Evaluating cell lines as models for metastatic breast cancer through integrative analysis of genomic data
Liu, Ke, Newbury, Patrick A., Glicksberg, Benjamin S., Zeng, William Z. D., Paithankar, Shreya, Andrechek, Eran R., Chen, Bin
Published in Nature communications (15.05.2019)
Published in Nature communications (15.05.2019)
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Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome
Klopocki, Eva, Schulze, Harald, Strauß, Gabriele, Ott, Claus-Eric, Hall, Judith, Trotier, Fabienne, Fleischhauer, Silke, Greenhalgh, Lynn, Newbury-Ecob, Ruth A., Neumann, Luitgard M., Habenicht, Rolf, König, Rainer, Seemanova, Eva, Megarbane, André, Ropers, Hans-Hilger, Ullmann, Reinhard, Horn, Denise, Mundlos, Stefan
Published in American journal of human genetics (01.02.2007)
Published in American journal of human genetics (01.02.2007)
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Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth
Steward, C. G., Newbury-Ecob, R. A., Hastings, R., Smithson, S. F., Tsai-Goodman, B., Quarrell, O. W., Kulik, W., Wanders, R., Pennock, M., Williams, M., Cresswell, J. L., Gonzalez, I. L., Brennan, P.
Published in Prenatal diagnosis (01.10.2010)
Published in Prenatal diagnosis (01.10.2010)
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Gene expression signatures identify paediatric patients with multiple organ dysfunction who require advanced life support in the intensive care unit
Shankar, Rama, Leimanis, Mara L., Newbury, Patrick A., Liu, Ke, Xing, Jing, Nedveck, Derek, Kort, Eric J., Prokop, Jeremy W, Zhou, Guoli, Bachmann, André S, Chen, Bin, Rajasekaran, Surender
Published in EBioMedicine (01.12.2020)
Published in EBioMedicine (01.12.2020)
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Mutation in myosin heavy chain 6 causes atrial septal defect
Brook, J David, Ching, Yung-Hao, Ghosh, Tushar K, Cross, Steve J, Packham, Elizabeth A, Honeyman, Louise, Loughna, Siobhan, Robinson, Thelma E, Dearlove, Andrew M, Ribas, Gloria, Bonser, Andrew J, Thomas, Neil R, Scotter, Andrew J, Caves, Leo S D, Tyrrell, Graham P, Newbury-Ecob, Ruth A, Munnich, Arnold, Bonnet, Damien
Published in Nature genetics (01.04.2005)
Published in Nature genetics (01.04.2005)
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Bilateral subcortical heterotopia with partial callosal agenesis in a mouse mutant
Rosen, G D, Azoulay, N G, Griffin, E G, Newbury, A, Koganti, L, Fujisaki, N, Takahashi, E, Grant, P E, Truong, D T, Fitch, R H, Lu, L, Williams, R W
Published in Cerebral cortex (New York, N.Y. 1991) (01.04.2013)
Published in Cerebral cortex (New York, N.Y. 1991) (01.04.2013)
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The phenotype of Floating-Harbor syndrome in 10 patients
White, Susan M., Morgan, Angela, Da Costa, Annette, Lacombe, Didier, Knight, Samantha J.L., Houlston, Richard, Whiteford, Margo L., Newbury-Ecob, Ruth A., Hurst, Jane A.
Published in American journal of medical genetics. Part A (01.04.2010)
Published in American journal of medical genetics. Part A (01.04.2010)
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The influence of age on aerosol deposition in children with cystic fibrosis
Chua, HL, Collis, GG, Newbury, AM, Chan, K, Bower, GD, Sly, PD, Le Souef, PN
Published in The European respiratory journal (01.12.1994)
Published in The European respiratory journal (01.12.1994)
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Ibrutinib Blocks YAP1 Activation and Reverses BRAF Inhibitor Resistance in Melanoma Cells
Misek, Sean A, Newbury, Patrick A, Chekalin, Evgenii, Paithankar, Shreya, Doseff, Andrea I, Chen, Bin, Gallo, Kathleen A, Neubig, Richard R
Published in Molecular pharmacology (01.01.2022)
Published in Molecular pharmacology (01.01.2022)
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Thrombocytopenia-absent radius syndrome: a clinical genetic study
Greenhalgh, K L, Howell, R T, Bottani, A, Ancliff, P J, Brunner, H G, Verschuuren-Bemelmans, C C, Vernon, E, Brown, K W, Newbury-Ecob, R A
Published in Journal of medical genetics (01.12.2002)
Published in Journal of medical genetics (01.12.2002)
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Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury ( T ) gene family
Young, Ian D, Robson, Stephen C, Bonnet, Damien, Bullen, Philip J, Newbury-Ecob, Ruth A, Gebuhr, Tom, Buckler, Alan J, Wilson, David I, Law, David J, Terrett, Jonathan A, Brook, J. David, Yi Li, Quan, Strachan, Tom, Curtis, Andrew R.J, Raeburn, J. Alexander, Lyonnet, Stanislas, Ho Yi, Cheong
Published in Nature genetics (01.01.1997)
Published in Nature genetics (01.01.1997)
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The Effects of Motorcycle Helmet Legislation on Craniomaxillofacial Injuries
Adams, Nicholas S, Newbury, Patrick A, Eichhorn, Mitchell G, Davis, Alan T, Mann, Robert J, Polley, John W, Girotto, John A
Published in Plastic and reconstructive surgery (1963) (01.06.2017)
Published in Plastic and reconstructive surgery (1963) (01.06.2017)
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MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome
van Bokhoven, Hans, Celli, Jacopo, van Reeuwijk, Jeroen, Rinne, Tuula, Glaudemans, Bob, van Beusekom, Ellen, Rieu, Paul, Newbury-Ecob, Ruth A, Chiang, Chin, Brunner, Han G
Published in Nature genetics (01.05.2005)
Published in Nature genetics (01.05.2005)
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Abstract No. 85 Splenic artery embolization for unstable patients with acute splenic injury
Zoppo, C., Valero, D. Alvarez, Murugan, V. Arumugam, Pavidapha, A., Flahive, J., Newbury, A., Harman, A.
Published in Journal of vascular and interventional radiology (01.06.2022)
Published in Journal of vascular and interventional radiology (01.06.2022)
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Genetic analysis of the G4.5 gene in families with suspected Barth syndrome
Cantlay, Ann M., Shokrollahi, Kayvan, Allen, John T., Lunt, Peter W., Newbury-Ecob, Ruth A., Steward, Colin G.
Published in The Journal of pediatrics (01.09.1999)
Published in The Journal of pediatrics (01.09.1999)
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