Author

Sabrina Nowak

Centre Hospitalier Universitaire Sainte-Justine

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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Genetics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Aurélie LabbeiD· 2 shared Catherine SchrammiD· 2 shared Celia M.T. GreenwoodiD· 2 shared David C. GlahniD· 2 shared Elise A. DouardiD· 2 shared Guillaume HuguetiD· 2 shared Günter SchumanniD· 2 shared Laura A. AlmasyiD· 2 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

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2 papers

Recent·Most cited

Effects-sizes of deletions and duplications on autism risk across the genome

Elise A. Douard, Abderrahim Zeribi, Catherine Schramm, Petra Tamer, Mor Absa Loum, Sabrina Nowak, Zohra Saci, Marie-Pier Lord, Borja Rodríguez‐Herreros, Martineau Jean‐Louis, Clara A. Moreau, Eva Loth, Günter Schumann, Zdenka Pausová, Mayada Elsabbagh, , Sébastien Jacquemont

The paper estimates the effect sizes of deletions and duplications on autism risk and IQ using statistical models applied to CNV data from multiple cohorts.

American Journal of Psychiatry · Sep 11, 2020Peer-reviewedGenetics

Genome wide analysis of gene dosage in 24,092 individuals shows that 10,000 genes modulate cognitive ability

Guillaume Huguet, Catherine Schramm, Elise A. Douard, Petra Tamer, Antoine Main, Pauline Monin, Jade England, Khadijé Jizi, Thomas Renne, Myriam Poirier, Sabrina Nowak, Charles-Olivier Martin, Nadine Younis, Inga Sophia Knoth, Martineau Jean‐Louis, , Sébastien Jacquemont

The paper quantifies the effect of copy number variants on cognitive ability using genomic data from 24,092 individuals, finding that 10,000 genes modulate intelligence.

bioRxiv · Apr 3, 2020 · PreprintGenetics