Irene Barrett
Impact in
-
- Prenatal Screening and Diagnostics
- Genetics top 2%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
Papers in
-
- Prenatal Screening and Diagnostics 22
- Genetics 22
- Genetic Syndromes and Imprinting 15
- Genomic variations and chromosomal abnormalities 10
- Co-authors
- Dagmar K. Kalousek (24 shared papers)Philip Hieter (6 shared papers)Sylvie Langlois (9 shared papers)P. N. Howard‐Peebles (4 shared papers)Wendy P. Robinson (10 shared papers)Kirk J. McManus (4 shared papers)R. Douglas Wilson (6 shared papers)Barbara McGillivray (2 shared papers)
- Journals
- Prenatal Diagnosis (9 papers)Human Genetics (4 papers)PLoS Genetics (3 papers)Journal of Enzyme Inhibition and Medicinal Chemistry (2 papers)Proceedings of the National Academy of Sciences (2 papers)
- Partner nations
- CanadaUnited StatesIreland
In The Last Decade
Irene Barrett
37 papers receiving 2.1k citations
Peers
Comparison fields: 5 of 86
- Pediatrics, Perinatology and Child Health 1.1k
- Genetics 1.0k
- Molecular Biology 1.1k
- Obstetrics and Gynecology 102
- Cell Biology 166
Countries citing papers authored by Irene Barrett
This map shows the geographic impact of Irene Barrett'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 Irene Barrett with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Irene Barrett more than expected).
Fields of papers citing papers by Irene Barrett
This network shows the impact of papers produced by Irene Barrett. 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 Irene Barrett. The network helps show where Irene Barrett may publish in the future.
Co-authors
The 25 scholars most cited alongside Irene Barrett, 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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 309 | |
| 2 | 2012 | 182 | |
| 3 | Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction. | 1997 | 164 |
| 4 | Uniparental disomy for chromosome 16 in humans. | 1993 | 155 |
| 5 | 1991 | 153 | |
| 6 | Placental mosaicism and intrauterine survival of trisomies 13 and 18. | 1989 | 124 |
| 7 | 2009 | 105 | |
| 8 | 2013 | 68 | |
| 9 | 2012 | 59 | |
| 10 | 1996 | 56 | |
| 11 | 2006 | 53 | |
| 12 | 1997 | 50 | |
| 13 | 2011 | 46 | |
| 14 | 1996 | 46 | |
| 15 | 2002 | 46 | |
| 16 | 2008 | 43 | |
| 17 | 2002 | 41 | |
| 18 | 1994 | 41 | |
| 19 | 1994 | 39 | |
| 20 | 1999 | 33 |
About Irene Barrett
Irene Barrett is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Organic Chemistry and Surgery, having authored 37 papers that have together received 2.1k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (22 papers), Genetic Syndromes and Imprinting (15 papers), Genomic variations and chromosomal abnormalities (10 papers), DNA Repair Mechanisms (5 papers), Synthesis and biological activity (4 papers), Genomics and Chromatin Dynamics (4 papers), Epigenetics and DNA Methylation (4 papers) and RNA Research and Splicing (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1.1k citations), Genetics (1.0k citations), Molecular Biology (1.1k citations), Obstetrics and Gynecology (102 citations) and Cell Biology (166 citations). Irene Barrett has collaborated with scholars based in Canada, United States and Ireland. Frequent co-authors include Dagmar K. Kalousek, Philip Hieter, Sylvie Langlois, P. N. Howard‐Peebles, Wendy P. Robinson, Kirk J. McManus, R. Douglas Wilson, Barbara McGillivray, Brenda Lomax and Adèle Telenius. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, PLoS Genetics, Journal of Enzyme Inhibition and Medicinal Chemistry and Proceedings of the National Academy of Sciences.
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.