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AGNES WILKIE, M.D.
M.D.
Child & Adolescent Psychiatry Physician
NPI: 1700098746Individual
Specialties, Licenses & Credentials
Psychiatry Physician
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
179811(NY)
Child & Adolescent Psychiatry PhysicianPrimary
Psychiatry & Neurology — Child & Adolescent Psychiatry
Code: 2084P0804X
179811(NY)
Research & Publications (20)
Duplications of noncoding elements 5' of SOX9 are associated with brachydactyly-anonychia.
PMID 19639023·Nat Genet·2009
7-preclinical
Reoperation for intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome: a 15-year review.
PMID 19483581·Plast Reconstr Surg·2009
6-review
Pitfalls in the phylogenomic evaluation of human disease-causing mutations.
PMID 19344491·J Biol·2009
6-review
Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily.
PMID 18726952·Hum Mutat·2009
5-case
Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.
PMID 19409524·Am J Hum Genet·2009
8-other
Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome.
PMID 19086028·Dev Dyn·2009
7-preclinical
Genetic screening of 202 individuals with congenital limb malformations and requiring reconstructive surgery.
PMID 19429598·J Med Genet·2009
8-other
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
PMID 18628315·J Med Genet·2008
8-other
Implications of a vertex bulge following modified strip craniectomy for sagittal synostosis.
PMID 18594408·Plast Reconstr Surg·2008
8-other
A variant in the sonic hedgehog regulatory sequence (ZRS) is associated with triphalangeal thumb and deregulates expression in the developing limb.
PMID 18463159·Hum Mol Genet·2008
7-preclinical
Bench-scale recovery of phosphorus from flushed dairy manure wastewater.
PMID 17884466·Bioresour Technol·2008
7-preclinical
Fibroblast growth factor receptor 3 (FGFR3) mutation in a verrucous epidermal naevus associated with mild facial dysmorphism.
PMID 17441958·Br J Dermatol·2007
5-case
Nonsense-mediated decay and the molecular pathogenesis of mutations in SALL1 and GLI3.
PMID 18000979·Am J Med Genet A·2007
7-preclinical
Clinical dividends from the molecular genetic diagnosis of craniosynostosis.
PMID 17621648·Am J Med Genet A·2007
6-review
Genetic aspects of birth defects: new understandings of old problems.
PMID 17585097·Arch Dis Child Fetal Neonatal Ed·2007
6-review
A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation.
PMID 17569090·Hum Genet·2007
4-observational
RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity.
PMID 17503333·Am J Hum Genet·2007
8-other
A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN.
PMID 17668388·Am J Hum Genet·2007
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
- 51 E 73RD ST, SUITE 5C
NEW YORK, NY 10021 - Phone
- (212) 722-1803
Quick Facts
- NPI
- 1700098746
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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