Contrasting synergistic heterobimetallic(Na-Mg) and homometallic (Na or Mg) bases in metallation reactions of dialkyl- phenylphosphines and -anilines: lateral vs ring selectivities von Stevens, Michael Andrew, Hashim, Fairuz H, Gwee, Eunice S H, Izgorodina, Ekaterina I, Mulvey, Robert E, Blair, Victoria Louise

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Evidence for 28 genetic disorders discovered by combining healthcare and research data von Kaplanis, Joanna, Samocha, Kaitlin E., Wiel, Laurens, Zhang, Zhancheng, Arvai, Kevin J., Eberhardt, Ruth Y., Gallone, Giuseppe, Lelieveld, Stefan H., Martin, Hilary C., McRae, Jeremy F., Short, Patrick J., Torene, Rebecca I., de Boer, Elke, Danecek, Petr, Gardner, Eugene J., Huang, Ni, Lord, Jenny, Martincorena, Iñigo, Pfundt, Rolph, Reijnders, Margot R. F., Yeung, Alison, Yntema, Helger G., Vissers, Lisenka E. L. M., Juusola, Jane, Wright, Caroline F., Brunner, Han G., Firth, Helen V., FitzPatrick, David R., Barrett, Jeffrey C., Hurles, Matthew E., Gilissen, Christian, Retterer, Kyle

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Effects of antiplatelet therapy after stroke due to intracerebral haemorrhage (RESTART): a randomised, open-label trial von Sullivan, Frank, Rojas, Javier, Lowe, Gordon, McGill, Connor, Palmer, Jeb, Parakramawansha, Ruwan, MacRaild, Allan, Parry-Jones, Adrian, Johnes, Mary, Wood, Edith, Owoyele, Emmanuelle, Ballantine, Robert, Maatouk, Ahmad, Dakin, Katy, Szabo, Susan, Tysoe, Sharon, Esson, Derek, Anjum, Talat, Quinn, Leanne, Chenna, Srikanth, Gainard, Glyn, Butler, Adrian, Shelton, Faye, Havard, Diane, Board, Joanne, Murali, Elodie, Adie, Katja, Bond, Kirsty, Mudd, Paul, Moreton, Fiona, Huang, Xuya, Gartrell, Imogen, Smith, Simon, Hewitt, Jonathan, Banaras, Azra, Bakawala, Rehana, Manoj, Aravind, Sharma, Nikhil, Gbadamoshi, Lukuman, Bell, Jo, Longland, Barbara, Harrison, Melanie, Stevenson, Sarah, Jagpal, Baljit, Nelson, Sandra, Webber, Adam, Tayler, Michelle, Clayton, Susan, Gamble, Ed, Grimwood, Gemma, Reckless, Ian, Finlay, Sarah, Hayhoe, Helen, Tallantyre, Emma, White, Susan, Reddan, Julie, Jarrett, David, Harrington-Davies, Yasmin, Shahmehri, Shahrzad, Henry, Margo, Hazel, Beth, Shah, Alex, Datta, Prabal, Thompson, Teresa, Herman, Jane, Howard, Joanne, Dhar, Saikat, Baird, Yolanda, Davies, Ruth, Little, Victoria, Cherian, Suja, Cunningham, Mishell, Zahoor, Tajammal, Webster, Timothy, Jenkins, Colin, Hughes, Claire, Whitcher, Alison, Ravenhill, Garth, Saada, Janak, Perfitt, Rebekah, Tauro, Suzanne, Cuddy, Sarah, Markova, Skarlet, Thomas, Isobel, Sekaran, Lakshmanan, Elfandi, Khaled, Salehin, Maqsud, Ghaly, George, Horton, Sarah, Bell, Murdina, Gilham, Ellie, Fuller, Tracy, Goorah, Neetish, Bell, Angela, Kelly, Christine, Tomlinson, Benjamin, Donaldson, Denise, Kenton, Antony, Subramonian, Santhosh, Owusu-Agyei, Peter

