Monitoring the emergence of community transmission of influenza A/H1N1 2009 in England: a cross sectional opportunistic survey of self sampled telephone callers to NHS Direct by Elliot, Alex J, Powers, Cassandra, Thornton, Alicia, Obi, Chinelo, Hill, Caterina, Simms, Ian, Waight, Pauline, Maguire, Helen, Foord, David, Povey, Enid, Wreghitt, Tim, Goddard, Nichola, Ellis, Joanna, Bermingham, Alison, Sebastianpillai, Praveen, Lackenby, Angie, Zambon, Maria, Brown, David, Smith, Gillian E, Gill, O Noel

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Erratum to “Influenza vaccine uptake in the elderly: results from a rapid assessment of new government policy in England for the winters 2000/2001 and 2001/2002” [Vaccine 21 (2003)... by Joseph, Carol, Goddard, Nichola

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Influenza vaccine uptake in the elderly: results from a rapid assessment of the effectiveness of new government policy in England for the winters 2000/2001 and 2001/2002 by Joseph, Carol, Goddard, Nichola

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Influenza vaccine uptake and distribution in England and Wales using data from the General Practice Research Database, 1989/90–2003/04 by Joseph, Carol, Goddard, Nichola, Gelb, David

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Influenza vaccine uptake and distribution in England and Wales using data from the General Practice Research Database, 1989/90-2003/04 by Joseph, Carol, Goddard, Nichola, Gelb, David

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Influenza present: the impact of the 1999/2000 epidemic on morbidity and mortality in the UK by Watson, John M, Goddard, Nichola, Joseph, Carol, Zambon, Maria

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The genetic interpretation of area under the ROC curve in genomic profiling by Wray, Naomi R, Yang, Jian, Goddard, Michael E, Visscher, Peter M

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ObStruct: a method to objectively analyse factors driving population structure using Bayesian ancestry profiles by Gayevskiy, Velimir, Klaere, Steffen, Knight, Sarah, Goddard, Matthew R

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Monocyte/Macrophage Suppression in CD11b Diphtheria Toxin Receptor Transgenic Mice Differentially Affects Atherogenesis and Established Plaques by Stoneman, Victoria, Braganza, Denise, Figg, Nichola, Mercer, John, Lang, Richard, Goddard, Martin, Bennett, Martin

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Chronic Apoptosis of Vascular Smooth Muscle Cells Accelerates Atherosclerosis and Promotes Calcification and Medial Degeneration by Clarke, Murray C.H, Littlewood, Trevor D, Figg, Nichola, Maguire, Janet J, Davenport, Anthony P, Goddard, Martin, Bennett, Martin R

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Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis by Lee, S Hong, Harold, Denise, Nyholt, Dale R, Goddard, Michael E, Zondervan, Krina T, Williams, Julie, Montgomery, Grant W, Wray, Naomi R, Visscher, Peter M

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Selenoprotein deficiency disorder predisposes to aortic aneurysm formation by Schoenmakers, Erik, Marelli, Federica, Jørgensen, Helle F., Visser, W. Edward, Moran, Carla, Groeneweg, Stefan, Avalos, Carolina, Jurgens, Sean J., Figg, Nichola, Finigan, Alison, Wali, Neha, Agostini, Maura, Wardle-Jones, Hannah, Lyons, Greta, Rusk, Rosemary, Gopalan, Deepa, Twiss, Philip, Visser, Jacob J., Goddard, Martin, Nashef, Samer A. M., Heijmen, Robin, Clift, Paul, Sinha, Sanjay, Pirruccello, James P., Ellinor, Patrick T., Busch-Nentwich, Elisabeth M., Ramirez-Solis, Ramiro, Murphy, Michael P., Persani, Luca, Bennett, Martin, Chatterjee, Krishna

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Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent by de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, John K., Goddard, Michael E., O’Donovan, Michael C., Purcell, Shaun M., Posthuma, Danielle, Visscher, Peter M., Wray, Naomi R., Keller, Matthew C.

