Dezsö David
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Hematology top 10%
- Hemophilia Treatment and Research
Papers in
- Hematology 13
- Hemophilia Treatment and Research 10
- Blood Coagulation and Thrombosis Mechanisms 3
- Genetics 16
- Genomic variations and chromosomal abnormalities 12
- Genomics and Rare Diseases 4
- Ocular Disorders and Treatments 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Andreas Gal (6 shared papers)Maria Guida Boavida (5 shared papers)Hans van Bokhoven (2 shared papers)Ulrike Orth (2 shared papers)Helger G. Yntema (1 shared paper)Ben C.J. Hamel (1 shared paper)Jean‐Pierre Fryns (1 shared paper)Kerstin Kutsche (1 shared paper)
- Journals
- Human Mutation (3 papers)Human Genetics (3 papers)Thrombosis and Haemostasis (2 papers)Nature Genetics (2 papers)Genomics (2 papers)
- Partner nations
- PortugalUnited StatesGermany
In The Last Decade
Dezsö David
36 papers receiving 927 citations
Peers
Comparison fields: 5 of 44
- Genetics 445
- Hematology 151
- Cellular and Molecular Neuroscience 87
- Molecular Biology 302
- Pediatrics, Perinatology and Child Health 58
Countries citing papers authored by Dezsö David
This map shows the geographic impact of Dezsö David'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 Dezsö David with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dezsö David more than expected).
Fields of papers citing papers by Dezsö David
This network shows the impact of papers produced by Dezsö David. 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 Dezsö David. The network helps show where Dezsö David may publish in the future.
Co-authors
The 25 scholars most cited alongside Dezsö David, 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 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 314 | |
| 2 | 2016 | 241 | |
| 3 | 1993 | 95 | |
| 4 | 2003 | 33 | |
| 5 | 2009 | 30 | |
| 6 | 1994 | 28 | |
| 7 | The spectrum of mutations and molecular pathogenesis of hemophilia A in 181 Portuguese patients. | 2006 | 27 |
| 8 | 2000 | 21 | |
| 9 | 2003 | 17 | |
| 10 | 1992 | 16 | |
| 11 | 2003 | 16 | |
| 12 | 2013 | 16 | |
| 13 | 1996 | 14 | |
| 14 | 2014 | 14 | |
| 15 | 1997 | 13 | |
| 16 | 2002 | 13 | |
| 17 | 2004 | 12 | |
| 18 | 1993 | 11 | |
| 19 | 1993 | 10 | |
| 20 | 2020 | 10 |
About Dezsö David
Dezsö David is a scholar working on Hematology, Genetics, Developmental Biology, Molecular Biology and Genetics, having authored 36 papers that have together received 1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Hemophilia Treatment and Research (10 papers), Genomics and Rare Diseases (4 papers), Ocular Disorders and Treatments (3 papers), Retinal Development and Disorders (3 papers), Blood Coagulation and Thrombosis Mechanisms (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Genetics (445 citations), Hematology (151 citations), Cellular and Molecular Neuroscience (87 citations), Molecular Biology (302 citations) and Pediatrics, Perinatology and Child Health (58 citations). Dezsö David has collaborated with scholars based in Portugal, United States and Germany. Frequent co-authors include Andreas Gal, Maria Guida Boavida, Hans van Bokhoven, Ulrike Orth, Helger G. Yntema, Ben C.J. Hamel, Jean‐Pierre Fryns, Kerstin Kutsche, Jamel Chelly and Hans‐Hilger Ropers. Their work appears in journals such as Human Mutation, Human Genetics, Thrombosis and Haemostasis, Nature Genetics and Genomics.
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.