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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	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 2024 ·Genetics in Medicine ·Patricia Birch, (unknown), (unknown), Cyrus Boelman, Mary Connolly, Michelle Demos, (unknown), (unknown), Sylvia Stöckler, Alison M. Elliott, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	1
2	Expanding the genotype-phenotype spectrum in SCN8A-related disorders 2024 ·BMC Neurology ·Malavika Hebbar, (unknown), (unknown), Cyrus Boelman, Richard A. Dean, Samuel J. Goodchild, Janette Mezeyova, Noah Gregory Shuart, J. P. Johnson, James Lee, Aspasia Michoulas, Linda Huh, Linlea Armstrong, Mary Connolly, Michelle Demos	2
3	Solving inherited white matter disorder etiologies in the neurology clinic: Challenges and lessons learned using next-generation sequencing 2023 ·Frontiers in Neurology ·(unknown), Kether Guerrero, Luan T. Tran, Mackenzie A. Michell‐Robinson, Geneviève Legault, Bernard Brais, Michel Sylvain, (unknown), Michelle Demos, Wolfgang Köhler, Tomi Pastinen, Isabelle Thiffault, Geneviève Bernard	3
4	Somatic mosaicism detected by genome-wide sequencing in 500 parent–child trios with suspected genetic disease: clinical and genetic counseling implications 2021 ·Molecular Case Studies ·(unknown), Linlea Armstrong, Cornelius F. Boerkoel, L. Clarke, Christèle du Souich, Michelle Demos, William T. Gibson, Harinder Gill, Elena Lopez‐Rangel, Millan S. Patel, Kathryn Selby, (unknown), (unknown), Alison M. Elliott, Jan M. Friedman	6
5	SETD1B-associated neurodevelopmental disorder 2020 ·Journal of Medical Genetics ·(unknown), (unknown), Harinder Gill, Margaret L. McKinnon, Bertrand Isidor, Benjamin Cogné, Jill Mwenifumbo, Clara van Karnebeek, Jianghong An, Steven J.M. Jones, Matthew J. Farrer, Michelle Demos, Mary Connolly, William T. Gibson, (unknown)	19
6	Pathophysiology of and therapeutic options for a GABRA1 variant linked to epileptic encephalopathy 2019 ·Molecular Brain ·Yunfei Bai, (unknown), (unknown), Peter Axerio-Cilies, Jie Lu, Linda Huh, Mary Connolly, Ilaria Guella, Matthew J. Farrer, Qing Xu, Lidong Liu, Michelle Demos, Yu Tian Wang	14
7	Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions 2018 ·Journal of Genetic Counseling ·Shelin Adam, Patricia Birch, (unknown), Nick Bansback, Adrian L. Jones, Mary Connolly, Michelle Demos, Eric Toyota, Matthew J. Farrer, Jan M. Friedman	28
8	An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2 2017 ·Pediatric Neurology ·(unknown), Sarah E. Buerki, Ilaria Guella, Eric Toyota, Daniel M. Evans, Marna B. McKenzie, Anita Datta, Aspasia Michoulas, Shelin Adam, Margot I. Van Allen, Tanya N. Nelson, Matthew J. Farrer, Mary Connolly, Michelle Demos	15
9	De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy 2016 ·Neurology Genetics ·Ilaria Guella, Linda Huh, Marna B. McKenzie, Eric Toyota, E. Martina Bebin, Michelle L. Thompson, Gregory M. Cooper, Daniel M. Evans, Sarah E. Buerki, Shelin Adam, Margot I. Van Allen, Tanya N. Nelson, Mary Connolly, Matthew J. Farrer, Michelle Demos	19
10	Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target? 2015 ·Molecular Genetics and Metabolism ·Gabriella Horváth, Michelle Demos, Casper Shyr, Allison Matthews, Linhua Zhang, (unknown), Sylvia Stöckler‐Ipsiroglu, Margot I. Van Allen, B. Ogan Mancarci, Lilah Toker, Paul Pavlidis, Colin J.D. Ross, Wyeth W. Wasserman, Natalie Trump, (unknown), Simon Pope, J. Helen Cross, Clara van Karnebeek	33
11	A novel recurrent mutation in ATP1A3 causes CAPOS syndrome 2014 ·Orphanet Journal of Rare Diseases ·Michelle Demos, Clara DM van Karnebeek, Colin J.D. Ross, Shelin Adam, Yaoqing Shen, Shing H. Zhan, Casper Shyr, Gabriella Horváth, Mohnish Suri, Alan Fryer, Steven J.M. Jones, Jan M. Friedman	135
12	Recurrent subacute post-viral onset of ataxia associated with a PRF1 mutation 2013 ·European Journal of Human Genetics ·Cristina Dias, (unknown), Murat Sincan, Rosemarie Rupps, Thomas C. Markello, Ramona Salvarinova, (unknown), Kamal Menghrajani, (unknown), Darren Sutherland, Edgardo S. Fortuno, Tobias R. Kollmann, Michelle Demos, Jan M. Friedman, David P. Speert, William A. Gahl, Cornelius F. Boerkoel	11
13	A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction 2009 ·Movement Disorders ·Michelle Demos, Vincenzo Macri, K Farrell, Tanya N. Nelson, Kristine Chapman, Eric A. Accili, Linlea Armstrong	41
14	Characterization of a new X‐linked mental retardation syndrome with microcephaly, cortical malformation, and thin habitus 2009 ·American Journal of Medical Genetics Part A ·Christèle du Souich, (unknown), (unknown), (unknown), Tanya N. Nelson, (unknown), Laura Arbour, (unknown), Barbara McGillivray, (unknown), Andreas Rump, Kenneth J. Poskitt, Michelle Demos, Margot I. Van Allen, Cornelius F. Boerkoel	23
15	Clinical study of two brothers with a novel 33 bp duplication in the ARX gene 2009 ·American Journal of Medical Genetics Part A ·Michelle Demos, Tod Fullston, M. W. Partington, Jozef Gécz, William T. Gibson	13
16	ELECTRO-CLINICAL STUDY OF FOUR FIRST NATIONS FAMILIES WITH BENIGN FAMILIAL INFANTILE SEIZURES 2006 ·Neuropediatrics ·Michelle Demos, Mary Connolly, Laura Arbour, K Farrell	1
17	Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: A unique patient or a novel metabolic disorder? 2005 ·Molecular Genetics and Metabolism ·Paula J. Waters, Minesh Khashu, Yolanda Lillquist, Christof Senger, André Mattman, Michelle Demos, Kenneth D.R. Setchell, (unknown), Patrick Scott, Nenad Blau, Hilary Vallance	4
18	6‐Pyruvoyl‐tetrahydropterin synthase deficiency with mild hyperphenylalaninemia 2005 ·Annals of Neurology ·Michelle Demos, Paula J. Waters, Hilary Vallance, Yolanda Lillquist, Nawal Makhseed, Keith Hyland, Nenad Blau, Mary Connolly	9
19	Erbstatin blocks platelet activating factor‐induced protein‐tyrosine phosphorylation, polyphosphoinositide hydrolysis, protein kinase C activation, serotonin secretion and aggregation of rabbit platelets 1990 ·FEBS Letters ·Hassan Salari, Vincent Duronio, (unknown), Michelle Demos, Kelvin E. Jones, (unknown), Alan T. Hudson, Steven Pelech	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 1990 ·Biochemical Journal ·H. Salari, Vincent Duronio, (unknown), Michelle Demos, Steven Pelech	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.

Explore authors with similar magnitude of impact