Zobrazeno 1 - 10
of 66
pro vyhledávání: '"J L, Haines"'
Autor:
Itay Chowers, Stacy M Meuer, R. Theodore Smith, Bamini Gopinath, Brendan J Vote, Thierry Léveillard, David A Mackey, Dwight Stambolian, Jamie E Craig, José-Alain Sahel, David J Hunter, Michael L Klein, Jane Romm, Robyn H Guymer, Mingyao Li, J. L. Haines, Emily L. Moore, J Allie McGrath, Chloe M. Stanton, Danni Lin, Jessica N Cooke Bailey, Anton Orlin, Anita Agarwal, Frank G Holz, Debra A Schaumberg, Valerie Kuan, Christine A. Curcio, Ken Flagg, Sudha K Iyengar, Sebanti Sengupta, Bal Dhillon, Joanna E. Merriam, Janette Hall, Bernhard H F Weber, Caroline Brandl, Donald Zack, Eric Souied, Yara T. E. Lechanteur, Christina A Rennie, Mathias Gorski, Murray H Brilliant, Denise J. Morgan, Barbara Truitt, Daniel E Weeks, Thomas Langmann, Aroon D. Hingorani, Gerald Liew, Andrea J Richardson, Neal S Peachey, John Blangero, Alasdair Warwick, Humma Shahid, Eiko K de Jong, Kari E Branham, S. V. Goverdhan, Paul Mitchell, Angela J Cree, Margaux A. Morrison, Rebecca J Sardell, Ian J Constable, Michael A. Hauser, Zhenglin Yang, Reneé Laux, G. Rudolph, David Cho, Jie Jin Wang, Albert Caramoy, Jaclyn L Kovach, Alexander Brucker, Frédéric Blond, Hongrong Luo, Michael B Gorin, Robert P Igo, Caroline C W Klaver, Lebriz Ersoy, Timothy Isaacs, Adnan Tufail, Gabriëlle H.S. Buitendijk, Nicholas Katsanis, Stephen Burgess, Carel B Hoyng, Reecha Sofat, Ivana K Kim, Mohammad Othman, Ian L McAllister, Giuliana Silvestri, Helena Hai Liang, Margaret DeAngelis, Matthew P Johnson, Ava G Tan, Felix Grassmann, Lindsay A Farrer, Alex W Hewitt, Hong Ouyang, Cindy Wen, Henry Ferreyra, Milam A Brantley, Melinda Cain, Caroline Hayward, Kristine E. Lee, Linn Gieser, Isabelle Audo, Evangelia E Tsironi, Nicole T.M. Saksens, Hendrik P N Scholl, Stephen G Schwartz, Matthias Olden, Saddek Mohand-Said, Scott J Hebbring, Joshua D Hoffman, Shira Hagbi-Levi, Anthony T Moore, Mustapha Benchaboune, Lars G Fritsche, Margaret A Pericak-Vance, Iris M Heid, Kyu Hyung Park, Jennifer L Bragg-Gresham, Hélène Blanché, Alexis Boleda, Rando Allikmets, John R Heckenlively, Kathryn P Burdon, Elisa Bala, Rinki Ratnapriya, Kimberly F Doheny, Xiaowei Zhan, Sascha Fauser, Claudia N von Strachwitz, Ronald Klein, Johanna R. Foerster, Wilmar Igl, Andrew J Lotery, Klaus Stark, Matthew Brooks, Jane C Khan, Emily Y Chew, Paul N Baird, Cornelia M Van Duijn, Chelsea E. Myers, Anneke I den Hollander, Monique D Courtenay, Zhiguang Su, Yingda Jiang, William K Scott, Tammy M Martin, Armin Wolf, Jeeyun Ahn, John C. Merriam, Eric A Postel, Guanping Mao, Emmanuelle Souzeau, Barbara E K Klein, Terrie Kitchner, Stewart Lake, Anand Swaroop, Valentina Cipriani, Tina Schick, Stephanie A. Hagstrom, Alan M. Kwong, Daniel Chen, Gonçalo R. Abecasis, Matthew Schu, Michelle Grunin, John R.W. Yates, Peter Campochiaro, Kang Zhang, Jean-François Deleuze
Publikováno v:
JAMA Ophthalmology. 139:1299
Importance Advanced age-related macular degeneration (AMD) is a leading cause of blindness in Western countries. Causal, modifiable risk factors need to be identified to develop preventive measures for advanced AMD. Objective To assess whether smokin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e94ddf71fb72de624f6c6439cbb037b
https://doi.org/10.1001/jamaophthalmol.2021.4601
https://doi.org/10.1001/jamaophthalmol.2021.4601
Autor:
D. A. S. Compston, J. L. Haines, Lisa F. Barcellos, Stephen L. Hauser, Margaret A. Pericak-Vance, Patricia P. Ramsay, Stacy J. Caillier, Jorge R. Oksenberg, Silke Schmidt, Stephen Sawcer, Pablo Gabatto
Publikováno v:
Genes & Immunity. 9:493-500
Multiple sclerosis (MS) is a chronic inflammatory disorder of the central nervous system with a strong genetic component. Variation in the major histocompatibility complex on chromosome 6p21, specifically the HLA-DRB1*15 haplotype, is the strongest g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4a215bd6aad2f44079b8fa2c5d99d35
https://doi.org/10.1038/gene.2008.41
https://doi.org/10.1038/gene.2008.41
Autor:
Marylyn D. Ritchie, Alison A. Motsinger, Lori Steiner, Jorge R. Oksenberg, Stacy J. Caillier, Henry A. Erlich, Silke Schmidt, Simon G. Gregory, Bruce A.C. Cree, Margaret A. Pericak-Vance, David Brassat, J. L. Haines, Lisa F. Barcellos, Karen Walker, Stephen L. Hauser
Publikováno v:
Genes & Immunity. 7:310-315
