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American Journal of Medical Genetics. Part A|February 14, 2018
Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and reviewSamantha N Hartin, Waheeda A Hossain, Nicolette Weisensel, et al.Plos One|May 5, 2015
A Synthetic Lethal Screen Identifies a Role for Lin-44/Wnt in C. elegans EmbryogenesisSamantha N Hartin, Martin L Hudson, Curtis Yingling, et al.Molecular Medicine (Cambridge, Mass.)|November 26, 2020
Expediting rare disease diagnosis: a call to bridge the gap between clinical and functional genomicsSamantha N Hartin, John C Means, Joseph T Alaimo, et al.Molecular Genetics & Genomic Medicine|February 23, 2019
Analysis of the Prader-Willi syndrome imprinting center using droplet digital PCR and next-generation whole-exome sequencingSamantha N Hartin, Waheeda A Hossain, David Francis, et al.Journal of Aggression, Maltreatment & Trauma|December 7, 2020
Relationship Between Body Habitus and Aggression Subtypes Among Healthy Young Adults from the American MidwestSamantha N Hartin, Waheeda A Hossain, Ann M Manzardo, et al.Scientific Reports|May 9, 2022
Massively parallel identification of functionally consequential noncoding genetic variants in undiagnosed rare disease patientsJasmine A McQuerry, Merry Mclaird, Samantha N Hartin, et al.Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|February 21, 2018
A descriptive study on selected growth parameters and growth hormone receptor gene in healthy young adults from the American MidwestSamantha N Hartin, Waheeda A Hossain, Ann M Manzardo, et al.Translational Psychiatry|October 29, 2020
Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disordersEmma K Baker, Merlin G Butler, Samantha N Hartin, et al.Journal of Medical Genetics|May 7, 2018
Molecular genetic classification in Prader-Willi syndrome: a multisite cohort studyMerlin G Butler, Samantha N Hartin, Waheeda A Hossain, et al.Pageof 1