Andreas Hehr
Impact in
- Genetics top 5%
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Connective tissue disorders research
- Neurogenetic and Muscular Disorders Research
- Developmental Biology top 10%
Papers in
-
- Prenatal Screening and Diagnostics 4
- Assisted Reproductive Technology and Twin Pregnancy 2
-
- Neuroscience and Neuropharmacology Research 2
- Co-authors
- Maximilian Muenke (3 shared papers)Nathaniel H. Robin (2 shared papers)William Reardon (1 shared paper)H. Wolfgang Losken (1 shared paper)Albert Schinzel (1 shared paper)Paul Rutland (1 shared paper)Sue Malcolm (1 shared paper)Robin M. Winter (1 shared paper)
- Journals
- Human Genetics (1 paper)Nature Genetics (1 paper)European Journal of Pediatrics (1 paper)Neurology (1 paper)Orphanet Journal of Rare Diseases (1 paper)
- Partner nations
- GermanyUnited StatesNetherlands
In The Last Decade
Andreas Hehr
16 papers receiving 980 citations
Peers
Comparison fields: 5 of 54
- Genetics 682
- Developmental Biology 36
- Molecular Biology 553
- Genetics 81
- Cellular and Molecular Neuroscience 118
Countries citing papers authored by Andreas Hehr
This map shows the geographic impact of Andreas Hehr'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 Hehr with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Hehr more than expected).
Fields of papers citing papers by Andreas Hehr
This network shows the impact of papers produced by Andreas Hehr. 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 Hehr. The network helps show where Andreas Hehr may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreas Hehr, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 540 | |
| 2 | 1995 | 208 | |
| 3 | 2007 | 100 | |
| 4 | 2013 | 48 | |
| 5 | 2004 | 46 | |
| 6 | 2007 | 38 | |
| 7 | 2010 | 38 | |
| 8 | 2021 | 12 | |
| 9 | Molecular basis for the stereoselective interactions of catecholamines with alpha-adrenoceptors. | 1998 | 5 |
| 10 | 2008 | 2 | |
| 11 | 2016 | 2 | |
| 12 | Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia | 2007 | 1 |
| 13 | 2011 | 1 | |
| 14 | 1994 | 1 | |
| 15 | 2014 | 1 | |
| 16 | 2007 | 1 |
About Andreas Hehr
Andreas Hehr is a scholar working on Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience, Genetics, Molecular Biology and Speech and Hearing, having authored 16 papers that have together received 1.0k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (4 papers), Cleft Lip and Palate Research (3 papers), Receptor Mechanisms and Signaling (3 papers), Assisted Reproductive Technology and Twin Pregnancy (2 papers), Hedgehog Signaling Pathway Studies (2 papers), RNA Research and Splicing (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Neuroscience and Neuropharmacology Research (2 papers). The work is most often cited by research in Genetics (682 citations), Developmental Biology (36 citations), Molecular Biology (553 citations), Genetics (81 citations) and Cellular and Molecular Neuroscience (118 citations). Andreas Hehr has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Maximilian Muenke, Nathaniel H. Robin, William Reardon, H. Wolfgang Losken, Albert Schinzel, Paul Rutland, Sue Malcolm, Robin M. Winter, Louise J. Pulleyn and David H. Viskochil. Their work appears in journals such as Human Genetics, Nature Genetics, European Journal of Pediatrics, Neurology and Orphanet Journal of Rare Diseases.
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.