Gerhard Binder

8.8k citations
226 papers · 5.8k · 1 hit paper · h-index 40

Impact in

    • Growth Hormone and Insulin-like Growth Factors
  • Genetics top 0.5%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetic Syndromes and Imprinting
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Genetic Syndromes and Imprinting 44
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 23
    • Epigenetics and DNA Methylation 24
    • Sexual Differentiation and Disorders 22

Gerhard Binder

208 papers receiving 5.4k citations

Gerhard Binder's Hit Papers

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome 1997 · 764 citations
7640+9+19Years since publication250500750

Peers

Gerhard Binder
Comparison fields: 5 of 151
  • Endocrinology, Diabetes and Metabolism 1.9k
  • Genetics 2.6k
  • Pediatrics, Perinatology and Child Health 802
  • Reproductive Medicine 265
  • Molecular Biology 2.1k
Replace R Stanhope with:
R Stanhope United Kingdom
Erica A. Eugster United States
Stenvert L. S. Drop Netherlands
Kirstine Stochholm Denmark
Peter C. Hindmarsh United Kingdom
Mehul Dattani United Kingdom
Felix A. Conte United States
Marsha L. Davenport United States
Unnur Þorsteinsdóttir Iceland
Ivo J.P. Arnhold Brazil
Gerhard Binder relative to R Stanhope United Kingdom R Stanhope's profile →
Citations per field
00.5×6.5×
R Stanhope · 1×
Citations per year

Countries citing papers authored by Gerhard Binder

Since Specialization
Citations

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

Fields of papers citing papers by Gerhard Binder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Gerhard Binder, 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 Gerhard Binder Line = papers co-authored together Gerhard Binder links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 226 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
Hit paper breakdown →
1997764
2 2011172
3 2015154
4 2011149
5 2006139
6 2005135
7 1998124
8 2008101
9 201093
10 200387
11 200984
12 199583
13 200081
14 200080
15 200577
16 201475
17 200769
18 200967
19 200167
20 200165

About Gerhard Binder

Gerhard Binder is a scholar working on Genetics, Molecular Biology, Endocrinology, Diabetes and Metabolism, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health, having authored 226 papers that have together received 5.8k indexed citations. Recurring topics across this work include Growth Hormone and Insulin-like Growth Factors (53 papers), Genetic Syndromes and Imprinting (44 papers), Epigenetics and DNA Methylation (24 papers), Prenatal Screening and Diagnostics (24 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (23 papers), Sexual Differentiation and Disorders (22 papers), Medical and Health Sciences Research (9 papers) and Fluid Dynamics and Turbulent Flows (9 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (1.9k citations), Genetics (2.6k citations), Pediatrics, Perinatology and Child Health (802 citations), Reproductive Medicine (265 citations) and Molecular Biology (2.1k citations). Gerhard Binder has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Michael B. Ranke, Roland Schweizer, Thomas Eggermann, David Martín, C. P. Schwarze, Matthias Begemann, Karin Weber, Sabrina Spengler, H Wollmann and Gunnar Blumenstock. Their work appears in journals such as Hormone Research in Paediatrics, The Journal of Clinical Endocrinology & Metabolism, Clinical Endocrinology, Growth Hormone & IGF Research and European Journal of Medical Genetics.

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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