S. Goodburn

541 total citations
12 papers, 336 citations indexed

About

S. Goodburn is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience. According to data from OpenAlex, S. Goodburn has authored 12 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in S. Goodburn's work include Mitochondrial Function and Pathology (3 papers), Prenatal Screening and Diagnostics (3 papers) and Genetic Neurodegenerative Diseases (3 papers). S. Goodburn is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Prenatal Screening and Diagnostics (3 papers) and Genetic Neurodegenerative Diseases (3 papers). S. Goodburn collaborates with scholars based in United Kingdom, India and South Sudan. S. Goodburn's co-authors include David C. Rubinsztein, Judy Rubinsztein, A J Holland, Howard Cuckle, M.A. Ferguson‐Smith, Peter J. McKenna, Malcolm Ferguson-Smith, P. J. D. Milton, James R. Yates and Ann Kershaw and has published in prestigious journals such as Journal of Neurology Neurosurgery & Psychiatry, Journal of Medical Genetics and Prenatal Diagnosis.

In The Last Decade

S. Goodburn

11 papers receiving 320 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
S. Goodburn United Kingdom	8	159	139	100	91	67	12	336
Po‐Cheng Hung Taiwan	12	125 0.8×	91 0.7×	39 0.4×	192 2.1×	31 0.5×	38	414
Michiko Torio Japan	10	55 0.3×	23 0.2×	75 0.8×	46 0.5×	41 0.6×	31	256
P. Boccella Italy	12	166 1.0×	77 0.6×	42 0.4×	149 1.6×	14 0.2×	13	456
Mehmet Canpolat Türkiye	12	97 0.6×	17 0.1×	47 0.5×	81 0.9×	16 0.2×	45	348
Isabelle Simon France	9	137 0.9×	48 0.3×	19 0.2×	17 0.2×	73 1.1×	15	286
Yuma Kitase United States	10	214 1.3×	28 0.2×	44 0.4×	19 0.2×	25 0.4×	28	337
R. Riel-Romero United States	10	65 0.4×	23 0.2×	20 0.2×	51 0.6×	16 0.2×	27	225
Morris W. Levinsohn United States	10	123 0.8×	45 0.3×	50 0.5×	66 0.7×	19 0.3×	14	311
Sarah Glatter Austria	10	115 0.7×	26 0.2×	32 0.3×	70 0.8×	35 0.5×	17	254
Rui Zhong China	11	106 0.7×	36 0.3×	47 0.5×	53 0.6×	21 0.3×	35	318

Countries citing papers authored by S. Goodburn

Since Specialization

Citations

This map shows the geographic impact of S. Goodburn'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 S. Goodburn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Goodburn more than expected).

Fields of papers citing papers by S. Goodburn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. Goodburn. 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 S. Goodburn. The network helps show where S. Goodburn may publish in the future.

Co-authorship network of co-authors of S. Goodburn

This figure shows the co-authorship network connecting the top 25 collaborators of S. Goodburn. A scholar is included among the top collaborators of S. Goodburn 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 S. Goodburn. S. Goodburn is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Lees, C., et al.. (2005). Prospective audit of a one-centre combined nuchal translucency and triple test programme for the detection of trisomy 21. Prenatal Diagnosis. 25(6). 465–469. 8 indexed citations

Cuckle, Howard, et al.. (2004). Age‐standardisation when target setting and auditing performance of Down syndrome screening programmes. Prenatal Diagnosis. 24(11). 851–856. 42 indexed citations

Jolly, Meenakshi, S. Goodburn, P. Cox, & Pamela Loughna. (2002). Congenital nephropathy and ventriculomegaly: a report of four cases. Prenatal Diagnosis. 23(1). 48–51. 4 indexed citations

Marteau, Theresa M., et al.. (2000). Numbers or words? A randomised controlled trial of presenting screen negative results to pregnant women. Journal of Medical Genetics. 37. 2 indexed citations

Rubinsztein, Judy, David C. Rubinsztein, S. Goodburn, & A J Holland. (1998). Apathy and hypersomnia are common features of myotonic dystrophy. Journal of Neurology Neurosurgery & Psychiatry. 64(4). 510–515. 91 indexed citations

Rubinsztein, Judy, David C. Rubinsztein, Peter J. McKenna, S. Goodburn, & A J Holland. (1997). Mild myotonic dystrophy is associated with memory impairment in the context of normal general intelligence.. Journal of Medical Genetics. 34(3). 229–233. 43 indexed citations

Rubinsztein, David C., Jayne Leggo, S. Goodburn, et al.. (1996). Genetic association between monoamine oxidase A microsatellite and RFLP alleles and bipolar affective disorder. Psychiatric Genetics. 6(3). 151–151.

Jain, Sanjeev, Jayne Leggo, Lynn E. DeLisi, et al.. (1996). Analysis of thirteen trinucleotide repeat loci as candidate genes for schizophrenia and bipolar disorder. Psychiatric Genetics. 6(3). 153–153. 2 indexed citations

Scott, Rosemary & S. Goodburn. (1995). Potter's syndrome in the second trimester—prenatal screening and pathological findings in 60 cases of oligohydramnios sequence. Prenatal Diagnosis. 15(6). 519–525. 12 indexed citations

10.

Goodburn, S., James R. Yates, P R Raggatt, et al.. (1994). Second‐trimester maternal serum screening using alpha‐fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: Experience of a regional programme. Prenatal Diagnosis. 14(5). 391–402. 83 indexed citations

11.

Rubinsztein, David C., Jayne Leggo, S. Goodburn, et al.. (1994). Study of the Huntington's disease (HD) gene CAG repeats in schizophrenic patients shows overlap of the normal and HD affected ranges but absence of correlation with schizophrenia.. Journal of Medical Genetics. 31(9). 690–693. 19 indexed citations

12.

Cuckle, Howard, et al.. (1990). Measurement of activity of urea resistant neutrophil alkaline phosphatase as an antenatal screening test for Down's syndrome.. BMJ. 301(6759). 1024–1026. 30 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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