Dynamic 3D Locus Organization and Its Drivers Underpin Immunoglobulin Recombination

por Rogers, Carolyn H., Mielczarek, Olga, Corcoran, Anne E.
Publicado en Front Immunol (2021)

Are We Ready for Fragile X Newborn Screening Testing?—Lessons Learnt from a Feasibility Study

por Wotton, Tiffany, Wiley, Veronica, Bennetts, Bruce, Christie, Louise, Wilcken, Bridget, Jenkins, Gemma, Rogers, Carolyn, Boyle, Jackie, Field, Michael
Publicado en Int J Neonatal Screen (2018)

Novel Vitamin K analogues suppress seizures in zebrafish and mouse models of epilepsy

por Rahn, Jennifer J., Bestman, Jennifer E., Josey, Benjamin J., Inks, Elizabeth S., Stackley, Krista D., Rogers, Carolyn E., Chou, C. James, Chan, Sherine S. L.
Publicado 2013

Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia

por Hwang, Yun Tae, Dudding, Tracy, Aliaga, Solange Mabel, Arpone, Marta, Francis, David, Li, Xin, Slater, Howard Robert, Rogers, Carolyn, Bretherton, Lesley, du Sart, Desirée, Heard, Robert, Godler, David Eugeny
Publicado en Genes (Basel) (2016)

Erratum: Hwang Y.T. et al. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes 2016, 7, 68

por Hwang, Yun Tae, Dudding, Tracy, Aliaga, Solange Mabel, Arpone, Marta, Francis, David, Li, Xin, Slater, Howard Robert, Rogers, Carolyn, Bretherton, Lesley, du Sart, Desirée, Heard, Robert, Godler, David Eugeny
Publicado en Genes (Basel) (2017)

Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders

por Baker, Emma K., Butler, Merlin G., Hartin, Samantha N., Ling, Ling, Bui, Minh, Francis, David, Rogers, Carolyn, Field, Michael J., Slee, Jennie, Gamage, Dinusha, Amor, David J., Godler, David E.
Publicado en Transl Psychiatry (2020)

The inducible costimulator augments Tc17 cell responses to self and tumor tissue

por Nelson, Michelle H., Kundimi, Sreenath, Bowers, Jacob S., Rogers, Carolyn E., Huff, Logan W., Schwartz, Kristina M., Thyagarajan, Krishnamurthy, Little, Elizabeth C., Mehrotra, Shikhar, Cole, David J., Rubinstein, Mark P., Paulos, Chrystal M.
Publicado en J Immunol (2015)

Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing

por Field, Michael, Dudding-Byth, Tracy, Arpone, Marta, Baker, Emma K., Aliaga, Solange M., Rogers, Carolyn, Hickerton, Chriselle, Francis, David, Phelan, Dean G., Palmer, Elizabeth E., Amor, David J., Slater, Howard, Bretherton, Lesley, Ling, Ling, Godler, David E.
Publicado en Int J Mol Sci (2019)

DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome

por Kraan, Claudine M, Baker, Emma K, Arpone, Marta, Bui, Minh, Ling, Ling, Gamage, Dinusha, Bretherton, Lesley, Rogers, Carolyn, Field, Michael J, Wotton, Tiffany L, Francis, David, Hunter, Matt F, Cohen, Jonathan, Amor, David J, Godler, David E
Publicado en Int J Mol Sci (2020)

Comparative microanatomy of the orbicularis oris muscle between chimpanzees and humans: evolutionary divergence of lip function

por Rogers, Carolyn R, Mooney, Mark P, Smith, Timothy D, Weinberg, Seth M, Waller, Bridget M, Parr, Lisa A, Docherty, Beth A, Bonar, Christopher J, Reinholt, Lauren E, Deleyiannis, Frederic W-B, Siegel, Michael I, Marazita, Mary L, Burrows, Anne M
Publicado 2009

Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X

por Arpone, Marta, Baker, Emma K., Bretherton, Lesley, Bui, Minh, Li, Xin, Whitaker, Simon, Dissanayake, Cheryl, Cohen, Jonathan, Hickerton, Chriselle, Rogers, Carolyn, Field, Mike, Elliott, Justine, Aliaga, Solange M., Ling, Ling, Francis, David, Hearps, Stephen J. C., Hunter, Matthew F., Amor, David J., Godler, David E.
Publicado en Sci Rep (2018)