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Prevalence and architecture of de novo mutations in developmental disorders von McRae, Jeremy F, Clayton, Stephen, Mason, Laura E, Tivey, Adrian R, Ahmed, Munaza, Awada, Jana, Balasubramanian, Meena, Banka, Siddharth, Bennett, Chris, Bernhard, Birgitta, Bevan, A. Paul, Blair, Edward, Blyth, Moira, Burn, John, Castle, Bruce, Clasper, Susan, Collins, Amanda, Collinson, Morag N, Dabir, Tabib, Davidson, Rosemarie, Davies, Sally, Dean, John, Donnai, Dian, Ellard, Sian, Ellis, Ian, Everest, Sarah, Foulds, Nicola, Fryer, Alan, Gaunt, Lorraine, Goudie, David, Gray, Emma, Greene, Philip, Gribble, Susan, Henderson, Alex, Hildyard, Lucy, Holden, Simon, Holder, Muriel, Ingram, Stuart, Jackson, Andrew, Kaemba, Beckie, Kazembe, Sandra, Kinning, Esther, Kraus, Alison, Kumar, V. K. Ajith, Lachlan, Katherine, Lam, Wayne, Lim, Derek, Longman, Cheryl, Lynch, Sally A, Maher, Eddy, Maye, Una, McKay, Kirsten, McWilliam, Catherine, Metcalfe, Kay, Morgan, Sian, Murday, Victoria, Murphy, Helen, Nemeth, Andrea, Nevitt, Louise, Newbury-Ecob, Ruth, Park, Soo-Mi, Paterson, Joan, Payne, Stewart, Perrett, Daniel, Pratt, Norman, Quarrell, Oliver, Randall, Josh, Rankin, Julia, Raymond, Lucy, Robert, Leema, Roberts, Paul, Saggar, Anand, Samant, Shalaka, Sampson, Julian, Sandford, Richard, Selby, Ann, Sequeira, Cheryl, Shearing, Emma, Smith, Audrey, Smith, Kath, Splitt, Miranda, Suri, Mohnish, Sutton, Vivienne, Tatton-Brown, Kate, Temple, I. Karen, Turner, Claire, Varghese, Vinod, Vasudevan, Pradeep, Vogt, Julie, Wakeling, Emma, Wilcox, Sarah, Williams, Denise, Williams, Nicola, Wilson, Louise, Wright, Michael, Yates, Laura, Yau, Michael, Wright, Caroline F, FitzPatrick, David R, Barrett, Jeffrey C

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Effects of fluoxetine on functional outcomes after acute stroke (FOCUS): a pragmatic, double-blind, randomised, controlled trial von Perry, David, Dinsmore, Lynn, Kambafwile, Mary, Idrovo, Luis, Hurley, Lisa, Kerwood, Lauriane, Merritt, Carley, Duty, Suzanna, Lindert, Ralf, Meegada, Madana, Maguire, Holly, Hiden, Joanne, Brodie, Fiona, Barcroft, Heather, Wightman, John, O Neill, Mark, Siddiqui, Amber, Rashmi, Sindhu, Wilson, Laura, Cullen, Claire, Keeling, Alison, Hindle, Julia, Maguire, Stuart, Hamid, Umair, Gaba, Waqar, Mohammed, Niaz, Robinson, Rianne, Mathieson, Philip, Jones, Val, Lush, Audrey, Bell, Jo, Badiani, Bhavna, Guo, Fenglin, Chamberlain, Angela, Donaldson, Dave, Melikyan, Elina, Oconnell, Susan, Hurdowar, Steve, Johnson, Matthew, Moore, Kimberley, Stevens, Angela, Burnip, Rachel, Beranova, Eva, Walker, Susannah, Cain, Rebecca, Willmot, Mark, Bates, Michelle, Pitt Ford, Alexandra, Aubrey, Beth, Howard, Joanne, Dhar, Saikat, Howard-Brown, Jennifer, Imam, Javed, Whitworth, Simon, Mcgee, Joanne, Hannon, Niamh, Mokoena, Langanani, Smart, Amanda, Donaldson, Fiona, Graham, Libby, Rowe, Joy, Munuswamy Vaiyapuri, Elangovan, Thomas, Lisa, Sharon, Storton, Jones, Paul, Johnston, Stuart, Pusalkar, Aparna, Broughton, David, Tryambake, Dinesh, Skotnicka, Agnieszka, Thompson, Jane, Annamalai, Arunkumar, Wilkinson, Peter, Young, Emma, Pereira, Rita, Drummond, Graham, Austin, Duncan, Funnell, Sarah, Jones, Stephanie, Vassallo, Joseph, Leonard, Dee, Wynter, Inez, Janbieh, Joumana, Wade, Lynne, Otter, Linda, Fleming, Amy, Jones, Rhian, Williams, Richard, Mavinamane, Sunanda, Hunt, Lorraine, Haque, Kashif, Gibson, Elspeth, Neves-Silva, Yara, Thompson, Alastair, Ritchings, Andrew, Mcredmond, Catherine, Goulding, Alicia, Punnoose, Sunil, Gordon, Laura, Tarkas, Tillana

