Matthew L. Warman

Matthew L. Warman, M.D.

Professor of Genetics

617-919-2371

Publications

The mutational spectrum of brachydactyly type C.

Authors: Authors: Everman DB, Bartels CF, Yang Y, Yanamandra N, Goodman FR, Mendoza-Londono JR, Savarirayan R, White SM, Graham JM, Gale RP, Svarch E, Newman WG, Kleckers AR, Francomano CA, Govindaiah V, Singh L, Morrison S, Thomas JT, Warman ML.
Am J Med Genet 2002-10-15
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A novel mutation in the IHH gene causes brachydactyly type A1: a 95-year-old mystery resolved.

Authors: Authors: McCready ME, Sweeney E, Fryer AE, Donnai D, Baig A, Racacho L, Warman ML, Hunter AG, Bulman DE.
Hum Genet 2002-10-01
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The gene for juvenile hyaline fibromatosis maps to chromosome 4q21.

Authors: Authors: Rahman N, Dunstan M, Teare MD, Hanks S, Edkins SJ, Hughes J, Bignell GR, Mancini G, Kleijer W, Campbell M, Keser G, Black C, Williams N, Arbour L, Warman M, Superti-Furga A, Futreal PA, Pope FM.
Am J Hum Genet 2002-10-01
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Significant difference of opinion regarding the role of noggin in fibrodysplasia ossificans progressiva.

Authors: Authors: Warman ML.
Am J Med Genet 2002-04-22
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Confirmation of existence of a new syndrome: LAPS syndrome.

Authors: Authors: Lindor NM, Kasperbauer JL, Hoffman AD, Parisi JE, Wang H, Warman M.
Am J Med Genet 2002-04-22
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Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas").

Authors: Authors: Brouillard P, Boon LM, Mulliken JB, Enjolras O, Ghassibé M, Warman ML, Tan OT, Olsen BR, Vikkula M.
Am J Hum Genet 2002-04-01
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LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development.

Authors: Authors: Gong Y, Slee RB, Fukai N, Rawadi G, Roman-Roman S, Reginato AM, Wang H, Cundy T, Glorieux FH, Lev D, Zacharin M, Oexle K, Marcelino J, Suwairi W, Heeger S, Sabatakos G, Apte S, Adkins WN, Allgrove J, Arslan-Kirchner M, Batch JA, Beighton P, Black GC, Boles RG, Boon LM, Borrone C, Brunner HG, Carle GF, Dallapiccola B, De Paepe A, Floege B, Halfhide ML, Hall B, Hennekam RC, Hirose T, Jans A, Jüppner H, Kim CA, Keppler-Noreuil K, Kohlschuetter A, LaCombe D, Lambert M, Lemyre E, Letteboer T, Peltonen L, Ramesar RS, Romanengo M, Somer H, Steichen-Gersdorf E, Steinmann B, Sullivan B, Superti-Furga A, Swoboda W, van den Boogaard MJ, Van Hul W, Vikkula M, Votruba M, Zabel B, Garcia T, Baron R, Olsen BR, Warman ML.
Cell 2001-11-16
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Bone brittleness varies with genetic background in A/J and C57BL/6J inbred mice.

Authors: Authors: Jepsen KJ, Pennington DE, Lee YL, Warman M, Nadeau J.
J Bone Miner Res 2001-10-01
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Human disease-causing NOG missense mutations: effects on noggin secretion, dimer formation, and bone morphogenetic protein binding.

Authors: Authors: Marcelino J, Sciortino CM, Romero MF, Ulatowski LM, Ballock RT, Economides AN, Eimon PM, Harland RM, Warman ML.
Proc Natl Acad Sci U S A 2001-09-25
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Human genetic insights into skeletal development, growth, and homeostasis.

Authors: Authors: Warman ML.
Clin Orthop Relat Res 2000-10-01
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