Matthew Warman headshot

Matthew L. Warman, M.D.

Professor of Genetics
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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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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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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Intramuscular fast-flow vascular anomaly contains somatic MAP2K1 and KRAS mutations.
Authors: Authors: Goss JA, Konczyk DJ, Smits PJ, Kozakewich HPW, Alomari AI, Al-Ibraheemi A, Taghinia AH, Dickie BH, Adams DM, Fishman SJ, Mulliken JB, Warman ML, Greene AK.
Angiogenesis
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Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta.
Authors: Authors: Moosa S, Yamamoto GL, Garbes L, Keupp K, Beleza-Meireles A, Moreno CA, Valadares ER, de Sousa SB, Maia S, Saraiva J, Honjo RS, Kim CA, Cabral de Menezes H, Lausch E, Lorini PV, Lamounier A, Carniero TCB, Giunta C, Rohrbach M, Janner M, Semler O, Beleggia F, Li Y, Yigit G, Reintjes N, Altmüller J, Nürnberg P, Cavalcanti DP, Zabel B, Warman ML, Bertola DR, Wollnik B, Netzer C.
Am J Hum Genet
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Expression of a Degradation-Resistant ß-Catenin Mutant in Osteocytes Protects the Skeleton From Mechanodeprivation-Induced Bone Wasting.
Authors: Authors: Bullock WA, Hoggatt AM, Horan DJ, Lewis KJ, Yokota H, Hann S, Warman ML, Sebastian A, Loots GG, Pavalko FM, Robling AG.
J Bone Miner Res
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Gain-of-function mutation of microRNA-140 in human skeletal dysplasia.
Authors: Authors: Grigelioniene G, Suzuki HI, Taylan F, Mirzamohammadi F, Borochowitz ZU, Ayturk UM, Tzur S, Horemuzova E, Lindstrand A, Weis MA, Grigelionis G, Hammarsjö A, Marsk E, Nordgren A, Nordenskjöld M, Eyre DR, Warman ML, Nishimura G, Sharp PA, Kobayashi T.
Nat Med
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Induction of Lrp5 HBM-causing mutations in Cathepsin-K expressing cells alters bone metabolism.
Authors: Authors: Kang KS, Hong JM, Horan DJ, Lim KE, Bullock WA, Bruzzaniti A, Hann S, Warman ML, Robling AG.
Bone
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Somatic mutations in intracranial arteriovenous malformations.
Authors: Authors: Goss JA, Huang AY, Smith E, Konczyk DJ, Smits PJ, Sudduth CL, Stapleton C, Patel A, Alexandrescu S, Warman ML, Greene AK.
PLoS One
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