Judith Goodship
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genetic and Kidney Cyst Diseases
- Molecular Biology top 5%
- Congenital heart defects research
Papers in
-
- Congenital heart defects research 19
- Mitochondrial Function and Pathology 3
- Genetics 16
- Congenital Ear and Nasal Anomalies 6
- Neurogenetic and Muscular Disorders Research 4
- Genomic variations and chromosomal abnormalities 3
- Genetic Syndromes and Imprinting 3
- Co-authors
- John Burn (16 shared papers)Peter Scambler (8 shared papers)David I. Wilson (7 shared papers)I Cross (5 shared papers)Jesse Li‐Ling (1 shared paper)R Wadey (4 shared papers)Miranda Splitt (2 shared papers)David A. Kelly (2 shared papers)
- Journals
- Journal of Medical Genetics (14 papers)Prenatal Diagnosis (3 papers)Human Genetics (3 papers)Circulation (2 papers)British Journal of Dermatology (1 paper)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Judith Goodship
47 papers receiving 2.7k citations
Peers
Comparison fields: 5 of 110
- Genetics 1.0k
- Molecular Biology 2.0k
- Epidemiology 634
- Developmental Biology 38
- Pulmonary and Respiratory Medicine 450
Countries citing papers authored by Judith Goodship
This map shows the geographic impact of Judith 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 Judith Goodship with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Judith Goodship more than expected).
Fields of papers citing papers by Judith Goodship
This network shows the impact of papers produced by Judith 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 Judith Goodship. The network helps show where Judith Goodship may publish in the future.
Co-authors
The 25 scholars most cited alongside Judith 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
Showing the 20 most-cited of 47 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1993 | 364 | |
| 2 | 1996 | 222 | |
| 3 | 1993 | 204 | |
| 4 | 1998 | 191 | |
| 5 | 1993 | 142 | |
| 6 | 2010 | 129 | |
| 7 | Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome. | 1992 | 124 |
| 8 | 2006 | 117 | |
| 9 | 2003 | 117 | |
| 10 | 1993 | 116 | |
| 11 | 1995 | 91 | |
| 12 | 1996 | 84 | |
| 13 | Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome. | 1996 | 83 |
| 14 | 1987 | 79 | |
| 15 | 2000 | 76 | |
| 16 | 1988 | 55 | |
| 17 | 2013 | 55 | |
| 18 | 1996 | 55 | |
| 19 | 1987 | 45 | |
| 20 | 2002 | 41 |
About Judith Goodship
Judith Goodship is a scholar working on Molecular Biology, Genetics, Genetics, Surgery and Pulmonary and Respiratory Medicine, having authored 47 papers that have together received 2.8k indexed citations. Recurring topics across this work include Congenital heart defects research (19 papers), Congenital Ear and Nasal Anomalies (6 papers), Neurogenetic and Muscular Disorders Research (4 papers), Tracheal and airway disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetic Syndromes and Imprinting (3 papers), Mitochondrial Function and Pathology (3 papers) and Congenital Heart Disease Studies (3 papers). The work is most often cited by research in Genetics (1.0k citations), Molecular Biology (2.0k citations), Epidemiology (634 citations), Developmental Biology (38 citations) and Pulmonary and Respiratory Medicine (450 citations). Judith Goodship has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include John Burn, Peter Scambler, David I. Wilson, I Cross, Jesse Li‐Ling, R Wadey, Miranda Splitt, David A. Kelly, Kazuo Momma and Atsuyoshi Takao. Their work appears in journals such as Journal of Medical Genetics, Prenatal Diagnosis, Human Genetics, Circulation and British Journal of Dermatology.
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.