Mathias Ehrich
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
Papers in
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- Epigenetics and DNA Methylation 23
- Cancer-related gene regulation 8
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- Prenatal Screening and Diagnostics 30
- Fetal and Pediatric Neurological Disorders 15
- Co-authors
- Dirk van den Boom (38 shared papers)Cosmin Deciu (17 shared papers)Allan T. Bombard (11 shared papers)Charles R. Cantor (6 shared papers)Glenn E. Palomaki (8 shared papers)Jacob A. Canick (6 shared papers)Geralyn Lambert‐Messerlian (6 shared papers)Edward M. Kloza (6 shared papers)
- Journals
- Clinical Chemistry (6 papers)American Journal of Obstetrics and Gynecology (5 papers)Prenatal Diagnosis (5 papers)Genetics in Medicine (4 papers)Oncogene (3 papers)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Mathias Ehrich
61 papers receiving 6.0k citations
Mathias Ehrich's Hit Papers
Peers
Comparison fields: 5 of 130
- Pediatrics, Perinatology and Child Health 2.9k
- Cancer Research 1.0k
- Infectious Diseases 1.1k
- Genetics 1.4k
- Molecular Biology 3.3k
Countries citing papers authored by Mathias Ehrich
This map shows the geographic impact of Mathias Ehrich'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 Mathias Ehrich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mathias Ehrich more than expected).
Fields of papers citing papers by Mathias Ehrich
This network shows the impact of papers produced by Mathias Ehrich. 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 Mathias Ehrich. The network helps show where Mathias Ehrich may publish in the future.
Co-authors
The 25 scholars most cited alongside Mathias Ehrich, 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 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Oct4-Induced Pluripotency in Adult Neural Stem Cells Hit paper breakdown → | 2009 | 704 |
| 2 | DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study Hit paper breakdown → | 2011 | 660 |
| 3 | Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometry Hit paper breakdown → | 2005 | 656 |
| 4 | DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study Hit paper breakdown → | 2012 | 392 |
| 5 | Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting Hit paper breakdown → | 2011 | 371 |
| 6 | 2009 | 227 | |
| 7 | 2007 | 217 | |
| 8 | 2015 | 160 | |
| 9 | 2013 | 156 | |
| 10 | 2014 | 142 | |
| 11 | 2016 | 134 | |
| 12 | 2012 | 125 | |
| 13 | 2009 | 117 | |
| 14 | 2008 | 112 | |
| 15 | 2015 | 112 | |
| 16 | 2010 | 112 | |
| 17 | 2009 | 109 | |
| 18 | 2013 | 108 | |
| 19 | 2006 | 103 | |
| 20 | 2007 | 98 |
About Mathias Ehrich
Mathias Ehrich is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics, Cancer Research and Infectious Diseases, having authored 61 papers that have together received 6.2k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (30 papers), Epigenetics and DNA Methylation (23 papers), Fetal and Pediatric Neurological Disorders (15 papers), Cancer Genomics and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (10 papers), Genetic Syndromes and Imprinting (8 papers), Parvovirus B19 Infection Studies (8 papers) and Cancer-related gene regulation (8 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (2.9k citations), Cancer Research (1.0k citations), Infectious Diseases (1.1k citations), Genetics (1.4k citations) and Molecular Biology (3.3k citations). Mathias Ehrich has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Dirk van den Boom, Cosmin Deciu, Allan T. Bombard, Charles R. Cantor, Glenn E. Palomaki, Jacob A. Canick, Geralyn Lambert‐Messerlian, Edward M. Kloza, James E. Haddow and Matthew R. Nelson. Their work appears in journals such as Clinical Chemistry, American Journal of Obstetrics and Gynecology, Prenatal Diagnosis, Genetics in Medicine and Oncogene.
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.