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Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.

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Title: Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.
Authors: Ratnapriya R; Neurobiology Neurodegeneration and Repair Laboratory., Zhan X; Center for Statistical Genetics, Department of Biostatistics and., Fariss RN; Biological Imaging Core., Branham KE; Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI 48109, USA., Zipprer D; Neurobiology Neurodegeneration and Repair Laboratory., Chakarova CF; Department of Genetics, UCL-Institute of Ophthalmology, Bath Street, London EC1V 9EL, UK., Sergeev YV; Ophthalmic Genetics and Visual Function Branch., Campos MM; Biological Imaging Core., Othman M; Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI 48109, USA., Friedman JS; Neurobiology Neurodegeneration and Repair Laboratory., Maminishkis A; Section of Epithelial and Retinal Physiology and Disease., Waseem NH; Department of Genetics, UCL-Institute of Ophthalmology, Bath Street, London EC1V 9EL, UK., Brooks M; Neurobiology Neurodegeneration and Repair Laboratory., Rajasimha HK; Neurobiology Neurodegeneration and Repair Laboratory., Edwards AO; Institute for Molecular Biology, University of Oregon and Oregon Retina, Eugene, OR 97401, USA., Lotery A; Faculty of Medicine, Clinical and Experimental Sciences, University of Southampton, Southampton SO16 6YD, UK., Klein BE; Department of Ophthalmology and Visual Sciences, University of Wisconsin School of Medicine and, Public Health, Madison, WI 53726, USA., Truitt BJ; Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, OH 44106, USA., Li B; Center for Human Genetics Research, Vanderbilt University, Nashville, TN 37232, USA., Schaumberg DA; Division of Preventive Medicine, Brigham and Women's Hospital, Boston, MA 02215, USA, Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah, Salt Lake City, UT 84132, USA., Morgan DJ; Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah, Salt Lake City, UT 84132, USA., Morrison MA; Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah, Salt Lake City, UT 84132, USA., Souied E; Hôpital Intercommunal de Créteil, Hôpital Henri Mondor - Université Paris Est Créteil 94000, France., Tsironi EE; Department of Ophthalmology, University of Thessaly School of Medicine, Larissa, Greece., Grassmann F; Institute of Human Genetics, University of Regensburg, Regensburg 93053, Germany., Fishman GA; Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, IL 60607, USA., Silvestri G; Centre for Vision and Vascular Science, Queen's University, Belfast, UK., Scholl HP; Wilmer Eye Institute, Johns Hopkins University, 600 N. Wolfe Street, Baltimore, MD 21287, USA., Kim IK; Retina Service and Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, MA 02114, USA., Ramke J; The Fred Hollows Foundation, Auckland, New Zealand, School of Social Sciences, University of New South Wales, Sydney, Australia., Tuo J; Section of Immunopathology and., Merriam JE; Department of Ophthalmology and., Merriam JC; Department of Ophthalmology and., Park KH; Department of Ophthalmology, Seoul National University Bundang Hospital, Seoul 463-707, Republic of Korea., Olson LM; Center for Human Genetics Research, Vanderbilt University, Nashville, TN 37232, USA., Farrer LA; Departments of Medicine (Section of Biomedical Genetics), Ophthalmology and Biostatistics, Neurology, Epidemiology, Boston University Schools of Medicine and Public Health, Boston, MA 02215, USA., Johnson MP; Texas Biomedical Research Institute, San Antonio, TX 78245, USA., Peachey NS; Cleveland Clinic Foundation, Cole Eye Institute, Cleveland, OH 44195, USA, Louis Stokes Cleveland VA Medical Center, Cleveland, OH 44195, USA., Lathrop M; Department of Genetics, Institut de la Vision - Inserm Université Pierre et Marie Curie UMR-S 968, Paris, France., Baron RV; Department of Human Genetics and., Igo RP Jr; Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, OH 44106, USA., Klein R; Department of Ophthalmology and Visual Sciences, University of Wisconsin School of Medicine and, Public Health, Madison, WI 53726, USA., Hagstrom SA; Cleveland Clinic Foundation, Cole Eye Institute, Cleveland, OH 44195, USA., Kamatani Y; Department of Genetics, Institut de la Vision - Inserm Université Pierre et Marie Curie UMR-S 968, Paris, France., Martin TM; Oregon Health & Science University, Portland, OR 97239, USA., Jiang Y; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA 15261, USA., Conley Y; Health Promotion and Development, School of Nursing, 440 Victoria Building, 3500 Victoria