Dr. Lisa Ann Schimmenti MD
Pediatrician
516 Delaware St Se Pwb Fourthfloor, Roo Minneapolis MN, 55455About
Dr. Lisa Schimmenti is a pediatrician practicing in Minneapolis, MN. Dr. Schimmenti is a doctor who specializes in the health care of children. As a pedicatrician, Dr. Schimmenti diagnoses and treats infections, injuries, diseases and other disorders in children. Pediatricians typically work with infants, children, teenagers and young adults up to age 21. They practice medical care as well as preventative health care. Dr. Schimmenti can oversee and manage the physical, mental and emotional health of their patients.
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Renal-coloboma syndrome: a multi-system developmental disorder caused by PAX2 mutations.
- Identification of two single nucleotide polymorphisms in exon 8 of PAX2.
- Optic nerve dysplasia and renal insufficiency in a family with a novel PAX2 mutation, Arg115X: further ophthalmologic delineation of the renal-coloboma syndrome.
- Duplication of the Down syndrome critical region does not predict facial phenotype in a baby with a ring chromosome 21.
- Prelingual siblings of children with GJB2 hearing loss: issues to consider.
- Genome-wide reverse genetics framework to identify novel functions of the vertebrate secretome.
- Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities.
- Ethnic differences in parental perceptions of genetic testing for deaf infants.
- Severe methylenetetrahydrofolate reductase (MTHFR) deficiency: a case report of nonclassical homocystinuria.
- Development and Notch signaling requirements of the zebrafish choroid plexus.
- A primer for morpholino use in zebrafish.
- A prospective, longitudinal study of the impact of GJB2/GJB6 genetic testing on the beliefs and attitudes of parents of deaf and hard-of-hearing infants.
- Cardiac conduction improvement in two heterozygotes for primary carnitine deficiency on L-carnitine supplementation.
- Next generation sequencing in research and diagnostics of ocular birth defects.
- A novel microdeletion/microduplication syndrome of 19p13.13.
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