Brenda J. Barry

5.1k total citations
33 papers, 2.1k citations indexed

About

Brenda J. Barry is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Brenda J. Barry has authored 33 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 15 papers in Molecular Biology and 6 papers in Cell Biology. Recurrent topics in Brenda J. Barry's work include Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (7 papers) and Microtubule and mitosis dynamics (6 papers). Brenda J. Barry is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (7 papers) and Microtubule and mitosis dynamics (6 papers). Brenda J. Barry collaborates with scholars based in United States, Saudi Arabia and United Kingdom. Brenda J. Barry's co-authors include Christopher A. Walsh, A. James Barkovich, William F. Hickey, Tammy Kielian, Annapurna Poduri, Srinivasa R. Nagalla, Ganeshwaran H. Mochida, R. Sean Hill, Xuyu Cai and E R Spindel and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Brenda J. Barry

33 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Brenda J. Barry United States 22 1.2k 743 361 336 249 33 2.1k
Takeshi Mizuguchi Japan 28 1.6k 1.3× 1.2k 1.6× 381 1.1× 266 0.8× 198 0.8× 126 2.7k
Marlène Rio France 33 2.2k 1.8× 1.7k 2.3× 237 0.7× 207 0.6× 263 1.1× 112 3.5k
Ghayda Mirzaa United States 22 873 0.7× 711 1.0× 171 0.5× 230 0.7× 312 1.3× 56 1.7k
Pascale Saugier-Véber France 28 1.1k 0.9× 672 0.9× 437 1.2× 156 0.5× 267 1.1× 82 2.3k
Fiorella Gurrieri Italy 27 1.4k 1.1× 1.3k 1.7× 131 0.4× 132 0.4× 345 1.4× 88 2.4k
Yuanyi Feng United States 22 1.8k 1.4× 634 0.9× 525 1.5× 1.2k 3.4× 305 1.2× 34 3.1k
Kaya Bilgüvar United States 27 992 0.8× 532 0.7× 217 0.6× 284 0.8× 128 0.5× 78 2.0k
Keiko Shimojima Japan 25 1.0k 0.8× 1.2k 1.6× 190 0.5× 190 0.6× 218 0.9× 125 1.9k
Grazia M.S. Mancini Netherlands 26 849 0.7× 681 0.9× 212 0.6× 285 0.8× 297 1.2× 46 1.9k
Marjolein H. Willemsen Netherlands 20 1.3k 1.1× 1.5k 2.0× 238 0.7× 203 0.6× 131 0.5× 43 2.4k

Countries citing papers authored by Brenda J. Barry

Since Specialization
Citations

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

Fields of papers citing papers by Brenda J. Barry

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brenda J. Barry. 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 Brenda J. Barry. The network helps show where Brenda J. Barry may publish in the future.

