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MARY LEPPERT, MD
MD
Pediatric Neurodevelopmental Disabilities Physician
NPI: 1720136344Individual
Specialties, Licenses & Credentials
Pediatric Neurodevelopmental Disabilities PhysicianPrimary
Pediatrics — Neurodevelopmental Disabilities
Code: 2080P0008X
D41387(MD)
Research & Publications (20)
The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study.
PMID 19265784·Am J Hypertens·2009
8-other
Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypes.
PMID 19436041·Nicotine Tob Res·2009
8-other
Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions.
PMID 19453707·Epilepsia·2009
7-preclinical
A high-density SNP genome-wide linkage scan in a large autism extended pedigree.
PMID 18283277·Mol Psychiatry·2009
8-other
High-sensitivity nanoLC-MS/MS analysis of urinary desmosine and isodesmosine.
PMID 19178285·Anal Chem·2009
8-other
Further genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22.
PMID 18923449·J Invest Dermatol·2009
8-other
Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study.
PMID 19153477·Am J Nephrol·2009
4-observational
A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22.
PMID 19318250·Neuromuscul Disord·2009
5-case
Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome.
PMID 18602572·J Allergy Clin Immunol·2008
8-other
Colonic adenoma risk in familial colorectal cancer--a study of six extended kindreds.
PMID 18671820·Am J Gastroenterol·2008
4-observational
Detailed genetic characterization of the interleukin-23 receptor in psoriasis.
PMID 18650833·Genes Immun·2008
8-other
Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysis.
PMID 19001137·J Exp Med·2008
8-other
Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization.
PMID 18483067·J Physiol·2008
7-preclinical
Neuropathy target esterase gene mutations cause motor neuron disease.
PMID 18313024·Am J Hum Genet·2008
8-other
Intra-individual change over time in DNA methylation with familial clustering.
PMID 18577732·JAMA·2008
8-other
From linkage maps to quantitative trait loci: the history and science of the Utah genetic reference project.
PMID 18544033·Annu Rev Genomics Hum Genet·2008
6-review
Absence of TGFBR1 and TGFBR2 mutations in patients with bicuspid aortic valve and aortic dilation.
PMID 18721526·Am J Cardiol·2008
4-observational
A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction.
PMID 18618000·PLoS Genet·2008
2-rct
The 5q31 variants associated with psoriasis and Crohn's disease are distinct.
PMID 18614543·Hum Mol Genet·2008
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
- 707 N BROADWAY, KENNEDY KRIEGER INSTITUTE
BALTIMORE, MD 21205 - Phone
- (443) 923-9200
Quick Facts
- NPI
- 1720136344
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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