Pieter J. de Jong

22.8k total citations · 6 hit papers
81 papers, 11.1k citations indexed

About

Pieter J. de Jong is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Pieter J. de Jong has authored 81 papers receiving a total of 11.1k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Molecular Biology, 30 papers in Genetics and 12 papers in Plant Science. Recurrent topics in Pieter J. de Jong's work include CRISPR and Genetic Engineering (19 papers), RNA Research and Splicing (15 papers) and Animal Genetics and Reproduction (13 papers). Pieter J. de Jong is often cited by papers focused on CRISPR and Genetic Engineering (19 papers), RNA Research and Splicing (15 papers) and Animal Genetics and Reproduction (13 papers). Pieter J. de Jong collaborates with scholars based in United States, United Kingdom and Canada. Pieter J. de Jong's co-authors include Charalampos Aslanidis, Chris T. Amemiya, Emmanuel Mignot, Hiroshi Kadotani, Juliette Faraco, Robin Li, Xiaohong Qiu, Seiji Nishino, William M. Rogers and Ling Lin and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Pieter J. de Jong

81 papers receiving 10.9k citations

Hit Papers

The Sleep Disorder Canine Narcolepsy Is Caused by a Mutat... 1990 2026 2002 2014 1999 1992 2011 1990 2004 500 1000 1.5k
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.

  1. The Sleep Disorder Canine Narcolepsy Is Caused by a Mutation in the Hypocretin (Orexin) Receptor 2 Gene
    1999 1.9k citations Ling Lin, Juliette Faraco et al. Cell profile →
  2. Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene
    1992 1.3k citations Pieter J. de Jong et al. profile →
  3. A conditional knockout resource for the genome-wide study of mouse gene function
    2011 1.2k citations Barry P. Rosen, Pieter J. de Jong et al. profile →
  4. Ligation-independent cloning of PCR products (LIC-PCR)
    1990 961 citations Charalampos Aslanidis, Pieter J. de Jong Nucleic Acids Research profile →
  5. Mutations in a new member of the chromodomain gene family cause CHARGE syndrome
    2004 876 citations Pieter J. de Jong et al. profile →
  6. A new bacteriophage P1–derived vector for the propagation of large human DNA fragments
    1994 681 citations Hiroaki Shizuya, Pieter J. de Jong et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pieter J. de Jong United States 40 6.8k 2.5k 2.0k 1.8k 1.5k 81 11.1k
David M. Virshup United States 66 8.5k 1.2× 1.3k 0.5× 1.4k 0.7× 646 0.4× 3.8k 2.5× 179 14.2k
Jean‐François Brunet France 58 5.4k 0.8× 1.5k 0.6× 2.3k 1.2× 902 0.5× 2.4k 1.6× 127 11.1k
Peter L. Oliver United Kingdom 36 6.5k 1.0× 1.2k 0.5× 953 0.5× 543 0.3× 262 0.2× 98 9.7k
Mark Lathrop France 25 3.2k 0.5× 2.9k 1.2× 554 0.3× 303 0.2× 534 0.3× 48 7.2k
Heiner Westphal United States 73 14.9k 2.2× 5.8k 2.3× 3.0k 1.5× 556 0.3× 491 0.3× 153 22.5k
Terry Magnuson United States 70 12.5k 1.8× 4.2k 1.7× 1.8k 0.9× 1.1k 0.6× 191 0.1× 198 18.0k
Christine Petit France 78 11.8k 1.7× 3.0k 1.2× 1.6k 0.8× 2.6k 1.5× 970 0.6× 334 19.9k
Evan Z. Macosko United States 33 10.6k 1.5× 801 0.3× 2.0k 1.0× 694 0.4× 1.1k 0.7× 45 16.0k
Masatsugu Ueda Japan 37 2.3k 0.3× 837 0.3× 758 0.4× 400 0.2× 1.5k 1.0× 169 6.0k
Kay E. Davies United Kingdom 79 19.3k 2.8× 6.9k 2.8× 3.8k 1.9× 1.2k 0.7× 258 0.2× 380 24.4k

Countries citing papers authored by Pieter J. de Jong

Since Specialization
Citations

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

Fields of papers citing papers by Pieter J. de Jong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pieter J. de Jong. 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 Pieter J. de Jong. The network helps show where Pieter J. de Jong may publish in the future.

