Matthew Warman headshot

Matthew L. Warman, M.D.

Professor of Genetics
617-919-2371
Matt Warman Website
Sox9 is upstream of microRNA-140 in cartilage.
Authors: Authors: Nakamura Y, He X, Kato H, Wakitani S, Kobayashi T, Watanabe S, Iida A, Tahara H, Warman ML, Watanapokasin R, Postlethwait JH.
Appl Biochem Biotechnol
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Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity.
Authors: Authors: Boyden ED, Campos-Xavier AB, Kalamajski S, Cameron TL, Suarez P, Tanackovic G, Tanackovich G, Andria G, Ballhausen D, Briggs MD, Hartley C, Cohn DH, Davidson HR, Hall C, Ikegawa S, Jouk PS, König R, Megarbané A, Nishimura G, Lachman RS, Mortier G, Rimoin DL, Rogers RC, Rossi M, Sawada H, Scott R, Unger S, Valadares ER, Bateman JF, Warman ML, Superti-Furga A, Bonafé L.
Am J Hum Genet
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High-bone-mass-producing mutations in the Wnt signaling pathway result in distinct skeletal phenotypes.
Authors: Authors: Niziolek PJ, Farmer TL, Cui Y, Turner CH, Warman ML, Robling AG.
Bone
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The mechanical properties of tail tendon fascicles from lubricin knockout, wild type and heterozygous mice.
Authors: Authors: Reuvers J, Thoreson AR, Zhao C, Zhang L, Jay GD, An KN, Warman ML, Amadio PC.
J Struct Biol
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Lrp5 functions in bone to regulate bone mass.
Authors: Authors: Cui Y, Niziolek PJ, MacDonald BT, Zylstra CR, Alenina N, Robinson DR, Zhong Z, Matthes S, Jacobsen CM, Conlon RA, Brommage R, Liu Q, Mseeh F, Powell DR, Yang QM, Zambrowicz B, Gerrits H, Gossen JA, He X, Bader M, Williams BO, Warman ML, Robling AG.
Nat Med
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Expansion thoracoplasty affects lung growth and morphology in a rabbit model: a pilot study.
Authors: Authors: Olson JC, Kurek KC, Mehta HP, Warman ML, Snyder BD.
Clin Orthop Relat Res
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Nosology and classification of genetic skeletal disorders: 2010 revision.
Authors: Authors: Warman ML, Cormier-Daire V, Hall C, Krakow D, Lachman R, LeMerrer M, Mortier G, Mundlos S, Nishimura G, Rimoin DL, Robertson S, Savarirayan R, Sillence D, Spranger J, Unger S, Zabel B, Superti-Furga A.
Am J Med Genet A
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Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome.
Authors: Authors: Bowen ME, Boyden ED, Holm IA, Campos-Xavier B, Bonafé L, Superti-Furga A, Ikegawa S, Cormier-Daire V, Bovée JV, Pansuriya TC, de Sousa SB, Savarirayan R, Andreucci E, Vikkula M, Garavelli L, Pottinger C, Ogino T, Sakai A, Regazzoni BM, Wuyts W, Sangiorgi L, Pedrini E, Zhu M, Kozakewich HP, Kasser JR, Seidman JG, Kurek KC, Warman ML.
PLoS Genet
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Tendon fascicle gliding in wild type, heterozygous, and lubricin knockout mice.
Authors: Authors: Kohrs RT, Zhao C, Sun YL, Jay GD, Zhang L, Warman ML, An KN, Amadio PC.
J Orthop Res
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Wwp2 is essential for palatogenesis mediated by the interaction between Sox9 and mediator subunit 25.
Authors: Authors: Nakamura Y, Yamamoto K, He X, Otsuki B, Kim Y, Murao H, Soeda T, Tsumaki N, Deng JM, Zhang Z, Behringer RR, Crombrugghe Bd, Postlethwait JH, Warman ML, Nakamura T, Akiyama H.
Nat Commun
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