J. Herrmann

1.7k citations
50 papers · 1.2k indexed · h-index 21

Impact in

    • Congenital limb and hand anomalies
  • Genetics top 5%
    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities
    • Connective tissue disorders research
    • Craniofacial Disorders and Treatments

Papers in

J. Herrmann

49 papers receiving 1.1k citations

Peers

J. Herrmann
Comparison fields: 5 of 81
  • Developmental Biology 162
  • Genetics 645
  • Pediatrics, Perinatology and Child Health 334
  • Genetics 96
  • Hematology 92
Replace Sevim Balcı with:
Sevim Balcı Türkiye
Walter Fuhrmann Germany
Frank Majewski Germany
Stephen E. Gellis United States
Laurence Taine France
Paulo Ricardo Gazzola Zen Brazil
R J Gorlin Australia
Giorgio Adriano Paskulin Brazil
Bertil Hall Sweden
Maria da Graça Dutra Brazil
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Citations per field
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Sevim Balcı · 1×
Citations per year

Countries citing papers authored by J. Herrmann

Since Specialization
Citations

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

Fields of papers citing papers by J. Herrmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown
#Work
1 20144
2 201346
3 20101
4
Ektoparasitosen Teil 1: Läuse und Flöhe
20093
5 20093
6 20094
7 20080
8 200518
9 19928
10
Clinical delineation of trisomy 9 syndrome.
198019
11 19797
12 19788
13 197826
14 197772
15
Studies of malformation syndromes in man XXXXII: a pleiotropic dominant mutation affecting skeletal, sexual and apocrine-mammary development.
197623
16 197618
17
The Stickler syndrome (hereditary arthroophthalmopathy).
197566
18 197476
19
Short rib-polydactyly syndromes and related conditions.
197411
20 19665

About J. Herrmann

J. Herrmann is a scholar working on Developmental Biology, Anatomy, Immunology and Allergy, Genetics and Hematology, having authored 50 papers that have together received 1.2k indexed citations. Recurring topics across this work include Nail Diseases and Treatments (6 papers), Congenital limb and hand anomalies (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Connective tissue disorders research (4 papers), Dermatological diseases and infestations (4 papers), Hedgehog Signaling Pathway Studies (4 papers), Prenatal Screening and Diagnostics (4 papers) and Genetic Syndromes and Imprinting (3 papers). The work is most often cited by research in Developmental Biology (162 citations), Genetics (645 citations), Pediatrics, Perinatology and Child Health (334 citations), Genetics (96 citations) and Hematology (92 citations). J. Herrmann has collaborated with scholars based in United States, Germany and Switzerland. Frequent co-authors include John M. Opitz, Enid F. Gilbert, JohnM. Opitz, Philip D. Pallister, Jürgen W. Spranger, Barbara McGillivray, R. Brian Lowry, Li‐Wen Lai, E.D. Thomas and Robert P. Erickson. Their work appears in journals such as European Journal of Pediatrics, Human Genetics, The Lancet, Blood and Journal of Cutaneous Pathology.

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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