Development and Testing of an Electronic Health Record‐Integrated Patient‐Reported Outcome Application and Intervention to Improve Efficiency of Rheumatoid Arthritis Care von Solomon, Daniel H., Dalal, Anuj K., Landman, Adam B., Santacroce, Leah, Altwies, Hallie, Stratton, Jackie, Rudin, Robert S.

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Mobile health applications for individuals with psoriatic arthritis von Awad, Rami, Pham, Tammy, Stratton, Jackie, Leibowitz, Evan, Solomon, Daniel H

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Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability von Proos, Anne, Gécz, Jozef, Hackett, Anna, Ramsden, Sarah L, Shoubridge, Cheryl, Gardner, Alison, Stratton, Michael R, Harvey, Robert J, Raymond, F Lucy, Field, Michael, Murphy, Jessica A, Puusepp, Helen, Schwartz, Charles E, Shaw, Marie, Turner, Gill, Abidi, Fatima, Walikonis, Randall S, Futreal, P Andrew, Tarpey, Patrick S, Stevenson, Roger E, Rujirabanjerd, Sinitdhorn, Boyle, Jackie

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Fine-Scale Survey of X Chromosome Copy Number Variants and Indels Underlying Intellectual Disability von Whibley, Annabel C., Plagnol, Vincent, Tarpey, Patrick S., Abidi, Fatima, Fullston, Tod, Choma, Maja K., Boucher, Catherine A., Shepherd, Lorraine, Willatt, Lionel, Parkin, Georgina, Smith, Raffaella, Futreal, P. Andrew, Shaw, Marie, Boyle, Jackie, Licata, Andrea, Skinner, Cindy, Stevenson, Roger E., Turner, Gillian, Field, Michael, Hackett, Anna, Schwartz, Charles E., Gecz, Jozef, Stratton, Michael R., Raymond, F. Lucy

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Influence of primary care practices on patients' uptake of diabetic retinopathy screening: a qualitative case study von Lindenmeyer, Antje, Sturt, Jackie A, Hipwell, Alison, Stratton, Irene M, Al-Athamneh, Nidal, Gadsby, Roger, O'Hare, Joseph Paul, Scanlon, Peter H

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A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A von Corbett, Mark A, Dudding-Byth, Tracy, Crock, Patricia A, Botta, Elena, Christie, Louise M, Nardo, Tiziana, Caligiuri, Giuseppina, Hobson, Lynne, Boyle, Jackie, Mansour, Albert, Friend, Kathryn L, Crawford, Jo, Jackson, Graeme, Vandeleur, Lucianne, Hackett, Anna, Tarpey, Patrick, Stratton, Michael R, Turner, Gillian, Gécz, Jozef, Field, Michael

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Mutations in CUL4B, Which Encodes a Ubiquitin E3 Ligase Subunit, Cause an X-linked Mental Retardation Syndrome Associated with Aggressive Outbursts, Seizures, Relative Macrocephaly... von Tarpey, Patrick S., Raymond, F. Lucy, O’Meara, Sarah, Edkins, Sarah, Teague, Jon, Butler, Adam, Dicks, Ed, Stevens, Claire, Tofts, Calli, Avis, Tim, Barthorpe, Syd, Buck, Gemma, Cole, Jennifer, Gray, Kristian, Halliday, Kelly, Harrison, Rachel, Hills, Katy, Jenkinson, Andrew, Jones, David, Menzies, Andrew, Mironenko, Tatiana, Perry, Janet, Raine, Keiran, Richardson, David, Shepherd, Rebecca, Small, Alexandra, Varian, Jennifer, West, Sofie, Widaa, Sara, Mallya, Uma, Moon, Jenny, Luo, Ying, Holder, Susan, Smithson, Sarah F., Hurst, Jane A., Clayton-Smith, Jill, Kerr, Bronwyn, Boyle, Jackie, Shaw, Marie, Vandeleur, Lucianne, Rodriguez, Jayson, Slaugh, Rachel, Easton, Douglas F., Wooster, Richard, Bobrow, Martin, Srivastava, Anand K., Stevenson, Roger E., Schwartz, Charles E., Turner, Gillian, Gecz, Jozef, Futreal, P. Andrew, Stratton, Michael R., Partington, Michael

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Widespread Myofascial Dysfunction and Regional Sensitization in Women with Endometriosis-associated Chronic Pelvic Pain (P2.096) von Karp, Barbara, Tandon, Hannah, Sinaii, Ninet, Shah, Jay, Aredo, Jackie, Stratton, Pamela

