Anna Buj‐Bello

3.8k total citations · 1 hit paper
27 papers, 2.9k citations indexed

About

Anna Buj‐Bello is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Anna Buj‐Bello has authored 27 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 12 papers in Cell Biology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Anna Buj‐Bello's work include Cellular transport and secretion (11 papers), Muscle Physiology and Disorders (10 papers) and Nerve injury and regeneration (6 papers). Anna Buj‐Bello is often cited by papers focused on Cellular transport and secretion (11 papers), Muscle Physiology and Disorders (10 papers) and Nerve injury and regeneration (6 papers). Anna Buj‐Bello collaborates with scholars based in France, United States and United Kingdom. Anna Buj‐Bello's co-authors include Alun M. Davies, Arnon Rosenthal, Vladimir L. Buchman, Antony Horton, Luzia G. P. Piñón, Jocelyn Laporte, Jean‐Louis Mandel, Donna M. Stone, Heidi Phillips and Mark W. Moore and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Neuron.

In The Last Decade

Anna Buj‐Bello

26 papers receiving 2.8k 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.

Characterization of a multicomponent receptor for GDNF

1996 893 citations James Treanor, Laurie J. Goodman et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anna Buj‐Bello France	21	1.7k	1.3k	719	637	346	27	2.9k
Stefan Britsch Germany	22	2.1k 1.2×	1.1k 0.9×	521 0.7×	447 0.7×	414 1.2×	46	3.6k
Horst H. Simon Germany	23	2.3k 1.4×	1.4k 1.1×	518 0.7×	363 0.6×	370 1.1×	30	3.6k
Quenten Schwarz Australia	27	2.1k 1.2×	809 0.6×	246 0.3×	434 0.7×	220 0.6×	65	3.1k
Stefano C. Previtali Italy	36	1.8k 1.1×	2.1k 1.7×	437 0.6×	941 1.5×	142 0.4×	104	4.0k
Hui Z. Sheng China	21	2.6k 1.5×	797 0.6×	449 0.6×	246 0.4×	744 2.2×	39	3.6k
Victor F. Rafuse Canada	30	1.6k 1.0×	1.2k 1.0×	674 0.9×	249 0.4×	121 0.3×	43	2.9k
Joshua R. Sanes United States	14	1.9k 1.1×	1.3k 1.0×	283 0.4×	734 1.2×	196 0.6×	15	2.9k
Lucien J. Houenou United States	25	1.3k 0.8×	1.7k 1.3×	953 1.3×	235 0.4×	177 0.5×	41	3.0k
Clas B. Johansson Sweden	19	2.1k 1.2×	1.6k 1.3×	2.5k 3.4×	306 0.5×	369 1.1×	22	4.4k
Tetsuji Mori Japan	26	1.6k 1.0×	1.1k 0.9×	1.3k 1.8×	513 0.8×	274 0.8×	66	3.2k

Countries citing papers authored by Anna Buj‐Bello

Since Specialization

Citations

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

Fields of papers citing papers by Anna Buj‐Bello

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna Buj‐Bello. 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 Anna Buj‐Bello. The network helps show where Anna Buj‐Bello may publish in the future.

Co-authorship network of co-authors of Anna Buj‐Bello

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Buj‐Bello. A scholar is included among the top collaborators of Anna Buj‐Bello 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 Anna Buj‐Bello. Anna Buj‐Bello 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

Lawlor, Michael W., Marissa G. Viola, Hui Meng, et al.. (2014). Differential Muscle Hypertrophy Is Associated with Satellite Cell Numbers and Akt Pathway Activation Following Activin Type IIB Receptor Inhibition in Mtm1 p.R69C Mice. American Journal Of Pathology. 184(6). 1831–1842. 26 indexed citations

Goddard, Melissa, Alan H. Beggs, Anna Buj‐Bello, et al.. (2014). Gait characteristics in a canine model of X-linked myotubular myopathy. Journal of the Neurological Sciences. 346(1-2). 221–226. 9 indexed citations

Lawlor, Michael W., Dustin Armstrong, Marissa G. Viola, et al.. (2013). Enzyme replacement therapy rescues weakness and improves muscle pathology in mice with X-linked myotubular myopathy. Human Molecular Genetics. 22(8). 1525–1538. 54 indexed citations

