Males with Familial Idiopathic Scoliosis: A Distinct Phenotypic Subgroup

מאת Clough, Mark, Justice, Cristina M., Marosy, Beth, Miller, Nancy H.
יצא לאור 2010

Critical values and variation in type I error along chromosomes in the COGA dataset using the applied pseudo-trait method

מאת Papanicolaou, George J, Justice, Cristina M, Kovac, Illija M, Sorant, Alexa JM, Wilson, Alexander F
יצא לאור 2005

CHD7 Gene Polymorphisms and Familial Idiopathic Scoliosis

מאת Tilley, Mera K., Justice, Cristina M., Swindle, Kandice, Marosy, Beth, Wilson, Alexander F., Miller, Nancy H.
יצא לאור 2013

Identification of Susceptibility Loci for Scoliosis in FIS Families With Triple Curves

מאת Marosy, Beth, Justice, Cristina M., Vu, Cuong, Zorn, Andrew, Nzegwu, Nneka, Wilson, Alexander F., Miller, Nancy H.
יצא לאור 2010

Type I error rates of rare single nucleotide variants are inflated in tests of association with non–normally distributed traits using simple linear regression methods

מאת Schwantes-An, Tae-Hwi, Sung, Heejong, Sabourin, Jeremy A., Justice, Cristina M., Sorant, Alexa J. M., Wilson, Alexander F.
הוצא לאור ב BMC Proc (2016)

Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study data

מאת Mathias, Rasika A, Roy-Gagnon, Marie-Hélène, Justice, Cristina M, Papanicolaou, George J, Fan, Yu Ti, Pugh, Elizabeth W, Wilson, Alexander F
יצא לאור 2003

Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis

מאת Justice, Cristina M., Bishop, Kevin, Carrington, Blake, Mullikin, Jim C., Swindle, Kandice, Marosy, Beth, Sood, Raman, Miller, Nancy H., Wilson, Alexander F.
הוצא לאור ב G3 (Bethesda) (2016)

Sequencing of the TBX6 Gene in Families with Familial Idiopathic Scoliosis

מאת Baschal, Erin E., Swindle, Kandice, Justice, Cristina M., Baschal, Robin M., Perera, Anoja, Wethey, Cambria I., Poole, Alex, Pourquié, Olivier, Tassy, Olivier, Miller, Nancy H.
הוצא לאור ב Spine Deform (2015)

Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data

מאת Simpson, Claire L, Justice, Cristina M, Krishnan, Mera, Wojciechowski, Robert, Sung, Heejong, Cai, Jerry, Green, Tiffany, Lewis, Deyana, Behneman, Dana, Wilson, Alexander F, Bailey-Wilson, Joan E
יצא לאור 2011

A Variant Associated with Sagittal Nonsyndromic Craniosynostosis Alters the Regulatory Function of a Non-Coding Element

מאת Justice, Cristina M., Kim, Jinoh, Kim, Sun-Don, Kim, Kyunhgho, Yagnik, Garima, Cuellar, Araceli, Carrington, Blake, Lu, Chung-Ling, Sood, Raman, Boyadjiev, Simeon A., Wilson, Alexander F.
הוצא לאור ב Am J Med Genet A (2017)

Intra-familial tests of association between Familial Idiopathic Scoliosis and markers on 9q31.3-q34.3 and 16p12.3-q22.2

מאת Miller, Nancy H., Justice, Cristina M., Marosy, Beth, Swindle, Kandice, Kim, Yoonhee, Roy-Gagnon, Marie-Hélène, Sung, Heejong, Behneman, Dana, Doheny, Kimberly F., Pugh, Elizabeth, Wilson, Alexander F.
יצא לאור 2012

Genetic associations with childhood brain growth, defined in two longitudinal cohorts

מאת Szekely, Eszter, Schwantes-An, Tae-Hwi Linus, Justice, Cristina M., Sabourin, Jeremy A., Jansen, Philip R., Muetzel, Ryan L., Sharp, Wendy, Tiemeier, Henning, Sung, Heejong, White, Tonya J., Wilson, Alexander F., Shaw, Philip
הוצא לאור ב Genet Epidemiol (2018)

Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis

מאת Cuellar, Araceli, Bala, Krithi, Di Pietro, Lorena, Barba, Marta, Yagnik, Garima, Liu, Jia Lie, Stevens, Christina, Hur, David J., Ingersoll, Roxann G., Justice, Cristina M., Drissi, Hicham, Kim, Jinoh, Lattanzi, Wanda, Boyadjiev, Simeon A.
הוצא לאור ב Bone (2020)

A genome-wide association study identifies susceptibility loci for non-syndromic sagittal craniosynostosis near BMP2 and within BBS9

מאת Justice, Cristina M., Yagnik, Garima, Kim, Yoonhee, Peter, Inga, Jabs, Ethylin Wang, Erazo, Monica, Ye, Xiaoqian, Ainehsazan, Edmond, Shi, Lisong, Cunningham, Michael L., Kimonis, Virginia, Roscioli, Tony, Wall, Steven A., Wilkie, Andrew O.M., Stoler, Joan, Richtsmeier, Joan T., Heuzé, Yann, Sanchez-Lara, Pedro A., Buckley, Michael F., Druschel, Charlotte M., Mills, James L., Caggana, Michele, Romitti, Paul A., Kay, Denise M., Senders, Craig, Taub, Peter J., Klein, Ophir D., Boggan, James, Zwienenberg-Lee, Marike, Naydenov, Cyril, Kim, Jinoh, Wilson, Alexander F., Boyadjiev, Simeon A.
יצא לאור 2012

A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis

מאת Justice, Cristina M, Cuellar, Araceli, Bala, Krithi, Sabourin, Jeremy A, Cunningham, Michael L, Crawford, Karen, Phipps, Julie M, Zhou, Yan, Cilliers, Deirdre, Byren, Jo C, Johnson, David, Wall, Steven A, Morton, Jenny E V, Noons, Peter, Sweeney, Elizabeth, Weber, Astrid, Rees, Katie E M, Wilson, Louise C, Simeonov, Emil, Kaneva, Radka, Yaneva, Nadezhda, Georgiev, Kiril, Bussarsky, Assen, Senders, Craig, Zwienenberg, Marike, Boggan, James, Roscioli, Tony, Tamburrini, Gianpiero, Barba, Marta, Conway, Kristin, Sheffield, Val C, Brody, Lawrence, Mills, James L, Kay, Denise, Sicko, Robert J, Langlois, Peter H, Tittle, Rachel K, Botto, Lorenzo D, Jenkins, Mary M, LaSalle, Janine M, Lattanzi, Wanda, Wilkie, Andrew O M, Wilson, Alexander F, Romitti, Paul A, Boyadjiev, Simeon A
הוצא לאור ב Hum Genet (2020)