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Effects of antiplatelet therapy on stroke risk by brain imaging features of intracerebral haemorrhage and cerebral small vessel diseases: subgroup analyses of the RESTART randomise... von Rinkel, Gabriel, Perry, David, Macleod, Malcolm, Adil-Smith, Jennifer, Perez, Jane, David, Anette, Bayliss, Pauline, Lindert, Ralf, Salih, Isam, Ayres, Georgina, Siddiqui, Amber, Beaty, Teresa, Davies, Caroline, Connor, Lynda, Slade, Peter, Denic, Hayley, Alipio, Francis, Barry, Adrian, Couser, Mandy, Parry, Anthea, Balian, Linda, Vickers, Carinna, Buckley, Clare, Tanate, Alfonso, van Someren, Chloe, Roughan, Caroline, Gregory, Bindu, Allen, Christopher, Pressly, Vanessa, Battersby-Wood, Emma, Blades, Alex, Smith, Fiona, Boxall, Cherish, Buckle, Steve, Elliott, Emma, Sigsworth, Andrew, Sharma, Nikhil, Shaw, Louise, Patel, Bhavini, Bell, Jo, Longland, Barbara, Caine, Sarah, Peters, Jenny, Stevenson, Sarah, Jagpal, Baljit, Krishnamurthy, Vinodh, Webber, Adam, Tayler, Michelle, Rogers, Gill, Clayton, Susan, Charles, Bethan, Kennedy, James, Francis, Jobbin, Finlay, Sarah, Hayhoe, Helen, White, Susan, Jarrett, David, McAlpine, Christine, Henry, Margo, Rudenko, Hannah, Hazel, Beth, Shah, Alex, Baker, John, Walker, Marion, Stanners, Andrew, Guy, Helen, Woodward, Stephen, Herman, Jane, Howard, Joanne, Clay, Caroline, Newton, Sophie, Rayessa, Rayessa, Davies, Ruth, Cherian, Suja, Zahoor, Tajammal, Webster, Timothy, Jenkins, Colin, Hughes, Claire, Homan, Jane, Khan, Mohammad, Ravenhill, Garth, Perfitt, Rebekah, Osborne, Emily, Cuddy, Sarah, Markova, Skarlet, Thomas, Isobel, Pettitt, Kerry, Salehin, Maqsud, Ghaly, George, Ball, Margaret, Bell, Murdina, Ahmed, Iman, Fuller, Tracy, Goorah, Neetish, Bell, Angela, Kelly, Christine, Donaldson, Denise, Kenton, Antony, Pusalkar, Aparna, Leggett, Jacqui

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Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts von Moll, Matthew, Sakornsakolpat, Phuwanat, Shrine, Nick, Hobbs, Brian D, DeMeo, Dawn L, John, Catherine, Guyatt, Anna L, McGeachie, Michael J, Gharib, Sina A, Obeidat, Ma'en, Lahousse, Lies, Wijnant, Sara R A, Brusselle, Guy, Meyers, Deborah A, Bleecker, Eugene R, Li, Xingnan, Tal-Singer, Ruth, Manichaikul, Ani, Rich, Stephen S, Won, Sungho, Kim, Woo Jin, Do, Ah Ra, Washko, George R, Barr, R Graham, Psaty, Bruce M, Bartz, Traci M, Hansel, Nadia N, Barnes, Kathleen, Hokanson, John E, Crapo, James D, Lynch, David, Bakke, Per, Gulsvik, Amund, Hall, Ian P, Wain, Louise, Soler Artigas, María, Jackson, Victoria E, Strachan, David P, Hui, Jennie, James, Alan L, Kerr, Shona M, Polasek, Ozren, Vitart, Veronique, Marten, Jonathan, Rudan, Igor, Kähönen, Mika, Surakka, Ida, Gieger, Christian, Karrasch, Stefan, Rawal, Rajesh, Schulz, Holger, Deary, Ian J, Harris, Sarah E, Enroth, Stefan, Gyllensten, Ulf, Imboden, Medea, Probst-Hensch, Nicole M, Lehtimäki, Terho, Raitakari, Olli T, Langenberg, Claudia, Luan, Jian'an, Wareham, Nick, Zhao, Jing Hua, Hayward, Caroline, Murray, Alison, Porteous, David J, Smith, Blair H, Jarvelin, Marjo-Riitta, Wielscher, Matthias, Joshi, Peter K, Kentistou, Katherine A, Timmers, Paul RHJ, Wilson, James F, Cook, James P, Lind, Lars, Mahajan, Anubha, Morris, Andrew P, Ewert, Ralf, Homuth, Georg, Stubbe, Beate, Weiss, Stefan, Zeggini, Eleftheria, Weiss, Scott T, Silverman, Edwin K, Dudbridge, Frank, Tobin, Martin D, Cho, Michael H

