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IAN GLASS, M.D.

M.D.

Internal Medicine Physician

NPI: 1821134255Individual

Specialties, Licenses & Credentials

Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

44710(OH)

Research & Publications (20)

Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis).
PMID 19574260·J Med Genet·2010
5-case
Eye movement abnormalities in Joubert syndrome.
PMID 19443711·Invest Ophthalmol Vis Sci·2009
8-other
MKS3-related ciliopathy with features of autosomal recessive polycystic kidney disease, nephronophthisis, and Joubert Syndrome.
PMID 19540516·J Pediatr·2009
5-case
Prevalence of ALDH7A1 mutations in 18 North American pyridoxine-dependent seizure (PDS) patients.
PMID 19128417·Epilepsia·2009
8-other
CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290.
PMID 18950740·Am J Hum Genet·2008
8-other
Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization.
PMID 18471320·Mol Cytogenet·2008
8-other
Prediction of clinical outcomes from rTMS in depressed patients with lateral visual field stimulation: a replication.
PMID 18451190·J Neuropsychiatry Clin Neurosci·2008
3-trial
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome.
PMID 18674751·Am J Hum Genet·2008
7-preclinical
Minimal heating of titanium skull plates during 1Hz repetitive transcranial magnetic stimulation.
PMID 17890148·Clin Neurophysiol·2007
8-other
A case of true hermaphroditism reveals an unusual mechanism of twinning.
PMID 17165045·Hum Genet·2007
5-case
Joubert syndrome (and related disorders) (OMIM 213300).
PMID 17377524·Eur J Hum Genet·2007
8-other
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
PMID 17558407·Nat Genet·2007
7-preclinical
Mutation analysis of NPHP6/CEP290 in patients with Joubert syndrome and Senior-Løken syndrome.
PMID 17617513·J Med Genet·2007
8-other
Senataxin, the yeast Sen1p orthologue: characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron disease.
PMID 16644229·Neurobiol Dis·2006
5-case
Ring chromosome 15: characterization by array CGH.
PMID 16267671·Hum Genet·2006
5-case
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4.
PMID 16682973·Nat Genet·2006
7-preclinical
AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome.
PMID 16155189·J Med Genet·2006
8-other
Prenatal diagnosis in pregnancies at risk for Joubert syndrome by ultrasound and MRI.
PMID 15966043·Prenat Diagn·2005
5-case
Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures.
PMID 16075246·Neurogenetics·2005
8-other
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus: a rare brain malformation syndrome associated with mental retardation and seizures.
PMID 15627943·Neuropediatrics·2004
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
6780 MAYFIELD RD, ADMIN
MAYFIELD HEIGHTS, OH 44124

Location

Practice Location

6780 MAYFIELD RD, MAYFIELD HEIGHTS, OH
(440) 312-6710

Quick Facts

NPI
1821134255
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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