Sarwal, Aarti, et al.. (2013). Neuromuscular Ultrasound for Diaphragm Assessment Following Gene Replacement Therapy in a Canine Model of X-Linked Myotubular Myopathy (XLMTM) (P05.083). Neurology. 80(7_supplement). 1 indexed citations

Sarwal, Aarti, et al.. (2013). A Novel Method for Targeting Intramuscular Diaphragm Injections Using Ultrasound and Electromyography (P02.220). Neurology. 80(7_supplement). 1 indexed citations

Pierson, Christopher R., Andrew Snyder, Jordan T. Gladman, et al.. (2011). Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotype. Human Molecular Genetics. 21(4). 811–825. 53 indexed citations

McClelland, Verity M., Thomas Cullup, István Bódi, et al.. (2010). Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy. American Journal of Medical Genetics Part A. 152A(3). 741–747. 35 indexed citations

Al‐Qusairi, Lama, Norbert Weiss, Anne Toussaint, et al.. (2009). T-tubule disorganization and defective excitation-contraction coupling in muscle fibers lacking myotubularin lipid phosphatase. Proceedings of the National Academy of Sciences. 106(44). 18763–18768. 142 indexed citations

Weiss, Norbert, Lama Al‐Qusairi, Bruno Allard, et al.. (2009). Impaired Sarcoplasmic Reticulum Calcium Release In Skeletal Muscle Fibers From Myotubularin-Deficient Mice. Biophysical Journal. 96(3). 10a–10a.

10.

Buj‐Bello, Anna, Françoise Fougerousse, Yannick Schwab, et al.. (2008). AAV-mediated intramuscular delivery of myotubularin corrects the myotubular myopathy phenotype in targeted murine muscle and suggests a function in plasma membrane homeostasis. Human Molecular Genetics. 17(14). 2132–2143. 90 indexed citations

11.

Jungbluth, Heinz, Haiyan Zhou, Caroline A. Sewry, et al.. (2007). Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene. Neuromuscular Disorders. 17(4). 338–345. 82 indexed citations

12.

Fukami, Maki, Yuka Wada, Kanako Miyabayashi, et al.. (2006). CXorf6 is a causative gene for hypospadias. Nature Genetics. 38(12). 1369–1371. 108 indexed citations

13.

Biancalana, Valérie, Olivier Caron, Sabina Gallati, et al.. (2003). Characterisation of mutations in 77 patients with X-linked myotubular myopathy, including a family with a very mild phenotype. Human Genetics. 112(2). 135–142. 90 indexed citations

14.

McEntagart, Meriel, Anna Buj‐Bello, Valérie Biancalana, et al.. (2002). Genotype–phenotype correlations in X-linked myotubular myopathy. Neuromuscular Disorders. 12(10). 939–946. 104 indexed citations

15.

Laporte, Jocelyn, Stephan M. Tanner, Wolfram Kreß, et al.. (2000). MTM1 mutations in X-linked myotubular myopathy. Human Mutation. 15(5). 393–409. 164 indexed citations

16.

Buj‐Bello, Anna, et al.. (1999). Identification of novel mutations in theMTM1 gene causing severe and mild forms of X-linked myotubular myopathy. Human Mutation. 14(4). 320–325. 35 indexed citations

17.

Forgie, Alison, Epaminondas Doxakis, Anna Buj‐Bello, Séan Wyatt, & Alun M. Davies. (1999). Differences and Developmental Changes in the Responsiveness of PNS Neurons to GDNF and Neurturin. Molecular and Cellular Neuroscience. 13(6). 430–440. 29 indexed citations

18.

Buj‐Bello, Anna, Jimi Adu, Luzia G. P. Piñón, et al.. (1997). Neurturin responsiveness requires a GPI-linked receptor and the Ret receptor tyrosine kinase. Nature. 387(6634). 721–724. 254 indexed citations

19.

Treanor, James, Laurie J. Goodman, Frédéric J. de Sauvage, et al.. (1996). Characterization of a multicomponent receptor for GDNF. Nature. 382(6586). 80–83. 893 indexed citations breakdown →

20.

Buj‐Bello, Anna, Vladimir L. Buchman, Antony Horton, Arnon Rosenthal, & Alun M. Davies. (1995). GDNF is an age-specific survival factor for sensory and autonomic neurons. Neuron. 15(4). 821–828. 352 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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