Publications by authors named "Stela Filipovic-Sadic"

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Multisite Verification of a Targeted CFTR Polymerase Chain Reaction/Capillary Electrophoresis Assay That Evaluates Pathogenic Variants Across Diverse Ethnic and Ancestral Groups.
Bradley Hall, John N Milligan, Kevin Kelnar, Elliot Hallmark, Jacob D Ashton, Stela Filipovic-Sadic

Arch Pathol Lab Med· October 2024

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Multisite Evaluation and Validation of a Sensitive Diagnostic and Screening System for Spinal Muscular Atrophy that Reports SMN1 and SMN2 Copy Number, along with Disease Modifier and Gene Duplication Variants.
John N Milligan, Jessica L Larson, Stela Filipovic-Sadic, Walairat Laosinchai-Wolf, Ya-Wen Huang

J Mol Diagn· June 2021

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A Genotype-Phenotype Study of High-Resolution Nucleic Acid and Protein Analyses in Fragile X Patients with Neurobehavioral Assessments.
Dejan B Budimirovic, Annette Schlageter, Stela Filipovic-Sadic, Dragana D Protic, Eran Bram

Brain Sci· September 2020

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A methylation PCR method determines activation ratios and differentiates premutation allele mosaicism in carrier siblings.
Andrew G Hadd, Stela Filipovic-Sadic, Lili Zhou, Arianna Williams, Gary J Latham

Clin Epigenetics· March 2017

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A novel methylation PCR that offers standardized determination of FMR1 methylation and CGG repeat length without southern blot analysis.
Marina Grasso, Elles M J Boon, Stela Filipovic-Sadic, Patrick A van Bunderen, Elena Gennaro

J Mol Diagn· January 2014

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High-resolution methylation polymerase chain reaction for fragile X analysis: evidence for novel FMR1 methylation patterns undetected in Southern blot analyses.
Liangjing Chen, Andrew Hadd, Sachin Sah, Jeffrey F Houghton, Stela Filipovic-Sadic

Genet Med· June 2011

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An information-rich CGG repeat primed PCR that detects the full range of fragile X expanded alleles and minimizes the need for southern blot analysis.
Liangjing Chen, Andrew Hadd, Sachin Sah, Stela Filipovic-Sadic, Julie Krosting

J Mol Diagn· September 2010

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A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome.
Stela Filipovic-Sadic, Sachin Sah, Liangjing Chen, Julie Krosting, Edward Sekinger

Clin Chem· March 2010

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