Search Results - Audrey E. Hendricks

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  1. 1
    Correction for multiple testing in a gene region

    Correction for multiple testing in a gene region by Audrey E. Hendricks, Josée Dupuis, Mark W. Logue, Richard H. Myers, Kathryn L. Lunetta

    Published 2013
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  2. 2
    Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset

    Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset by Meera Swami, Audrey E. Hendricks, Tammy Gillis, Tiffany Massood, Jayalakshmi Srinidhi Mysore, Richard H. Myers, Vanessa C. Wheeler

    Published 2009
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  3. 3
    Iron in Micronutrient Powder Promotes an Unfavorable Gut Microbiota in Kenyan Infants

    Iron in Micronutrient Powder Promotes an Unfavorable Gut Microbiota in Kenyan Infants by Minghua Tang, Daniel N. Frank, Audrey E. Hendricks, Diana Ir, Fabian Esamai, Edward A. Liechty, K. Michael Hambidge, Nancy F. Krebs

    Published 2017
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  4. 4
    Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes

    Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes by Ella Dragileva, Audrey E. Hendricks, Allison Teed, Tammy Gillis, Edith Lopez, Errol C. Friedberg, Raju Kucherlapati, Winfried Edelmann, Kathryn L. Lunetta, Marcy E. MacDonald, Vanessa C. Wheeler

    Published 2008
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  5. 5
    Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes

    Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes by Xiaoling Zhang, Andrew D. Johnson, Audrey E. Hendricks, Shih-Jen Hwang, Kahraman Tanrıverdi, Santhi K. Ganesh, Nicholas L. Smith, Patricia A. Peyser, Jane E. Freedman, Christopher J. O’Donnell

    Published 2013
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  6. 6
    Characterizing substructure via mixture modeling in large-scale genetic summary statistics

    Characterizing substructure via mixture modeling in large-scale genetic summary statistics by Hayley R Stoneman, Adelle Price, Nikole Scribner Trout, Riley Lamont, Souha Tifour, Nikita Pozdeyev, Kristy Crooks, Meng Lin, Nicholas Rafaels, Christopher R. Gignoux, Katie M. Marker, Audrey E. Hendricks

    Published 2025
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  7. 7
    Genetic architecture of human thinness compared to severe obesity

    Genetic architecture of human thinness compared to severe obesity by Fernando Riveros-Mckay, Vanisha Mistry, Rebecca Bounds, Audrey E. Hendricks, Julia M. Keogh, H. Thomas, Elana Henning, Laura J. Corbin, Stephen O’Rahilly, Eleftheria Zeggini, Eleanor Wheeler, Inês Barroso, I. Sadaf Farooqi

    Published 2019
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  8. 8
    Assessment of cortical and striatal involvement in 523 Huntington disease brains

    Assessment of cortical and striatal involvement in 523 Huntington disease brains by Tiffany C. Hadzi, Audrey E. Hendricks, Jeanne C. Latourelle, Kathryn L. Lunetta, L. Adrienne Cupples, Tammy Gillis, Jayalakshmi Srinidhi Mysore, James F. Gusella, Marcy E. MacDonald, Richard H. Myers, Jean‐Paul Vonsattel

    Published 2012
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  9. 9
    Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription

    Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription by Gaëlle Marenne, Audrey E. Hendricks, Aliki Perdikari, Rebecca Bounds, Felicity Payne, Julia M. Keogh, Christopher J. Lelliott, Elana Henning, Saad Pathan, Sofie Ashford, Elena G. Bochukova, Vanisha Mistry, Allan Daly, Caroline Hayward, Nicholas J. Wareham, Stephen O’Rahilly, Claudia Langenberg, Eleanor Wheeler, Eleftheria Zeggini, I. Sadaf Farooqi, Inês Barroso

    Published 2020
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  10. 10
    Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance

    Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance by Agatha A. van der Klaauw, Sophie Croizier, Edson Mendes de Oliveira, Lukas Kurt Josef Stadler, Soyoung Park, Youxin Kong, Matthew C. Banton, Panna Tandon, Audrey E. Hendricks, Julia M. Keogh, Susanna E. Riley, Sofia Papadia, Elana Henning, Rebecca Bounds, Elena G. Bochukova, Vanisha Mistry, Stephen O’Rahilly, Richard B. Simerly, James E. N. Minchin, Inês Barroso, E. Yvonne Jones, Sébastien G. Bouret, I. Sadaf Farooqi

    Published 2019
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  11. 11
    Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis

    Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis by Jian Yang, Agatha A. van der Klaauw, Liangru Zhu, Tessa Cacciottolo, Yanlin He, Lukas Kurt Josef Stadler, Chunmei Wang, Pingwen Xu, Kenji Saito, Antentor Hinton, Xiaofeng Yan, Julia M. Keogh, Elana Henning, Matthew C. Banton, Audrey E. Hendricks, Elena G. Bochukova, Vanisha Mistry, Katherine Lawler, Lan Liao, Jianming Xu, Stephen O’Rahilly, Qingchun Tong, Inês Barroso, Bert W. O’Malley, I. Sadaf Farooqi, Yong Xu

    Published 2019
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  12. 12
    KSR2 Mutations Are Associated with Obesity, Insulin Resistance, and Impaired Cellular Fuel Oxidation

    KSR2 Mutations Are Associated with Obesity, Insulin Resistance, and Impaired Cellular Fuel Oxidation by Laura R. Pearce, Neli Atanassova, Matthew C. Banton, Bill Bottomley, Agatha A. van der Klaauw, Jean‐Pierre Revelli, Audrey E. Hendricks, Julia M. Keogh, Elana Henning, Deon Doree, Sabrina Jeter‐Jones, Sumedha Garg, Elena G. Bochukova, Rebecca Bounds, Sofie Ashford, Emma L. Gayton, Peter C. Hindmarsh, Julian Hamilton‐Shield, Elizabeth Crowne, David Barford, Nicholas J. Wareham, Stephen O’Rahilly, Michael P. Murphy, David R. Powell, Inês Barroso, I. Sadaf Farooqi

    Published 2013
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  13. 13
    The UK10K project identifies rare variants in health and disease

    The UK10K project identifies rare variants in health and disease by Klaudia Walter, Josine L. Min, Jie Huang, Lucy Crooks, Yasin Memari, Shane McCarthy, John R. B. Perry, Changjiang Xu, Marta Futema, Daniel Lawson, Valentina Iotchkova, Stephan Schiffels, Audrey E. Hendricks, Petr Danecek, Rui Li, James S. Floyd, Louise V. Wain, Inês Barroso, Steve E. Humphries, Matthew E. Hurles, Eleftheria Zeggini, Jeffrey C. Barrett, Vincent Plagnol, J. Brent Richards, Celia M. T. Greenwood, Nicholas J. Timpson, Richard Durbin, Nicole Soranzo, Senduran Bala, Peter Clapham, Guy Coates, Tony Cox, Allan Daly, Petr Danecek, Yuanping Du, Richard Durbin, Sarah Edkins, Peter Ellis, Paul Flicek, Xiaosen Guo, Xueqin Guo, Jie Huang, David K. Jackson, Christopher Joyce, Thomas Keane, Anja Kolb-Kokocinski, Cordelia Langford, Rui Li, Jieqin Liang, Hong Lin, Ryan Liu, John Maslen, Shane McCarthy, Dawn Muddyman, Michael A. Quail, Jim Stalker, Jianping Sun, Jing Tian, Guangbiao Wang, Jun Wang, Yu Wang, Kim Wong, Pingbo Zhang, Inês Barroso, Ewan Birney, Chris Boustred, Lu Chen, Gail Clement, Massimiliano Cocca, Petr Danecek, George Davey Smith, Ian N.M. Day, Aaron Day-Williams, Thomas A. Down, Ian Dunham, Richard Durbin, David M. Evans, Tom R. Gaunt, Matthias Geihs, Celia M. T. Greenwood, Deborah Hart, Audrey E. Hendricks, Bryan Howie, Jie Huang, Tim Hubbard, Pirro G. Hysi, Valentina Iotchkova, Yalda Jamshidi, Konrad J. Karczewski, John P. Kemp, Geneviève Lachance, Daniel Lawson, Monkol Lek, Margarida Lopes, Daniel G. MacArthur, Jonathan Marchini, Massimo Mangino, Iain Mathieson, Shane McCarthy, Yasin Memari

    Published 2015
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  14. 14
    Haplotypes and gene expression implicate the <i>MAPT</i> region for Parkinson disease

    Haplotypes and gene expression implicate the <i>MAPT</i> region for Parkinson disease by Jennifer E. Tobin, Jeanne C. Latourelle, Mark Lew, Christine Klein, Oksana Suchowersky, H. A. Shill, Lawrence I. Golbe, M. H. Mark, John H. Growdon, G. Frederick Wooten, Brad A. Racette, J. S. Perlmutter, Ray L. Watts, Mark Guttman, Kenneth B. Baker, Stefano Goldwurm, Gianni Pezzoli, Carlos Singer, Marie Saint‐Hilaire, Audrey E. Hendricks, Sally Williamson, Michael W. Nagle, Jemma B. Wilk, Tiffany Massood, Jason M. Laramie, Anita L. DeStefano, Irene Litvan, Garth A. Nicholson, Alastair Corbett, Stuart Isaacson, David J. Burn, Patrick F. Chinnery, Peter P. Pramstaller, Scott J. Sherman, Jomana T. Al‐Hinti, Edward Drasby, Martha Nance, Anette Torvin Møller, Karen Østergaard, Richard Roxburgh, B. J. Snow, John T. Slevin, Franca Cambi, James F. Gusella, Richard H. Myers

