Peter de Knijff

23.5k citations

198 papers · 11.1k indexed · h-index 58

Impact in

Genetics top 0.1%
- Forensic and Genetic Research
- Genetic diversity and population structure
- Genetic Associations and Epidemiology
- Race, Genetics, and Society
Endocrinology, Diabetes and Metabolism top 0.5%
- Diabetes, Cardiovascular Risks, and Lipoproteins

Papers in

Genetics 105
- Forensic and Genetic Research 64
- Genetic diversity and population structure 38
- Genetic Associations and Epidemiology 31
- Race, Genetics, and Society 20
Endocrinology, Diabetes and Metabolism 26
- Diabetes, Cardiovascular Risks, and Lipoproteins 22

Co-authors: Manfred Kayser Louis M. Havekes Kristiaan J. van der Gaag Cornelia M. van Duijn Lutz Roewer Christine Van Broeckhoven John J.P. Kastelein Sofia B. Zuniga
Journals: Forensic Science International Genetics (21 papers)European Journal of Human Genetics (10 papers)Forensic Science International (9 papers)The American Journal of Human Genetics (8 papers)Human Mutation (7 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Peter de Knijff

195 papers receiving 10.7k citations

Peers

Countries citing papers authored by Peter de Knijff

Since Specialization

Citations

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

Fields of papers citing papers by Peter de Knijff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Survival in Patients with Uveal Melanoma Is Linked to Genetic Variation at HERC2 Single Nucleotide Polymorphism rs12913832 Ophthalmology ·Maria Chiara Gelmi, Peninah J Limo, Annemijn P. A. Wierenga, Robert Henzel, Bastiaan T. Heijmans, Gregorius P. M. Luyten, Peter de Knijff, K. M. Wu, Rick H. de Leeuw, Martine J. Jager	2024	0
2	Mitochondrial Transport from Mesenchymal Stromal Cells to Chondrocytes Increases DNA Content and Proteoglycan Deposition In Vitro in 3D Cultures Cartilage ·Jasmijn V. Korpershoek, Kyoko Totake, Edwin Chavarria Lindo, Clarence W. Hopkins, K. M. Wu, Peter de Knijff, Daniël B.F. Saris, Luciënne A. Vonk	2022	19
3	Large-scale pedigree analysis highlights rapidly mutating Y-chromosomal short tandem repeats for differentiating patrilineal relatives and predicting their degrees of consanguinity Human Genetics ·Arwin Ralf, Diego Montiel González, Salazar Martinez, Andrew J. Ryan, Ting Cheng Chang, Peter de Knijff, Atif Adnan, Mazurov V.I. Mazurov, Mohsen Ghanbari, Maarten Larmuseau, Manfred Kayser	2022	10
4	DNA metabarcoding quantifies the relative biomass of arthropod taxa in songbird diets: Validation with camera‐recorded diets Ecology and Evolution ·Yvonne I. Verkuil, Marion Nicolaus, Richard Ubels, Maurine W. Dietz, Jelmer M. Samplonius, Lan Hua Zhou, Z.T. Li, Peter de Knijff, Christiaan Both	2022	34
5	On the Forensic Use of Y-Chromosome Polymorphisms Genes ·Peter de Knijff	2022	14
6	The Dutch Y-chromosomal landscape European Journal of Human Genetics ·Eveline Altena, Gurvich Se, Kristiaan J. van der Gaag, Maarten Larmuseau, Ronny Decorte, Óscar Lao, Manfred Kayser, Thirsa Kraaijenbrink, Peter de Knijff	2019	8
7	From next generation sequencing to now generation sequencing in forensics Forensic Science International Genetics ·Peter de Knijff	2018	53
8	Short hypervariable microhaplotypes: A novel set of very short high discriminating power loci without stutter artefacts Forensic Science International Genetics ·Kristiaan J. van der Gaag, Rick H. de Leeuw, Jeroen F. J. Laros, Johan T. den Dunnen, Peter de Knijff	2018	35
9	A SNP panel for identification of DNA and RNA specimens BMC Genomics ·Soheil Yousefi, Tooba Abbassi‐Daloii, Thirsa Kraaijenbrink, Martijn Vermaat, Hailiang Mei, Peter van ‘t Hof, Maarten van Iterson, Daria V. Zhernakova, Annique Claringbould, Lude Franke, Leen M. ‘t Hart, Roderick C. Slieker, Amber van der Heijden, Peter de Knijff, Peter A.C. ’t Hoen	2018	36
10	Effect of APOE ε4 allele on survival and fertility in an adverse environment PLoS ONE ·Eric van Exel, Jacob J.E. Koopman, David van Bodegom, Elisa Camps, Peter de Knijff, Juventus B. Ziem, Caleb E. Finch, Rudi G. J. Westendorp	2017	56
11	Fusion Transcripts without Corresponding Cytogenetic Abnormalities in Acute Myeloid Leukemia: Implications for AML Pathogenesis Blood ·Е.В. Овчарова, Wibowo Arindrarto, Daniel Borràs, M. Willy Honders, Rick H. de Leeuw, Wilma G. M. Kroes, Peter de Knijff, Cornelis A.M. van Bergen, Peter A.C. ’t Hoen, Szymon M. Kiełbasa, Jeroen F. J. Laros, Marieke Griffioen, Hendrik Veelken	2017	2
