Irén Haltrich
Impact in
-
- Acute Myeloid Leukemia Research
- Chronic Myeloid Leukemia Treatments
-
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genetic Syndromes and Imprinting 3
- Genomics and Rare Diseases 3
-
- Congenital heart defects research 3
- Co-authors
- György Fekete (25 shared papers)Tatjana Bierhals (1 shared paper)Inga Nagel (1 shared paper)G. Fekete (1 shared paper)Georg Rosenberger (1 shared paper)Kerstin Kutsche (1 shared paper)Hengameh Abdollahpour (1 shared paper)Zoltán Szállási (1 shared paper)
In The Last Decade
Irén Haltrich
28 papers receiving 238 citations
Peers
Comparison fields: 5 of 58
- Hematology 40
- Genetics 87
- Cognitive Neuroscience 32
- Genetics 15
- Cancer Research 21
Countries citing papers authored by Irén Haltrich
This map shows the geographic impact of Irén Haltrich'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 Irén Haltrich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Irén Haltrich more than expected).
Fields of papers citing papers by Irén Haltrich
This network shows the impact of papers produced by Irén Haltrich. 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 Irén Haltrich. The network helps show where Irén Haltrich may publish in the future.
Co-authors
The 25 scholars most cited alongside Irén Haltrich, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 53 | |
| 2 | 2012 | 42 | |
| 3 | 2013 | 17 | |
| 4 | 2003 | 17 | |
| 5 | 2012 | 11 | |
| 6 | 2021 | 9 | |
| 7 | 2005 | 9 | |
| 8 | 2017 | 9 | |
| 9 | 2019 | 9 | |
| 10 | 2005 | 8 | |
| 11 | 2012 | 7 | |
| 12 | 2015 | 6 | |
| 13 | 2020 | 5 | |
| 14 | 2020 | 5 | |
| 15 | 2014 | 5 | |
| 16 | 2022 | 4 | |
| 17 | 2019 | 4 | |
| 18 | 2019 | 3 | |
| 19 | 2020 | 3 | |
| 20 | 2015 | 3 |
About Irén Haltrich
Irén Haltrich is a scholar working on Genetics, Molecular Biology, Hematology, Public Health, Environmental and Occupational Health and Genetics, having authored 33 papers that have together received 241 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (6 papers), Acute Myeloid Leukemia Research (6 papers), Congenital heart defects research (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Acute Lymphoblastic Leukemia research (3 papers), Genetic Syndromes and Imprinting (3 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Hematology (40 citations), Genetics (87 citations), Cognitive Neuroscience (32 citations), Genetics (15 citations) and Cancer Research (21 citations). Irén Haltrich has collaborated with scholars based in Hungary, Sweden and Germany. Frequent co-authors include György Fekete, Tatjana Bierhals, Inga Nagel, G. Fekete, Georg Rosenberger, Kerstin Kutsche, Hengameh Abdollahpour, Zoltán Szállási, Balázs Győrffy and István Likó. Their work appears in journals such as Molecular Cytogenetics, BMC Pediatrics, Modern Pathology, European Journal of Medical Genetics and PLoS ONE.
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.