I D Young
Impact in
- Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
- Connective tissue disorders research
- Reproductive Medicine top 2%
- Sperm and Testicular Function
Papers in
- Genetics 42
- Connective tissue disorders research 8
- Genomic variations and chromosomal abnormalities 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetics and Neurodevelopmental Disorders 6
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- Congenital heart defects research 7
- Sexual Differentiation and Disorders 6
- Co-authors
- P.S. Harper (8 shared papers)J. David Brook (3 shared papers)Sahar Mansour (3 shared papers)Silvana Guioli (3 shared papers)Cheni Kwok (3 shared papers)M. Dominguez-Steglich (3 shared papers)Jamie W. Foster (2 shared papers)Alan J. Schafer (2 shared papers)
- Journals
- Journal of Medical Genetics (17 papers)Clinical Genetics (6 papers)Journal of Intellectual Disability Research (4 papers)Developmental Medicine & Child Neurology (3 papers)The Lancet (3 papers)
- Partner nations
- United KingdomUnited StatesIndia
In The Last Decade
I D Young
78 papers receiving 3.5k citations
I D Young's Hit Papers
Peers
Comparison fields: 5 of 105
- Genetics 2.1k
- Reproductive Medicine 332
- Developmental Biology 77
- Rheumatology 427
- Molecular Biology 1.9k
Countries citing papers authored by I D Young
This map shows the geographic impact of I D Young'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 I D Young with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites I D Young more than expected).
Fields of papers citing papers by I D Young
This network shows the impact of papers produced by I D Young. 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 I D Young. The network helps show where I D Young may publish in the future.
Co-authors
The 25 scholars most cited alongside I D Young, 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 79 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene Hit paper breakdown → | 1994 | 1237 |
| 2 | 1995 | 177 | |
| 3 | Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal. | 1995 | 157 |
| 4 | 2003 | 153 | |
| 5 | 1983 | 125 | |
| 6 | 1982 | 110 | |
| 7 | 1998 | 97 | |
| 8 | 1982 | 92 | |
| 9 | 1994 | 89 | |
| 10 | 2000 | 87 | |
| 11 | 1988 | 63 | |
| 12 | 1994 | 60 | |
| 13 | 1987 | 50 | |
| 14 | 2003 | 48 | |
| 15 | 1982 | 48 | |
| 16 | 1986 | 47 | |
| 17 | 1985 | 44 | |
| 18 | 1988 | 43 | |
| 19 | 1996 | 42 | |
| 20 | 1982 | 41 |
About I D Young
I D Young is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Rheumatology and Surgery, having authored 79 papers that have together received 3.6k indexed citations. Recurring topics across this work include Connective tissue disorders research (8 papers), Congenital heart defects research (7 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Prenatal Screening and Diagnostics (7 papers), Sexual Differentiation and Disorders (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Hereditary Neurological Disorders (4 papers). The work is most often cited by research in Genetics (2.1k citations), Reproductive Medicine (332 citations), Developmental Biology (77 citations), Rheumatology (427 citations) and Molecular Biology (1.9k citations). I D Young has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include P.S. Harper, J. David Brook, Sahar Mansour, Silvana Guioli, Cheni Kwok, M. Dominguez-Steglich, Jamie W. Foster, Alan J. Schafer, Milena Stevanović and Peter N. Goodfellow. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Journal of Intellectual Disability Research, Developmental Medicine & Child Neurology and The Lancet.
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.