Хайлтын үр дүнгүүд - James Floyd

  • 14-н 1 - 14 үр дүнгүүдийг харуулж байна
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  1. 1
    optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variants

    optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variants -н Tejas Shah, J. Z. Liu, James Floyd, James Morris, Nicolas T. Wirth, Jeffrey C. Barrett, Carl A. Anderson

    Хэвлэсэн 2012
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    Artigo
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  2. 2
    De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability

    De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability -н Detelina Grozeva, Keren Carss, Olivera Spasić-Bošković, Michael Parker, Hayley Archer, Helen V. Firth, Soo‐Mi Park, Natalie Canham, Susan Holder, Meredith Wilson, Anna Hackett, Michael Field, James Floyd, Matthew E. Hurles, F. Lucy Raymond

    Хэвлэсэн 2014
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    Artigo
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  3. 3
    Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects

    Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects -н Kathleen A. Williamson, Joe Rainger, James Floyd, Morad Ansari, Alison Meynert, Kishan V. Aldridge, Jacqueline K. Rainger, Carl A. Anderson, Anthony T. Moore, Matthew E. Hurles, Angus Clarke, Veronica van Heyningen, Alain Verloès, Martin S. Taylor, Andrew O.M. Wilkie, David Fitzpatrick

    Хэвлэсэн 2014
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    Artigo
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  4. 4
    A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma

    A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma -н Chunqiao Liu, Sonya A. Widen, Kathleen A. Williamson, Rinki Ratnapriya, Christina Gerth‐Kahlert, Joe Rainger, Ramakrishna P. Alur, Erin Strachan, Souparnika H. Manjunath, Archana Balakrishnan, James Floyd, Tiansen Li, Andrew J. Waskiewicz, Brian P. Brooks, Ordan J. Lehmann, David Fitzpatrick, Anand Swaroop

    Хэвлэсэн 2016
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    Artigo
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  5. 5
    Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

    Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis -н George Mells, James Floyd, Katherine I. Morley, Heather J. Cordell, Christopher Franklin, So–Youn Shin, Michael A. Heneghan, James Neuberger, Peter T. Donaldson, Darren B. Day, Samantha Ducker, Agnes W Muriithi, Elizabeth F Wheater, Christopher J. Hammond, Muhammad F. Dawwas, D. I. Jones, Leena Peltonen, Graeme Alexander, Richard Sandford, Carl A. Anderson

    Хэвлэсэн 2011
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  6. 6
    Targeted Next‐Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability

    Targeted Next‐Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability -н Detelina Grozeva, Keren Carss, Olivera Spasić-Bošković, María‐Isabel Tejada, Jozef Gécz, Marie Shaw, Mark Corbett, Eric Haan, Elizabeth Thompson, Kathryn Friend, Zaamin B. Hussain, Anna Hackett, Michael Field, Alessandra Renieri, Roger E. Stevenson, Charles E. Schwartz, James Floyd, Jamie Bentham, Catherine Cosgrove, Bernard Keavney, Shoumo Bhattacharya, Matthew E. Hurles, F. Lucy Raymond

    Хэвлэсэн 2015
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    Artigo
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  7. 7
    Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations

    Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations -н Ayşe Demirkan, Cornelia M. van Duijn, Péter Ugocsai, Aaron Isaacs, Peter P. Pramstaller, Gerhard Liebisch, James F. Wilson, Åsa Johansson, Igor Rudan, Yurii S. Aulchenko, Anatoly V. Kirichenko, A. Cecile J.W. Janssens, Ritsert C. Jansen, Carsten Gnewuch, Francisco S. Domingues, Cristian Pattaro, Sarah H. Wild, Inger Jonasson, Ozren Polašek, Irina V. Zorkoltseva, Albert Hofman, Lennart C. Karssen, Maksim Struchalin, James Floyd, Wilmar Igl, Zrinka Biloglav, Linda Broer, Arne Pfeufer, Irene Pichler, Susan Campbell, Ghazal Zaboli, Ivana Kolčić, Fernando Rivadeneira, Jennifer E. Huffman, Nicholas D. Hastie, André G. Uitterlinden, Lude Franke, Christopher Franklin, Véronique Vitart, Christopher P. Nelson, Michael Preuß, Joshua C. Bis, Christopher J. O’Donnell, Nora Franceschini, Jacqueline C.M. Witteman, Tatiana I. Axenovich, Ben A. Oostra, Thomas Meitinger, Andrew A. Hicks, Caroline Hayward, Alan F. Wright, Ulf Gyllensten, Harry Campbell, Gerd Schmitz

