Publications by authors named "Meagan Cochran"

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Novel variant alters splicing of in family with features of Loeys-Dietz syndrome.
Emily R Gordon, Stephanie A Felker, Tanner F Coleman, Nadiya Sosonkina, Jada Pugh, Meagan E Cochran

Front Genet· December 2024

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Errors in genome sequencing result disclosures: A randomized controlled trial comparing neonatology non-genetics healthcare professionals and genetic counselors.
Tanner F Coleman, Jada Pugh, Whitley V Kelley, Kelly M East, Veronica Greve, Meagan E Cochran

Genet Med· September 2024

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Does genetic testing offer utility as a supplement to traditional family health history intake for inherited disease risk?
Thomas May, Crystal L Smith, Whitley Kelley, Kelly East, Lori Orlando, Meagan Cochran

Fam Pract· December 2023

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Medical and psychosocial outcomes of state-funded population genomic screening.
Ashley Cannon, Olivia McMillan, Whitley V Kelley, Kelly M East, Meagan E Cochran

Clin Genet· October 2023

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Contributions of rare and common variation to early-onset and atypical dementia risk.
Carter A Wright, Jared W Taylor, Meagan Cochran, James M J Lawlor, Belle A Moyers, J Nicholas Cochran

Cold Spring Harb Mol Case Stud· June 2023

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Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit.
Amy A Lemke, Michelle L Thompson, Emily C Gimpel, Katelyn C McNamara, Carla A Rich, Meagan E Cochran

J Pers Med· June 2023

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Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype.
Susan M Hiatt, Slavica Trajkova, Matteo Rossi Sebastiano, E Christopher Partridge, Fatima E Abidi, Meagan E Cochran

Am J Hum Genet· February 2023

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Contributions of rare and common variation to early-onset and atypical dementia risk.
Carter A Wright, Jared W Taylor, Meagan Cochran, James M J Lawlor, Belle A Moyers, J Nicholas Cochran

medRxiv· February 2023

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Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing: further evidence of validity.
Robin Z Hayeems, Stephanie Luca, Anna C E Hurst, Meagan Cochran, Chelsea Owens

Eur J Hum Genet· December 2022

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Genome sequencing as a first-line diagnostic test for hospitalized infants.
Kevin M Bowling, Michelle L Thompson, Candice R Finnila, Susan M Hiatt, Donald R Latner, Meagan E Cochran

Genet Med· April 2022

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Education and Training of Non-Genetics Providers on the Return of Genome Sequencing Results in a NICU Setting.
Kelly M East, Meagan E Cochran, Whitley V Kelley, Veronica Greve, Candice R Finnila

J Pers Med· March 2022

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A study of elective genome sequencing and pharmacogenetic testing in an unselected population.
Meagan Cochran, Kelly East, Veronica Greve, Melissa Kelly, Whitley Kelley

Mol Genet Genomic Med· September 2021

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A state-based approach to genomics for rare disease and population screening.
Kelly M East, Whitley V Kelley, Ashley Cannon, Meagan E Cochran, Irene P Moss

Genet Med· April 2021

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Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles.
J Nicholas Cochran, Emily C McKinley, Meagan Cochran, Michelle D Amaral, Bryan A Moyers

Cold Spring Harb Mol Case Stud· December 2019

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Understanding the present and preparing for the future: Exploring the needs of diagnostic and elective genomic medicine patients.
Kelly M East, Meagan Cochran, Whitley V Kelley, Veronica Greve, Kristina Emmerson, Jesse Nicholas Cochran

J Genet Couns· April 2019

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High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation.
Kitiwan Rojnueangnit, Jing Xie, Alicia Gomes, Angela Sharp, Tom Callens, Meagan Cochran

Hum Mutat· November 2015

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International adoption of children with birth defects: current knowledge and areas for further research.
Meagan E Cochran, Katherine R Nelson, Nathaniel H Robin

Curr Opin Pediatr· December 2014

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