Sarojini Budden

2.5k total citations
30 papers, 1.7k citations indexed

About

Sarojini Budden is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Sarojini Budden has authored 30 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 13 papers in Cognitive Neuroscience and 9 papers in Molecular Biology. Recurrent topics in Sarojini Budden's work include Genetics and Neurodevelopmental Disorders (18 papers), Autism Spectrum Disorder Research (13 papers) and Family and Disability Support Research (7 papers). Sarojini Budden is often cited by papers focused on Genetics and Neurodevelopmental Disorders (18 papers), Autism Spectrum Disorder Research (13 papers) and Family and Disability Support Research (7 papers). Sarojini Budden collaborates with scholars based in United States, Italy and Australia. Sarojini Budden's co-authors include Angela J. McArthur, John M. Opitz, James F. Reynolds, Stephen LaFranchi, Michael G. Brown, N. Carolyn Schanen, Uta Francke, M. Gunness, Huda Y. Zoghbi and H.-R. Song and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain Research and The American Journal of Human Genetics.

In The Last Decade

Sarojini Budden

30 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarojini Budden United States 22 1.2k 794 788 271 237 30 1.7k
Sarika U. Peters United States 29 2.1k 1.7× 915 1.2× 1.3k 1.6× 208 0.8× 213 0.9× 63 2.7k
Jennifer Reichert United States 15 1.5k 1.2× 1.6k 2.0× 869 1.1× 166 0.6× 256 1.1× 17 2.3k
Sabine M. Klauck Germany 22 996 0.8× 849 1.1× 746 0.9× 125 0.5× 173 0.7× 36 1.8k
Pamela Sklar United States 8 1.3k 1.1× 587 0.7× 735 0.9× 110 0.4× 199 0.8× 8 1.9k
Christiane Cox United States 21 445 0.4× 888 1.1× 502 0.6× 236 0.9× 509 2.1× 24 1.8k
Sabrina Signorini Italy 20 386 0.3× 357 0.4× 543 0.7× 115 0.4× 352 1.5× 78 1.7k
Ronald L. Thibert United States 24 1.2k 1.0× 360 0.5× 759 1.0× 38 0.1× 379 1.6× 53 1.7k
Tamar Green United States 20 382 0.3× 286 0.4× 632 0.8× 85 0.3× 147 0.6× 51 1.2k
Lan Xiong Canada 24 298 0.2× 436 0.5× 263 0.3× 142 0.5× 340 1.4× 58 1.5k
Mark D. Shen United States 17 390 0.3× 769 1.0× 166 0.2× 126 0.5× 180 0.8× 35 1.1k

Countries citing papers authored by Sarojini Budden

Since Specialization
Citations

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

Fields of papers citing papers by Sarojini Budden

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarojini Budden

This figure shows the co-authorship network connecting the top 25 collaborators of Sarojini Budden. A scholar is included among the top collaborators of Sarojini Budden 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 Sarojini Budden. Sarojini Budden 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.
Matagne, Valérie, Joyce Wondolowski, Matthew Frerking, et al.. (2018). Correcting deregulated Fxyd1 expression rescues deficits in neuronal arborization and potassium homeostasis in MeCP2 deficient male mice. Brain Research. 1697. 45–52. 6 indexed citations
2.
Fabio, Rosa Angela, Antonio Gangemi, Tindara Caprì, Sarojini Budden, & Alessandra Falzone. (2018). Neurophysiological and cognitive effects of Transcranial Direct Current Stimulation in three girls with Rett Syndrome with chronic language impairments. Research in Developmental Disabilities. 76. 76–87. 36 indexed citations
3.
Matagne, Valérie, Sarojini Budden, Sergio R. Ojeda, & Jacob Raber. (2012). Correcting deregulated Fxyd1 expression ameliorates a behavioral impairment in a mouse model of Rett syndrome. Brain Research. 1496. 104–114. 7 indexed citations
4.
Fabio, Rosa Angela, et al.. (2008). The role of stereotypies in overselectivity process in Rett syndrome. Research in Developmental Disabilities. 30(1). 136–145. 38 indexed citations
5.
Matagne, Valérie, Fatima Banine, Matthew Frerking, et al.. (2007). FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice. Human Molecular Genetics. 16(6). 640–650. 111 indexed citations
6.
Budden, Sarojini, et al.. (2005). Clinical profile of a male with Rett syndrome. Brain and Development. 27. S69–S71. 33 indexed citations
7.
Budden, Sarojini & M. Gunness. (2001). Bone histomorphometry in three females with Rett syndrome. Brain and Development. 23. S133–S137. 22 indexed citations
8.
Wan, Mimi, Xianyu Zhang, Elisa J. F. Houwink, et al.. (1999). Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots. The American Journal of Human Genetics. 65(6). 1520–1529. 369 indexed citations
9.
Schanen, N. Carolyn, et al.. (1997). Is Rett Syndrome Caused by a Triplet Repeat Expansion?. Neuropediatrics. 28(3). 179–183. 9 indexed citations
10.
Budden, Sarojini. (1995). Management of Rett Syndrome: A Ten Year Experience. Neuropediatrics. 26(2). 75–77. 43 indexed citations
11.
Kaufmann, Walter E., S. Naidu, & Sarojini Budden. (1995). Abnormal Expression of Microtubule-Associated Protein 2 (MAP-2) in Neocortex in Rett Syndrome. Neuropediatrics. 26(2). 109–113. 63 indexed citations
12.
McLaughlin, John F., et al.. (1993). WOMEN WITH CEREBRAL PALSY: OBSTETRIC EXPERIENCE AND NEONATAL OUTCOME. Developmental Medicine & Child Neurology. 35(11). 974–982. 11 indexed citations
13.
Magenis, R.E., Leland Allen, Mary Helen Black, et al.. (1990). Comparison of the 15q deletions in Prader‐Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences. American Journal of Medical Genetics. 35(3). 333–349. 158 indexed citations
14.
Budden, Sarojini, et al.. (1990). Communication and Oral‐Motor Function in Rett Syndrome. Developmental Medicine & Child Neurology. 32(1). 51–55. 25 indexed citations
15.
Budden, Sarojini, Edwin C. Myer, & Ian J. Butler. (1990). Cerebrospinal fluid studies in the Rett syndrome: Biogenic amines and β-endorphins. Brain and Development. 12(1). 81–84. 28 indexed citations
16.
Magenis, R. Ellen, Michael G. Brown, Sarojini Budden, et al.. (1987). Is angelman syndrome an alternate result of del(15)(qllql3)?. American Journal of Medical Genetics. 28(4). 829–838. 190 indexed citations
17.
Budden, Sarojini. (1987). The role of the physician in the care of the child with Rett syndrome. Brain and Development. 9(5). 532–534. 2 indexed citations
18.
Budden, Sarojini, et al.. (1987). Auditory brainstem response findings in rett syndrome. Brain and Development. 9(5). 514–516. 19 indexed citations
19.
Budden, Sarojini, Nancy G. Kennaway, Neil R.M. Buist, A. Poulos, & Richard G. Weleber. (1986). Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: Studies in four children. The Journal of Pediatrics. 108(1). 33–39. 55 indexed citations
20.
Tongue, Andrea Cibis, et al.. (1984). Ophthalmic Manifestations of Infantile Phytanic Acid Storage Disease. Archives of Ophthalmology. 102(9). 1317–1321. 33 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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