Danielle M. Andrade

6.9k total citations
111 papers, 2.5k citations indexed

About

Danielle M. Andrade is a scholar working on Psychiatry and Mental health, Genetics and Molecular Biology. According to data from OpenAlex, Danielle M. Andrade has authored 111 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Psychiatry and Mental health, 40 papers in Genetics and 30 papers in Molecular Biology. Recurrent topics in Danielle M. Andrade's work include Epilepsy research and treatment (47 papers), Genetics and Neurodevelopmental Disorders (31 papers) and Glycogen Storage Diseases and Myoclonus (17 papers). Danielle M. Andrade is often cited by papers focused on Epilepsy research and treatment (47 papers), Genetics and Neurodevelopmental Disorders (31 papers) and Glycogen Storage Diseases and Myoclonus (17 papers). Danielle M. Andrade collaborates with scholars based in Canada, United States and Netherlands. Danielle M. Andrade's co-authors include Richard Wennberg, Anne S. Bassett, Andrés M. Lozano, Clement Hamani, Felippe Borlot, Berge A. Minassian, Mojgan Hodaie, Eva W.C. Chow, Anthony E. Lang and Dominik Zumsteg and has published in prestigious journals such as Neurology, Annals of Neurology and The British Journal of Psychiatry.

In The Last Decade

Danielle M. Andrade

103 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Danielle M. Andrade Canada 30 869 769 717 614 588 111 2.5k
Bruria Ben‐Zeev Israel 33 892 1.0× 1.3k 1.7× 994 1.4× 737 1.2× 268 0.5× 105 3.4k
Jennifer M. Kwon United States 29 280 0.3× 1.2k 1.5× 634 0.9× 861 1.4× 316 0.5× 77 3.4k
Hans Stroink Netherlands 35 1.6k 1.8× 1.1k 1.4× 485 0.7× 491 0.8× 365 0.6× 70 3.3k
Onno van Nieuwenhuizen Netherlands 33 1.5k 1.8× 687 0.9× 372 0.5× 772 1.3× 354 0.6× 117 3.5k
Raili Riikonen Finland 36 1.8k 2.1× 647 0.8× 1.2k 1.7× 597 1.0× 258 0.4× 115 3.9k
W.O. Renier Netherlands 32 1.4k 1.7× 1.1k 1.4× 472 0.7× 858 1.4× 424 0.7× 116 3.5k
Mårten Kyllerman Sweden 34 444 0.5× 1.2k 1.6× 759 1.1× 350 0.6× 266 0.5× 88 3.1k
Olivier Dulac France 22 797 0.9× 574 0.7× 232 0.3× 367 0.6× 296 0.5× 78 2.0k
Andrew Bleasel Australia 30 2.1k 2.5× 417 0.5× 543 0.8× 961 1.6× 1.0k 1.8× 92 3.6k
Lucia Fusco Italy 28 1.5k 1.7× 449 0.6× 454 0.6× 587 1.0× 277 0.5× 87 2.2k

Countries citing papers authored by Danielle M. Andrade

Since Specialization
Citations

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

Fields of papers citing papers by Danielle M. Andrade

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Danielle M. Andrade. 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 Danielle M. Andrade. The network helps show where Danielle M. Andrade may publish in the future.

Co-authorship network of co-authors of Danielle M. Andrade

This figure shows the co-authorship network connecting the top 25 collaborators of Danielle M. Andrade. A scholar is included among the top collaborators of Danielle M. Andrade 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 Danielle M. Andrade. Danielle M. Andrade 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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2.
Ali, Quratulain Zulfiqar, et al.. (2024). P.049 Acetazolamide use for myoclonus: case report of 2 patients with progressive myoclonic epilepsy and literature review. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 51(s1). S29–S29.
3.
Ali, Quratulain Zulfiqar, Ángel Aledo‐Serrano, Allan Bayat, et al.. (2024). Adult Phenotype of CHD2 -Associated Disorders. Neurology Genetics. 10(6). e200194–e200194.
4.
Andrade, Danielle M., Hans Katzberg, Steven P. Miller, et al.. (2023). Building the Bridge From Pediatric to Adult Neurological Care. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 51(5). 690–692. 2 indexed citations
5.
Andrade, Danielle M., et al.. (2023). Abstracts. Epilepsia. 64(S2). 7–570.
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Perucca, Piero, Kate E. Stanley, Anne M. McIntosh, et al.. (2022). Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe Epilepsy. Annals of Neurology. 93(4). 752–761. 4 indexed citations
8.
Berg, Anne T., Kelly G. Knupp, Sookyong Koh, et al.. (2022). COVID‐19 vaccine in patients with Dravet syndrome: Observations and real‐world experiences. Epilepsia. 63(7). 1778–1786. 14 indexed citations
9.
House, Andrew A., Danielle M. Andrade, Mary Connolly, et al.. (2021). Adults with tuberous sclerosis complex: A distinct patient population. Epilepsia. 63(3). 663–671. 3 indexed citations
10.
Sadoway, Tara, Yue Yin, Quratulain Zulfiqar Ali, et al.. (2021). Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox–Gastaut syndrome. Brain Communications. 3(3). fcab207–fcab207. 8 indexed citations
11.
Andrade, Danielle M., Anne T. Berg, Kelly G. Knupp, et al.. (2021). Dravet syndrome: A quick transition guide for the adult neurologist. Epilepsy Research. 177. 106743–106743. 15 indexed citations
12.
Borlot, Felippe, et al.. (2019). Clinical utility of multigene panel testing in adults with epilepsy and intellectual disability. Epilepsia. 60(8). 1661–1669. 35 indexed citations
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14.
Sen, Arjune, Patricia Dugan, Piero Perucca, et al.. (2018). The phenotype of bilateral hippocampal sclerosis and its management in “real life” clinical settings. Epilepsia. 59(7). 1410–1420. 5 indexed citations
15.
Fasano, Alfonso, Carlo Di Bonaventura, Francesco Bove, et al.. (2018). Movement disorders phenomenology in focal motor seizures. Parkinsonism & Related Disorders. 61. 161–165. 6 indexed citations
16.
Wissel, Benjamin D., Alok Dwivedi, Tyler E. Gaston, et al.. (2016). Which patients with epilepsy are at risk for psychogenic nonepileptic seizures (PNES)? A multicenter case–control study. Epilepsy & Behavior. 61. 180–184. 25 indexed citations
17.
Vasli, Nasim, Kirti Mittal, Anna Mikhailov, et al.. (2015). Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability. Psychiatric Genetics. 26(2). 66–73. 17 indexed citations
18.
George, Susan R., et al.. (2013). Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome. Genetics in Medicine. 16(1). 40–44. 60 indexed citations
19.
Espay, Alberto J., Danielle M. Andrade, Richard Wennberg, & Anthony E. Lang. (2005). Atypical absences and recurrent absence status in an adult with Angelman syndrome due to the UBE3A mutation. Epileptic Disorders. 7(3). 227–230. 14 indexed citations
20.
Chan, Elayne M., Danielle M. Andrade, Silvana Franceschetti, & Berge A. Minassian. (2005). Progressive myoclonus epilepsies: EPM1, EPM2A, EPM2B.. PubMed. 95. 47–57. 26 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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