Genome-wide Association Scan for Childhood Caries Implicates Novel Genes von Shaffer, J.R., Wang, X., Feingold, E., Lee, M., Begum, F., Weeks, D.E., Cuenco, K.T., Barmada, M.M., Wendell, S.K., Crosslin, D.R., Laurie, C.C., Doheny, K.F., Pugh, E.W., Zhang, Q., Feenstra, B., Geller, F., Boyd, H.A., Zhang, H., Melbye, M., Murray, J.C., Weyant, R.J., Crout, R., McNeil, D.W., Levy, S.M., Slayton, R.L., Willing, M.C., Broffitt, B., Vieira, A.R., Marazita, M.L.

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Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations von Tran-Fadulu, V, Pannu, H, Kim, D H, Vick, G W, Lonsford, C M, Lafont, A L, Boccalandro, C, Smart, S, Peterson, K L, Hain, J Zenger, Willing, M C, Coselli, J S, LeMaire, S A, Ahn, C, Byers, P H, Milewicz, D M

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Genetic Association of MMP10, MMP14, and MMP16 with Dental Caries von Reis, Steven E., Crout, Richard, Weyant, R. J., Levy, Steven M., Vieira, Alexandre Rezende, Marazita, Mary L., Willing, M. C., Slayton, R. L., Maher, B. S., Vanyukov, M. M., Cooper, Margaret E., Feingold, Eleanor, Shaffer, John R., Lewis, D. D., McNeil, Daniel W.

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Genetic and Environmental Factors Associated with Dental Caries in Children: The Iowa Fluoride Study von Wang, X., Willing, M.C., Marazita, M.L., Wendell, S., Warren, J.J., Broffitt, B., Smith, B., Busch, T., Lidral, A.C., Levy, S.M.

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Premature chain termination is a unifying mechanism for COL1A1 null alleles in osteogenesis imperfecta type I cell strains von WILLING, M. C, DESCHENES, S. P, SLAYTON, R. L, ROBERTS, E. J

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Genetic Association of MPPED2 and ACTN2 with Dental Caries von Stanley, B.O.C., Feingold, E., Cooper, M., Vanyukov, M.M., Maher, B.S., Slayton, R.L., Willing, M.C., Reis, S.E., McNeil, D.W., Crout, R.J., Weyant, R.J., Levy, S.M., Vieira, A.R., Marazita, M.L., Shaffer, J.R.

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COL5A1 Haploinsufficiency Is a Common Molecular Mechanism Underlying the Classical Form of EDS von Wenstrup, Richard J., Florer, Jane B., Willing, Marcia C., Giunta, Cecilia, Steinmann, Beat, Young, Felix, Susic, Miki, Cole, William G.

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Osteogenesis imperfecta type I : molecular heterogeneity for COL1A1 null alleles of type I collagen von WILLING, M. C, DESCHENES, S. P, SCOTT, D. A, BYERS, P. H, SLAYTON, R. L, PITTS, S. H, ARIKAT, H, ROBERTS, E. J

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Mapping a locus for familial thoracic aortic aneurysms and dissections (TAAD2) to 3p24-25 von HASHAM, Sumera N, WILLING, Marcia C, GUO, Dong-Chuan, MUILENBURG, Ann, RUMIN HE, TRAN, Van T, SCHERER, Steven E, SHETE, Sanjay S, MILEWICZ, Dianna M

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Physical Activity and Bone Measures in Young Children: The Iowa Bone Development Study von Janz, Kathleen F, Burns, Trudy L, Torner, James C, Levy, Steven M, Paulos, Richard, Willing, Marcia C, Warren, John J

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Everyday activity predicts Bone geometry in children: The Iowa Bone development study von JANZ, Kathleen F, BURNS, Trudy L, LEVY, Steven M, TORNER, James C, WILLING, Marcia C, BECK, Thomas J, GILMORE, Julie M, MARSHALL, Teresa A

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Osteocalcin: Genetic and Physical Mapping of the Human Gene BGLAP and Its Potential Role in Postmenopausal Osteoporosis von Raymond, Michael H., Schutte, Brian C., Torner, James C., Burns, Trudy L., Willing, Marcia C.

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Heterogeneous basis of the type VIB form of Ehlers-Danlos syndrome (EDS VIB) that is unrelated to decreased collagen lysyl hydroxylation von Walker, L.C., Overstreet, M.A., Willing, M.C., Marini, J.C., Cabral, W.A., Pals, G., Bristow, J., Atsawasuwan, P., Yamauchi, M., Yeowell, Heather N.

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Gene polymorphisms, bone mineral density and bone mineral content in young children: the Iowa bone development study von WILLING, Marcia C, TORNER, James C, BURNS, Trudy L, JANZ, Kathleen F, MARSHALL, Teresa, GILMORE, Julie, DESCHENES, Sachi P, WARREN, John J, LEVY, Steven M

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Osteogenesis imperfecta type I is commonly due to a COL1A1 null allele of type I collagen von WILLING, M. C, PRUCHNO, C. J, ATKINSON, M, BYERS, P. H

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Distinct biochemical phenotypes predict clinical severity in nonlethal variants of osteogenesis imperfecta von WENSTRUP, R. J, WILLING, M. C, STARMAN, B. J, BYERS, P. H

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Determinants of Bone Mineral Density in Postmenopausal White Iowans von Willing, Marcia C., Torner, James C., Burns, Trudy L., Segar, Ellen T., Werner, Joanna R.

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Mutations of the alpha 2(V) chain of type V collagen impair matrix assembly and produce Ehlers-Danlos syndrome type I von Michalickova, K, Susic, M, Willing, M C, Wenstrup, R J, Cole, W G

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Deletions and duplications of Gly-Xaa-Yaa triplet repeats in the triple helical domains of type I collagen chains disrupt helix formation and result in several types of osteogenesi... von Pace, James M., Atkinson, Mary, Willing, Marcia C., Wallis, Gillian, Byers, Peter H.

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Frameshift mutation near the 3' end of the COL1A1 gene of type I collagen predicts an elongated Pro alpha 1(I) chain and results in osteogenesis imperfecta type I von Willing, M C, Cohn, D H, Byers, P H

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