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Patterns of opioid use after surgical discharge: a multicentre, prospective cohort study in 25 countries by Elhadi, Muhammed, Ohis, Christina, Raubenheimer, Kyle, Ludbrook, Isabella, Watson, David, Wong, Samantha, Stevens, Sean, Gunn, Emma, Rigby, Naomi, Byrnes, Lauren, Jin, Rong, Tu, Hien, Soni, Akshay, Patel, Diya, Laura, Sharon, Brown, Matthew, Swan, Daniel, Sritharan, Mithra, Tan, Wen Po Jonathan, Gan, Siang Wei, Markovic, Aleksandra, Foo, Jonathon, Morgan, Monica, Loder, Rebecca, Kanczuk, Marcelo, Clanfield, Matthew, Lew, Chen, Koh, Imogen, Donaldson, Olivia, Vidanagama, Sasini, Edwards, Liam, Lai, Sherman, Hou, Zhen, Diab, Menna, Hussien, Aya, Roshdy, Mo'men, Elnagar, Rahma, Laymon, Mahmoud, Teema, Eman, Ads, Alaa Mohamed, Valaroutsou, Olga Maria, Arnaoutoglou, Eleni, Traina, Francesco, Cerinic, Pietro Matucci, Massadeh, Noor, Alatefi, Dawood, Muqbel, Ro‐a, Al‐Haek, Safa', Ghemmied, Malak, Alharam, Abtisam, Swalem, Aisha, Ahmed, Habeeba, Abozid, Anwaar, Alaqoubi, Retaj, Alkchr, Mohamd A A, Alsari, Najah, Zakaria, Andee Dzulkarnaen, Zakaria, Mohd Zaim, Noor, Zaidatul Husna Mohamad, Ren, Seifei, Jinu, Puja, Liu, Yizhuo, Casciola, Francesca, Hakak, Fatima, Quek, Nicholas, Lam, Charles, Walsh, Eamon, Maxwell, Temiloluwa Peace, Ifoto, Oghenekaro, Okon, Seubong‐Abasi Imoh, Mohammed, Caleb, umar, Abubakar, Okunlola, Abiodun, Sulaiman, Bilal, Akpamgbo, Chukwunonso Nnamdi, Sani, Samuel Ali, Ammar, Ahmed Siddique, Butyrskii, Aleksandr, Azhari, Malaz, Babekir, Enas Mohammedtom Abdulhameed, Ali, Rzan Ali Hamedelneel, Yassin, Mohamed, Hilal, Nadir, Mohammed, Omeralfarouk, Osman, Walaa, Alnour, Ammar, Babiker, Afra, Elhadi, Rawan Elnoman, Osman, Fatima, Abdalla, Mohamed Galal Ali, Demirkiran, Mehmet Ali, Ozkan, Esin, Benek, Duygu Ece, Capar, Mehmet Ali, Bozkir, Haktan Ovul, Yuzgec, Ayse Nilufer, Ozbilen, Melis, Aral, Canan, Certel, Alperen Taha, Durdu, Beyza

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SARS-CoV-2 Vaccine Responses in Individuals with Antibody Deficiency: Findings from the COV-AD Study by Shields, Adrian M., Faustini, Sian E., Hill, Harriet J., Al-Taei, Saly, Tanner, Chloe, Ashford, Fiona, Workman, Sarita, Moreira, Fernando, Verma, Nisha, Wagg, Hollie, Heritage, Gail, Campton, Naomi, Stamataki, Zania, Klenerman, Paul, Thaventhiran, James E. D., Goddard, Sarah, Johnston, Sarah, Huissoon, Aarnoud, Bethune, Claire, Elcombe, Suzanne, Lowe, David M., Patel, Smita Y., Savic, Sinisa, Burns, Siobhan O., Richter, Alex G.

