Melissa Hill
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Ethics and Legal Issues in Pediatric Healthcare
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
-
- Prenatal Screening and Diagnostics 55
- Fetal and Pediatric Neurological Disorders 12
- Ethics and Legal Issues in Pediatric Healthcare 6
- Genetics 28
- Genomics and Rare Diseases 16
- BRCA gene mutations in cancer 10
- Co-authors
- Lyn S. Chitty (78 shared papers)Celine Lewis (56 shared papers)Stephen Morris (12 shared papers)Rebecca Daley (9 shared papers)Heather Skirton (4 shared papers)Fiona McKay (9 shared papers)Lucy Jenkins (8 shared papers)Rhiannon Mellis (7 shared papers)
- Journals
- Prenatal Diagnosis (18 papers)European Journal of Human Genetics (10 papers)Genetics in Medicine (5 papers)BJOG An International Journal of Obstetrics & Gynaecology (5 papers)PLoS ONE (4 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Melissa Hill
109 papers receiving 2.9k citations
Melissa Hill's Hit Papers
Peers
Comparison fields: 5 of 115
- Pediatrics, Perinatology and Child Health 1.8k
- Genetics 618
- Infectious Diseases 318
- Virology 79
- Cancer Research 128
Countries citing papers authored by Melissa Hill
This map shows the geographic impact of Melissa Hill'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 Melissa Hill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Melissa Hill more than expected).
Fields of papers citing papers by Melissa Hill
This network shows the impact of papers produced by Melissa Hill. 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 Melissa Hill. The network helps show where Melissa Hill may publish in the future.
Co-authors
The 25 scholars most cited alongside Melissa Hill, 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 114 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta‐analysis Hit paper breakdown → | 2022 | 129 |
| 2 | 2010 | 124 | |
| 3 | 2016 | 110 | |
| 4 | 2013 | 101 | |
| 5 | 2012 | 101 | |
| 6 | 2015 | 86 | |
| 7 | 2017 | 85 | |
| 8 | 2014 | 84 | |
| 9 | 2014 | 81 | |
| 10 | 2010 | 68 | |
| 11 | 2016 | 64 | |
| 12 | 2015 | 64 | |
| 13 | 2015 | 61 | |
| 14 | 2014 | 61 | |
| 15 | 2012 | 59 | |
| 16 | 1999 | 58 | |
| 17 | 2005 | 51 | |
| 18 | 2012 | 49 | |
| 19 | 2013 | 47 | |
| 20 | 2017 | 47 |
About Melissa Hill
Melissa Hill is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Infectious Diseases, Molecular Biology and Public Health, Environmental and Occupational Health, having authored 114 papers that have together received 2.9k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (55 papers), Genomics and Rare Diseases (16 papers), Fetal and Pediatric Neurological Disorders (12 papers), Parvovirus B19 Infection Studies (11 papers), BRCA gene mutations in cancer (10 papers), Ethics in Clinical Research (8 papers), Autopsy Techniques and Outcomes (6 papers) and Ethics and Legal Issues in Pediatric Healthcare (6 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1.8k citations), Genetics (618 citations), Infectious Diseases (318 citations), Virology (79 citations) and Cancer Research (128 citations). Melissa Hill has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Lyn S. Chitty, Celine Lewis, Stephen Morris, Rebecca Daley, Heather Skirton, Fiona McKay, Lucy Jenkins, Rhiannon Mellis, Sarah Mason and Angela N. Barrett. Their work appears in journals such as Prenatal Diagnosis, European Journal of Human Genetics, Genetics in Medicine, BJOG An International Journal of Obstetrics & Gynaecology 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.