Back to Search

RICHARD SCHROER, MD

MD

Clinical Genetics (M.D.) Physician

NPI: 1669463220IndividualAccepts Medicare

Specialties, Licenses & Credentials

Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

9091(SC)

CMS Specialties

PrimaryPEDIATRIC MEDICINE

Education

OTHER

Class of 1975

Research & Publications (18)

Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability.
PMID 19012874·Am J Hum Genet·2008
8-other
Analysis of the neuroligin 4Y gene in patients with autism.
PMID 18628683·Psychiatr Genet·2008
8-other
Neurexin 1alpha structural variants associated with autism.
PMID 18490107·Neurosci Lett·2008
8-other
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
PMID 18278044·Nat Genet·2008
5-case
Expanded newborn screening identifies maternal primary carnitine deficiency.
PMID 17126586·Mol Genet Metab·2007
8-other
High frequency of neurexin 1beta signal peptide structural variants in patients with autism.
PMID 17034946·Neurosci Lett·2006
8-other
Epimerase-deficiency galactosemia is not a binary condition.
PMID 16385452·Am J Hum Genet·2006
4-observational
Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements.
PMID 16284940·Am J Med Genet A·2005
8-other
The formation of spikes in the displacement of miscible fluids.
PMID 15644364·Ann N Y Acad Sci·2004
8-other
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A.
PMID 15389703·Am J Med Genet A·2004
8-other
Genetic syndromes among individuals with mental retardation.
PMID 14556243·Am J Med Genet A·2003
8-other
The HOXA1 A218G polymorphism and autism: lack of association in white and black patients from the South Carolina Autism Project.
PMID 12908836·J Autism Dev Disord·2003
8-other
Absence of MeCP2 mutations in patients from the South Carolina autism project.
PMID 12555243·Am J Med Genet B Neuropsychiatr Genet·2003
8-other
Genomic rearrangements of EYA1 account for a large fraction of families with BOR syndrome.
PMID 12404110·Eur J Hum Genet·2002
8-other
Longitudinal changes in cognitive and adaptive behavior scores in children and adolescents with the fragile X mutation or autism.
PMID 12058838·J Autism Dev Disord·2002
8-other
X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28.
PMID 11898126·Am J Hum Genet·2002
8-other
Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism.
PMID 11449390·Am J Med Genet·2001
8-other
The HOPA gene dodecamer duplication is not a significant etiological factor in autism.
PMID 11039861·J Autism Dev Disord·2000
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
3520 W MONTAGUE AVE STE 104
NORTH CHARLESTON, SC 29418

Location

Practice Location

3520 W MONTAGUE AVE STE 104, NORTH CHARLESTON, SC
(843) 746-1001

Quick Facts

NPI
1669463220
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
51
Publications
18

Are you this provider?

Claim Your Profile