Author

Kayla A. Quirin

Observed names: K. Quirin, Kayla Quirin

Institution: Parent Project Muscular Dystrophy

Observed institutions: Emory University, Inserm, Washington University in St. Louis, Sorbonne Université, Parent Project Muscular Dystrophy, Institut de Myologie, Indiana University Indianapolis, Centre de Recherche en Myologie, Indiana University School of Medicine

ORCID: 0000-0003-2671-5461

Observed ORCID: 0000-0003-2671-5461

OpenAlex ID: A5089394668

Novel role of miR-29a in pancreatic cancer autophagy and its therapeutic potential

2016 · Jason J. Kwon, Jeffrey A. Willy, et al. · Oncotarget · 75

Safety and Efficacy of AAV Retrograde Pancreatic Ductal Gene Delivery in Normal and Pancreatic Cancer Mice

2017 · Kayla A. Quirin, Jason J. Kwon, et al. · Molecular Therapy — Methods & Clinical Development · 35

Genetic counseling for advanced paternal age: A survey of genetic counselors' current practice

2020 · Kayla Quirin, Karrie A. Hines, et al. · Journal of Genetic Counseling · 8

OBGYN providers’ lack of knowledge and management of genetic risks due to advanced paternal age underscore the need for updated practice guidance

2022 · Joseph F. Biddle, Leah Wetherill, et al. · Journal of Community Genetics · 1

Abstract 528: Identification of MYC as a novel repressor of miR-29 in pancreatic ductal adenocarcinoma

2018 · Jason Kwon, Kayla Quirin, et al. · Cancer Research · 1

Abstract LB-327: Restoration of MYC-repressed miR-29 in pancreatic cancer cells leads to increased reactive oxygen species and gemcitabine sensitization

2017 · Jason J. Kwon, Kayla Quirin, et al. · Cancer Research · 1

P643: Unveiling noncoding DMD variants: Synergizing RNA sequencing and DNA sequencing for enhanced molecular diagnosis

2024 · Yinghong Pan, Fen Guo, et al. · Genetics in Medicine Open

P194 The Duchenne registry: key milestones and advances of a patient-report registry

2023 · A. Martin, N. Armstrong, et al. · Neuromuscular Disorders

A study to identify individuals at risk to be affected by Pompe disease who had previously been given a non-specific or tentative diagnosis for their muscle weakness (Pompe PURSUE)

2022 · Kayla A. Quirin, Eleanor G. Botha, et al. · Molecular Genetics and Metabolism

A Novel Wnt5a Variant in Context of Maternal Diabetes Leading to a Severe Phenotypic Presentation

2022 · Prapti Singh, Juliette J. Kahle, et al. · SSRN Electronic Journal

WNT5A haploinsufficiency and gestational diabetes in a newborn with multiple congenital anomalies: a likely gene-environment interaction

2021 · Juliette Kahle, Prapti Singh, et al. · Molecular Genetics and Metabolism

A distal 12p duplication in an adult with dysmorphic characteristics and neurodevelopmental impairments

2021 · Ying Chen Hou, Patricia Dickson, et al. · Molecular Genetics and Metabolism

Works count: 12

Citation count: 121

H-index: 3

I10-index: 2