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Matthew L. Warman, M.D.

Professor of Genetics
617-919-2371
Matt Warman Website
Significant difference of opinion regarding the role of noggin in fibrodysplasia ossificans progressiva.
Authors: Authors: Warman ML.
Am J Med Genet
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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
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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
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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
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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
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Human genetic insights into skeletal development, growth, and homeostasis.
Authors: Authors: Warman ML.
Clin Orthop Relat Res
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Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT).
Authors: Authors: Truett GE, Heeger P, Mynatt RL, Truett AA, Walker JA, Warman ML.
Biotechniques
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Autosomal recessive disorder otospondylomegaepiphyseal dysplasia is associated with loss-of-function mutations in the COL11A2 gene.
Authors: Authors: Melkoniemi M, Brunner HG, Manouvrier S, Hennekam R, Superti-Furga A, Kääriäinen H, Pauli RM, van Essen T, Warman ML, Bonaventure J, Miny P, Ala-Kokko L.
Am J Hum Genet
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CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
Authors: Authors: Marcelino J, Carpten JD, Suwairi WM, Gutierrez OM, Schwartz S, Robbins C, Sood R, Makalowska I, Baxevanis A, Johnstone B, Laxer RM, Zemel L, Kim CA, Herd JK, Ihle J, Williams C, Johnson M, Raman V, Alonso LG, Brunoni D, Gerstein A, Papadopoulos N, Bahabri SA, Trent JM, Warman ML.
Nat Genet
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Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes.
Authors: Authors: Annunen S, Körkkö J, Czarny M, Warman ML, Brunner HG, Kääriäinen H, Mulliken JB, Tranebjaerg L, Brooks DG, Cox GF, Cruysberg JR, Curtis MA, Davenport SL, Friedrich CA, Kaitila I, Krawczynski MR, Latos-Bielenska A, Mukai S, Olsen BR, Shinno N, Somer M, Vikkula M, Zlotogora J, Prockop DJ, Ala-Kokko L.
Am J Hum Genet
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