Alternative Funding Plans and Alternative Relationship Plans: Saviours of Academic Medicine or Just the Last Gasp?

Autor: Ron Bridges, Des Leddin, William Paterson, Hugh O’Brodovich, Jon Meddings, Stephen Vanner

Publikováno v: Canadian Journal of Gastroenterology, Vol 21, Iss 11, Pp 699-703 (2007)

Externí odkaz: https://doaj.org/article/013dab71a473449a99ca8e787181f7f3

Contributors

Autor: Robin Abel, Steven H. Abman, Eric Alton, Daniel R. Ambruso, William Carl Anderson, Karthik Balakrishnan, Ian Michael Balfour-Lynn, Anna Bamford, Ronen Bar-Yoseph, Erika Berman-Rosenzweig, Deepika Bhatla, Joshua A. Blatter, R. Paul Boesch, Matias Bruzoni, Andrew Bush, Michael Bye, Kai Håkon Carlsen, Anne B. Chang, Stephanie D. Chao, Michelle Chatwin, Bimal Pankaj Chaudhari, Lyn Chitty, Nicola Collins, Dan M. Cooper, Jonathan Corren, Robin T. Cotton, Andrea Coverstone, Suzanne Crowley, Steve Cunningham, Garry R. Cutting, Dorottya Czovek, Charles L. Daley, Gwyneth Davies, Jane C. Davies, Alessandro de Alarcòn, Emily M. DeBoer, Marietta Morales De Guzman, Sharon D. Dell, Robin Deterding, Gail H. Deutsch, Sunalene Devadason, William Graham Fox Ditcham, Jill Dorsey, Francine M. Ducharme, John Engelhardt, Mark L. Everard, Leland L. Fan, Albert Faro, Thomas Ferkol, Louise Fleming, Angela Mary Fonceca, Hammad A. Ganatra, Amy Michelle Garcia, David Gozal, Diane Gray, Anne Greenough, Uta Griesenbach, Jonathan Grigg, James S. Hagood, Jürg Hammer, Aaron Hamvas, Jonny Harcourt, Pia J. Hauk, Ulrich Heininger, Alexander John Henderson, Marianna M. Henry, Richard J. Hewitt, Heather Young Highsmith, Noah H. Hillman, Heather Ellen Hoch, Jeong S. Hyun, Mas Suhaila Isa, Adam Jaffé, Lance C. Jennings, Alan H. Jobe, Ankur A. Kamdar, Bhushan Katira, Brian P. Kavanagh, James Kemp, Carolyn M. Kercsmar, Leila Kheirandish-Gozal, Wilson King, Paul Kingma, Jennifer Knight-Madden, Alan Paul Knutsen, Alik Kornecki, Usha Krishnan, Geoffrey Kurland, Hugh Simon Lam, Claire Langston, Ada Lee, Margaret W. Leigh, Daniel Lesser, Clare M. Lloyd, Anna Maria Mandalakas, Paulo J.C. Marostica, Stacey L. Martiniano, Jennifer Maybee, Karen M. McDowell, Peter Michelson, Aaron Samuel Miller, Claire Kane Miller, Ayesha Mirza, David R. Murdoch, Christopher J.L. Newth, Andrew Gordon Nicholson, Jerry A. Nick, Christina J. Nicolais, Terry L. Noah, Lawrence M. Nogee, Blakeslee Noyes, Andrew H. Numa, Ann-Christine Nyquist, Hugh O'Brodovich, Matthias Ochs, J. Tod Olin, Øystein Olsen, Catherine Owens, Howard B. Panitch, Hans Pasterkamp, Donald Payne, Scott Pentiuk, Jeremy Prager, Jean-Paul Praud, Andrew P. Prayle, Bernadette Prentice, Philip E. Putnam, Alexandra L. Quittner, Shlomit Radom-Aizik, Suchitra Rao, Mobeen Rathore, Gregory J. Redding, Michael Rutter, Estefany Saez-Flores, Sejal Saglani, Rayfel Schneider, Kenneth O. Schowengerdt, Marcelo C. Scotta, Thomas Semple, Laurie Sherlock, Ram N. Singh, Raymond G. Slavin, Peter Sly, Bjarne Smevik, Keely Garrett Smith, Jonathan Spahr, James M. Stark, Jeffrey R. Starke, Renato T. Stein, Paul C. Stillwell, Dennis C. Stokes, Daniel T. Swarr, Stuart Charles Sweet, Stanley James Szefler, Paul Tambyah, Christelle Xian-Ting Tan, James Temprano, Chad M. Thorson, Bruce C. Trapnell, Brian Michael Varisco, Timothy J. Vece, Harish G. Vyas, Ruth Wakeman, Colin Wallis, Jennifer Wambach, Daniel J. Weiner, Anja M. Werno, Susan E. Wert, Jeffrey A. Whitsett, Robert William Wilmott, Robert E. Wood, Christopher Todd Wootten, Marie Wright, Sarah Wright, Rae S.M. Yeung, Takeshi Yoshida, Carolyn Young, Lisa R. Young, Heather J. Zar, Pamela Leslie Zeitlin, David Zielinski

