Annika Lindblom

49.7k citations
194 papers · 8.3k indexed · 1 hit paper · h-index 47
    • Genetic factors in colorectal cancer 110
    • Cancer Genomics and Diagnostics 53
  • Oncology top 0.5%
    • Colorectal Cancer Screening and Detection 53
    • Colorectal Cancer Treatments and Studies 23
  • Genetics top 0.5%
    • BRCA gene mutations in cancer 47
    • Genomic variations and chromosomal abnormalities 20
    • Digestive system and related health 14
    • DNA Repair Mechanisms 20

Annika Lindblom

185 papers receiving 8.0k citations

Hit Papers

Mutation in the DNA mismatch repair gene homologue hMLH 1...1.6k199420262004201550010001.5k

Peers

Annika Lindblom
Comparison fields: 5 of 145
  • Pathology and Forensic Medicine 4.9k
  • Cancer Research 2.6k
  • Oncology 3.9k
  • Genetics 1.9k
  • Molecular Biology 2.8k
Replace David Malkin with:
David Malkin Canada
Alisa M. Goldstein United States
Wendell G. Yarbrough United States
Georgia Chenevix‐Trench Australia
Brenda L. Gallie Canada
Ilan R. Kirsch United States
Thierry Jo Molina France
Marshall E. Kadin United States
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Citations per field
00.5×3.7×
David Malkin · 1×
Citations per year

Countries citing papers authored by Annika Lindblom

Since Specialization
Citations

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

Fields of papers citing papers by Annika Lindblom

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 20251
2 20250
3 20251
4 20241
5 20240
6 20232
7 20234
8 20225
9 20212
10 201810
11 201538
12 200530
13 200416
14 200110
15 19997
16 199941
17
A study of the PTEN/MMAC1 gene in 136 breast cancer families.
199835
18 199715
19
Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families.
199590
20
Predisposition for breast cancer in carriers of constitutional translocation 11q;22q.
199440

About Annika Lindblom

Annika Lindblom is a scholar working on Pathology and Forensic Medicine, Cancer Research and Oncology, having authored 194 papers that have together received 8.3k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (110 papers), Cancer Genomics and Diagnostics (53 papers), Colorectal Cancer Screening and Detection (53 papers), BRCA gene mutations in cancer (47 papers), Colorectal Cancer Treatments and Studies (23 papers), DNA Repair Mechanisms (20 papers), Genomic variations and chromosomal abnormalities (20 papers) and Digestive system and related health (14 papers). The work is most often cited by research in Pathology and Forensic Medicine (4.9k citations), Cancer Research (2.6k citations) and Oncology (3.9k citations). Annika Lindblom has collaborated with scholars based in Sweden, United States and United Kingdom. Frequent co-authors include Pia Tannergård, Magnus Nordenskjöld, Barbro Werelius, Carlos Rubio-Terrés, Richard D. Kolodner, J. Russell Lipford, Magnus Nordenskj�ld, Christian Bronner, David C. Ward and Michael Kane. Their work appears in journals such as Familial Cancer, International Journal of Cancer, Endoscopy, Genes Chromosomes and Cancer and British Journal of Cancer.

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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