Matthew L. Warman - Publications

Affiliations: 
Biology: Medical Sciences, Division of Harvard University, Cambridge, MA, United States 
Area:
Genetics, Human Development

50 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 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, ... ... Warman ML, et al. Gain-of-function mutation of microRNA-140 in human skeletal dysplasia. Nature Medicine. PMID 30804514 DOI: 10.1038/s41591-019-0353-2  0.48
2018 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. SHP2 regulates skeletal cell fate by modifying SOX9 expression and transcriptional activity. Bone Research. 6: 12. PMID 29644115 DOI: 10.1038/s41413-018-0013-z  0.48
2017 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. SHP2 Regulates the Osteogenic Fate of Growth Plate Hypertrophic Chondrocytes. Scientific Reports. 7: 12699. PMID 28983104 DOI: 10.1038/s41598-017-12767-9  0.48
2017 Couto JA, Ayturk UM, Konczyk DJ, Goss JA, Huang AY, Hann S, Reeve JL, Liang MG, Bischoff J, Warman ML, Greene AK. A somatic GNA11 mutation is associated with extremity capillary malformation and overgrowth. Angiogenesis. PMID 28120216 DOI: 10.1007/s10456-016-9538-1  0.48
2016 Jacobsen CM, Schwartz MA, Roberts HJ, Lim KE, Spevak L, Boskey AL, Zurakowski D, Robling AG, Warman ML. Enhanced Wnt signaling improves bone mass and strength, but not brittleness, in the Col1a1(+/mov13) mouse model of type I Osteogenesis Imperfecta. Bone. PMID 27297606 DOI: 10.1016/j.bone.2016.06.005  0.48
2016 Ayturk UM, Couto JA, Hann S, Mulliken JB, Williams KL, Huang AY, Fishman SJ, Boyd TK, Kozakewich HP, Bischoff J, Greene AK, Warman ML. Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma. American Journal of Human Genetics. 98: 1271. PMID 27259057 DOI: 10.1016/j.ajhg.2016.05.010  0.48
2016 Masci M, Wang M, Imbert L, Barnes AM, Spevak L, Lukashova L, Huang Y, Ma Y, Marini JC, Jacobsen CM, Warman ML, Boskey AL. Bone mineral properties in growing Col1a2(+/G610C) mice, an animal model of osteogenesis imperfecta. Bone. PMID 27083399 DOI: 10.1016/j.bone.2016.04.011  0.48
2016 Ayturk UM, Couto JA, Hann S, Mulliken JB, Williams KL, Huang AY, Fishman SJ, Boyd TK, Kozakewich HP, Bischoff J, Greene AK, Warman ML. Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma. American Journal of Human Genetics. 98: 789-95. PMID 27058448 DOI: 10.1016/j.ajhg.2016.03.009  0.48
2016 Huang W, Li Q, Amiry-Moghaddam M, Hokama M, Sardi SH, Nagao M, Warman ML, Olsen BR. Critical Endothelial Regulation by LRP5 during Retinal Vascular Development. Plos One. 11: e0152833. PMID 27031698 DOI: 10.1371/journal.pone.0152833  0.48
2015 Hill A, Waller KA, Cui Y, Allen JM, Smits P, Zhang LX, Ayturk UM, Hann S, Lessard SG, Zurakowski D, Warman ML, Jay GD. Lubricin restoration in a mouse model of congenital deficiency. Arthritis & Rheumatology (Hoboken, N.J.). PMID 26216721 DOI: 10.1002/art.39276  0.48
2015 Niziolek PJ, MacDonald BT, Kedlaya R, Zhang M, Bellido T, He X, Warman ML, Robling AG. High-bone-mass causing mutant LRP5 receptors are resistant to endogenous inhibitors in vivo. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 25808845 DOI: 10.1002/jbmr.2514  0.48
2015 Couto JA, Vivero MP, Kozakewich HP, Taghinia AH, Mulliken JB, Warman ML, Greene AK. A somatic MAP3K3 mutation is associated with verrucous venous malformation. American Journal of Human Genetics. 96: 480-6. PMID 25728774 DOI: 10.1016/j.ajhg.2015.01.007  0.48
2015 Wang SR, Jacobsen CM, Carmichael H, Edmund AB, Robinson JW, Olney RC, Miller TC, Moon JE, Mericq V, Potter LR, Warman ML, Hirschhorn JN, Dauber A. Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short stature. Human Mutation. 36: 474-81. PMID 25703509 DOI: 10.1002/humu.22773  0.48
