Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Wiggs, Janey L."'
Autor:
King, Rebecca, Struebing, Felix L., Li, Ying, Wang, Jiaxing, Koch, Allison Ashley, Cooke Bailey, Jessica N., Gharahkhani, Puya, MacGregor, Stuart, Allingham, Rand, Hauser, Michael, Wiggs, Janey L., Geisert, Eldon E., Brilliant, Murray, Budenz, Don, Bailey, Jessica N.Cooke, Fingert, John, Gaasterland, Douglas, Gaasterland, Teresa, Haines, Jonathan L., Hark, Lisa, Igo, Rob, Kang, Jae Hee, Kraft, Peter, Lee, Richard, Lichter, Paul, Liu, Yutao, Moroi, Syoko, Pasquale, Louis R., Pericak-Vance, Margaret, Realini, Anthony, Rhee, Doug, Richards, Julia R., Ritch, Robert, Schuman, Joel, Scott, William K., Singh, Kuldev, Sit, Arthur, Vollrath, Douglas, Weinreb, Robert N., Wollstein, Gadi, Zack, Don, Aung, Tin, Burdon, Kathryn P., Cheng, Ching Yu, Craig, Jamie E., Cree, Angela J., Hammond, Christopher J.
Publikováno v:
PLoS Genetics, 14(1):e1007145. Public Library of Science
PLoS genetics, vol 14, iss 1
PLoS Genetics, Vol 14, Iss 1, p e1007145 (2018)
PLoS Genetics
PLoS genetics, vol 14, iss 1
PLoS Genetics, Vol 14, Iss 1, p e1007145 (2018)
PLoS Genetics
Central corneal thickness (CCT) is one of the most heritable ocular traits and it is also a phenotypic risk factor for primary open angle glaucoma (POAG). The present study uses the BXD Recombinant Inbred (RI) strains to identify novel quantitative t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f31d79ff99f00ae7be0acdaa10e2834
https://pure.eur.nl/en/publications/e4f26832-4193-4695-b82d-ebd7ebb9a785
https://pure.eur.nl/en/publications/e4f26832-4193-4695-b82d-ebd7ebb9a785
Publikováno v:
Molecular Vision
Purpose To investigate whether associations with the nitric oxide synthase gene (NOS3) variants and risk of primary open-angle glaucoma (POAG) depend on female reproductive factors. Methods Two functional and two tagging single nucleotide polymorphis
Autor:
Verma, Shefali Setia, Cooke Bailey, Jessica N., Lucas, Anastasia, Bradford, Yuki, Linneman, James G., Hauser, Michael A., Pasquale, Louis R., Peissig, Peggy L., Brilliant, Murray H., McCarty, Catherine A., Haines, Jonathan L., Wiggs, Janey L., Vrabec, Tamara R., Tromp, Gerard, Ritchie, Marylyn D., null, null
Publikováno v:
PLoS Genetics; 9/13/2016, Vol. 12 Issue 9, p1-21, 21p
Publikováno v:
PLoS ONE; 6/7/2016, Vol. 11 Issue 6, p1-11, 11p
Autor:
Stein, Joshua D., Talwar, Nidhi, Kang, Jae H., Okereke, Olivia I., Wiggs, Janey L., Pasquale, Louis R.
Publikováno v:
PLoS ONE; Apr2015, Vol. 10 Issue 4, p1-11, 11p
Autor:
Ulmer Carnes, Megan, Liu, Yangfan P., Allingham, R. Rand, Whigham, Benjamin T., Havens, Shane, Garrett, Melanie E., Qiao, Chunyan, Katsanis, Nicholas, Wiggs, Janey L., Pasquale, Louis R., Ashley-Koch, Allison, Oh, Edwin C., Hauser, Michael A.
Publikováno v:
PLoS Genetics; May2014, Vol. 10 Issue 5, p1-10, 10p
Autor:
Hewitt, Alex W., Samples, John R., Rand Allingham, R., Irma Järvelä, George Kitsos, Krishnadas, Subbiah R., Richards, Julia E., Lichter, Paul R., Petersen, Michael B., Periasamy Sundaresan, Wiggs, Janey L., Mackey, David A., Wirtz, Mary K.
Publikováno v:
University of Helsinki
Molecular Vision
Molecular Vision
Purpose The aim of this study was to determine if there is a common founder for the Thr377Met myocilin mutation in primary open angle glaucoma (POAG) families with various ethnic backgrounds. Methods Genomic DNA of 24 POAG-affected individuals from n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2f555a8bcd98b4d67c97eb9033b09d74
https://researchportal.helsinki.fi/en/publications/60c66808-5256-41e3-abb7-4a821e569853
https://researchportal.helsinki.fi/en/publications/60c66808-5256-41e3-abb7-4a821e569853