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::34d96ab4068e695d68baf2fc1b6f5cab
https://doi.org/10.1016/b978-0-323-44887-1.00085-7

A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth

Autor: Xiaobin Wang, Jeffrey B. Gould, Ronald J. Wong, Marina Sirota, Jason A. Reuter, John Oehlert, Nikolaos A. Patsopoulos, Scott Huntsman, Jonathan Toung, Christopher R. Gignoux, Louis J. Muglia, Gary L. Darmstadt, Dale L. Bodian, Esteban G. Burchard, Michael Snyder, Carlos Bustamante, Nadav Rappoport, Gary M. Shaw, Xiumei Hong, John E. Niederhuber, Weronika Sikora-Wohfeld, Sam S. Oh, Kazumichi Fujioka, David K. Stevenson, Dexter Hadley, Laura L. Jelliffe-Pawlowski, Atul J. Butte, Donglei Hu, Hui Wang, Celeste Eng, Hugh O'Brodovich, Charles Abbott, Ge Zhang, Elad Ziv

Publikováno v: Scientific reports, vol 8, iss 1
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)

Preterm birth (PTB), or the delivery prior to 37 weeks of gestation, is a significant cause of infant morbidity and mortality. Although twin studies estimate that maternal genetic contributions account for approximately 30% of the incidence of PTB, a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec4e57184e680b0b51da38733af22e0d
https://escholarship.org/uc/item/2tb285m4

Determinants of chronic lung disease severity in the first year of life; A population based study

Autor: Susan Gage, Jeffrey B. Gould, John Oehlert, Gary M. Shaw, David K. Stevenson, Peiyi Kan, Hugh O'Brodovich

Publikováno v: Pediatric Pulmonology. 50:878-888

Summary Objectives First, create a clinical severity score for patients with chronic lung disease of infancy (CLDi) following neonatal intensive care unit (NICU) stay. Second, using California wide population-based data, identify factors associated w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a7b09acc9473637b0fb7f35fdd32a112
https://doi.org/10.1002/ppul.23148

A Genome-Wide Association Study (GWAS) for Bronchopulmonary Dysplasia

Autor: Jeffrey B. Gould, Laura L. Jelliffe-Pawlowski, John Oehlert, Krystal R. St. Julien, Hugh O'Brodovich, Laura C. Lazzeroni, Thomas J. Hoffmann, Cecele C. Quaintance, John S. Witte, Hui Wang, David K. Stevenson, Gary M. Shaw, Mark A. Krasnow

Publikováno v: Pediatrics, vol 132, iss 2

OBJECTIVE: Twin studies suggest that heritability of moderate-severe bronchopulmonary dysplasia (BPD) is 53% to 79%, we conducted a genome-wide association study (GWAS) to identify genetic variants associated with the risk for BPD. METHODS: The disco

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8076fed7c176303b18a97e53662cbe1
https://doi.org/10.1542/peds.2013-0533