Maryse Chalifoux

725 total citations
14 papers, 477 citations indexed

About

Maryse Chalifoux is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Maryse Chalifoux has authored 14 papers receiving a total of 477 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Cognitive Neuroscience. Recurrent topics in Maryse Chalifoux's work include Genetics and Neurodevelopmental Disorders (11 papers), Autism Spectrum Disorder Research (7 papers) and Genomic variations and chromosomal abnormalities (4 papers). Maryse Chalifoux is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Autism Spectrum Disorder Research (7 papers) and Genomic variations and chromosomal abnormalities (4 papers). Maryse Chalifoux collaborates with scholars based in Canada, United States and Cyprus. Maryse Chalifoux's co-authors include Jeanette J. A. Holden, Jiangxin Wan, Mónika Kuzma, Jifeng Ying, Yafan Huang, David T. Dennis, Peter McCourt, Yang Wang, Gene S. Fisch and Bradley N. White and has published in prestigious journals such as The Plant Journal, Molecular Plant and American Journal of Medical Genetics.

In The Last Decade

Maryse Chalifoux

14 papers receiving 449 citations

Peers

Countries citing papers authored by Maryse Chalifoux

Since Specialization

Citations

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

Fields of papers citing papers by Maryse Chalifoux

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maryse Chalifoux

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Activation tagging identifies Arabidopsis transcription factor AtMYB68 for heat and drought tolerance at yield determining reproductive stages 2020 ·The Plant Journal ·(unknown), Yang Wang, Mónika Kuzma, Maryse Chalifoux, (unknown), Shujun Yang, Jifeng Ying, (unknown), (unknown), Rebecca E. Griffiths, (unknown), Xurong Tang, Gang Tian, (unknown), David T. Dennis, Peter McCourt, Yafan Huang, Jiangxin Wan	26
2	Shoot-Specific Down-Regulation of Protein Farnesyltransferase (α-Subunit) for Yield Protection against Drought in Canola 2009 ·Molecular Plant ·Yang Wang, (unknown), Maryse Chalifoux, Jifeng Ying, (unknown), (unknown), Rebecca E. Griffiths, Mónika Kuzma, Jiangxin Wan, Yafan Huang	76
3	Molecular tailoring of farnesylation for plant drought tolerance and yield protection 2005 ·The Plant Journal ·Yang Wang, Jifeng Ying, Mónika Kuzma, Maryse Chalifoux, (unknown), (unknown), (unknown), (unknown), Jiangxin Wan, David T. Dennis, Peter McCourt, Yafan Huang	149
4	Autism and the X chromosome: No linkage to microsatellite loci detected using the affected sibling pair method 2002 ·American Journal of Medical Genetics ·(unknown), (unknown), Paula D. Robinson, Maryse Chalifoux, Fabìo Macciardi, Bradley N. White, Jeanette J. A. Holden	10
5	Frequencies of “grey‐zone” and premutation‐size FMR1 CGG‐repeat alleles in patients with developmental disability in Cyprus and Canada 1999 ·American Journal of Medical Genetics ·Philippos C. Patsalis, Carolina Sismani, (unknown), Jeanette J. A. Holden, J. S. Lawson, Maryse Chalifoux, (unknown), Melissa Walker, Jayne Leggo	1
6	FMR1 in global populations. 1996 ·PubMed ·Catherine B. Kunst, (unknown), (unknown), Evan E. Eichler, James M. Bullard, Maryse Chalifoux, Jeanette J. A. Holden, Antonio Torroni, David L. Nelson, Stephen T. Warren	65
7	Lack of expansion of triplet repeats in the FMR1, FRAXE, and FRAXF loci in male multiplex families with autism and pervasive developmental disorders 1996 ·American Journal of Medical Genetics ·Jeanette J. A. Holden, (unknown), Maryse Chalifoux, (unknown), (unknown), Paula D. Robinson, Péter Szatmári, Bradley N. White	13
8	Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38) 1996 ·American Journal of Medical Genetics ·(unknown), Elizabeth Ives, Maryse Chalifoux, (unknown), Sandra A. Farrell, Paula D. Robinson, Bradley N. White, Jeanette J. A. Holden	15
9	Longitudinal study of cognitive abilities and adaptive behavior levels in fragile X males: A prospective multicenter analysis 1996 ·American Journal of Medical Genetics ·Gene S. Fisch, Richard J. Simensen, Jack Tarleton, Maryse Chalifoux, Jeanette J. A. Holden, Nancy J. Carpenter, Patricia N. Howard‐Peebles, Anne Maddalena	67
10	Lack of association between mutation size and cognitive/behavior deficits in fragile X males: A brief report 1996 ·American Journal of Medical Genetics ·Gene S. Fisch, Nancy J. Carpenter, Patricia N. Howard‐Peebles, Anne Maddalena, Richard J. Simensen, Jack Tarleton, (unknown), Maryse Chalifoux, Jeanette J. A. Holden	8
11	Trinucleotide repeats at the FRAXF locus: Frequency and distribution in the general population 1996 ·American Journal of Medical Genetics ·J.J.A. Holden, Melissa Walker, Maryse Chalifoux, Bradley N. White	4
12	A rapid, reliable, and inexpensive method for detection of di- and trinucleotide repeat markers and disease loci from dried blood spots 1996 ·American Journal of Medical Genetics ·Jeanette J. A. Holden, Maryse Chalifoux, (unknown), (unknown), Bradley N. White	15
13	Trinucleotide repeat expansion in the FRAXE locus is not common among institutionalized individuals with non-specific developmental disabilities 1996 ·American Journal of Medical Genetics ·Jeanette J. A. Holden, (unknown), Maryse Chalifoux, (unknown), Elizabeth Scott, (unknown), (unknown), (unknown), Samantha J.L. Knight, Kay E. Davies, Bradley N. White	16
14	Reliability of diagnostic assessment of normal and premutation status in the fragile X syndrome using DNA testing 1994 ·American Journal of Medical Genetics ·Gene S. Fisch, David L. Nelson, Karen Snow, Stephen N. Thibodeau, Maryse Chalifoux, Jeanette J. A. Holden	12

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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