H.‐J. Lüdecke

823 total citations
12 papers, 279 citations indexed

About

H.‐J. Lüdecke is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, H.‐J. Lüdecke has authored 12 papers receiving a total of 279 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 3 papers in Plant Science. Recurrent topics in H.‐J. Lüdecke's work include Genomic variations and chromosomal abnormalities (9 papers), RNA regulation and disease (5 papers) and RNA modifications and cancer (3 papers). H.‐J. Lüdecke is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), RNA regulation and disease (5 papers) and RNA modifications and cancer (3 papers). H.‐J. Lüdecke collaborates with scholars based in Germany, United States and United Kingdom. H.‐J. Lüdecke's co-authors include Bernhard Horsthemke, Judith Nardmann, Dan E. Wells, Peter Meinecke, M.J. Wagner, Lisbeth Tranebjærg, C Turleau, Anna Latos‐Bieleńska, Niels Tommerup and Bernhard Zabel and has published in prestigious journals such as Journal of Dental Research, Genomics and Human Genetics.

In The Last Decade

H.‐J. Lüdecke

12 papers receiving 263 citations

Peers

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

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

#	Work	Indexed citations
1	Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype 2017 ·Human Genetics ·Nuria C. Bramswig, Oana Caluseriu, H.‐J. Lüdecke, François V. Bolduc, Nicole C. L. Noel, Thomas Wieland, Harald Surowy, H.‐J. Christen, Hartmut Engels, Tim M. Strom, Dagmar Wieczorek	46
2	DYT16 mimics metabolic disease with fever associated beginning of dystonia and MRI abnormalities 2017 ·European Journal of Paediatric Neurology ·Heike Kölbel, A. Kuechler, (unknown), H.‐J. Lüdecke, (unknown), (unknown), (unknown), Ulrike Schara	2
3	Tricho-Rhino-Phalangeal Syndrome with Supernumerary Teeth 2008 ·Journal of Dental Research ·Piranit Nik Kantaputra, Isabelle Milétich, H.‐J. Lüdecke, (unknown), Verayuth Praphanphoj, Ramesh A. Shivdasani, Manuela Wuelling, Andrea Vortkamp, Dobrawa Napierala, Paul T. Sharpe	34
4	Pronounced short stature in a girl with tricho‐rhino‐phalangeal syndrome II (TRPS II, Langer–Giedion syndrome) and growth hormone deficiency 2004 ·American Journal of Medical Genetics Part A ·Stefan Riedl, A Giedion, Karin Schweitzer, Andrea Müllner-Eidenböck, Franz Grill, H Frisch, H.‐J. Lüdecke	20
5	Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8 1999 ·Human Genetics ·H.‐J. Lüdecke, O. Schmidt, Judith Nardmann, (unknown), Peter Meinecke, Maximilian Muenke, Bernhard Horsthemke	23
6	The EIF3S3 gene encoding the p40 subunit of the translation initiation factor eIF3 has eight exons and maps to the Langer-Giedion syndrome chromosome region on 8q24, but is not the TRPS1 gene 1999 ·Human Genetics ·O. Schmidt, (unknown), Stefanie Groß, Bernhard Horsthemke, H.‐J. Lüdecke	2
7	Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8 1999 ·Human Genetics ·H.‐J. Lüdecke, (unknown), (unknown), (unknown), (unknown), Maximilian Muenke, (unknown)	6
8	The tricho-rhino-phalangeal syndromes: frequency and parental origin of 8q deletions 1997 ·Human Genetics ·Judith Nardmann, Lisbeth Tranebjærg, Bernhard Horsthemke, H.‐J. Lüdecke	28
9	A 4-Megabase YAC Contig That Spans the Langer-Giedion Syndrome Region on Human Chromosome 8q24.1: Use in Refining the Location of the Trichorhinophalangeal Syndrome and Multiple Exostoses Genes (TRPS1 and EXT1) 1995 ·Genomics ·Jiakai Hou, Julia Parrish, H.‐J. Lüdecke, (unknown), Y. Wang, Wen‐Shan Chen, (unknown), J. Siegel‐Bartelt, Hope Northrup, (unknown), Craig Chinault, Bernhard Horsthemke, M.J. Wagner, Dan E. Wells	39
10	11p15.5-Specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis 1992 ·Genomics ·Anne Puech, (unknown), H.‐J. Lüdecke, Gabriele Senger, Alasdair Ivens, Marc Jeanpierre, Peter Little, Bernhard Horsthemke, U. Claussen, C. Jones, Claudine Junien, Isabelle Henry	7
11	Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome. 1991 ·PubMed ·H.‐J. Lüdecke, Colin A. Johnson, M.J. Wagner, Dan E. Wells, C Turleau, Niels Tommerup, Anna Latos‐Bieleńska, (unknown), Peter Meinecke, Bernhard Zabel	59
12	Comparative chromosome band mapping in primates byin situ suppression hybridization of band specific DNA microlibraries 1991 ·Human Evolution ·Christoph Lengauer, Johannes Wienberg, Thomas Cremer, H.‐J. Lüdecke, Bernhard Horsthemke	13

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