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1
Determinants of medication adherence to antihypertensive medications among a Chinese population using Morisky Medication Adherence Scale
Determinants of medication adherence to antihypertensive medications among a Chinese population using Morisky Medication Adherence Scale
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Determinants of medication adherence to antihypertensive medications among a Chinese population using Morisky Medication Adherence Scale

Lee, Gabrielle K Y ; Wang, Harry H X ; Liu, Kirin Q L ; Cheung, Yu ; Morisky, Donald E ; Wong, Martin C S Cameron, D. William

PloS one, 2013-04, Vol.8 (4), p.e62775-e62775 [Periódico revisado por pares]

United States: Public Library of Science

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2
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk
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Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk

Salyakina, Daria ; Cukier, Holly N ; Lee, Joycelyn M ; Sacharow, Stephanie ; Nations, Laura D ; Ma, Deqiong ; Jaworski, James M ; Konidari, Ioanna ; Whitehead, Patrice L ; Wright, Harry H ; Abramson, Ruth K ; Williams, Scott M ; Menon, Ramkumar ; Haines, Jonathan L ; Gilbert, John R ; Cuccaro, Michael L ; Pericak-Vance, Margaret A Zwick, Michael Edward

PloS one, 2011-10, Vol.6 (10), p.e26049-e26049 [Periódico revisado por pares]

United States: Public Library of Science

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3
Effectiveness of non-adjuvanted pandemic influenza A vaccines for preventing pandemic influenza acute respiratory illness visits in 4 U.S. communities
Effectiveness of non-adjuvanted pandemic influenza A vaccines for preventing pandemic influenza acute respiratory illness visits in 4 U.S. communities
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Effectiveness of non-adjuvanted pandemic influenza A vaccines for preventing pandemic influenza acute respiratory illness visits in 4 U.S. communities

Griffin, Marie R ; Monto, Arnold S ; Belongia, Edward A ; Treanor, John J ; Chen, Qingxia ; Chen, Jufu ; Talbot, H Keipp ; Ohmit, Suzanne E ; Coleman, Laura A ; Lofthus, Gerry ; Petrie, Joshua G ; Meece, Jennifer K ; Hall, Caroline Breese ; Williams, John V ; Gargiullo, Paul ; Berman, LaShondra ; Shay, David K Jin, Xia

PloS one, 2011-08, Vol.6 (8), p.e23085-e23085 [Periódico revisado por pares]

United States: Public Library of Science

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4
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Weiner, Daniel J ; Wigdor, Emilie M ; Ripke, Stephan ; Walters, Raymond K ; Kosmicki, Jack A ; Grove, Jakob ; Samocha, Kaitlin E ; Goldstein, Jacqueline I ; Okbay, Aysu ; Bybjerg-Grauholm, Jonas ; Werge, Thomas ; Hougaard, David M ; Taylor, Jacob ; Skuse, David ; Devlin, Bernie ; Anney, Richard ; Sanders, Stephan J ; Bishop, Somer ; Mortensen, Preben Bo ; Børglum, Anders D ; Smith, George Davey ; Daly, Mark J ; Robinson, Elise B

Nature genetics, 2017-07, Vol.49 (7), p.978-985 [Periódico revisado por pares]

United States: Nature Publishing Group

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5
Hemifield effects in multiple identity tracking
Hemifield effects in multiple identity tracking
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Hemifield effects in multiple identity tracking

Hudson, Charlotte ; Howe, Piers D L ; Little, Daniel R Williams, Mark Alexander

PloS one, 2012-08, Vol.7 (8), p.e43796-e43796 [Periódico revisado por pares]

United States: Public Library of Science

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6
Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families
Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families
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Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families

Cruchaga, Carlos ; Haller, Gabe ; Chakraverty, Sumitra ; Mayo, Kevin ; Vallania, Francesco L M ; Mitra, Robi D ; Faber, Kelley ; Williamson, Jennifer ; Bird, Tom ; Diaz-Arrastia, Ramon ; Foroud, Tatiana M ; Boeve, Bradley F ; Graff-Radford, Neill R ; St Jean, Pamela ; Lawson, Michael ; Ehm, Margaret G ; Mayeux, Richard ; Goate, Alison M Toft, Mathias

PloS one, 2012-02, Vol.7 (2), p.e31039-e31039 [Periódico revisado por pares]

United States: Public Library of Science

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7
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci
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Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