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Biologic therapy in rare eosinophil-associated disorders: remaining questions and translational research opportunities by Khoury, Paneez, Roufosse, Florence, Kuang, Fei Li, Ackerman, Steven J, Akuthota, Praveen, Bochner, Bruce S, Johansson, Mats W, Mathur, Sameer K, Ogbogu, Princess U, Spencer, Lisa A, Wechsler, Michael E, Zimmermann, Nives, Klion, Amy D

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Reanalysis of RNA sequencing data ends diagnostic odyssey and expands the phenotypic spectrum of congenital titinopathy by McNamee, Lucy, Huang, Alden, Wang, Lee‐kai, Buckley, Anne F., Adams, David R., Afzali, Ben, Allworth, Aimee, Alvey, Justin, Andrews, Ashley, Bacino, Carlos A., Bademci, Guney, Baldridge, Dustin, Bale, Jim, Barbouth, Deborah, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Borja, Nicholas, Briere, Lauren C., Callaway, Kaitlin, Chanprasert, Sirisak, Coggins, Matthew, Craigen, William J., Cuddapah, Vishnu, Darr, Kahlen, Dipple, Katrina, Doherty, Daniel, Douglas, Jessica, Emrick, Lisa T., Eng, Christine M., Fogel, Brent L., Fu, Jiayu, Glass, Ian, Gropman, Andrea, Halley, Meghan C., Hassey, Kelly, Hayes, Nichole, Hing, Anne, Horike‐Pyne, Martha, Huang, Alden, Huang, Yan, Karasozen, Yigit, Ketkar, Shamika, Kilich, Gonench, Klee, Eric, Kohler, Jennefer N., Korrick, Susan, Kravets, Elijah, Lalani, Seema R., Latchman, Kumarie, LeBlanc, Kimberly, Liu, Pengfei, Longo, Nicola, MacRae, Calum A., Maghiro, AudreyStephannie, Mahoney, Rachel, Malicdan, May Christine V., Martin, Beth A., Miller, Danny, Moretti, Paolo, Mulvihill, Lindsay, Neumann, Serena, Novacic, Donna, Orengo, James P., Pace, Laura, Pak, Stephen, Parker, Neil H., Pinto e Vairo, Filippo, Posey, Jennifer E., Potocki, Lorraine, Rader, Daniel J., Rosenfeld, Jill A., Ruzhnikov, Maura, Sampson, Jacinda B., Schoch, Kelly, Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Skelton, Tammi, Spillmann, Rebecca C., Stergachis, Andrew, Stoler, Joan M., Sutton, Shirley, Sweetser, David A., Tabor, Holly K., Tan, Queenie, Tan, Amelia L. M., Tifft, Cynthia J., Viskochil, Dave, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wood, Heidi, Worley, Kim

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Advancing Equity in Rare Disease Research: Insights From the Undiagnosed Disease Network by Borja, Nicholas A, Tinker, Rory J, Bivona, Stephanie A, Smith, Carson A, Locker, Theodore Krijnse, Fernandes, Samuela, Phillips, 3rd, John A, Stoler, Justin, Taylor, Herman, Zuchner, Stephan, Tekin, Mustafa