2015 Luks VL, Kamitaki N, Vivero MP, Uller W, Rab R, Bovée JV, Rialon KL, Guevara CJ, Alomari AI, Greene AK, Fishman SJ, Kozakewich HP, Maclellan RA, Mulliken JB, Rahbar R, ... ... Warman ML, et al. Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA. The Journal of Pediatrics. 166: 1048-54.e1-5. PMID 25681199 DOI: 10.1016/j.jpeds.2014.12.069  0.48
2015 Ai M, Cui Y, Sy MS, Lee DM, Zhang LX, Larson KM, Kurek KC, Jay GD, Warman ML. Anti-lubricin monoclonal antibodies created using lubricin-knockout mice immunodetect lubricin in several species and in patients with healthy and diseased joints. Plos One. 10: e0116237. PMID 25642942 DOI: 10.1371/journal.pone.0116237  0.48
2015 Kozhemyakina E, Zhang M, Ionescu A, Ayturk UM, Ono N, Kobayashi A, Kronenberg H, Warman ML, Lassar AB. Identification of a Prg4-expressing articular cartilage progenitor cell population in mice. Arthritis & Rheumatology (Hoboken, N.J.). 67: 1261-73. PMID 25603997 DOI: 10.1002/art.39030  0.48
2015 Boscolo E, Coma S, Luks VL, Greene AK, Klagsbrun M, Warman ML, Bischoff J. AKT hyper-phosphorylation associated with PI3K mutations in lymphatic endothelial cells from a patient with lymphatic malformation. Angiogenesis. 18: 151-62. PMID 25424831 DOI: 10.1007/s10456-014-9453-2  0.48
2014 Cui Y, Niziolek PJ, MacDonald BT, Alenina N, Matthes S, Jacobsen CM, Conlon RA, Brommage R, Powell DR, He X, Bader M, Williams BO, Warman ML, Robling AG. Reply to Lrp5 regulation of bone mass and gut serotonin synthesis. Nature Medicine. 20: 1229-30. PMID 25375917 DOI: 10.1038/nm.3697  0.48
2014 Bennike T, Ayturk U, Haslauer CM, Froehlich JW, Proffen BL, Barnaby O, Birkelund S, Murray MM, Warman ML, Stensballe A, Steen H. A normative study of the synovial fluid proteome from healthy porcine knee joints. Journal of Proteome Research. 13: 4377-87. PMID 25160569 DOI: 10.1021/pr500587x  0.48
2014 Bowen ME, Ayturk UM, Kurek KC, Yang W, Warman ML. SHP2 regulates chondrocyte terminal differentiation, growth plate architecture and skeletal cell fates. Plos Genetics. 10: e1004364. PMID 24875294 DOI: 10.1371/journal.pgen.1004364  0.48
2014 Jacobsen CM, Barber LA, Ayturk UM, Roberts HJ, Deal LE, Schwartz MA, Weis M, Eyre D, Zurakowski D, Robling AG, Warman ML. Targeting the LRP5 pathway improves bone properties in a mouse model of osteogenesis imperfecta. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 29: 2297-306. PMID 24677211 DOI: 10.1002/jbmr.2198  0.48
2014 Maclellan RA, Luks VL, Vivero MP, Mulliken JB, Zurakowski D, Padwa BL, Warman ML, Greene AK, Kurek KC. PIK3CA activating mutations in facial infiltrating lipomatosis. Plastic and Reconstructive Surgery. 133: 12e-9e. PMID 24374682 DOI: 10.1097/01.prs.0000436822.26709.7c  0.48
2013 Kedlaya R, Veera S, Horan DJ, Moss RE, Ayturk UM, Jacobsen CM, Bowen ME, Paszty C, Warman ML, Robling AG. Sclerostin inhibition reverses skeletal fragility in an Lrp5-deficient mouse model of OPPG syndrome. Science Translational Medicine. 5: 211ra158. PMID 24225945 DOI: 10.1126/scitranslmed.3006627  0.48
2013 Hann S, Kvenvold L, Newby BN, Hong M, Warman ML. A Wisp3 Cre-knockin Allele Produces Efficient Recombination in Spermatocytes during Early Prophase of Meiosis I Plos One. 8. PMID 24040393 DOI: 10.1371/journal.pone.0075116  0.48
2013 Allen JM, McGlinn E, Hill A, Warman ML. Autopodial development is selectively impaired by misexpression of chordin-like 1 in the chick limb. Developmental Biology. 381: 159-69. PMID 23764427 DOI: 10.1016/j.ydbio.2013.06.003  0.48
2013 Ayturk UM, Jacobsen CM, Christodoulou DC, Gorham J, Seidman JG, Seidman CE, Robling AG, Warman ML. An RNA-seq protocol to identify mRNA expression changes in mouse diaphyseal bone: applications in mice with bone property altering Lrp5 mutations. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 28: 2081-93. PMID 23553928 DOI: 10.1002/jbmr.1946  0.48
