Lea Lahnstein

49 papers receiving 1.4k citations

Lea Lahnstein's Hit Papers

Substitution mutational signatures in whole-genome–sequenced cancers in the UK population 2022 · 190 citations
1900+1+2Years since publication50100150

Peers

Lea Lahnstein
Comparison fields: 5 of 91
  • Cancer Research 254
  • Genetics 337
  • Molecular Biology 699
  • Pathology and Forensic Medicine 164
  • Genetics 87
Replace Matthew J. Welland with:
Matthew J. Welland United Kingdom
Chris A. Odhams United Kingdom
John C. Ambrose United Kingdom
Ivonne U. S. Leong United Kingdom
Alexa Kidd New Zealand
Nilah M. Ioannidis United States
Ana Lisa Taylor Tavares United Kingdom
François-Olivier Desmet France
Jean‐Pierre Desvignes France
Tadbir K. Bariana United Kingdom
Lea Lahnstein relative to Matthew J. Welland United Kingdom Matthew J. Welland's profile →
Citations per field
00.5×1.5×
Matthew J. Welland · 1×
Citations per year

Countries citing papers authored by Lea Lahnstein

Since Specialization
Citations

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

Fields of papers citing papers by Lea Lahnstein

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 17 scholars most cited alongside Lea Lahnstein, 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 Lea Lahnstein Line = papers co-authored together Lea Lahnstein links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Substitution mutational signatures in whole-genome–sequenced cancers in the UK population
Hit paper breakdown →
2022190
2 2021105
3 202081
4 202066
5 202252
6 202150
7 202348
8 202247
9 202247
10 202142
11 202342
12 202038
13 202037
14 202036
15 202236
16 202234
17 202331
18 202230
19 202228
20 202227

About Lea Lahnstein

Lea Lahnstein is a scholar working on Genetics, Cancer Research, Cellular and Molecular Neuroscience, Molecular Biology and Genetics, having authored 50 papers that have together received 1.5k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (6 papers), Genomics and Rare Diseases (6 papers), Genetic Neurodegenerative Diseases (5 papers), Mitochondrial Function and Pathology (4 papers), RNA modifications and cancer (4 papers), Genetic factors in colorectal cancer (3 papers), RNA Research and Splicing (3 papers) and RNA and protein synthesis mechanisms (3 papers). The work is most often cited by research in Cancer Research (254 citations), Genetics (337 citations), Molecular Biology (699 citations), Pathology and Forensic Medicine (164 citations) and Genetics (87 citations). Lea Lahnstein has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Fiona Maleady-Crowe, Philippa Clare Matthews, Ghanasyam Rallapalli, Jean Lutamyo Mbisa, Effy Vayena, Gkikas Magiorkinis, Tom Fowler, Peter Simmonds, Colin S. Cooper and Richard S. Tedder. Their work appears in journals such as Genetics in Medicine, Brain, Scientific Reports, Nature Communications and Nature Genetics.

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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