Christine Fauth
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 5%
- Genomics and Chromatin Dynamics
- RNA Research and Splicing
- DNA Repair Mechanisms
- Epigenetics and DNA Methylation
Papers in
- Genetics 39
- Genomic variations and chromosomal abnormalities 27
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 6
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- Genomics and Chromatin Dynamics 11
- Mitochondrial Function and Pathology 4
- Co-authors
- Michael R. Speicher (14 shared papers)Thomas Cremer (4 shared papers)Roland Eils (4 shared papers)Kaan Saracoglu (3 shared papers)Andreas Bolzer (2 shared papers)Irina Solovei (1 shared paper)Christoph Cremer (1 shared paper)Gregor Kreth (1 shared paper)
- Journals
- European Journal of Human Genetics (6 papers)European Journal of Medical Genetics (4 papers)Clinical Genetics (4 papers)The American Journal of Human Genetics (3 papers)Human Genetics (3 papers)
- Partner nations
- AustriaGermanyUnited States
In The Last Decade
Christine Fauth
64 papers receiving 2.2k citations
Christine Fauth's Hit Papers
Peers
Comparison fields: 5 of 109
- Genetics 790
- Molecular Biology 1.5k
- Developmental Neuroscience 68
- Cell Biology 234
- Plant Science 522
Countries citing papers authored by Christine Fauth
This map shows the geographic impact of Christine Fauth'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 Christine Fauth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christine Fauth more than expected).
Fields of papers citing papers by Christine Fauth
This network shows the impact of papers produced by Christine Fauth. 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 Christine Fauth. The network helps show where Christine Fauth may publish in the future.
Co-authors
The 25 scholars most cited alongside Christine Fauth, 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 66 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Three-Dimensional Maps of All Chromosomes in Human Male Fibroblast Nuclei and Prometaphase Rosettes Hit paper breakdown → | 2005 | 611 |
| 2 | 1999 | 237 | |
| 3 | Targeted inactivation of p53 in human cells does not result in aneuploidy. | 2002 | 153 |
| 4 | 2011 | 104 | |
| 5 | 2009 | 91 | |
| 6 | 1999 | 72 | |
| 7 | 2012 | 62 | |
| 8 | 2000 | 57 | |
| 9 | 1994 | 51 | |
| 10 | 2016 | 50 | |
| 11 | 1990 | 43 | |
| 12 | 2001 | 42 | |
| 13 | 2006 | 40 | |
| 14 | 2015 | 34 | |
| 15 | 2000 | 34 | |
| 16 | 2001 | 33 | |
| 17 | 1988 | 31 | |
| 18 | 2015 | 30 | |
| 19 | 2012 | 25 | |
| 20 | 2010 | 24 |
About Christine Fauth
Christine Fauth is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Pathology and Forensic Medicine, having authored 66 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (27 papers), Chromosomal and Genetic Variations (17 papers), Prenatal Screening and Diagnostics (12 papers), Genomics and Chromatin Dynamics (11 papers), Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Cancer Genomics and Diagnostics (5 papers) and Mitochondrial Function and Pathology (4 papers). The work is most often cited by research in Genetics (790 citations), Molecular Biology (1.5k citations), Developmental Neuroscience (68 citations), Cell Biology (234 citations) and Plant Science (522 citations). Christine Fauth has collaborated with scholars based in Austria, Germany and United States. Frequent co-authors include Michael R. Speicher, Thomas Cremer, Roland Eils, Kaan Saracoglu, Andreas Bolzer, Irina Solovei, Christoph Cremer, Gregor Kreth, Daniela Koehler and Stefan Müller. Their work appears in journals such as European Journal of Human Genetics, European Journal of Medical Genetics, Clinical Genetics, The American Journal of Human Genetics and Human 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.