Eva Holmberg
Impact in
- Genetics top 2%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Neurogenetic and Muscular Disorders Research
- Diabetes and associated disorders
- Immunology top 10%
- Immunodeficiency and Autoimmune Disorders
Papers in
- Genetics 18
- Genomic variations and chromosomal abnormalities 6
- Diabetes and associated disorders 3
- BRCA gene mutations in cancer 3
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
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- Genetic factors in colorectal cancer 3
- Co-authors
- Ulf Kristoffersson (3 shared papers)Elisabeth Blennow (3 shared papers)Magnus Nordenskjöld (4 shared papers)Åke Lernmark (4 shared papers)Ingrid Skelton Kockum (4 shared papers)Ralf Waßmuth (3 shared papers)Göran Annerén (3 shared papers)Birgitte Koch Michelsen (2 shared papers)
- Journals
- Clinical Genetics (5 papers)Journal of Clinical Investigation (2 papers)Neuromuscular Disorders (2 papers)European Journal of Human Genetics (2 papers)Matrix Biology (1 paper)
- Partner nations
- SwedenUnited StatesBelgium
In The Last Decade
Eva Holmberg
35 papers receiving 2k citations
Peers
Comparison fields: 5 of 76
- Genetics 955
- Genetics 148
- Immunology 215
- Pediatrics, Perinatology and Child Health 117
- Oncology 198
Countries citing papers authored by Eva Holmberg
This map shows the geographic impact of Eva Holmberg'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 Eva Holmberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eva Holmberg more than expected).
Fields of papers citing papers by Eva Holmberg
This network shows the impact of papers produced by Eva Holmberg. 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 Eva Holmberg. The network helps show where Eva Holmberg may publish in the future.
Co-authors
The 25 scholars most cited alongside Eva Holmberg, 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 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 239 | |
| 2 | 2016 | 228 | |
| 3 | 2014 | 174 | |
| 4 | Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer. | 1997 | 152 |
| 5 | 2000 | 147 | |
| 6 | 1995 | 122 | |
| 7 | 2006 | 102 | |
| 8 | 1994 | 95 | |
| 9 | HLA-DQ primarily confers protection and HLA-DR susceptibility in type I (insulin-dependent) diabetes studied in population-based affected families and controls. | 1993 | 90 |
| 10 | 2013 | 77 | |
| 11 | 2000 | 76 | |
| 12 | 2008 | 75 | |
| 13 | 2001 | 67 | |
| 14 | New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndrome. | 1995 | 55 |
| 15 | 2008 | 50 | |
| 16 | 1988 | 49 | |
| 17 | 2009 | 44 | |
| 18 | 2010 | 35 | |
| 19 | 1995 | 33 | |
| 20 | 2018 | 28 |
About Eva Holmberg
Eva Holmberg is a scholar working on Genetics, Pathology and Forensic Medicine, Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 35 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Diabetes and associated disorders (3 papers), Genetic factors in colorectal cancer (3 papers), BRCA gene mutations in cancer (3 papers), Muscle Physiology and Disorders (3 papers), Genomics and Rare Diseases (3 papers), Hereditary Neurological Disorders (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Genetics (955 citations), Genetics (148 citations), Immunology (215 citations), Pediatrics, Perinatology and Child Health (117 citations) and Oncology (198 citations). Eva Holmberg has collaborated with scholars based in Sweden, United States and Belgium. Frequent co-authors include Ulf Kristoffersson, Elisabeth Blennow, Magnus Nordenskjöld, Åke Lernmark, Ingrid Skelton Kockum, Ralf Waßmuth, Göran Annerén, Birgitte Koch Michelsen, Geert R. Mortier and Niklas Dahl. Their work appears in journals such as Clinical Genetics, Journal of Clinical Investigation, Neuromuscular Disorders, European Journal of Human Genetics and Matrix 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.