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CATHERINE MASLEN, M.D.
M.D.
Family Medicine Physician
NPI: 1861435604Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
D0055499(MD)
Research & Publications (15)
An expressed fgf4 retrogene is associated with breed-defining chondrodysplasia in domestic dogs.
PMID 19608863·Science·2009
7-preclinical
The FBN2 gene: new mutations, locus-specific database (Universal Mutation Database FBN2), and genotype-phenotype correlations.
PMID 18767143·Hum Mutat·2009
8-other
Report of the National Heart, Lung, and Blood Institute and National Marfan Foundation Working Group on research in Marfan syndrome and related disorders.
PMID 18695204·Circulation·2008
8-other
GATA4 sequence variants in patients with congenital heart disease.
PMID 18055909·J Med Genet·2007
8-other
CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome.
PMID 17036335·Am J Med Genet A·2006
8-other
CRELD2: gene mapping, alternate splicing, and comparative genomic identification of the promoter region.
PMID 16919896·Gene·2006
4-observational
PTPN11 mutations play a minor role in isolated congenital heart disease.
PMID 15940693·Am J Med Genet A·2005
4-observational
Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects.
PMID 12632326·Am J Hum Genet·2003
7-preclinical
Prenatal ultrasound findings in a fetus with congenital contractural arachnodactyly.
PMID 12383326·Ultrasound Obstet Gynecol·2002
5-case
Identification, genomic organization and mRNA expression of CRELD1, the founding member of a unique family of matricellular proteins.
PMID 12137942·Gene·2002
7-preclinical
RPR203494 a pyrimidine analogue of the p38 inhibitor RPR200765A with an improved in vitro potency.
PMID 11266171·Bioorg Med Chem Lett·2001
7-preclinical
The discovery of RPR 200765A, a p38 MAP kinase inhibitor displaying a good oral anti-arthritic efficacy.
PMID 11249145·Bioorg Med Chem·2001
7-preclinical
Carrier frequency of the common mutation IVS8-1G>C in DHCR7 and estimate of the expected incidence of Smith-Lemli-Opitz syndrome.
PMID 11161831·Mol Genet Metab·2001
8-other
Mutation analysis and description of sixteen RSH/Smith-Lemli-Opitz syndrome patients: polymerase chain reaction-based assays to simplify genotyping.
PMID 10995508·Am J Med Genet·2000
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
- 1040 PARK AVE STE 200
BALTIMORE, MD 21201 - Phone
- (443) 738-0300
Quick Facts
- NPI
- 1861435604
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
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