Kathy Mann
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
Papers in
- Genetics 27
- Genomic variations and chromosomal abnormalities 19
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Genomics and Rare Diseases 3
- Hemoglobinopathies and Related Disorders 2
-
- Prenatal Screening and Diagnostics 25
- Fetal and Pediatric Neurological Disorders 8
- Co-authors
- Caroline Mackie Ogilvie (24 shared papers)Zoe Docherty (9 shared papers)Celia Donaghue (12 shared papers)Shu C. Yau (2 shared papers)Joo Wook Ahn (8 shared papers)Stephen Abbs (1 shared paper)Paul N. Scriven (1 shared paper)Alison Hills (5 shared papers)
- Journals
- Prenatal Diagnosis (10 papers)Molecular Cytogenetics (6 papers)European Journal of Human Genetics (2 papers)Nature (2 papers)Blood (1 paper)
- Partner nations
- United KingdomAustraliaCanada
In The Last Decade
Kathy Mann
41 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 94
- Pediatrics, Perinatology and Child Health 800
- Genetics 862
- Infectious Diseases 123
- Genetics 54
- Molecular Biology 330
Countries citing papers authored by Kathy Mann
This map shows the geographic impact of Kathy Mann'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 Kathy Mann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kathy Mann more than expected).
Fields of papers citing papers by Kathy Mann
This network shows the impact of papers produced by Kathy Mann. 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 Kathy Mann. The network helps show where Kathy Mann may publish in the future.
Co-authors
The 25 scholars most cited alongside Kathy Mann, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 160 | |
| 2 | 2004 | 112 | |
| 3 | 2018 | 92 | |
| 4 | 2005 | 76 | |
| 5 | 2004 | 66 | |
| 6 | 2010 | 57 | |
| 7 | 2003 | 53 | |
| 8 | 2005 | 52 | |
| 9 | 2012 | 47 | |
| 10 | 2005 | 45 | |
| 11 | 2013 | 43 | |
| 12 | 2007 | 39 | |
| 13 | 2010 | 38 | |
| 14 | 2006 | 34 | |
| 15 | 2009 | 32 | |
| 16 | 2010 | 32 | |
| 17 | 2005 | 31 | |
| 18 | 2007 | 27 | |
| 19 | 2020 | 24 | |
| 20 | 2012 | 23 |
About Kathy Mann
Kathy Mann is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Plant Science, Molecular Biology and Infectious Diseases, having authored 41 papers that have together received 1.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (25 papers), Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (13 papers), Fetal and Pediatric Neurological Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Parvovirus B19 Infection Studies (3 papers), Genomics and Rare Diseases (3 papers) and Hemoglobinopathies and Related Disorders (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (800 citations), Genetics (862 citations), Infectious Diseases (123 citations), Genetics (54 citations) and Molecular Biology (330 citations). Kathy Mann has collaborated with scholars based in United Kingdom, Australia and Canada. Frequent co-authors include Caroline Mackie Ogilvie, Zoe Docherty, Celia Donaghue, Shu C. Yau, Joo Wook Ahn, Stephen Abbs, Paul N. Scriven, Alison Hills, Roland G. Roberts and Ros Hastings. Their work appears in journals such as Prenatal Diagnosis, Molecular Cytogenetics, European Journal of Human Genetics, Nature and Blood.
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.