Lucy R. Osborne

5.9k total citations
69 papers, 3.1k citations indexed

About

Lucy R. Osborne is a scholar working on Developmental Neuroscience, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Lucy R. Osborne has authored 69 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Developmental Neuroscience, 31 papers in Molecular Biology and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Lucy R. Osborne's work include Williams Syndrome Research (35 papers), Congenital heart defects research (15 papers) and Nuclear Receptors and Signaling (8 papers). Lucy R. Osborne is often cited by papers focused on Williams Syndrome Research (35 papers), Congenital heart defects research (15 papers) and Nuclear Receptors and Signaling (8 papers). Lucy R. Osborne collaborates with scholars based in Canada, United States and United Kingdom. Lucy R. Osborne's co-authors include Carolyn Β. Mervis, Stephen W. Scherer, George Santis, Barbara R. Pober, Colleen A. Morris, M.E. Hodson, Richard A. Knight, Edwin J. Young, Lap‐Chee Tsui and Ariane Mandel and has published in prestigious journals such as Science, New England Journal of Medicine and The Lancet.

In The Last Decade

Lucy R. Osborne

69 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lucy R. Osborne Canada 32 1.3k 1.1k 931 385 300 69 3.1k
Aparna Bhaduri United States 27 2.6k 2.0× 580 0.5× 442 0.5× 104 0.3× 296 1.0× 58 4.1k
Anne Schaefer United States 22 1.7k 1.3× 181 0.2× 553 0.6× 350 0.9× 324 1.1× 34 4.3k
Giuseppe Merla Italy 35 1.6k 1.3× 326 0.3× 746 0.8× 142 0.4× 168 0.6× 97 2.9k
Robert Lachmann Germany 19 1.3k 1.0× 524 0.5× 256 0.3× 533 1.4× 275 0.9× 39 2.9k
Takumi Takizawa Japan 20 1.5k 1.2× 539 0.5× 345 0.4× 102 0.3× 328 1.1× 68 2.2k
Abdel G. Elkahloun United States 26 1.5k 1.1× 216 0.2× 433 0.5× 157 0.4× 176 0.6× 39 3.4k
Anna Falk Sweden 30 2.0k 1.5× 533 0.5× 328 0.4× 65 0.2× 588 2.0× 79 3.2k
François D. Boussin France 33 2.0k 1.6× 668 0.6× 157 0.2× 174 0.5× 301 1.0× 93 3.6k
Paul R. Borghesani United States 17 1.0k 0.8× 409 0.4× 260 0.3× 139 0.4× 553 1.8× 25 3.1k
Angelo Selicorni Italy 29 2.5k 2.0× 173 0.2× 1.8k 2.0× 125 0.3× 191 0.6× 176 3.8k

Countries citing papers authored by Lucy R. Osborne

Since Specialization
Citations

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

Fields of papers citing papers by Lucy R. Osborne

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lucy R. Osborne. 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 Lucy R. Osborne. The network helps show where Lucy R. Osborne may publish in the future.

