Dawn Cordeiro

1.4k total citations
15 papers, 484 citations indexed

About

Dawn Cordeiro is a scholar working on Clinical Biochemistry, Molecular Biology and Genetics. According to data from OpenAlex, Dawn Cordeiro has authored 15 papers receiving a total of 484 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Clinical Biochemistry, 7 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Dawn Cordeiro's work include Metabolism and Genetic Disorders (9 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Dawn Cordeiro is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Dawn Cordeiro collaborates with scholars based in Canada, United Kingdom and Netherlands. Dawn Cordeiro's co-authors include Saadet Mercimek‐Andrews, Saadet Mercimek‐Mahmutoglu, Komudi Siriwardena, Gregory Costain, Jeff Kobayashi, Shelly K. Weiss, Jaina Patel, Pekka Kannus, Mahendranath Moharir and Eduard A. Struys and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neuroscience and Epilepsia.

In The Last Decade

Dawn Cordeiro

14 papers receiving 477 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dawn Cordeiro Canada	10	233	200	173	145	61	15	484
Jaina Patel Canada	8	193 0.8×	118 0.6×	125 0.7×	109 0.8×	43 0.7×	17	389
Suzanne D. DeBrosse United States	12	115 0.5×	246 1.2×	182 1.1×	55 0.4×	55 0.9×	17	422
Christine Makowski Germany	10	51 0.2×	229 1.1×	143 0.8×	116 0.8×	51 0.8×	18	480
Léna Damaj France	11	109 0.5×	186 0.9×	108 0.6×	38 0.3×	71 1.2×	19	479
Sabine Grønborg Denmark	11	69 0.3×	207 1.0×	74 0.4×	61 0.4×	64 1.0×	25	330
Hiroko Shimbo Japan	12	73 0.3×	192 1.0×	101 0.6×	22 0.2×	33 0.5×	33	315
Tessa Wassenberg Netherlands	11	61 0.3×	112 0.6×	156 0.9×	27 0.2×	28 0.5×	19	372
Kae Munakata Japan	9	127 0.5×	366 1.8×	161 0.9×	126 0.9×	41 0.7×	9	535
Kathrin Jeltsch Germany	9	84 0.4×	160 0.8×	198 1.1×	17 0.1×	50 0.8×	18	387
Thatjana Gardeitchik Netherlands	13	162 0.7×	233 1.2×	105 0.6×	11 0.1×	78 1.3×	19	419

Countries citing papers authored by Dawn Cordeiro

Since Specialization

Citations

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

Fields of papers citing papers by Dawn Cordeiro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dawn Cordeiro

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

All Works

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15 of 15 papers shown

Cordeiro, Dawn, et al.. (2023). NKX6-2 Disease in Two Unrelated Patients with Early-Onset Spastic Quadriplegia and Diffuse Hypomyelinating Leukodystrophy. SHILAP Revista de lepidopterología. 9. 100069–100069.

Bourque, Danielle K., Dawn Cordeiro, Graeme Nimmo, Jeff Kobayashi, & Saadet Mercimek‐Andrews. (2021). Phenotypic and Genotypic Spectrum of Glucose Transporter-1 Deficiency Syndrome. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 48(6). 1–5. 8 indexed citations

Cordeiro, Dawn, et al.. (2021). Prevalence of Congenital Disorders of Glycosylation in Childhood Epilepsy and Effects of Anti-Epileptic Drugs on the Transferrin Isoelectric Focusing Test. Genes. 12(8). 1227–1227. 9 indexed citations

Cordeiro, Dawn, et al.. (2020). Urine creatine metabolite panel as a screening test in neurodevelopmental disorders. Orphanet Journal of Rare Diseases. 15(1). 339–339. 10 indexed citations

Costain, Gregory, et al.. (2019). Clinical Application of Targeted Next-Generation Sequencing Panels and Whole Exome Sequencing in Childhood Epilepsy. Neuroscience. 418. 291–310. 70 indexed citations

Veenma, Danielle, Dawn Cordeiro, Neal Sondheimer, & Saadet Mercimek‐Andrews. (2018). DNAJC12-associated developmental delay, movement disorder, and mild hyperphenylalaninemia identified by whole-exome sequencing re-analysis. European Journal of Human Genetics. 26(12). 1867–1870. 21 indexed citations

Cordeiro, Dawn, et al.. (2018). Outcome of Patients With Inherited Neurotransmitter Disorders. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 45(5). 571–576. 3 indexed citations

Cordeiro, Dawn, et al.. (2018). Genetic landscape of pediatric movement disorders and management implications. Neurology Genetics. 4(5). e265–e265. 28 indexed citations

Bruun, Theodora U. J., Dawn Cordeiro, Ronald D. Cohn, et al.. (2017). Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type II. Molecular Genetics and Metabolism. 120(3). 235–242. 40 indexed citations

10.

Nimmo, Graeme, Resham Ejaz, Dawn Cordeiro, Pekka Kannus, & Saadet Mercimek‐Andrews. (2017). Riboflavin transporter deficiency mimicking mitochondrial myopathy caused by complex II deficiency. American Journal of Medical Genetics Part A. 176(2). 399–403. 21 indexed citations

11.

Barmherzig, Rebecca, et al.. (2017). A New Patient With Intermediate Severe Salla Disease With Hypomyelination: A Literature Review for Salla Disease. Pediatric Neurology. 74. 87–91.e2. 19 indexed citations

12.

Bruun, Theodora U. J., Dawn Cordeiro, Jaina Patel, et al.. (2016). Phenotype, biochemical features, genotype and treatment outcome of pyridoxine-dependent epilepsy. Metabolic Brain Disease. 32(2). 443–451. 37 indexed citations

13.

Patel, Jaina, et al.. (2015). Diagnostic yield of genetic testing in epileptic encephalopathy in childhood. Journal of the Neurological Sciences. 357. e31–e31. 3 indexed citations

14.

Mercimek‐Mahmutoglu, Saadet, Jaina Patel, Dawn Cordeiro, et al.. (2015). Diagnostic yield of genetic testing in epileptic encephalopathy in childhood. Epilepsia. 56(5). 707–716. 164 indexed citations

15.

Mercimek‐Mahmutoglu, Saadet, Dawn Cordeiro, Keith Hyland, et al.. (2014). Novel therapy for pyridoxine dependent epilepsy due to ALDH7A1 genetic defect: l-arginine supplementation alternative to lysine-restricted diet. European Journal of Paediatric Neurology. 18(6). 741–746. 51 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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