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Jeffrey Ming, MD, PhD

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.

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