Ledia Brunga

1.3k total citations
6 papers, 79 citations indexed

About

Ledia Brunga is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Rheumatology. According to data from OpenAlex, Ledia Brunga has authored 6 papers receiving a total of 79 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Rheumatology. Recurrent topics in Ledia Brunga's work include Glycogen Storage Diseases and Myoclonus (1 paper), Tuberous Sclerosis Complex Research (1 paper) and Acute Lymphoblastic Leukemia research (1 paper). Ledia Brunga is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (1 paper), Tuberous Sclerosis Complex Research (1 paper) and Acute Lymphoblastic Leukemia research (1 paper). Ledia Brunga collaborates with scholars based in Canada, Netherlands and United Kingdom. Ledia Brunga's co-authors include Cyrus Boelman, Adam Shlien, Stephen W. Scherer, Mohammed Uddin, Sylvia Lamoureux, Bailey Gallinger, Giovanna Pellecchia, Harvey B. Sarnat, Mary Connolly and Anita Villani and has published in prestigious journals such as Genetics in Medicine, Journal of Child Neurology and Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

In The Last Decade

Ledia Brunga

6 papers receiving 79 citations

Peers

Ledia Brunga

GENET

MB

PPCH

PHYSI

PMH

Ahlam A. Hamed Sudan

Alice Dica Romania

Chontelle King New Zealand

Linn Öijerstedt Sweden

Sara Ellingwood United States

Jennifer McEvoy‐Venneri United States

Danique R.M. Vlaskamp Netherlands

Amy Kritzer United States

Kamer Tezcan United States

Stefanie Beck‐Woedl Germany

Ahlam A. Hamed Sudan

Ledia Brunga

19 ×0.4

GENET

33 ×1.0

MB

18 ×0.9

PPCH

15 ×0.9

PHYSI

24 ×1.5

PMH

Citations per year, relative to Ledia Brunga Ledia Brunga (= 1×) peers Ahlam A. Hamed

Countries citing papers authored by Ledia Brunga

Since Specialization

Citations

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

Fields of papers citing papers by Ledia Brunga

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ledia Brunga

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Davidson, Scott, Karin P.S. Langenberg, Fabio Fuligni, et al.. (2023). Myeloproliferative Neoplasm Driven by ETV6-ABL1 in an Adolescent with Recent History of Burkitt Leukemia. Current Oncology. 30(7). 5946–5952. 1 indexed citations

2.

Hancock, Kelly, Bailey Gallinger, Ledia Brunga, et al.. (2022). Perspectives and Experiences of Parents and Adolescents Who Participate in a Pediatric Precision Oncology Program: "When You Feel Helpless, This Kind of Thing Is Very Helpful". JCO Precision Oncology. 6(6). e2100444–e2100444. 13 indexed citations

3.

Wong, Derek, Leslie E. Oldfield, Jeffrey P. Bruce, et al.. (2022). OP015: Multi-omic analysis of circulating tumour DNA for the early detection of cancer in patients with Li-Fraumeni syndrome. Genetics in Medicine. 24(3). S346–S347. 1 indexed citations

4.

Xu, Qi, Christopher Dunham, Harvey B. Sarnat, et al.. (2018). mTOR Inhibitors as a New Therapeutic Strategy in Treatment Resistant Epilepsy in Hemimegalencephaly: A Case Report. Journal of Child Neurology. 34(3). 132–138. 23 indexed citations

5.

Hewson, Stacy, Ledia Brunga, Jaina Patel, et al.. (2017). Prevalence of Genetic Disorders and GLUT1 Deficiency in a Ketogenic Diet Clinic. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 45(1). 93–96. 6 indexed citations

6.

Uddin, Mohammed, Marc Woodbury‐Smith, Ada J. S. Chan, et al.. (2017). Germline and somatic mutations in STXBP1 with diverse neurodevelopmental phenotypes. Neurology Genetics. 3(6). e199–e199. 35 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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