Daniela Buhaş

1.3k total citations
24 papers, 286 citations indexed

About

Daniela Buhaş is a scholar working on Clinical Biochemistry, Molecular Biology and Genetics. According to data from OpenAlex, Daniela Buhaş has authored 24 papers receiving a total of 286 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Clinical Biochemistry, 12 papers in Molecular Biology and 10 papers in Genetics. Recurrent topics in Daniela Buhaş's work include Metabolism and Genetic Disorders (15 papers), Mitochondrial Function and Pathology (7 papers) and Genomics and Rare Diseases (6 papers). Daniela Buhaş is often cited by papers focused on Metabolism and Genetic Disorders (15 papers), Mitochondrial Function and Pathology (7 papers) and Genomics and Rare Diseases (6 papers). Daniela Buhaş collaborates with scholars based in Canada, United States and Denmark. Daniela Buhaş's co-authors include Chantal Poulin, Nathalie Alos, Joaquim Miró, Gilles Chabot, Frank Rutsch, Thomas Édouard, Chantale Lapierre, Yvonne Nitschke, Paula J. Waters and Jeremy Schwartzentruber and has published in prestigious journals such as Neurology, Biochemical and Biophysical Research Communications and Movement Disorders.

In The Last Decade

Daniela Buhaş

23 papers receiving 285 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniela Buhaş Canada 10 157 109 107 44 36 24 286
Rebecca Mardach United States 11 193 1.2× 164 1.5× 40 0.4× 53 1.2× 100 2.8× 17 351
Loreta Cimbalistienė Lithuania 11 121 0.8× 60 0.6× 53 0.5× 40 0.9× 79 2.2× 22 233
Patricia Galvin‐Parton United States 11 192 1.2× 93 0.9× 84 0.8× 36 0.8× 47 1.3× 13 313
Ohad Wormser Israel 11 173 1.1× 31 0.3× 65 0.6× 11 0.3× 24 0.7× 28 275
Silvio Ferraris Italy 12 262 1.7× 198 1.8× 42 0.4× 27 0.6× 43 1.2× 12 370
Heiko Brennenstuhl Germany 11 180 1.1× 99 0.9× 74 0.7× 12 0.3× 30 0.8× 25 315
Magalie Barth France 12 274 1.7× 171 1.6× 35 0.3× 23 0.5× 92 2.6× 32 378
Sirisak Chanprasert United States 8 158 1.0× 96 0.9× 33 0.3× 17 0.4× 33 0.9× 13 228
Claudia Soler‐Alfonso United States 12 197 1.3× 129 1.2× 135 1.3× 55 1.3× 45 1.3× 21 333
Jeannette Gootjes Netherlands 12 446 2.8× 129 1.2× 25 0.2× 17 0.4× 93 2.6× 17 497

Countries citing papers authored by Daniela Buhaş

Since Specialization
Citations

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

Fields of papers citing papers by Daniela Buhaş

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Buhaş

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela Buhaş. A scholar is included among the top collaborators of Daniela Buhaş 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 Daniela Buhaş. Daniela Buhaş 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
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Sahly, Ahmed N., Myriam Srour, Daniela Buhaş, Ingrid E. Scheffer, & Kenneth A. Myers. (2023). The epileptology of Wiedemann-Steiner syndrome: Electroclinical findings in five patients with KMT2A pathogenic variants. European Journal of Paediatric Neurology. 44. 46–50. 2 indexed citations
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Carter, Melissa T., Myriam Srour, Daniela Buhaş, et al.. (2023). Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG). Journal of Medical Genetics. 60(6). 523–532. 18 indexed citations
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Chrestian, Nicolas, et al.. (2022). Case report: PLPHP deficiency, a rare but important cause of B6-responsive disorders: A report of three novel individuals and review of 51 cases. Frontiers in Neurology. 13. 913652–913652. 1 indexed citations
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Tseng, Laura A., José E. Abdenur, Ashley Andrews, et al.. (2022). Timing of therapy and neurodevelopmental outcomes in 18 families with pyridoxine-dependent epilepsy. Molecular Genetics and Metabolism. 135(4). 350–356. 17 indexed citations
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Mariño, Tania Cruz, Philippe Caron, Charles Morin, et al.. (2021). French-Canadian families from Saguenay-Lac-Saint-Jean: a new founder population for APECED. Endocrine. 75(1). 48–58. 1 indexed citations
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Guay, Simon‐Pierre, Najma Ahmed, Christine Saint‐Martin, et al.. (2021). Clinical utility of methionine restriction in adenosine kinase deficiency. JIMD Reports. 61(1). 52–59. 5 indexed citations
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Buhaş, Daniela, et al.. (2021). Enhancing the Impact of Genomics Research in Autism through Integration of Research Results into Routine Care Pathways—A Case Series. Journal of Personalized Medicine. 11(8). 755–755. 1 indexed citations
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Abraham, Joseph R., John Barnard, Heng Wang, et al.. (2019). Proteomic investigations of human HERC2 mutants: Insights into the pathobiology of a neurodevelopmental disorder. Biochemical and Biophysical Research Communications. 512(2). 421–427. 11 indexed citations
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Kitzler, Thomas M., Indra R. Gupta, Chantal Poulin, et al.. (2018). Acute and Chronic Management in an Atypical Case of Ethylmalonic Encephalopathy. JIMD Reports. 45. 57–63. 16 indexed citations
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Altassan, Ruqaiah, Stéphanie Fox, Chantal Poulin, & Daniela Buhaş. (2018). Hyperphosphatasia with mental retardation syndrome, expanded phenotype of PIGL related disorders. Molecular Genetics and Metabolism Reports. 15. 46–49. 13 indexed citations
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Waters, Paula J., Daniela Buhaş, Sébastien Lévesque, et al.. (2018). Combined malonic and methylmalonic aciduria due to ACSF3 mutations: benign clinical course in an unselected cohort. Journal of Inherited Metabolic Disease. 3 indexed citations
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Anastasio, Natascia, Maja Tarailo‐Graovac, Reem Al Khalifah, et al.. (2016). Mitochondrial Complex III Deficiency with Ketoacidosis and Hyperglycemia Mimicking Neonatal Diabetes. JIMD Reports. 31. 57–62. 5 indexed citations
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Jain‐Ghai, Shailly, et al.. (2015). Contiguous Gene Deletion of Chromosome Xp in Three FamiliesEncompassing OTC, RPGR and TSPAN7 Genes. 1(1). 1 indexed citations
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Srour, Myriam, Jeremy Schwartzentruber, Véronique Bolduc, et al.. (2014). Mutations in riboflavin transporter present with severe sensory loss and deafness in childhood. Muscle & Nerve. 50(5). 775–779. 20 indexed citations
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Édouard, Thomas, Gilles Chabot, Joaquim Miró, et al.. (2011). Efficacy and safety of 2-year etidronate treatment in a child with generalized arterial calcification of infancy. European Journal of Pediatrics. 170(12). 1585–1590. 52 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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