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Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders von Faundes, Víctor, Demos, Michelle K., Goldman, Amy, Lehman, Anna, McKee, Shane, Morton, Jenny, Rankin, Julia, Temple, I. Karen, Adam, Shelin, van Karnebeek, Clara, Aitken, Stuart, Alvi, Mohsan, Ambridge, Kirsty, Jones, Philip, Jones, Wendy D., Mason, Laura E., Tivey, Adrian R., Ahmed, Munaza, Balasubramanian, Meena, Barnicoat, Angela, Bitner-Glindzicz, Maria, Bourdon, Louise, Bradley, Lisa, Burn, John, Colgiu, Irina, Collins, Amanda, Collinson, Morag N., Connell, Fiona, Crow, Yanick, Dabir, Tabib, Davidson, Rosemarie, de Vries, Dylan, Deshpande, Charu, Dixit, Abhijit, Dobbie, Angus, Douzgou, Sofia, Duncan, Alexis, Eason, Jacqueline, Ellard, Sian, Elmslie, Frances, Evans, Karenza, Everest, Sarah, Flinter, Frances, Foulds, Nicola, Ghali, Neeti, Gibbons, Richard, Gill, Harinder, Greene, Philip, Gribble, Susan, Holder, Muriel, Hollingsworth, Georgina, Ingram, Stuart, Jenkins, Lucy, Joss, Shelagh, Kerr, Bronwyn, Kini, Usha, Kraus, Alison, Lachlan, Katherine, Marks, Karen, McConnell, Vivienne, McEntagart, Meriel, McGowan, Ruth, Middleton, Anna, Mohammed, Shehla, O’Shea, Rosie, Ogilvie, Caroline, Ong, Kai-Ren, Parker, Michael J., Patel, Chirag, Paterson, Joan, Payne, Stewart, Prescott, Katrina, Procter, Annie, Purnell, Hellen, Randall, Josh, Rankin, Julia, Raymond, Lucy, Rice, Debbie, Robert, Leema, Samant, Shalaka, Selby, Ann, Sequeira, Cheryl, Shears, Debbie, Smith, Audrey, Smith, Kath, Splitt, Miranda, Squires, Miranda, Tomkins, Susan, Treacy, Becky, Tysoe, Carolyn, Vasudevan, Pradeep, Vijayarangakannan, Parthiban, Vogt, Julie, Wakeling, Emma, Whiteford, Margo, Wilcox, Sarah, Wilkinson, Emily, Firth, Helen V., Wright, Caroline F., FitzPatrick, David R.

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CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

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Effects of Antiplatelet Therapy After Stroke Caused by Intracerebral Hemorrhage: Extended Follow-up of the RESTART Randomized Clinical Trial von Al-Shahi Salman, Rustam, Dennis, Martin S, Sandercock, Peter A. G, Sudlow, Cathie L. M, Wardlaw, Joanna M, Whiteley, William N, Murray, Gordon D, Stephen, Jacqueline, Rodriguez, Aryelly, Lewis, Steff, Werring, David J, White, Phil M

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Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12 von Jackson, Victoria E, Ntalla, Ioanna, Sayers, Ian, Morris, Richard, Whincup, Peter, Casas, Juan-Pablo, Amuzu, Antoinette, Choi, Minkyoung, Dale, Caroline, Kumari, Meena, Engmann, Jorgen, Kalsheker, Noor, Chappell, Sally, Guetta-Baranes, Tamar, McKeever, Tricia M, Palmer, Colin N A, Tavendale, Roger, Holloway, John W, Sayer, Avan A, Dennison, Elaine M, Cooper, Cyrus, Bafadhel, Mona, Barker, Bethan, Brightling, Chris, Bolton, Charlotte E, John, Michelle E, Parker, Stuart G, Moffat, Miriam F, Wardlaw, Andrew J, Connolly, Martin J, Porteous, David J, Smith, Blair H, Padmanabhan, Sandosh, Hocking, Lynne, Stirrups, Kathleen E, Deloukas, Panos, Strachan, David P, Hall, Ian P, Tobin, Martin D, Wain, Louise V

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Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy von Abou Jamra, Rami, Accogli, Andrea, Amburgey, Kimberly, Basinger, Alice A., Ceulemans, Sophia, Charles, Perrine, McRae, Jeremy F., Rajan, Diana, Ambridge, Kirsty, Jones, Philip, Jones, Wendy D., Ahmed, Munaza, Anjum, Uruj, Armstrong, Ruth, Barnicoat, Angela, Bennett, Chris, Blair, Edward, Blyth, Moira, Bourdon, Louise, Brady, Angela, Burn, John, Canham, Natalie, Cilliers, Deirdre, Clayton-Smith, Jill, Coates, Andrea, Cooper, Nicola, Dabir, Tabib, Davies, Sally, Dean, John, Devlin, Gemma, Donnai, Dian, Donnelly, Carina, Evans, Karenza, Fendick, Tina, Goodship, Judith, Green, Andrew, Harrison, Lucy, Holden, Simon, Jarvis, Joanna, Johnson, Diana, Jones, Elizabeth, Kumar, V. K. Ajith, Lachlan, Katherine, Langman, Caroline, Maye, Una, McMullan, Dominic J., McWilliam, Catherine, Metcalfe, Kay, Norman, Andrew, Ogilvie, Caroline, Park, Soo-Mi, Phipps, Julie, Prescott, Katrina, Procter, Annie, Purnell, Hellen, Ross, Alison, Sampson, Julian, Shannon, Nora, Skitt, Zara, Stewart, Fiona, Stewart, Helen, Swaminathan, Ganesh Jawahar, Taylor, Cat, Tein, Mark, Treacy, Becky, Vandersteen, Anthony, Wallwark, Sarah, Waters, Jonathon, Weber, Astrid, Whiteford, Margo, Widaa, Sara, Wilcox, Sarah, Wilkinson, Emily, Parker, Michael, FitzPatrick, David R., Demurger, Florence, Eiset, Saga Elise, Ferrarini, Alessandra, Haack, Tobias B., Hashim, Mona, Jonasson, Amy R., Kok, Fernando, Marcelis, Carlo L.M., McWalter, Kirsty, Mercimek-Andrews, Saadet, Person, Richard, Ramelli, Gian Paolo, Rauch, Anita, Sanchez-Valle, Amarilis, Sattar, Shifteh, Saunders, Carol, Steindl, Katharina, Syrbe, Steffen, Taylor, Jenny C., Trauner, Doris A., Vogel, Ida, Widjaja, Elysa, Zak, Jaroslav, Banka, Siddharth, Rodan, Lance H.

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Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia von Reich, Adi, Cross, J. Helen, Scheffer, Ingrid E., Krishnappa, Netravathi, Awada, Jana, Baralle, Diana, Bernhard, Birgitta, Clasper, Susan, Clayton-Smith, Jill, Cresswell, Lara, Donaldson, Alan, Ellis, Ian, Gaunt, Lorraine, He, Liu, Hewitt, Sarah, Hurst, Jane, Kirk, Claire, Kivuva, Emma, Kumar, Dhavendra, Mansour, Sahar, McCann, Emma, McKee, Shane, Mugalaasi, Hood, Murphy, Helen, Newbury-Ecob, Ruth, Pilz, Daniela T., Pollard, Martin, Pridham, Abigail, Saggar, Anand, Scott, Richard, Shearing, Emma, Smithson, Sarah, Sneddon, Linda, Suri, Mohnish, Tatton-Brown, Kate, Thomson, Jenny, Torokwa, Audrey, Varghese, Vinod, Yau, Michael, Artigas, Maria Soler, Boustred, Chris, Evans, David, Flicek, Paul, Hart, Deborah, Langford, Cordelia, Lawson, Daniel, Li, Rui, O'Donnovan, Michael, Parker, Victoria, Parr, Jeremy R., Paunio, Tiina, Rehnström, Karola, Sun, Jianping, Suvisaari, Jaana, Tachmazidou, Ionna, Williamson, Kathleen A., Wong, Kim, Alachkar, Hana, Ambegaonkar, Gautum, Attwood, Antony, Austin, Steve, Bennett, David, Bibi, Shahnaz, Bleda, Marta, Boggard, Harm, Bradley, John R., Browning, Michael, Clement, Emma, Doffinger, Rainer, Drewe, Elizabeth, Frary, Amy, Ghataorhe, Pavandeep K., Greenhalgh, Alan, Hackett, Scott, Hadinnapola, Charaka, Heemskerk, Johan W.M., Humbert, Marc, James, Roger, Krishnakumar, Deepa, Lawrie, Allan, Lentaigne, Claire, Maimaris, Jesmeen, Maw, Anna, Megy, Karyn, Moledina, Shahin, Morrell, Nicholas, Nejentsev, Sergey, Polwarth, Gary, Quinti, Isabella, Raymond, F. Lucy, Samarghitean, Crina, Sanchis-Juan, Alba, Southgate, Laura, Stauss, Hans, Thrasher, Adrian, Trembath, Richard, Turro, Ernest, Williamson, Catherine, Yeatman, Nigel, Millichap, John J.

