Georg Melmer

4.0k citations
39 papers · 3.0k indexed · 1 hit paper · h-index 16

Impact in

    • Cystic Fibrosis Research Advances
    • Neonatal Respiratory Health Research
    • Tracheal and airway disorders
  • Genetics top 5%
    • Congenital Ear and Nasal Anomalies
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Genomic variations and chromosomal abnormalities 5
    • Toxin Mechanisms and Immunotoxins 6

Georg Melmer

38 papers receiving 2.9k citations

Hit Papers

Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping 1989 · 2.4k citations
2.4k198920262001201350010001.5k2.0k

Peers

Georg Melmer
Comparison fields: 5 of 116
  • Pulmonary and Respiratory Medicine 1.9k
  • Genetics 313
  • Genetics 550
  • Molecular Biology 983
  • Biotechnology 81
Replace Zsuzsa Bebők with:
Zsuzsa Bebők United States
D. Markiewicz Canada
Jeffery L. Cole United States
M. Zsiga Canada
Harry Cuppens Belgium
Tara Cox United States
R. Ratcliff United Kingdom
Jan Bijman Netherlands
Lesley Heptinstall United Kingdom
Neil A. Bradbury United States
Georg Melmer relative to Zsuzsa Bebők United States Zsuzsa Bebők's profile →
Citations per field
00.5×1.5×
Zsuzsa Bebők · 1×
Citations per year

Countries citing papers authored by Georg Melmer

Since Specialization
Citations

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

Fields of papers citing papers by Georg Melmer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown
#Work
1 201939
2 201541
3 20142
4 201219
5 200914
6 200953
7 200916
8 199712
9 19944
10 199334
11 19933
12 19933
13 19939
14 199315
15 199219
16 199213
17
Linkage analysis in a large pedigree multiply affected with Gilles de la Tourette syndrome
19911
18 19917
19 19905
20 19908

About Georg Melmer

Georg Melmer is a scholar working on Genetics, Genetics, Immunology, Molecular Biology and Behavioral Neuroscience, having authored 39 papers that have together received 3.0k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (6 papers), Toxin Mechanisms and Immunotoxins (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Monoclonal and Polyclonal Antibodies Research (4 papers), RNA and protein synthesis mechanisms (4 papers), CRISPR and Genetic Engineering (3 papers), Molecular Biology Techniques and Applications (3 papers) and Advanced biosensing and bioanalysis techniques (3 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (1.9k citations), Genetics (313 citations), Genetics (550 citations), Molecular Biology (983 citations) and Biotechnology (81 citations). Georg Melmer has collaborated with scholars based in Germany, United Kingdom and Canada. Frequent co-authors include Manuel Buchwald, Johanna M. Rommens, M. Zsiga, Richard Rozmahel, Bat-Sheva Kerem, Michael Dean, Francis S. Collins, John R. Riordan, Michael C. Iannuzzi and Jeffery L. Cole. Their work appears in journals such as Electrophoresis, Psychiatric Genetics, Annals of Human Genetics, Human Molecular Genetics and DNA and Cell Biology.

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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