Thorleifsson, Gudmar ; Haripriya, Aravind ; Burdon, Kathryn P ; Abu-Amero, Khaled ; Hauser, Michael ; Li, Zheng ; Prakadeeswari, Gopalakrishnan ; Inoue, Kenji ; Park, Ki Ho ; Perera, Shamira A ; Vijaya, Lingam ; Do, Tan ; Edward, Deepak P ; de Juan Marcos, Lourdes ; Ideta, Ryuichi ; Thomas, Samuel ; Greer, Wenda L ; Jia, Liyun ; Qiao, Chunyan ; Wang, Ya-Xing ; Leruez, Stéphanie ; Uebe, Steffen ; Zenkel, Matthias ; Hoja, Ursula ; Mardin, Christian ; Founti, Panayiota ; Chatzikyriakidou, Anthi ; Pappas, Theofanis ; Sarangapani, Sripriya ; Dallorto, Laura ; Ishiko, Satoshi ; Kiuchi, Yoshiaki ; Ohashi, Tsutomu ; Chuman, Hideki ; Miyake, Masahiro ; Matsuda, Fumihiko ; Park, Kyu Hyung ; Cruz-Aguilar, Marisa ; Yong, Victor H K ; Ashaye, Adeyinka O ; Ugbede, Idakwo ; Teekhasaenee, Chaiwat ; Asimadu, Ifeoma ; Kosior-Jarecka, Ewa ; Roy, Sylvain ; Dervan, Edward ; Rao, Aparna ; Sivori, Delia ; Souzeau, Emmanuelle ; Astakhov, Sergei Y ; Emelyanov, Anton ; Kazakbaeva, Gyulli ; Fayzrakhmanov, Rinat ; Chowbay, Balram ; Peh, Su Qin ; Heng, Khai Koon ; Ho, Su-Ling ; Hillmer, Axel M ; Salas, Antonio ; Kitnarong, Naris ; Sakuntabhai, Anavaj ; Nguyn, Giang T T ; Zenz, Werner ; Binder, Alexander ; Hibberd, Martin L ; Nöthen, Markus M ; Rautenbach, Robyn M ; Carmichael, Trevor R ; Álvarez, Lydia ; Fernández-Vega Cueto, Luis ; Oguz, Çilingir ; Atalay, Eray ; Batu, Bilge ; Aktas, Dilek ; Kasım, Burcu ; Coleman, Anne L ; Challa, Pratap ; Curtin, Karen ; Chaya, Craig J ; Zangwill, Linda M ; Wong, Tien Yin ; Kinoshita, Shigeru ; Fingert, John H ; Lee, Richard K ; Sit, Arthur J ; Kraft, Peter ; Pericak-Vance, Margaret A ; Kruse, Friedrich E ; Weinreb, Robert N ; Pasquale, Louis R ; Haines, Jonathan L ; Thorsteinsdottir, Unnur ; Jonasson, Fridbert ; Ritch, Robert ; Kubota, Toshiaki ; Micheal, Shazia ; Topouzis, Fotis ; Craig, Jamie E ; Sundaresan, Periasamy ; Stefansson, Kari

Nature genetics, 2017-07, Vol.49 (7), p.993-1004 [Periódico revisado por pares]

United States: Nature Publishing Group

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8
Serum cholesterol and the progression of Parkinson's disease: results from DATATOP
Serum cholesterol and the progression of Parkinson's disease: results from DATATOP
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Serum cholesterol and the progression of Parkinson's disease: results from DATATOP

Huang, Xuemei ; Auinger, Peggy ; Eberly, Shirley ; Oakes, David ; Schwarzschild, Michael ; Ascherio, Alberto ; Mailman, Richard ; Chen, Honglei Combs, Colin

PloS one, 2011-08, Vol.6 (8), p.e22854-e22854 [Periódico revisado por pares]

United States: Public Library of Science

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9
MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms
MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms
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MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms

Velez Edwards, Digna R ; Tacconelli, Alessandra ; Wejse, Christian ; Hill, Philip C ; Morris, Gerard A J ; Edwards, Todd L ; Gilbert, John R ; Myers, Jamie L ; Park, Yo Son ; Stryjewski, Martin E ; Abbate, Eduardo ; Estevan, Rosa ; Rabna, Paulo ; Novelli, Giuseppe ; Hamilton, Carol D ; Adegbola, Richard ; Østergaar, Lars ; Williams, Scott M ; Scott, William K ; Sirugo, Giorgio Zealand, Pere-Joan

PloS one, 2012-02, Vol.7 (2), p.e32275-e32275 [Periódico revisado por pares]

United States: Public Library of Science

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10
Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation
Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation
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Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation

Rowe, Steven M ; Liu, Bo ; Hill, Aubrey ; Hathorne, Heather ; Cohen, Morty ; Beamer, John R ; Accurso, Frank J ; Dong, Qunming ; Ordoñez, Claudia L ; Stone, Anne J ; Olson, Eric R ; Clancy, John P Boyaka, Prosper N.

PloS one, 2013-07, Vol.8 (7), p.e66955 [Periódico revisado por pares]

United States: Public Library of Science

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