Shelagh Joss

746 total citations
6 papers, 59 citations indexed

About

Shelagh Joss is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Shelagh Joss has authored 6 papers receiving a total of 59 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 1 paper in Surgery. Recurrent topics in Shelagh Joss's work include Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Shelagh Joss is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Shelagh Joss collaborates with scholars based in United Kingdom, Denmark and Italy. Shelagh Joss's co-authors include Pamela Magini, Л. П. Назаренко, N. A. Skryabin, А. А. Кашеварова, Claudio Graziano, G. Cara Romeo, Zeynep Tümer, Е. Н. Толмачева, И. Н. Лебедев and Bart Loeys and has published in prestigious journals such as Scientific Reports, European Journal of Human Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Shelagh Joss

5 papers receiving 58 citations

Peers

Countries citing papers authored by Shelagh Joss

Since Specialization

Citations

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

Fields of papers citing papers by Shelagh Joss

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shelagh Joss

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

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	SOX5: Lamb–Shaffer syndrome—A case series further expanding the phenotypic spectrum 2023 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Lucy Hanington, (unknown), Shelagh Joss, Anne Lampe, Isabelle Maystadt, Deborah Osio, Ruth Richardson, (unknown), Francis H. Sansbury, Ingrid Scurr, Helen Stewart, (unknown), Karen Low	3
2	Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients 2022 ·Scientific Reports ·Nanna Dahl Rendtorff, (unknown), Marianne Lodahl, John Tolmie, Catherine McWilliam, Mads Bak, Niels Tommerup, Lusine Nazaryan‐Petersen, Henricus P. M. Kunst, Melanie Wong, Shelagh Joss, Valério Carelli, Lisbeth Tranebjærg	3
3	Transcriptome: from laboratory to clinic room 2019 ·Archives of Disease in Childhood Education & Practice ·(unknown), Shelagh Joss	0
4	Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability 2014 ·Molecular Cytogenetics ·А. А. Кашеварова, Л. П. Назаренко, (unknown), N. A. Skryabin, (unknown), (unknown), Е. Н. Толмачева, (unknown), Pamela Magini, Claudio Graziano, G. Cara Romeo, Shelagh Joss, Zeynep Tümer, И. Н. Лебедев	43
5	Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions 2011 ·European Journal of Human Genetics ·Sarah Vergult, (unknown), Bart Loeys, Stanislas Lyonnet, (unknown), Britt‐Marie Anderlid, (unknown), Shelagh Joss, Geert Mortier, Björn Menten	8
6	Nasopharyngeal teratoma associated with a complex congenital cardiac anomaly 2007 ·Clinical Dysmorphology ·(unknown), Emma Hobson, Shelagh Joss	2

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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