Matthew L. Warman

Matthew L. Warman, M.D.

Professor of Genetics

617-919-2371

Publications

An RNA-seq protocol to identify mRNA expression changes in mouse diaphyseal bone: applications in mice with bone property altering Lrp5 mutations.

Authors: Authors: Ayturk UM, Jacobsen CM, Christodoulou DC, Gorham J, Seidman JG, Seidman CE, Robling AG, Warman ML.
J Bone Miner Res 2013-10-01
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Autopodial development is selectively impaired by misexpression of chordin-like 1 in the chick limb.

Authors: Authors: Allen JM, McGlinn E, Hill A, Warman ML.
Dev Biol 2013-09-01
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Role of lubricin and boundary lubrication in the prevention of chondrocyte apoptosis.

Authors: Authors: Waller KA, Zhang LX, Elsaid KA, Fleming BC, Warman ML, Jay GD.
Proc Natl Acad Sci U S A 2013-04-09
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Presphenoidal synchondrosis fusion in DBA/2J mice.

Authors: Authors: Adams A, McBratney-Owen B, Newby B, Bowen ME, Olsen BR, Warman ML.
Mamm Genome 2013-02-01
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A Wisp3 Cre-knockin allele produces efficient recombination in spermatocytes during early prophase of meiosis I.

Authors: Authors: Hann S, Kvenvold L, Newby BN, Hong M, Warman ML.
PLoS One 2013-01-01
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Craniofacial abnormalities result from knock down of nonsyndromic clefting gene, crispld2, in zebrafish.

Authors: Authors: Yuan Q, Chiquet BT, Devault L, Warman ML, Nakamura Y, Swindell EC, Hecht JT.
Genesis 2012-12-01
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Mechanotransduction in bone tissue: The A214V and G171V mutations in Lrp5 enhance load-induced osteogenesis in a surface-selective manner.

Authors: Authors: Niziolek PJ, Warman ML, Robling AG.
Bone 2012-09-01
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The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): a review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals.

Authors: Authors: Garcia Segarra N, Mittaz L, Campos-Xavier AB, Bartels CF, Tuysuz B, Alanay Y, Cimaz R, Cormier-Daire V, Di Rocco M, Duba HC, Elcioglu NH, Forzano F, Hospach T, Kilic E, Kuemmerle-Deschner JB, Mortier G, Mrusek S, Nampoothiri S, Obersztyn E, Pauli RM, Selicorni A, Tenconi R, Unger S, Utine GE, Wright M, Zabel B, Warman ML, Superti-Furga A, Bonafé L.
Am J Med Genet C Semin Med Genet 2012-08-15
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Somatic mosaic activating mutations in PIK3CA cause CLOVES syndrome.

Authors: Authors: Kurek KC, Luks VL, Ayturk UM, Alomari AI, Fishman SJ, Spencer SA, Mulliken JB, Bowen ME, Yamamoto GL, Kozakewich HP, Warman ML.
Am J Hum Genet 2012-06-08
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Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity.

Authors: Authors: Korvala J, Jüppner H, Mäkitie O, Sochett E, Schnabel D, Mora S, Bartels CF, Warman ML, Deraska D, Cole WG, Hartikka H, Ala-Kokko L, Männikkö M.
BMC Med Genet 2012-04-10
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