Boris Lenhard

41.5k citations
132 papers · 12.7k indexed · 6 hit papers · h-index 52
    • Genomics and Chromatin Dynamics 67
    • RNA Research and Splicing 32
    • RNA modifications and cancer 31
    • RNA and protein synthesis mechanisms 28
    • Genomics and Phylogenetic Studies 26
    • Epigenetics and DNA Methylation 19
    • Cancer-related molecular mechanisms research 12
  • Genetics top 0.5%
  • Aging top 2%
  • Immunology top 2%
    • Chromosomal and Genetic Variations 17

Boris Lenhard

129 papers receiving 12.6k citations

Hit Papers

JASPAR 2024...33420072026201320194008001.2k

Peers

Boris Lenhard
Comparison fields: 5 of 159
  • Molecular Biology 10.4k
  • Cancer Research 1.7k
  • Genetics 2.2k
  • Aging 118
  • Immunology 969
Replace Simon Andrews with:
Simon Andrews United Kingdom
Albin Sandelin Denmark
Kelly A. Frazer United States
Wouter de Laat Netherlands
David S. Johnson United States
Martha L. Bulyk United States
Sumio Sugano Japan
Laurie A. Boyer United States
Krishna M. Roskin United States
Gang Wei China
Boris Lenhard relative to Simon Andrews United Kingdom Simon Andrews's profile →
Citations per field
00.5×1.5×
Simon Andrews · 1×
Citations per year

Countries citing papers authored by Boris Lenhard

Since Specialization
Citations

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

Fields of papers citing papers by Boris Lenhard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Boris Lenhard. 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 Boris Lenhard. The network helps show where Boris Lenhard may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Boris Lenhard, 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 Boris Lenhard Line = papers co-authored together Boris Lenhard links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20254
2 20241
3 20241
4
JASPAR 2024: 20th anniversary of the open-access database of transcription factor binding profilesbreakdown →
2023334
5 202023
6 202059
7 202029
8 20188
9 2018181
10 201814
11 2014142
12 201373
13 201381
14 201249
15 201148
16
The genome-wide dynamics of the binding of Ldb1 complexes during erythroid differentiation (Genes & Development (2010) 24, (277-289))
201025
17 200975
18 2007388
19 2006127
20 200442

About Boris Lenhard

Boris Lenhard is a scholar working on Molecular Biology, Cancer Research and Genetics, having authored 132 papers that have together received 12.7k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (67 papers), RNA Research and Splicing (32 papers), RNA modifications and cancer (31 papers), RNA and protein synthesis mechanisms (28 papers), Genomics and Phylogenetic Studies (26 papers), Epigenetics and DNA Methylation (19 papers), Chromosomal and Genetic Variations (17 papers) and Cancer-related molecular mechanisms research (12 papers). The work is most often cited by research in Molecular Biology (10.4k citations), Cancer Research (1.7k citations) and Genetics (2.2k citations). Boris Lenhard has collaborated with scholars based in United Kingdom, Norway and United States. Frequent co-authors include Albin Sandelin, Wyeth W. Wasserman, Ge Tan, Piero Carninci, François Parcy, Anthony Mathelier, David J. Arenillas, Oriol Fornés, Pär G. Engström and Damir Baranas̆ić. Their work appears in journals such as Nucleic Acids Research, Genome Research, Nature Communications, BMC Genomics and Genome biology.

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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