Concepedia

Samantha N. Hartin

SN

Statistics

Publications

4

Citations

224

H-Index

4

Active since

2018

Affiliations

University of Kansas Medical Center(Current)

Murdoch Children's Research Institute

Royal Children's Hospital

Victorian Clinical Genetics Services

Samantha N. Hartin is an author at University of Kansas Medical Center specializing in public health, molecular diagnostics, and molecular genetics.

Top concepts

Publications per year

2018–2020

4

Publications

4

Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study

Merlin G. Butler, Samantha N. Hartin, Waheeda A. Hossain et al. · Journal of Medical Genetics · 2018 · 164 citations · Full text

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Analysis of the Prader–Willi syndrome imprinting center using droplet digital PCR and next‐generation whole‐exome sequencing

Samantha N. Hartin, Waheeda A. Hossain, David Francis et al. · Molecular Genetics & Genomic Medicine · 2019 · 22 citations · Full text

Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders

Emma K. Baker, Merlin G. Butler, Samantha N. Hartin et al. · Translational Psychiatry · 2020 · 20 citations · Full text

Three siblings with Prader–Willi syndrome caused by imprinting center microdeletions and review

Samantha N. Hartin, Waheeda A. Hossain, Nicolette Weisensel et al. · American Journal of Medical Genetics Part A · 2018 · 18 citations

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