Gerhard Binder

8.5k citations
211 papers · 5.1k · 1 hit paper · h-index 37

Impact in

Papers in

    • Sexual Differentiation and Disorders 43
    • Epigenetics and DNA Methylation 32
    • Genetic Syndromes and Imprinting 49
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 30

Gerhard Binder

199 papers receiving 4.9k citations

Hit Papers

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome 1997 · 701 citations
7010+9+19Years since publication200400600

Peers

Gerhard Binder
Comparison fields: 5 of 146
  • Endocrinology, Diabetes and Metabolism 1.8k
  • Genetics 2.7k
  • Pediatrics, Perinatology and Child Health 1.0k
  • Molecular Biology 2.5k
  • Reproductive Medicine 277
Replace William Greulich with:
William Greulich United States
R Stanhope United Kingdom
Stenvert L. S. Drop Netherlands
Erica A. Eugster United States
Kirstine Stochholm Denmark
Wilma Oostdijk Netherlands
Charmian A. Quigley United States
Raja Brauner France
Mohamad Maghnie Italy
Guy Van Vliet Canada
Gerhard Binder relative to William Greulich United States William Greulich's profile →
Citations per field
00.5×3.4×
William Greulich · 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 211 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 →
1997701
2 2011166
3 2015148
4 2011138
5 2006131
6 2005126
7 200384
8 200879
9 200078
10 199578
11 201072
12 200071
13 201470
14 200966
15 200563
16 200161
17 200960
18 200160
19 200456
20 201154

About Gerhard Binder

Gerhard Binder is a scholar working on Molecular Biology, Genetics, Endocrinology, Diabetes and Metabolism, Pediatrics, Perinatology and Child Health and Physiology, having authored 211 papers that have together received 5.1k indexed citations. Recurring topics across this work include Growth Hormone and Insulin-like Growth Factors (63 papers), Genetic Syndromes and Imprinting (49 papers), Sexual Differentiation and Disorders (43 papers), Prenatal Screening and Diagnostics (33 papers), Epigenetics and DNA Methylation (32 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (30 papers), Birth, Development, and Health (16 papers) and Gender Studies in Language (9 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (1.8k citations), Genetics (2.7k citations), Pediatrics, Perinatology and Child Health (1.0k citations), Molecular Biology (2.5k citations) and Reproductive Medicine (277 citations). Gerhard Binder has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Michael B. Ranke, Roland Schweizer, David Martín, Thomas Eggermann, C. P. Schwarze, Karin Weber, Matthias Begemann, H Wollmann, Gunnar Blumenstock and Sabrina Spengler. Their work appears in journals such as Hormone Research in Paediatrics, The Journal of Clinical Endocrinology & Metabolism, Clinical Endocrinology, Growth Hormone & IGF Research and Clinical Epigenetics.

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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