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Author Details
Full Name
Karynne E Patterson
Affiliation
University of Washington
ORCID
Career Start Year
2014
Papers
9
H Index
7
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37603195
Caspase 5 depletion is linked to hyper-inflammatory response and progeroid syndrome.
Geroscience
2024
37972748
Lisch Epithelial Corneal Dystrophy Is Caused by Heterozygous Loss-of-Function Variants in MCOLN1.
Am J Ophthalmol
2024
34216551
Targeted long-read sequencing identifies missing disease-causing variation.
Am J Hum Genet
2021
29875422
Stargazer: a software tool for calling star alleles from next-generation sequencing data using CYP2D6 as a model.
Genet Med
2019
28748635
Copy Number Changes Identified Using Whole Exome Sequencing in Nonsyndromic Cleft Lip and Palate in a Honduran Population.
Birth Defects Res
2017
28332277
Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.
Am J Med Genet B Neuropsychiatr Genet
2017
26656649
Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features.
Genet Med
2016
26166479
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities.
Am J Hum Genet
2015
25363768
The contribution of de novo coding mutations to autism spectrum disorder.
Nature
2014
1 - 9 of 9
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