Works matching AU Fishman, Gerald

Results: 65

Noncoding mutation in RPGRIP1 contributes to inherited retinal degenerations.

Published in:

Molecular Vision, 2021, v. 27, p. 95

By:

Gang Zou;
Tao Zhang;
Xuesen Cheng;
Igelman, Austin D.;
Jun Wang;
Xinye Qian;
Shangyi Fu;
Keqing Wang;
Koenekoop, