M. Leppert

8.0k total citations · 2 hit papers
169 papers, 6.1k citations indexed

About

M. Leppert is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, M. Leppert has authored 169 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 86 papers in Molecular Biology, 50 papers in Genetics and 9 papers in Pathology and Forensic Medicine. Recurrent topics in M. Leppert's work include DNA and Nucleic Acid Chemistry (48 papers), Genomic variations and chromosomal abnormalities (33 papers) and DNA Repair Mechanisms (29 papers). M. Leppert is often cited by papers focused on DNA and Nucleic Acid Chemistry (48 papers), Genomic variations and chromosomal abnormalities (33 papers) and DNA Repair Mechanisms (29 papers). M. Leppert collaborates with scholars based in United States, Belgium and Canada. M. Leppert's 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 and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

M. Leppert

169 papers receiving 5.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17

1987 520 citations Yusuke Nakamura, P. O’Connell et al. profile →
The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5

1987 502 citations M. Leppert, P. O’Connell et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
M. Leppert United States	40	2.8k	1.4k	1.4k	1.3k	658	169	6.1k
Elias I. Traboulsi United States	45	3.8k 1.3×	954 0.7×	2.1k 1.5×	433 0.3×	563 0.9×	289	7.5k
Colette Dib France	11	3.1k 1.1×	749 0.5×	2.5k 1.8×	572 0.4×	409 0.6×	23	6.0k
Lauren A. Langford United States	34	2.9k 1.0×	766 0.5×	258 0.2×	867 0.7×	524 0.8×	70	5.4k
A. Westerveld Netherlands	44	4.3k 1.5×	297 0.2×	1.4k 1.0×	575 0.4×	245 0.4×	153	6.1k
Irene H. Maumenee United States	47	3.4k 1.2×	544 0.4×	1.9k 1.4×	365 0.3×	408 0.6×	143	6.3k
Martijn H. Breuning Netherlands	50	6.2k 2.2×	1.4k 1.0×	5.9k 4.3×	791 0.6×	735 1.1×	160	11.0k
Mireille Claustres France	46	4.3k 1.5×	255 0.2×	1.8k 1.3×	354 0.3×	427 0.6×	221	8.2k
Margaret Robertson United States	29	2.2k 0.8×	1.6k 1.1×	567 0.4×	1.4k 1.1×	383 0.6×	46	5.7k
David Viskochil United States	48	2.6k 0.9×	893 0.6×	1.2k 0.9×	617 0.5×	810 1.2×	159	8.6k
Vijaya Ramesh United States	48	2.7k 0.9×	440 0.3×	716 0.5×	773 0.6×	339 0.5×	113	6.6k

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-authorship network of co-authors of M. Leppert

This figure shows the co-authorship network connecting the top 25 collaborators of M. Leppert. A scholar is included among the top collaborators of M. Leppert based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M. Leppert. M. Leppert is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Jurynec, Michael J., Allen D. Sawitzke, Timothy C. Beals, et al.. (2018). A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis. Osteoarthritis and Cartilage. 26. S159–S159. 1 indexed citations

Zimprich, Fritz, Gabriel M. Ronen, Christian Baumgärtner, et al.. (2006). Andreas Rett and benign familial neonatal convulsions revisited. Neurology. 67(5). 864–866. 23 indexed citations

Hall, Margaret A., Paul J. Norman, Bonnie Thiel, et al.. (2002). Quantitative-Trait Loci on Chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 Control Variation in Levels of T and B Lymphocyte Subpopulations. The American Journal of Human Genetics. 70(5). 1172–1182. 37 indexed citations

Bejjani, Bassem A., Richard A. Lewis, Karim F. Tomey, et al.. (1998). Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi Arabia. The American Journal of Human Genetics. 62(2). 325–333. 255 indexed citations

Leppert, M., et al.. (1997). Gastric adenocarcinoma and dysplasia in fundic gland polyps of a patient with attenuated adenomatous polyposis coli. Gastroenterology. 113(2). 659–663. 125 indexed citations

Curran, Michael A., Donald L. Atkinson, K Timothy, et al.. (1993). Locus heterogeneity of autosomal dominant long QT syndrome.. Journal of Clinical Investigation. 92(2). 799–803. 51 indexed citations

Odelberg, Shannon J., R. Plaetke, L. Ballard, et al.. (1989). Characterization of eight VNTR loci by agarose gel electrophoresis. Genomics. 5(4). 915–924. 73 indexed citations

Nakamura, Yusuke, Melanie Culver, M. Leppert, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p [D1S57]. Nucleic Acids Research. 16(10). 4747–4747. 30 indexed citations

Nakamura, Yusuke, Melanie Culver, P. O’Connell, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pYNZ15) on chromosome 2 [D2S50]. Nucleic Acids Research. 16(12). 5702–5702. 1 indexed citations

10.

Hoff, M., Yusuke Nakamura, T. Holm, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pHHH208) on chromosome 14 [D14S19]. Nucleic Acids Research. 16(21). 10400–10400. 2 indexed citations

11.

Fujimoto, E., Yusuke Nakamura, P. O’Connell, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pEFD70.3) on chromosome 18 [D18S23]. Nucleic Acids Research. 16(10). 4748–4748. 2 indexed citations

12.

Fujimoto, E., Yusuke Nakamura, L. Ballard, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pEFD49.2) on chromosome 15 [Dl5S38]. Nucleic Acids Research. 16(22). 10943–10943. 3 indexed citations

13.

Nakamura, Yusuke, Mark Lathrop, M. Leppert, et al.. (1988). Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5.. PubMed. 43(5). 638–44. 155 indexed citations

14.

Nakamura, Yusuke, E. Fujimoto, Cindy M. Martin, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence pEFD33.2 on chromosome 12 [D12S14]. Nucleic Acids Research. 16(2). 778–778. 13 indexed citations

15.

Martin, Cindy M., Yusuke Nakamura, L. Ballard, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pCMM62) on chromosome 14 [D14S21]. Nucleic Acids Research. 16(11). 5220–5220. 3 indexed citations

16.

Nakamura, Yusuke, K. Krapcho, P. O’Connell, et al.. (1987). Isolation and mapping of a polymorphic DNA sequence pEKZlOS on chromosome 2 (D2S55). Nucleic Acids Research. 15(23). 10076–10076. 3 indexed citations

17.

Carlson, M., Yusuke Nakamura, K. Krapcho, et al.. (1987). Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S10). Nucleic Acids Research. 15(24). 10613–10613. 7 indexed citations

18.

Nakamura, Yusuke, P. O’Connell, M. Leppert, et al.. (1987). Isolation and mapping of a polymorphic DNA sequence pEKZ130 on chromosome 9 (D9S9). Nucleic Acids Research. 15(24). 10611–10611. 1 indexed citations

19.

Nakamura, Yusuke, P. O’Connell, M. Leppert, et al.. (1987). Isolation and mapping of a polymorphic DNA sequence pTBABS.7 on chromosome 2 (D2S47). Nucleic Acids Research. 15(23). 10072–10072. 1 indexed citations

20.

Leppert, M., Webster K. Cavenee, T. Holm, et al.. (1986). A primary genetic map of chromosome 13q.. PubMed. 39(4). 425–37. 63 indexed citations

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.

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