Alessandra Baumer
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 50
- Genomic variations and chromosomal abnormalities 27
- Genetic Syndromes and Imprinting 19
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 7
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- Epigenetics and DNA Methylation 11
- Congenital heart defects research 8
- Co-authors
- Albert Schinzel (41 shared papers)Phillip Nagley (5 shared papers)Chunfang Zhang (4 shared papers)A. W. Linnane (3 shared papers)Mariluce Riegel (16 shared papers)Anthony W. Linnane (3 shared papers)Ronald J. Maxwell (2 shared papers)Anita Rauch (15 shared papers)
- Journals
- European Journal of Human Genetics (11 papers)Prenatal Diagnosis (5 papers)Human Mutation (5 papers)Human Genetics (4 papers)European Journal of Pediatrics (3 papers)
- Partner nations
- SwitzerlandGermanyAustralia
In The Last Decade
Alessandra Baumer
85 papers receiving 2.8k citations
Peers
Comparison fields: 5 of 105
- Clinical Biochemistry 280
- Genetics 1.2k
- Aging 59
- Pediatrics, Perinatology and Child Health 430
- Molecular Biology 1.6k
Countries citing papers authored by Alessandra Baumer
This map shows the geographic impact of Alessandra Baumer'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 Alessandra Baumer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alessandra Baumer more than expected).
Fields of papers citing papers by Alessandra Baumer
This network shows the impact of papers produced by Alessandra Baumer. 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 Alessandra Baumer. The network helps show where Alessandra Baumer may publish in the future.
Co-authors
The 25 scholars most cited alongside Alessandra Baumer, 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 88 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 307 | |
| 2 | 2006 | 225 | |
| 3 | 1992 | 182 | |
| 4 | 2010 | 180 | |
| 5 | 2011 | 140 | |
| 6 | Mitochondrial gene mutation: the ageing process and degenerative diseases. | 1990 | 132 |
| 7 | 1992 | 102 | |
| 8 | 1998 | 94 | |
| 9 | 2007 | 82 | |
| 10 | 2001 | 76 | |
| 11 | Age-related human mtDNA deletions: a heterogeneous set of deletions arising at a single pair of directly repeated sequences. | 1994 | 62 |
| 12 | 2000 | 55 | |
| 13 | 2013 | 49 | |
| 14 | 2001 | 48 | |
| 15 | 1998 | 46 | |
| 16 | 2008 | 43 | |
| 17 | 1998 | 41 | |
| 18 | 1992 | 40 | |
| 19 | 1995 | 39 | |
| 20 | 2019 | 39 |
About Alessandra Baumer
Alessandra Baumer is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Cellular and Molecular Neuroscience, having authored 88 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (27 papers), Prenatal Screening and Diagnostics (25 papers), Genetic Syndromes and Imprinting (19 papers), Epigenetics and DNA Methylation (11 papers), Metabolism and Genetic Disorders (9 papers), Congenital heart defects research (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Clinical Biochemistry (280 citations), Genetics (1.2k citations), Aging (59 citations), Pediatrics, Perinatology and Child Health (430 citations) and Molecular Biology (1.6k citations). Alessandra Baumer has collaborated with scholars based in Switzerland, Germany and Australia. Frequent co-authors include Albert Schinzel, Phillip Nagley, Chunfang Zhang, A. W. Linnane, Mariluce Riegel, Anthony W. Linnane, Ronald J. Maxwell, Anita Rauch, Damina Balmer and Franz Binkert. Their work appears in journals such as European Journal of Human Genetics, Prenatal Diagnosis, Human Mutation, Human Genetics and European Journal of Pediatrics.
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.