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Current Opinion in Genetics & Development|July 1, 2025
The HNRNPs and neurodevelopmental disordersMadelyn A GillentineBiochemical Pharmacology|June 23, 2015
The human clinical phenotypes of altered CHRNA7 copy numberMadelyn A Gillentine, Christian P SchaafAmerican Journal of Medical Genetics. Part A|June 21, 2017
The importance of phase analysis in multiexon copy number variation detected by aCGH in autosomal recessive disorder lociMadelyn A Gillentine, Christian P Schaaf, Ankita PatelBiomedicines|November 11, 2022
Estimating the Prevalence of De Novo Monogenic Neurodevelopmental Disorders from Large Cohort StudiesMadelyn A Gillentine, Tianyun Wang, Evan E EichlerJournal of Human Genetics|April 26, 2018
An estimation of the prevalence of genomic disorders using chromosomal microarray dataMadelyn A Gillentine, Philip J Lupo, Pawel Stankiewicz, et al.American Journal of Human Genetics|November 14, 2017
Functional Consequences of CHRNA7 Copy-Number Alterations in Induced Pluripotent Stem Cells and Neural Progenitor CellsMadelyn A Gillentine, Jiani Yin, Aleksandar Bajic, et al.Journal of Child and Adolescent Psychopharmacology|August 18, 2017
CHRNA7 Deletions are Enriched in Risperidone-Treated Children and AdolescentsMadelyn A Gillentine, Janson J White, Christopher M Grochowski, et al.Molecular Biology and Evolution|December 24, 2013
Asynchronous evolutionary origins of Aβ and BACE1D Blaine Moore, Madelyn A Gillentine, Nathalie M Botezatu, et al.Journal of Affective Disorders|July 21, 2018
CHRNA7 copy number gains are enriched in adolescents with major depressive and anxiety disordersMadelyn A Gillentine, Ricardo Lozoya, Jiani Yin, et al.Proceedings of the National Academy of Sciences of the United States of America|November 9, 2022
Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disordersTianyun Wang, Chang N Kim, Trygve E Bakken, et al.Pageof 3