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Author Details
Full Name
Karen Ouyang
Affiliation
Invitae Corporation
ORCID
Career Start Year
2013
Papers
14
H Index
5
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36933558
Patterns of mosaicism for sequence and copy-number variants discovered through clinical deep sequencing of disease-related genes in one million individuals.
Am J Hum Genet
2023
37255402
FH Variant Pathogenicity Promotes Purine Salvage Pathway Dependence in Kidney Cancer.
Cancer Discov
2023
36773955
Fumarate Hydratase Variants and Their Association With Paraganglioma/Pheochromocytoma.
Urology
2023
34724198
Fumarate hydratase variant prevalence and manifestations among individuals receiving germline testing.
Cancer
2022
35570716
Systematic use of phenotype evidence in clinical genetic testing reduces the frequency of variants of uncertain significance.
Am J Med Genet A
2022
33743207
Spectrum of splicing variants in disease genes and the ability of RNA analysis to reduce uncertainty in clinical interpretation.
Am J Hum Genet
2021
32229555
Measuring the predictability of life outcomes with a scientific mass collaboration.
Proc Natl Acad Sci U S A
2020
31610925
Frequency of Cystic Fibrosis Transmembrane Conductance Regulator Variants in Individuals Evaluated for Primary Ciliary Dyskinesia.
J Pediatr
2019
29531232
Genetic analyses in a bonobo (Pan paniscus) with arrhythmogenic right ventricular cardiomyopathy.
Sci Rep
2018
28766213
Expanded Gene Panel Use for Women With Breast Cancer: Identification and Intervention Beyond Breast Cancer Risk.
Ann Surg Oncol
2017
28592622
Li-Fraumeni versus Pseudo-Li-Fraumeni Syndrome: Key Insights for Interpreting Next-Generation Sequencing Reports in Patients with Suspected Cancer Predisposition Syndromes.
Oncologist
2017
26798524
Intermediate MCAD Deficiency Associated with a Novel Mutation of the ACADM Gene: c.1052C>T.
Case Rep Genet
2015
22800289
A case of pediatric γ/δ T-cell malignancy with t(8;14)(q24;q11)/MYC-TCR successfully treated with pulse type chemotherapy followed by stem cell transplant.
Leuk Lymphoma
2013
22997192
Two cases of localized neuroblastoma with multiple segmental chromosomal alterations and metastatic progression.
Pediatr Blood Cancer
2013
1 - 14 of 14
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row(s) 1 - 30 of 30
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