Peter vanTuinen

3.1k citations
25 papers · 2.5k indexed · 1 hit paper · h-index 14

Peter vanTuinen

25 papers receiving 2.4k citations

Hit Papers

Chromosome 17 Deletions and p53 Gene Mutations in Colorec...1.7k198920262001201350010001.5k

Peers

Peter vanTuinen
Comparison fields: 5 of 87
  • Oncology 1.3k
  • Cancer Research 584
  • Pathology and Forensic Medicine 602
  • Biotechnology 242
  • Molecular Biology 1.1k
Replace Simon J. Leedham with:
Simon J. Leedham United Kingdom
Dahmane Oukrif United Kingdom
Torben F. Ørntoft Denmark
Kenji Hibi Japan
A L Børresen Norway
Yasushi Kasai Japan
Jim Heighway United Kingdom
Kurt Grünewald Austria
M Terada Japan
Camilla Pilati France
Peter vanTuinen relative to Simon J. Leedham United Kingdom Simon J. Leedham's profile →
Citations per field
00.5×4.2×
Simon J. Leedham · 1×
Citations per year

Countries citing papers authored by Peter vanTuinen

Since Specialization
Citations

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

Fields of papers citing papers by Peter vanTuinen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1
Mosaic Trisomy 9p in a Patient with Mild Dysmorphic Features and Normal Intelligence.
20171
2 20162
3 20161
4 20164
5 20157
6 2012144
7 20114
8 20098
9 200313
10 199645
11
Chromosome 17 Deletions and p53 Gene Mutations in Colorectal Carcinomasbreakdown →
19891664
12 1988162
13
Mapping of human methylmalonyl CoA mutase (MUT) on chromosome 6
19882
14
Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome.
198881
15 198851
16 19879
17 19872
18 198744
19
Molecular cloning and characterization of a cDNA for human granulocyte colony-stimulating factor (G-CSF) from a glioblastoma multiforme cell line and localization of the G-CSF gene to chromosome band 17q21.
198731
20 198627

About Peter vanTuinen

Peter vanTuinen is a scholar working on Clinical Biochemistry, Hematology, Genetics, Immunology and Pathology and Forensic Medicine, having authored 25 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Metabolism and Genetic Disorders (3 papers), Genomics and Chromatin Dynamics (3 papers), Immunodeficiency and Autoimmune Disorders (3 papers), Lymphoma Diagnosis and Treatment (3 papers), Multiple Myeloma Research and Treatments (2 papers), RNA Interference and Gene Delivery (2 papers) and Biochemical and Molecular Research (2 papers). The work is most often cited by research in Oncology (1.3k citations), Cancer Research (584 citations), Pathology and Forensic Medicine (602 citations), Biotechnology (242 citations) and Molecular Biology (1.1k citations). Peter vanTuinen has collaborated with scholars based in United States, Australia and Mexico. Frequent co-authors include David H. Ledbetter, Yusuke Nakamura, David F. Barker, Stanley R. Hamilton, R. White, Bert Vogelstein, J. Milburn Jessup, Eric R. Fearon, Suzanne J. Baker and Janice Nigro. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research, Genomics, Journal of Virology and Biochemical and Biophysical Research Communications.

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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