2013 Adams A, McBratney-Owen B, Newby B, Bowen ME, Olsen BR, Warman ML. Presphenoidal synchondrosis fusion in DBA/2J mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 24: 54-62. PMID 23179633 DOI: 10.1007/s00335-012-9437-8  0.48
2012 Kurek KC, Luks VL, Ayturk UM, Alomari AI, Fishman SJ, Spencer SA, Mulliken JB, Bowen ME, Yamamoto GL, Kozakewich HP, Warman ML. Somatic mosaic activating mutations in PIK3CA cause CLOVES syndrome. American Journal of Human Genetics. 90: 1108-15. PMID 22658544 DOI: 10.1016/j.ajhg.2012.05.006  0.48
2012 Bowen ME, Henke K, Siegfried KR, Warman ML, Harris MP. Efficient mapping and cloning of mutations in zebrafish by low-coverage whole-genome sequencing. Genetics. 190: 1017-24. PMID 22174069 DOI: 10.1534/genetics.111.136069  0.48
2012 Nakamura Y, He X, Kato H, Wakitani S, Kobayashi T, Watanabe S, Iida A, Tahara H, Warman ML, Watanapokasin R, Postlethwait JH. Sox9 is upstream of microRNA-140 in cartilage. Applied Biochemistry and Biotechnology. 166: 64-71. PMID 22052544 DOI: 10.1007/s12010-011-9404-y  0.48
2011 Boyden ED, Campos-Xavier AB, Kalamajski S, Cameron TL, Suarez P, Tanackovic G, Tanackovich G, Andria G, Ballhausen D, Briggs MD, Hartley C, Cohn DH, Davidson HR, Hall C, Ikegawa S, ... ... Warman ML, et al. Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity. American Journal of Human Genetics. 89: 767-72. PMID 22152678 DOI: 10.1016/j.ajhg.2011.10.016  0.48
2011 Cui Y, Niziolek PJ, MacDonald BT, Zylstra CR, Alenina N, Robinson DR, Zhong Z, Matthes S, Jacobsen CM, Conlon RA, Brommage R, Liu Q, Mseeh F, Powell DR, Yang QM, ... ... Warman ML, et al. Lrp5 functions in bone to regulate bone mass. Nature Medicine. 17: 684-91. PMID 21602802 DOI: 10.1038/nm.2388  0.48
2011 Bowen ME, Boyden ED, Holm IA, Campos-Xavier B, Bonafé L, Superti-Furga A, Ikegawa S, Cormier-Daire V, Bovée JV, Pansuriya TC, de Sousa SB, Savarirayan R, Andreucci E, Vikkula M, Garavelli L, ... ... Warman ML, et al. Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome. Plos Genetics. 7: e1002050. PMID 21533187 DOI: 10.1371/journal.pgen.1002050  0.48
2011 Warman ML, Cormier-Daire V, Hall C, Krakow D, Lachman R, LeMerrer M, Mortier G, Mundlos S, Nishimura G, Rimoin DL, Robertson S, Savarirayan R, Sillence D, Spranger J, Unger S, et al. Nosology and classification of genetic skeletal disorders: 2010 revision. American Journal of Medical Genetics. Part A. 155: 943-68. PMID 21438135 DOI: 10.1002/ajmg.a.33909  0.48
2011 Nakamura Y, Yamamoto K, He X, Otsuki B, Kim Y, Murao H, Soeda T, Tsumaki N, Deng JM, Zhang Z, Behringer RR, Crombrugghe Bd, Postlethwait JH, Warman ML, Nakamura T, et al. Wwp2 is essential for palatogenesis mediated by the interaction between Sox9 and mediator subunit 25. Nature Communications. 2: 251. PMID 21427722 DOI: 10.1038/ncomms1242  0.48
2010 Coles JM, Zhang L, Blum JJ, Warman ML, Jay GD, Guilak F, Zauscher S. Loss of cartilage structure, stiffness, and frictional properties in mice lacking PRG4. Arthritis and Rheumatism. 62: 1666-74. PMID 20191580 DOI: 10.1002/art.27436  0.48
2010 Kiener HP, Watts GF, Cui Y, Wright J, Thornhill TS, Sköld M, Behar SM, Niederreiter B, Lu J, Cernadas M, Coyle AJ, Sims GP, Smolen J, Warman ML, Brenner MB, et al. Synovial fibroblasts self-direct multicellular lining architecture and synthetic function in three-dimensional organ culture. Arthritis and Rheumatism. 62: 742-52. PMID 20131230 DOI: 10.1002/art.27285  0.48
2010 Smits P, Bolton AD, Funari V, Hong M, Boyden ED, Lu L, Manning DK, Dwyer ND, Moran JL, Prysak M, Merriman B, Nelson SF, Bonafé L, Superti-Furga A, Ikegawa S, ... ... Warman ML, et al. Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210. The New England Journal of Medicine. 362: 206-16. PMID 20089971 DOI: 10.1056/NEJMoa0900158  0.48
