Irma Kluijt

4.4k total citations · 1 hit paper
42 papers, 2.4k citations indexed

About

Irma Kluijt is a scholar working on Oncology, Genetics and Molecular Biology. According to data from OpenAlex, Irma Kluijt has authored 42 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Oncology, 15 papers in Genetics and 11 papers in Molecular Biology. Recurrent topics in Irma Kluijt's work include Pancreatic and Hepatic Oncology Research (12 papers), BRCA gene mutations in cancer (10 papers) and Genetic factors in colorectal cancer (10 papers). Irma Kluijt is often cited by papers focused on Pancreatic and Hepatic Oncology Research (12 papers), BRCA gene mutations in cancer (10 papers) and Genetic factors in colorectal cancer (10 papers). Irma Kluijt collaborates with scholars based in Netherlands, United States and United Kingdom. Irma Kluijt's co-authors include Paul Fockens, Marco J. Bruno, Femme Harinck, Yung Nio, Eveline M. A. Bleiker, Claudio Bassi, G. Johan A. Offerhaus, Marcia Irene Canto, Amitabh Chak and Jan–Werner Poley and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Clinical Oncology and Gastroenterology.

In The Last Decade

Irma Kluijt

41 papers receiving 2.3k 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.

International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer

2012 525 citations Marcia Irene Canto, Femme Harinck et al. Gut profile →

Peers

Irma Kluijt

ONCOL

GENET

PFM

Olivier Caron France

Ronald P. Zweemer Netherlands

Melyssa Aronson Canada

Fabíola Medeiros United States

Sonja C. Henzen‐Logmans Netherlands

J. Kærn Norway

Satoru Sagae Japan

Victoria A. Murday United Kingdom

Marion Gauthier‐Villars France

Michael C. Luce United States

Olivier Caron France

Irma Kluijt

842 ×0.7

ONCOL

721 ×1.0

GENET

1.0k ×1.6

657 ×1.1

746 ×1.3

PFM

Citations per year, relative to Irma Kluijt Irma Kluijt (= 1×) peers Olivier Caron

Countries citing papers authored by Irma Kluijt

Since Specialization

Citations

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

Fields of papers citing papers by Irma Kluijt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irma Kluijt

This figure shows the co-authorship network connecting the top 25 collaborators of Irma Kluijt. A scholar is included among the top collaborators of Irma Kluijt 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 Irma Kluijt. Irma Kluijt 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

Stoep, Nienke van der, Irma Kluijt, Cora M. Aalfs, et al.. (2015). High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations. Familial Cancer. 14(2). 247–257. 14 indexed citations

Aaronson, Neil K., et al.. (2014). The efficacy of a standardized questionnaire in facilitating personalized communication about problems encountered in cancer genetic counseling: design of a randomized controlled trial. BMC Cancer. 14(1). 26–26. 6 indexed citations

Mathijssen, Inge B., Frank Baas, Johanna I. de Vries, et al.. (2014). Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence. European Journal of Human Genetics. 23(9). 1151–1157. 29 indexed citations

Harinck, Femme, Irma Kluijt, Nienke van der Stoep, et al.. (2012). Indication for CDKN2A-mutation analysis in familial pancreatic cancer families without melanomas. Journal of Medical Genetics. 49(6). 362–365. 29 indexed citations

Kluijt, Irma, Rolf H. Sijmons, Nicoline Hoogerbrugge, et al.. (2012). Familial gastric cancer: guidelines for diagnosis, treatment and periodic surveillance. Familial Cancer. 11(3). 363–369. 57 indexed citations

Canto, Marcia Irene, Femme Harinck, Ralph H. Hruban, et al.. (2012). International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer. Gut. 62(3). 339–347. 525 indexed citations breakdown →

Harinck, Femme, Irma Kluijt, Cora M. Aalfs, et al.. (2011). Feasibility of a pancreatic cancer surveillance program from a psychological point of view. Genetics in Medicine. 13(12). 1015–1024. 32 indexed citations

Kluijt, Irma, Ester Siemerink, Margreet G.E.M. Ausems, et al.. (2011). CDH1‐related hereditary diffuse gastric cancer syndrome: Clinical variations and implications for counseling. International Journal of Cancer. 131(2). 367–376. 90 indexed citations

Harinck, Femme, Irma Kluijt, Saskia E. van Mil, et al.. (2011). Routine testing for PALB2 mutations in familial pancreatic cancer families and breast cancer families with pancreatic cancer is not indicated. European Journal of Human Genetics. 20(5). 577–579. 28 indexed citations

10.

Adank, Muriel A., Marianne A. Jonker, Irma Kluijt, et al.. (2011). CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women. Journal of Medical Genetics. 48(12). 860–863. 53 indexed citations

11.

Riel, E. van, Margreet G.E.M. Ausems, Frans B.L. Hogervorst, et al.. (2010). A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome. Hereditary Cancer in Clinical Practice. 8(1). 7–7. 16 indexed citations

12.

Manders, Peggy, Anouk Pijpe, Maartje J. Hooning, et al.. (2010). Body weight and risk of breast cancer in BRCA1/2 mutation carriers. Breast Cancer Research and Treatment. 126(1). 193–202. 43 indexed citations

13.

Kluijt, Irma, et al.. (2010). Hereditary causes of kidney tumours. European Journal of Clinical Investigation. 40(5). 433–439. 23 indexed citations

14.

Kluijt, Irma, Annemieke Cats, Paul Fockens, et al.. (2009). Atypical Familial Presentation of FAMMM Syndrome With a High Incidence of Pancreatic Cancer. Journal of Clinical Gastroenterology. 43(9). 853–857. 21 indexed citations

15.

Kluijt, Irma, Daphne de Jong, Gilles Thomas, et al.. (2009). Early onset of renal cancer in a family with Birt–Hogg–Dubé syndrome. Clinical Genetics. 75(6). 537–543. 24 indexed citations

16.

Harinck, Femme, Irma Kluijt, Jan‐Werner Poley, et al.. (2009). 965 Comparative Yield of Endosonography and Magnetic Resonance Imaging in Individuals At High-Risk for Pancreatic Cancer. Gastroenterology. 136(5). A–147. 2 indexed citations

17.

Bleiker, Eveline M. A., Fred H. Menko, Irma Kluijt, et al.. (2007). Colorectal Cancer in the Family: Psychosocial Distress and Social Issues in the Years Following Genetic Counselling. Hereditary Cancer in Clinical Practice. 5(2). 59–59. 25 indexed citations

18.

Bleiker, Eveline M. A., Fred H. Menko, Babs G. Taal, et al.. (2005). Screening behavior of individuals at high risk for colorectal cancer. Gastroenterology. 128(2). 280–287. 89 indexed citations

19.

Steensel, Maurice A. M. Van, Frances J.D. Smith, Peter M. Steijlen, et al.. (1999). The Gene for Hypotrichosis of Marie Unna Maps between D8S258 and D8S298: Exclusion of the hr Gene by cDNA and Genomic Sequencing. The American Journal of Human Genetics. 65(2). 413–419. 37 indexed citations

20.

Kluijt, Irma, et al.. (1995). Ophthalmologic abnormalities in encephalocraniocutaneous lipomatosis. Documenta Ophthalmologica. 90(1). 87–98. 26 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.

Explore authors with similar magnitude of impact