Kris G. Samsom

469 total citations
13 papers, 153 citations indexed

About

Kris G. Samsom is a scholar working on Cancer Research, Oncology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Kris G. Samsom has authored 13 papers receiving a total of 153 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cancer Research, 8 papers in Oncology and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Kris G. Samsom's work include Cancer Genomics and Diagnostics (10 papers), Genetic factors in colorectal cancer (4 papers) and Genomics and Rare Diseases (3 papers). Kris G. Samsom is often cited by papers focused on Cancer Genomics and Diagnostics (10 papers), Genetic factors in colorectal cancer (4 papers) and Genomics and Rare Diseases (3 papers). Kris G. Samsom collaborates with scholars based in Netherlands and Ireland. Kris G. Samsom's co-authors include Paul Roepman, Kim Monkhorst, Gerrit A. Meijer, Edwin Cuppen, Emile E. Voest, Luuk J. Schipper, Ewart de Bruijn, Jacobus J. M. van der Hoeven, Linda J.W. Bosch and Willemina R.R. Geurts-Giele and has published in prestigious journals such as Journal of Clinical Oncology, Annals of Oncology and Cancers.

In The Last Decade

Kris G. Samsom

11 papers receiving 152 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kris G. Samsom Netherlands	7	92	71	61	33	30	13	153
Alicia Latham United States	7	84 0.9×	75 1.1×	46 0.8×	112 3.4×	31 1.0×	26	209
Abirami Sivapiragasam United States	8	41 0.4×	107 1.5×	40 0.7×	23 0.7×	37 1.2×	33	178
Satoshi Okada Japan	7	75 0.8×	121 1.7×	43 0.7×	59 1.8×	78 2.6×	16	245
Joshua Kapp Switzerland	9	96 1.0×	75 1.1×	156 2.6×	24 0.7×	70 2.3×	14	269
Carlijn van de Water Netherlands	6	27 0.3×	69 1.0×	43 0.7×	19 0.6×	24 0.8×	11	144
Shiangjiin Leaw China	8	55 0.6×	166 2.3×	48 0.8×	39 1.2×	87 2.9×	13	237
Benjamin Powers United States	6	34 0.4×	118 1.7×	97 1.6×	19 0.6×	30 1.0×	15	171
Eric Q. Konnick United States	4	80 0.9×	79 1.1×	62 1.0×	65 2.0×	34 1.1×	21	162
Matthew Labriola United States	6	82 0.9×	137 1.9×	159 2.6×	15 0.5×	72 2.4×	23	238
Veronica R. Holley United States	4	67 0.7×	55 0.8×	51 0.8×	37 1.1×	45 1.5×	14	169

Countries citing papers authored by Kris G. Samsom

Since Specialization

Citations

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

Fields of papers citing papers by Kris G. Samsom

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kris G. Samsom. 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 Kris G. Samsom. The network helps show where Kris G. Samsom may publish in the future.

Co-authorship network of co-authors of Kris G. Samsom

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

All Works

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13 of 13 papers shown

Koster, Roelof, Luuk J. Schipper, Daphne M. van Beek, et al.. (2023). Impact of genetic counseling strategy on diagnostic yield and workload for genome-sequencing-based tumor diagnostics. Genetics in Medicine. 26(2). 101032–101032. 2 indexed citations

Schipper, Luuk J., Kris G. Samsom, Pétur Snæbjörnsson, et al.. (2022). Complete genomic characterization in patients with cancer of unknown primary origin in routine diagnostics. ESMO Open. 7(6). 100611–100611. 15 indexed citations

Schipper, Luuk J., Kim Monkhorst, Kris G. Samsom, et al.. (2022). Clinical Impact of Prospective Whole Genome Sequencing in Sarcoma Patients. Cancers. 14(2). 436–436. 12 indexed citations

Schipper, Luuk J., Pétur Snæbjörnsson, Kris G. Samsom, et al.. (2021). 1133P Whole genome sequencing can classify diagnostically challenging tumors. Annals of Oncology. 32. S924–S925.

Roepman, Paul, Ewart de Bruijn, Stef van Lieshout, et al.. (2021). Clinical Validation of Whole Genome Sequencing for Cancer Diagnostics. Journal of Molecular Diagnostics. 23(7). 816–833. 39 indexed citations

Radonic, Teodora, Willemina R.R. Geurts-Giele, Kris G. Samsom, et al.. (2021). RET Fluorescence In Situ Hybridization Analysis Is a Sensitive but Highly Unspecific Screening Method for RET Fusions in Lung Cancer. Journal of Thoracic Oncology. 16(5). 798–806. 25 indexed citations

Samsom, Kris G., Kim Monkhorst, Luuk J. Schipper, et al.. (2021). Feasibility of whole-genome sequencing in routine clinical practice.. Journal of Clinical Oncology. 39(15_suppl). 3013–3013. 3 indexed citations

Schipper, Luuk J., Kim Monkhorst, Kris G. Samsom, et al.. (2021). Whole-genome sequencing to improve sarcoma diagnosis and patient care.. Journal of Clinical Oncology. 39(15_suppl). 11540–11540.

Samsom, Kris G., Linda J.W. Bosch, Luuk J. Schipper, et al.. (2020). Study protocol: Whole genome sequencing Implementation in standard Diagnostics for Every cancer patient (WIDE). BMC Medical Genomics. 13(1). 169–169. 24 indexed citations

10.

Monkhorst, Kim, Kris G. Samsom, Luuk J. Schipper, et al.. (2020). 1189O Validation of whole genome sequencing in routine clinical practice. Annals of Oncology. 31. S784–S784. 5 indexed citations

11.

Samsom, Kris G., Paul Roepman, Liudmila L. Kodach, et al.. (2020). Driver mutations occur frequently in metastases of well‐differentiated small intestine neuroendocrine tumours. Histopathology. 78(4). 556–566. 13 indexed citations

12.

Roepman, Paul, L. Van den Bosch, Kris G. Samsom, et al.. (2019). WGS implementation in standard cancer diagnostics for every cancer patient (WIDE). Annals of Oncology. 30. v575–v575. 3 indexed citations

13.

Samsom, Kris G., et al.. (2019). Molecular prognostic factors in small-intestinal neuroendocrine tumours. Endocrine Connections. 8(7). 906–922. 12 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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