Aiden E. Shearer

Pediatrics

300 Longwood Ave
Boston, MA 02115

Last Updated: 09/26/2026

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Found 56 publications

Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorder.

Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorder.

Journal: American journal of human genetics

Published: February 15, 2026

DB-OTO Gene Therapy for Inherited Deafness.

DB-OTO Gene Therapy for Inherited Deafness.

Journal: The New England journal of medicine

Published: October 14, 2025

A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic Targets.

A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic Targets.

Journal: medRxiv : the preprint server for health sciences

Published: March 10, 2025

A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic Targets.

A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic Targets.

Journal: American journal of medical genetics. Part C, Seminars in medical genetics

Published: January 21, 2025

Sex Differences in B Cells From the Joints of Children With Oligoarticular Juvenile Idiopathic Arthritis.

Sex Differences in B Cells From the Joints of Children With Oligoarticular Juvenile Idiopathic Arthritis.

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: January 07, 2025

Novel Phenotypes and Genotype-Phenotype Correlations in a Large Clinical Cohort of Patients With Kleefstra Syndrome.

Novel Phenotypes and Genotype-Phenotype Correlations in a Large Clinical Cohort of Patients With Kleefstra Syndrome.

Journal: Clinical genetics

Published: October 10, 2024

Predictors of Posttransplant Lymphoproliferative Disease in Pediatric Patients.

Predictors of Posttransplant Lymphoproliferative Disease in Pediatric Patients.

Journal: The Laryngoscope

Published: September 25, 2024

Pediatric sporadic Burkitt lymphoma of the head and neck: A case series and analysis of national trends.

Pediatric sporadic Burkitt lymphoma of the head and neck: A case series and analysis of national trends.

Journal: International journal of pediatric otorhinolaryngology

Published: September 04, 2024

Endocochlear potential contributes to hair cell death in TMPRSS3 hearing loss.

Endocochlear potential contributes to hair cell death in TMPRSS3 hearing loss.

Journal: The Journal of clinical investigation

Published: August 30, 2024

Genetic testing for pediatric sensorineural hearing loss in the era of gene therapy.

Genetic testing for pediatric sensorineural hearing loss in the era of gene therapy.

Journal: Current opinion in otolaryngology & head and neck surgery

Published: August 15, 2024

Pediatric cerebrospinal fluid rhinorrhea caused by low flow vascular anomaly of the temporal bone: A case series.

Pediatric cerebrospinal fluid rhinorrhea caused by low flow vascular anomaly of the temporal bone: A case series.

Journal: International journal of pediatric otorhinolaryngology

Published: February 06, 2024

PKHD1L1, A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss.

PKHD1L1, A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss.

Journal: medRxiv : the preprint server for health sciences

Published: October 24, 2023

Showing 1-12 of 56

Last Updated: 09/26/2026