National Lipid Association Recommendations for Patient-Centered Management of Dyslipidemia: Part 2

by Jacobson, Terry A., MD, Maki, Kevin C., PhD, Orringer, Carl E., MD, Jones, Peter H., MD, Kris-Etherton, Penny, PhD, Sikand, Geeta, MA, La Forge, Ralph, MSc, Daniels, Stephen R., MD, PhD, Wilson, Don P., MD, Morris, Pamela B., MD, Wild, Robert A., MD, PhD, MPH, Grundy, Scott M., MD, PhD, Daviglus, Martha, MD, PhD, Ferdinand, Keith C., MD, Vijayaraghavan, Krishnaswami, MD, Deedwania, Prakash C., MD, Aberg, Judith A., MD, Liao, Katherine P., MD, MPH, McKenney, James M., PharmD, Ross, Joyce L., MSN, CRNP, Braun, Lynne T., PhD, CNP, Ito, Matthew K., PharmD, Bays, Harold E., MD, Brown, W. Virgil, MD
Published in Journal of clinical lipidology

Assessment of culture and environment in the Adolescent Brain and Cognitive Development Study: Rationale, description of measures, and early data

by Zucker, Robert A., Gonzalez, Raul, Feldstein Ewing, Sarah W., Paulus, Martin P., Arroyo, Judith, Fuligni, Andrew, Morris, Amanda Sheffield, Sanchez, Mariana, Wills, Thomas
Published in Developmental cognitive neuroscience

Docosahexaenoic acid supplementation of preterm infants and parent-reported symptoms of allergic disease at 7 years corrected age: follow-up of a randomized controlled trial

by Gunaratne, Anoja W, Makrides, Maria, Collins, Carmel T, Gibson, Robert A, McPhee, Andrew J, Sullivan, Thomas R, Gould, Jacqueline F, Green, Tim J, Doyle, Lex W, Davis, Peter G, French, Noel P, Colditz, Paul B, Simmer, Karen, Morris, Scott A, Best, Karen P
Published in The American journal of clinical nutrition

All-trans-retinoic acid, idarubicin, and IV arsenic trioxide as initial therapy in acute promyelocytic leukemia (APML4)

by Iland, Harry J., Bradstock, Ken, Supple, Shane G., Catalano, Alberto, Collins, Marnie, Hertzberg, Mark, Browett, Peter, Grigg, Andrew, Firkin, Frank, Hugman, Amanda, Reynolds, John, Di Iulio, Juliana, Tiley, Campbell, Taylor, Kerry, Filshie, Robin, Seldon, Michael, Taper, John, Szer, Jeff, Moore, John, Bashford, John, Seymour, John F.
Published in Blood

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

by Wang, Sheng, Mandell, Jeffrey D., Kumar, Yogesh, Sun, Nawei, Nasello, Cara, Dong, Shan, Duhn, Clif, Zhao, Xin, Yang, Zhiyu, Padmanabhuni, Shanmukha S., Yu, Dongmei, King, Robert A., Dietrich, Andrea, Dahl, Niklas, Huang, Alden Y., Neale, Benjamin M., Mathews, Carol A., Abdulkadir, Mohamed, Arbelaez, Juan, Bodmer, Benjamin, Coffey, Barbara J., Deng, Li, Dietrich, Andrea, Duhn, Clif, Fernandez, Thomas V., Fremer, Carolin, Gilbert, Donald L., Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heiman, Gary A., Hong, Hyun Ju, Huyser, Chaim, Kim, Eun-Joo, Kim, Young Key, Kim, Young-Shin, King, Robert A., Kuperman, Samuel, Mandell, Jeffrey D., Maras, Athanasios, Müller-Vahl, Kirsten, Münchau, Alexander, Nasello, Cara, Plessen, Kerstin J., Poisner, Hannah, Roessner, Veit, Sanders, Stephan J., Song, Jungeun, State, Matthew W., Tischfield, Jay A., Wanderer, Sina, Wang, Sheng, Willsey, A Jeremy, Xing, Jinchuan, Zhang, Yeting, Zhao, Xin, Zinner, Samuel H., Androutsos, Christos, Barta, Csaba, Farkas, Luca, Janik, Piotr, Karagiannidis, Iordanis, Koumoula, Anastasia, Nagy, Peter, Rizzo, Renata, Szymanska, Urszula, Tarnok, Zsanett, Tsironi, Vaia, Zekanowski, Cezary, Batterson, James R., Berlin, Cheston, Bruun, Ruth D., Budman, Cathy L., Chouinard, Sylvain, Coppola, Giovanni, Darrow, Sabrina, Dion, Yves, Freimer, Nelson B., Grados, Marco A., Hirschtritt, Matthew E., Kurlan, Roger, Lyon, Gholson J., Malaty, Irene A., MacMahon, William M., Neale, Benjamin M., Pauls, David L., Ramensky, Vasily, Robertson, Mary M., Scharf, Jeremiah M., Singer, Harvey S., Smit, Jan, Sul, Jae-Hoon, Yu, Dongmei, Fernandez, Thomas V., De Rubeis, Silvia, Xing, Jinchuan, Tischfield, Jay A., Paschou, Peristera, Willsey, A. Jeremy, State, Matthew W.
Published in Cell reports (Cambridge)