St, Pittsburgh, PA 15261, USA., Sahel JA; Department of Genetics, Institut de la Vision - Inserm Université Pierre et Marie Curie UMR-S 968, Paris, France., Zack DJ; Wilmer Eye Institute, Johns Hopkins University, 600 N. Wolfe Street, Baltimore, MD 21287, USA., Chan CC; Section of Immunopathology and., Pericak-Vance MA; Bascom Palmer Eye Institute and Human Genomics, University of Miami Miller School of Medicine, Miami, FL 33125, USA., Jacobson SG; Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, PA 19104, USA., Gorin MB; Department of Ophthalmology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA., Klein ML; Macular Degeneration Center, Casey Eye Institute, Oregon Health and Science, University, Portland, OR 97201, USA., Allikmets R; Department of Ophthalmology and Department of Pathology and Cell Biology, Columbia University, New York, NY 10032, USA., Iyengar SK; Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, OH 44106, USA., Weber BH; Institute of Human Genetics, University of Regensburg, Regensburg 93053, Germany., Haines JL; Center for Human Genetics Research, Vanderbilt University, Nashville, TN 37232, USA., Léveillard T; Department of Genetics, Institut de la Vision - Inserm Université Pierre et Marie Curie UMR-S 968, Paris, France., Deangelis MM; Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah, Salt Lake City, UT 84132, USA., Stambolian D; Department of Ophthalmology, and Department of Genetics, University of Pennsylvania, Philadelphia, PA 9104, USA., Weeks DE; Department of Human Genetics and Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA 15261, USA., Bhattacharya SS; Department of Genetics, UCL-Institute of Ophthalmology, Bath Street, London EC1V 9EL, UK., Chew EY; Clinical Trials Branch, Division of Epidemiology and Clinical Applications, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA., Heckenlively JR; Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI 48109, USA., Abecasis GR; Center for Statistical Genetics, Department of Biostatistics and., Swaroop A; Neurobiology Neurodegeneration and Repair Laboratory, swaroopa@nei.nih.gov.
Source: Human molecular genetics [Hum Mol Genet] 2014 Nov 01; Vol. 23 (21), pp. 5827-37. Date of Electronic Publication: 2014 Jun 04.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.
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      – TitleFull: Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.
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      – PersonEntity:
          Name:
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      – PersonEntity:
          Name:
            NameFull: Conley Y
      – PersonEntity:
          Name:
            NameFull: Sahel JA
      – PersonEntity:
          Name:
            NameFull: Zack DJ
      – PersonEntity:
          Name:
            NameFull: Chan CC
      – PersonEntity:
          Name:
            NameFull: Pericak-Vance MA
      – PersonEntity:
          Name:
            NameFull: Jacobson SG
      – PersonEntity:
          Name:
            NameFull: Gorin MB
      – PersonEntity:
          Name:
            NameFull: Klein ML
      – PersonEntity:
          Name:
            NameFull: Allikmets R
      – PersonEntity:
          Name:
            NameFull: Iyengar SK
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          Name:
            NameFull: Weber BH
      – PersonEntity:
          Name:
            NameFull: Haines JL
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            NameFull: Léveillard T
      – PersonEntity:
          Name:
            NameFull: Deangelis MM
      – PersonEntity:
          Name:
            NameFull: Stambolian D
      – PersonEntity:
          Name:
            NameFull: Weeks DE
      – PersonEntity:
          Name:
            NameFull: Bhattacharya SS
      – PersonEntity:
          Name:
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      – PersonEntity:
          Name:
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          Name:
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      – PersonEntity:
          Name:
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    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 11
              Text: 2014 Nov 01
              Type: published
              Y: 2014
          Identifiers:
            – Type: issn-electronic
              Value: 1460-2083
          Numbering:
            – Type: volume
              Value: 23
            – Type: issue
              Value: 21
          Titles:
            – TitleFull: Human molecular genetics
              Type: main
ResultId 1