Lars E. Beckman
Impact in
- Genetics top 1%
- Forensic and Genetic Research
- Genetic diversity and population structure
- Race, Genetics, and Society
- Genetic Associations and Epidemiology
- BRCA gene mutations in cancer
- Cancer Research top 5%
Papers in
-
- Alkaline Phosphatase Research Studies 25
- Genetics 30
- Genetic and phenotypic traits in livestock 7
- Co-authors
- Gunhild Beckman (61 shared papers)Ingrid Nordenson (24 shared papers)Richard Birgander (2 shared papers)Björn Tavelin (7 shared papers)Stefan Nordström (9 shared papers)Camilla Thellenberg Karlsson (7 shared papers)Nirmalya Saha (1 shared paper)Anders Widmark (7 shared papers)
- Journals
- Human Heredity (75 papers)Hereditas (36 papers)Nature (8 papers)Clinical Genetics (6 papers)The Lancet (5 papers)
- Partner nations
- SwedenUnited StatesEstonia
In The Last Decade
Lars E. Beckman
195 papers receiving 6.7k citations
Lars E. Beckman's Hit Papers
Peers
Comparison fields: 5 of 172
- Genetics 2.4k
- Cancer Research 688
- Archeology 438
- Genetics 336
- Oncology 768
Countries citing papers authored by Lars E. Beckman
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
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.
All Works
Showing the 20 most-cited of 210 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 → | 2013 | 908 |
| 2 | VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death Hit paper breakdown → | 2003 | 743 |
| 3 | Ultra-hypofractionated versus conventionally fractionated radiotherapy for prostate cancer: 5-year outcomes of the HYPO-RT-PC randomised, non-inferiority, phase 3 trial Hit paper breakdown → | 2019 | 655 |
| 4 | The Genetic Legacy of Paleolithic Homo sapiens sapiens in Extant Europeans: A Y Chromosome Perspective Hit paper breakdown → | 2000 | 627 |
| 5 | 2000 | 512 | |
| 6 | 1994 | 315 | |
| 7 | 2004 | 245 | |
| 8 | 2004 | 190 | |
| 9 | 1996 | 178 | |
| 10 | 2003 | 142 | |
| 11 | 1991 | 124 | |
| 12 | 2021 | 108 | |
| 13 | 1964 | 71 | |
| 14 | 2001 | 63 | |
| 15 | 1999 | 61 | |
| 16 | 2003 | 58 | |
| 17 | 1963 | 55 | |
| 18 | 1986 | 54 | |
| 19 | 1964 | 53 | |
| 20 | 1998 | 51 |
About Lars E. Beckman
Lars E. Beckman is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics, Hematology, Cancer Research and Rheumatology, having authored 210 papers that have together received 7.2k indexed citations. Recurring topics across this work include Alkaline Phosphatase Research Studies (25 papers), Carcinogens and Genotoxicity Assessment (11 papers), Parathyroid Disorders and Treatments (9 papers), Blood groups and transfusion (8 papers), Folate and B Vitamins Research (8 papers), Prostate Cancer Diagnosis and Treatment (8 papers), Genetic and phenotypic traits in livestock (7 papers) and Hemoglobin structure and function (7 papers). The work is most often cited by research in Genetics (2.4k citations), Cancer Research (688 citations), Archeology (438 citations), Genetics (336 citations) and Oncology (768 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, Björn Tavelin, Stefan Nordström, Camilla Thellenberg Karlsson, Nirmalya Saha, Anders Widmark, Frank M. Johnson and Jon Kindblom. 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.