MARKUS WEISSERT
Impact in
- Hematology top 5%
- Blood Coagulation and Thrombosis Mechanisms
- Neurology top 10%
- Cerebral Venous Sinus Thrombosis
Papers in
-
- Blood Coagulation and Thrombosis Mechanisms 5
-
- Peripheral Neuropathies and Disorders 1
- Co-authors
- Eugen Boltshauser (9 shared papers)Maja I. Steinlin (5 shared papers)Thomas Schmitt‐Mechelke (5 shared papers)Danielle Mercati (3 shared papers)Gianpaolo Ramelli (2 shared papers)Andrea Capone Mori (2 shared papers)Emanuela, Elisabeth, Sophia Keller (2 shared papers)Emmanuelle Roulet (2 shared papers)
- Journals
- Developmental Medicine & Child Neurology (4 papers)Neuropediatrics (4 papers)European Journal of Paediatric Neurology (3 papers)Molecular Genetics and Metabolism (1 paper)Journal of Inherited Metabolic Disease (1 paper)
- Partner nations
- SwitzerlandUnited StatesGermany
In The Last Decade
MARKUS WEISSERT
20 papers receiving 799 citations
Peers
Comparison fields: 5 of 63
- Hematology 230
- Neurology 196
- Clinical Biochemistry 70
- Internal Medicine 29
- Pediatrics, Perinatology and Child Health 131
Countries citing papers authored by MARKUS WEISSERT
This map shows the geographic impact of MARKUS WEISSERT'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 MARKUS WEISSERT with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites MARKUS WEISSERT more than expected).
Fields of papers citing papers by MARKUS WEISSERT
This network shows the impact of papers produced by MARKUS WEISSERT. 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 MARKUS WEISSERT. The network helps show where MARKUS WEISSERT may publish in the future.
Co-authors
The 25 scholars most cited alongside MARKUS WEISSERT, 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 | 2005 | 160 | |
| 2 | 1998 | 99 | |
| 3 | 2006 | 93 | |
| 4 | 2010 | 89 | |
| 5 | 2009 | 66 | |
| 6 | 2009 | 56 | |
| 7 | 1994 | 45 | |
| 8 | 2003 | 43 | |
| 9 | 2002 | 34 | |
| 10 | 2012 | 26 | |
| 11 | 1992 | 19 | |
| 12 | 2012 | 19 | |
| 13 | 1999 | 17 | |
| 14 | 2010 | 16 | |
| 15 | 2006 | 14 | |
| 16 | 1999 | 12 | |
| 17 | 1994 | 9 | |
| 18 | Polymyositis, myasthenic syndrome and thymoma in a patient with defective cell-mediated immunity. | 1979 | 5 |
| 19 | 1989 | 5 | |
| 20 | 1980 | 1 |
About MARKUS WEISSERT
MARKUS WEISSERT is a scholar working on Hematology, Neurology, Pediatrics, Perinatology and Child Health, Epidemiology and Infectious Diseases, having authored 20 papers that have together received 828 indexed citations. Recurring topics across this work include Blood Coagulation and Thrombosis Mechanisms (5 papers), Cerebrospinal fluid and hydrocephalus (2 papers), Fetal and Pediatric Neurological Disorders (2 papers), Spinal Dysraphism and Malformations (2 papers), Mitochondrial Function and Pathology (2 papers), Infectious Encephalopathies and Encephalitis (2 papers), RNA modifications and cancer (2 papers) and Peripheral Neuropathies and Disorders (1 paper). The work is most often cited by research in Hematology (230 citations), Neurology (196 citations), Clinical Biochemistry (70 citations), Internal Medicine (29 citations) and Pediatrics, Perinatology and Child Health (131 citations). MARKUS WEISSERT has collaborated with scholars based in Switzerland, United States and Germany. Frequent co-authors include Eugen Boltshauser, Maja I. Steinlin, Thomas Schmitt‐Mechelke, Danielle Mercati, Gianpaolo Ramelli, Andrea Capone Mori, Emanuela, Elisabeth, Sophia Keller, Emmanuelle Roulet, Juerg Luetschg and Vincent Th. Ramaekers. Their work appears in journals such as Developmental Medicine & Child Neurology, Neuropediatrics, European Journal of Paediatric Neurology, Molecular Genetics and Metabolism and Journal of Inherited Metabolic Disease.
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.