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Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant by Gulsevin, Alican, Hamid, Rizwan, Neumann, Serena, Phillips, John A., Adams, David R., Afzali, Ben, Andrews, Ashley, Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bayrak‐Toydemir, Pinar, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Bonner, Devon, Borja, Nicholas, Butte, Manish J., Byrd, William E., Callaway, Kaitlin, Carvalho, George, Chanprasert, Sirisak, Chinn, Ivan, Clark, Gary D., Cogan, Joy D., Coggins, Matthew, Corner, Brian, Dipple, Katrina, Doherty, Daniel, Douglas, Jessica, Emrick, Lisa T., Eng, Christine M., Fogel, Brent L., Fu, Jiayu, Glass, Ian, Gropman, Andrea, Halley, Meghan C., Hassey, Kelly, Hayes, Nichole, Hing, Anne, Horike‐Pyne, Martha, Huang, Alden, Huang, Yan, Kaitryn, Emerald, Kanca, Oguz, Kohler, Jennefer N., Krakow, Deborah, Lam, Christina, Lanpher, Brendan C., Lanza, Ian R., Liu, Pengfei, Longo, Nicola, Mahoney, Rachel, Marth, Gabor, McCray, Alexa T., Might, Matthew, Miller, Danny, Moretti, Paolo, Mulvihill, John J., Mulvihill, Lindsay, Neumann, Serena, Novacic, Donna, Orengo, James P., Pace, Laura, Pak, Stephen, Parker, Neil H., Pinto e Vairo, Filippo, Posey, Jennifer E., Potocki, Lorraine, Rader, Daniel J., Rosenfeld, Jill A., Ruzhnikov, Maura, Sampson, Jacinda B., Schoch, Kelly, Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Skelton, Tammi, Spillmann, Rebecca C., Stergachis, Andrew, Stoler, Joan M., Sutton, Shirley, Sweetser, David A., Tabor, Holly K., Tan, Queenie, Tan, Amelia L. M., Tifft, Cynthia J., Viskochil, Dave, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wood, Heidi, Worley, Kim

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Immunological and hematological findings as major features in a patient with a new germline pathogenic CBL variant by Stellacci, Emilia, Stevenson, David, Moslehi, Dorsa, Adams, David R., Afzali, Ben, Allworth, Aimee, Alvey, Justin, Ashley, Euan A., Bacino, Carlos A., Baldwin, Erin, Bale, Jim, Beggs, Alan H., Behrens, Edward, Bejerano, Gill, Bernstein, Jonathan A., Blue, Elizabeth, Burke, Elizabeth A., Burrage, Lindsay C., Byrd, William E., Carey, John, Cassini, Thomas, Coakley, Terra R., Cobban, Laurel A., Cogan, Joy D., Coggins, Matthew, Corona, Rosario I., Cuddapah, Vishnu, D'Souza, Precilla, Dasari, Surendra, Dell'Angelica, Esteban C., Dipple, Katrina, Doherty, Daniel, Dorrani, Naghmeh, Earl, Dawn, Esteves, Cecilia, Ezell, Kimberly, Fieg, Elizabeth L., Fisher, Paul G., Gahl, William A., Gonzalez, Joanna M., Gropman, Andrea, Hamid, Rizwan, Hassey, Kelly, Holm, Ingrid A., Hom, Jason, Horike‐Pyne, Martha, Hurst, Anna, Jean‐Marie, Orpa, Jobanputra, Vaidehi, Kanca, Oguz, Kiley, Dana, Korf, Bruce, Krakow, Deborah, Lam, Christina, Lee, Brendan H., Leppig, Kathleen A., Longo, Nicola, Macnamara, Ellen F., Mao, Rong, Marth, Gabor, Martínez‐Agosto, Julian A., McConkie‐Rosell, Allyn, McMinn, Ashley, Mikati, Mohamad, Mitchell, Breanna, Morimoto, Marie, Mulvihill, John J., Orengo, James P., Petcharet, Leoyklang, Phillips, John A., Swerdzewski, Barbara N. Pusey, Quinlan, Aaron, Rajagopalan, Ramakrishnan, Rao, Deepak A., Raper, Anna, Rebelo, Adriana, Reuter, Chloe M., Rives, Lynette, Rosenthal, Elizabeth, Sampson, Jacinda B., Schedl, Timothy, Schoch, Kelly, Seto, Elaine, Shashi, Vandana, Sheppeard, Sam, Sirugo, Giorgio, Smith, Carson A., Solomon, Ben, Sullivan, Kathleen, Sybert, Virginia, Taylor, Herman, Tekin, Mustafa, Toro, Camilo, Ungar, Rachel A., Wahl, Colleen E., Walker, Melissa, Wegner, Daniel, Hubshman, Monika Weisz, Wheeler, Matthew T., Bernstein, Jonathan A.

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