S. Kammerer

523 citations
12 papers · 390 · h-index 7

Impact in

  • Genetics top 10%
    • Coagulation, Bradykinin, Polyphosphates, and Angioedema
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetic Associations and Epidemiology
    • Genomic variations and chromosomal abnormalities

Papers in

    • Peroxisome Proliferator-Activated Receptors 1
    • Coagulation, Bradykinin, Polyphosphates, and Angioedema 4
    • Genetics and Neurodevelopmental Disorders 1
    • Animal Genetics and Reproduction 1

S. Kammerer

12 papers receiving 380 citations

Peers

S. Kammerer
Comparison fields: 5 of 59
  • Genetics 113
  • Genetics 121
  • Physiology 17
  • Reproductive Medicine 26
  • Hematology 31
Replace Sarah Opie-Martin with:
Sarah Opie-Martin United Kingdom
Marie Coutelier France
Jean Welssenbach France
Catherine A. Sei United States
Galynn Zitnik United States
Samira Ait-El-Mkadem France
Genki Tohnai Japan
Vincenzo Lupo Spain
Seyedeh Sedigheh Abedini Iran
Anju A. Roy Canada
S. Kammerer relative to Sarah Opie-Martin United Kingdom Sarah Opie-Martin's profile →
Citations per field
00.5×10×15.5×
Sarah Opie-Martin · 1×
Citations per year

Countries citing papers authored by S. Kammerer

Since Specialization
Citations

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

Fields of papers citing papers by S. Kammerer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

12 of 12 papers shown
#Work
1 2006107
2
True hermaphroditism in a 46,XY individual, caused by a postzygotic somatic point mutation in the male gonadal sex-determining locus (SRY): molecular genetics and histological findings in a sporadic case.
199365
3 199564
4 199549
5
Mutations in the gene for X-linked adrenoleukodystrophy in patients with different clinical phenotypes.
199540
6 199622
7 199422
8 19966
9 19956
10 19956
11 19932
12 20041

About S. Kammerer

S. Kammerer is a scholar working on Molecular Biology, Genetics, Hematology, Genetics and Oncology, having authored 12 papers that have together received 390 indexed citations. Recurring topics across this work include Coagulation, Bradykinin, Polyphosphates, and Angioedema (4 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers), Peptidase Inhibition and Analysis (2 papers), Hippo pathway signaling and YAP/TAZ (1 paper), Hemophilia Treatment and Research (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Peroxisome Proliferator-Activated Receptors (1 paper) and Animal Genetics and Reproduction (1 paper). The work is most often cited by research in Genetics (113 citations), Genetics (121 citations), Physiology (17 citations), Reproductive Medicine (26 citations) and Hematology (31 citations). S. Kammerer has collaborated with scholars based in Germany, Japan and Australia. Frequent co-authors include Andreas Braun, A. Roscher, Norbert Arnold, Hartwig Clevė, B. Müller, Ursula Kuhnle, U. Löhrs, Hans‐Peter Schwarz, Herlina Y. Handoko and Michael R. James. Their work appears in journals such as Human Genetics, Biochemical and Biophysical Research Communications, Gene, Molecular Psychiatry and Human Molecular Genetics.

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