Mark Charles Hannibal MD PhD
Clinical Genetics, Pediatric Medical Genetics
Clinical Associate Professor at Michigan Medicine
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D5240 Medical Professional Bldg1500 E Medical Center DrAnn Arbor, MI 48109
Phone+1 734-764-0579
Fax+1 734-763-6561
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Summary
- Dr. Mark Hannibal is a medical geneticist based in Ann Arbor, MI, specializing in clinical and pediatric medical genetics. He completed residencies in both Medical Genetics and Genomics, and Pediatrics at the University of Washington after obtaining his medical degree from the University of Michigan Medical School in 1994. Dr. Hannibal has contributed to several peer-reviewed publications, covering topics such as Sifrim-Hitz-Weiss syndrome, TCF3-related diseases, and SMARCC2-associated neurodevelopmental disorders. His work has been widely cited, and he has received recognition as a Top MD from Consumers Checkbook.
Education & Training
University of WashingtonResidency, Medical Genetics and Genomics, 1997 - 2000- University of WashingtonResidency, Pediatrics, 1994 - 1997
University of Michigan Medical SchoolClass of 1994
Certifications & Licensure
MI State Medical License 2011 - 2025
AK State Medical License Active through 2012
WA State Medical License 1999 - 2012
ID State Medical License 1995 - 1995
American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Awards, Honors, & Recognition
- Top MD Consumers Checkbook
Publications & Presentations
PubMed
- Discovery of a DNA methylation profile in individuals with Sifrim-Hitz-Weiss syndrome.Karim Karimi, Yael Lichtenstein, Jack Reilly, Haley McConkey, Raissa Relator
American Journal of Human Genetics. 2025-02-06 - Heterozygous TCF3-related disease presenting as X-linked agammaglobulinemia mimicry in a male toddler with B-cell aplasia, agammaglobulinemia, and severe neutropenia.Laura M Bou-Maroun, Kelly J Walkovich, Lauren Frazier, Mark Hannibal, Thomas F Michniacki
Pediatric Blood & Cancer. 2024-06-01 - 7 citationsElucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals.Elisabeth Bosch, Bernt Popp, Esther Güse, Cindy Skinner, Pleuntje J van der Sluijs
Genetics in Medicine. 2023-11-01
Grant Support
- Molecular Basis Of Hereditary Neuralgic AmyotrophyNational Institute Of Neurological Disorders And Stroke2008
- Analysis Of Susceptibility Genes For Arthritis In MiceNational Institute Of Arthritis And Musculoskeletal And Skin Diseases2000–2004
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