Multiple sclerosis (MS) is a common disease of the central nervous system characterized by inflammation, myelin loss, gliosis, varying degrees of axonal pathology, and progressive neurological dysfunction. Multiple sclerosis exhibits many of the char
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1964b095b528d830f423bb3efd81241
https://doi.org/10.1038/sj.gene.6364299
https://doi.org/10.1038/sj.gene.6364299
Autor:
Janey L. Wiggs, Lana M. Olson, E. A. Del Bono, S. Lynch, J. Auguste, G. Ynagi, M. Maselli, J. L. Haines
Publikováno v:
The American Journal of Human Genetics. 74:1314-1320
Glaucoma is a leading cause of blindness worldwide. The disease is characterized by a degeneration of the optic nerve, which is usually associated with elevated intraocular pressure. The common form of adult-onset primary open-angle glaucoma is inher
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ed06fd5e7baa52b3291d41ec93d760f
https://doi.org/10.1086/421533
https://doi.org/10.1086/421533
Autor:
null The Multiple Sclerosis Genetics Group, L. F. Barcellos, J. R. Oksenberg, A. J. Green, P. Bucher, J. B. Rimmler, S. Schmidt, M. E. Garcia, R. R Lincoln, M. A. Pericak‐Vance, J. L. Haines, S. L. Hauser
Publikováno v:
Brain. 125:150-158
Multiple sclerosis is a clinically heterogeneous demyelinating disease and an important cause of acquired neurological disability. An underlying complex genetic susceptibility plays an important role in multiple sclerosis aetiology; however, the role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d6a0af7e3e40ad059c2746893a55909
https://doi.org/10.1093/brain/awf009
https://doi.org/10.1093/brain/awf009
Publikováno v:
Journal of Clinical Investigation. 100:74-83
Relationships among plasma lipoprotein cholesterol, cholesterol secretion by the isolated, perfused liver, and coronary artery atherosclerosis were examined in African green monkeys fed diets containing cholesterol and 35% of calories as fat enriched
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::063aed552d594be8a3da5c64a1531789
https://doi.org/10.1172/jci119524
https://doi.org/10.1172/jci119524
Publikováno v:
Genes, brain, and behavior. 13(3)
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with strong evidence for genetic susceptibility. However, the effect sizes for implicated chromosomal loci are small, hard to replicate and current evidence does not explain the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aed6dca720973ed22b4b1e49bae37c91
https://pubmed.ncbi.nlm.nih.gov/24373520
https://pubmed.ncbi.nlm.nih.gov/24373520
Autor:
J L, Wiggs, G R, Howell, K, Linkroum, W, Abdrabou, E, Hodges, C E, Braine, L R, Pasquale, G J, Hannon, J L, Haines, S W M, John
Publikováno v:
Clinical genetics. 84(2)
Primary open angle glaucoma (POAG) is a genetically and phenotypically complex disease that is a leading cause of blindness worldwide. Previously we completed a genome-wide scan for early-onset POAG that identified a locus on 9q22 (GLC1J). To identif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::67562691858f03180e7ff391c513f18f
https://pubmed.ncbi.nlm.nih.gov/23621901
https://pubmed.ncbi.nlm.nih.gov/23621901
Autor:
J. K. Fink, T. Heiman-Patterson, T. Bird, F. Cambi, M.-P. Dube, D. A. Figlewicz, J. L. Haines, A. Hentati, M. A. Pericak-Vance, W. Raskind, G. A. Rouleau, T. Siddique
Publikováno v:
Neurology. 46:1507-1514
Hereditary spastic paraplegia (HSP) is a diverse group of inherited disorders characterized by progressive lower-extremity spasticity and weakness. Insight into the genetic basis of these disorders is expanding rapidly. Uncomplicated autosomal domina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccb5cda779835b8258fd1fb448359b52
https://doi.org/10.1212/wnl.46.6.1507
https://doi.org/10.1212/wnl.46.6.1507
Autor:
T, Desronvil, D, Logan-Wyatt, W, Abdrabou, M, Triana, R, Jones, S, Taheri, E, Del Bono, L R, Pasquale, M, Olivier, J L, Haines, B J, Fan, J L, Wiggs
Publikováno v:
Molecular Vision
Purpose One approach to identify genes that contribute to common complex ocular disorders such as primary open angle glaucoma (POAG) is to study the genetic determinates of endophenotypes that are defined by underlying pre-disposing heritable quantit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b6d3a1ced71cb8ffb609fd9e9edc60e5
https://pubmed.ncbi.nlm.nih.gov/21139683
https://pubmed.ncbi.nlm.nih.gov/21139683