Precilla D’Souza

1.3k total citations
24 papers, 336 citations indexed

About

Precilla D’Souza is a scholar working on Genetics, Molecular Biology and Clinical Psychology. According to data from OpenAlex, Precilla D’Souza has authored 24 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Clinical Psychology. Recurrent topics in Precilla D’Souza's work include Genomic variations and chromosomal abnormalities (5 papers), Lysosomal Storage Disorders Research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Precilla D’Souza is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Lysosomal Storage Disorders Research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Precilla D’Souza collaborates with scholars based in United States, Czechia and Türkiye. Precilla D’Souza's co-authors include Susan E. Swedo, Paul Grant, James F. Leckman, Rebecca Hommer, Cristan Farmer, Cynthia J. Tifft, Ellen F. Macnamara, Kyle A. Williams, Liliya Katsovich and Robert A. King and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Precilla D’Souza

22 papers receiving 328 citations

Peers

Precilla D’Souza
Precilla D’Souza
Citations per year, relative to Precilla D’Souza Precilla D’Souza (= 1×) peers Makiko Nakagawa

Countries citing papers authored by Precilla D’Souza

Since Specialization
Citations

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

Fields of papers citing papers by Precilla D’Souza

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Precilla D’Souza. 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 Precilla D’Souza. The network helps show where Precilla D’Souza may publish in the future.

Co-authorship network of co-authors of Precilla D’Souza

This figure shows the co-authorship network connecting the top 25 collaborators of Precilla D’Souza. A scholar is included among the top collaborators of Precilla D’Souza 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 Precilla D’Souza. Precilla D’Souza 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.
Kühn, Anna Luisa, Jean M. Johnston, Precilla D’Souza, et al.. (2025). Differential tractography: an imaging marker for tissue degeneration in neurodegenerative diseases. Brain Communications. 7(3). fcaf198–fcaf198.
2.
Filippi, Courtney A., Elizabeth G. Smith, Elizabeth Redcay, et al.. (2025). Brain Morphometry of Toddlers With Language Delay: An Exploratory Study. Infant and Child Development. 34(1).
3.
Johnston, Jean M., Precilla D’Souza, Anna Luisa Kühn, et al.. (2025). Natural history progression of MRI brain volumetrics in type II late-infantile and juvenile GM1 gangliosidosis patients. Molecular Genetics and Metabolism. 144(3). 109025–109025. 1 indexed citations
4.
Johnston, Jean M., Sílvia Zaragoza Domingo, Gilbert Vézina, et al.. (2025). Retrospective assessment of clinical global impression of severity and change in GM1 gangliosidosis: a tool to score natural history data in rare disease cohorts. Orphanet Journal of Rare Diseases. 20(1). 125–125. 3 indexed citations
5.
Johnston, Jean M., Precilla D’Souza, Anna Luisa Kühn, et al.. (2024). Quantitative reliability assessment of brain MRI volumetric measurements in type II GM1 gangliosidosis patients. SHILAP Revista de lepidopterología. 3. 1410848–1410848. 2 indexed citations
6.
Grant, Natalie, Jin Yun Chen, Precilla D’Souza, et al.. (2024). The spectrum of neurological presentation in individuals affected by TBL1XR1 gene defects. Orphanet Journal of Rare Diseases. 19(1). 79–79. 2 indexed citations
7.
Corti, Manuela, Kirsten E. Coleman, Julie Berthy, et al.. (2023). Thrombotic microangiopathy following systemic AAV administration is dependent on anti-capsid antibodies. Journal of Clinical Investigation. 134(1). 67 indexed citations
8.
Kell, Pamela, Rohini Sidhu, Mingxing Qian, et al.. (2023). A pentasaccharide for monitoring pharmacodynamic response to gene therapy in GM1 gangliosidosis. EBioMedicine. 92. 104627–104627. 8 indexed citations
9.
Macnamara, Ellen F., Yvonne L. Latour, Precilla D’Souza, et al.. (2023). Risks and benefits of anesthesia for combined pediatric procedures in the NIH undiagnosed diseases program. Molecular Genetics and Metabolism. 140(3). 107707–107707. 1 indexed citations
10.
Acosta, Maria T., Precilla D’Souza, Jean M. Johnston, et al.. (2023). P094: Clinical and MRI correlations in GM1 patients: Finding biomarkers to predict treatment response with gene therapy*. SHILAP Revista de lepidopterología. 1(1). 100123–100123. 1 indexed citations
11.
Smith, Elizabeth G., Yaqiong Xiao, Hua Xie, et al.. (2023). Posterior superior temporal cortex connectivity is related to social communication in toddlers. Infant Behavior and Development. 71. 101831–101831. 2 indexed citations
12.
Tifft, Cynthia J., Precilla D’Souza, Michael F. Wangler, et al.. (2022). Complex effects on CaV2.1 channel gating caused by a CACNA1A variant associated with a severe neurodevelopmental disorder. Scientific Reports. 12(1). 9186–9186. 12 indexed citations
13.
Macnamara, Ellen F., et al.. (2019). The undiagnosed diseases program: Approach to diagnosis. PubMed. 4(3-4). 179–188. 13 indexed citations
14.
D’Souza, Precilla, et al.. (2019). Incontinence in Phelan‐McDermid Syndrome. Journal of Pediatric Gastroenterology and Nutrition. 69(2). e39–e42. 2 indexed citations
15.
Khan, Omar, Xiangping Zhou, Riley Kessler, et al.. (2018). Prospective longitudinal overnight video-EEG evaluation in Phelan–McDermid Syndrome. Epilepsy & Behavior. 80. 312–320. 10 indexed citations
16.
Hommer, Rebecca, Paul Grant, Cristan Farmer, et al.. (2017). Longitudinal outcomes of children with pediatric autoimmune neuropsychiatric disorder associated with streptococcal infections (PANDAS). European Child & Adolescent Psychiatry. 27(5). 637–643. 14 indexed citations
17.
Williams, Kyle A., Susan E. Swedo, Cristan Farmer, et al.. (2016). Randomized, Controlled Trial of Intravenous Immunoglobulin for Pediatric Autoimmune Neuropsychiatric Disorders Associated With Streptococcal Infections. Journal of the American Academy of Child & Adolescent Psychiatry. 55(10). 860–867.e2. 69 indexed citations
18.
Thurm, Audrey, Precilla D’Souza, Owen M. Rennert, et al.. (2016). Creatine Transporter Deficiency. Journal of Developmental & Behavioral Pediatrics. 37(4). 322–326. 10 indexed citations
19.
Zhou, Xiangping, Andrea Gropman, Precilla D’Souza, Audrey Thurm, & Sara K. Inati. (2015). Epilepsy and Electroencephalographic Features in Patients with Phelan McDermid Syndrome (P6.270). Neurology. 84(14_supplement). 2 indexed citations
20.
Hommer, Rebecca, Paul Grant, Precilla D’Souza, et al.. (2014). Disordered Eating and Food Restrictions in Children with PANDAS/PANS. Journal of Child and Adolescent Psychopharmacology. 25(1). 48–56. 42 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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