Jenny Morton

1.1k total citations
8 papers, 236 citations indexed

About

Jenny Morton is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Jenny Morton has authored 8 papers receiving a total of 236 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Surgery and 2 papers in Molecular Biology. Recurrent topics in Jenny Morton's work include Genomic variations and chromosomal abnormalities (3 papers), RNA modifications and cancer (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Jenny Morton is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), RNA modifications and cancer (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Jenny Morton collaborates with scholars based in United Kingdom, Denmark and Japan. Jenny Morton's co-authors include Sarah Bundey, T. Webb, Fiona MacDonald, Sarah Bullock, Dominic McMullan, Val Davison, Lisa Cooper‐Charles, Chirag Patel, Mark D. Kilby and Dagan Jenkins and has published in prestigious journals such as PLoS Genetics, Journal of Medical Genetics and Ultrasound in Obstetrics and Gynecology.

In The Last Decade

Jenny Morton

8 papers receiving 233 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jenny Morton United Kingdom	6	122	90	68	40	31	8	236
Igor Albizua United States	5	291 2.4×	173 1.9×	198 2.9×	26 0.7×	62 2.0×	7	420
Valerie Drasinover Israel	8	214 1.8×	172 1.9×	114 1.7×	15 0.4×	9 0.3×	8	374
Vera Beyer Germany	9	168 1.4×	181 2.0×	61 0.9×	11 0.3×	14 0.5×	15	318
Tania Radziewic Australia	6	189 1.5×	276 3.1×	98 1.4×	10 0.3×	14 0.5×	8	378
EdmundC. Jenkins United States	9	98 0.8×	65 0.7×	58 0.9×	7 0.2×	24 0.8×	13	237
Matthew F. Hunter Australia	13	273 2.2×	225 2.5×	105 1.5×	11 0.3×	23 0.7×	35	478
Stephen Amoah United States	7	97 0.8×	355 3.9×	48 0.7×	10 0.3×	23 0.7×	14	476
Barbara Wiśniowiecka‐Kowalnik Poland	8	306 2.5×	214 2.4×	155 2.3×	13 0.3×	18 0.6×	11	445
Pia Bernardo Italy	9	91 0.7×	77 0.9×	39 0.6×	20 0.5×	4 0.1×	33	236
Anna Stittrich Germany	6	141 1.2×	123 1.4×	13 0.2×	11 0.3×	30 1.0×	11	285

Countries citing papers authored by Jenny Morton

Since Specialization

Citations

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

Fields of papers citing papers by Jenny Morton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jenny Morton

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

All Works

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8 of 8 papers shown

1.

Kato, Kohji, Seiji Mizuno, Jenny Morton, et al.. (2020). Expanding the phenotype of biallelic loss‐of‐function variants in the NSUN2 gene: Description of four individuals with juvenile cataract, chronic nephritis, or brain anomaly as novel complications. American Journal of Medical Genetics Part A. 185(1). 282–285. 5 indexed citations

2.

Munye, Mustafa M., Anna Dı́az-Font, Louise Ocaka, et al.. (2017). COLEC10 is mutated in 3MC patients and regulates early craniofacial development. PLoS Genetics. 13(3). e1006679–e1006679. 60 indexed citations

3.

Foster, Alison, Hannah Titheradge, & Jenny Morton. (2015). Genetics of learning disability. Paediatrics and Child Health. 25(10). 450–457. 3 indexed citations

4.

Patel, Chirag, et al.. (2011). Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome. European Journal of Human Genetics. 19(6). 634–639. 59 indexed citations

5.

Kilby, Mark D., et al.. (2001). First‐trimester prenatal diagnosis of a familial subtelomeric translocation. Ultrasound in Obstetrics and Gynecology. 17(6). 531–533. 7 indexed citations

6.

Kilby, Mark D., et al.. (1999). A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation. Prenatal Diagnosis. 19(6). 570–574. 27 indexed citations

7.

Morton, Jenny, et al.. (1998). A new lethal autosomal recessive skeletal dysplasia with associated dysmorphic features. Clinical Dysmorphology. 7(2). 109–114. 2 indexed citations

8.

Morton, Jenny, et al.. (1997). Fragile X syndrome is less common than previously estimated.. Journal of Medical Genetics. 34(1). 1–5. 73 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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