Marie Stenmark Askmalm

642 total citations
14 papers, 366 citations indexed

About

Marie Stenmark Askmalm is a scholar working on Cancer Research, Oncology and Genetics. According to data from OpenAlex, Marie Stenmark Askmalm has authored 14 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cancer Research, 7 papers in Oncology and 6 papers in Genetics. Recurrent topics in Marie Stenmark Askmalm's work include Cancer Genomics and Diagnostics (6 papers), BRCA gene mutations in cancer (5 papers) and Genetic factors in colorectal cancer (5 papers). Marie Stenmark Askmalm is often cited by papers focused on Cancer Genomics and Diagnostics (6 papers), BRCA gene mutations in cancer (5 papers) and Genetic factors in colorectal cancer (5 papers). Marie Stenmark Askmalm collaborates with scholars based in Sweden, Russia and Norway. Marie Stenmark Askmalm's co-authors include Lambert Skoog, Karin Söderlund, Bo Nordenskjöld, Olle Stål, Lars Erik Rutqvist, Tommy� Fornander, Emma Tham, Magnus Tengvar, Joakim Crona and Andreas Muth and has published in prestigious journals such as SHILAP Revista de lepidopterología, Cancer Research and Annals of Surgery.

In The Last Decade

Marie Stenmark Askmalm

14 papers receiving 356 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Marie Stenmark Askmalm Sweden	11	148	141	136	108	91	14	366
Mauricio Camus Chile	13	143 1.0×	187 1.3×	79 0.6×	211 2.0×	169 1.9×	49	487
Shulamit Rizel Israel	11	129 0.9×	113 0.8×	96 0.7×	91 0.8×	127 1.4×	24	408
Silvia Pecchio Italy	8	143 1.0×	105 0.7×	49 0.4×	58 0.5×	67 0.7×	13	306
Jane P. Hasselby Denmark	8	88 0.6×	79 0.6×	86 0.6×	83 0.8×	58 0.6×	12	271
C. Brumm Germany	7	155 1.0×	86 0.6×	52 0.4×	105 1.0×	98 1.1×	19	332
Luca Giuseppe Sgrò Italy	11	145 1.0×	152 1.1×	55 0.4×	71 0.7×	105 1.2×	31	447
Robyn Sayer United States	10	79 0.5×	87 0.6×	128 0.9×	143 1.3×	21 0.2×	17	404
W. Bradford Carter United States	8	130 0.9×	169 1.2×	90 0.7×	60 0.6×	21 0.2×	10	318
Gloria Peiró Spain	9	164 1.1×	128 0.9×	47 0.3×	78 0.7×	25 0.3×	12	347
Chan Seok Yoon South Korea	9	170 1.1×	200 1.4×	77 0.6×	48 0.4×	47 0.5×	19	377

Countries citing papers authored by Marie Stenmark Askmalm

Since Specialization

Citations

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

Fields of papers citing papers by Marie Stenmark Askmalm

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marie Stenmark Askmalm. 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 Marie Stenmark Askmalm. The network helps show where Marie Stenmark Askmalm may publish in the future.

Co-authorship network of co-authors of Marie Stenmark Askmalm

This figure shows the co-authorship network connecting the top 25 collaborators of Marie Stenmark Askmalm. A scholar is included among the top collaborators of Marie Stenmark Askmalm 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 Marie Stenmark Askmalm. Marie Stenmark Askmalm is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Zagoras, Theofanis, Marie Stenmark Askmalm, Erik Björck, et al.. (2022). Merged testing for colorectal cancer syndromes and re‐evaluation of genetic variants improve diagnostic yield: Results from a nationwide prospective cohort. Genes Chromosomes and Cancer. 61(10). 585–591. 2 indexed citations

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

Muth, Andreas, Joakim Crona, Oliver Gimm, et al.. (2018). Genetic testing and surveillance guidelines in hereditary pheochromocytoma and paraganglioma. Journal of Internal Medicine. 285(2). 187–204. 79 indexed citations

Soller, Maria, Marie Stenmark Askmalm, Theofanis Zagoras, et al.. (2015). The gynecological surveillance of women with Lynch syndrome in Sweden. Gynecologic Oncology. 138(3). 717–722. 19 indexed citations

Ignatova, Simone, et al.. (2015). A NovelSMAD4Mutation Causing Severe Juvenile Polyposis Syndrome with Protein Losing Enteropathy, Immunodeficiency, and Hereditary Haemorrhagic Telangiectasia. SHILAP Revista de lepidopterología. 2015. 1–5. 15 indexed citations

Fornander, Tommy�, et al.. (2014). The RAD51 135G>C polymorphism is related to the effect of adjuvant therapy in early breast cancer. Journal of Cancer Research and Clinical Oncology. 141(5). 797–804. 7 indexed citations

Arver, Brita, Karin Isaksson, Leif Bergkvist, et al.. (2011). Bilateral Prophylactic Mastectomy in Swedish Women at High Risk of Breast Cancer. Annals of Surgery. 253(6). 1147–1154. 51 indexed citations

Lampic, Claudia, et al.. (2011). What Information Do Cancer Genetic Counselees Prioritize?. Journal of Genetic Counseling. 21(4). 510–526. 14 indexed citations

Isaksson, Karolin, Brita Arver, Yvonne Brandberg, et al.. (2010). Abstract P6-10-03: Bilateral Prophylactic Mastectomy in Swedish Women at High Risk of Breast Cancer — A National Survey. Cancer Research. 70(24_Supplement). P6–10. 1 indexed citations

10.

Söderlund, Karin, Lambert Skoog, Tommy� Fornander, & Marie Stenmark Askmalm. (2007). The BRCA1/BRCA2/Rad51 complex is a prognostic and predictive factor in early breast cancer. Radiotherapy and Oncology. 84(3). 242–251. 47 indexed citations

11.

Söderlund, Karin, Olle Stål, Lambert Skoog, et al.. (2007). Intact Mre11/Rad50/Nbs1 Complex Predicts Good Response to Radiotherapy in Early Breast Cancer. International Journal of Radiation Oncology*Biology*Physics. 68(1). 50–58. 53 indexed citations

12.

Wegman, Pia, Olle Stål, Marie Stenmark Askmalm, et al.. (2006). p53 polymorphic variants at codon 72 and the outcome of therapy in randomized breast cancer patients. Pharmacogenetics and Genomics. 16(5). 347–351. 21 indexed citations

13.

Askmalm, Marie Stenmark, John Carstensen, Bo Nordenskjöld, et al.. (2004). Mutation and accumulation of p53 related to results of adjuvant therapy of postmenopausal breast cancer patients. Acta Oncologica. 43(3). 235–244. 15 indexed citations

14.

Stål, Olle, Marie Stenmark Askmalm, Sten Wingren, et al.. (1995). P53 Expression and the Result of Adjuvant Therapy of Breast Cancer. Acta Oncologica. 34(6). 767–770. 32 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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