M. Leppert
Impact in
- Pathology and Forensic Medicine top 0.5%
- Genetic factors in colorectal cancer
- Ophthalmology top 1%
Papers in
-
- DNA and Nucleic Acid Chemistry 48
- DNA Repair Mechanisms 29
- Genomics and Chromatin Dynamics 10
- CRISPR and Genetic Engineering 7
- Genetics 50
- Genomic variations and chromosomal abnormalities 33
- Genomics and Rare Diseases 9
- Neurogenetic and Muscular Disorders Research 6
- Co-authors
- P. O’Connell (108 shared papers)R. White (75 shared papers)J.-M. Lalouel (57 shared papers)G.M. Lathrop (107 shared papers)Yusuke Nakamura (95 shared papers)Lisa Spirio (5 shared papers)Yusuke Nakamura (14 shared papers)M. 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 StatesBelgiumCanada
In The Last Decade
M. Leppert
169 papers receiving 5.9k citations
M. Leppert's Hit Papers
Peers
Comparison fields: 5 of 115
- Pathology and Forensic Medicine 1.4k
- Ophthalmology 561
- Genetics 602
- Genetics 1.4k
- Oncology 1.3k
Countries citing papers authored by M. Leppert
This map shows the geographic impact of M. 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 M. Leppert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Leppert more than expected).
Fields of papers citing papers by M. Leppert
This network shows the impact of papers produced by M. 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 M. Leppert. The network helps show where M. Leppert may publish in the future.
Co-authors
The 25 scholars most cited alongside M. 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 169 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17 Hit paper breakdown → | 1987 | 520 |
| 2 | The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5 Hit paper breakdown → | 1987 | 502 |
| 3 | 1993 | 456 | |
| 4 | 1990 | 449 | |
| 5 | 1998 | 255 | |
| 6 | 1999 | 250 | |
| 7 | 1993 | 161 | |
| 8 | Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5. | 1988 | 155 |
| 9 | 1997 | 125 | |
| 10 | 1997 | 122 | |
| 11 | 1992 | 118 | |
| 12 | 1995 | 117 | |
| 13 | Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region. | 1994 | 114 |
| 14 | Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus. | 1991 | 111 |
| 15 | Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q. | 1995 | 102 |
| 16 | 1988 | 90 | |
| 17 | 2000 | 84 | |
| 18 | Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q. | 1996 | 83 |
| 19 | 1991 | 82 | |
| 20 | 1988 | 81 |
About M. Leppert
M. Leppert is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Cardiology and Cardiovascular Medicine and Genetics, having authored 169 papers that have together received 6.1k 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), Genetic factors in colorectal cancer (9 papers), Genomics and Rare Diseases (9 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 (1.4k citations), Ophthalmology (561 citations), Genetics (602 citations), Genetics (1.4k citations) and Oncology (1.3k citations). M. Leppert has collaborated with scholars based in United States, Belgium and Canada. Frequent co-authors include P. O’Connell, R. White, J.-M. Lalouel, G.M. Lathrop, Yusuke Nakamura, Lisa Spirio, Yusuke Nakamura, M. Carlson, R. White and Mark Lathrop. 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.