David Konecki

4.3k citations
60 papers · 3.6k · 1 hit paper · h-index 30

Impact in

    • Metabolism and Genetic Disorders
    • Biochemical and Molecular Research
    • RNA modifications and cancer
    • RNA and protein synthesis mechanisms
    • Mitochondrial Function and Pathology

Papers in

David Konecki

58 papers receiving 3.5k citations

David Konecki's Hit Papers

Structure, expression, and mutation of the hypoxanthine phosphoribosyltransferase gene. 1984 · 395 citations
3950+14+28Years since publication100200300

Peers

David Konecki
Comparison fields: 5 of 106
  • Clinical Biochemistry 812
  • Molecular Biology 2.5k
  • Cell Biology 588
  • Genetics 738
  • Rheumatology 348
Replace Eric F. Wawrousek with:
Eric F. Wawrousek United States
A Kahn France
Giuseppe Borsani Italy
Petra Kioschis Germany
Catherine Caillaud France
H. Galjaard Netherlands
R S Sparkes United States
Valentino Romano Italy
Ikuo Goto Japan
Nathan Fischel‐Ghodsian United States
David Konecki relative to Eric F. Wawrousek United States Eric F. Wawrousek's profile →
Citations per field
00.5×3.3×
Eric F. Wawrousek · 1×
Citations per year

Countries citing papers authored by David Konecki

Since Specialization
Citations

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

Fields of papers citing papers by David Konecki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 60 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Structure, expression, and mutation of the hypoxanthine phosphoribosyltransferase gene.
Hit paper breakdown →
1984395
2 1982270
3 1987266
4 1986243
5 1987210
6 1991207
7 2003118
8 1993114
9 1982111
10 199299
11
Associations between mutations and a VNTR in the human phenylalanine hydroxylase gene.
199294
12 199591
13 198390
14 199387
15 197786
16 197581
17
Multiple origins for phenylketonuria in Europe.
199273
18
Metaphase and interphase cytogenetics with Alu-PCR-amplified yeast artificial chromosome clones containing the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erbB-2.
199271
19 199968
20 198857

About David Konecki

David Konecki is a scholar working on Molecular Biology, Clinical Biochemistry, Rheumatology, Genetics and Cell Biology, having authored 60 papers that have together received 3.6k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (24 papers), Biochemical and Molecular Research (17 papers), Folate and B Vitamins Research (13 papers), RNA modifications and cancer (8 papers), RNA and protein synthesis mechanisms (7 papers), Cellular transport and secretion (6 papers), Muscle metabolism and nutrition (5 papers) and Amino Acid Enzymes and Metabolism (5 papers). The work is most often cited by research in Clinical Biochemistry (812 citations), Molecular Biology (2.5k citations), Cell Biology (588 citations), Genetics (738 citations) and Rheumatology (348 citations). David Konecki has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include John Brennand, C. Thomas Caskey, Uta Lichter‐Konecki, David W. Melton, Wieland Β. Huttner, A. Craig Chinault, H. Gerdes, Friedrich K. Trefz, Savio L.C. Woo and C. Thomas Caskey. Their work appears in journals such as Human Genetics, Journal of Biological Chemistry, Human Molecular Genetics, Molecular Genetics and Metabolism and Archives of Biochemistry and Biophysics.

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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