2009 Neilson DE, Adams MD, Orr CM, Schelling DK, Eiben RM, Kerr DS, Anderson J, Bassuk AG, Bye AM, Childs AM, Clarke A, Crow YJ, Di Rocco M, Dohna-Schwake C, Dueckers G, ... ... Warman ML, et al. Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2. American Journal of Human Genetics. 84: 44-51. PMID 19118815 DOI: 10.1016/j.ajhg.2008.12.009  0.48
2008 Balemans W, Piters E, Cleiren E, Ai M, Van Wesenbeeck L, Warman ML, Van Hul W. The binding between sclerostin and LRP5 is altered by DKK1 and by high-bone mass LRP5 mutations. Calcified Tissue International. 82: 445-53. PMID 18521528 DOI: 10.1007/s00223-008-9130-9  0.48
2007 Nakamura Y, Weidinger G, Liang JO, Aquilina-Beck A, Tamai K, Moon RT, Warman ML. The CCN family member Wisp3, mutant in progressive pseudorheumatoid dysplasia, modulates BMP and Wnt signaling. The Journal of Clinical Investigation. 117: 3075-86. PMID 17823661 DOI: 10.1172/JCI32001  0.48
2006 Sawakami K, Robling AG, Ai M, Pitner ND, Liu D, Warden SJ, Li J, Maye P, Rowe DW, Duncan RL, Warman ML, Turner CH. The Wnt co-receptor LRP5 is essential for skeletal mechanotransduction but not for the anabolic bone response to parathyroid hormone treatment. The Journal of Biological Chemistry. 281: 23698-711. PMID 16790443 DOI: 10.1074/jbc.M601000200  0.48
2006 Okajima K, Warman ML, Byrne LC, Kerr DS. Somatic mosaicism in a male with an exon skipping mutation in PDHA1 of the pyruvate dehydrogenase complex results in a milder phenotype. Molecular Genetics and Metabolism. 87: 162-8. PMID 16412675 DOI: 10.1016/j.ymgme.2005.09.023  0.48
2005 Ai M, Holmen SL, Van Hul W, Williams BO, Warman ML. Reduced affinity to and inhibition by DKK1 form a common mechanism by which high bone mass-associated missense mutations in LRP5 affect canonical Wnt signaling. Molecular and Cellular Biology. 25: 4946-55. PMID 15923613 DOI: 10.1128/MCB.25.12.4946-4955.2005  0.48
2004 Holmen SL, Giambernardi TA, Zylstra CR, Buckner-Berghuis BD, Resau JH, Hess JF, Glatt V, Bouxsein ML, Ai M, Warman ML, Williams BO. Decreased BMD and limb deformities in mice carrying mutations in both Lrp5 and Lrp6. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 19: 2033-40. PMID 15537447 DOI: 10.1359/JBMR.040907  0.48
2004 Falk MJ, Feiler HS, Neilson DE, Maxwell K, Lee JV, Segall SK, Robin NH, Wilhelmsen KC, Träskelin AL, Kolehmainen J, Lehesjoki AE, Wiznitzer M, Warman ML. Cohen syndrome in the Ohio Amish. American Journal of Medical Genetics. Part A. 128: 23-8. PMID 15211651 DOI: 10.1002/ajmg.a.30033  0.48
2004 Neilson DE, Feiler HS, Wilhelmsen KC, Lynn A, Eiben RM, Kerr DS, Warman ML. Autosomal dominant acute necrotizing encephalopathy maps to 2q12.1-2q13. Annals of Neurology. 55: 291-4. PMID 14755735 DOI: 10.1002/ana.10849  0.48
2003 Falk MJ, Heeger S, Lynch KA, DeCaro KR, Bohach D, Gibson KS, Warman ML. Intravenous bisphosphonate therapy in children wih osteogenesis imperfecta Pediatrics. 111: 573-578. PMID 12612238 DOI: 10.1542/peds.111.3.573  0.48
2003 Van Wesenbeeck L, Cleiren E, Gram J, Beals RK, Bénichou O, Scopelliti D, Key L, Renton T, Bartels C, Gong Y, Warman ML, De Vernejoul MC, Bollerslev J, Van Hul W. Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density American Journal of Human Genetics. 72: 763-771. PMID 12579474 DOI: 10.1086/368277  0.48
2002 Brouillard P, Boon LM, Mulliken JB, Enjolras O, Ghassibé M, Warman ML, Tan OT, Olsen BR, Vikkula M. Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas"). American Journal of Human Genetics. 70: 866-74. PMID 11845407 DOI: 10.1086/339492  0.48
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