Albert Schinzel
Impact in
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Craniofacial Disorders and Treatments
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 196
- Genomic variations and chromosomal abnormalities 131
- Genetic Syndromes and Imprinting 50
- Genetics and Neurodevelopmental Disorders 20
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- Prenatal Screening and Diagnostics 106
- Fetal and Pediatric Neurological Disorders 20
- Co-authors
- Wendy P. Robinson (25 shared papers)Franz Binkert (31 shared papers)Werner Schmid (24 shared papers)Alessandra Baumer (41 shared papers)James R. Miller (1 shared paper)David W. Smith (1 shared paper)Mariluce Riegel (35 shared papers)John M. Opitz (7 shared papers)
- Journals
- Human Genetics (29 papers)Journal of Medical Genetics (28 papers)European Journal of Human Genetics (19 papers)Prenatal Diagnosis (13 papers)Clinical Genetics (12 papers)
- Partner nations
- SwitzerlandUnited StatesGermany
In The Last Decade
Albert Schinzel
296 papers receiving 11.9k citations
Albert Schinzel's Hit Papers
Peers
Comparison fields: 5 of 133
- Genetics 8.1k
- Pediatrics, Perinatology and Child Health 3.7k
- Developmental Biology 459
- Molecular Biology 5.6k
- Genetics 527
Countries citing papers authored by Albert Schinzel
This map shows the geographic impact of Albert Schinzel'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 Albert Schinzel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Albert Schinzel more than expected).
Fields of papers citing papers by Albert Schinzel
This network shows the impact of papers produced by Albert Schinzel. 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 Albert Schinzel. The network helps show where Albert Schinzel may publish in the future.
Co-authors
The 25 scholars most cited alongside Albert Schinzel, 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 303 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Catalogue of Unbalanced Chromosome Aberrations in Man Hit paper breakdown → | 1983 | 595 |
| 2 | 1994 | 467 | |
| 3 | 2006 | 424 | |
| 4 | 1997 | 421 | |
| 5 | 1979 | 409 | |
| 6 | 2006 | 307 | |
| 7 | 1995 | 270 | |
| 8 | 1991 | 229 | |
| 9 | 1983 | 223 | |
| 10 | 1988 | 218 | |
| 11 | 1995 | 216 | |
| 12 | 1992 | 213 | |
| 13 | 2010 | 180 | |
| 14 | 2003 | 165 | |
| 15 | 1998 | 155 | |
| 16 | 1981 | 153 | |
| 17 | 1992 | 150 | |
| 18 | 1999 | 148 | |
| 19 | 1999 | 123 | |
| 20 | 1993 | 122 |
About Albert Schinzel
Albert Schinzel is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Surgery, having authored 303 papers that have together received 12.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (131 papers), Prenatal Screening and Diagnostics (106 papers), Genetic Syndromes and Imprinting (50 papers), Chromosomal and Genetic Variations (40 papers), Congenital limb and hand anomalies (21 papers), Fetal and Pediatric Neurological Disorders (20 papers), Epigenetics and DNA Methylation (20 papers) and Genetics and Neurodevelopmental Disorders (20 papers). The work is most often cited by research in Genetics (8.1k citations), Pediatrics, Perinatology and Child Health (3.7k citations), Developmental Biology (459 citations), Molecular Biology (5.6k citations) and Genetics (527 citations). Albert Schinzel has collaborated with scholars based in Switzerland, United States and Germany. Frequent co-authors include Wendy P. Robinson, Franz Binkert, Werner Schmid, Alessandra Baumer, James R. Miller, David W. Smith, Mariluce Riegel, John M. Opitz, Stylianos E. Antonarakis and Dieter Kotzot. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, European Journal of Human Genetics, Prenatal Diagnosis and Clinical 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.