Caroline Alby

860 total citations
13 papers, 113 citations indexed

About

Caroline Alby is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Caroline Alby has authored 13 papers receiving a total of 113 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Cell Biology and 5 papers in Genetics. Recurrent topics in Caroline Alby's work include Skin and Cellular Biology Research (4 papers), Fetal and Pediatric Neurological Disorders (3 papers) and Hedgehog Signaling Pathway Studies (2 papers). Caroline Alby is often cited by papers focused on Skin and Cellular Biology Research (4 papers), Fetal and Pediatric Neurological Disorders (3 papers) and Hedgehog Signaling Pathway Studies (2 papers). Caroline Alby collaborates with scholars based in France, United Kingdom and Hungary. Caroline Alby's co-authors include Michel Vekemans, Tania Attié‐Bitach, Sophie Thomas, Nadia Elkhartoufi, Bettina Bessières, Valérie Malan, S. Hadj‐Rabia, Férechté Encha‐Razavi, Lucile Boutaud and Amale Ichkou and has published in prestigious journals such as British Journal of Dermatology, Journal of Medical Genetics and Experimental Dermatology.

In The Last Decade

Caroline Alby

12 papers receiving 110 citations

Peers

Caroline Alby
Elham Al Mardawi Saudi Arabia
Nada Alsahan Saudi Arabia
Kai Muru Estonia
Danielle R. Little United States
Christopher Hugge United States
Elham Al Mardawi Saudi Arabia
Caroline Alby
Citations per year, relative to Caroline Alby Caroline Alby (= 1×) peers Elham Al Mardawi

Countries citing papers authored by Caroline Alby

Since Specialization
Citations

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

Fields of papers citing papers by Caroline Alby

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Alby

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

All Works

13 of 13 papers shown
1.
Fertitta, L., Fabienne Charbit‐Henrion, Stéphanie Leclerc‐Mercier, et al.. (2022). Bothnian Palmoplantar Keratoderma: Further Delineation of the Associated Phenotype. Genes. 13(12). 2360–2360. 2 indexed citations
2.
Chartier, Suzanne, Lucile Boutaud, Caroline Alby, et al.. (2021). Prenatal‐onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation. Birth Defects Research. 113(18). 1324–1332. 2 indexed citations
3.
Nagy, Nándor, Conor J. McCann, Dipa Natarajan, et al.. (2021). TALPID3/KIAA0586 Regulates Multiple Aspects of Neuromuscular Patterning During Gastrointestinal Development in Animal Models and Human. Frontiers in Molecular Neuroscience. 14. 757646–757646. 3 indexed citations
4.
Kettunen, K, Outi Elomaa, Elísabet Einarsdóttir, et al.. (2020). Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma. Acta Dermato Venereologica. 100(4). 0–0. 2 indexed citations
5.
Bellon, N., S. Hadj‐Rabia, Florence Moulin, et al.. (2020). The challenging management of a series of 43 infants with Netherton syndrome: unexpected complications and novel mutations*. British Journal of Dermatology. 184(3). 532–537. 13 indexed citations
6.
Alby, Caroline, Éric Gabison, Serge Doan, et al.. (2019). P63‐related disorders: Dermatological characteristics in 22 patients. Experimental Dermatology. 28(10). 1190–1195. 10 indexed citations
7.
Chartier, Suzanne, Caroline Alby, Lucile Boutaud, et al.. (2018). A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern. Birth Defects Research. 110(7). 598–602. 7 indexed citations
8.
Boutaud, Lucile, Bettina Bessières, Maryse Bonnière, et al.. (2017). Fetal Cerebral Ventricular Dilatation: Etiopathogenic Study of 130 Observations. Birth Defects Research. 109(19). 1586–1595. 2 indexed citations
9.
Alby, Caroline, Valérie Malan, Lucile Boutaud, et al.. (2015). Clinical, genetic and neuropathological findings in a series of 138 fetuses with a corpus callosum malformation. Birth Defects Research Part A Clinical and Molecular Teratology. 106(1). 36–46. 30 indexed citations
10.
Alby, Caroline, Bettina Bessières, Éric Bieth, et al.. (2013). Contiguous gene deletion of TBX5 and TBX3 leads to a varible phenotype with combined features of holt‐oram and ulnar‐mammary syndromes. American Journal of Medical Genetics Part A. 161(7). 1797–1802. 9 indexed citations
11.
Putoux, Audrey, Sheela Nampoothiri, Nicole Laurent, et al.. (2012). Novel KIF7 mutations extend the phenotypic spectrum of acrocallosal syndrome. Journal of Medical Genetics. 49(11). 713–720. 26 indexed citations
13.
Picone, Olivier, Caroline Alby, R. Frydman, & Xavier Mariette. (2006). Syndrome de Gougerot-Sjögren en gynécologie obstétrique. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 35(2). 169–175. 7 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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