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JOHN VAN HAGEN, PH.D
PH.D
Psychologist
NPI: 1821109018Individual
Specialties, Licenses & Credentials
PsychologistPrimary
Psychologist
Code: 103T00000X
PSY4469(CA)
Research & Publications (20)
Comparing two diagnostic laboratory tests for Williams syndrome: fluorescent in situ hybridization versus multiplex ligation-dependent probe amplification.
PMID 17949295·Genet Test·2007
4-observational
Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome.
PMID 17270452·Neurobiol Dis·2007
7-preclinical
[From gene to disease; EVC, EVC2, and Ellis-van Creveld syndrome].
PMID 15884406·Ned Tijdschr Geneeskd·2005
6-review
[Williams syndrome: new insights into genetic etiology, pathogenesis and clinical aspects].
PMID 11253493·Ned Tijdschr Geneeskd·2001
6-review
Variable phenotypic manifestation of IRF6 mutations in the Van der Woude syndrome and popliteal pterygium syndrome: implications for genetic counseling.
PMID 19623037·Clin Dysmorphol·2009
5-case
A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.
PMID 19225462·Eur J Hum Genet·2009
8-other
Rendu-Osler-Weber disease: update of medical and dental considerations.
PMID 18230376·Oral Surg Oral Med Oral Pathol Oral Radiol Endod·2008
6-review
Feasibility and outcomes of multiplex ligation-dependent probe amplification on buccal smears as a screening method for microdeletions and duplications among 300 adults with an intellectual disability of unknown aetiology.
PMID 18173573·J Intellect Disabil Res·2008
8-other
Cellular and clinical impact of haploinsufficiency for genes involved in ATR signaling.
PMID 17564965·Am J Hum Genet·2007
8-other
A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype-phenotype correlations in type XI collagenopathies.
PMID 17236192·Am J Med Genet A·2007
5-case
Classic pseudoxanthoma elasticum in a patient with sickle cell disease.
PMID 17190641·J Am Acad Dermatol·2007
5-case
Regional underreporting of associated congenital anomalies in cleft patients in the Netherlands.
PMID 17105333·Cleft Palate Craniofac J·2006
4-observational
Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 gene.
PMID 16679492·J Med Genet·2006
5-case
CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene.
PMID 16155193·J Med Genet·2006
8-other
R561C missense mutation in the SMARCAL1 gene associated with mild Schimke immuno-osseous dysplasia.
PMID 16237566·Pediatr Nephrol·2005
5-case
Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy.
PMID 16297189·J Invest Dermatol·2005
8-other
Increased prevalences of left-handedness and left-eye sighting dominance in individuals with Williams-Beuren syndrome.
PMID 16207621·J Clin Exp Neuropsychol·2005
8-other
[Restrictive dermopathy: a rare, lethal genodermatosis].
PMID 16184949·Ned Tijdschr Geneeskd·2005
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
- 35 VICENTE ST
SAN FRANCISCO, CA 94127 - Phone
- (415) 282-1210
Quick Facts
- NPI
- 1821109018
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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