Celia Moss

10.9k total citations · 1 hit paper
135 papers, 4.2k citations indexed

About

Celia Moss is a scholar working on Genetics, Cell Biology and Molecular Biology. According to data from OpenAlex, Celia Moss has authored 135 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Genetics, 46 papers in Cell Biology and 40 papers in Molecular Biology. Recurrent topics in Celia Moss's work include Skin and Cellular Biology Research (37 papers), Genetic and rare skin diseases. (28 papers) and Hedgehog Signaling Pathway Studies (12 papers). Celia Moss is often cited by papers focused on Skin and Cellular Biology Research (37 papers), Genetic and rare skin diseases. (28 papers) and Hedgehog Signaling Pathway Studies (12 papers). Celia Moss collaborates with scholars based in United Kingdom, United States and Germany. Celia Moss's co-authors include Peter S. Friedmann, Sam Shuster, Judy M. Simpson, Meena Upadhyaya, N. H. Thomas, Harry Willshaw, Christoph Steiger, M. Gleeson, D. Gareth Evans and Richard Towers and has published in prestigious journals such as The Lancet, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Celia Moss

131 papers receiving 4.0k 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.

Guidelines for the diagnosis and management of individuals with neurofibromatosis 1

2006 652 citations Celia Moss, Meena Upadhyaya et al. profile →

Peers

Countries citing papers authored by Celia Moss

Since Specialization

Citations

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

Fields of papers citing papers by Celia Moss

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Celia Moss

This figure shows the co-authorship network connecting the top 25 collaborators of Celia Moss. A scholar is included among the top collaborators of Celia Moss 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 Celia Moss. Celia Moss 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

#	Work	Indexed citations
1	Thermally Robust 1D Cu(I) Phosphonate Coordination Polymer Exhibiting Enhanced Proton Conductivity via Humidity‐Driven Pathways 2025 ·Zeitschrift für anorganische und allgemeine Chemie ·(unknown), (unknown), Celia Moss, Biswajit Bhattacharya, Franziska Emmerling	0
2	Classification of aplasia cutis congenita: a 25‐year review of cases presenting to a tertiary paediatric dermatology department 2020 ·Clinical and Experimental Dermatology ·(unknown), Malobi Ogboli, Celia Moss	9
3	Happle–Tinschert, Curry–Jones and segmental basal cell naevus syndromes, overlapping disorders caused by somatic mutations in hedgehog signalling genes: the mosaic hedgehog spectrum 2019 ·British Journal of Dermatology ·(unknown), Yan Zhou, (unknown), (unknown), Isabel Colmenero, Stephen R.F. Twigg, Celia Moss	8
4	Mosaic SMO mutation in a patient with linear basal follicular hamartomas confirms Happle-Tinschert syndrome as a variant of Curry-Jones syndrome 2018 ·British Journal of Dermatology ·(unknown), (unknown), Celia Moss	1
5	Topical therapy in atopic dermatitis in children 2016 ·Indian Journal of Dermatology ·Celia Moss, (unknown)	22
6	Steroid sulfatase contributes to systemic androgen activation in pre-pubertal boys: lessons from steroid sulfatase deficiency 2014 ·Endocrine Abstracts ·Jan Idkowiak, Angela E. Taylor, Donna O’Neil, (unknown), Raymon Vijzelaar, Renuka Dias, Rakesh Amin, Timothy Barrett, (unknown), Cedric Shackleton, Celia Moss, Wiebke Arlt	1
7	Intrafamilial phenotypic variability of dominant and recessive dystrophic epidermolysis bullosa resulting from a novel glycine substitution, p.G1770S, in type VII collagen. 2007 ·British Journal of Dermatology ·(unknown), John A. McGrath, (unknown), Celia Moss	1
8	EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype–phenotype correlation? 2007 ·American Journal of Medical Genetics Part A ·Kenneth N. Maclean, (unknown), Elizabeth Gilmour, Mark G. Taylor, Hans Scheffer, Nicole Graf, Grahame Smith, Ella Onikul, Hans van Bokhoven, Celia Moss, Lesley C. Adès	10
9	The cardio-facio-cutaneous syndrome: a manifestation of the Noonan syndrome? 2006 ·British Journal of Dermatology ·Ken Ward, Celia Moss, C McKeown	6
10	Epidermal naevus in Proteus syndrome showing loss of heterozygosity for an inherited PTEN mutation 2006 ·British Journal of Dermatology ·(unknown), (unknown), Theresa Cole, Stewart J. Payne, Dominique Fricker, Celia Moss	37
11	Tuberculous cold abscess resembling a lymphatic malformation 2005 ·Clinical and Experimental Dermatology ·S. Laube, (unknown), Dhruv Parikh, Celia Moss	2
12	Gonosomal Mosaicism for a Nonsense Mutation (R1947X) in the NF1 Gene in Segmental Neurofibromatosis Type 1 2005 ·Journal of Investigative Dermatology ·Claudia Consoli, Celia Moss, Stuart A. Green, (unknown), D.N. Cooper, Meena Upadhyaya	44
13	Two families with Greither's syndrome caused by a keratin 1 mutation 2005 ·Journal of the American Academy of Dermatology ·J. E. Gach, Colin S. Munro, E. Birgitte Lane, Neil Wilson, Celia Moss	12
14	Evolving lesions of phakomatosis pigmentokeratotica 2004 ·Journal of the American Academy of Dermatology ·(unknown), Celia Moss	3
15	Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome 2004 ·Journal of Investigative Dermatology ·G H S Ashton, W.H. Irwin McLean, Andrew P. South, Noritaka Oyama, Frances J.D. Smith, (unknown), (unknown), David J. Atherton, Catherine Harwood, Irene M. Leigh, Celia Moss, Biagio Didona, Giovanna Zambruno, Annalisa Patrizi, Robin A.J. Eady, John A. McGrath	65
16	Neurocutaneous Melanosis with Leptomeningeal Melanoma 2001 ·Pediatric Neurosurgery ·(unknown), (unknown), Celia Moss, Richard G. Grundy, (unknown)	12
17	Hereditary bullous disorders 1995 ·Current Paediatrics ·Celia Moss	6
18	What is segmental neurofibromatosis? 1994 ·British Journal of Dermatology ·Celia Moss, (unknown)	55
19	Susceptibility and amplification of sensitivity in contact dermatitis. 1985 ·PubMed Central ·Celia Moss, Peter S. Friedmann, Sam Shuster, Judy M. Simpson	82
20	Antipyrine clearance in psoriasis. 1981 ·BMJ ·P. H. Chapman, (unknown), M. D. Rawlins, Celia Moss, Sam Shuster	11

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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