Back to Search
ARTHUR BEAUDET, MD
MD
Pediatrics Physician
NPI: 1649350067Individual
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) Physician
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
D9939(TX)
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
D9939(TX)
Research & Publications (20)
Allan Award lecture: Rare patients leading to epigenetics and back to genetics.
PMID 18468009·Am J Hum Genet·2008
8-other
Epigenetics and complex human disease: is there a role in IBD?
PMID 18354324·J Pediatr Gastroenterol Nutr·2008
6-review
A rheostat model for a rapid and reversible form of imprinting-dependent evolution.
PMID 11992247·Am J Hum Genet·2002
7-preclinical
Efficient, long-term hepatic gene transfer using clinically relevant HDAd doses by balloon occlusion catheter delivery in nonhuman primates.
PMID 19050700·Mol Ther·2009
7-preclinical
Increased LIS1 expression affects human and mouse brain development.
PMID 19136950·Nat Genet·2009
7-preclinical
Subcellular dynamics of somatostatin receptor subtype 1 in the rat arcuate nucleus: receptor localization and synaptic connectivity vary in parallel with the ultradian rhythm of growth hormone secretion.
PMID 19553459·J Neurosci·2009
7-preclinical
Epigenetic profiling at mouse imprinted gene clusters reveals novel epigenetic and genetic features at differentially methylated regions.
PMID 19542493·Genome Res·2009
7-preclinical
The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations.
PMID 19455642·Autism Res·2009
8-other
Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders.
PMID 19289393·J Med Genet·2009
8-other
Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
PMID 19012303·Prenat Diagn·2009
8-other
Current controversies in prenatal diagnosis 3: For prenatal diagnosis, should we offer less or more than metaphase karyotyping?
PMID 19012273·Prenat Diagn·2009
8-other
Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNA.
PMID 19324990·J Mol Diagn·2009
8-other
Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.
PMID 18752307·Hum Mutat·2008
4-observational
Identification of chromatin remodeling genes Arid4a and Arid4b as leukemia suppressor genes.
PMID 18728284·J Natl Cancer Inst·2008
7-preclinical
Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH.
PMID 18792925·Prenat Diagn·2008
8-other
Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.
PMID 19047251·Pediatrics·2008
4-observational
Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.
PMID 18663743·Am J Med Genet A·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 6701 FANNIN ST
HOUSTON, TX 77030 - Phone
- (832) 822-4280
Quick Facts
- NPI
- 1649350067
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile