Suchergebnisse - Hashem A. Shihab
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HIPred: an integrative approach to predicting haploinsufficient genes von Hashem A. Shihab, Mark F. Rogers, Colin Campbell, Tom R. Gaunt
Veröffentlicht 2017Artigo -
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CScape: a tool for predicting oncogenic single-point mutations in the cancer genome von Mark F. Rogers, Hashem A. Shihab, Tom R. Gaunt, Colin Campbell
Veröffentlicht 2017Artigo -
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Predicting the functional consequences of cancer-associated amino acid substitutions von Hashem A. Shihab, Julian Gough, D.N. Cooper, Ian N.M. Day, Tom R. Gaunt
Veröffentlicht 2013Artigo -
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Ranking non-synonymous single nucleotide polymorphisms based on disease concepts von Hashem A. Shihab, Julian Gough, Matthew Mort, D.N. Cooper, Ian N.M. Day, Tom R. Gaunt
Veröffentlicht 2014Artigo -
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Maternal pre-pregnancy BMI and gestational weight gain, offspring DNA methylation and later offspring adiposity: findings from the Avon Longitudinal Study of Parents and Children von Gemma C. Sharp, Debbie A. Lawlor, Rebecca C. Richmond, Abigail Fraser, Andrew J. Simpkin, Matthew Suderman, Hashem A. Shihab, Oliver Lyttleton, Wendy L. McArdle, Susan M. Ring, Tom R. Gaunt, George Davey Smith, Caroline L. Relton
Veröffentlicht 2015Artigo -
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Systematic identification of genetic influences on methylation across the human life course von Tom R. Gaunt, Hashem A. Shihab, Gibran Hemani, Josine L. Min, Geoff Woodward, Oliver Lyttleton, Jie Zheng, Aparna Duggirala, Wendy L. McArdle, Karen Ho, Susan M. Ring, David M. Evans, George Davey Smith, Caroline L. Relton
Veröffentlicht 2016Artigo -
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MR-Base: a platform for systematic causal inference across the phenome using billions of genetic associations von Gibran Hemani, Jie Zheng, Kaitlin H. Wade, Charles Laurin, Benjamin Elsworth, Stephen Burgess, Jack Bowden, Ryan Langdon, Vanessa Y. Tan, James Yarmolinsky, Hashem A. Shihab, Nicholas J. Timpson, David M. Evans, Caroline L. Relton, Richard M. Martin, George Davey Smith, Tom R. Gaunt, Philip Haycock
Veröffentlicht 2016Pré-impressão -
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Data Resource Profile: Accessible Resource for Integrated Epigenomic Studies (ARIES) von Caroline L. Relton, Tom R. Gaunt, Wendy L. McArdle, Karen Ho, Aparna Duggirala, Hashem A. Shihab, Geoff Woodward, Oliver Lyttleton, David M. Evans, Wolf Reik, Yu‐Lee Paul, Gabriella Ficz, Susan E. Ozanne, Anil Wipat, Keith Flanagan, Allyson Lister, Bastiaan T. Heijmans, Susan M. Ring, George Davey Smith
Veröffentlicht 2015Artigo -
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The MR-Base platform supports systematic causal inference across the human phenome von Gibran Hemani, Jie Zheng, Benjamin Elsworth, Kaitlin H. Wade, Valeriia Haberland, Denis Baird, Charles Laurin, Stephen Burgess, Jack Bowden, Ryan Langdon, Vanessa Y. Tan, James Yarmolinsky, Hashem A. Shihab, Nicholas J. Timpson, David M. Evans, Caroline L. Relton, Richard M. Martin, George Davey Smith, Tom R. Gaunt, Philip Haycock
Veröffentlicht 2018Artigo -
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Author response: The MR-Base platform supports systematic causal inference across the human phenome von Gibran Hemani, Jie Zheng, Benjamin Elsworth, Kaitlin H. Wade, Valeriia Haberland, Denis Baird, Charles Laurin, Stephen Burgess, Jack Bowden, Ryan Langdon, Vanessa Y. Tan, James Yarmolinsky, Hashem A. Shihab, Nicholas J. Timpson, David M. Evans, Caroline L. Relton, Richard M. Martin, George Davey Smith, Tom R. Gaunt, Philip Haycock
Veröffentlicht 2018Revisão por Pares -
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Copy Number Variations and Cognitive Phenotypes in Unselected Populations von Katrin Männik, Reedik Mägi, Aurélien Mace, Ben Cole, Anna L. Guyatt, Hashem A. Shihab, Anne Maillard, Helene Alavere, Anneli Kolk, Anu Reigo, Evelin Mihailov, Liis Leitsalu, Anne-Maud Ferreira, Margit Nõukas, Alexander Teumer, Erika Salvi, Daniele Cusi, Matt McGue, William G. Iacono, Tom R. Gaunt, J. Beckmann, Sébastien Jacquemont, Zoltán Kutalik, Nathan Pankratz, Nicholas J. Timpson, Andres Metspalu, Alexandre Reymond
Veröffentlicht 2015Artigo -
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Mosaic structural variation in children with developmental disorders von Daniel A. King, Wendy D. Jones, Yanick J. Crow, Anna F. Dominiczak, N Foster, Tom R. Gaunt, Jade Harris, Stephen Hellens, Tessa Homfray, Josie Innes, Elizabeth A. Jones, Shelagh Joss, Abhijit Kulkarni, Sahar Mansour, Andrew D. Morris, Michael Parker, David J. Porteous, Hashem A. Shihab, Blair H. Smith, Katrina Tatton‐Brown, John Tolmie, Maciej Trzaskowski, Pradeep Vasudevan, Emma Wakeling, Michael Wright, Robert Plomin, Nicholas J. Timpson, Matthew E. Hurles
Veröffentlicht 2015Artigo -
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Whole-genome sequence-based analysis of thyroid function von Peter Taylor, Eleonora Porcu, Shelby Chew, Purdey J. Campbell, Michela Traglia, Suzanne J. Brown, Benjamin H. Mullin, Hashem A. Shihab, Josine L. Min, Klaudia Walter, Yasin Memari, Jie Huang, Michael R. Barnes, John Beilby, Pimphen Charoen, Petr Danecek, Frank Dudbridge, Vincenzo Forgetta, Celia M.T. Greenwood, Elin Grundberg, Andrew D. Johnson, Jennie Hui, Ee Mun Lim, Shane McCarthy, Dawn Muddyman, Vijay Panicker, John R. B. Perry, Jordana T. Bell, Yuan Wei, Caroline L. Relton, Tom R. Gaunt, David Schlessinger, Gonçalo R. Abecasis, Francesco Cucca, Gabriela Surdulescu, Wolfram Woltersdorf, Eleftheria Zeggini, Hou‐Feng Zheng, Daniela Toniolo, Colin Dayan, Silvia Naitza, John P. Walsh, Tim D. Spector, George Davey Smith, Richard Durbin, J. Brent Richards, Serena Sanna, Nicole Soranzo, Nicholas J. Timpson, Scott G. Wilson, Saeed Al Turki, Carl A. Anderson, Richard Anney, Dinu Antony, María Soler Artigas, Muhammad Ayub, Senduran Balasubramaniam, Jeffrey C. Barrett, Inês Barroso, Phil Beales, Jamie Bentham, Shoumo Bhattacharya, Ewan Birney, Douglas Blackwood, Martin Bobrow, Elena G. Bochukova, Patrick Bolton, Rebecca Bounds, Chris Boustred, Gerome Breen, Mattia Calissano, Keren Carss, Krishna Chatterjee, Lu Chen, Antonio Ciampi, Sebhattin Cirak, Peter Clapham, Gail Clement, Guy Coates, David Collier, Catherine Cosgrove, Tony Cox, Nick Craddock, Lucy Crooks, Sarah Curran, David Curtis, Allan Daly, Aaron Day-Williams, Ian N. M. Day, Thomas A. Down, Yuanping Du, Ian Dunham, Sarah Edkins, Peter Ellis, David M. Evans, Sadaf Faroogi, Ghazaleh Fatemifar, David Fitzpatrick, Paul Flicek, James Flyod
Veröffentlicht 2015Revisão -
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Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits von Ioanna Tachmazidou, Dániel Süveges, Josine L. Min, Graham R. S. Ritchie, Julia Steinberg, Klaudia Walter, Valentina Iotchkova, Jeremy Schwartzentruber, Jie Huang, Yasin Memari, Shane McCarthy, Andrew Crawford, Cristina Bombieri, Massimiliano Cocca, Aliki-Eleni Farmaki, Tom R. Gaunt, Jari Lahti, Marjolein N. Kooijman, Benjamin Lehne, Giovanni Malerba, Satu Männistö, Angela Matchan, Carolina Medina‐Gómez, Sarah Metrustry, Abhishek Nag, Ιωάννα Ντάλλα, Lavinia Paternoster, Nigel W. Rayner, Cinzia Sala, William R. Scott, Hashem A. Shihab, Lorraine Southam, Beaté St Pourcain, Michela Traglia, Katerina Trajanoska, Gianluigi Zaza, Weihua Zhang, María Soler Artigas, Narinder Bansal, Marianne Benn, Zhongsheng Chen, Petr Danecek, Wei‐Yu Lin, Adam E. Locke, Jian’an Luan, Alisa K. Manning, Antonella Mulas, Carlo Sidore, Anne Tybjærg‐Hansen, Anette Varbo, Magdalena Żołędziewska, Chris Finan, Konstantinos Hatzikotoulas, Audrey E. Hendricks, John P. Kemp, Alireza Moayyeri, Kalliope Panoutsopoulou, Michał Szpak, Scott G. Wilson, Michael Boehnke, Francesco Cucca, Emanuele Di Angelantonio, Claudia Langenberg, Cecilia M. Lindgren, Mark I. McCarthy, Andrew P. Morris, Børge G. Nordestgaard, Robert A. Scott, Martin D. Tobin, Nicholas J. Wareham, Paul R. Burton, John C. Chambers, George Davey Smith, George Dedoussis, Janine F. Felix, Oscar H. Franco, Giovanni Gambaro, Paolo Gasparini, Christopher J. Hammond, Albert Hofman, Vincent W. V. Jaddoe, Marcus E. Kleber, Jaspal S. Kooner, Markus Perola, Caroline L. Relton, Susan M. Ring, Fernando Rivadeneira, Veikko Salomaa, Timothy D. Spector, Oliver Stegle, Daniela Toniolo, André G. Uitterlinden, Inês Barroso, Celia M.T. Greenwood, John R. B. Perry, Brian R. Walker, Adam S. Butterworth, Yali Xue, Richard Durbin, Kerrin S. Small
Veröffentlicht 2017Artigo
Suchwerkzeuge:
Ähnliche Schlagworte
Biology
Gene
Genetics
Computational biology
Computer science
Genome
Genotype
Medicine
Single-nucleotide polymorphism
Artificial intelligence
Mathematics
Mutation
Phenotype
Bioinformatics
Exome sequencing
Gene expression
Genome-wide association study
Pathology
Causal inference
DNA methylation
Data science
Exome
Inference
Phenome
Programming language
Statistics
Trait
Allele
Cancer
Coding (social sciences)