David Konecki

4.3k total citations · 1 hit paper
60 papers, 3.6k citations indexed

About

David Konecki is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, David Konecki has authored 60 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 24 papers in Clinical Biochemistry and 13 papers in Rheumatology. Recurrent topics in David Konecki's work include Metabolism and Genetic Disorders (24 papers), Biochemical and Molecular Research (17 papers) and Folate and B Vitamins Research (13 papers). David Konecki is often cited by papers focused on Metabolism and Genetic Disorders (24 papers), Biochemical and Molecular Research (17 papers) and Folate and B Vitamins Research (13 papers). David Konecki collaborates with scholars based in United States, Germany and United Kingdom. David Konecki's 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 and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

David Konecki

58 papers receiving 3.5k citations

Hit Papers

align trajectories

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.

Structure, expression, and mutation of the hypoxanthine phosphoribosyltransferase gene.

1984 396 citations David Konecki et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David Konecki United States	30	2.6k	815	755	606	380	60	3.6k
Hitoshi Osaka Japan	37	3.0k 1.2×	566 0.7×	1.3k 1.8×	724 1.2×	316 0.8×	235	5.0k
Giuseppe Borsani Italy	37	3.1k 1.2×	282 0.3×	1.2k 1.6×	624 1.0×	191 0.5×	90	4.7k
R S Sparkes United States	37	2.9k 1.1×	173 0.2×	2.1k 2.7×	238 0.4×	190 0.5×	142	5.1k
Valentino Romano Italy	23	1.1k 0.4×	595 0.7×	686 0.9×	310 0.5×	83 0.2×	71	2.1k
Catherine Caillaud France	32	1.5k 0.6×	333 0.4×	789 1.0×	803 1.3×	711 1.9×	107	3.6k
Tamae Ohye Japan	27	1.4k 0.5×	581 0.7×	569 0.8×	108 0.2×	221 0.6×	71	2.6k
Thomas Braulke Germany	43	3.1k 1.2×	304 0.4×	471 0.6×	2.5k 4.1×	1.1k 2.8×	174	6.5k
Ohad S. Birk Israel	33	2.1k 0.8×	158 0.2×	1.2k 1.6×	421 0.7×	208 0.5×	121	3.7k
Michal Minczuk United Kingdom	48	5.3k 2.0×	1.2k 1.5×	377 0.5×	138 0.2×	266 0.7×	99	5.8k
Pio D’Adamo Italy	24	1.6k 0.6×	597 0.7×	349 0.5×	92 0.2×	80 0.2×	84	2.8k

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-authorship network of co-authors of David Konecki

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

All Works

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20 of 20 papers shown

Arcos‐Burgos, Mauricio, F. Xavier Castellanos, David Konecki, et al.. (2004). Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolate. Molecular Psychiatry. 9(3). 252–259. 52 indexed citations

Lichter‐Konecki, Uta, Karl W. Broman, Richard A. Dart, Edward B. Blau, & David Konecki. (2000). The locus for autosomal dominant renal Fanconi Syndrome maps to the long arm of chromosome 15. Genetics in Medicine. 2(1). 106–106.

Matsumoto, Naomichi, Donna E. David, Eric W. Johnson, et al.. (2000). Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome. European Journal of Human Genetics. 8(11). 875–883. 26 indexed citations

Rivera, Isabel, Manuela Almeida, Paula Leandro, et al.. (2000). The Correlation of Genotype and Phenotype in Portuguese Hyperphenylalaninemic Patients. Molecular Genetics and Metabolism. 69(3). 195–203. 14 indexed citations

Lichter‐Konecki, Uta, et al.. (1999). Expression patterns of murine lysosome-associated membrane protein 2 (Lamp-2) transcripts during morphogenesis. Differentiation. 65(1). 43–58. 23 indexed citations

Konecki, David, Ewald Münstermann, PF Bolton, et al.. (1996). Point mutation analysis of the FMR-1 gene in autism.. PubMed. 1(3). 227–31. 16 indexed citations

Burgard, Peter, André Rupp, David Konecki, et al.. (1996). Phenylalanine hydroxylase genotypes, predicted residual enzyme activity and phenotypic parameters of diagnosis and treatment of phenylketonuria. European Journal of Pediatrics. 155(S1). S11–S15. 29 indexed citations

McDowell, Geraldine A., Takao Isogai, Akira Tanigami, et al.. (1996). Fine Mapping of the Cystinosis Gene Using an Integrated Genetic and Physical Map of a Region within Human Chromosome Band 17p13. Biochemical and Molecular Medicine. 58(2). 135–141. 19 indexed citations

Konecki, David, Kay Foetisch, Magdalena Schlotter, & Uta Lichter‐Konecki. (1994). Complete cDNA Sequence of Human Lysosome-Associated Membrane Protein-2. Biochemical and Biophysical Research Communications. 205(1). 1–5. 12 indexed citations

10.

Sedláček, Zdeněk, David Konecki, Bernd Korn, Sabine M. Klauck, & Annemarie Poustka. (1994). Evolutionary conservation and genomic organization of XAP-4, an Xq28 located gene coding for a human rab GDP-dissociation inhibitor (GDI). Mammalian Genome. 5(10). 633–639. 15 indexed citations

11.

Verkerk, Annemieke J.M.H., Esther de Graaff, Kristel De Boulle, et al.. (1993). Alternative splicing in the fragile X gene FMR1. Human Molecular Genetics. 2(8). 1348–1348. 114 indexed citations

12.

Verkerk, Annemieke J.M.H., Esther de Graaff, Kristel De Boulle, et al.. (1993). Alternative splicing in the fragile X gene FMR1. Human Molecular Genetics. 2(4). 399–404. 86 indexed citations

13.

Trefz, Friedrich K., Peter Burgard, Thomas König, et al.. (1993). Genotype-phenotype correlations in phenylketonuria. Clinica Chimica Acta. 217(1). 15–21. 33 indexed citations

14.

Konecki, David, Yibin Wang, Friedrich K. Trefz, Uta Lichter‐Konecki, & Savio L.C. Woo. (1992). Structural characterization of the 5' regions of the human phenylalanine hydroxylase gene. Biochemistry. 31(35). 8363–8368. 45 indexed citations

15.

Korn, Bernhard, Zdeněk Sedláček, Antonella Manca, et al.. (1992). A strategy for the selection of transcribed sequences in the Xq28 region. Human Molecular Genetics. 1(4). 235–242. 99 indexed citations

16.

Okano, Yoshiyuki, Randy C. Eisensmith, Flemming Güttler, et al.. (1991). Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria. New England Journal of Medicine. 324(18). 1232–1238. 206 indexed citations

17.

Konecki, David, Magdalena Schlotter, Friedrich K. Trefz, & Uta Lichter‐Konecki. (1991). The identification of two mis-sense mutations at the PAH gene locus in a Turkish patient with phenylketonuria. Human Genetics. 87(4). 389–93. 16 indexed citations

18.

Lichter‐Konecki, Uta, Magdalena Schlotter, Meral Özgüç, et al.. (1989). DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population. Human Genetics. 81(4). 373–376. 28 indexed citations

19.

Lichter‐Konecki, Uta, Magdalena Schlotter, Friedrich K. Trefz, & David Konecki. (1989). Direct detection of a major mutation responsible for phenylketonuria in the population of the Federal Republic of Germany. European Journal of Pediatrics. 149(2). 120–123. 7 indexed citations

20.

Krawczak, Michael, et al.. (1988). Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families. Human Genetics. 80(1). 78–80. 46 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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