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Matthew L. Warman, M.D.

Professor of Genetics
617-919-2371
Matt Warman Website
Endothelial Cells from Capillary Malformations Are Enriched for Somatic GNAQ Mutations.
Authors: Authors: Couto JA, Huang L, Vivero MP, Kamitaki N, Maclellan RA, Mulliken JB, Bischoff J, Warman ML, Greene AK.
Plast Reconstr Surg
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Nosology and classification of genetic skeletal disorders: 2015 revision.
Authors: Authors: Bonafe L, Cormier-Daire V, Hall C, Lachman R, Mortier G, Mundlos S, Nishimura G, Sangiorgi L, Savarirayan R, Sillence D, Spranger J, Superti-Furga A, Warman M, Unger S.
Am J Med Genet A
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Lubricin restoration in a mouse model of congenital deficiency.
Authors: Authors: Hill A, Waller KA, Cui Y, Allen JM, Smits P, Zhang LX, Ayturk UM, Hann S, Lessard SG, Zurakowski D, Warman ML, Jay GD.
Arthritis Rheumatol
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High Bone Mass-Causing Mutant LRP5 Receptors Are Resistant to Endogenous Inhibitors In Vivo.
Authors: Authors: Niziolek PJ, MacDonald BT, Kedlaya R, Zhang M, Bellido T, He X, Warman ML, Robling AG.
J Bone Miner Res
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Facial Infiltrating Lipomatosis Contains Somatic PIK3CA Mutations in Multiple Tissues.
Authors: Authors: Couto JA, Vivero MP, Upton J, Padwa BL, Warman ML, Mulliken JB, Greene AK.
Plast Reconstr Surg
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Mechanistic and therapeutic insights gained from studying rare skeletal diseases.
Authors: Authors: Tosi LL, Warman ML.
Bone
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Identification of a Prg4-expressing articular cartilage progenitor cell population in mice.
Authors: Authors: Kozhemyakina E, Zhang M, Ionescu A, Ayturk UM, Ono N, Kobayashi A, Kronenberg H, Warman ML, Lassar AB.
Arthritis Rheumatol
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Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short stature.
Authors: Authors: Wang SR, Jacobsen CM, Carmichael H, Edmund AB, Robinson JW, Olney RC, Miller TC, Moon JE, Mericq V, Potter LR, Warman ML, Hirschhorn JN, Dauber A.
Hum Mutat
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Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA.
Authors: Authors: Luks VL, Kamitaki N, Vivero MP, Uller W, Rab R, Bovée JV, Rialon KL, Guevara CJ, Alomari AI, Greene AK, Fishman SJ, Kozakewich HP, Maclellan RA, Mulliken JB, Rahbar R, Spencer SA, Trenor CC, Upton J, Zurakowski D, Perkins JA, Kirsh A, Bennett JT, Dobyns WB, Kurek KC, Warman ML, McCarroll SA, Murillo R.
J Pediatr
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AKT hyper-phosphorylation associated with PI3K mutations in lymphatic endothelial cells from a patient with lymphatic malformation.
Authors: Authors: Boscolo E, Coma S, Luks VL, Greene AK, Klagsbrun M, Warman ML, Bischoff J.
Angiogenesis
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