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JAYNE MULVIHILL, PHD
PHD
Mental Health Counselor
NPI: 1770311011Individual
Specialties, Licenses & Credentials
Mental Health CounselorPrimary
Counselor — Mental Health
Code: 101YM0800X
6609(NC)
Research & Publications (20)
Celebrating the structure of DNA: 50 years and beyond.
PMID 12733207·J Okla State Med Assoc·2003
8-other
Expanding metabolic screening of newborns: can the health care industry do better than public health?
PMID 14619602·J Okla State Med Assoc·2003
5-case
Replication of association between a common variant near melanocortin-4 receptor gene and obesity-related traits in Asian Sikhs.
PMID 19680233·Obesity (Silver Spring)·2010
8-other
Testing the association of novel meta-analysis-derived diabetes risk genes with type II diabetes and related metabolic traits in Asian Indian Sikhs.
PMID 19247373·J Hum Genet·2009
8-other
Radiotherapy for childhood cancer and risk for congenital malformations in offspring: a population-based cohort study.
PMID 19021636·Clin Genet·2009
8-other
Tonic-clonic seizures in a fetus with Pena-Shokeir syndrome.
PMID 19643800·J Ultrasound Med·2009
5-case
Ovarian failure and reproductive outcomes after childhood cancer treatment: results from the Childhood Cancer Survivor Study.
PMID 19364956·J Clin Oncol·2009
6-review
Population-based clinical epidemiology of familial cancer: lessons for oncologists.
PMID 19410189·Lancet Oncol·2009
8-other
The Childhood Cancer Survivor Study: a National Cancer Institute-supported resource for outcome and intervention research.
PMID 19364948·J Clin Oncol·2009
6-review
Quality assurance in medical and public health genetics services: a systematic review.
PMID 19621459·Am J Med Genet C Semin Med Genet·2009
1-meta
Automated classification of metaphase chromosomes: optimization of an adaptive computerized scheme.
PMID 18585097·J Biomed Inform·2009
8-other
Low adherence to national guidelines for thyroid screening in Down syndrome.
PMID 19506481·Genet Med·2009
8-other
Prenatal identification of a novel R937P L1CAM missense mutation.
PMID 19594370·Genet Test Mol Biomarkers·2009
5-case
Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk.
PMID 18598350·BMC Med Genet·2008
8-other
De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia.
PMID 18203189·Am J Med Genet A·2008
5-case
A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0).
PMID 18262051·Cancer Genet Cytogenet·2008
5-case
The global network on dental education: a new vision for IFDEA.
PMID 18289279·Eur J Dent Educ·2008
8-other
TCF7L2 polymorphisms are associated with type 2 diabetes in Khatri Sikhs from North India: genetic variation affects lipid levels.
PMID 18397358·Ann Hum Genet·2008
8-other
Deletion of 14q24.1 approximately q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization.
PMID 18656693·Cancer Genet Cytogenet·2008
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 9266 WASHAM POTTS RD
CORNELIUS, NC 28031 - Phone
- (312) 480-8211
Quick Facts
- NPI
- 1770311011
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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