Assistant Professor, Molecular and Human Genetics, Baylor College of Medicine

Medical Genetics

Dr. Ayelet Erez, MD

Ayelet Erez practices Medical Genetics. She researched medicine at Baylor College of Medicine. Ayelet Erez, MD is a published doctor and has 30 publications published. The lastest was: 'Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27.'

Publications

Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27.
Proteoglycan 4 expression protects against the development of osteoarthritis.
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders.
Argininosuccinic aciduria: from a monogenic to a complex disorder.
Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function.
Response to srilatha et Al.
Nitric-Oxide Supplementation for Treatment of Long-Term Complications in Argininosuccinic Aciduria.
The right to ignore genetic status of late onset genetic disease in the genomic era; Prenatal testing for Huntington disease as a paradigm.
Mosaic deletion 11p13 in a child with dopamine beta-hydroxylase deficiency--case report and review of the literature.
Requirement of argininosuccinate lyase for systemic nitric oxide production.
Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43-q44.
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements.
Insights into the pathogenesis and treatment of cancer from inborn errors of metabolism.
Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications.
One NOTCH Further: Jagged 1 in Bone Metastasis.
Argininosuccinate lyase deficiency-argininosuccinic aciduria and beyond.
Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two females.
Phenotypic manifestations of copy number variation in chromosome 16p13.11.
Phenylbutyrate therapy for maple syrup urine disease.
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12.
Systemic hypertension in two patients with ASL deficiency: a result of nitric oxide deficiency?
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder.
Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss.
The mitotic checkpoint gene, SIL is regulated by E2F1.
Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q.
Interaction between murine spf-ash mutation and genetic background yields different metabolic phenotypes.
The SIL gene is essential for mitotic entry and survival of cancer cells.
Sil overexpression in lung cancer characterizes tumors with increased mitotic activity.
GLI3 is not mutated commonly in sporadic medulloblastomas.

Doctors Specialties

Clinical Genetics
Medical Genetics

Accepted Insurances

Education

Baylor College of Medicine

Hospital

Texas Children's Hospital

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