S. Adolph

1.6k citations
45 papers · 1.2k indexed · h-index 21

Impact in

  • Genetics top 5%
    • Genetic Mapping and Diversity in Plants and Animals
    • Genetic diversity and population structure
    • Genomic variations and chromosomal abnormalities
    • Genomics and Chromatin Dynamics
    • DNA Repair Mechanisms

Papers in

    • Genomics and Chromatin Dynamics 11
    • DNA Repair Mechanisms 6
    • DNA and Nucleic Acid Chemistry 4
    • Genomic variations and chromosomal abnormalities 7
    • Genetic diversity and population structure 6
    • Chronic Lymphocytic Leukemia Research 3

S. Adolph

44 papers receiving 1.1k citations

Peers

S. Adolph
Comparison fields: 5 of 103
  • Genetics 416
  • Molecular Biology 664
  • Hematology 87
  • Oceanography 82
  • Oncology 168
Replace Kjell Petersen with:
Kjell Petersen Norway
James L. Sherley United States
Raffaella Melfi Italy
Chia‐Lin Wei Singapore
Hiroshi Kagoshima Japan
A Robertson United States
Giuseppe Petrosino Italy
Pierre Hutter Switzerland
John Longshore United States
Panagiotis Pantazis United States
S. Adolph relative to Kjell Petersen Norway Kjell Petersen's profile →
Citations per field
00.5×1.5×2.5×
Kjell Petersen · 1×
Citations per year

Countries citing papers authored by S. Adolph

Since Specialization
Citations

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

Fields of papers citing papers by S. Adolph

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 45 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2002119
2
Inducible acceleration of G1 progression through tetracycline-regulated expression of human cyclin E.
1994114
3 198157
4 198451
5 198951
6 198948
7 200646
8 199446
9 198746
10 198745
11 199045
12 199541
13 199239
14 198437
15 198334
16 198530
17 198830
18 199324
19 199023
20 198923

About S. Adolph

S. Adolph is a scholar working on Molecular Biology, Genetics, Plant Science, Oncology and Pathology and Forensic Medicine, having authored 45 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (11 papers), Chromosomal and Genetic Variations (10 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetic diversity and population structure (6 papers), DNA Repair Mechanisms (6 papers), Lymphoma Diagnosis and Treatment (5 papers), DNA and Nucleic Acid Chemistry (4 papers) and Chronic Lymphocytic Leukemia Research (3 papers). The work is most often cited by research in Genetics (416 citations), Molecular Biology (664 citations), Hematology (87 citations), Oceanography (82 citations) and Oncology (168 citations). S. Adolph has collaborated with scholars based in Germany, France and United States. Frequent co-authors include H. Hameister, Jan Klein, Heinz Winking, Rolf Müller, Anja Wimmel, Frances C. Lucibello, A. Sewing, Carl L. Schildkraut, Walther Traut and C. Klett. Their work appears in journals such as Cytogenetic and Genome Research, Chromosoma, Human Genetics, Genetics Research and Hereditas.

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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