Dallas A. Reed

Obstetrics and Gynecology | Medical Genetics

800 Washigton St
Boston, MA 02111

Last Updated: 09/26/2026

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Found 14 publications

Case Report With Biallelic Variants in GCNT2 Implicates Exon 1B in Congenital Cataracts.

Case Report With Biallelic Variants in GCNT2 Implicates Exon 1B in Congenital Cataracts.

Journal: American journal of medical genetics. Part A

Published: December 02, 2025

Rapid Genome Sequencing Compared to a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic Evaluation.

Rapid Genome Sequencing Compared to a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic Evaluation.

Journal: medRxiv : the preprint server for health sciences

Published: April 29, 2025

Rapid Genome Sequencing Compared with a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic Evaluation.

Rapid Genome Sequencing Compared with a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic Evaluation.

Journal: The Journal of pediatrics

Published: April 22, 2025

Screening Positive for Rare Autosomal Aneuploidies Increases Frequency of Adverse Pregnancy Outcomes and Alters Clinical Management.

Screening Positive for Rare Autosomal Aneuploidies Increases Frequency of Adverse Pregnancy Outcomes and Alters Clinical Management.

Journal: Prenatal diagnosis

Published: November 27, 2024

Rapid Whole-Genomic Sequencing and a Targeted Neonatal Gene Panel in Infants With a Suspected Genetic Disorder.

Rapid Whole-Genomic Sequencing and a Targeted Neonatal Gene Panel in Infants With a Suspected Genetic Disorder.

Journal: JAMA

Published: July 11, 2023

Tarui Disease Caused by a Novel PFKM Genetic Variant in a Sub-Saharan African Patient.

Tarui Disease Caused by a Novel PFKM Genetic Variant in a Sub-Saharan African Patient.

Journal: Journal of clinical neuromuscular disease

Published: February 21, 2022

Ocular phenotype in a patient with PAX2 gene mutation-associated papillorenal syndrome.

Ocular phenotype in a patient with PAX2 gene mutation-associated papillorenal syndrome.

Journal: Ophthalmic genetics

Published: December 10, 2021

Novel Variant Findings and Challenges Associated With the Clinical Integration of Genomic Testing: An Interim Report of the Genomic Medicine for Ill Neonates and Infants (GEMINI) Study.

Novel Variant Findings and Challenges Associated With the Clinical Integration of Genomic Testing: An Interim Report of the Genomic Medicine for Ill Neonates and Infants (GEMINI) Study.

Journal: JAMA pediatrics

Published: February 15, 2021

Unlearning, Undoing, and Uplifting: An Organized Approach to Ending Health Disparities Affecting Black Women.

Unlearning, Undoing, and Uplifting: An Organized Approach to Ending Health Disparities Affecting Black Women.

Journal: Obstetrics and gynecology

Published: January 08, 2021

Maternal genetic diseases: potential concerns for mother and baby.

Maternal genetic diseases: potential concerns for mother and baby.

Journal: Human genetics

Published: April 24, 2019

Aggressive-Variant Microsatellite-Stable POLE Mutant Prostate Cancer With High Mutation Burden and Durable Response to Immune Checkpoint Inhibitor Therapy.

Aggressive-Variant Microsatellite-Stable POLE Mutant Prostate Cancer With High Mutation Burden and Durable Response to Immune Checkpoint Inhibitor Therapy.

Journal: JCO precision oncology

Published: November 01, 2018

Ocular and systemic manifestations of beta-propeller protein-associated neurodegeneration.

Ocular and systemic manifestations of beta-propeller protein-associated neurodegeneration.

Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus

Published: November 27, 2017

Showing 1-12 of 14

Last Updated: 09/26/2026