Annika Lindblom

49.7k total citations · 1 hit paper
194 papers, 8.3k citations indexed

About

Annika Lindblom is a scholar working on Pathology and Forensic Medicine, Genetics and Oncology. According to data from OpenAlex, Annika Lindblom has authored 194 papers receiving a total of 8.3k indexed citations (citations by other indexed papers that have themselves been cited), including 112 papers in Pathology and Forensic Medicine, 82 papers in Genetics and 81 papers in Oncology. Recurrent topics in Annika Lindblom's work include Genetic factors in colorectal cancer (110 papers), Cancer Genomics and Diagnostics (53 papers) and Colorectal Cancer Screening and Detection (53 papers). Annika Lindblom is often cited by papers focused on Genetic factors in colorectal cancer (110 papers), Cancer Genomics and Diagnostics (53 papers) and Colorectal Cancer Screening and Detection (53 papers). Annika Lindblom collaborates with scholars based in Sweden, United States and United Kingdom. Annika Lindblom's 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 and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Annika Lindblom

185 papers receiving 8.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer

1994 1.6k citations J. Russell Lipford, Annika Lindblom et al. profile →

Peers

Annika Lindblom

PFM

ONCOL

GENET

Georgia Chenevix‐Trench Australia

Nathan A. Ellis United States

Bertil Johansson Sweden

Elizabeth M. Swisher United States

Sverre Heim Norway

Michael D. Walsh Australia

Brigitte Schlegelberger Germany

David Malkin Canada

Ilan R. Kirsch United States

Sharon E. Plon United States

Georgia Chenevix‐Trench Australia

Annika Lindblom

1.7k ×0.3

PFM

2.2k ×0.6

ONCOL

5.2k ×1.8

1.8k ×0.7

3.3k ×1.7

GENET

Citations per year, relative to Annika Lindblom Annika Lindblom (= 1×) peers Georgia Chenevix‐Trench

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 of co-authors of Annika Lindblom

This figure shows the co-authorship network connecting the top 25 collaborators of Annika Lindblom. A scholar is included among the top collaborators of Annika Lindblom based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Annika Lindblom. Annika Lindblom is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Møller, Pål, Aysel Ahadova, Matthias Kloor, et al.. (2025). Colorectal carcinogenesis in the Lynch syndromes and familial adenomatous polyposis: trigger events and downstream consequences. Hereditary Cancer in Clinical Practice. 23(1). 3–3. 1 indexed citations

Liu, Wen, Xue Min Wang, Hafdís T. Helgadóttir, et al.. (2025). A Swedish genome-wide haplotype association analysis identifies novel candidate loci associated with endometrial cancer risk. PLoS ONE. 20(3). e0316086–e0316086.

Prizment, Anna E., Conghui Qu, Shuo Wang, et al.. (2025). Functional variants in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are associated with increased risk of colorectal cancer. Human Molecular Genetics. 34(7). 617–625. 1 indexed citations

Wolk, Alicja, et al.. (2024). A GWAS Suggesting Genetic Modifiers to Increase the Risk of Colorectal Cancer from Antibiotic Use. Cancers. 17(1). 12–12. 1 indexed citations

Liu, Wen, et al.. (2024). Swedish Genome-Wide Haplotype Association Analysis Suggests Breast Cancer Loci with Varying Risk-Modifying Effects. Genes. 15(12). 1616–1616.

Ghazi, Sam, et al.. (2023). The prognostic significance of microsatellite instability in colorectal cancer: a Swedish multi-center study. International Journal of Colorectal Disease. 38(1). 197–197. 2 indexed citations

Liu, Wen, Patrick Bryant, Jessada Thutkawkorapin, et al.. (2023). A Swedish Familial Genome-Wide Haplotype Analysis Identified Five Novel Breast Cancer Susceptibility Loci on 9p24.3, 11q22.3, 15q11.2, 16q24.1 and Xq21.31. International Journal of Molecular Sciences. 24(5). 4468–4468. 4 indexed citations

Liu, Wen, Hafdís T. Helgadóttir, Kyriaki Michailidou, et al.. (2022). A Swedish Genome-Wide Haplotype Association Analysis Identifies a Novel Breast Cancer Susceptibility Locus in 8p21.2 and Characterizes Three Loci on Chromosomes 10, 11 and 16. Cancers. 14(5). 1206–1206. 5 indexed citations

Helgadóttir, Hafdís T., Jessada Thutkawkorapin, Anna Rohlin, et al.. (2021). Identification of known and novel familial cancer genes in Swedish colorectal cancer families. International Journal of Cancer. 149(3). 627–634. 2 indexed citations

10.

Karimi, Masoud, Jenny von Salomé, Gustav Silander, et al.. (2018). A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families. Hereditary Cancer in Clinical Practice. 16(1). 16–16. 10 indexed citations

11.

Bruun, Jarle, Matthias Kolberg, Terje Ahlquist, et al.. (2015). Regulator of Chromosome Condensation 2 Identifies High-Risk Patients within Both Major Phenotypes of Colorectal Cancer. Clinical Cancer Research. 21(16). 3759–3770. 38 indexed citations

12.

Djureinovic, Tatjana, et al.. (2005). Germline Mutations in the MYH Gene in Swedish Familial and Sporadic Colorectal Cancer. Genetic Testing. 9(2). 147–151. 30 indexed citations

13.

Margolin, Sara, Barbro Werelius, Tommy� Fornander, & Annika Lindblom. (2004). BRCA1 Mutations in a Population-based Study of Breast Cancer in Stockholm County. Genetic Testing. 8(2). 127–132. 16 indexed citations

14.

Arver, Brita, Åke Borg, & Annika Lindblom. (2001). First BRCA1 and BRCA2 Gene Testing Implemented in the Health Care System of Stockholm. Genetic Testing. 5(1). 1–8. 10 indexed citations

15.

Langerød, Anita, et al.. (1999). BRCAl Screening in Patients with a Family History of Breast or Ovarian Cancer. Genetic Testing. 3(2). 223–226. 7 indexed citations

16.

Wahlberg, Siobhan, Tao Liu, Per Henrik Lindblom, & Annika Lindblom. (1999). Various Mutation Screening Techniques in the DNA Mismatch Repair Genes hMSH2 and hMLH1. Genetic Testing. 3(3). 259–264. 41 indexed citations

17.

Chen, Jinxin, Per Henrik Lindblom, & Annika Lindblom. (1998). A study of the PTEN/MMAC1 gene in 136 breast cancer families.. PubMed. 102(1). 124–5. 35 indexed citations

18.

Zelada-Hedman, M, et al.. (1997). Screening for TP53 mutations in patients and tumours from 109 Swedish breast cancer families. British Journal of Cancer. 75(8). 1201–1204. 15 indexed citations

19.

Tannergård, Pia, J. Russell Lipford, Richard D. Kolodner, et al.. (1995). Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families.. PubMed. 55(24). 6092–6. 90 indexed citations

20.

Lindblom, Annika, Kerstin Sandelin, Lennart Iselius, et al.. (1994). Predisposition for breast cancer in carriers of constitutional translocation 11q;22q.. PubMed. 54(5). 871–6. 40 indexed citations

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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