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Integration of pre-hospital electrocardiograms and ST-elevation myocardial infarction receiving center (SRC) networks: impact on Door-to-Balloon times across 10 independent regions von Rokos, Ivan C, French, William J, Koenig, William J, Stratton, Samuel J, Nighswonger, Beverly, Strunk, Brian, Jewell, Jackie, Mahmud, Ehtisham, Dunford, James V, Hokanson, Jon, Smith, Stephen W, Baran, Kenneth W, Swor, Robert, Berman, Aaron, Wilson, B Hadley, Aluko, Akinyele O, Gross, Brian W, Rostykus, Paul S, Salvucci, Angelo, Dev, Vishva, McNally, Bryan, Manoukian, Steven V, King, 3rd, Spencer B

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CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes von Hackett, Anna, Tarpey, Patrick S, Licata, Andrea, Cox, James, Whibley, Annabel, Boyle, Jackie, Rogers, Carolyn, Grigg, John, Partington, Michael, Stevenson, Roger E, Tolmie, John, Yates, John RW, Turner, Gillian, Wilson, Meredith, Futreal, Andrew P, Corbett, Mark, Shaw, Marie, Gecz, Jozef, Raymond, F Lucy, Stratton, Michael R, Schwartz, Charles E, Abidi, Fatima E

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Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans von Wu, Ye, Arai, Amy C, Rumbaugh, Gavin, Srivastava, Anand K, Turner, Gillian, Hayashi, Takashi, Suzuki, Erika, Jiang, Yuwu, Zhang, Lilei, Rodriguez, Jayson, Boyle, Jackie, Tarpey, Patrick, Raymond, F. Lucy, Nevelsteen, Joke, Froyen, Guy, Stratton, Mike, Futreal, Andy, Gecz, Jozef, Stevenson, Roger, Schwartz, Charles E, Valle, David, Huganir, Richard L, Wang, Tao

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Mutations in ZDHHC9, Which Encodes a Palmitoyltransferase of NRAS and HRAS, Cause X-Linked Mental Retardation Associated with a Marfanoid Habitus von Raymond, F. Lucy, Tarpey, Patrick S., Edkins, Sarah, Tofts, Calli, O’Meara, Sarah, Teague, Jon, Butler, Adam, Stevens, Claire, Barthorpe, Syd, Buck, Gemma, Cole, Jennifer, Dicks, Ed, Gray, Kristian, Halliday, Kelly, Hills, Katy, Hinton, Jonathon, Jones, David, Menzies, Andrew, Perry, Janet, Raine, Keiran, Shepherd, Rebecca, Small, Alexandra, Varian, Jennifer, Widaa, Sara, Mallya, Uma, Moon, Jenny, Luo, Ying, Shaw, Marie, Boyle, Jackie, Kerr, Bronwyn, Turner, Gillian, Quarrell, Oliver, Cole, Trevor, Easton, Douglas F., Wooster, Richard, Bobrow, Martin, Schwartz, Charles E., Gecz, Jozef, Stratton, Michael R., Futreal, P. Andrew

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Gene-gene interactions in breast cancer susceptibility von Turnbull, Clare, Seal, Sheila, Renwick, Anthony, Warren-Perry, Margaret, Hughes, Deborah, Elliott, Anna, Pernet, David, Peock, Susan, Adlard, Julian W., Barwell, Julian, Berg, Jonathan, Brady, Angela F., Brewer, Carole, Brice, Glen, Chapman, Cyril, Cook, Jackie, Davidson, Rosemarie, Donaldson, Alan, Douglas, Fiona, Greenhalgh, Lynn, Henderson, Alex, Izatt, Louise, Kumar, Ajith, Lalloo, Fiona, Miedzybrodzka, Zosia, Morrison, Patrick J, Paterson, Joan, Porteous, Mary, Rogers, Mark T., Shanley, Susan, Walker, Lisa, Ahmed, Munaza, Eccles, Diana, Evans, D. Gareth, Donnelly, Peter, Easton, Douglas F., Stratton, Michael R., Rahman, Nazneen

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Integration of Pre-Hospital Electrocardiograms and ST-Elevation Myocardial Infarction Receiving Center (SRC) Networks von Rokos, Ivan C., MD, French, William J., MD, Koenig, William J., MD, Stratton, Samuel J., MD, MPH, Nighswonger, Beverly, RN, Strunk, Brian, MD, Jewell, Jackie, RN, Mahmud, Ehtisham, MD, Dunford, James V., MD, Hokanson, Jon, MD, Smith, Stephen W., MD, Baran, Kenneth W., MD, Swor, Robert, DO, Berman, Aaron, MD, Wilson, B. Hadley, MD, Aluko, Akinyele O., MD, Gross, Brian W., MD, Rostykus, Paul S., MD, MPH, Salvucci, Angelo, MD, Dev, Vishva, MD, McNally, Bryan, MD, MPH, Manoukian, Steven V., MD, King, Spencer B., MD

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The Physical Activity Signposting Scheme (PASS): the A-CLASS project von Hepples, J, Stratton, G

