Michelle Demos

2.0k total citations
23 papers, 482 citations indexed

About

Michelle Demos is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Michelle Demos has authored 23 papers receiving a total of 482 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Michelle Demos's work include Genomics and Rare Diseases (7 papers), Ion channel regulation and function (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Michelle Demos is often cited by papers focused on Genomics and Rare Diseases (7 papers), Ion channel regulation and function (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Michelle Demos collaborates with scholars based in Canada, United States and United Kingdom. Michelle Demos's co-authors include Shelin Adam, Jan M. Friedman, Steven J.M. Jones, Gabriella Horváth, Casper Shyr, Colin J.D. Ross, Steven Pelech, Vincent Duronio, Alan Fryer and Mohnish Suri and has published in prestigious journals such as Annals of Neurology, Biochemical Journal and FEBS Letters.

In The Last Decade

Michelle Demos

23 papers receiving 478 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michelle Demos Canada 13 270 145 97 64 50 23 482
Monica Traverso Italy 13 348 1.3× 122 0.8× 66 0.7× 53 0.8× 38 0.8× 32 488
Moeenaldeen AlSayed Saudi Arabia 15 254 0.9× 183 1.3× 35 0.4× 36 0.6× 86 1.7× 49 737
Nathalie Van der Aa Belgium 19 412 1.5× 388 2.7× 84 0.9× 22 0.3× 43 0.9× 26 809
Takahito Inoue Japan 12 185 0.7× 124 0.9× 81 0.8× 188 2.9× 34 0.7× 30 604
Marc D’Hooghe Belgium 12 337 1.2× 63 0.4× 95 1.0× 123 1.9× 25 0.5× 18 580
Ardinger Hh United States 6 192 0.7× 124 0.9× 37 0.4× 12 0.2× 56 1.1× 287 402
Delphine Héron France 11 201 0.7× 157 1.1× 138 1.4× 60 0.9× 14 0.3× 27 421
K N Harikrishnan Australia 12 552 2.0× 249 1.7× 63 0.6× 58 0.9× 33 0.7× 16 722
Takeshi Okinaga Japan 14 160 0.6× 74 0.5× 58 0.6× 99 1.5× 18 0.4× 27 411
Bean Ljh 6 180 0.7× 113 0.8× 37 0.4× 12 0.2× 56 1.1× 285 386

Countries citing papers authored by Michelle Demos

Since Specialization
Citations

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

Fields of papers citing papers by Michelle Demos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michelle Demos

This figure shows the co-authorship network connecting the top 25 collaborators of Michelle Demos. A scholar is included among the top collaborators of Michelle Demos 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 Michelle Demos. Michelle Demos 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.
Birch, Patricia, Cyrus Boelman, Mary Connolly, et al.. (2024). Where there is no genetic counselor: An online decision-aid supports the majority of parents’ diagnostic genomic testing choices for their children. Genetics in Medicine. 26(9). 101173–101173. 1 indexed citations
2.
Hebbar, Malavika, Cyrus Boelman, Richard A. Dean, et al.. (2024). Expanding the genotype-phenotype spectrum in SCN8A-related disorders. BMC Neurology. 24(1). 31–31. 2 indexed citations
3.
Guerrero, Kether, Luan T. Tran, Mackenzie A. Michell‐Robinson, et al.. (2023). Solving inherited white matter disorder etiologies in the neurology clinic: Challenges and lessons learned using next-generation sequencing. Frontiers in Neurology. 14. 1148377–1148377. 3 indexed citations
4.
Armstrong, Linlea, Cornelius F. Boerkoel, L. Clarke, et al.. (2021). Somatic mosaicism detected by genome-wide sequencing in 500 parent–child trios with suspected genetic disease: clinical and genetic counseling implications. Molecular Case Studies. 7(6). a006125–a006125. 6 indexed citations
5.
Gill, Harinder, Margaret L. McKinnon, Bertrand Isidor, et al.. (2020). SETD1B-associated neurodevelopmental disorder. Journal of Medical Genetics. 58(3). 196–204. 19 indexed citations
6.
Bai, Yunfei, Peter Axerio-Cilies, Jie Lu, et al.. (2019). Pathophysiology of and therapeutic options for a GABRA1 variant linked to epileptic encephalopathy. Molecular Brain. 12(1). 92–92. 14 indexed citations
7.
Adam, Shelin, Patricia Birch, Nick Bansback, et al.. (2018). Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions. Journal of Genetic Counseling. 28(1). 10–17. 28 indexed citations
8.
Buerki, Sarah E., Ilaria Guella, Eric Toyota, et al.. (2017). An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2. Pediatric Neurology. 75. 87–90. 15 indexed citations
9.
Guella, Ilaria, Linda Huh, Marna B. McKenzie, et al.. (2016). De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy. Neurology Genetics. 2(6). e120–e120. 19 indexed citations
10.
Horváth, Gabriella, Michelle Demos, Casper Shyr, et al.. (2015). Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target?. Molecular Genetics and Metabolism. 117(1). 42–48. 33 indexed citations
11.
Demos, Michelle, Clara DM van Karnebeek, Colin J.D. Ross, et al.. (2014). A novel recurrent mutation in ATP1A3 causes CAPOS syndrome. Orphanet Journal of Rare Diseases. 9(1). 15–15. 135 indexed citations
12.
Dias, Cristina, Murat Sincan, Rosemarie Rupps, et al.. (2013). Recurrent subacute post-viral onset of ataxia associated with a PRF1 mutation. European Journal of Human Genetics. 21(11). 1232–1239. 11 indexed citations
13.
Demos, Michelle, Vincenzo Macri, K Farrell, et al.. (2009). A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction. Movement Disorders. 24(5). 778–782. 41 indexed citations
14.
Souich, Christèle du, Tanya N. Nelson, Laura Arbour, et al.. (2009). Characterization of a new X‐linked mental retardation syndrome with microcephaly, cortical malformation, and thin habitus. American Journal of Medical Genetics Part A. 149A(11). 2469–2478. 23 indexed citations
15.
Demos, Michelle, Tod Fullston, M. W. Partington, Jozef Gécz, & William T. Gibson. (2009). Clinical study of two brothers with a novel 33 bp duplication in the ARX gene. American Journal of Medical Genetics Part A. 149A(7). 1482–1486. 13 indexed citations
16.
Demos, Michelle, Mary Connolly, Laura Arbour, & K Farrell. (2006). ELECTRO-CLINICAL STUDY OF FOUR FIRST NATIONS FAMILIES WITH BENIGN FAMILIAL INFANTILE SEIZURES. Neuropediatrics. 37(S 1). 1 indexed citations
17.
Waters, Paula J., Minesh Khashu, Yolanda Lillquist, et al.. (2005). Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: A unique patient or a novel metabolic disorder?. Molecular Genetics and Metabolism. 86. 148–152. 4 indexed citations
18.
Demos, Michelle, Paula J. Waters, Hilary Vallance, et al.. (2005). 6‐Pyruvoyl‐tetrahydropterin synthase deficiency with mild hyperphenylalaninemia. Annals of Neurology. 58(1). 164–167. 9 indexed citations
19.
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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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