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Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries von Shrine, Nick, Guyatt, Anna L., Erzurumluoglu, A. Mesut, Jackson, Victoria E., Hobbs, Brian D., Melbourne, Carl A., Batini, Chiara, Fawcett, Katherine A., Song, Kijoung, Sakornsakolpat, Phuwanat, Boxall, Ruth, Reeve, Nicola F., Obeidat, Ma’en, Zhao, Jing Hua, Wielscher, Matthias, Weiss, Stefan, Kentistou, Katherine A., Cook, James P., Sun, Benjamin B., Zhou, Jian, Hui, Jennie, Karrasch, Stefan, Imboden, Medea, Harris, Sarah E., Marten, Jonathan, Enroth, Stefan, Kerr, Shona M., Surakka, Ida, Vitart, Veronique, Lehtimäki, Terho, Allen, Richard J., Bakke, Per S., Beaty, Terri H., Bossé, Yohan, Brandsma, Corry-Anke, Chen, Zhengming, Crapo, James D., Danesh, John, DeMeo, Dawn L., Dudbridge, Frank, Ewert, Ralf, Gieger, Christian, Gulsvik, Amund, Hansell, Anna L., Hao, Ke, Hokanson, John E., Homuth, Georg, Langenberg, Claudia, Li, Liming, Lin, Kuang, Lind, Lars, Locantore, Nicholas, Luan, Jian’an, Mahajan, Anubha, Maranville, Joseph C., Murray, Alison, Packer, Richard, Parker, Margaret M., Paynton, Megan L., Porteous, David J., Prokopenko, Dmitry, Qiao, Dandi, Rawal, Rajesh, Runz, Heiko, Sayers, Ian, Sin, Don D., Smith, Blair H., Sparrow, David, Tal-Singer, Ruth, Timmers, Paul R. H. J., Van den Berge, Maarten, Whittaker, John C., Woodruff, Prescott G., Yerges-Armstrong, Laura M., Troyanskaya, Olga G., Raitakari, Olli T., Kähönen, Mika, Polašek, Ozren, Gyllensten, Ulf, Rudan, Igor, Deary, Ian J., Probst-Hensch, Nicole M., Schulz, Holger, James, Alan L., Wilson, James F., Zeggini, Eleftheria, Jarvelin, Marjo-Riitta, Wareham, Nick, Silverman, Edwin K., Hayward, Caroline, Morris, Andrew P., Butterworth, Adam S., Scott, Robert A., Walters, Robin G., Meyers, Deborah A., Cho, Michael H., Strachan, David P., Hall, Ian P., Tobin, Martin D., Wain, Louise V.

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

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Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries von Shrine, Nick, Guyatt, Anna L., Erzurumluoglu, A. Mesut, Jackson, Victoria E., Hobbs, Brian D., Melbourne, Carl A., Batini, Chiara, Fawcett, Katherine A., Song, Kijoung, Boxall, Ruth, Reeve, Nicola F., Obeidat, Ma’en, Zhao, Jing Hua, Wielscher, Matthias, Weiss, Stefan, Kentistou, Katherine A., Cook, James P., Sun, Benjamin B., Zhou, Jian, Hui, Jennie, Karrasch, Stefan, Imboden, Medea, Harris, Sarah E, Marten, Jonathan, Enroth, Stefan, Kerr, Shona M., Surakka, Ida, Vitart, Veronique, Lehtimäki, Terho, Allen, Richard J., Bakke, Per S., Beaty, Terri H., Bossé, Yohan, Brandsma, Corry-Anke, Chen, Zhengming, Crapo, James D., Danesh, John, DeMeo, Dawn L., Dudbridge, Frank, Ewert, Ralf, Gieger, Christian, Gulsvik, Amund, Hansell, Anna L., Hao, Ke, Hokanson, John E., Homuth, Georg, Joubert, Philippe, Langenberg, Claudia, Li, Liming, Lin, Kuang, Lind, Lars, Locantore, Nicholas, Luan, Jian’an, Mahajan, Anubha, Maranville, Joseph C., Murray, Alison, Packer, Richard, Parker, Margaret M., Paynton, Megan L., Porteous, David J., Prokopenko, Dmitry, Qiao, Dandi, Rawal, Rajesh, Runz, Heiko, Sayers, Ian, Sin, Don D, Smith, Blair H, Sparrow, David, Tal-Singer, Ruth, Timmers, Paul R. H. J., Van den Berge, Maarten, Whittaker, John C., Woodruff, Prescott G., Yerges-Armstrong, Laura M., Troyanskaya, Olga G., Raitakari, Olli T., Kähönen, Mika, Polašek, Ozren, Gyllensten, Ulf, Rudan, Igor, Deary, Ian J., Probst-Hensch, Nicole M., Schulz, Holger, James, Alan L, Wilson, James F., Zeggini, Eleftheria, Jarvelin, Marjo-Riitta, Wareham, Nick, Silverman, Edwin K., Hayward, Caroline, Morris, Andrew P., Butterworth, Adam S., Scott, Robert A., Walters, Robin G., Meyers, Deborah A., Cho, Michael H., Strachan, David P., Hall, Ian P., Tobin, Martin D., Wain, Louise V.

