H. Enders

2.5k total citations
40 papers, 1.5k citations indexed

About

H. Enders is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, H. Enders has authored 40 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 19 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in H. Enders's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (11 papers) and Chromosomal and Genetic Variations (8 papers). H. Enders is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (11 papers) and Chromosomal and Genetic Variations (8 papers). H. Enders collaborates with scholars based in Germany, France and Poland. H. Enders's co-authors include Michael B. Ranke, J. R. Bierich, W. Rosendahl, F. Majewski, P. Stubbe, Andreas Dufke, H. A. Wollmann, M A Preece, A. A. Schmaltz and P Heidemann and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and The Journal of Pediatrics.

In The Last Decade

H. Enders

40 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H. Enders Germany 18 933 899 313 113 102 40 1.5k
Jean‐Pierre Fryns Belgium 21 909 1.0× 1.2k 1.3× 202 0.6× 83 0.7× 127 1.2× 25 2.0k
Holger Tönnies Germany 23 833 0.9× 927 1.0× 179 0.6× 180 1.6× 79 0.8× 55 1.6k
Véronique David France 29 749 0.8× 1.1k 1.2× 327 1.0× 70 0.6× 75 0.7× 70 2.2k
Daniela del Gaudio United States 18 1.0k 1.1× 854 0.9× 388 1.2× 129 1.1× 72 0.7× 47 1.8k
Lawrence C. Layman United States 23 841 0.9× 825 0.9× 188 0.6× 147 1.3× 122 1.2× 54 1.8k
M.H. Breuning Netherlands 16 1.7k 1.8× 1.4k 1.5× 207 0.7× 89 0.8× 40 0.4× 26 2.1k
Maureen Bocian United States 18 1.4k 1.5× 1.2k 1.4× 241 0.8× 55 0.5× 36 0.4× 35 2.1k
Susan Holder United Kingdom 21 1.2k 1.3× 1.1k 1.2× 265 0.8× 102 0.9× 61 0.6× 43 2.2k
Gholamali Tariverdian Germany 18 812 0.9× 721 0.8× 212 0.7× 23 0.2× 70 0.7× 64 1.3k
Almuth Caliebe Germany 23 678 0.7× 655 0.7× 324 1.0× 46 0.4× 74 0.7× 66 1.4k

Countries citing papers authored by H. Enders

Since Specialization
Citations

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

Fields of papers citing papers by H. Enders

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Enders

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

All Works

20 of 20 papers shown
1.
Nguyen, Huu Phuc, et al.. (2009). Mosaic Trisomy 21/Monosomy 21 in a Living Female Infant. Cytogenetic and Genome Research. 125(1). 26–32. 10 indexed citations
2.
Grzeschik, Karl‐Heinz, Dorothea Bornholdt, Frank Oeffner, et al.. (2007). Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia. Nature Genetics. 39(7). 833–835. 181 indexed citations
3.
Dufke, Andreas, Sylke Singer, Ulrike A. Mau‐Holzmann, et al.. (2006). De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies. Cytogenetic and Genome Research. 114(3-4). 342–350. 11 indexed citations
4.
Robinson, Peter N., Luitgard M. Neumann, Stephanie Demuth, et al.. (2005). Shprintzen–Goldberg syndrome: Fourteen new patients and a clinical analysis. American Journal of Medical Genetics Part A. 135A(3). 251–262. 54 indexed citations
5.
Binder, Gerhard, Thomas Eggermann, H. Enders, Michael B. Ranke, & Andreas Dufke. (2001). Tall stature, gonadal dysgenesis, and stigmata of Turner’s syndrome caused by a structurally altered X chromosome. The Journal of Pediatrics. 138(2). 285–287. 19 indexed citations
6.
Dufke, Andreas, et al.. (2001). Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23). Cytogenetic and Genome Research. 93(3-4). 168–170. 22 indexed citations
7.
Kühl, Hjalmar S., et al.. (2001). Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs). Chromosome Research. 9(3). 215–222. 44 indexed citations
8.
Dufke, Andreas, M. Schöning, Christina Kelbova, et al.. (2000). Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome. Cytogenetic and Genome Research. 91(1-4). 81–84. 7 indexed citations
9.
Mielke, G., et al.. (1997). Prenatal detection of double aneuploidy trisomy 10/monosomy X in a liveborn twin with exclusively monosomy X in blood. Clinical Genetics. 51(4). 275–277. 10 indexed citations
10.
Eggermann, Thomas, H Wollmann, Ruprecht Kuner, et al.. (1997). Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy. Human Genetics. 100(3-4). 415–419. 110 indexed citations
11.
Wollmann, H. A., et al.. (1995). Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients. European Journal of Pediatrics. 154(12). 958–968. 131 indexed citations
12.
13.
14.
Rudolph, Günter, Werner Blum, M. Schöning, et al.. (1994). Growth hormone (GH), insulin‐like growth factors (IGFs), and IGF‐binding protein‐3 (IGFBP‐3) in a child with Proteus syndrome. American Journal of Medical Genetics. 50(2). 204–210. 16 indexed citations
15.
Haas, Kurt, et al.. (1994). Das Cardio-Facio-Cutane Syndrom - Blickdiagnose eines seltenen Syndroms. Klinische Pädiatrie. 206(3). 181–183. 5 indexed citations
16.
Steinbach, Peter, Gholamali Tariverdian, Ingo Kennerknecht, et al.. (1993). Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families. Human Genetics. 92(5). 491–498. 12 indexed citations
17.
Majewski, F., H. Enders, MB Ranke, & Thomas Voït. (1993). Serpentine fibula — polycystic kidney syndrome and Melnick-Needles syndrome are different disorders. European Journal of Pediatrics. 152(11). 916–921. 19 indexed citations
18.
Schmid, Michael, et al.. (1992). A 47,XXY female with unusual genitalia. Human Genetics. 90(4). 346–9. 6 indexed citations
19.
Ranke, Michael B., et al.. (1988). Noonan syndrome: growth and clinical manifestations in 144 cases. European Journal of Pediatrics. 148(3). 220–227. 156 indexed citations
20.
Blum, Werner F., et al.. (1987). Growth hormone, somatomedin levels and growth regulation in Turner's syndrome. European Journal of Endocrinology. 116(2). 305–313. 57 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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