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

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

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20 of 20 papers shown

#	Title	Journal	Authors	Indexed citations
1	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	Patricia Birch, Cyrus Boelman et al.	1
2	Expanding the genotype-phenotype spectrum in SCN8A-related disorders	BMC Neurology	Malavika Hebbar, Cyrus Boelman et al.	2
3	Solving inherited white matter disorder etiologies in the neurology clinic: Challenges and lessons learned using next-generation sequencing	Frontiers in Neurology	Kether Guerrero, Luan T. Tran et al.	3
4	Somatic mosaicism detected by genome-wide sequencing in 500 parent–child trios with suspected genetic disease: clinical and genetic counseling implications	Molecular Case Studies	Linlea Armstrong, Cornelius F. Boerkoel et al.	6
5	SETD1B-associated neurodevelopmental disorder	Journal of Medical Genetics	Harinder Gill, Margaret L. McKinnon et al.	19
6	Pathophysiology of and therapeutic options for a GABRA1 variant linked to epileptic encephalopathy	Molecular Brain	Yunfei Bai, Peter Axerio-Cilies et al.	14
7	Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions	Journal of Genetic Counseling	Shelin Adam, Patricia Birch et al.	28
8	An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2	Pediatric Neurology	Sarah E. Buerki, Ilaria Guella et al.	15
9	De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy	Neurology Genetics	Ilaria Guella, Linda Huh et al.	19
10	Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target?	Molecular Genetics and Metabolism	Gabriella Horváth, Michelle Demos et al.	33
11	A novel recurrent mutation in ATP1A3 causes CAPOS syndrome	Orphanet Journal of Rare Diseases	Michelle Demos, Clara DM van Karnebeek et al.	135
12	Recurrent subacute post-viral onset of ataxia associated with a PRF1 mutation	European Journal of Human Genetics	Cristina Dias, Murat Sincan et al.	11
13	A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction	Movement Disorders	Michelle Demos, Vincenzo Macri et al.	41
14	Characterization of a new X‐linked mental retardation syndrome with microcephaly, cortical malformation, and thin habitus	American Journal of Medical Genetics Part A	Christèle du Souich, Tanya N. Nelson et al.	23
15	Clinical study of two brothers with a novel 33 bp duplication in the ARX gene	American Journal of Medical Genetics Part A	Michelle Demos, Tod Fullston et al.	13
16	ELECTRO-CLINICAL STUDY OF FOUR FIRST NATIONS FAMILIES WITH BENIGN FAMILIAL INFANTILE SEIZURES	Neuropediatrics	Michelle Demos, Mary Connolly et al.	1
17	Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: A unique patient or a novel metabolic disorder?	Molecular Genetics and Metabolism	Paula J. Waters, Minesh Khashu et al.	4
18	6‐Pyruvoyl‐tetrahydropterin synthase deficiency with mild hyperphenylalaninemia	Annals of Neurology	Michelle Demos, Paula J. Waters et al.	9
19	Erbstatin blocks platelet activating factor‐induced protein‐tyrosine phosphorylation, polyphosphoinositide hydrolysis, protein kinase C activation, serotonin secretion and aggregation of rabbit platelets	FEBS Letters	Hassan Salari, Vincent Duronio et al.	59
20	Translocation-independent activation of protein kinase C by platelet-activating factor, thrombin and prostacyclin. Lack of correlation with polyphosphoinositide hydrolysis in rabbit platelets	Biochemical Journal	H. Salari, Vincent Duronio et al.	24

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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