Jeffrey Ming, MD, PhD
Areas of expertise: Genetics of brain development
Locations: Main Building
About Jeffrey Ming, MD, PhD
Titles
Attending Physician
Certifications
Clinical Genetics and Genomics – American Board of Medical Genetics and Genomics
Pediatrics – American Board of Pediatrics
Education & training
Medical Degree
Cornell University Medical College, New York, NY
Publications
Publications
2015
Weaver DD, Norby AR, Rosenfeld JA, Proud VK, Spangler BE, Ming JE, Chisholm E, Zackai, Lee BH, Edelmann L, Desnick RJ. Chromosome 1p36.22p36.21 duplications/ triplication causes Setleis syndrome (focal facial dermal dysplasia type III). Am J Med Genet A 167A:1061-70, 2015.
2012
Srivastava K, Hu P, Solomon BD, Ming JE, Roessler E, Muenke M. Molecular analysis of the Noggin (NOG) gene in holoprosencephaly patients. Mol Genet Metab 106:241-3, 2012.
2011
Hannibal MC, Buckingham KJ, Ng SB, Ming JE, Beck AE, McMillin MJ, Gildersleeve HI, Bigham AW, Tabor HK, Mefford HC, Cook J, Yoshiura K, Matsumoto T, Matsumoto N, Miyake N, Tonoki H, Naritomi K, Kaname T, Nagai T, Ohashi H, Kurosawa K, Hou JW, Ohta T, Liang D, Sudo A, Morris CA, Banka S, Black GC, Clayton-Smith J, Nickerson DA, Zackai EH, Shaikh TH, Donnai D, Niikawa N, Shendure J, Bamshad MJ. Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome. Am J Med Genet A 155:1511-1516, 2011.