The genotypic and phenotypic spectrum of MTO1 deficiency

by O'Byrne, James J., Tarailo-Graovac, Maja, Ghani, Aisha, Champion, Michael, Deshpande, Charu, Dursun, Ali, Ozgul, Riza K., Freisinger, Peter, Garber, Ian, Haack, Tobias B., Horvath, Rita, Barić, Ivo, Husain, Ralf A., Kluijtmans, Leo A.J., Kotzaeridou, Urania, Morris, Andrew A., Ross, Colin J., Santra, Saikat, Smeitink, Jan, Tarnopolsky, Mark, Wortmann, Saskia B., Mayr, Johannes A., Brunner-Krainz, Michaela, Prokisch, Holger, Wasserman, Wyeth W., Wevers, Ron A., Engelke, Udo F., Rodenburg, Richard J., Ting, Teck Wah, McFarland, Robert, Taylor, Robert W., Salvarinova, Ramona, van Karnebeek, Clara D.M.
Published in Molecular genetics and metabolism

International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome

by Dimitrova, Dimana, Nademi, Zohreh, Maccari, Maria Elena, Ehl, Stephan, Uzel, Gulbu, Tomoda, Takahiro, Okano, Tsubasa, Imai, Kohsuke, Carpenter, Benjamin, Ip, Winnie, Rao, Kanchan, Worth, Austen J.J., Laberko, Alexandra, Mukhina, Anna, Néven, Bénédicte, Moshous, Despina, Speckmann, Carsten, Warnatz, Klaus, Wehr, Claudia, Abolhassani, Hassan, Aghamohammadi, Asghar, Bleesing, Jacob J., Dara, Jasmeen, Dvorak, Christopher C., Ghosh, Sujal, Kang, Hyoung Jin, Markelj, Gašper, Modi, Arunkumar, Bayer, Diana K., Notarangelo, Luigi D., Schulz, Ansgar, Garcia-Prat, Marina, Soler-Palacín, Pere, Karakükcü, Musa, Yilmaz, Ebru, Gambineri, Eleonora, Menconi, Mariacristina, Masmas, Tania N., Holm, Mette, Bonfim, Carmem, Prando, Carolina, Hughes, Stephen, Jolles, Stephen, Morris, Emma C., Kapoor, Neena, Koltan, Sylwia, Paneesha, Shankara, Steward, Colin, Wynn, Robert, Duffner, Ulrich, Gennery, Andrew R., Lankester, Arjan C., Slatter, Mary, Kanakry, Jennifer A.
Published in Journal of allergy and clinical immunology

Diversity of Canadian meningococcal serogroup B isolates and estimated coverage by an investigational meningococcal serogroup B vaccine (4CMenB)

by Bettinger, Julie A, Scheifele, David W, Halperin, Scott A, Vaudry, Wendy, Findlow, Jamie, Borrow, Ray, Medini, Duccio, Tsang, Raymond
Published in Vaccine

MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load

by Ng, Yi Shiau, Lax, Nichola Z., Maddison, Paul, Alston, Charlotte L., Blakely, Emma L., Hepplewhite, Philippa D., Riordan, Gillian, Meldau, Surita, Chinnery, Patrick F., Pierre, Germaine, Chronopoulou, Efstathia, Du, Ailian, Hughes, Imelda, Morris, Andrew A., Kamakari, Smaragda, Chrousos, Georgia, Rodenburg, Richard J., Saris, Christiaan G.J., Feeney, Catherine, Hardy, Steven A., Sakakibara, Takafumi, Sudo, Akira, Okazaki, Yasushi, Murayama, Kei, Mundy, Helen, Hanna, Michael G., Ohtake, Akira, Schaefer, Andrew M., Champion, Mike P., Turnbull, Doug M., Taylor, Robert W., Pitceathly, Robert D.S., McFarland, Robert, Gorman, Gráinne S.
Published in EBioMedicine

Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

by 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.
Published in American journal of human genetics

