Herbert Reichenbach

694 citations
12 papers · 578 · h-index 7

Impact in

    • Congenital limb and hand anomalies
  • Genetics top 10%
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities

Papers in

    • Congenital limb and hand anomalies 3
    • Genomic variations and chromosomal abnormalities 4
    • Genomics and Rare Diseases 2

Herbert Reichenbach

12 papers receiving 539 citations

Peers

Herbert Reichenbach
Comparison fields: 5 of 42
  • Developmental Biology 70
  • Genetics 189
  • Urology 35
  • Sensory Systems 18
  • Molecular Biology 216
Replace Martine Sinico with:
Martine Sinico France
Aleksander Jamsheer Poland
Giangiorgio Crisponi Italy
Hartmut Engel Germany
Yousef Shafeghati Iran
H.-J. Lüdecke Germany
Lisa Ewans Australia
Katarina Lehmann Germany
Misa Kimura Japan
Kouji Narahara Japan
Herbert Reichenbach relative to Martine Sinico France Martine Sinico's profile →
Citations per field
00.5×2×2.9×
Martine Sinico · 1×
Citations per year

Countries citing papers authored by Herbert Reichenbach

Since Specialization
Citations

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

Fields of papers citing papers by Herbert Reichenbach

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 21 scholars most cited alongside Herbert Reichenbach, 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 Herbert Reichenbach Line = papers co-authored together Herbert Reichenbach links everyone, so they are left out of the graph.

All Works

12 of 12 papers shown
#Work
1 1998389
2 200650
3
[The heart-hand syndrome. A new variant of disorders of heart conduction and syndactylia including osseous changes in hands and feet].
199249
4 199932
5 201116
6 199514
7 202210
8
[Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication].
19935
9 20005
10 20005
11
[A further case with Baller-Gerold syndrome (craniosynostosis--radial aplasia syndrome)--overview and new viewpoints on a rare syndrome].
19932
12 20001

About Herbert Reichenbach

Herbert Reichenbach is a scholar working on Developmental Biology, Genetics, Clinical Biochemistry, Rehabilitation and Urology, having authored 12 papers that have together received 578 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Congenital limb and hand anomalies (3 papers), Genomics and Rare Diseases (2 papers), Glycogen Storage Diseases and Myoclonus (1 paper), Immunodeficiency and Autoimmune Disorders (1 paper), Hair Growth and Disorders (1 paper), Metabolism and Genetic Disorders (1 paper) and Elbow and Forearm Trauma Treatment (1 paper). The work is most often cited by research in Developmental Biology (70 citations), Genetics (189 citations), Urology (35 citations), Sensory Systems (18 citations) and Molecular Biology (216 citations). Herbert Reichenbach has collaborated with scholars based in Germany, Israel and United States. Frequent co-authors include Ursula G. Froster, Jürgen Kohlhase, Wolfgang Engel, Heidrun Holland, Uwe Claussen, Johannes R. Lemke, Ilse Chudoba, Barbara Thamm, Nadezda Kosyakova and Bernward Lauer. Their work appears in journals such as Molecular Cytogenetics, JAMA Dermatology, Journal of Inherited Metabolic Disease, Nature Genetics and Human Mutation.

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.

Explore authors with similar magnitude of impact