Matthew Warman headshot

Matthew L. Warman, M.D.

Professor of Genetics
617-919-2371
Matt Warman Website
[Mapping the gene responsible for Smith-Fineman-Myers syndrome to Xq25].
Authors: Authors: Gong Y, Wei J, Shao C, Guo Y, Chen B, Guo C, Warman M.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
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Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia.
Authors: Authors: Hurvitz JR, Suwairi WM, Van Hul W, El-Shanti H, Superti-Furga A, Roudier J, Holderbaum D, Pauli RM, Herd JK, Van Hul EV, Rezai-Delui H, Legius E, Le Merrer M, Al-Alami J, Bahabri SA, Warman ML.
Nat Genet
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Complete sequence of the 23-kilobase human COL9A3 gene. Detection of Gly-X-Y triplet deletions that represent neutral variants.
Authors: Authors: Paassilta P, Pihlajamaa T, Annunen S, Brewton RG, Wood BM, Johnson CC, Liu J, Gong Y, Warman ML, Prockop DJ, Mayne R, Ala-Kokko L.
J Biol Chem
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Clinical and molecular studies of brachydactyly type D.
Authors: Authors: Robin NH, Hurvitz J, Warman ML, Morrison S.
Am J Med Genet
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A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22.
Authors: Authors: Boon LM, Brouillard P, Irrthum A, Karttunen L, Warman ML, Rudolph R, Mulliken JB, Olsen BR, Vikkula M.
Am J Hum Genet
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Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis.
Authors: Authors: Gong Y, Krakow D, Marcelino J, Wilkin D, Chitayat D, Babul-Hirji R, Hudgins L, Cremers CW, Cremers FP, Brunner HG, Reinker K, Rimoin DL, Cohn DH, Goodman FR, Reardon W, Patton M, Francomano CA, Warman ML.
Nat Genet
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Brachydactyly type B: clinical description, genetic mapping to chromosome 9q, and evidence for a shared ancestral mutation.
Authors: Authors: Gong Y, Chitayat D, Kerr B, Chen T, Babul-Hirji R, Pal A, Reiss M, Warman ML.
Am J Hum Genet
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A member of a family of sulfate-activating enzymes causes murine brachymorphism.
Authors: Authors: Kurima K, Warman ML, Krishnan S, Domowicz M, Krueger RC, Deyrup A, Schwartz NB.
Proc Natl Acad Sci U S A
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Acromesomelic dysplasia Maroteaux type maps to human chromosome 9.
Authors: Authors: Kant SG, Polinkovsky A, Mundlos S, Zabel B, Thomeer RT, Zonderland HM, Shih L, van Haeringen A, Warman ML.
Am J Hum Genet
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Marshall syndrome associated with a splicing defect at the COL11A1 locus.
Authors: Authors: Griffith AJ, Sprunger LK, Sirko-Osadsa DA, Tiller GE, Meisler MH, Warman ML.
Am J Hum Genet
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