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
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- Tracheal and airway disorders 2
- Renal cell carcinoma treatment 1
- Co-authors
- Jane Wolstenholme (3 shared papers)Alison L. Webb (2 shared papers)Stephen N. Sturgiss (1 shared paper)Paul Warwicker (1 shared paper)Stephen C. Robson (1 shared paper)Diana Johnson (1 shared paper)John Burn (4 shared papers)Tara Montgomery (1 shared paper)
- Journals
- Heart (2 papers)Prenatal Diagnosis (2 papers)The American Journal of Human Genetics (2 papers)Clinical & Experimental Immunology (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United KingdomNetherlandsHungary
In The Last Decade
JA Goodship
11 papers receiving 254 citations
Peers
Comparison fields: 5 of 33
- Genetics 48
- Genetics 103
- Pediatrics, Perinatology and Child Health 51
- Epidemiology 73
- Immunology 42
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 | 86 | |
| 2 | 1996 | 50 | |
| 3 | 2010 | 49 | |
| 4 | 2010 | 37 | |
| 5 | A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation. | 1992 | 27 |
| 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, Genetics, Pediatrics, Perinatology and Child Health and Epidemiology, having authored 11 papers that have together received 265 indexed citations. Recurring topics across this work include Congenital heart defects research (4 papers), Prenatal Screening and Diagnostics (3 papers), Tracheal and airway disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Multiple and Secondary Primary Cancers (1 paper), Hermeneutics and Narrative Identity (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Renal cell carcinoma treatment (1 paper). The work is most often cited by research in Genetics (48 citations), Genetics (103 citations), Pediatrics, Perinatology and Child Health (51 citations), Epidemiology (73 citations) and Immunology (42 citations). JA Goodship has collaborated with scholars based in United Kingdom, Netherlands and Hungary. Frequent co-authors include Jane Wolstenholme, Alison L. Webb, Stephen N. Sturgiss, Paul Warwicker, Stephen C. Robson, Diana Johnson, John Burn, Tara Montgomery, Ana Töpf and Andrew R. Gennery. Their work appears in journals such as Heart, Prenatal Diagnosis, The American Journal of Human Genetics, 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.