Lars E. Beckman

8.8k citations
192 papers · 6.2k · 2 hit papers · h-index 30

Impact in

  • Genetics top 0.5%
    • Forensic and Genetic Research
    • Genetic Associations and Epidemiology
    • BRCA gene mutations in cancer
  • Neurology top 5%
    • Amyotrophic Lateral Sclerosis Research

Papers in

Lars E. Beckman

179 papers receiving 5.8k citations

Lars E. Beckman's Hit Papers

Large-scale genotyping identifies 41 new loci associated with breast cancer risk 2013 · 913 citations
9130+7+15Years since publication250500750

Peers

Lars E. Beckman
Comparison fields: 5 of 114
  • Genetics 2.1k
  • Neurology 367
  • Cancer Research 252
  • Environmental Chemistry 143
  • Endocrinology, Diabetes and Metabolism 239
Replace Gunhild Beckman with:
Gunhild Beckman Sweden
Mitchell J. Machiela United States
Athena Matakidou United Kingdom
Marina V. Bibikova United States
M. Stephen Meyn Canada
Sandra Andersson Sweden
Gudrun E. Moore United Kingdom
Kristinn Pétur Magnússon Iceland
Gary Walters United States
Lars E. Beckman relative to Gunhild Beckman Sweden Gunhild Beckman's profile →
Citations per field
00.5×2×4×6×8×9.4×
Gunhild Beckman · 1×
Citations per year

Countries citing papers authored by Lars E. Beckman

Since Specialization
Citations

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

Fields of papers citing papers by Lars E. Beckman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lars E. Beckman. 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 Lars E. Beckman. The network helps show where Lars E. Beckman may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 192 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Hit paper breakdown →
2013913
2
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death
Hit paper breakdown →
2003743
3 2000625
4 2000505
5 1994311
6 2004245
7 2004189
8 1996178
9 2003140
10 1991124
11 196469
12 200163
13 199960
14 200358
15 196354
16 198653
17 196452
18 199850
19 197747
20 199647

About Lars E. Beckman

Lars E. Beckman is a scholar working on Endocrinology, Diabetes and Metabolism, Hematology, Cancer Research, Genetics and Rheumatology, having authored 192 papers that have together received 6.2k indexed citations. Recurring topics across this work include Alkaline Phosphatase Research Studies (23 papers), Carcinogens and Genotoxicity Assessment (14 papers), Forensic and Genetic Research (14 papers), Iron Metabolism and Disorders (9 papers), Rheumatoid Arthritis Research and Therapies (7 papers), Blood groups and transfusion (7 papers), Complement system in diseases (4 papers) and Glutathione Transferases and Polymorphisms (3 papers). The work is most often cited by research in Genetics (2.1k citations), Neurology (367 citations), Cancer Research (252 citations), Environmental Chemistry (143 citations) and Endocrinology, Diabetes and Metabolism (239 citations). Lars E. Beckman has collaborated with scholars based in Sweden, United States and Estonia. Frequent co-authors include Gunhild Beckman, Ingrid Nordenson, Richard Birgander, Stefan Nordström, Nirmalya Saha, Frank M. Johnson, Giuseppe Passarino, Dragan Primorac, Svetlana Arbuzova and Svetlana Limborska. Their work appears in journals such as Human Heredity, Hereditas, Nature, Clinical Genetics and The Lancet.

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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