Tessa Homfray
- Developmental Neuroscience top 0.5%
- Molecular Biology top 2%
- Genetics top 2%
- Genomic variations and chromosomal abnormalities 6
- Aging top 5%
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- Prenatal Screening and Diagnostics 17
- Fetal and Pediatric Neurological Disorders 9
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- Cardiovascular Effects of Exercise 8
- Cardiomyopathy and Myosin Studies 8
- Cardiac electrophysiology and arrhythmias 7
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- Genetic factors in colorectal cancer 8
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- Parvovirus B19 Infection Studies 7
- Co-authors
- Matthew E. HurlesJosef PenningerMagdalena RennerJuergen A. KnoblichLouise S. BicknellCarol-Anne MartinD. WénzelAndrew P. Jackson
- Journals
- Ultrasound in Obstetrics and Gynecology (8 papers)Prenatal Diagnosis (5 papers)Journal of Medical Genetics (4 papers)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
Tessa Homfray
65 papers receiving 5.7k citations
Hit Papers
Peers
Comparison fields: 5 of 135
- Developmental Neuroscience 616
- Molecular Biology 3.3k
- Cellular and Molecular Neuroscience 787
- Genetics 1.1k
- Aging 57
Countries citing papers authored by Tessa Homfray
This map shows the geographic impact of Tessa Homfray'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 Tessa Homfray with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tessa Homfray more than expected).
Fields of papers citing papers by Tessa Homfray
This network shows the impact of papers produced by Tessa Homfray. 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 Tessa Homfray. The network helps show where Tessa Homfray may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Tessa Homfray, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 0 | |
| 2 | 2023 | 8 | |
| 3 | 2023 | 3 | |
| 4 | 2023 | 0 | |
| 5 | 2022 | 6 | |
| 6 | 2020 | 7 | |
| 7 | 2020 | 4 | |
| 8 | 2017 | 38 | |
| 9 | 2017 | 5 | |
| 10 | 2016 | 11 | |
| 11 | 2015 | 9 | |
| 12 | 2008 | 47 | |
| 13 | 2007 | 150 | |
| 14 | 2007 | 59 | |
| 15 | 2003 | 17 | |
| 16 | 2001 | 3 | |
| 17 | 1999 | 3 | |
| 18 | 1999 | 325 | |
| 19 | 1997 | 17 | |
| 20 | 1997 | 47 |
About Tessa Homfray
Tessa Homfray is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Cardiology and Cardiovascular Medicine, having authored 69 papers that have together received 5.8k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (17 papers), Fetal and Pediatric Neurological Disorders (9 papers), Cardiovascular Effects of Exercise (8 papers), Cardiomyopathy and Myosin Studies (8 papers), Genetic factors in colorectal cancer (8 papers), Cardiac electrophysiology and arrhythmias (7 papers), Parvovirus B19 Infection Studies (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). The work is most often cited by research in Developmental Neuroscience (616 citations), Molecular Biology (3.3k citations) and Cellular and Molecular Neuroscience (787 citations). Tessa Homfray has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Matthew E. Hurles, Josef Penninger, Magdalena Renner, Juergen A. Knoblich, Louise S. Bicknell, Carol-Anne Martin, D. Wénzel, Andrew P. Jackson, Madeline A. Lancaster and B. Thilaganathan. Their work appears in journals such as Ultrasound in Obstetrics and Gynecology, Prenatal Diagnosis, Journal of Medical Genetics, Fetal Diagnosis and Therapy and Human 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.