Eva Holmberg
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Neurogenetic and Muscular Disorders Research
- Diabetes and associated disorders
Papers in
- Genetics 18
- Genomic variations and chromosomal abnormalities 8
- Diabetes and associated disorders 3
- Neurogenetic and Muscular Disorders Research 3
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- Receptor Mechanisms and Signaling 3
- Co-authors
- Bertil Waldeck (8 shared papers)Ulf Kristoffersson (3 shared papers)Elisabeth Blennow (3 shared papers)Magnus Nordenskjöld (4 shared papers)Ingrid Kockum (4 shared papers)Åke Lernmark (4 shared papers)Göran Annerén (3 shared papers)Ralf Waßmuth (3 shared papers)
- Journals
- Clinical Genetics (4 papers)European Journal of Pediatrics (1 paper)Neuromuscular Disorders (1 paper)Prenatal Diagnosis (1 paper)Human Genetics (1 paper)
- Partner nations
- SwedenUnited StatesBelgium
In The Last Decade
Eva Holmberg
40 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 88
- Genetics 650
- Genetics 164
- Molecular Biology 614
- Oncology 224
- Animal Science and Zoology 81
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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 210 | |
| 2 | Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer. | 1997 | 142 |
| 3 | 1995 | 96 | |
| 4 | 2006 | 94 | |
| 5 | 1994 | 91 | |
| 6 | HLA-DQ primarily confers protection and HLA-DR susceptibility in type I (insulin-dependent) diabetes studied in population-based affected families and controls. | 1993 | 84 |
| 7 | 2008 | 64 | |
| 8 | 2001 | 64 | |
| 9 | 2013 | 64 | |
| 10 | New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndrome. | 1995 | 57 |
| 11 | 1980 | 55 | |
| 12 | 2008 | 46 | |
| 13 | 1988 | 44 | |
| 14 | 2009 | 40 | |
| 15 | 1977 | 32 | |
| 16 | 1995 | 30 | |
| 17 | 2010 | 29 | |
| 18 | 1998 | 23 | |
| 19 | 1980 | 23 | |
| 20 | 2004 | 23 |
About Eva Holmberg
Eva Holmberg is a scholar working on Genetics, Molecular Biology, Animal Science and Zoology, Physiology and Surgery, having authored 41 papers that have together received 1.5k indexed citations. Recurring topics across this work include Pharmacological Effects and Assays (8 papers), Genomic variations and chromosomal abnormalities (8 papers), Diabetes and associated disorders (3 papers), Receptor Mechanisms and Signaling (3 papers), Pain Mechanisms and Treatments (3 papers), Neurogenetic and Muscular Disorders Research (3 papers), Prenatal Screening and Diagnostics (3 papers) and Cancer Genomics and Diagnostics (3 papers). The work is most often cited by research in Genetics (650 citations), Genetics (164 citations), Molecular Biology (614 citations), Oncology (224 citations) and Animal Science and Zoology (81 citations). Eva Holmberg has collaborated with scholars based in Sweden, United States and Belgium. Frequent co-authors include Bertil Waldeck, Ulf Kristoffersson, Elisabeth Blennow, Magnus Nordenskjöld, Ingrid Kockum, Åke Lernmark, Göran Annerén, Ralf Waßmuth, B Michelsen and Niklas Dahl. Their work appears in journals such as Clinical Genetics, European Journal of Pediatrics, Neuromuscular Disorders, Prenatal Diagnosis and Human 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.