Mark Leppert
Impact in
- Developmental Neuroscience top 0.5%
- Williams Syndrome Research
-
- Cardiac electrophysiology and arrhythmias
Papers in
-
- Ion channel regulation and function 5
- RNA and protein synthesis mechanisms 5
- Genetics 24
- Genomic variations and chromosomal abnormalities 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetics and Neurodevelopmental Disorders 6
- Co-authors
- Mark Keating (3 shared papers)G. Michael Vincent (2 shared papers)Katherine W. Timothy (2 shared papers)Donald L. Atkinson (2 shared papers)Mark T. Keating (1 shared paper)Patricia Spallone (1 shared paper)Keith L. Sternes (1 shared paper)Colleen A. Morris (1 shared paper)
- Journals
- Human Genetics (5 papers)Nature Genetics (4 papers)Journal of Proteome Research (3 papers)Nucleic Acids Research (3 papers)Genomics (3 papers)
- Partner nations
- United StatesCanadaPoland
In The Last Decade
Mark Leppert
63 papers receiving 5.7k citations
Mark Leppert's Hit Papers
Peers
Comparison fields: 5 of 135
- Developmental Neuroscience 683
- Cardiology and Cardiovascular Medicine 1.4k
- Genetics 1.7k
- Cellular and Molecular Neuroscience 1.0k
- Molecular Biology 3.1k
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 63 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns Hit paper breakdown → | 1998 | 939 |
| 2 | Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome Hit paper breakdown → | 1993 | 809 |
| 3 | 1992 | 471 | |
| 4 | 2003 | 411 | |
| 5 | 1991 | 391 | |
| 6 | 1985 | 259 | |
| 7 | Precise localization of NF1 to 17q11.2 by balanced translocation. | 1989 | 172 |
| 8 | Heritability of X chromosome--inactivation phenotype in a large family. | 1996 | 148 |
| 9 | 1994 | 134 | |
| 10 | 1993 | 131 | |
| 11 | Cytogenetic and molecular analysis of sex-chromosome monosomy. | 1988 | 121 |
| 12 | 2003 | 112 | |
| 13 | 1995 | 110 | |
| 14 | 1977 | 107 | |
| 15 | 1993 | 106 | |
| 16 | 1987 | 106 | |
| 17 | 1999 | 94 | |
| 18 | 2016 | 94 | |
| 19 | 1996 | 88 | |
| 20 | 2005 | 72 |
About Mark Leppert
Mark Leppert is a scholar working on Molecular Biology, Genetics, Cardiology and Cardiovascular Medicine, Plant Science and Pediatrics, Perinatology and Child Health, having authored 63 papers that have together received 5.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Cardiac electrophysiology and arrhythmias (5 papers), Prenatal Screening and Diagnostics (5 papers), Chromosomal and Genetic Variations (5 papers), Ion channel regulation and function (5 papers) and RNA and protein synthesis mechanisms (5 papers). The work is most often cited by research in Developmental Neuroscience (683 citations), Cardiology and Cardiovascular Medicine (1.4k citations), Genetics (1.7k citations), Cellular and Molecular Neuroscience (1.0k citations) and Molecular Biology (3.1k citations). Mark Leppert has collaborated with scholars based in United States, Canada and Poland. Frequent co-authors include Mark Keating, G. Michael Vincent, Katherine W. Timothy, Donald L. Atkinson, Mark T. Keating, Patricia Spallone, Keith L. Sternes, Colleen A. Morris, A.D. Stock and Andy Peiffer. Their work appears in journals such as Human Genetics, Nature Genetics, Journal of Proteome Research, Nucleic Acids 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.