Denise A. Batista

Medical Genetics

600 N Wolfe St
Park Building, Sb 202
Baltimore, MD 21287

Last Updated: 09/26/2026

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Found 5 publications

Analysis of an NGS retinopathy panel detects chromosome 1 uniparental isodisomy in a patient with RPE65-related leber congenital amaurosis.

Analysis of an NGS retinopathy panel detects chromosome 1 uniparental isodisomy in a patient with RPE65-related leber congenital amaurosis.

Journal: Ophthalmic genetics

Published: June 23, 2021

Generation of 10 patient-specific induced pluripotent stem cells (iPSCs) to model Pitt-Hopkins Syndrome.

Generation of 10 patient-specific induced pluripotent stem cells (iPSCs) to model Pitt-Hopkins Syndrome.

Journal: Stem cell research

Published: June 04, 2020

A non-mosaic transchromosomic mouse model of down syndrome carrying the long arm of human chromosome 21.

A non-mosaic transchromosomic mouse model of down syndrome carrying the long arm of human chromosome 21.

Journal: eLife

Published: February 20, 2020

Bone Marrow Findings in Patients With Acute Promyelocytic Leukemia Treated With Arsenic Trioxide.

Bone Marrow Findings in Patients With Acute Promyelocytic Leukemia Treated With Arsenic Trioxide.

Journal: American journal of clinical pathology

Published: July 16, 2019

Loss of the mismatched human leukocyte antigen haplotype in two acute myelogenous leukemia relapses after haploidentical bone marrow transplantation with post-transplantation cyclophosphamide.

Loss of the mismatched human leukocyte antigen haplotype in two acute myelogenous leukemia relapses after haploidentical bone marrow transplantation with post-transplantation cyclophosphamide.

Journal: Leukemia

Published: May 24, 2016

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Last Updated: 09/26/2026