Co-authorship network of co-authors of Brenda J. Barry

This figure shows the co-authorship network connecting the top 25 collaborators of Brenda J. Barry. A scholar is included among the top collaborators of Brenda J. Barry 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 Brenda J. Barry. Brenda J. Barry 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.
Jurgens, Julie A., Brenda J. Barry, Gabrielle Lemire, et al.. (2021). Novel variants in TUBA1A cause congenital fibrosis of the extraocular muscles with or without malformations of cortical brain development. European Journal of Human Genetics. 29(5). 816–826. 12 indexed citations
2.
Thiffault, Isabelle, Laura Cross, Shivarajan Amudhavalli, et al.. (2019). MAGEL2 ‐related disorders: A study and case series. Clinical Genetics. 96(6). 493–505. 27 indexed citations
3.
Heidary, Gena, et al.. (2019). Outcomes of strabismus surgery in genetically confirmed congenital fibrosis of the extraocular muscles. Journal of American Association for Pediatric Ophthalmology and Strabismus. 23(5). 253.e1–253.e6. 5 indexed citations
4.
Tischfield, Max A., Caroline D. Robson, Shek Man Chim, et al.. (2017). Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura. Developmental Cell. 42(5). 445–461.e5. 35 indexed citations
5.
Papandreou, Apostolos, Mandy Ma, Brenda J. Barry, et al.. (2015). Familial recurrences of FOXG1‐related disorder: Evidence for mosaicism. American Journal of Medical Genetics Part A. 167(12). 3096–3102. 11 indexed citations
6.
Mutch, Christopher A., Annapurna Poduri, Mustafa Şahin, et al.. (2015). Disorders of Microtubule Function in Neurons: Imaging Correlates. American Journal of Neuroradiology. 37(3). 528–535. 43 indexed citations
7.
D’Gama, Alissa M., Ying Geng, Javier Couto, et al.. (2015). Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia. Annals of Neurology. 77(4). 720–725. 183 indexed citations
8.
9.
Poduri, Annapurna, Edward Neilan, Princess C. Elhosary, et al.. (2012). Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy. Epilepsia. 53(8). e146–50. 68 indexed citations
10.
Poduri, Annapurna, Gilad D. Evrony, Xuyu Cai, et al.. (2012). Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations. Neuron. 74(1). 41–48. 319 indexed citations
11.
González, Germán, Leonardo Vedolin, Brenda J. Barry, et al.. (2012). Location of Periventricular Nodular Heterotopia Is Related to the Malformation Phenotype on MRI. American Journal of Neuroradiology. 34(4). 877–883. 32 indexed citations
12.
Yang, Yawei J., Andrew E. Baltus, Elisabeth A. Murphy, et al.. (2012). Microcephaly Gene Links Trithorax and REST/NRSF to Control Neural Stem Cell Proliferation and Differentiation. Cell. 151(5). 1097–1112. 119 indexed citations
13.
Alkuraya, Fowzan S., Xuyu Cai, Ganeshwaran H. Mochida, et al.. (2011). Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly. The American Journal of Human Genetics. 88(5). 677–677. 2 indexed citations
14.
Sheen, Volney, et al.. (2010). Mutation in PQBP1 is associated with periventricular heterotopia. American Journal of Medical Genetics Part A. 152A(11). 2888–2890. 14 indexed citations
15.
Manzini, M. Chiara, Anna Rajab, Thomas M. Maynard, et al.. (2009). Developmental and degenerative features in a complicated spastic paraplegia. Annals of Neurology. 67(4). 516–525. 27 indexed citations
16.
Poduri, Annapurna, Vida Chitsazzadeh, Stefano D’Arrigo, et al.. (2009). The syndrome of perisylvian polymicrogyria with congenital arthrogryposis. Brain and Development. 32(7). 550–555. 13 indexed citations
17.
Manzini, M. Chiara, Danielle Gleason, Bernard S. Chang, et al.. (2008). Ethnically diverse causes of Walker-Warburg syndrome (WWS):FCMDmutations are a more common cause of WWS outside of the Middle East. Human Mutation. 29(11). E231–E241. 49 indexed citations
18.
Kielian, Tammy, Brenda J. Barry, & William F. Hickey. (2001). CXC Chemokine Receptor-2 Ligands Are Required for Neutrophil-Mediated Host Defense in Experimental Brain Abscesses. The Journal of Immunology. 166(7). 4634–4643. 162 indexed citations
19.
Ratcliffe, Nora, John G. B. Hutchins, Brenda J. Barry, & William F. Hickey. (2000). Chronic Myocarditis Induced by T Cells Reactive to a Single Cardiac Myosin Peptide: Persistent Inflammation, Cardiac Dilatation, Myocardial Scarring and Continuous Myocyte Apoptosis. Journal of Autoimmunity. 15(3). 359–367. 23 indexed citations
20.
Nagalla, Srinivasa R., Brenda J. Barry, Arnold M. Falick, et al.. (1996). There Are Three Distinct Forms of Bombesin. Journal of Biological Chemistry. 271(13). 7731–7737. 54 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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