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MARY PRIEUR, PH.D.

PH.D.

Clinical Psychologist

NPI: 1245581040IndividualAccepts Medicare

Specialties, Licenses & Credentials

Clinical PsychologistPrimary

Psychologist — Clinical

Code: 103TC0700X

102990(NC)
Clinical Child & Adolescent Psychologist

Psychologist — Clinical Child & Adolescent

Code: 103TC2200X

102990(NC)

CMS Specialties

PrimaryCLINICAL PSYCHOLOGIST

Education

UNIVERSITY OF MIAMI, LM MILLER SCHOOL OF MEDICINE

Class of 2011

Research & Publications (20)

Sotos syndrome caused by a paracentric inversion disrupting the NSD1 gene.
PMID 18042263·Clin Genet·2008
5-case
Classification of human chromosome 21 gene-expression variations in Down syndrome: impact on disease phenotypes.
PMID 17701894·Am J Hum Genet·2007
8-other
Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterization.
PMID 16892304·Am J Med Genet A·2006
5-case
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders.
PMID 16840569·J Med Genet·2006
8-other
Paraoxonase-1 expression is up-regulated in Down syndrome fetal liver.
PMID 16806076·Biochem Biophys Res Commun·2006
8-other
Stem cell research in a Catholic institution: yes or no?
PMID 16770888·Kennedy Inst Ethics J·2006
8-other
Intrachromosomal insertion mimicking a pericentric inversion: molecular cytogenetic characterization of a three break rearrangement of chromosome 20.
PMID 16158442·Am J Med Genet A·2005
5-case
Failure to detect an 8p22-8p23.1 duplication in patients with Kabuki (Niikawa-Kuroki) syndrome.
PMID 15770228·Eur J Hum Genet·2005
6-review
Functional disomy of the Xq28 chromosome region.
PMID 15741994·Eur J Hum Genet·2005
5-case
Long-term survival in severe combined immune deficiency: the role of persistent maternal engraftment.
PMID 15644840·J Pediatr·2005
5-case
NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome.
PMID 15591270·J Med Genet·2004
8-other
Genome-wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation.
PMID 15253762·Clin Genet·2004
4-observational
Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations.
PMID 12960216·J Med Genet·2003
8-other
Spectrum of NSD1 mutations in Sotos and Weaver syndromes.
PMID 12807965·J Med Genet·2003
4-observational
Parathyroid function and growth in 22q11.2 deletion syndrome.
PMID 12756381·J Pediatr·2003
8-other
Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature.
PMID 12404101·Eur J Hum Genet·2002
8-other
Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype.
PMID 12161602·J Med Genet·2002
5-case
Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation.
PMID 11950856·J Med Genet·2002
8-other
Chromosome 10p11.2-p12.2 duplication: report of a patient and review of the literature.
PMID 11754045·Am J Med Genet·2001
5-case
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structures.
PMID 11595972·Am J Hum Genet·2001
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
CB # 7160, DEPARTMENT OF PSYCHIATRY, UNC SCHOOL OF MEDICINE
CHAPEL HILL, NC 27599

Location

Practice Location

CB # 7160, CHAPEL HILL, NC
(919) 843-3209

Quick Facts

NPI
1245581040
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
2
Locations
1
Years in Practice
15
Publications
20

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