Showing 1 - 20 results of 22 for search 'T Boyadjiev', query time: 0.03s
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Hankel transform and series representation in Laguerre polynomials by L. Boyadjiev
Published 2011-02-01
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Numerical investigation of the magnetic flux static distributions in layered josephson junctions by I Hristov, S Dimova, T Boyadjiev
Published 2016-04-01
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The genetic overlap between osteoporosis and craniosynostosis by Erika Kague, Carolina Medina-Gomez, Simeon A. Boyadjiev, Fernando Rivadeneira
Published 2022-09-01
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A STATISTICAL APPROACH TO THE DETERMINATION OF THE MAJOR CONTRIBUTING ANTHROPOMETRIC PARAMETER(S) FOR REGIONAL VARIATION IN BODY MASS INDEX IN COASTAL AND PLAIN REGIONS OF INDIA: A... by J. P. Verma, Harinder Jaseja, Nikolay Boyadjiev, Priti Gurjar, Amey Bhojane, Ajeet Singh
Published 2018-07-01
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Selective Androgen Receptor Modulators Combined with Treadmill Exercise Have No Bone Benefit in Healthy Adult Rats by Marina Komrakova, Arndt Friedrich Schilling, Wolfgang Lehmann, Veselin Vasilev, Katerina Georgieva, Fanka Gerginska, Nikolay Boyadjiev, Slavi Delchev
Published 2023-09-01
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Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients. by Jehee, F, Alonso, L, Cavalcanti, D, Kim, C, Wall, SA, Mulliken, J, Sun, M, Jabs, E, Boyadjiev, SA, Wilkie, A, Passos-Bueno, MR
Published 2006Journal article -
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Growth and Characterization of Graphene Layers on Different Kinds of Copper Surfaces by Peter M. Rafailov, Peter K. Sveshtarov, Vladimir B. Mehandzhiev, Ivalina Avramova, Penka Terziyska, Minko Petrov, Boyko Katranchev, Haritun Naradikian, Stefan I. Boyadjiev, Csaba Cserháti, Zoltán Erdélyi, Imre M. Szilágyi
Published 2022-03-01
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Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly. by Jehee, F, Johnson, D, Alonso, L, Cavalcanti, D, de Sá Moreira, E, Alberto, F, Kok, F, Kim, C, Wall, SA, Jabs, E, Boyadjiev, SA, Wilkie, A, Passos-Bueno, MR
Published 2005Journal article -
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Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic Craniosynostosis by Cristina M. Justice, Anthony M. Musolf, Araceli Cuellar, Wanda Lattanzi, Emil Simeonov, Radka Kaneva, Justin Paschall, Michael Cunningham, Andrew O. M. Wilkie, Alexander F. Wilson, Paul A. Romitti, Simeon A. Boyadjiev
Published 2022-05-01
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Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape by Seppe Goovaerts, Hanne Hoskens, Ryan J. Eller, Noah Herrick, Anthony M. Musolf, Cristina M. Justice, Meng Yuan, Sahin Naqvi, Myoung Keun Lee, Dirk Vandermeulen, Heather L. Szabo-Rogers, Paul A. Romitti, Simeon A. Boyadjiev, Mary L. Marazita, John R. Shaffer, Mark D. Shriver, Joanna Wysocka, Susan Walsh, Seth M. Weinberg, Peter Claes
Published 2023-11-01
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Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428 by Anthony M. Musolf, Cristina M. Justice, Zeynep Erdogan-Yildirim, Seppe Goovaerts, Araceli Cuellar, John R. Shaffer, Mary L. Marazita, Peter Claes, Seth M. Weinberg, Jae Li, Craig Senders, Marike Zwienenberg, Emil Simeonov, Radka Kaneva, Tony Roscioli, Lorena Di Pietro, Marta Barba, Wanda Lattanzi, Michael L. Cunningham, Paul A. Romitti, Simeon A. Boyadjiev
Published 2024-04-01
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A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis by Justice, CM, Cuellar, A, Bala, K, Sabourin, JA, Cunningham, ML, Crawford, K, Phipps, JM, Zhou, Y, Cilliers, D, Byren, JC, Johnson, D, Wall, SA, Morton, JEV, Noons, P, Sweeney, E, Weber, A, Rees, KEM, Wilson, LC, Simeonov, E, Kaneva, R, Yaneva, N, Georgiev, K, Bussarsky, A, Senders, C, Zwienenberg, M, Boggan, J, Roscioli, T, Tamburrini, G, Barba, M, Conway, K, Sheffield, VC, Brody, L, Mills, JL, Kay, D, Sicko, RJ, Langlois, PH, Tittle, RK, Botto, LD, Jenkins, MM, LaSalle, JM, Lattanzi, W, Wilkie, AOM, Wilson, AF, Romitti, PA, Boyadjiev, SA, National Birth Defects Prevention Study
Published 2020Journal article -
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TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities by Wiszniewski, W, Hunter, J, Hanchard, N, Willer, JR, Shaw, C, Tian, Q, Illner, A, Wang, X, Cheung, S, Patel, A, Campbell, I, Gelowani, V, Hixson, P, Ester, A, Azamian, MS, Potocki, L, Zapata, G, Hernandez, P, Ramocki, M, Santos-Cortez, R, Wang, G, York, M, Justice, M, Chu, Z, Bader, P, Omo-Griffith, L, Madduri, N, Scharer, G, Crawford, H, Yanatatsaneejit, P, Eifert, A, Kerr, J, Bacino, C, Franklin, A, Goin-Kochel, R, Simpson, G, Immken, L, Haque, M, Stosic, M, Williams, MD, Morgan, T, Pruthi, S, Omary, R, Boyadjiev, SA, Win, K, Thida, A, Hurles, M, Hibberd, M, Khor, C, Van Vinh Chau, N, Gallagher, T, Mutirangura, A, Stankiewicz, P, Beaudet, A, Maletic-Savatic, M, Rosenfeld, J, Shaffer, L, Davis, E, Belmont, J, Dunstan, S, Simmons, C, Bonnen, P, Leal, S, Katsanis, N, Lupski, JR, Lalani, SR
Published 2013Journal article