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Corrigendum to: CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes von Hackett, Anna, Tarpey, Patrick S, Licata, Andrea, Cox, James, Whibley, Annabel, Boyle, Jackie, Rogers, Carolyn, Grigg, John, Partington, Michael, Stevenson, Roger E, Tolmie, John, Yates, John R W, Turner, Gillian, Wilson, Meredith, Futreal, Andrew P, Corbett, Mark, Shaw, Marie, Gecz, Jozef, Raymond, F Lucy, Stratton, Michael R, Schwartz, Charles E, Abidi, Fatima E

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Erratum: Corrigendum to: CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes von Hackett, Anna, Tarpey, Patrick S, Licata, Andrea, Cox, James, Whibley, Annabel, Boyle, Jackie, Rogers, Carolyn, Grigg, John, Partington, Michael, Stevenson, Roger E, Tolmie, John, Yates, John R W, Turner, Gillian, Wilson, Meredith, Futreal, Andrew P, Corbett, Mark, Shaw, Marie, Gecz, Jozef, Raymond, F Lucy, Stratton, Michael R, Schwartz, Charles E, Abidi, Fatima E

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Correction: Corrigendum to: CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes von Hackett, Anna, Tarpey, Patrick S, Licata, Andrea, Cox, James, Whibley, Annabel, Boyle, Jackie, Rogers, Carolyn, Grigg, John, Partington, Michael, Stevenson, Roger E, Tolmie, John, Yates, John R W, Turner, Gillian, Wilson, Meredith, Futreal, Andrew P, Corbett, Mark, Shaw, Marie, Gecz, Jozef, Raymond, F Lucy, Stratton, Michael R, Schwartz, Charles E, Abidi, Fatima E

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Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans von Wu, Ye, Arai, Amy C, Rumbaugh, Gavin, Srivastava, Anand K, Turner, Gillian, Hayashi, Takashi, Suzuki, Erika, Jiang, Yuwu, Zhang, Lilei, Rodriguez, Jayson, Boyle, Jackie, Tarpey, Patrick, Raymond, F. Lucy, Nevelsteen, Joke, Froyen, Guido, Stratton, Mike, Futreal, Andy, Gecz, Jozef, Stevenson, Roger, Schwartz, Charles E, Valle, David, Huganir, Richard L, Wang, Tao

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Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants von Newport, Melanie, Sirugo, Giorgio, Lyons, Emily, Vannberg, Fredrik, Hill, Adrian V.S, Bradbury, Linda A, Farrar, Claire, Pointon, Jennifer J, Wordsworth, Paul, Brown, Matthew A, Franklyn, Jayne A, Heward, Joanne M, Simmonds, Matthew J, Gough, Stephen C.L, Seal, Sheila, Stratton, Michael R, Rahman, Nazneen, Ban, Maria, Goris, An, Sawcer, Stephen J, Compston, Alastair, Conway, David, Jallow, Muminatou, Rockett, Kirk A, Kwiatkowski, Dominic P, Bumpstead, Suzannah J, Chaney, Amy, Downes, Kate, Ghori, Mohammed J.R, Gwilliam, Rhian, Hunt, Sarah E, Inouye, Michael, Keniry, Andrew, King, Emma, McGinnis, Ralph, Potter, Simon, Ravindrarajah, Rathi, Whittaker, Pamela, Widden, Claire, Withers, David, Deloukas, Panos, Leung, Hin-Tak, Nutland, Sarah, Stevens, Helen E, Walker, Neil M, Todd, John A, Easton, Doug, Clayton, David G, Burton, Paul R, Tobin, Martin D, Barrett, Jeffrey C, Evans, David M, Morris, Andrew P, Cardon, Lon R, Cardin, Niall J, Davison, Dan, Ferreira, Teresa, Pereira-Gale, Joanne, Hallgrimsdottir, Ingeleif B, Howie, Bryan N, Marchini, Jonathan L, Spencer, Chris C.A, Su, Zhan, Teo, Yik Ying, Vukcevic, Damjan, Donnelly, Peter, Bentley, David, Caulfield, Mark, Craddock, Nick, Farrall, Martin, Hall, Alistair S, Hattersley, Andrew T, Matthew, Christopher G, McCarthy, Mark I, Ouwehand, Willem H, Parkes, Miles, Pembrey, Marcus, Samani, Nilesh J, Worthington, Jane, Mitchell, Sarah L, Newby, Paul R, Brand, Oliver J, Carr-Smith, Jackie, Pearce, Simon H.S, McGinnis, R, Keniry, A, Deloukas, P, Reveille, John D, Zhou, Xiaodong, Sims, Anne-Marie, Dowling, Alison, Taylor, Jacqueline, Doan, Tracy, Davis, John C, Savage, Laurie, Ward, Michael M, Learch, Thomas L, Weisman, Michael H

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