H.-J. Lüdecke

835 total citations
10 papers, 345 citations indexed

About

H.-J. Lüdecke is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, H.-J. Lüdecke has authored 10 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in H.-J. Lüdecke's work include RNA regulation and disease (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and dental development and anomalies (1 paper). H.-J. Lüdecke is often cited by papers focused on RNA regulation and disease (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and dental development and anomalies (1 paper). H.-J. Lüdecke collaborates with scholars based in Germany, United States and Netherlands. H.-J. Lüdecke's co-authors include Bernhard Horsthemke, Olaf Pongs, E Haan, Ralf Janknecht, Julia Parrish, Guus Hamers, M.J. Wagner, Moshe Frydman, Patrick J. Willems and U. Claussen and has published in prestigious journals such as Nucleic Acids Research, Human Molecular Genetics and Genomics.

In The Last Decade

H.-J. Lüdecke

10 papers receiving 336 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
H.-J. Lüdecke Germany	9	211	169	70	43	37	10	345
Guus Hamers Netherlands	12	193 0.9×	258 1.5×	32 0.5×	20 0.5×	21 0.6×	19	393
E. Redeker Netherlands	17	571 2.7×	284 1.7×	49 0.7×	34 0.8×	31 0.8×	29	808
Tara R. St. Amand United States	7	523 2.5×	156 0.9×	54 0.8×	66 1.5×	14 0.4×	8	606
Christiane Spaich Germany	8	304 1.4×	269 1.6×	23 0.3×	59 1.4×	11 0.3×	8	432
Man-Chun Ting United States	9	426 2.0×	289 1.7×	35 0.5×	15 0.3×	20 0.5×	10	558
Esther Geán Spain	13	294 1.4×	258 1.5×	20 0.3×	21 0.5×	12 0.3×	20	434
Rodrigo Cuervo Mexico	8	354 1.7×	263 1.6×	27 0.4×	23 0.5×	26 0.7×	10	521
Gabriele Gillessen-Kaesbach Germany	5	349 1.7×	265 1.6×	25 0.4×	14 0.3×	41 1.1×	5	506
Chris Showell United States	8	304 1.4×	72 0.4×	31 0.4×	16 0.4×	50 1.4×	10	385
Andrew J. Bendall Canada	12	454 2.2×	156 0.9×	48 0.7×	56 1.3×	7 0.2×	20	560

Countries citing papers authored by H.-J. Lüdecke

Since Specialization

Citations

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

Fields of papers citing papers by H.-J. Lüdecke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H.-J. Lüdecke. 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 H.-J. Lüdecke. The network helps show where H.-J. Lüdecke may publish in the future.

Co-authorship network of co-authors of H.-J. Lüdecke

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

All Works

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10 of 10 papers shown

Bramswig, Nuria C., Charlotte W. Ockeloen, Johanna Christina Czeschik, et al.. (2015). ‘Splitting versus lumping’: Temple–Baraitser and Zimmermann–Laband Syndromes. Human Genetics. 134(10). 1089–1097. 25 indexed citations

Kuechler, A., Julia Hentschel, Ingo Kurth, et al.. (2012). A Novel Homozygous <b><i>WDR72</i></b> Mutation in Two Siblings with Amelogenesis Imperfecta and Mild Short Stature. Molecular Syndromology. 3(5). 223–229. 13 indexed citations

Beygo, Jasmin, Karin Buiting, Saskia Seland, et al.. (2011). First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome. Molecular Syndromology. 2(2). 53–59. 16 indexed citations

Kaiser, Frank J., Peter H. Byers, Sabina Gallati, et al.. (2003). Novel missense mutations in the TRPS1 transcription factor define the nuclear localization signal. European Journal of Human Genetics. 12(2). 121–126. 48 indexed citations

Lüdecke, H.-J., Jung Ahn, Xin Lin, et al.. (1997). Genomic Organization and Promoter Structure of the Human EXT1 Gene. Genomics. 40(2). 351–354. 45 indexed citations

Lüdecke, H.-J., M.J. Wagner, Julia Parrish, et al.. (1995). Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer--Giedion syndrome. Human Molecular Genetics. 4(1). 31–36. 95 indexed citations

Klink, Albrecht, K. Schiebel, M. Winkelmann, et al.. (1995). The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability. Human Molecular Genetics. 4(5). 869–878. 52 indexed citations

Bardenheuer, Walter, Andreas Lux, H.-J. Lüdecke, et al.. (1994). Characterization of a Microdissection Library from Human Chromosome Region 3p14. Genomics. 19(2). 291–297. 13 indexed citations

Karpiński, Stanisław, et al.. (1993). Detailed characterization of a human 8q24.1 microdissection library and generation of ‘‘sequence-tagged sites”. Cytogenetic and Genome Research. 63(3). 185–188. 1 indexed citations

10.

Janknecht, Ralf, et al.. (1989). Characterization of a putative transcription factor gene expressed in the 20-OH-ecdysone inducible puff 74EF inDrosophila melanogaster. Nucleic Acids Research. 17(12). 4455–4464. 37 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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