JA Goodship
Impact in
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- Genomic variations and chromosomal abnormalities
- Congenital Ear and Nasal Anomalies
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
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- Congenital heart defects research 4
- Signaling Pathways in Disease 1
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- Coronary Artery Anomalies 2
- Tracheal and airway disorders 2
- Co-authors
- Jane Wolstenholme (3 shared papers)Alison L. Webb (2 shared papers)Stephen N. Sturgiss (1 shared paper)Stephen C. Robson (1 shared paper)Paul Warwicker (1 shared paper)John Burn (4 shared papers)D Barge (1 shared paper)Mary Slatter (1 shared paper)
- Journals
- The American Journal of Human Genetics (2 papers)Heart (2 papers)Prenatal Diagnosis (2 papers)Clinical & Experimental Immunology (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United KingdomNetherlandsSwitzerland
In The Last Decade
JA Goodship
11 papers receiving 240 citations
Peers
Comparison fields: 5 of 36
- Genetics 45
- Genetics 107
- Pediatrics, Perinatology and Child Health 52
- Epidemiology 80
- Pulmonary and Respiratory Medicine 64
Countries citing papers authored by JA Goodship
This map shows the geographic impact of JA Goodship'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 JA Goodship with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites JA Goodship more than expected).
Fields of papers citing papers by JA Goodship
This network shows the impact of papers produced by JA Goodship. 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 JA Goodship. The network helps show where JA Goodship may publish in the future.
Co-authors
The 25 scholars most cited alongside JA Goodship, 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 | 2008 | 76 | |
| 2 | 2010 | 46 | |
| 3 | 1996 | 46 | |
| 4 | 2010 | 33 | |
| 5 | A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation. | 1992 | 26 |
| 6 | MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES | 1991 | 4 |
| 7 | Comparison of facial features of DiGeorge syndrome (DGS) due to deletion 10p13-10pter with DGS due to 22q11 deletion | 1994 | 4 |
| 8 | A family with X-linked epilepsy mapping to Xp11-Xq13 | 1999 | 3 |
| 9 | IS MONOSOMY FOR THE DIGEORGE LOCUS ON CHROMOSOME-22 RESPONSIBLE FOR ISOLATED HEART MALFORMATIONS | 1991 | 2 |
| 10 | 1998 | 2 | |
| 11 | 1998 | 1 |
About JA Goodship
JA Goodship is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine, Epidemiology, Genetics and Pediatrics, Perinatology and Child Health, having authored 11 papers that have together received 243 indexed citations. Recurring topics across this work include Congenital heart defects research (4 papers), Prenatal Screening and Diagnostics (3 papers), Congenital Heart Disease Studies (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Coronary Artery Anomalies (2 papers), Tracheal and airway disorders (2 papers), Hermeneutics and Narrative Identity (1 paper) and Signaling Pathways in Disease (1 paper). The work is most often cited by research in Genetics (45 citations), Genetics (107 citations), Pediatrics, Perinatology and Child Health (52 citations), Epidemiology (80 citations) and Pulmonary and Respiratory Medicine (64 citations). JA Goodship has collaborated with scholars based in United Kingdom, Netherlands and Switzerland. Frequent co-authors include Jane Wolstenholme, Alison L. Webb, Stephen N. Sturgiss, Stephen C. Robson, Paul Warwicker, John Burn, D Barge, Mary Slatter, Tara Montgomery and Jason Rice. Their work appears in journals such as The American Journal of Human Genetics, Heart, Prenatal Diagnosis, Clinical & Experimental Immunology 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.