Author

Molly C. Losh

Northwestern UniversityORCID 0000-0002-9823-8249Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 1 Assay:electronic health records· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Anna K. KähleriD· 1 shared Annette K. Taylor· 1 shared Bharath ChandrasekaraniD· 1 shared Craig A. StockmeieriD· 1 shared Edwin H. CookiD· 1 shared Felicia Mou· 1 shared Greg E. Crawford· 1 shared Jacie R. McHaneyiD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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1 shared paperGenetics

Anna K. KählerORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Neurophysiological Evidence for Reduced Use of Prior Sound Patterns to Shape Speech Processing in Autism

Joseph C. Y. Lau, Jacie R. McHaney, Lindsay Goldman, Kylie Robinshaw, Felicia Mou, Kailyn McFarlane, Bharath Chandrasekaran, Molly C. Losh

This study finds that autistic adults show reduced context-dependent modulation of speech encoding compared to non-autistic adults, linked to differences in auditory and social-communicative function.

bioRxiv · Jul 10, 2026 · PreprintNeuroscience

Elevated polygenic burden for ASD is associated with the broad autism phenotype

Kritika Nayar, Julia Sealock, Nell Maltman, Linda A. Bush, Edwin H. Cook, Lea Karatheodoris Davis, Molly C. Losh

The paper investigates the association between polygenic scores for ASD and the broad autism phenotype (BAP) in parents and their children, finding domain- and sex-specific links.

bioRxiv · Nov 12, 2019 · PreprintGenetics

Common Variant Associations with Fragile X Syndrome

James J. Crowley, Jin Szatkiewicz, Anna K. Kähler, Paola Giusti‐Rodríguez, NaEshia Ancalade, Jessica K. Booker, Jennifer L. Carr, Greg E. Crawford, Molly C. Losh, Craig A. Stockmeier, Annette K. Taylor, Joseph Piven, Patrick F. Sullivan

This study identifies genome-wide significant associations near FMR1 with Fragile X Syndrome in males, highlighting the complexity of monogenetic disorders.

Molecular Psychiatry · Dec 7, 2018Peer-reviewedGenetics