Andreas Speer
Impact in
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
-
- Muscle Physiology and Disorders
- RNA Research and Splicing
Papers in
-
- Muscle Physiology and Disorders 15
- Nuclear Structure and Function 4
- RNA Research and Splicing 4
- Philosophy 26
- Medieval Philosophy and Theology 20
- Co-authors
- K. E. Davies (5 shared papers)S. M. Forrest (7 shared papers)Gareth Cross (4 shared papers)Tracey Flint (4 shared papers)D. Gardner‐Medwin (1 shared paper)John Burn (1 shared paper)Kathryn Robson (1 shared paper)R. Hanke (15 shared papers)
- Journals
- Journal of Medical Genetics (5 papers)Nucleic Acids Research (3 papers)Genomics (3 papers)Analytical Biochemistry (2 papers)Prenatal Diagnosis (2 papers)
- Partner nations
- GermanyUnited KingdomUnited States
In The Last Decade
Andreas Speer
68 papers receiving 933 citations
Peers
Comparison fields: 5 of 99
- Genetics 168
- Molecular Biology 650
- Clinical Biochemistry 61
- Immunology and Allergy 51
- Cardiology and Cardiovascular Medicine 191
Countries citing papers authored by Andreas Speer
This map shows the geographic impact of Andreas Speer'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 Andreas Speer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Speer more than expected).
Fields of papers citing papers by Andreas Speer
This network shows the impact of papers produced by Andreas Speer. 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 Andreas Speer. The network helps show where Andreas Speer may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreas Speer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 95 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1987 | 164 | |
| 2 | 1988 | 147 | |
| 3 | 1983 | 58 | |
| 4 | 1997 | 50 | |
| 5 | 1988 | 49 | |
| 6 | 1991 | 48 | |
| 7 | 1985 | 48 | |
| 8 | 1999 | 42 | |
| 9 | 1987 | 41 | |
| 10 | 1989 | 26 | |
| 11 | 1988 | 25 | |
| 12 | Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLP. | 1986 | 17 |
| 13 | 1987 | 16 | |
| 14 | 1989 | 15 | |
| 15 | 1993 | 13 | |
| 16 | 1986 | 13 | |
| 17 | 1989 | 13 | |
| 18 | 1995 | 12 | |
| 19 | 1994 | 12 | |
| 20 | 1995 | 12 |
About Andreas Speer
Andreas Speer is a scholar working on Molecular Biology, Philosophy, Classics, History and Genetics, having authored 95 papers that have together received 1000 indexed citations. Recurring topics across this work include Historical, Literary, and Cultural Studies (22 papers), Medieval Philosophy and Theology (20 papers), Muscle Physiology and Disorders (15 papers), Neurogenetic and Muscular Disorders Research (7 papers), Reformation and Early Modern Christianity (6 papers), Metabolism and Genetic Disorders (5 papers), Nuclear Structure and Function (4 papers) and RNA Research and Splicing (4 papers). The work is most often cited by research in Genetics (168 citations), Molecular Biology (650 citations), Clinical Biochemistry (61 citations), Immunology and Allergy (51 citations) and Cardiology and Cardiovascular Medicine (191 citations). Andreas Speer has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include K. E. Davies, S. M. Forrest, Gareth Cross, Tracey Flint, D. Gardner‐Medwin, John Burn, Kathryn Robson, R. Hanke, Terry Smith and Jan A. Aertsen. Their work appears in journals such as Journal of Medical Genetics, Nucleic Acids Research, Genomics, Analytical Biochemistry and Prenatal Diagnosis.
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.