Hartmut Engel

890 total citations
15 papers, 518 citations indexed

About

Hartmut Engel is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Hartmut Engel has authored 15 papers receiving a total of 518 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 3 papers in Pathology and Forensic Medicine and 3 papers in Oncology. Recurrent topics in Hartmut Engel's work include Hedgehog Signaling Pathway Studies (3 papers), Cancer and Skin Lesions (2 papers) and Ion channel regulation and function (2 papers). Hartmut Engel is often cited by papers focused on Hedgehog Signaling Pathway Studies (3 papers), Cancer and Skin Lesions (2 papers) and Ion channel regulation and function (2 papers). Hartmut Engel collaborates with scholars based in Germany, United States and Italy. Hartmut Engel's co-authors include Karl‐Heinz Grzeschik, Dorothea Bornholdt, Rudolf Happle, Karl‐Heinz Grzeschik, Stylianos E. Antonarakis, Uppala Radhakrishna, Colette Rossier, Armand Bottani, Hamish S. Scott and Jean-Louis Blouin and has published in prestigious journals such as Oncogene, FEBS Letters and Journal of the American Society of Nephrology.

In The Last Decade

Hartmut Engel

14 papers receiving 490 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hartmut Engel Germany 9 380 182 71 69 52 15 518
E. M. Bleeker‐Wagemakers Netherlands 17 719 1.9× 235 1.3× 35 0.5× 104 1.5× 9 0.2× 50 904
Morad Khayat Israel 16 422 1.1× 162 0.9× 37 0.5× 73 1.1× 3 0.1× 50 664
Syed Irfan Raza Pakistan 14 259 0.7× 97 0.5× 13 0.2× 146 2.1× 8 0.2× 29 439
Bader Alhaddad Germany 15 331 0.9× 174 1.0× 16 0.2× 24 0.3× 46 0.9× 29 516
Patricio Barros‐Núñez Mexico 15 359 0.9× 302 1.7× 28 0.4× 99 1.4× 8 0.2× 71 688
Sahar Mansour United Kingdom 11 575 1.5× 288 1.6× 81 1.1× 43 0.6× 36 0.7× 15 854
Deborah Morrogh United Kingdom 9 247 0.7× 299 1.6× 34 0.5× 83 1.2× 2 0.0× 13 542
Julie S. Fryburg United States 12 341 0.9× 412 2.3× 59 0.8× 42 0.6× 18 0.3× 25 790
Lauréane Mittaz Switzerland 10 211 0.6× 180 1.0× 40 0.6× 93 1.3× 7 0.1× 10 586
Luisa Nanni Italy 10 741 1.9× 515 2.8× 81 1.1× 32 0.5× 73 1.4× 14 958

Countries citing papers authored by Hartmut Engel

Since Specialization
Citations

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

Fields of papers citing papers by Hartmut Engel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hartmut Engel

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

All Works

15 of 15 papers shown
1.
Derst, Christian, Christine Karschin, Erhard Wischmeyer, et al.. (2001). Genetic and functional linkage of Kir5.1 and Kir2.1 channel subunits. FEBS Letters. 491(3). 305–311. 53 indexed citations
2.
3.
Weber, Stefanie, Karl P. Schlingmann, Melanie Peters, et al.. (2001). Primary Gene Structure and Expression Studies of Rodent Paracellin-1. Journal of the American Society of Nephrology. 12(12). 2664–2672. 41 indexed citations
4.
5.
Derst, Christian, et al.. (2000). Genomic structure and chromosome mapping of human and mouse RAMP genes. Cytogenetic and Genome Research. 90(1-2). 115–118. 11 indexed citations
6.
Lisch, Walter, Andreas Büttner, Frank Oeffner, et al.. (2000). Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to Xp22.3. American Journal of Ophthalmology. 130(4). 461–468. 29 indexed citations
7.
Pietro, Cinzia Di, Marina Scalia, Amanda de Souza da Motta, et al.. (2000). Genomic localization of the human genes TAF1A, TAF1B and TAF1C, encoding TAF<sub>I</sub>48, TAF<sub>I</sub>63 and TAF<sub>I</sub>110 subunits of class I general transcription initiation factor SL1. Cytogenetic and Genome Research. 89(1-2). 133–136. 3 indexed citations
8.
Happle, Rudolf, et al.. (2000). Mutations in the NSDHL gene, encoding a 3?-hydroxysteroid dehydrogenase, cause CHILD syndrome. American Journal of Medical Genetics. 90(4). 339–346. 204 indexed citations
9.
König, Arne, Rudolf Happle, Dorothea Bornholdt, Hartmut Engel, & Karl‐Heinz Grzeschik. (2000). Mutations in the NSDHL gene, encoding a 3β-hydroxysteroid dehydrogenase, cause CHILD syndrome. American Journal of Medical Genetics. 90(4). 339–339. 2 indexed citations
10.
Radhakrishna, Uppala, Dorothea Bornholdt, Hamish S. Scott, et al.. (1999). The Phenotypic Spectrum of GLI3 Morphopathies Includes Autosomal Dominant Preaxial Polydactyly Type-IV and Postaxial Polydactyly Type-A/B; No Phenotype Prediction from the Position of GLI3 Mutations. The American Journal of Human Genetics. 65(3). 645–655. 127 indexed citations
11.
Gilbert, Debra J., Hartmut Engel, Karl‐Heinz Grzeschik, et al.. (1999). The neurobeachin gene ( Nbea ) identifies a new region of homology between mouse central Chromosome 3 and human Chromosome 13q13. Mammalian Genome. 10(10). 1030–1031. 8 indexed citations
12.
Pietro, Cinzia Di, Hartmut Engel, Marina Scalia, et al.. (1999). Genomics of the human genes encoding four TAFII subunits of TFIID, the three subunits of TFIIA, as well as CDK8 and SURB7.. Somatic Cell and Molecular Genetics. 25(3). 185–189. 1 indexed citations
13.
Derst, Christian, Frank Döring, Regina Preisig‐Müller, et al.. (1998). Partial Gene Structure and Assignment to Chromosome 2q37 of the Human Inwardly Rectifying K+Channel (Kir7.1) Gene (KCNJ13). Genomics. 54(3). 560–563. 19 indexed citations
14.
Engel, Hartmut. (1990). SAA - Standard der Zukunft.. WIRTSCHAFTSINFORMATIK. 32. 422–428. 1 indexed citations
15.
Ruprecht, A, H Wagner, & Hartmut Engel. (1988). Osteopetrosis: Report of a case and discussion of the differential diagnosis. Oral Surgery Oral Medicine Oral Pathology. 66(6). 674–679. 7 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 E. M. Bleeker‐Wagemakers Breakdown of academic impact, for papers by Morad Khayat Breakdown of academic impact, for papers by Syed Irfan Raza Breakdown of academic impact, for papers by Bader Alhaddad Breakdown of academic impact, for papers by Patricio Barros‐Núñez Breakdown of academic impact, for papers by Sahar Mansour Breakdown of academic impact, for papers by Deborah Morrogh Breakdown of academic impact, for papers by Julie S. Fryburg Breakdown of academic impact, for papers by Lauréane Mittaz Breakdown of academic impact, for papers by Luisa Nanni
Rankless by CCL
2026