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Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations von Sakornsakolpat, Phuwanat, Prokopenko, Dmitry, Lamontagne, Maxime, Reeve, Nicola F, Guyatt, Anna L, Jackson, Victoria E, Shrine, Nick, Qiao, Dandi, Bartz, Traci M, Kim, Deog Kyeom, Lee, Mi Kyeong, Latourelle, Jeanne C, Li, Xingnan, Morrow, Jarrett D, Obeidat, Ma'en, Wyss, Annah B, Bakke, Per, Barr, R. Graham, Beaty, Terri H, Belinsky, Steven A, Brusselle, Guy G, Crapo, James D, de Jong, Kim, DeMeo, Dawn L, Fingerlin, Tasha E, Gharib, Sina A, Gulsvik, Amund, Hall, Ian P, Hokanson, John E, Kim, Woo Jin, Lomas, David A, London, Stephanie J, Meyers, Deborah A, O'Connor, George T, Rennard, Stephen, Schwartz, David A, Sliwinski, Pawel, Sparrow, David, Strachan, David P, Tal-Singer, Ruth, Tesfaigzi, Yohannes, Vestbo, Jorgen, Vonk, Judith M, Yim, Jae-Joon, Zhou, Xiaobo, Bosse, Yohan, Manichaikul, Ani, Lahousse, Lies, Silverman, Edwin K, Boezen, H. Marike, Wain, Louise, Tobin, Martin D, Hobbs, Brian D, Cho, Michael H, Batini, Chiara, Zhao, Jing Hua, Wielscher, Matthias, Weiss, Stefan, Kentistou, Katherine A, Cook, James P, Hui, Jennie, Karrasch, Stefan, Imboden, Medea, Harris, Sarah E, Marten, Jonathan, Enroth, Stefan, Kerr, Shona M, Surakka, Ida, Vitart, Veronique, Lehtimaki, Terho, Ewert, Ralf, Gieger, Christian, Homuth, Georg, Joshi, Peter K, Langenberg, Claudia, Lind, Lars, Luan, Jianan, Mahajan, Anubha, Murray, Alison, Porteous, David J, Rawal, Rajesh, Smith, Blair H, Timmers, Paul R.H.J, Raitakari, Olli T, Kahonen, Mika, Polasek, Ozren, Gyllensten, Ulf, Rudan, Igor, Deary, Ian J, Probst-Hensch, Nicole M, Schulz, Holger, James, Alan L, Wilson, James F, Stubbe, Beate, Zeggini, Eleftheria, Jarvelin, Marjo-Riitta, Wareham, Nick, Hayward, Caroline, Morris, Andrew P, Agusti, Alvar

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Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12 von Jackson, Victoria E, Ntalla, Ioanna, Sayers, Ian, Morris, Richard, Whincup, Peter, Casas, Juan-Pablo, Amuzu, Antoinette, Choi, Minkyoung, Dale, Caroline, Kumari, Meena, Engmann, Jorgen, Kalsheker, Noor, Chappell, Sally, Guetta-Baranes, Tamar, McKeever, Tricia M, Palmer, Colin NA, Tavendale, Roger, Holloway, John W, Sayer, Avan A, Dennison, Elaine M, Cooper, Cyrus, Bafadhel, Mona, Barker, Bethan, Brightling, Chris, Bolton, Charlotte E, John, Michelle E, Parker, Stuart G, Moffat, Miriam F, Wardlaw, Andrew J, Connolly, Martin J, Porteous, David J, Smith, Blair H, Padmanabhan, Sandosh, Hocking, Lynne, Stirrups, Kathleen E, Deloukas, Panos, Strachan, David P, Hall, Ian P, Tobin, Martin D, Wain, Louise V