    Published 2008
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  15. 15
    The Gly2019Ser mutation in LRRK2is not fully penetrant in familial Parkinson's disease: the GenePD study

    The Gly2019Ser mutation in LRRK2is not fully penetrant in familial Parkinson's disease: the GenePD study by Jeanne C. Latourelle, Mei Sun, Mark Lew, Oksana Suchowersky, Christine Klein, Lawrence I. Golbe, Margery H. Mark, John H. Growdon, G. Frederick Wooten, Ray L. Watts, Mark Guttman, Brad A. Racette, Joel S. Perlmutter, Anwar Ahmed, Holly A. Shill, Carlos Singer, Stefano Goldwurm, Gianni Pezzoli, Michela Zini, Marie Saint‐Hilaire, Audrey E. Hendricks, Sally Williamson, Michael W. Nagle, Jemma B. Wilk, Tiffany Massood, Karen W. Huskey, Jason M. Laramie, Anita L. DeStefano, Kenneth B. Baker, Ilia Itin, Irene Litvan, Garth A. Nicholson, Alastair Corbett, Martha Nance, Edward Drasby, Stuart Isaacson, David J. Burn, Patrick F. Chinnery, Peter P. Pramstaller, Jomana T. Al‐Hinti, Anette Torvin Møller, Karen Østergaard, Scott J. Sherman, Richard Roxburgh, Barry Snow, John T. Slevin, Franca Cambi, James F. Gusella, Richard H. Myers

    Published 2008
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  16. 16
    Body mass index is negatively associated with telomere length: a collaborative cross-sectional meta-analysis of 87 observational studies

    Body mass index is negatively associated with telomere length: a collaborative cross-sectional meta-analysis of 87 observational studies by Marij Gielen, Geja J. Hageman, Evangelia E. Antoniou, Katarina Nordfjäll, Massimo Mangino, Muthuswamy Balasubramanyam, Tim De Meyer, Audrey E. Hendricks, Erik J. Giltay, Steven C. Hunt, Jennifer A. Nettleton, Klelia D. Salpea, Vanessa Diaz, Ramin Farzaneh‐Far, Gil Atzmon, Sarah E. Harris, Lifang Hou, David Gilley, Iiris Hovatta, Jeremy D. Kark, Hisham Nassar, David J. Kurz, Karen A. Mather, Peter Willeit, Yun‐Ling Zheng, Sofia Pavanello, Ellen W. Demerath, Line Rode, Daniel Bunout, Andrew Steptoe, Lisa A. Boardman, Amelia Martí, Belinda L. Needham, Wei Zheng, Rosalind Ramsey‐Goldman, Andrew J. Pellatt, Jaakko Kaprio, Jonathan N. Hofmann, Christian Gieger, Giuseppe Paolisso, Jacob Hjelmborg, Kari G. Rabe, Teresa E. Seeman, Jason Wong, Pim van der Harst, Linda Broer, Florian Kronenberg, Barbara Kollerits, Timo Strandberg, Dan T. A. Eisenberg, Catherine Duggan, Josine E. Verhoeven, Roxanne Schaakxs, Raffaela Zannolli, Rosana M. R. dos Reis, Fadi J. Charchar, Maciej Tomaszewski, Ute Mons, Ilja Demuth, Andrea Elena Iglesias Molli, Guo Cheng, Dmytro Krasnienkov, Bianca D’Antono, Marek Kasielski, Barry J. McDonnell, Richard P. Ebstein, Kristina Sundquist, Guillaume Paré, Michael Chong, Maurice P. Zeegers

    Published 2018
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  17. 17
    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 by 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

    Published 2015
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  18. 18
    Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

    Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity by Audrey E. Hendricks, Elena G. Bochukova, Gaëlle Marenne, Julia M. Keogh, Neli Atanassova, Rebecca Bounds, Eleanor Wheeler, Vanisha Mistry, Elana Henning, Antje Körner, Dawn Muddyman, Shane McCarthy, Anke Hinney, Johannes Hebebrand, Robert A. Scott, Claudia Langenberg, Nicholas J. Wareham, Praveen Surendran, Joanna M. M. Howson, Adam S. Butterworth, John Danesh, Børge G. Nordestgaard, Sune F. Nielsen, Shoaib Afzal, Sofia Papadia, Sofie Ashford, Sumedha Garg, Glenn L. Millhauser, Rafael I. Palomino, Alexandra Kwasniewska, Ioanna Tachmazidou, Stephen O’Rahilly, Eleftheria Zeggini, Inês Barroso, I. Sadaf Farooqi, Michaela Benzeval, Jonathan Burton, Nicholas Buck, Annette Jäckle, Meena Kumari, Heather Laurie, Peter Lynn, Stephen Pudney, Birgitta Rabe, Dieter Wolke, Kim Overvad, Anne Tjønneland, Francoise Clavel-Chapelon, Rudolf Kaaks, Heiner Boeing, Antonia Trichopoulou, Pietro Ferrari, Domenico Palli, Vittorio Krogha, Salvatore Panico, Rosario Tuminoa, Giuseppe Matullo, Jolanda M.A. Boer, Yvonne T. van der Schouw, Elisabete Weiderpass, J. Ramón Quirós, María‐José Sánchez, Carmen Navarro, Conchi Moreno‐Iribas, Larraitz Arriola, Olle Melander, Patrik Wennberg, Timothy J. Key, Elio Ríboli, Saeed Al Turki, Carl A. Anderson, Richard Anney, Dinu Antony, María Soler Artigas, Muhammad Ayub, Senduran Bala, Jeffrey C. Barrett, Phil Beales, Jamie Bentham, Shoumo Bhattacharyaa, Ewan Birney, Douglas Blackwooda, Martin Bobrow, Patrick Bolton, Chris Boustred, Gerome Breen, Mattia Calissanoa, Keren Carss, Ruth Charlton, Krishna Chatterjee, Lu Chen, Antonio Ciampia, Sebahattin Çırak, Peter Clapham, Gail Clement, Guy Coates, Massimiliano Coccaa, David Collier, Catherine Cosgrove, Tony Coxa

    Published 2017
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  19. 19
    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 by 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

    Published 2019
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  20. 20
    TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

    TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport by Miriam Schmidts, Yuqing Hou, Claudio R. Cortés, Dorus A. Mans, Céline Huber, Karsten Boldt, Mitali Patel, Jeroen van Reeuwijk, Jean-Marc Plaza, Sylvia E. C. van Beersum, Zhi Min Yap, Stef J.F. Letteboer, S. Paige Taylor, Warren Herridge, Colin A. Johnson, Peter Scambler, Marius Ueffing, Hülya Kayserili, Deborah Krakow, Stephen M. King, Philip L. Beales, Lihadh Al‐Gazali, Carol Wicking, Valérie Cormier‐Daire, Ronald Roepman, Hannah M. Mitchison, George B. Witman, Saeed Al-Turki, Carl E. Anderson, Richard Anney, Dinu Antony, Jennifer L. Asimit, Muhammad Ayub, J. M. Barrett, Inês Barroso, Jamie Bentham, Shoumo Bhattacharya, Douglas Blackwood, Martin Bobrow, Elena G. Bochukova, Patrick Bolton, Chris Boustred, Gerome Breen, Marie‐Jo Brion, Andrew H. Brown, Mattia Calissano, Keren Carss, Krishna Chatterjee, Lu Chen, Sebhattin Cirak, Peter Clapham, Gail Clement, Guy Coates, David Collier, Catherine Cosgrove, Tony Cox, Nick Craddock, Lucy Crooks, Sarah Curran, Allan Daly, Petr Danecek, George Davey Smith, Aaron Day-Williams, Ian N.M. Day, Richard Durbin, Sarah Edkins, Peter Ellis, David A. Evans, I. Sadaf Farooqi, Ghazaleh Fatemifar, David Fitzpatrick, Paul Flicek, Jamie Floyd, A. Reghan Foley, Chris Franklin, Marta Futema, Louise Gallagher, Tom R. Gaunt, Daniel H. Geschwind, Celia M.T. Greenwood, Detelina Grozeva, Xiaosen Guo, Hugh Gurling, Deborah Hart, Audrey E. Hendricks, Peter Holmans, Jie Huang, Steve E. Humphries, Matt Hurles, Pirro G. Hysi, David H. Jackson, Yalda Jamshidi, David Jewell, J. Janse Chris, J. F. Kaye, Thomas Keane, John P. Kemp, Karen L. Kennedy, Alastair Kent, Anja Kolb‐Kokocinski

    Published 2015
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