Co-authorship network of co-authors of Lucy R. Osborne

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

All Works

20 of 20 papers shown
1.
Tobon, Alejandro, Reinald Shyti, Carlo Emanuele Villa, et al.. (2023). GTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders. Science Advances. 9(48). eadh2726–eadh2726. 15 indexed citations
2.
Mervis, Carolyn Β., et al.. (2023). DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number. npj Genomic Medicine. 8(1). 25–25. 2 indexed citations
3.
Yin, Yue, Carolyn Β. Mervis, Colleen A. Morris, et al.. (2021). Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype. Orphanet Journal of Rare Diseases. 16(1). 6–6. 4 indexed citations
4.
Deurloo, Marielle, Ekaterina Turlova, Wenliang Chen, et al.. (2018). Transcription Factor 2I Regulates Neuronal Development via TRPC3 in 7q11.23 Disorder Models. Molecular Neurobiology. 56(5). 3313–3325. 14 indexed citations
5.
Fernandes, Darren, Jacob Ellegood, Rand Askalan, et al.. (2017). Spatial gene expression analysis of neuroanatomical differences in mouse models. NeuroImage. 163. 220–230. 12 indexed citations
6.
Zhu, Dan, Li Xie, Youhou Kang, et al.. (2017). Syntaxin 2 Acts as Inhibitory SNARE for Insulin Granule Exocytosis. Diabetes. 66(4). 948–959. 18 indexed citations
7.
Liang, Tao, Tairan Qin, Li Xie, et al.. (2016). New Roles of Syntaxin-1A in Insulin Granule Exocytosis and Replenishment. Journal of Biological Chemistry. 292(6). 2203–2216. 29 indexed citations
8.
Morris, Colleen A., Carolyn Β. Mervis, Omar Abdul‐Rahman, et al.. (2015). 7q11.23 Duplication syndrome: Physical characteristics and natural history. American Journal of Medical Genetics Part A. 167(12). 2916–2935. 63 indexed citations
9.
Mervis, Carolyn Β., Bonnie Klein-Tasman, Shelley L. Velleman, et al.. (2015). Children with 7q11.23 duplication syndrome: Psychological characteristics. American Journal of Medical Genetics Part A. 167(7). 1436–1450. 47 indexed citations
10.
Butcher, Darci T., Rajat Singhania, Carolyn Β. Mervis, et al.. (2015). Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23. The American Journal of Human Genetics. 97(2). 216–227. 49 indexed citations
11.
Flenniken, Ann M., Celeste Owen, Irina Voronov, et al.. (2011). The V–ATPase a3 subunit mutation R740S is dominant negative and results in osteopetrosis in mice. Journal of Bone and Mineral Research. 26(7). 1484–1493. 30 indexed citations
12.
Hughes, Michael R., Nicole Anderson, Steven Maltby, et al.. (2010). A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis. Experimental Hematology. 39(3). 305–320.e2. 23 indexed citations
13.
Pikor, Natalia, Georgina Galicia, Lesley A. Ward, et al.. (2010). Substrain Differences Reveal Novel Disease-Modifying Gene Candidates That Alter the Clinical Course of a Rodent Model of Multiple Sclerosis. The Journal of Immunology. 184(6). 3174–3185. 25 indexed citations
14.
Young, Edwin J., Tatiana V. Lipina, Ariane Mandel, et al.. (2007). Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1‐targeted mice. Genes Brain & Behavior. 7(2). 224–234. 83 indexed citations
15.
Scherer, Stephen W., Karen W. Gripp, Linda K. Nicholson, et al.. (2005). Observation of a parental inversion variant in a rare Williams–Beuren syndrome family with two affected children. Human Genetics. 117(4). 383–388. 34 indexed citations
16.
Gruszka, Alicja, Rifat Hamoudi, Lucy R. Osborne, Estella Matutes, & Daniel Catovsky. (2002). Deletion mapping on the long arm of chromosome 7 in splenic lymphoma with villous lymphocytes. Genes Chromosomes and Cancer. 36(1). 57–69. 26 indexed citations
17.
Metcalfe, Kay, Leslie Smoot, Pascal McKeown, et al.. (2000). Elastin: mutational spectrum in supravalvular aortic stenosis. European Journal of Human Genetics. 8(12). 955–963. 110 indexed citations
18.
Osborne, Lucy R., Tracey Campbell, A. Daradich, Stephen W. Scherer, & Lap‐Chee Tsui. (1999). Identification of a Putative Transcription Factor Gene (WBSCR11) That Is Commonly Deleted in Williams–Beuren Syndrome. Genomics. 57(2). 279–284. 53 indexed citations
19.
Jadayel, Dalal, Lucy R. Osborne, Lionel Coignet, et al.. (1998). The BCL7 gene family: deletion of BCL7B in Williams syndrome. Gene. 224(1-2). 35–44. 38 indexed citations
20.
Munkonge, Felix M., Lucy R. Osborne, Duncan M. Geddes, & Eric W.F.W. Alton. (1994). Lack of inhibition by dideoxy-forskolin and verapamil of DIDS-sensitive volume-activated Cl− secretion in human squamous lung carcinoma epithelial cells. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1224(3). 342–348. 6 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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