Mark S. Lechner

2.4k citations
21 papers · 2.0k indexed · h-index 15
Topics
Genomics and Chromatin Dynamics (7 papers)Renal and related cancers (5 papers)Chromosomal and Genetic Variations (3 papers)

In The Last Decade

Mark S. Lechner

20 papers receiving 1.9k citations

Peers

Mark S. Lechner
Comparison fields: 5 of 91
  • Molecular Biology 1.5k
  • Genetics 403
  • Oncology 305
  • Epidemiology 250
  • Plant Science 182
Replace Mark Leonard with:
Mark Leonard United States
Ignacio Moreno de Alborán Spain
Anne E. Griep United States
Tilman Borggrefe Germany
Stuart H. Johnston United States
Sarah De Clercq Belgium
Cordelia Langford United Kingdom
Silvia Fré France
Hans Teunissen Netherlands
Fong‐Ying Tsai United States
Mark S. Lechner relative to Mark Leonard United States Mark Leonard's profile →
Citations per field
00.5×4.8×
Mark Leonard · 1×
Citations per year

Countries citing papers authored by Mark S. Lechner

Since Specialization
Citations

This map shows the geographic impact of Mark S. Lechner'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 S. Lechner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark S. Lechner more than expected).

Fields of papers citing papers by Mark S. Lechner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark S. Lechner. 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 S. Lechner. The network helps show where Mark S. Lechner may publish in the future.

Co-authorship network of co-authors of Mark S. Lechner

This figure shows the co-authorship network connecting the top 25 collaborators of Mark S. Lechner. A scholar is included among the top collaborators of Mark S. Lechner 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 Mark S. Lechner. Mark S. Lechner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 0
2 21
3 21
4
Insights Into Cornelia de Lange Syndrome From the Nipbl-Mutant Mouse
3
5 190
6 28
7 168
8 11
9 297
10 72
11 176
12 65
13 3
14 52
15 157
16 56
17 199
18 174
19 234
20 14

About Mark S. Lechner

Mark S. Lechner is a scholar working on Aging, Molecular Biology and Sensory Systems, having authored 21 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (7 papers), Renal and related cancers (5 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Molecular Biology (1.5k citations), Genetics (403 citations) and Aging (25 citations). Mark S. Lechner has collaborated with scholars based in United States, Canada and Austria. Frequent co-authors include Gregory R. Dressler, Laimonis A. Laimins, Frank J. Rauscher, D. Schultz, Gerd G. Maul, David W. Speicher, Gillian E. Begg, J.E. Dixon, Quinn Vega and Carolyn A. Worby. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

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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