H. Enders

2.5k citations
40 papers · 1.5k · h-index 18

Impact in

  • Genetics top 2%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities
    • Genetic and rare skin diseases.

Papers in

    • Genomic variations and chromosomal abnormalities 12
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
    • Genetic Syndromes and Imprinting 4
    • Genetics and Neurodevelopmental Disorders 2
    • Sexual Differentiation and Disorders 4
    • Genomics and Chromatin Dynamics 3

H. Enders

40 papers receiving 1.4k citations

Peers

H. Enders
Comparison fields: 5 of 74
  • Genetics 901
  • Developmental Biology 39
  • Pediatrics, Perinatology and Child Health 269
  • Molecular Biology 790
  • Dermatology 52
Replace Susan Holder with:
Susan Holder United Kingdom
Beate Albrecht Germany
M.H. Breuning Netherlands
Sarina G. Kant Netherlands
Emma Wakeling United Kingdom
Holger Tönnies Germany
Serdar Ceylaner Türkiye
Jean‐Pierre Fryns Belgium
Kwame Anyane‐Yeboa United States
Ann Haskins Olney United States
H. Enders relative to Susan Holder United Kingdom Susan Holder's profile →
Citations per field
00.5×3.7×
Susan Holder · 1×
Citations per year

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-authors

The 25 scholars most cited alongside H. Enders, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with H. Enders Line = papers co-authored together H. Enders links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 40 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1983249
2 2007181
3 1988156
4 1995133
5 1997109
6 199574
7 200471
8 198757
9 200555
10 200144
11 198229
12 200128
13 199625
14 199425
15 200122
16 200020
17 200119
18 199319
19 201817
20 199817

About H. Enders

H. Enders is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 40 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (10 papers), Chromosomal and Genetic Variations (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Sexual Differentiation and Disorders (4 papers), Genetic Syndromes and Imprinting (4 papers), Genomics and Chromatin Dynamics (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Genetics (901 citations), Developmental Biology (39 citations), Pediatrics, Perinatology and Child Health (269 citations), Molecular Biology (790 citations) and Dermatology (52 citations). H. Enders has collaborated with scholars based in Germany, Poland and France. Frequent co-authors include Michael B. Ranke, J. R. Bierich, W. Rosendahl, F. Majewski, P. Stubbe, Andreas Dufke, M A Preece, H. A. Wollmann, A. A. Schmaltz and P Heidemann. Their work appears in journals such as European Journal of Pediatrics, Cytogenetic and Genome Research, Human Genetics, Clinical Genetics and The Journal of Pediatrics.

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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