Strong positive selection and recombination drive the antigenic variation of the PilE protein of the human pathogen Neisseria meningitidis.

Autor Andrews, T Daniel, Gojobori, Takashi
Vydáno 2004

Efficacy of computational predictions of the functional effect of idiosyncratic pharmacogenetic variants

Autor McConnell, Hannah, Andrews, T. Daniel, Field, Matt A.
Vydáno v PeerJ (2021)

Reliably Detecting Clinically Important Variants Requires Both Combined Variant Calls and Optimized Filtering Strategies

Autor Field, Matthew A., Cho, Vicky, Andrews, T. Daniel, Goodnow, Chris C.
Vydáno v PLoS One (2015)

Molecular Evolution and Functional Characterization of Drosophila Insulin-Like Peptides

Autor Grönke, Sebastian, Clarke, David-Francis, Broughton, Susan, Andrews, T. Daniel, Partridge, Linda
Vydáno 2010

DeepSNVMiner: a sequence analysis tool to detect emergent, rare mutations in subsets of cell populations

Autor Andrews, T. Daniel, Jeelall, Yogesh, Talaulikar, Dipti, Goodnow, Christopher C., Field, Matthew A.
Vydáno v PeerJ (2016)

The Ensembl Automatic Gene Annotation System

Autor Curwen, Val, Eyras, Eduardo, Andrews, T. Daniel, Clarke, Laura, Mongin, Emmanuel, Searle, Steven M.J., Clamp, Michele
Vydáno 2004

Interplay of dFOXO and Two ETS-Family Transcription Factors Determines Lifespan in Drosophila melanogaster

Autor Alic, Nazif, Giannakou, Maria E., Papatheodorou, Irene, Hoddinott, Matthew P., Andrews, T. Daniel, Bolukbasi, Ekin, Partridge, Linda
Vydáno 2014

The RNA-binding protein hnRNPLL induces a T cell alternative splicing program delineated by differential intron retention in polyadenylated RNA

Autor Cho, Vicky, Mei, Yan, Sanny, Arleen, Chan, Stephanie, Enders, Anselm, Bertram, Edward M, Tan, Andy, Goodnow, Christopher C, Andrews, T Daniel
Vydáno 2014

Reducing the search space for causal genetic variants with VASP

Autor Field, Matthew A., Cho, Vicky, Cook, Matthew C., Enders, Anselm, Vinuesa, Carola G., Whittle, Belinda, Andrews, T. Daniel, Goodnow, Chris C.
Vydáno v Bioinformatics (2015)

Recurrent miscalling of missense variation from short-read genome sequence data

Autor Field, Matthew A., Burgio, Gaetan, Chuah, Aaron, Al Shekaili, Jalila, Hassan, Batool, Al Sukaiti, Nashat, Foote, Simon J., Cook, Matthew C., Andrews, T. Daniel
Vydáno v BMC Genomics (2019)

Genome-wide dFOXO targets and topology of the transcriptomic response to stress and insulin signalling

Autor Alic, Nazif, Andrews, T Daniel, Giannakou, Maria E, Papatheodorou, Irene, Slack, Cathy, Hoddinott, Matthew P, Cochemé, Helena M, Schuster, Eugene F, Thornton, Janet M, Partridge, Linda
Vydáno 2011

Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization

Autor Marioni, John C, Thorne, Natalie P, Valsesia, Armand, Fitzgerald, Tomas, Redon, Richard, Fiegler, Heike, Andrews, T Daniel, Stranger, Barbara E, Lynch, Andrew G, Dermitzakis, Emmanouil T, Carter, Nigel P, Tavaré, Simon, Hurles, Matthew E
Vydáno 2007

Zinc-finger protein ZFP318 is essential for expression of IgD, the alternatively spliced Igh product made by mature B lymphocytes

Autor Enders, Anselm, Short, Alanna, Miosge, Lisa A., Bergmann, Hannes, Sontani, Yovina, Bertram, Edward M., Whittle, Belinda, Balakishnan, Bhavani, Yoshida, Kaoru, Sjollema, Geoff, Field, Matthew A., Andrews, T. Daniel, Hagiwara, Hiromi, Goodnow, Christopher C.
Vydáno 2014

Heterogeneity of Human Neutrophil CD177 Expression Results from CD177P1 Pseudogene Conversion

