Author

Hanad Sharmarke

Institut Universitaire de Gériatrie de Montréal

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2 Neuroscience· 2

Signature Assays, Organisms & Methods

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Assay:imaging· 4 Organism:human· 3 Approach:statistical model· 3 Research Focus:benchmarking· 2 Research Focus:gene regulatory network inference· 2 Approach:benchmark study· 1 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

Pierre BelleciD· 4 shared Pierre OrbaniD· 3 shared Sebastian Georg Wenzel UrchsiD· 3 shared Ana Isabel SilvaiD· 2 shared Anne Manuela MaillardiD· 2 shared Aurélie LabbeiD· 2 shared Carrie E. BeardeniD· 2 shared Charles-Olivier MartiniD· 2 shared

Activity by Year

2019-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersNeuroscience

Pierre BellecORCID

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4 papers

Recent·Most cited

Continuous Evaluation of Denoising Strategies in Resting-State fMRI Connectivity Using fMRIPrep and Nilearn

Hao-Ting Wang, Steven L. Meisler, Hanad Sharmarke, Natasha Clarke, Nicolas Gensollen, Christopher Johnson Markiewicz, François Paugam, Bertrand Thirion, Pierre Bellec

This paper evaluates denoising strategies in resting-state fMRI using fMRIPrep and Nilearn, finding that scrubbing combined with global signal regression is effective but may disrupt continuous sampling.

PLoS Computational Biology · Mar 18, 2024Peer-reviewedNeuroscience

Atlas of functional connectivity relationships across rare and common genetic variants, traits, and psychiatric conditions

Clara A. Moreau, Kuldeep Kumar, Annabelle Harvey, Guillaume Huguet, Sebastian Georg Wenzel Urchs, Elise A. Douard, Laura M. Schultz, Hanad Sharmarke, Khadijé Jizi, Charles-Olivier Martin, Nadine Younis, Petra Tamer, Thomas Rolland, Martineau Jean‐Louis, Pierre Orban, , Sébastien Jacquemont

The paper examines how rare and common genomic variants affect brain functional connectivity, revealing how polygenicity and pleiotropy influence psychiatric conditions and brain networks.

medRxiv · May 21, 2021 · PreprintGenetic & Genomic Medicine

The general impact of haploinsufficiency on brain connectivity underlies the pleiotropic effect of neuropsychiatric CNVs

Clara A. Moreau, Guillaume Huguet, Sebastian Georg Wenzel Urchs, Elise A. Douard, Hanad Sharmarke, Pierre Orban, Aurélie Labbe, Claudia Modenato, Sandra Martin‐Brevet, Kuldeep Kumar, Charles-Olivier Martin, Khadijé Jizi, Nadine Younis, Petra Tamer, Martineau Jean‐Louis, , Sébastien Jacquemont

Neuropsychiatric CNVs reorganize brain connectivity along shared patterns linked to cognitive traits and disorder severity.

Biological Psychiatry · Apr 27, 2021Peer-reviewedGenetic & Genomic Medicine

A highly predictive signature of cognition and brain atrophy for progression to Alzheimer’s dementia

Angela Tam, Christian L. Dansereau, Yasser Iturria‐Medina, Sebastian Georg Wenzel Urchs, Pierre Orban, Hanad Sharmarke, John C.S. Breitner, Pierre Bellec, Alzheimer’s Disease Neuroimaging Initiative

The paper identifies a predictive signature of cognition and brain atrophy for progression to Alzheimer’s dementia using machine learning, validated in two MCI cohorts with high positive predictive value.

GigaScience · May 1, 2019Peer-reviewedNeuroscience