Matthew Warman headshot

Matthew L. Warman, M.D.

Professor of Genetics
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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Causal somatic mutations in urine DNA from persons with the CLOVES subgroup of the PIK3CA-related overgrowth spectrum.
Authors: Authors: Michel ME, Konczyk DJ, Yeung KS, Murillo R, Vivero MP, Hall AM, Zurakowski D, Adams D, Gupta A, Huang AY, Chung BHY, Warman ML.
Clin Genet
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The skeletal phenotype of achondrogenesis type 1A is caused exclusively by cartilage defects.
Authors: Authors: Bird IM, Kim SH, Schweppe DK, Caetano-Lopes J, Robling AG, Charles JF, Gygi SP, Warman ML, Smits PJ.
Development
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SHP2 regulates skeletal cell fate by modifying SOX9 expression and transcriptional activity.
Authors: Authors: Zuo C, Wang L, Kamalesh RM, Bowen ME, Moore DC, Dooner MS, Reginato AM, Wu Q, Schorl C, Song Y, Warman ML, Neel BG, Ehrlich MG, Yang W.
Bone Res
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Clcn7F318L/+ as a new mouse model of Albers-Schönberg disease.
Authors: Authors: Caetano-Lopes J, Lessard SG, Hann S, Espinoza K, Kang KS, Lim KE, Horan DJ, Noonan HR, Hu D, Baron R, Robling AG, Warman ML.
Bone
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Somatic PIK3CA mutations are present in multiple tissues of facial infiltrating lipomatosis.
Authors: Authors: Couto JA, Konczyk DJ, Vivero MP, Kozakewich HPW, Upton J, Fu X, Padwa BL, Mulliken JB, Warman ML, Greene AK.
Pediatr Res
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SHP2 Regulates the Osteogenic Fate of Growth Plate Hypertrophic Chondrocytes.
Authors: Authors: Wang L, Huang J, Moore DC, Zuo C, Wu Q, Xie L, von der Mark K, Yuan X, Chen D, Warman ML, Ehrlich MG, Yang W.
Sci Rep
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Mice maintain predominantly maternal Gas expression throughout life in brown fat tissue (BAT), but not other tissues.
Authors: Authors: Tafaj O, Hann S, Ayturk U, Warman ML, Jüppner H.
Bone
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A somatic GNA11 mutation is associated with extremity capillary malformation and overgrowth.
Authors: Authors: Couto JA, Ayturk UM, Konczyk DJ, Goss JA, Huang AY, Hann S, Reeve JL, Liang MG, Bischoff J, Warman ML, Greene AK.
Angiogenesis
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