    Хэвлэсэн 2012
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  8. 8
    Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations

    Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations -н Joe Rainger, Davut Pehli̇van, Stefan Johansson, Hemant Bengani, Luis Sánchez‐Pulido, Kathleen A. Williamson, Mehmet Türe, Heather Barker, Karen Rosendahl, Jürgen W. Spranger, Denise Horn, Alison Meynert, James Floyd, Trine Prescott, Carl A. Anderson, Jacqueline K. Rainger, Ender Karaca, Claudia Gonzaga‐Jauregui, Shalini N. Jhangiani, Donna M. Muzny, Anne Seawright, Dinesh C. Soares, Mira Kharbanda, Victoria Murday, Andrew J. Finch, Richard A. Gibbs, Veronica van Heyningen, Martin S. Taylor, Tahsin Yakut, Per M. Knappskog, Matthew E. Hurles, Chris P. Ponting, James R. Lupski, Gunnar Houge, David Fitzpatrick, Matthew E. Hurles, David Fitzpatrick, Saeed Al-Turki, Carl A. Anderson, Inês Barroso, Philip L. Beales, Jamie Bentham, Shoumo Bhattacharya, Keren Carss, Krishna Chatterjee, Sebhattin Cirak, Catherine Cosgrove, Allan Daly, Jamie Floyd, Chris Franklin, Marta Futema, Steve E. Humphries, Shane McCarthy, Hannah M. Mitchison, Francesco Muntoni, Alexandros Onoufriadis, Victoria Parker, Felicity Payne, Vincent Plagnol, Lucy Raymond, David B. Savage, Peter Scambler, Miriam Schmidts, Robert K. Semple, Eva Serra, Jim Stalker, Margriet van Kogelenberg, Parthiban Vijayarangakannan, Klaudia Walter, G Black Wood

    Хэвлэсэн 2014
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    Artigo
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  9. 9
    Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

    Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel -н Jie Huang, Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min, Petr Danecek, Giovanni Malerba, Elisabetta Trabetti, Hou‐Feng Zheng, Saeed Al Turki, Antoinette Amuzu, Carl A. Anderson, Richard Anney, Dinu Antony, María Soler Artigas, Muhammad Ayub, Senduran Bala, Jeffrey C. Barrett, Inês Barroso, Phil Beales, Marianne Benn, 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, Juan P. Casas, John C. Chambers, Ruth Charlton, Krishna Chatterjee, Lu Chen, Antonio Ciampi, Sebahattin Çırak, Peter Clapham, Gail Clement, Guy Coates, Massimiliano Cocca, David Collier, Catherine Cosgrove, Tony Cox, Nick Craddock, Lucy Crooks, Sarah Curran, David Curtis, Allan Daly, Ian N.M. Day, Aaron Day-Williams, George Dedoussis, Thomas A. Down, Yuanping Du, Cornelia M. van Duijn, Ian Dunham, Sarah Edkins, Rosemary Ekong, Peter Ellis, David M. Evans, I. Sadaf Farooqi, David Fitzpatrick, Paul Flicek, James Floyd, A. Reghan Foley, Christopher S. Franklin, Marta Futema, Louise Gallagher, Paolo Gasparini, Tom R. Gaunt, Matthias Geihs, Daniel H. Geschwind, Celia M.T. Greenwood, Heather Griffin, Detelina Grozeva, Xiaosen Guo, Xueqin Guo, Hugh Gurling, Deborah Hart, Audrey E. Hendricks, Peter Holmans, Jie Huang, Tim Hubbard, Steve E. Humphries, Matthew E. Hurles, Pirro G. Hysi, Valentina Iotchkova, Aaron Isaacs, David K. Jackson, Yalda Jamshidi, Jon Johnson, Christopher Joyce, Konrad J. Karczewski, Jane Kaye, Thomas Keane, John P. Kemp

    Хэвлэсэн 2015
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    Artigo
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  10. 10
    International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways

    International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways -н Heather J. Cordell, Younghun Han, George Mells, Yafang Li, Gideon M. Hirschfield, Casey S. Greene, Gang Xie, Brian D. Juran, Dakai Zhu, David C. Qian, James Floyd, Katherine I. Morley, Daniele Prati, Ana Lleó, Daniele Cusi, Erik M. Schlicht, Craig Lammert, Elizabeth J. Atkinson, Landon L. Chan, Mariza de Andrade, Tobias Balschun, Andrew L. Mason, Robert P. Myers, Jinyi Zhang, Piotr Milkiewicz, Jia Qu, Joseph A. Odin, Velimir A. Luketic, Bruce R. Bacon, Henry C. Bodenheimer, Valentina Liakina, Catherine Vincent, Cynthia Levy, Peter K. Gregersen, Piero Luigi Almasio, Domenico Alvaro, Pietro Andreoné, Angelo Andriulli, Cristina Barlassina, Pier Maria Battezzati, A. Benedetti, Francesca Bernuzzi, Ilaria Bianchi, Maria Consiglia Bragazzi, Maurizia Rossana Brunetto, Savino Bruno, Giovanni Casella, B. Coco, Agostino Colli, Massimo Colombo, Sílvia Colombo, Carmela Cursaro, Lory Saveria Crocè, Andrea Crosignani, Maria Francesca Donato, G. Elia, Luca Fabris, Carlo Ferrari, Annarosa Floreani, Barbara Foglieni, Rosanna Fontana, Andrea Galli, Roberta Lazzari, Fabio Salvatore Macaluso, Federica Malinverno, Fabio Marra, Marco Marzioni, Alberto Mattalia, R. Montanari, Lorenzo Morini, Filomena Morisco, Hani S. Mousa, Luigi Muratori, Paolo Muratori, Grazia Anna Niro, Vincenzo Ostilio Palmieri, A. Picciotto, Mauro Podda, Piero Portincasa, Vincenzo Ronca, F. Rosina, Sonia Rossi, Ilaria Sogno, Giancarlo Spinzi, Marta Spreafico, Mario Strazzabosco, Sonia Tarallo, Mirko Tarocchi, Claudio Tiribelli, Pierluigi Toniutto, Maria Cristina Vinci, Massimo Zuin, Chin Lye Ch’ng, Mesbah Rahman, Tom Yapp, Richard Sturgess, Christopher Healey, Marek Czajkowski, Anton Gunasekera, Pranab Gyawali

    Хэвлэсэн 2015
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  11. 11
    Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

    Low-frequency variation in TP53 has large effects on head circumference and intracranial volume -н Simon Haworth, Chin Yang Shapland, Caroline Hayward, Bram P. Prins, Janine F. Felix, Carolina Medina‐Gómez, Fernando Rivadeneira, Carol A. Wang, Tarunveer S. Ahluwalia, Martine Vrijheid, Mònica Guxens, Jordi Sunyer, Ioanna Tachmazidou, Klaudia Walter, Valentina Iotchkova, Andrew P. Jackson, Louise Cleal, Jennifer Huffmann, Josine L. Min, Lærke Sass, Paul R. H. J. Timmers, Saeed Al Turki, Carl A. Anderson, Richard Anney, Dinu Antony, María Soler Artigas, Muhammad Ayub, Senduran Bala, 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, Ruth Charlton, Krishna Chatterjee, Lu Chen, Antonio Ciampi, Sebahattin Çırak, Peter Clapham, Gail Clement, Guy Coates, Massimiliano Cocca, David Collier, Catherine Cosgrove, Tony Cox, Nick Craddock, Lucy Crooks, Sarah Curran, David Curtis, Allan Daly, Petr Danecek, Ian N. M. Day, Aaron Day-Williams, Anna F. Dominiczak, Thomas A. Down, Yuanping Du, Ian Dunham, Richard Durbin, Sarah Edkins, Rosemary Ekong, Peter Ellis, David M. Evans, I. Sadaf Farooqi, David Fitzpatrick, Paul Flicek, James Floyd, A. Reghan Foley, Christopher S. Franklin, Marta Futema, Louise Gallagher, Tom R. Gaunt, Matthias Geihs, Daniel Geschwind, Celia M.T. Greenwood, Heather Griffin, Detelina Grozeva, Xiaosen Guo, Xueqin Guo, Hugh Gurling, Deborah Hart, Audrey E. Hendricks, Peter Holmans, Bryan Howie, Jie Huang, Jie Huang, Tim Hubbard, Steve E. Humphries, Matthew E. Hurles, Pirro G. Hysi, David K. Jackson