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Meta-analysis of exome array data identifies six novel genetic loci for lung function von Jackson, Victoria E., Latourelle, Jeanne C., Wain, Louise V., Smith, Albert V., Grove, Megan L., Bartz, Traci M., Obeidat, Ma'en, Province, Michael A., Gao, Wei, Qaiser, Beenish, Porteous, David J., Cassano, Patricia A., Ahluwalia, Tarunveer S., Grarup, Niels, Li, Jin, Altmaier, Elisabeth, Marten, Jonathan, Harris, Sarah E., Manichaikul, Ani, Pottinger, Tess D., Li-Gao, Ruifang, Lind-Thomsen, Allan, Mahajan, Anubha, Lahousse, Lies, Imboden, Medea, Teumer, Alexander, Prins, Bram, Lyytikäinen, Leo-Pekka, Eiriksdottir, Gudny, Franceschini, Nora, Sitlani, Colleen M., Brody, Jennifer A., Bossé, Yohan, Timens, Wim, Kraja, Aldi, Loukola, Anu, Tang, Wenbo, Liu, Yongmei, Bork-Jensen, Jette, Justesen, Johanne M., Linneberg, Allan, Lange, Leslie A., Rawal, Rajesh, Karrasch, Stefan, Huffman, Jennifer E., Smith, Blair H., Davies, Gail, Burkart, Kristin M., Mychaleckyj, Josyf C., Bonten, Tobias N., Enroth, Stefan, Lind, Lars, Brusselle, Guy G., Kumar, Ashish, Stubbe, Beate, Kähönen, Mika, Wyss, Annah B., Psaty, Bruce M., Heckbert, Susan R., Hao, Ke, Rantanen, Taina, Kritchevsky, Stephen B., Lohman, Kurt, Skaaby, Tea, Pisinger, Charlotta, Hansen, Torben, Schulz, Holger, Polasek, Ozren, Campbell, Archie I., Starr, John M., Rich, Stephen S., Mook-Kanamori, Dennis O., Johansson, Åsa, Ingelsson, Erik, Uitterlinden, André G., Weiss, Stefan, Raitakari, Olli T., Gudnason, Vilmundur, North, Kari E., Gharib, Sina A., Sin, Don D., Taylor, Kent D., O'Connor, George T., Kaprio, Jaakko, Harris, Tamara B., Pederson, Oluf, Vestergaard, Henrik, Wilson, James G., Strauch, Konstantin, Hayward, Caroline, Kerr, Shona M., Deary, Ian J., Barr, R. Graham, de Mutsert, Renée, Gyllensten, Ulf, Morris, Andrew P., Ikram, M. Arfan, Probst-Hensch, Nicole, Gläser, Sven, Zeggini, Eleftheria

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The contribution of X-linked coding variation to severe developmental disorders von Gardner, Eugene J, Sifrim, Alejandro, Neville, Matthew D. C, Gallone, Giuseppe, FitzPatrick, David R, Firth, Helen V, Borras, Silvia, Clark, Caroline, Miedzybrodzka, Zosia, Donnelly, Deirdre, Magee, Alex, McKee, Shane, Morrison, Patrick J, Stewart, Fiona, Cooper, Nicola, Islam, Lily, Jarvis, Joanna, Lim, Derek, Morton, Jenny, Ong, Kai-Ren, Turton, Sarah, Vogt, Julie, Hills, Alison, Low, Karen, Newbury-Ecob, Ruth, Scurr, Ingrid, Tooley, Madeleine, Armstrong, Ruth, Holden, Simon, Reid, Evan, Woods, Geoff, Bradley, Lisa, Comerford, Joanne, Mavrak, Eleni, Cleary, Elaine, Baple, Emma, Brewer, Carole, Kivuva, Emma, Turnpenny, Peter, Bradley, Therese, Davidson, Rosemarie, Whiteford, Margo, Barnicoat, Angela, Hurst, Jane, Jenkins, Lucy, Jones, Wendy, Kumar, V.K.Ajith, Lees, Melissa, Male, Alison, Rosser, Elisabeth, Josifova, Dragana, Roworth, Wendy, Ryten, Mina, Yau, Shu, Campbell, Jennifer, Coates, Andrea, Dobbie, Angus, Jewell, Rosalyn, Dixit, Abhijit, Harrison, Rachel, Sharif, Abid, Suri, Mohnish, Vasudevan, Pradeep, Canham, Natalie, Howard, Emma, Weber, Astrid, Clayton-Smith, Jill, Douzgou, Sofia, Kerr, Bronwyn, Wright, Ronnie, Bourn, David, Hellens, Steve, Montgomery, Tara, Straub, Volker, Allen, Zoe, Bernhard, Birgitta, Brady, Angela, Brooks, Claire, Holder, Susan, Carmichael, Jenny, Kini, Usha, Nemeth, Andrea, Wilkie, Andrew, Albaba, Shadi, Baker, Duncan, Balasubramanian, Meena, Johnson, Diana, Stewart, Alison, Crosby, Charlene, Jin, Huilin, Lahiri, Nayana, Kamath, Arveen, Mugalaasi, Hood, Pottinger, Caroline, Procter, Annie, Varghese, Vinod, Daniels, Stacey, Hunt, David, Lachlan, Katherine, Wellesley, Diana

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