M. Leppert

8.0k citations
169 papers · 6.4k · 2 hit papers · h-index 40

Impact in

Papers in

    • DNA and Nucleic Acid Chemistry 48
    • DNA Repair Mechanisms 29
    • Genomics and Chromatin Dynamics 10
    • CRISPR and Genetic Engineering 7
    • Genomic variations and chromosomal abnormalities 33
    • Genomics and Rare Diseases 9
    • Neurogenetic and Muscular Disorders Research 6

M. Leppert

167 papers receiving 6.1k citations

M. Leppert's Hit Papers

Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17 1987 · 560 citations
5600+13+26Years since publication100200300400500

Peers

M. Leppert
Comparison fields: 5 of 120
  • Pathology and Forensic Medicine 1.4k
  • Genetics 606
  • Ophthalmology 456
  • Genetics 1.4k
  • Oncology 1.2k
Replace Colette Dib with:
Colette Dib France
Hans Scheffer Netherlands
Elias I. Traboulsi United States
Fowzan S. Alkuraya Saudi Arabia
Niklas Dahl Sweden
Mireille Claustres France
Junkoh Yamashita Japan
Irene H. Maumenee United States
Didier Lacombe France
Stefan Isenmann Germany
M. Leppert relative to Colette Dib France Colette Dib's profile →
Citations per field
00.5×4.0×
Colette Dib · 1×
Citations per year

Countries citing papers authored by M. Leppert

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with M. Leppert Line = papers co-authored together M. Leppert links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

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 →
1987560
2
The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5
Hit paper breakdown →
1987555
3 1993486
4 1990472
5 1998272
6 1999262
7 1993186
8
Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5.
1988165
9 1997138
10 1997130
11 1995127
12 1992119
13
Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.
1991119
14
Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region.
1994117
15
Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.
1995108
16
Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q.
199699
17 200096
18 198890
19 198785
20 198885

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 6.4k 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 (9 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 (1.4k citations), Genetics (606 citations), Ophthalmology (456 citations), Genetics (1.4k citations) and Oncology (1.2k 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, Mark Lathrop and R. White. 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.

Explore authors with similar magnitude of impact