Autor Wu, Zuopeng, Liang, Rong, Ohnesorg, Thomas, Cho, Vicky, Lam, Wesley, Abhayaratna, Walter P., Gatenby, Paul A., Perera, Chandima, Zhang, Yafei, Whittle, Belinda, Sinclair, Andrew, Goodnow, Christopher C., Field, Matthew, Andrews, T. Daniel, Cook, Matthew C.
Vydáno v PLoS Genet (2016)

Comparison of predicted and actual consequences of missense mutations

Autor Miosge, Lisa A., Field, Matthew A., Sontani, Yovina, Cho, Vicky, Johnson, Simon, Palkova, Anna, Balakishnan, Bhavani, Liang, Rong, Zhang, Yafei, Lyon, Stephen, Beutler, Bruce, Whittle, Belinda, Bertram, Edward M., Enders, Anselm, Goodnow, Christopher C., Andrews, T. Daniel
Vydáno v Proc Natl Acad Sci U S A (2015)

A point mutation in IKAROS ZF1 causes a B cell deficiency in mice

Autor Boast, Brigette, Miosge, Lisa A., Kuehn, Hye Sun, Cho, Vicky, Athanasopoulos, Vicki, McNamara, Hayley A., Sontani, Yovina, Mei, Yan, Howard, Debbie, Sutton, Henry J., Omari, Sofia A., Yu, Zhijia, Nasreen, Mariam, Andrews, T. Daniel, Cockburn, Ian A., Goodnow, Christopher C., Rosenzweig, Sergio D., Enders, Anselm
Vydáno v J Immunol (2021)

B cell survival, surface BCR and BAFFR expression, CD74 metabolism, and CD8(−) dendritic cells require the intramembrane endopeptidase SPPL2A

Autor Bergmann, Hannes, Yabas, Mehmet, Short, Alanna, Miosge, Lisa, Barthel, Nadine, Teh, Charis E., Roots, Carla M., Bull, Katherine R., Jeelall, Yogesh, Horikawa, Keisuke, Whittle, Belinda, Balakishnan, Bhavani, Sjollema, Geoff, Bertram, Edward M., Mackay, Fabienne, Rimmer, Andrew J., Cornall, Richard J., Field, Matthew A., Andrews, T. Daniel, Goodnow, Christopher C., Enders, Anselm
Vydáno 2013

Gain-of-function IKBKB mutation causes human combined immune deficiency

Autor Cardinez, Chelisa, Miraghazadeh, Bahar, Tanita, Kay, da Silva, Elizabeth, Hoshino, Akihiro, Okada, Satoshi, Chand, Rochna, Asano, Takaki, Tsumura, Miyuki, Yoshida, Kenichi, Ohnishi, Hidenori, Kato, Zenichiro, Yamazaki, Masahide, Okuno, Yusuke, Miyano, Satoru, Kojima, Seiji, Ogawa, Seishi, Andrews, T. Daniel, Field, Matthew A., Burgio, Gaetan, Morio, Tomohiro, Vinuesa, Carola G., Kanegane, Hirokazu, Cook, Matthew C.
Vydáno v J Exp Med (2018)

Rasgrp1 mutation increases naïve T-cell CD44 expression and drives mTOR-dependent accumulation of Helios(+) T cells and autoantibodies

Autor Daley, Stephen R, Coakley, Kristen M, Hu, Daniel Y, Randall, Katrina L, Jenne, Craig N, Limnander, Andre, Myers, Darienne R, Polakos, Noelle K, Enders, Anselm, Roots, Carla, Balakishnan, Bhavani, Miosge, Lisa A, Sjollema, Geoff, Bertram, Edward M, Field, Matthew A, Shao, Yunli, Andrews, T Daniel, Whittle, Belinda, Barnes, S Whitney, Walker, John R, Cyster, Jason G, Goodnow, Christopher C, Roose, Jeroen P
Vydáno 2013

Origins and functional impact of copy number variation in the human genome

Autor Conrad, Donald F., Pinto, Dalila, Redon, Richard, Feuk, Lars, Gokcumen, Omer, Zhang, Yujun, Aerts, Jan, Andrews, T. Daniel, Barnes, Chris, Campbell, Peter, Fitzgerald, Tomas, Hu, Min, Ihm, Chun Hwa, Kristiansson, Kati, MacArthur, Daniel G., MacDonald, Jeffrey R., Onyiah, Ifejinelo, Pang, Andy Wing Chun, Robson, Sam, Stirrups, Kathy, Valsesia, Armand, Walter, Klaudia, Wei, John, Tyler-Smith, Chris, Carter, Nigel P., Lee, Charles, Scherer, Stephen W., Hurles, Matthew E.
Vydáno 2009