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HOPE NORTHRUP, M.D.
M.D.
NPI: 1740218296IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
H4843(TX)
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
H4843(TX)
CMS Specialties
PrimaryPEDIATRIC MEDICINE
Education
MEDICAL UNIVERSITY OF SOUTH CAROLINA COLLEGE OF MEDICINE
Class of 1983
Research & Publications (20)
Expanded newborn screening in Texas: a survey and educational module addressing the knowledge of pediatric residents.
PMID 19367189·Genet Med·2009
8-other
Tuberous sclerosis complex: disease modifiers and treatments.
PMID 19005330·Curr Opin Pediatr·2008
6-review
Regression of subependymal giant cell astrocytoma with rapamycin in tuberous sclerosis complex.
PMID 18952591·J Child Neurol·2008
5-case
Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals.
PMID 18937358·Birth Defects Res A Clin Mol Teratol·2008
8-other
The impact of BRCA1 on spina bifida meningomyelocele lesions.
PMID 17640328·Ann Hum Genet·2007
8-other
Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States.
PMID 17304050·Genet Med·2007
4-observational
Identification of 54 large deletions/duplications in TSC1 and TSC2 using MLPA, and genotype-phenotype correlations.
PMID 17287951·Hum Genet·2007
8-other
Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families.
PMID 16799052·Invest Ophthalmol Vis Sci·2006
8-other
Asymptomatic isolated human glycerol kinase deficiency associated with splice-site mutations and nonsense-mediated decay of mutant RNA.
PMID 16549535·Pediatr Res·2006
7-preclinical
Tuberous sclerosis complex and polycystic kidney disease together: an exception to the contiguous gene syndrome.
PMID 16540757·Genet Med·2006
5-case
Promotor genotype of the platelet-derived growth factor receptor-alpha gene shows population stratification but not association with spina bifida meningomyelocele.
PMID 16283668·Am J Med Genet A·2005
4-observational
An assessment of risk understanding in Hispanic genetic counseling patients.
PMID 16047094·J Genet Couns·2005
8-other
Spinal lesion level in spina bifida: a source of neural and cognitive heterogeneity.
PMID 15881750·J Neurosurg·2005
4-observational
Molecular genetic basis of tuberous sclerosis complex: from bench to bedside.
PMID 15563017·J Child Neurol·2004
6-review
Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation.
PMID 15338008·Nat Genet·2004
7-preclinical
FBN2 mutation associated with manifestations of Marfan syndrome and congenital contractural arachnodactyly.
PMID 15121784·J Med Genet·2004
8-other
Deletion 12q: a second patient with 12q24.31q24.32 deletion.
PMID 12687666·Am J Med Genet A·2003
5-case
Identification of a mutation in the Indian Hedgehog (IHH) gene causing brachydactyly type A1 and evidence for a third locus.
PMID 12525541·J Med Genet·2003
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
- 6410 FANNIN ST, 500
HOUSTON, TX 77030 - Phone
- (832) 325-7111
Quick Facts
- NPI
- 1740218296
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 43
- Publications
- 20
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