Ultrasound assessment of acute appendicitis in paediatric patients: methodology and pictorial overview of findings seen

por Quigley, Alan J., Stafrace, Samuel
Publicado 2013

The Characterisation of the Craniofacial Morphology of Infants Born With Zika Virus; Innovative Approach for Public Health Surveillance and Broad Clinical Applications

por Ayoub, Ashraf, de Freitas Silva, Leonardo, Mossey, Peter, Al-Rudainy, Dhelal, de Mattos, Adriana Marques, Garcia Júnior, Idelmo Rangel, Quigley, Alan, Ju, Xiangyang
Publicado 2021

Prenatal methadone exposure is associated with altered neonatal brain development

por Monnelly, Victoria J., Anblagan, Devasuda, Quigley, Alan, Cabez, Manuel Blesa, Cooper, E. Sarah, Mactier, Helen, Semple, Scott I., Bastin, Mark E., Boardman, James P.
Publicado 2017

Neonatal morphometric similarity mapping for predicting brain age and characterizing neuroanatomic variation associated with preterm birth

por Galdi, Paola, Blesa, Manuel, Stoye, David Q., Sullivan, Gemma, Lamb, Gillian J., Quigley, Alan J., Thrippleton, Michael J., Bastin, Mark E., Boardman, James P.
Publicado 2020

A latent measure explains substantial variance in white matter microstructure across the newborn human brain

por Telford, Emma J., Cox, Simon R., Fletcher-Watson, Sue, Anblagan, Devasuda, Sparrow, Sarah, Pataky, Rozalia, Quigley, Alan, Semple, Scott I., Bastin, Mark E., Boardman, James P.
Publicado 2017

Peak Width of Skeletonized Water Diffusion MRI in the Neonatal Brain

por Blesa, Manuel, Galdi, Paola, Sullivan, Gemma, Wheater, Emily N., Stoye, David Q., Lamb, Gillian J., Quigley, Alan J., Thrippleton, Michael J., Bastin, Mark E., Boardman, James P.
Publicado 2020

Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner

por Stoye, David Q, Blesa, Manuel, Sullivan, Gemma, Galdi, Paola, Lamb, Gillian J, Black, Gill S, Quigley, Alan J, Thrippleton, Michael J, Bastin, Mark E, Reynolds, Rebecca M, Boardman, James P
Publicado 2020

Hierarchical Complexity of the Macro-Scale Neonatal Brain

por Blesa, Manuel, Galdi, Paola, Cox, Simon R, Sullivan, Gemma, Stoye, David Q, Lamb, Gillian J, Quigley, Alan J, Thrippleton, Michael J, Escudero, Javier, Bastin, Mark E, Smith, Keith M, Boardman, James P
Publicado 2020

Association of Preterm Birth and Socioeconomic Status With Neonatal Brain Structure

por Mckinnon, Katie, Galdi, Paola, Blesa-Cábez, Manuel, Sullivan, Gemma, Vaher, Kadi, Corrigan, Amy, Hall, Jill, Jiménez-Sánchez, Lorena, Thrippleton, Michael, Bastin, Mark E., Quigley, Alan J., Valavani, Evdoxia, Tsanas, Athanasios, Richardson, Hilary, Boardman, James P.
Publicado 2023

Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy

por Parry, David A., Martin, Carol-Anne, Greene, Philip, Marsh, Joseph A., Blyth, Moira, Cox, Helen, Donnelly, Deirdre, Greenhalgh, Lynn, Greville-Heygate, Stephanie, Harrison, Victoria, Lachlan, Katherine, McKenna, Caoimhe, Quigley, Alan J., Rea, Gillian, Robertson, Lisa, Suri, Mohnish, Jackson, Andrew P.
Publicado 2020

PRIM1 deficiency causes a distinctive primordial dwarfism syndrome

por Parry, David A., Tamayo-Orrego, Lukas, Carroll, Paula, Marsh, Joseph A., Greene, Philip, Murina, Olga, Uggenti, Carolina, Leitch, Andrea, Káposzta, Rita, Merő, Gabriella, Nagy, Andrea, Orlik, Brigitta, Kovács-Pászthy, Balázs, Quigley, Alan J., Riszter, Magdolna, Rankin, Julia, Reijns, Martin A.M., Szakszon, Katalin, Jackson, Andrew P.
Publicado 2020

DNA methylation in relation to gestational age and brain dysmaturation in preterm infants

por Wheater, Emily N. W., Galdi, Paola, McCartney, Daniel L., Blesa, Manuel, Sullivan, Gemma, Stoye, David Q., Lamb, Gillian, Sparrow, Sarah, Murphy, Lee, Wrobel, Nicola, Quigley, Alan J., Semple, Scott, Thrippleton, Michael J., Wardlaw, Joanna M., Bastin, Mark E., Marioni, Riccardo E., Cox, Simon R., Boardman, James P.
Publicado 2022

Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis

por Martin, Carol-Anne, Murray, Jennie E., Carroll, Paula, Leitch, Andrea, Mackenzie, Karen J., Halachev, Mihail, Fetit, Ahmed E., Keith, Charlotte, Bicknell, Louise S., Fluteau, Adeline, Gautier, Philippe, Hall, Emma A., Joss, Shelagh, Soares, Gabriela, Silva, João, Bober, Michael B., Duker, Angela, Wise, Carol A., Quigley, Alan J., Phadke, Shubha R., Wood, Andrew J., Vagnarelli, Paola, Jackson, Andrew P.
Publicado 2016

PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins

por Hall, Emma A., Nahorski, Michael S., Murray, Lyndsay M., Shaheen, Ranad, Perkins, Emma, Dissanayake, Kosala N., Kristaryanto, Yosua, Jones, Ross A., Vogt, Julie, Rivagorda, Manon, Handley, Mark T., Mali, Girish R., Quidwai, Tooba, Soares, Dinesh C., Keighren, Margaret A., McKie, Lisa, Mort, Richard L., Gammoh, Noor, Garcia-Munoz, Amaya, Davey, Tracey, Vermeren, Matthieu, Walsh, Diana, Budd, Peter, Aligianis, Irene A., Faqeih, Eissa, Quigley, Alan J., Jackson, Ian J., Kulathu, Yogesh, Jackson, Mandy, Ribchester, Richard R., von Kriegsheim, Alex, Alkuraya, Fowzan S., Woods, C. Geoffrey, Maher, Eamonn R., Mill, Pleasantine
Publicado 2017

A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect

por McEntagart, Meriel, Williamson, Kathleen A., Rainger, Jacqueline K., Wheeler, Ann, Seawright, Anne, De Baere, Elfride, Verdin, Hannah, Bergendahl, L. Therese, Quigley, Alan, Rainger, Joe, Dixit, Abhijit, Sarkar, Ajoy, López Laso, Eduardo, Sanchez-Carpintero, Rocio, Barrio, Jesus, Bitoun, Pierre, Prescott, Trine, Riise, Ruth, McKee, Shane, Cook, Jackie, McKie, Lisa, Ceulemans, Berten, Meire, Françoise, Temple, I. Karen, Prieur, Fabienne, Williams, Jonathan, Clouston, Penny, Németh, Andrea H., Banka, Siddharth, Bengani, Hemant, Handley, Mark, Freyer, Elisabeth, Ross, Allyson, van Heyningen, Veronica, Marsh, Joseph A., Elmslie, Frances, FitzPatrick, David R.
Publicado 2016