    Хэвлэсэн 2019
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    Artigo
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  12. 12
    Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

    Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index -н Anke Hinney, Miriam Kesselmeier, Sigrid Jall, A-L Volckmar, Manuel Föcker, Jochen Antel, Vesna Boraska Perica, C. Franklin, James Floyd, Laura M. Thornton, Laura M. Huckins, Lorraine Southam, N. William Rayner, Ioanna Tachmazidou, Kelly L. Klump, Janet Treasure, Cathryn M. Lewis, Ulrike Schmidt, Federica Tozzi, Kirsty iezebrink, Johannes Hebebrand, Philip Gorwood, Roger A.H. Adan, Martien J. Kas, Angela Favaro, Paolo Santonastaso, Fernando Fernández‐Aranda, Mónica Gratacòs, Filip Rybakowski, Monika Dmitrzak‐Węglarz, Jaakko Kaprio, Anna Keski‐Rahkonen, Anu Raevuori, Eric F. van Furth, M Landt, James I. Hudson, Ted Reichborn‐Kjennerud, Gun Peggy Knudsen, Palmiero Monteleone, Allan S. Kaplan, Andreas Karwautz, Hákon Hákonarson, Wade H. Berrettini, Yiran Guo, Dong Li, Nicholas J. Schork, Gen Komaki, Tetsuya Ando, Hidetoshi Inoko, Tõnu Esko, Krista Fischer, Katrin Männik, Andres Metspalu, Jessica H. Baker, Roger D. Cone, Jennifer Dackor, Janiece E. DeSocio, Christopher Hilliard, Julie K. O’Toole, Jacques Pantel, Jin P. Szatkiewicz, Chrysecolla Taico, Stephanie Zerwas, Sara E. Trace, Oliver S. P. Davis, Sietske G. Helder, Katharina Bühren, Roland Burghardt, Martina de Zwaan, Karin Egberts, Stefan Ehrlich, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Hartmut Imgart, André Scherag, Susann Scherag, Stephan Zipfel, Claudette Boni, Nicolás Ramoz, Audrey Versini, Marek K. Brandys, Unna N. Danner, Carolien de Kove, Judith Hendriks, Bobby P.C. Koeleman, Roel A. Ophoff, Eric Strengman, Annemarie Elburg, Alice Bruson, Maurizio Clementi, Daniela Degortes, Monica Forzan, Elena Tenconi, Elisa Docampo, Geòrgia Escaramí, Susana Jiménez‐Múrcia, Jolanta Lissowska, Andrzej Rajewski, Neonila Szeszenia‐Dąbrowska, Agnieszka Slopien

    Хэвлэсэн 2016
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  13. 13
    Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa

    Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa -н Laramie Duncan, Zeynep Yılmaz, Helena Gaspar, Raymond K. Walters, Jackie Goldstein, Verneri Anttila, Brendan Bulik‐Sullivan, Stephan Ripke, Laura Thornton, Anke Hinney, Mark J. Daly, Patrick F. Sullivan, Eleftheria Zeggini, Gerome Breen, Cynthia M. Bulik, Laramie Duncan, Zeynep Yılmaz, Héléna A. Gaspar, Raymond K. Walters, Jackie Goldstein, Verneri Anttila, Brendan Bulik‐Sullivan, Stephan Ripke, Roger A.H. Adan, Lars Alfredsson, Tetsuya Ando, Ole A. Andreassen, H.N. Aschauer, Jessica H. Baker, Jeffrey C. Barrett, Vladimír Bencko, Andrew W. Bergen, Wade Berrettini, Andreas Birgegård, Claudette Boni, Vesna Boraska Perica, Harry Brandt, Roland Burghardt, Laura Carlberg, Matteo Cassina, Carolyn E. Cesta, Sven Cichon, Maurizio Clementi, Sarah Cohen‐Woods, Jonathan R. I. Coleman, Roger D. Cone, Philippe Courtet, Steven Crawford, Scott J. Crow, James L. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Bo Ding, Monika Dmitrzak‐Węglarz, Elisa Docampo, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Thomas Espeseth, Xavier Estivill, Angela Favaro, Fernando Fernández‐Aranda, Manfred Fichter, Chris Finan, Krista Fischer, James Floyd, Manuel Föcker, Lenka Foretová, Monica Forzan, Caroline S. Fox, C. Franklin, Valérie Gaborieau, Steven Gallinger, Giovanni Gambaro, Ina Giegling, Fragiskos Gonidakis, Philip Gorwood, Mónica Gratacòs, Sébastien Guillaume, Yiran Guo, Hakon Hakonarson, Katherine A. Halmi, Rebecca Harrison, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Judith Hendriks, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Christopher Hilliard

    Хэвлэсэн 2017
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  14. 14
    Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

    Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 -н Carl A. Anderson, Gabrielle Boucher, Charlie W. Lees, André Franke, Mauro D’Amato, Kent D. Taylor, James Lee, Philippe Goyette, Marcin Imieliński, Anna Latiano, Caroline Lagacé, Regan Scott, Leila Amininejad, Suzannah Bumpstead, Leonard Baidoo, Robert N. Baldassano, Murray L. Barclay, Theodore M. Bayless, Stephan Brand, Carsten Büning, Jean‐Frédéric Colombel, Lee A. Denson, Martine De Vos, Marla C. Dubinsky, Cathryn Edwards, David Ellinghaus, Rudolf S.N. Fehrmann, James Floyd, Timothy H. Florin, Denis Franchimont, Lude Franke, Michel Georges, Jürgen Glas, Nicole L. Glazer, Stephen L. Guthery, Talin Haritunians, Nicholas K. Hayward, Jean‐Pierre Hugot, Gilles Jobin, Debby Laukens, Ian C. Lawrance, Marc Lémann, Arie Levine, Cécile Libioulle, Édouard Louis, Dermot McGovern, Mónica Milla, Grant W. Montgomery, Katherine I. Morley, Craig Mowat, Aylwin Ng, William G. Newman, Roel A. Ophoff, Laura Papi, Orazio Palmieri, Laurent Peyrin–Biroulet, Julián Panés, Anne Phillips, Natalie J. Prescott, Deborah D. Proctor, Rebecca Roberts, Richard K. Russell, Paul Rutgeerts, Jeremy Sanderson, Miquel Sans, L. Philip Schumm, Frank Seibold, Yashoda Sharma, Lisa A. Simms, Mark Seielstad, A. Hillary Steinhart, Stephan R. Targan, Leonard H. van den Berg, Morten Vatn, Hein W. Verspaget, Thomas D. Walters, Cisca Wijmenga, David C. Wilson, Harm-Jan Westra, Ramnik J. Xavier, Zhen Zhao, Cyriel Y. Ponsioen, Vibeke Andersen, Leif Törkvist, Maria Gazouli, Nicholas P. Anagnou, Tom H. Karlsen, Limas Kupčinskas, Jurgita Šventoraitytė, John Mansfield, Subra Kugathasan, Mark S. Silverberg, Jonas Halfvarson, Jerome I. Rotter, Christopher G. Mathew, Anne M. Griffiths, Richard B. Gearry, Tariq Ahmad, Steven R. Brant, Mathias Chamaillard

    Хэвлэсэн 2011
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