Suchergebnisse - "Cochran, Meagan"

PubPharm (22)

1

Contributions of rare and common variation to early-onset and atypical dementia risk

enthalten in: bioRxiv.org | 2024

von Wright, C. | Taylor, J. | Cochran, M. | +12

2

Does genetic testing offer utility as a supplement to traditional family health history intake for inherited disease risk?

enthalten in: Family practice | 2023

von May, T. | Smith, C. | Kelley, W. | +8

3

Medical and psychosocial outcomes of state-funded population genomic screening

enthalten in: Clinical genetics | 2023

von Cannon, A. | McMillan, O. | Kelley, W. | +9

4

Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit

enthalten in: Journal of personalized medicine | 2023

von Lemke, A. | Thompson, M. | Gimpel, E. | +38

5

Contributions of rare and common variation to early-onset and atypical dementia risk

enthalten in: Cold Spring Harbor molecular case studies | 2023

von Wright, C. | Taylor, J. | Cochran, M. | +12

UpdateOf: medRxiv. 2023 Feb 08;:. - PMID 36798301

6

Contributions of rare and common variation to early-onset and atypical dementia risk

enthalten in: medRxiv : the preprint server for health sciences | 2023

von Wright, C. | Taylor, J. | Cochran, M. | +12

UpdateIn: Cold Spring Harb Mol Case Stud. 2023 Jun 12;:. - PMID 37308299

7

Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype

enthalten in: American journal of human genetics | 2023

von Hiatt, S. | Trajkova, S. | Sebastiano, M. | +81

8

Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing : further evidence of validity

enthalten in: European journal of human genetics : EJHG | 2022

von Hayeems, R. | Luca, S. | Hurst, A. | +8

9

Genome sequencing as a first-line diagnostic test for hospitalized infants

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2022

von Bowling, K. | Thompson, M. | Finnila, C. | +36

10

Education and Training of Non-Genetics Providers on the Return of Genome Sequencing Results in a NICU Setting

enthalten in: Journal of personalized medicine | 2022

von East, K. | Cochran, M. | Kelley, W. | +10