Co-authorship network of co-authors of Pieter J. de Jong

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

All Works

20 of 20 papers shown
1.
Heizer, Patrick J., Yiping Tu, Paul H. Kim, et al.. (2020). Deficiency in ZMPSTE24 and resulting farnesyl–prelamin A accumulation only modestly affect mouse adipose tissue stores. Journal of Lipid Research. 61(3). 413–421. 8 indexed citations
2.
Jung, Chris, Junli Zhang, K. C. Kent Lloyd, et al.. (2016). Efficient gene targeting in mouse zygotes mediated by CRISPR/Cas9-protein. Transgenic Research. 26(2). 263–277. 19 indexed citations
3.
Degagné, Émilie, Ashok Kumar Pandurangan, Padmavathi Bandhuvula, et al.. (2014). Sphingosine-1-phosphate lyase downregulation promotes colon carcinogenesis through STAT3-activated microRNAs. Journal of Clinical Investigation. 124(12). 5368–5384. 126 indexed citations
4.
Lee, John M., Yiping Tu, Angelica Tatar, et al.. (2014). Reciprocal knock-in mice to investigate the functional redundancy of lamin B1 and lamin B2. Molecular Biology of the Cell. 25(10). 1666–1675. 22 indexed citations
5.
Park, Chong Yon, Lukas T. Jeker, Karen Carver-Moore, et al.. (2012). A Resource for the Conditional Ablation of microRNAs in the Mouse. Cell Reports. 1(4). 385–391. 152 indexed citations
6.
Yang, Shao H., Sandy Y. Chang, Liya Yin, et al.. (2011). An absence of both lamin B1 and lamin B2 in keratinocytes has no effect on cell proliferation or the development of skin and hair. Human Molecular Genetics. 20(18). 3537–3544. 80 indexed citations
7.
Abi-Rached, Laurent, Heiner Kuhl, Christian Roos, et al.. (2009). A Small, Variable, and Irregular Killer Cell Ig-Like Receptor Locus Accompanies the Absence of MHC-C and MHC-G in Gibbons. The Journal of Immunology. 184(3). 1379–1391. 40 indexed citations
8.
Romanov, Michael N, Oliver A. Ryder, Maxim Koriabine, et al.. (2007). Genomic resources and tools to investigate factors associated with chondrodystrophy in California condors. Kent Academic Repository (University of Kent). 1 indexed citations
9.
Osoegawa, Kazutoyo, Roger A. Hoskins, José P. Abad, et al.. (2006). BAC clones generated from sheared DNA. Genomics. 89(2). 291–299. 21 indexed citations
10.
Goidts, Violaine, Pieter J. de Jong, D.N. Cooper, et al.. (2005). Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16. Genome Research. 15(9). 1232–1242. 37 indexed citations
11.
Geel, Michel van, J.C.T. van Deutekom, Richard J.L.F. Lemmers, et al.. (2000). Identification of a novel β-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35. Cytogenetic and Genome Research. 88(3-4). 316–321. 27 indexed citations
12.
Lin, Ling, Juliette Faraco, Robin Li, et al.. (1999). The Sleep Disorder Canine Narcolepsy Is Caused by a Mutation in the Hypocretin (Orexin) Receptor 2 Gene. Cell. 98(3). 365–376. 1892 indexed citations breakdown →
13.
Osoegawa, Kazutoyo, Peng Yeong Woon, Baohui Zhao, et al.. (1998). An Improved Approach for Construction of Bacterial Artificial Chromosome Libraries. Genomics. 52(1). 1–8. 251 indexed citations
14.
Cooper, Paul R., Norma J. Nowak, Michael J. Higgins, et al.. (1997). A Sequence-Ready High-Resolution Physical Map of the Best Macular Dystrophy Gene Region in 11q12–q13. Genomics. 41(2). 185–192. 18 indexed citations
15.
Lafrenière, Ronald G., Pieter J. de Jong, & Guy A. Rouleau. (1995). A 405-kb Cosmid Contig and HindIII Restriction Map of the Progressive Myoclonus Epilepsy Type 1 (EPM1) Candidate Region in 21q22.3. Genomics. 29(1). 288–290. 15 indexed citations
16.
Aslanidis, Charalampos, Pieter J. de Jong, & Gerd Schmitz. (1994). Minimal length requirement of the single-stranded tails for ligation-independent cloning (LIC) of PCR products.. Genome Research. 4(3). 172–177. 50 indexed citations
17.
Kim, Ung‐Jin, Hiroaki Shizuya, Pieter J. de Jong, Bruce W. Birren, & M I Simon. (1992). Stable propagation of cosmid sized human DNA inserts in an F factor based vector. Nucleic Acids Research. 20(5). 1083–1085. 195 indexed citations
18.
Carrano, A.V., Elbert Branscomb, Pieter J. de Jong, et al.. (1990). The interaction of high-resolution electrophoresis and computational analysis in genome mapping. OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information). 19(16). 3 indexed citations
19.
Aslanidis, Charalampos & Pieter J. de Jong. (1990). Ligation-independent cloning of PCR products (LIC-PCR). Nucleic Acids Research. 18(20). 6069–6074. 961 indexed citations breakdown →
20.
Carrano, A.V., et al.. (1989). Constructing chromosome- and region-specific cosmid maps of the human genome. Genome. 31(2). 1059–1065. 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

Breakdown of academic impact, for papers by David M. Virshup Breakdown of academic impact, for papers by Jean‐François Brunet Breakdown of academic impact, for papers by Peter L. Oliver Breakdown of academic impact, for papers by Mark Lathrop Breakdown of academic impact, for papers by Heiner Westphal Breakdown of academic impact, for papers by Terry Magnuson Breakdown of academic impact, for papers by Christine Petit Breakdown of academic impact, for papers by Evan Z. Macosko Breakdown of academic impact, for papers by Masatsugu Ueda Breakdown of academic impact, for papers by Kay E. Davies
Rankless by CCL
2026