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Office
10104 Frederick Ave
Kensington, MD 20895Phone+1 301-962-6441
Summary
- Dr. Donna Krasnewich, MD is a board certified medical geneticist in Kensington, Maryland. She is currently licensed to practice medicine in Maryland, District of Columbia, and Virginia.
Education & Training
- National Capital ConsortiumResidency, Pediatrics, 1989 - 1991
- Children's National HospitalResidency, Pediatrics, 1987 - 1989
- University of MinnesotaInternship, Transitional Year, 1986 - 1987
- Wayne State University School of MedicineClass of 1986
Certifications & Licensure
- DC State Medical License 1989 - 2018
- MD State Medical License 1996 - 2018
- VA State Medical License 1900 - 1900
- American Board of Medical Genetics and Genomics Clinical Biochemical Genetics
- American Board of Pediatrics Pediatrics
Publications & Presentations
PubMed
- 40 citationsPartial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling.Brett V. Johnson, Raman Kumar, Sabrina Oishi, Suzy Alexander, Maria Kasherman
Biological Psychiatry. 2020-01-15 - 41 citationsExpanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors.Christina Lam, Gretchen Golas, Mariska Davids, Marjan Huizing, Megan S. Kane
Molecular Genetics and Metabolism. 2015-06-01 - 98 citationsProspective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylationChristina Lam, Carlos Ferreira, Donna M. Krasnewich, Camilo Toro, Lea Latham
Genetics in Medicine. 2017-02-01
Grant Support
- Clinical Heterogenity In Patients With Congenital DisordNational Human Genome Research Institute2002–2006
- Characterization Of A Familial Presenile Dementia With NNational Human Genome Research Institute2002–2005
- Clinical Heterogenity:Congenital Glycosylation DisordersNational Human Genome Research Institute2004
- Heterogenity In Patients With Congenital GlycosylatioinNational Human Genome Research Institute2003
- Familial Presenile Dementia W/ Neuronal Inclusion BodiesNational Human Genome Research Institute2003
- Heterogenity In Congenital Disorders Of GlycosylationNational Human Genome Research Institute2001
- Familial Presenile Dementia With Neuronal Inclusion BodyNational Human Genome Research Institute2001
- Clinical Heterogenity In Patients With Congenital Disorders Of GlycosylationNational Human Genome Research Institute2000
- Characterization Of A Familial Presenile DementiaNational Human Genome Research Institute2000
- Clinical Heterogenity In Patients With Carbohydrate Deficient Glycoprotein SYNNational Human Genome Research Institute1997–1999