Matthew Warman headshot

Matthew L. Warman, M.D.

Professor of Genetics
617-919-2371
Matt Warman Website
Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma.
Authors: Authors: Ayturk UM, Couto JA, Hann S, Mulliken JB, Williams KL, Huang AY, Fishman SJ, Boyd TK, Kozakewich HP, Bischoff J, Greene AK, Warman ML.
Am J Hum Genet
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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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Critical Endothelial Regulation by LRP5 during Retinal Vascular Development.
Authors: Authors: Huang W, Li Q, Amiry-Moghaddam M, Hokama M, Sardi SH, Nagao M, Warman ML, Olsen BR.
PLoS One
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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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