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Matthew L. Warman, M.D.

Professor of Genetics
617-919-2371
Matt Warman Website
The camptodactyly-arthropathy-coxa vara-pericarditis syndrome: clinical features and genetic mapping to human chromosome 1.
Authors: Authors: Bahabri SA, Suwairi WM, Laxer RM, Polinkovsky A, Dalaan AA, Warman ML.
Arthritis Rheum
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Gene symbol: COL11A1. Disease: Marshall syndrome.
Authors: Authors: Meisler MH, Griffith AJ, Warman M, Tiller G, Sprunger LK.
Hum Genet
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Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2(XI) chain of type XI collagen.
Authors: Authors: Sirko-Osadsa DA, Murray MA, Scott JA, Lavery MA, Warman ML, Robin NH.
J Pediatr
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Physical and linkage mapping of the gene for the alpha3 chain of type IX collagen, COL9A3, to human chromosome 20q13.3.
Authors: Authors: Tiller GE, Warman ML, Gong Y, Knoll JH, Mayne R, Brewton RG.
Cytogenet Cell Genet
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Mutations in CDMP1 cause autosomal dominant brachydactyly type C.
Authors: Authors: Polinkovsky A, Robin NH, Thomas JT, Irons M, Lynn A, Goodman FR, Reardon W, Kant SG, Brunner HG, van der Burgt I, Chitayat D, McGaughran J, Donnai D, Luyten FP, Warman ML.
Nat Genet
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Hemangioma in twins.
Authors: Authors: Cheung DS, Warman ML, Mulliken JB.
Ann Plast Surg
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Clinical and locus heterogeneity in brachydactyly type C.
Authors: Authors: Robin NH, Gunay-Aygun M, Polinkovsky A, Warman ML, Morrison S.
Am J Med Genet
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Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2.
Authors: Authors: Vikkula M, Boon LM, Carraway KL, Calvert JT, Diamonti AJ, Goumnerov B, Pasyk KA, Marchuk DA, Warman ML, Cantley LC, Mulliken JB, Olsen BR.
Cell
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Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13.
Authors: Authors: Gong Y, Vikkula M, Boon L, Liu J, Beighton P, Ramesar R, Peltonen L, Somer H, Hirose T, Dallapiccola B, De Paepe A, Swoboda W, Zabel B, Superti-Furga A, Steinmann B, Brunner HG, Jans A, Boles RG, Adkins W, van den Boogaard MJ, Olsen BR, Warman ML.
Am J Hum Genet
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A mutation in COL9A2 causes multiple epiphyseal dysplasia (EDM2).
Authors: Authors: Muragaki Y, Mariman EC, van Beersum SE, Perälä M, van Mourik JB, Warman ML, Hamel BC, Olsen BR.
Ann N Y Acad Sci
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