Author

Marion Jeanne

GenentechORCID 0000-0001-7334-3061Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Research Focus:gene regulatory network inference· 2 Approach:statistical model· 2 Organism:human· 1 Organism:mouse· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Amy Stockwell· 1 shared Arthur WüsteriD· 1 shared Brian L. YaspaniD· 1 shared Douglas B. GouldiD· 1 shared Han Qin· 1 shared Ivaylo Stoilov· 1 shared Kendall HoffiD· 1 shared Mao MaoiD· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Amy Stockwell

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintJun 22, 2022

Age-related Macular Degeneration patient deep phenotyping and whole genome sequencing analysis identifies coding variants linking small low-luminance visual deficit to fat storage defects

Sehyun Kim, Amy Stockwell, Han Qin…·Marion Jeanne

The paper identifies coding variants in the CIDEC gene associated with small low-luminance visual deficit in AMD patients, showing an indirect effect on fat storage and lipid droplet fusion.

DOI 10.1101/2022.06.22.497149

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsDisease Models & MechanismsPeer-reviewedMar 10, 2021

Identification of Fibronectin 1 as a candidate genetic modifier in a Col4a mutant mouse model of Gould syndrome

Mao Mao, Tanav A. Popli, Marion Jeanne…·Douglas B. Gould

The paper identifies Fibronectin 1 as a genetic modifier in a Col4a1 mutant mouse model of Gould syndrome, showing it suppresses ocular and muscular phenotypes through increased expression and integrin signaling.

20 citations

mousestatistical model

𝕏 PostBluesky