Mark Leppert
Impact in
- Developmental Neuroscience top 0.5%
- Williams Syndrome Research
- Genetics top 0.5%
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 24
- Genomic variations and chromosomal abnormalities 9
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetics and Neurodevelopmental Disorders 6
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- RNA and protein synthesis mechanisms 5
- Ion channel regulation and function 4
- Co-authors
- Mark E. Keating (3 shared papers)Katherine W. Timothy (2 shared papers)G. Michael Vincent (2 shared papers)Donald L. Atkinson (2 shared papers)Patricia Spallone (1 shared paper)A. DEAN STOCK (1 shared paper)Colleen A. Morris (1 shared paper)Mark T. Keating (1 shared paper)
- Journals
- Human Genetics (5 papers)Nature Genetics (4 papers)Nucleic Acids Research (3 papers)Journal of Proteome Research (3 papers)Genomics (3 papers)
- Partner nations
- United StatesPolandCanada
In The Last Decade
Mark Leppert
67 papers receiving 11.5k citations
Mark Leppert's Hit Papers
Peers
Comparison fields: 5 of 170
- Developmental Neuroscience 729
- Genetics 4.2k
- Molecular Biology 5.3k
- Cardiology and Cardiovascular Medicine 1.6k
- Cellular and Molecular Neuroscience 1.1k
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 67 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The International HapMap Project Hit paper breakdown → | 2003 | 4921 |
| 2 | A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns Hit paper breakdown → | 1998 | 1031 |
| 3 | Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome Hit paper breakdown → | 1993 | 903 |
| 4 | Localization of an ataxia-telangiectasia gene to chromosome 11q22–23 Hit paper breakdown → | 1988 | 579 |
| 5 | The Spectrum of Symptoms and QT Intervals in Carriers of the Gene for the Long-QT Syndrome Hit paper breakdown → | 1992 | 530 |
| 6 | 2003 | 445 | |
| 7 | 1991 | 433 | |
| 8 | 1985 | 281 | |
| 9 | Precise localization of NF1 to 17q11.2 by balanced translocation. | 1989 | 181 |
| 10 | 1994 | 155 | |
| 11 | Heritability of X chromosome--inactivation phenotype in a large family. | 1996 | 152 |
| 12 | 1993 | 144 | |
| 13 | Cytogenetic and molecular analysis of sex-chromosome monosomy. | 1988 | 135 |
| 14 | 1995 | 128 | |
| 15 | 2003 | 123 | |
| 16 | 1977 | 115 | |
| 17 | 2016 | 112 | |
| 18 | 1993 | 110 | |
| 19 | 1987 | 106 | |
| 20 | 1999 | 100 |
About Mark Leppert
Mark Leppert is a scholar working on Genetics, Molecular Biology, Cardiology and Cardiovascular Medicine, Pediatrics, Perinatology and Child Health and Immunology, having authored 67 papers that have together received 12.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), RNA and protein synthesis mechanisms (5 papers), Prenatal Screening and Diagnostics (5 papers), Cardiac electrophysiology and arrhythmias (5 papers), Chromosomal and Genetic Variations (5 papers) and Ion channel regulation and function (4 papers). The work is most often cited by research in Developmental Neuroscience (729 citations), Genetics (4.2k citations), Molecular Biology (5.3k citations), Cardiology and Cardiovascular Medicine (1.6k citations) and Cellular and Molecular Neuroscience (1.1k citations). Mark Leppert has collaborated with scholars based in United States, Poland and Canada. Frequent co-authors include Mark E. Keating, Katherine W. Timothy, G. Michael Vincent, Donald L. Atkinson, Patricia Spallone, A. DEAN STOCK, Colleen A. Morris, Mark T. Keating, Keith L. Sternes and Andy P. Peiffer. Their work appears in journals such as Human Genetics, Nature Genetics, Nucleic Acids Research, Journal of Proteome Research and Genomics.
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.