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DAVID YAEGER, MD
MD
Pediatrics Physician
NPI: 1609824689Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
0047511(FL)
Research & Publications (18)
Poor neonatal adaptation after in utero exposure to duloxetine.
PMID 18450948·Am J Psychiatry·2008
5-case
Fine-mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals.
PMID 18257100·Am J Med Genet A·2008
8-other
Assessing parental attitudes toward genetic testing for childhood hearing loss: before and after genetic consultation.
PMID 17542006·Am J Med Genet A·2007
8-other
Additional clinical manifestations in children with sensorineural hearing loss and biallelic GJB2 mutations: who should be offered GJB2 testing?
PMID 17455295·Am J Med Genet A·2007
8-other
Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation.
PMID 17273969·Am J Hum Genet·2007
8-other
Tactile hallucinations associated with therapeutic doses of bupropion in 2 patients.
PMID 17196068·J Clin Psychiatry·2006
5-case
Posttraumatic stress disorder in female veterans with military and civilian sexual trauma.
PMID 17195980·J Trauma Stress·2006
8-other
Atypical antipsychotics in the treatment of schizophrenia during pregnancy and the postpartum.
PMID 17151155·Am J Psychiatry·2006
5-case
DSM-IV diagnosed posttraumatic stress disorder in women veterans with and without military sexual trauma.
PMID 16637949·J Gen Intern Med·2006
4-observational
Ophthalmologic findings in Cornelia de Lange syndrome: a genotype-phenotype correlation study.
PMID 16606884·Arch Ophthalmol·2006
8-other
Outcomes of clinical examination and genetic testing of 500 individuals with hearing loss evaluated through a genetics of hearing loss clinic.
PMID 16532460·Am J Med Genet A·2006
8-other
Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome.
PMID 16100726·Am J Med Genet A·2005
8-other
Chromosome rearrangements in cornelia de Lange syndrome (CdLS): report of a der(3)t(3;12)(p25.3;p13.3) in two half sibs with features of CdLS and review of reported CdLS cases with chromosome rearrangements.
PMID 16075459·Am J Med Genet A·2005
5-case
Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome.
PMID 15704124·Am J Med Genet A·2005
5-case
Hyponatremia associated with bupropion, a case verified by rechallenge.
PMID 15643110·J Clin Psychopharmacol·2005
3-trial
NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations.
PMID 15318302·Am J Hum Genet·2004
4-observational
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B.
PMID 15146186·Nat Genet·2004
4-observational
A ligand-reversible dimerization system for controlling protein-protein interactions.
PMID 10852943·Proc Natl Acad Sci U S A·2000
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
- 414 N MILLS AVE
ORLANDO, FL 32803 - Phone
- (407) 841-7290
Quick Facts
- NPI
- 1609824689
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 18
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