Recent Publications
(2005) Rhee DK, Marcelino J, Al-Mayouf S, Schelling DK, Bartels CF, Cui Y,
Laxer R, Goldbach-Mansky R, Warman ML. Related Articles, Links
J Biol Chem. 2005 Jul 5; (Epub)
(2005) Rhee DK, Marcelino J, Baker M, Gong Y, Smits P, Lefebvre V, Jay GD,
Stewart M, Wang H, Warman ML, Carpten JD
J Clin Invest. 2005 Mar; 115(3):622-631
(2005) Kutz WE, Gong Y, Warman ML
Mol Cell Biol. 2005 Jan; 25(1):414-421
(2004) Bartels CF, Bukulmez H, Padayatti P, Rhee DK, van Ravenswaaij-Arts C, Pauli RM, Mundlos S, Chitayat D, Shih LY, Al-Gazali LI, Kant S, Cole T, Morton J, Cormier-Daire V, Faivre L, Lees M, Kirk J, Mortier GR, Leroy J, Zabel B, Kim CA, Crow Y, Braverman NE, van den Akker F, Warman ML
"Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux"
Am J Hum Genet. 2004 Jul;75(1):27-34
(2004) Falk MJ, Feiler HS, Neilson DE, Maxwell K, Lee JV, Segall SK, Robin NH, Wilhelmsen KC, Kolehmainen J, Lehesjoki AE, Wiznitzer M, Warman ML
"Cohen syndrome in the Ohio Amish"
Am J Med Genet. 2004 Jul 1;128A(1):23-8
(2004) Neilson DE, Feiler HS, Wilhelmsen KC, Lynn A, Eiben RM, Warman ML
"Autosomal dominant acute necrotizing encephalopathy maps to 2q12.1-2q13"
Ann Neurol. 2004 Feb;55(2):291-4
(2003) Neilson DE, Eiben RM, Waniewski S, Hoppel CL, Warman ML, Kerr DS.
"Autosomal dominant acute necrotizing encephalopathy"
Neurology. 2003 Jul 22;61(2):226-30.
(2003) Van Wesenbeeck L, Cleiren E, Gram J, Beals RK, Benichou 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"
Am J Hum Genet. 2003 Mar;72(3):763-71. Epub 2003 Feb 10.
(2003) Falk MJ, Heeger S, Lynch K, DeCaro K, Bohach D, Warman ML
"Intravenous bisphosphonate therapy in children with osteogenesis imperfecta"
Pediatrics. 2003 Mar;111(3):573-8.
(2003) Everman DB, Bartels CF, Yang Y, Yanamandra N, Goodman FR, Mendoza-Londono JR, Savarirayan R, White SM, Graham JM Jr, Gale RP, Svarch E, Newman WG, Kleckers AR, Francomano CA, Govindaiah V, Singh L, Morrison S, Thomas JT, Warman, M.L.
"The mutational spectrum of Brachydactyly type C"
Am J Med Genet. 2002 Oct 15;112(3):291-6.
(2001) Jepsen, K.J., Pennington, D.E., Lee, Y.-L., Warman, M., Nadeau, J.
"Bone brittleness varies with genetic background in A/J and C57BL/6J inbred mice"
J. Bone Miner. Res. 16:1854-1862.
(2001) Gong Y, Slee RB, Fukai N, Rawadi G, Roman-Roman S, Reginato AM, Wang H, Cundy T, Glorieux FH, Lev D, Zacharin M, Oexle K, Marcelino J, Suwairi W, Heeger S, Sabatakos G, Apte S, Adkins WN, Allgrove J, Arslan-Kirchner M, Batch JA, Beighton P, Black GC, Boles RG, Boon LM, Borrone C, Brunner HG, Carle GF, Dallapiccola B, De Paepe A, Floege B, Halfhide ML, Hall B, Hennekam RC, Hirose T, Jans A, Juppner H, Kim CA, Keppler-Noreuil K, Kohlschuetter A, LaCombe D, Lambert M, Lemyre E, Letteboer T, Peltonen L, Ramesar RS, Romanengo M, Somer H, Steichen-Gersdorf E, Steinmann B, Sullivan B, Superti-Furga A, Swoboda W, van den Boogaard MJ, Van Hul W, Vikkula M, Votruba M, Zabel B, Garcia T, Baron R, Olsen BR, Warman ML
"LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development"
Cell. 2001 Nov 16;107(4):513-23.
(2001) Marcelino J, Sciortino CM, Romero MF, Ulatowski LM, Ballock RT, Economides AN, Eimon PM, Harland RM, Warman ML.
"Human disease-causing NOG missense mutations: effects on noggin secretion, dimer formation, and bone morphogenetic protein binding"
Proc Natl Acad Sci U S A. 2001 Sep 25;98(20):11353-8. Epub 2001 Sep 18.
(2000) Truett GE, Heeger P, Mynatt RL, Truett AA, Walker JA, Warman ML.
"Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT)"
Biotechniques. 2000 Jul;29(1):52, 54.
(1999) Gong Y, Chitayat D, Kerr B, Chen T, Babul-Hirji R, Pal A, Reiss M, Warman, M.L.
"Brachydactyly type B: Clinical description, genetic mapping to chromosome 9q, and evidence for a shared ancestral mutation">
Am. J. Hum. Genet. 64:570-577.
(1999) Gong Y, Krakow D, Marcelino J, Wilkin D, Chitayat D, Babul-Hirji R, Hudgins L, Cremers CW, Cremers FP, Brunner HG, Reinker K, Rimoin DL, Cohn DH, Goodman FR, Reardon W, Patton M, Francomano CA, Warman, M.L.
"Heterozygous mutations in the gene encoding NOGGIN affect human joint morphogenesis"
Nature Genet. 21:302-304.
(1999) Hurvitz JR, Suwairi WM, Van Hul W, El-Shanti H, Superti-Furga A, Roudier J, Holderbaum D, Pauli RM, Herd JK, Van Hul EV, Rezai-Delui H, Legius E, Le Merrer M, Al-Alami J, Bahabri SA, Warman.M.L.
"Mutations in the CCN family member WISP3 cause progressive pseudorheumatoid dysplasia"
Nature Genet. 23:94-98.
(1999) Marcelino J, Carpten JD, Suwairi WM, Gutierrez OM, Schwartz S, Robbins C, Sood R, Makalowska I, Baxevanis A, Johnstone B, Laxer RM, Zemel L, Kim CA, Herd JK, Ihle J, Williams C, Johnson M, Raman V, Alonso LG, Brunoni D, Gerstein A, Papadopoulos N, Bahabri SA, Trent JM, Warman, M.L.
"CACP encodes a secreted proteoglycan that is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome"
Nature Genet. 24:319-322.
|
