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Marwan Shinawi, M.D. | | 
Assistant Professor of Pediatrics Genetics and Genomic Medicine Dr. Shinawi has been an assistant professor at the department of molecular and human genetics at Baylor College of Medicine in Houston since 2005. He is Board certified in Clinical Genetics and Medical Biochemical Genetics. With his clinical and laboratory research experiences, he has been primary author on many publications. His special interests over the past few years were in autism spectrum disorders, cytogenetic abnormalities, microarray technology, and metabolic conditions. He joined the division of genetics and genomic medicine at St. Louis Children’s Hospital in September 2009. In addition to his efforts in expanding his previous research interests and his involvement in clinical work, Dr. Shinawi is establishing the skeletal dysplasia multidisciplinary clinic to serve the needs of children with skeletal abnormalities. |
Marwan Shinawi, M.D. | |
Assistant Professor of Pediatrics Genetics and Genomic Medicine Dr. Shinawi has been an assistant professor at the department of molecular and human genetics at Baylor College of Medicine in Houston since 2005. He is Board certified in Clinical Genetics and Medical Biochemical Genetics. With his clinical and laboratory research experiences, he has been primary author on many publications. His special interests over the past few years were in autism spectrum disorders, cytogenetic abnormalities, microarray technology, and metabolic conditions. He joined the division of genetics and genomic medicine at St. Louis Children’s Hospital in September 2009. In addition to his efforts in expanding his previous research interests and his involvement in clinical work, Dr. Shinawi is establishing the skeletal dysplasia multidisciplinary clinic to serve the needs of children with skeletal abnormalities. |
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- B.S., Biology, The Hebrew University of Jerusalem, Israel, 1989
- M.D., Technion-Faculty of Medicine, Israel, 1996
- B.S., Biology, The Hebrew University of Jerusalem, Israel, 1989
- M.D., Technion-Faculty of Medicine, Israel, 1996
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- Resident in Pediatrics, Rambam Medical Center, Haifa, Israel, 1996-2000
- Post-doctoral Fellowship in Genetics, Baylor College of Medicine, Houston, 2003-2005
- Residency in Clinical Genetics, Baylor College of Medicine, Houston, 2003-2005
- Resident in Pediatrics, Rambam Medical Center, Haifa, Israel, 1996-2000
- Post-doctoral Fellowship in Genetics, Baylor College of Medicine, Houston, 2003-2005
- Residency in Clinical Genetics, Baylor College of Medicine, Houston, 2003-2005
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- Israeli Board of Pediatrics, 2000
- Clinical Genetics, American Board of Medcal Genetics, 2005
- Medical Biochemical Genetics, American Board of Medical Genetics, 2009
- State of Texas, 2005
- State of Missouri, 2009
- Israeli Board of Pediatrics, 2000
- Clinical Genetics, American Board of Medcal Genetics, 2005
- Medical Biochemical Genetics, American Board of Medical Genetics, 2009
- State of Texas, 2005
- State of Missouri, 2009
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- Young Investigator Award, Cure Autism Now Foundation, 2005
- The Simons Young Investigator Award, Columbia University, 2007
- Young Investigator Award, Cure Autism Now Foundation, 2005
- The Simons Young Investigator Award, Columbia University, 2007
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- Shinawi M, Schaaf CP, Bhatt SS, Xia Z, Patel A, Cheung SW, Lanpher B, Nagl S, HerdingHS, Nevinny-Stickel C, Immken LL, Patel GS, German JR, Beaudet AL, Stankiewicz P. A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. Nature Genetics (in press)
- Shaibani A, Shchelochkov OA, Zhang S, Katsonis P, Lichtarge O, Wong LJ, Shinawi M. Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B. Arch Neurol 2009, 66:1028-32
- Shinawi M, Patel A, Panichkul P, Zascavage R, Peters S, Scaglia F. The Xp contiguous gene deletion syndrome and autism. Am J Med Genet A 2009; 149A:1138-1148
- Shchelochkov O, Wong LJ, Shaibani A, Shinawi M. Atypical presentation of VLCAD deficiency associated with a novel ACADVL splicing mutation. Muscle Nerve. 2009; 39: 374-382
- Shinawi M, Cheung SW. The array CGH and its clinical applications. Drug Discovery Today 2008; 13: 760-770
- Brunetti-Pierri N, Trilochan S, Chinault C, Peters S, Shinawi M. 15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization. Am J Med Genet A 2008; 146A: 1933-1941
- Shinawi M, Erez A, Shardy DL, Lee B, Naeem R, Cheung SW, Chinault C, Plon SE. Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia (AML) caused by constitutional microdeletions on chromosome 21q. Blood 2008 15; 112: 1042-1047
More Publications (PubMed)
- Shinawi M, Schaaf CP, Bhatt SS, Xia Z, Patel A, Cheung SW, Lanpher B, Nagl S, HerdingHS, Nevinny-Stickel C, Immken LL, Patel GS, German JR, Beaudet AL, Stankiewicz P. A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. Nature Genetics (in press)
- Shaibani A, Shchelochkov OA, Zhang S, Katsonis P, Lichtarge O, Wong LJ, Shinawi M. Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B. Arch Neurol 2009, 66:1028-32
- Shinawi M, Patel A, Panichkul P, Zascavage R, Peters S, Scaglia F. The Xp contiguous gene deletion syndrome and autism. Am J Med Genet A 2009; 149A:1138-1148
- Shchelochkov O, Wong LJ, Shaibani A, Shinawi M. Atypical presentation of VLCAD deficiency associated with a novel ACADVL splicing mutation. Muscle Nerve. 2009; 39: 374-382
- Shinawi M, Cheung SW. The array CGH and its clinical applications. Drug Discovery Today 2008; 13: 760-770
- Brunetti-Pierri N, Trilochan S, Chinault C, Peters S, Shinawi M. 15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization. Am J Med Genet A 2008; 146A: 1933-1941
- Shinawi M, Erez A, Shardy DL, Lee B, Naeem R, Cheung SW, Chinault C, Plon SE. Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia (AML) caused by constitutional microdeletions on chromosome 21q. Blood 2008 15; 112: 1042-1047
More Publications (PubMed)
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