12	Massively parallel sequencing of short tandem repeats—Population data and mixture analysis results for the PowerSeq™ system Forensic Science International Genetics ·Kristiaan J. van der Gaag, Rick H. de Leeuw, Jerry Hoogenboom, Jaynish Patel, Douglas R. Storts, Jeroen F. J. Laros, Peter de Knijff	2016	112
13	Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck Genome Research ·Mingkun Li, Rebecca Rothwell, Martijn Vermaat, Manja Wachsmuth, Roland Schröder, Jeroen F. J. Laros, Mannis van Oven, Paul I. W. de Bakker, Jasper Bovenberg, Cornelia M. van Duijn, Gert‐Jan B. van Ommen, P. Eline Slagboom, Morris A. Swertz, Cisca Wijmenga, Manfred Kayser, Dorret I. Boomsma, Sebastian Zöllner, Peter de Knijff, Mark Stoneking	2016	64
14	Analysis of 36 Y-STR marker units including a concordance study among 2085 Dutch males Forensic Science International Genetics ·Antoinette A. Westen, Thirsa Kraaijenbrink, 山内忠行, Fatemeh Beigom Hosseini, みどり高崎, Sofia B. Zuniga, Anika Tahsin Odri, L Ganchimeg, Kristiaan J. van der Gaag, Natalie Weiler, Arnoud J. Kal, Manfred Kayser, Titia Sijen, Peter de Knijff	2014	31
15	Developmental validation of the HIrisPlex system: DNA-based eye and hair colour prediction for forensic and anthropological usage Forensic Science International Genetics ·Susan Walsh, Lakshmi Chaitanya, 山内忠行, 양명헌, Tiago Feitosa Gondim, Leda Kovatsi, Hitoshi Maeda, Takaki Ishikawa, Titia Sijen, Peter de Knijff, Wojciech Branicki, Fan Liu, Manfred Kayser	2014	140
16	Annexin A5: genotypic risk marker for clinical restenosis after percutaneous coronary intervention European Heart Journal ·M.M. Ewing, Jeffrey J. W. Verschuren, M. Lourdes Sampietro, Margreet R. de Vries, Peter de Knijff, Paul H.A. Quax, J. Wouter Jukema	2010	1
17	Patterns of inter- and intra-group genetic diversity in the Vlax Roma as revealed by Y chromosome and mitochondrial DNA lineages European Journal of Human Genetics ·Luba Kalaydjieva, Francesc Calafell, Mark A. Jobling, Dora Angelicheva, Peter de Knijff, Roxane Abdel-Gawad, Matthew E. Hurles, Peter A. Underhill, Ivailo Tournev, Elena Marushiaková, Vesselin Popov	2001	53
18	The lipoprotein lipase (Asn291 → Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia Atherosclerosis ·Mariëtte J.V. Hoffer, S.J.H. Bredie, Dorret I. Boomsma, Paul W.A. Reymer, Johannes J.P. Kastelein, Peter de Knijff, Pierre N.M. Demacker, Anton F. H. Stalenhoef, Louis M. Havekes, Rune R. Frants	1996	63
19	Variable expression of familial dysbetalipoproteinemia in apolipoprotein E2 (Lys146-->Gln) Allele carriers. Journal of Clinical Investigation* ·Peter de Knijff, Arn M. J. M. van den Maagdenberg, García Rubiano Mónica, Anton F. H. Stalenhoef, A.H.M. Smelt, John J.P. Kastelein, A. David Marais, Rune R. Frants, Louis M. Havekes	1994	18
20	Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigree. Journal of Clinical Investigation ·Peter de Knijff, Arn M. J. M. van den Maagdenberg, A.F.H. Stalenhoef, J.A. Gevers Leuven, Pierre N.M. Demacker, L. P. Kuyt, Rune R. Frants, Louis M. Havekes	1991	84

About Peter de Knijff

Peter de Knijff is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism, Cancer Research, Molecular Biology and Surgery, having authored 198 papers that have together received 11.1k indexed citations. Recurring topics across this work include Forensic and Genetic Research (64 papers), Genetic diversity and population structure (38 papers), Genetic Associations and Epidemiology (31 papers), Lipoproteins and Cardiovascular Health (27 papers), Molecular Biology Techniques and Applications (26 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (22 papers), Race, Genetics, and Society (20 papers) and Genomics and Phylogenetic Studies (14 papers). The work is most often cited by research in Genetics (5.8k citations), Endocrinology, Diabetes and Metabolism (1.3k citations), Archeology (656 citations), Molecular Biology (4.4k citations) and Cancer Research (695 citations). Peter de Knijff has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Manfred Kayser, Louis M. Havekes, Kristiaan J. van der Gaag, Cornelia M. van Duijn, Lutz Roewer, Christine Van Broeckhoven, John J.P. Kastelein, Sofia B. Zuniga, Titia Sijen and Jan Albert Kuivenhoven. Their work appears in journals such as Forensic Science International Genetics, European Journal of Human Genetics, Forensic Science International, The American Journal of Human Genetics and Human Mutation.

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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