Maj Hultén
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 84
- Genomic variations and chromosomal abnormalities 32
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 18
- Genetics and Neurodevelopmental Disorders 12
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- DNA Repair Mechanisms 25
- Genomics and Chromatin Dynamics 23
- Epigenetics and DNA Methylation 17
- Co-authors
- D. A. Laurie (8 shared papers)J. Lindsten (30 shared papers)E. Viégas-Pèquignot (2 shared papers)Déborah Bourc’his (2 shared papers)Merete Bugge (1 shared paper)Timothy H. Bestor (1 shared paper)Chih-Lin Hsieh (1 shared paper)Niels Tommerup (1 shared paper)
- Journals
- Annals of Human Genetics (16 papers)Hereditas (13 papers)Journal of Medical Genetics (12 papers)Cytogenetic and Genome Research (9 papers)Clinical Genetics (7 papers)
- Partner nations
- United KingdomSwedenItaly
In The Last Decade
Maj Hultén
139 papers receiving 4.5k citations
Maj Hultén's Hit Papers
Peers
Comparison fields: 5 of 141
- Genetics 2.4k
- Pediatrics, Perinatology and Child Health 1.2k
- Molecular Biology 2.8k
- Reproductive Medicine 288
- Plant Science 1.1k
Countries citing papers authored by Maj Hultén
This map shows the geographic impact of Maj Hultén'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 Maj Hultén with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maj Hultén more than expected).
Fields of papers citing papers by Maj Hultén
This network shows the impact of papers produced by Maj Hultén. 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 Maj Hultén. The network helps show where Maj Hultén may publish in the future.
Co-authors
The 25 scholars most cited alongside Maj Hultén, 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 145 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene Hit paper breakdown → | 1999 | 884 |
| 2 | 2000 | 134 | |
| 3 | 1985 | 126 | |
| 4 | 2002 | 114 | |
| 5 | 2002 | 112 | |
| 6 | 1984 | 102 | |
| 7 | 1985 | 97 | |
| 8 | 1998 | 94 | |
| 9 | 2007 | 93 | |
| 10 | 2004 | 93 | |
| 11 | 2009 | 91 | |
| 12 | 2004 | 88 | |
| 13 | 1970 | 74 | |
| 14 | 2008 | 72 | |
| 15 | 1994 | 70 | |
| 16 | 2007 | 69 | |
| 17 | 1985 | 69 | |
| 18 | 1985 | 63 | |
| 19 | 1989 | 59 | |
| 20 | 1985 | 57 |
About Maj Hultén
Maj Hultén is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health, having authored 145 papers that have together received 4.8k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (47 papers), Prenatal Screening and Diagnostics (37 papers), Genomic variations and chromosomal abnormalities (32 papers), DNA Repair Mechanisms (25 papers), Genomics and Chromatin Dynamics (23 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers), Epigenetics and DNA Methylation (17 papers) and Genetics and Neurodevelopmental Disorders (12 papers). The work is most often cited by research in Genetics (2.4k citations), Pediatrics, Perinatology and Child Health (1.2k citations), Molecular Biology (2.8k citations), Reproductive Medicine (288 citations) and Plant Science (1.1k citations). Maj Hultén has collaborated with scholars based in United Kingdom, Sweden and Italy. Frequent co-authors include D. A. Laurie, J. Lindsten, E. Viégas-Pèquignot, Déborah Bourc’his, Merete Bugge, Timothy H. Bestor, Chih-Lin Hsieh, Niels Tommerup, James J. Russo and Guoliang Xu. Their work appears in journals such as Annals of Human Genetics, Hereditas, Journal of Medical Genetics, Cytogenetic and Genome Research and Clinical 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.