FMR1 mRNA from full mutation alleles is associated with ABC-C(FX) scores in males with fragile X syndrome

por Baker, Emma K., Arpone, Marta, Kraan, Claudine, Bui, Minh, Rogers, Carolyn, Field, Michael, Bretherton, Lesley, Ling, Ling, Ure, Alexandra, Cohen, Jonathan, Hunter, Matthew F., Santa María, Lorena, Faundes, Victor, Curotto, Bianca, Morales, Paulina, Trigo, Cesar, Salas, Isabel, Alliende, Angelica, Amor, David J., Godler, David E.
Publicado en Sci Rep (2020)

CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes

por Hackett, Anna, Tarpey, Patrick S, Licata, Andrea, Cox, James, Whibley, Annabel, Boyle, Jackie, Rogers, Carolyn, Grigg, John, Partington, Michael, Stevenson, Roger E, Tolmie, John, Yates, John RW, Turner, Gillian, Wilson, Meredith, Futreal, Andrew P, Corbett, Mark, Shaw, Marie, Gecz, Jozef, Raymond, F Lucy, Stratton, Michael R, Schwartz, Charles E, Abidi, Fatima E
Publicado 2010

Corrigendum to: CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes

por Hackett, Anna, Tarpey, Patrick S, Licata, Andrea, Cox, James, Whibley, Annabel, Boyle, Jackie, Rogers, Carolyn, Grigg, John, Partington, Michael, Stevenson, Roger E, Tolmie, John, Yates, John R W, Turner, Gillian, Wilson, Meredith, Futreal, Andrew P, Corbett, Mark, Shaw, Marie, Gecz, Jozef, Raymond, F Lucy, Stratton, Michael R, Schwartz, Charles E, Abidi, Fatima E
Publicado 2010

Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome

por Baker, Emma K., Arpone, Marta, Vera, Solange Aliaga, Bretherton, Lesley, Ure, Alexandra, Kraan, Claudine M., Bui, Minh, Ling, Ling, Francis, David, Hunter, Matthew F., Elliott, Justine, Rogers, Carolyn, Field, Michael J., Cohen, Jonathan, Maria, Lorena Santa, Faundes, Victor, Curotto, Bianca, Morales, Paulina, Trigo, Cesar, Salas, Isabel, Alliende, Angelica M., Amor, David J., Godler, David E.
Publicado en J Neurodev Disord (2019)

Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features

por Baker, Emma K., Arpone, Marta, Aliaga, Solange M., Bretherton, Lesley, Kraan, Claudine M., Bui, Minh, Slater, Howard R., Ling, Ling, Francis, David, Hunter, Matthew F., Elliott, Justine, Rogers, Carolyn, Field, Michael, Cohen, Jonathan, Cornish, Kim, Santa Maria, Lorena, Faundes, Victor, Curotto, Bianca, Morales, Paulina, Trigo, Cesar, Salas, Isabel, Alliende, Angelica M., Amor, David J., Godler, David E.
Publicado en Mol Autism (2019)

THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability

por Kumar, Raman, Corbett, Mark A., van Bon, Bregje W.M., Woenig, Joshua A., Weir, Lloyd, Douglas, Evelyn, Friend, Kathryn L., Gardner, Alison, Shaw, Marie, Jolly, Lachlan A., Tan, Chuan, Hunter, Matthew F., Hackett, Anna, Field, Michael, Palmer, Elizabeth E., Leffler, Melanie, Rogers, Carolyn, Boyle, Jackie, Bienek, Melanie, Jensen, Corinna, Van Buggenhout, Griet, Van Esch, Hilde, Hoffmann, Katrin, Raynaud, Martine, Zhao, Huiying, Reed, Robin, Hu, Hao, Haas, Stefan A., Haan, Eric, Kalscheuer, Vera M., Gecz, Jozef
Publicado en Am J Hum Genet (2015)