JA Goodship

492 total citations
11 papers, 243 citations indexed

About

JA Goodship is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Epidemiology. According to data from OpenAlex, JA Goodship has authored 11 papers receiving a total of 243 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Pulmonary and Respiratory Medicine and 4 papers in Epidemiology. Recurrent topics in JA Goodship's work include Congenital heart defects research (4 papers), Congenital Heart Disease Studies (3 papers) and Prenatal Screening and Diagnostics (3 papers). JA Goodship is often cited by papers focused on Congenital heart defects research (4 papers), Congenital Heart Disease Studies (3 papers) and Prenatal Screening and Diagnostics (3 papers). JA Goodship collaborates with scholars based in United Kingdom, Netherlands and Switzerland. JA Goodship's co-authors include Jane Wolstenholme, Stephen C. Robson, Stephen N. Sturgiss, Paul Warwicker, Alison L. Webb, John Burn, Jason Rice, Andrew R. Gennery, Andrew McLean‐Tooke and Mary Slatter and has published in prestigious journals such as The American Journal of Human Genetics, Heart and Journal of Medical Genetics.

In The Last Decade

JA Goodship

11 papers receiving 240 citations

Peers

JA Goodship

GENET

EPIDE

PRM

PPCH

N. Logghe Belgium

Suzanne Demczuk France

Milena Simioni Brazil

Társis Paiva Vieira Brazil

Rocío Mena Spain

Margrethe Flesvig Holt Norway

Florence Amblard France

Nicole Corsten‐Janssen Netherlands

L.C. Stranc Canada

Annie Levy‐Mozziconacci France

N. Logghe Belgium

JA Goodship

104 ×0.8

85 ×0.8

GENET

48 ×0.6

EPIDE

26 ×0.4

PRM

37 ×0.7

PPCH

Citations per year, relative to JA Goodship JA Goodship (= 1×) peers N. Logghe

Countries citing papers authored by JA Goodship

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of JA Goodship

This figure shows the co-authorship network connecting the top 25 collaborators of JA Goodship. A scholar is included among the top collaborators of JA Goodship based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with JA Goodship. JA Goodship is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Griffin, Helen, Ana Töpf, Elise Glen, et al.. (2010). Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants. Heart. 96(20). 1651–1655. 46 indexed citations

Engelen, Klaartje van, Ana Töpf, Bernard Keavney, et al.. (2010). 22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia: Table 1. Heart. 96(8). 621–624. 33 indexed citations

Gennery, Andrew R., Mary Slatter, Jason Rice, et al.. (2008). Mutations in CHD7 in patients with CHARGE syndrome cause T–B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome. Clinical & Experimental Immunology. 153(1). 75–80. 76 indexed citations

Goodship, JA, et al.. (1999). A family with X-linked epilepsy mapping to Xp11-Xq13. The American Journal of Human Genetics. 3 indexed citations

Ryan, C. Anthony, JA Goodship, & David I. Wilson. (1998). Reply to letters regarding clinical features of chromosome 22q11 deletion. Journal of Medical Genetics. 35(4). 347–347. 2 indexed citations

Webb, Alison L., et al.. (1998). Prenatal diagnosis of mosaic trisomy 8 with investigations of the extent and origin of trisomic cells. Prenatal Diagnosis. 18(7). 737–741. 1 indexed citations

Webb, Alison L., Stephen N. Sturgiss, Paul Warwicker, et al.. (1996). MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME 2 IN ASSOCIATION WITH CONFINED PLACENTAL MOSAICISM FOR TRISOMY 2 AND SEVERE INTRAUTERINE GROWTH RETARDATION. Prenatal Diagnosis. 16(10). 958–962. 46 indexed citations

Goodship, JA, Sally Ann Lynch, & Jill M. Brown. (1994). Comparison of facial features of DiGeorge syndrome (DGS) due to deletion 10p13-10pter with DGS due to 22q11 deletion. The American Journal of Human Genetics. 55. 4 indexed citations

Goodship, JA, Ann Curtis, Ismael Cross, et al.. (1992). A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.. PubMed. 29(7). 451–4. 26 indexed citations

10.

Scambler, Peter, Stephanie Halford, R Wadey, et al.. (1991). MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES. UCL Discovery (University College London). 4 indexed citations

11.

Wilson, David I., et al.. (1991). IS MONOSOMY FOR THE DIGEORGE LOCUS ON CHROMOSOME-22 RESPONSIBLE FOR ISOLATED HEART MALFORMATIONS. UCL Discovery (University College London). 2 indexed citations

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.

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