Author

Nisrine Tarik

Centre Hospitalier Universitaire de Rabat-Salé

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

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Neuroscience· 1

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Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aude-Marie Lepagnol-BesteliD· 1 shared Christine PlançoniD· 1 shared Gabriel SantpereiD· 1 shared Hassan Kisra· 1 shared Imane Benhima· 1 shared Jean-Marc PlazaiD· 1 shared Jean‐François DeleuzeiD· 1 shared Jean‐Marie Moalic· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperNeuroscience

Aude-Marie Lepagnol-BestelORCID

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1 paper

Recent·Most cited

Multi-hit autism genomic architecture evidenced from consanguineous families with involvement of FEZF2 and mutations in high-risk genes

Mounia Bensaid, Yann Loe-Mie, Aude-Marie Lepagnol-Bestel, Wenqi Han, Gabriel Santpere, Thomas Klarić, Christine Plançon, Rim Roudies, Imane Benhima, Nisrine Tarik, Patrick Nitschké, Jean-Marc Plaza, Hassan Kisra, Jean‐François Deleuze, Nenad Šestan, , Michel Simonneau

The paper identifies a multi-hit genomic architecture for ASD in consanguineous families, involving FEZF2 deletions and mutations in high-risk genes.

bioRxiv · Sep 11, 2019 · PreprintNeuroscience