genetics (5 papers)Genomics (5 papers)Human Heredity (3 papers)
- Partner nations
- United StatesBelgiumUnited Kingdom
In The Last Decade
Mark Leppert
169 papers receiving 6.4k citations
Mark Leppert's Hit Papers
Peers
Comparison fields: 5 of 123
- Pathology and Forensic Medicine 1.5k
- Genetics 631
- Ophthalmology 477
- Genetics 1.5k
- Oncology 1.3k
Countries citing papers authored by Mark Leppert
This map shows the geographic impact of Mark Leppert'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 Leppert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark Leppert more than expected).
Fields of papers citing papers by Mark Leppert
This network shows the impact of papers produced by Mark Leppert. 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 Leppert. The network helps show where Mark Leppert may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark Leppert, 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 171 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5 Hit paper breakdown → | 1987 | 576 |
| 2 | Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17 Hit paper breakdown → | 1987 | 571 |
| 3 | Alleles of the APC gene: An attenuated form of familial polyposis Hit paper breakdown → | 1993 | 516 |
| 4 | 1990 | 487 | |
| 5 | 1998 | 280 | |
| 6 | 1999 | 270 | |
| 7 | 1993 | 196 | |
| 8 | Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5. | 1988 | 171 |
| 9 | 2012 | 165 | |
| 10 | 1997 | 145 | |
| 11 | 1997 | 131 | |
| 12 | 1995 | 126 | |
| 13 | 1992 | 125 | |
| 14 | Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus. | 1991 | 124 |
| 15 | Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q. | 1995 | 120 |
| 16 | Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region. | 1994 | 118 |
| 17 | 2000 | 103 | |
| 18 | Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q. | 1996 | 101 |
| 19 | 1991 | 95 | |
| 20 | Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11. | 1991 | 92 |
About Mark Leppert
Mark Leppert is a scholar working on Genetics, Molecular Biology, Genetics, Pathology and Forensic Medicine and Ophthalmology, having authored 171 papers that have together received 6.8k indexed citations. Recurring topics across this work include DNA and Nucleic Acid Chemistry (48 papers), Genomic variations and chromosomal abnormalities (33 papers), DNA Repair Mechanisms (29 papers), Genomics and Chromatin Dynamics (10 papers), Genomics and Rare Diseases (8 papers), Genetic factors in colorectal cancer (8 papers), CRISPR and Genetic Engineering (7 papers) and Neurogenetic and Muscular Disorders Research (6 papers). The work is most often cited by research in Pathology and Forensic Medicine (1.5k citations), Genetics (631 citations), Ophthalmology (477 citations), Genetics (1.5k citations) and Oncology (1.3k citations). Mark Leppert has collaborated with scholars based in United States, Belgium and United Kingdom. Frequent co-authors include Peter O'Connell, Gregory Mark Lathrop, Ray L. White, J.-M. Lalouel, Yusuke Nakamura, Lisa N. Spirio, Yusuke Nakamura, Mary L. Carlson, Jean-Marc Lalouel and Geoff Joslyn. Their work appears in journals such as Nucleic Acids Research, Neurology, The American Journal of Human Genetics, Genomics and Human Heredity.
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.