The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project

by Blokland, Gabriëlla A.M., del Re, Elisabetta C., Mesholam-Gately, Raquelle I., Jovicich, Jorge, Trampush, Joey W., Keshavan, Matcheri S., DeLisi, Lynn E., Walters, James T.R., Turner, Jessica A., Malhotra, Anil K., Lencz, Todd, Shenton, Martha E., Voineskos, Aristotle N., Rujescu, Dan, Giegling, Ina, Kahn, René S., Roffman, Joshua L., Holt, Daphne J., Ehrlich, Stefan, Kikinis, Zora, Dazzan, Paola, Murray, Robin M., Di Forti, Marta, Lee, Jimmy, Sim, Kang, Lam, Max, Wolthusen, Rick P.F., de Zwarte, Sonja M.C., Walton, Esther, Cosgrove, Donna, Kelly, Sinead, Maleki, Nasim, Osiecki, Lisa, Picchioni, Marco M., Bramon, Elvira, Russo, Manuela, David, Anthony S., Mondelli, Valeria, Reinders, Antje A.T.S., Falcone, M. Aurora, Hartmann, Annette M., Konte, Bettina, Morris, Derek W., Gill, Michael, Corvin, Aiden P., Cahn, Wiepke, Ho, New Fei, Liu, Jian Jun, Keefe, Richard S.E., Gollub, Randy L., Manoach, Dara S., Calhoun, Vince D., Schulz, S. Charles, Sponheim, Scott R., Goff, Donald C., Buka, Stephen L., Cherkerzian, Sara, Thermenos, Heidi W., Kubicki, Marek, Nestor, Paul G., Dickie, Erin W., Vassos, Evangelos, Ciufolini, Simone, Reis Marques, Tiago, Crossley, Nicolas A., Purcell, Shaun M., Smoller, Jordan W., van Haren, Neeltje E.M., Toulopoulou, Timothea, Donohoe, Gary, Goldstein, Jill M., Seidman, Larry J., McCarley, Robert W., Petryshen, Tracey L.
Published in Schizophrenia research

Towards stratified treatment of JIA: machine learning identifies subtypes in response to methotrexate from four UK cohorts

by Shoop-Worrall, Stephanie J.W., Lawson-Tovey, Saskia, Wedderburn, Lucy R., Hyrich, Kimme L., Geifman, Nophar, Kimonyo, Aline, McNeece, Alyssia, Dick, Andrew, Morris, Andrew, Yarwood, Annie, Ramanan, Athimalaipet, Jebson, Bethany R., Wallace, Chris, Dastros-Pitei, Daniela, Tarasek, Damian, Ralph, Elizabeth, Carlsson, Emil, Robinson, Emily, Sumner, Emma, Merali, Fatema, Dekaj, Fatjon, Neale, Helen, Al-Mossawi, Hussein, Roberts, Jacqui, Gritzfeld, Jenna F., Fairlie, Joanna, Bowes, John, Ioannou, John, Hyrich, Kimme L., Wedderburn, Lucy R., Kartawinata, Melissa, Tordoff, Melissa, Barnes, Michael, Beresford, Michael W., Stadler, Michael, Geifman, Nophar, Martin, Paul, Kallala, Rami, Ng, Sandra, Smith, Samantha, Clarke, Sarah, Lawson-Tovey, Saskia, Raychaudhuri, Soumya, Shoop-Worrall, Stephanie J.W., Eyre, Stephen, Mukherjee, Sumanta, Duerr, Teresa, Sornasse, Thierry, Alexiou, Vasiliki, Burton, Victoria J., Lin, Wei-Yu, Thomson, Wendy, Wanstall, Zoe
Published in EBioMedicine

Clobetasol propionate emulsion formulation foam 0.05%: Review of phase II open-label and phase III randomized controlled trials in steroid-responsive dermatoses in adults and adole...

by Kimball, Alexa Boer, MD, MPH, Gold, Michael H., MD, Zib, Beth, Davis, Mark W., MS
Published in Journal of the American Academy of Dermatology

Clinicopathologic features and treatment outcome of children with large-cell lymphoma and the t(2;5)(p23;q35)

by Sandlund, J T, Pui, C H, Roberts, W M, Santana, V M, Morris, S W, Berard, C W, Hutchison, R E, Ribeiro, R C, Mahmoud, H, Crist, W M
Published in Blood

Immunization monitoring program, active: a model of active surveillance of vaccine safety

by Scheifele, David W, Halperin, Scott A
Published in Seminars in pediatric infectious diseases

Totally implantable vascular access devices in cystic fibrosis: A four-year experience with fifty-eight patients

by Morris, Jon B., Occhionero, Maria E., Gauderer, Michael W.L., Stern, Robert C., Doershuk, Carl F.
Published in The Journal of pediatrics

Endarterial urokinase in childhood hemolytic uremic syndrome

by Jones, Robert W. A, Morris, Max C., Maisey, Michael N., Saxton, Hugh M., Chantler, Cyril
Published in Kidney international

Differentiation of lymphoma from histoplasmosis in children with mediastinal masses

by Gaebler, John W., Kleiman, Martin B., Cohen, Mervyn, French, Morris L.V., Grosfeld, J.L., Weber, Thomas R., Weetman, Robert
Published in The Journal of pediatrics

T-cell subsets in healthy teenagers: Transition to the adult phenotype

by Tollerud, David J., Ildstad, Suzanne T., Brown, Linda Morris, Clark, Jeffrey W., Blattner, William A., Mann, Dean L., Neuland, Carolyn Y., Pankiw-Trost, Luba, Hoover, Robert N.
Published in Clinical immunology and immunopathology

Facilitation of exchange transfusions with Scribner shunts in Reye's syndrome

by Strauss, Ronald A., Kling, Thomas F., Levinsohn, Morris W., Danielson, Robert A.
Published in The American journal of surgery