R. A. Pfeiffer

968 citations
39 papers · 714 indexed · h-index 14
Topics
Congenital limb and hand anomalies (7 papers)Genomic variations and chromosomal abnormalities (7 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers)
Partner nations
GermanyUnited States

In The Last Decade

R. A. Pfeiffer

39 papers receiving 647 citations

Peers

R. A. Pfeiffer
Comparison fields: 5 of 79
  • Genetics 405
  • Molecular Biology 293
  • Developmental Biology 140
  • Pediatrics, Perinatology and Child Health 120
  • Surgery 95
Replace Walter Fuhrmann with:
Walter Fuhrmann Germany
K Imaizumi Japan
B. Rafael Elejalde United States
Donna L. Daentl United States
Richard C. Juberg United States
I D Young United Kingdom
Atsuko Fujimoto United States
R. A. Pfeiffer Germany
H.‐D. Rott Germany
Janet M. Stewart United States
R. A. Pfeiffer relative to Walter Fuhrmann Germany Walter Fuhrmann's profile →
Citations per field
00.5×1.5×2.5×
Walter Fuhrmann · 1×
Citations per year

Countries citing papers authored by R. A. Pfeiffer

Since Specialization
Citations

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

Fields of papers citing papers by R. A. Pfeiffer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R. A. Pfeiffer. 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 R. A. Pfeiffer. The network helps show where R. A. Pfeiffer may publish in the future.

Co-authorship network of co-authors of R. A. Pfeiffer

This figure shows the co-authorship network connecting the top 25 collaborators of R. A. Pfeiffer. A scholar is included among the top collaborators of R. A. Pfeiffer based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with R. A. Pfeiffer. R. A. Pfeiffer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 9
2
Comparative study on lymphocyte subpopulations in cancer patients after immunostimulation with propionibacteria and in renal transplant patients after combined immunosuppression.
2
3 8
4 3
5 5
6 61
7 8
8 7
9 62
10 13
11 13
12 6
13
Karyotyp und Phänotyp der autosomalen Chromosomenaberrationen beim Menschen = The karyotype and the phenotype of autosomal aberrations in man
16
14 13
15 14
16
[Familial cardiomyopathy with congenital webbed neck].
3
17 2
18 37
19 12
20 6

About R. A. Pfeiffer

R. A. Pfeiffer is a scholar working on Developmental Biology, Genetics and Clinical Biochemistry, having authored 39 papers that have together received 714 indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). The work is most often cited by research in Developmental Biology (140 citations), Genetics (405 citations) and Clinical Biochemistry (43 citations). R. A. Pfeiffer has collaborated with scholars based in Germany and United States. Frequent co-authors include W. Lenz, F. Majewski, Gerhard Feil, R. Seiler, Th. Büchner, H Gröbe, D. B. v. Bassewitz, J. Peiffer, Ralph Müller and L. Diekmann. Their work appears in journals such as Nature, The Lancet and The Journal of Pediatrics.

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

Rankless by CCL
2026