Ian Porter
Impact in
-
- Prenatal Screening and Diagnostics
- Neonatal Health and Biochemistry
- Assisted Reproductive Technology and Twin Pregnancy
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Papers in
-
- Neonatal Health and Biochemistry 4
- Genetics 10
- Genomic variations and chromosomal abnormalities 5
- Hemoglobinopathies and Related Disorders 3
- Co-authors
- Ernest B. Hook (4 shared papers)Samuel H. Boyer (2 shared papers)José M Valderas (17 shared papers)Jaheeda Gangannagaripalli (7 shared papers)Chris Sidey‐Gibbons (5 shared papers)Ignacio Ricci‐Cabello (4 shared papers)Joanne Greenhalgh (4 shared papers)Daniela C. Gonçalves (3 shared papers)
- Journals
- Pediatric Research (3 papers)BMJ Quality & Safety (2 papers)The Lancet (2 papers)Medical History (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesSpain
In The Last Decade
Ian Porter
73 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 143
- Pediatrics, Perinatology and Child Health 363
- Clinical Biochemistry 89
- Genetics 296
- Hematology 103
- Developmental Biology 16
Countries citing papers authored by Ian Porter
This map shows the geographic impact of Ian Porter'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 Ian Porter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ian Porter more than expected).
Fields of papers citing papers by Ian Porter
This network shows the impact of papers produced by Ian Porter. 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 Ian Porter. The network helps show where Ian Porter may publish in the future.
Co-authors
The 25 scholars most cited alongside Ian Porter, 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 76 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Human embryonic and fetal death | 1980 | 245 |
| 2 | 1962 | 168 | |
| 3 | 2016 | 155 | |
| 4 | 2021 | 129 | |
| 5 | 1964 | 100 | |
| 6 | 2018 | 70 | |
| 7 | 1962 | 53 | |
| 8 | 2017 | 42 | |
| 9 | 2018 | 37 | |
| 10 | 2021 | 34 | |
| 11 | 1972 | 33 | |
| 12 | 2021 | 31 | |
| 13 | 1962 | 31 | |
| 14 | Perinatal Genetics: Diagnosis and Treatment | 1986 | 31 |
| 15 | 2015 | 30 | |
| 16 | Monitoring, birth defects and environment | 1971 | 29 |
| 17 | 1986 | 28 | |
| 18 | 1970 | 27 | |
| 19 | 1996 | 26 | |
| 20 | 2019 | 26 |
About Ian Porter
Ian Porter is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, General Health Professions, Epidemiology and Molecular Biology, having authored 76 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Neonatal Health and Biochemistry (4 papers), Metabolism and Genetic Disorders (4 papers), Primary Care and Health Outcomes (3 papers), Health Systems, Economic Evaluations, Quality of Life (3 papers), Ethics in medical practice (3 papers), Hemoglobinopathies and Related Disorders (3 papers) and Chronic Disease Management Strategies (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (363 citations), Clinical Biochemistry (89 citations), Genetics (296 citations), Hematology (103 citations) and Developmental Biology (16 citations). Ian Porter has collaborated with scholars based in United Kingdom, United States and Spain. Frequent co-authors include Ernest B. Hook, Samuel H. Boyer, José M Valderas, Jaheeda Gangannagaripalli, Chris Sidey‐Gibbons, Ignacio Ricci‐Cabello, Joanne Greenhalgh, Daniela C. Gonçalves, Jonathan P Evans and Ray Fitzpatrick. Their work appears in journals such as Pediatric Research, BMJ Quality & Safety, The Lancet, Medical History and Journal of Medical 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.