Matthew Warman headshot

Matthew L. Warman, M.D.

Professor of Genetics
617-919-2371
Matt Warman Website
Single-Cell RNA Sequencing of Calvarial and Long-Bone Endocortical Cells.
Authors: Authors: Ayturk UM, Scollan JP, Goz Ayturk D, Suh ES, Vesprey A, Jacobsen CM, Divieti Pajevic P, Warman ML.
J Bone Miner Res
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Ocular Manifestations of Chordin-like 1 Knockout Mice.
Authors: Authors: Chen D, Liu Y, Shu G, Chen C, Sullivan DA, Kam WR, Hann S, Fowler M, Warman ML.
Cornea
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Independent validation of experimental results requires timely and unrestricted access to animal models and reagents.
Authors: Authors: Diegel CR, Hann S, Ayturk UM, Hu JCW, Lim KE, Droscha CJ, Madaj ZB, Foxa GE, Izaguirre I, Robling AG, Warman ML, Williams BO.
PLoS Genet
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Correction: Unique and non-redundant function of csf1r paralogues in regulation and evolution of post-embryonic development of the zebrafish.
Authors: Authors: Caetano-Lopes J, Henke K, Urso K, Duryea J, Charles JF, Warman ML, Harris MP.
Development
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An osteocalcin-deficient mouse strain without endocrine abnormalities.
Authors: Authors: Diegel CR, Hann S, Ayturk UM, Hu JCW, Lim KE, Droscha CJ, Madaj ZB, Foxa GE, Izaguirre I, Transgenics Core VVA, Paracha N, Pidhaynyy B, Dowd TL, Robling AG, Warman ML, Williams BO.
PLoS Genet
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Combination therapy in the Col1a2G610C mouse model of Osteogenesis Imperfecta reveals an additive effect of enhancing LRP5 signaling and inhibiting TGFß signaling on trabecular bone but not on cortical bone.
Authors: Authors: Kaupp S, Horan DJ, Lim KE, Feldman HA, Robling AG, Warman ML, Jacobsen CM.
Bone
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Unique and non-redundant function of csf1r paralogues in regulation and evolution of post-embryonic development of the zebrafish.
Authors: Authors: Caetano-Lopes J, Henke K, Urso K, Duryea J, Charles JF, Warman ML, Harris MP.
Development
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Proteolysis and cartilage development are activated in the synovium after surgical induction of post traumatic osteoarthritis.
Authors: Authors: Ayturk UM, Sieker JT, Haslauer CM, Proffen BL, Weissenberger MH, Warman ML, Fleming BC, Murray MM.
PLoS One
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Arteriovenous malformation associated with a HRAS mutation.
Authors: Authors: Konczyk DJ, Goss JA, Smits PJ, Huang AY, Al-Ibraheemi A, Sudduth CL, Warman ML, Greene AK.
Hum Genet
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Nosology and classification of genetic skeletal disorders: 2019 revision.
Authors: Authors: Mortier GR, Cohn DH, Cormier-Daire V, Hall C, Krakow D, Mundlos S, Nishimura G, Robertson S, Sangiorgi L, Savarirayan R, Sillence D, Superti-Furga A, Unger S, Warman ML.

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