Judith A. Goodship

11.1k total citations · 1 hit paper
64 papers, 6.0k citations indexed

About

Judith A. Goodship is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Judith A. Goodship has authored 64 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 25 papers in Genetics and 22 papers in Immunology. Recurrent topics in Judith A. Goodship's work include Complement system in diseases (20 papers), Genetic and Kidney Cyst Diseases (15 papers) and Hedgehog Signaling Pathway Studies (12 papers). Judith A. Goodship is often cited by papers focused on Complement system in diseases (20 papers), Genetic and Kidney Cyst Diseases (15 papers) and Hedgehog Signaling Pathway Studies (12 papers). Judith A. Goodship collaborates with scholars based in United Kingdom, United States and Spain. Judith A. Goodship's co-authors include Timothy H.J. Goodship, Víctor L. Ruiz‐Pérez, Mark O’Driscoll, C. Geoffrey Woods, Penny A. Jeggo, Anna Richards, Roy Ward, Yves Pirson, Rosemary L. Donne and Paul Warwicker and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Judith A. Goodship

64 papers receiving 5.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A splicing mutation affecting expression of ataxia–telangiectasia and Rad3–related protein (ATR) results in Seckel syndrome

2003 595 citations Víctor L. Ruiz‐Pérez, Judith A. Goodship et al. profile →

Peers

Judith A. Goodship

IMMUN

GENET

NEPHR

HEMAT

Jordan A. Kreidberg United States

Yanick J. Crow United Kingdom

Carol A. Wise United States

J.G. Seidman United States

E. D. Albert Germany

Peter D. Turnpenny United Kingdom

Philippe Duquesnoy France

Lies H. Hoefsloot Netherlands

Stacie M. Anderson United States

Stephen J. Richards United Kingdom

Jordan A. Kreidberg United States

Judith A. Goodship

6.4k ×2.2

753 ×0.3

IMMUN

1.8k ×1.0

GENET

1.3k ×1.1

NEPHR

435 ×0.4

HEMAT

Citations per year, relative to Judith A. Goodship Judith A. Goodship (= 1×) peers Jordan A. Kreidberg

Countries citing papers authored by Judith A. Goodship

Since Specialization

Citations

This map shows the geographic impact of Judith A. 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 A. 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 A. Goodship more than expected).

Fields of papers citing papers by Judith A. Goodship

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judith A. 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 A. Goodship. The network helps show where Judith A. Goodship may publish in the future.

Co-authorship network of co-authors of Judith A. Goodship

This figure shows the co-authorship network connecting the top 25 collaborators of Judith A. Goodship. A scholar is included among the top collaborators of Judith A. 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 Judith A. Goodship. Judith A. 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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20 of 20 papers shown

Caparrós‐Martín, José A., Alessandro De Luca, François Cartault, et al.. (2015). Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium. Human Molecular Genetics. 24(14). 4126–4137. 42 indexed citations

Glen, Elise, Ana Töpf, Darroch Hall, et al.. (2012). Nonsynonymous variants in theSMAD6gene predispose to congenital cardiovascular malformation. Human Mutation. 33(4). 720–727. 87 indexed citations

Twigg, Stephen R.F., Dagan Jenkins, C.D.O. Cooper, et al.. (2012). Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization. The American Journal of Human Genetics. 91(5). 897–905. 56 indexed citations

Siddle, Katherine J., Judith A. Goodship, Bernard Keavney, & Mauro Santibanez‐Koref. (2011). Bases adjacent to mononucleotide repeats show an increased single nucleotide polymorphism frequency in the human genome. Bioinformatics. 27(7). 895–898. 13 indexed citations

Pacheco, María, Eulalia Valencia, José A. Caparrós‐Martín, et al.. (2011). Evc works in chondrocytes and osteoblasts to regulate multiple aspects of growth plate development in the appendicular skeleton and cranial base. Bone. 50(1). 28–41. 35 indexed citations

Cordell, Heather J., Rebecca Darlay, Pimphen Charoen, et al.. (2009). Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux. Journal of the American Society of Nephrology. 21(1). 113–123. 42 indexed citations

Ruiz‐Pérez, Víctor L. & Judith A. Goodship. (2009). Ellis–van Creveld syndrome and Weyers acrodental dysostosis are caused by cilia‐mediated diminished response to hedgehog ligands. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 151C(4). 341–351. 86 indexed citations

Blom, Anna M., Matthew Edey, Martha Diaz-Torres, et al.. (2008). A Novel Non-Synonymous Polymorphism (p.Arg240His) in C4b-Binding Protein Is Associated with Atypical Hemolytic Uremic Syndrome and Leads to Impaired Alternative Pathway Cofactor Activity. The Journal of Immunology. 180(9). 6385–6391. 48 indexed citations

Fantes, Judith A., Jacqueline Ramsay, Dian Donnai, et al.. (2008). FISH Mapping of De Novo Apparently Balanced Chromosome Rearrangements Identifies Characteristics Associated with Phenotypic Abnormality. The American Journal of Human Genetics. 82(4). 916–926. 31 indexed citations

10.

Kavanagh, David, Anna Richards, Marina Noris, et al.. (2007). Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome. Molecular Immunology. 45(1). 95–105. 119 indexed citations

11.

Pan‐Hammarström, Qiang, Aleksi Lähdesmäki, Yaofeng Zhao, et al.. (2006). Disparate roles of ATR and ATM in immunoglobulin class switch recombination and somatic hypermutation. The Journal of Experimental Medicine. 203(1). 99–110. 39 indexed citations

12.

Crow, Yanick J., Judith A. Goodship, Chris Wright, et al.. (2006). A newly recognized, likely autosomal recessive syndrome comprising agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis, and other features. American Journal of Medical Genetics Part A. 140A(11). 1131–1135. 1 indexed citations

13.

Heinen, Stefan, Pilar Sánchez‐Corral, Michael S. Jackson, et al.. (2006). De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome. Human Mutation. 27(3). 292–293. 125 indexed citations

14.

Richards, Anna, Judith A. Goodship, & Timothy H.J. Goodship. (2002). The genetics and pathogenesis of haemolytic uraemic syndrome and thrombotic thrombocytopenic purpura. Current Opinion in Nephrology & Hypertension. 11(4). 431–435. 31 indexed citations

15.

Richards, Anna, M. Buddles, Rosemary L. Donne, et al.. (2001). Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell Recognition. The American Journal of Human Genetics. 68(2). 485–490. 254 indexed citations

16.

Wolstenholme, Jackie, et al.. (2001). Maternal uniparental heterodisomy for chromosome 2: detection through ‘atypical’ maternal AFP/hCG levels, with an update on a previous case. Prenatal Diagnosis. 21(10). 813–817. 37 indexed citations

17.

Warwicker, Paul, Timothy H.J. Goodship, Rosemary L. Donne, et al.. (1998). Genetic studies into inherited and sporadic hemolytic uremic syndrome. Kidney International. 53(4). 836–844. 373 indexed citations

18.

Wolstenholme, Jackie, et al.. (1992). Prenatal detection of multiple copies of a familial supernumerary marker chromosome. Prenatal Diagnosis. 12(12). 1067–1071. 16 indexed citations

19.

Scambler, Peter, David A. Kelly, Elizabeth Lindsay, et al.. (1992). Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus. The Lancet. 339(8802). 1138–1139. 333 indexed citations

20.

Malcolm, S, Geneviève de Saint Basile, Benoı̂t Arveiler, et al.. (1987). Close linkage of random DNA fragments from Xq 21.3–22 to X-linked agammaglobulinaemia (XLA). Human Genetics. 77(2). 172–174. 50 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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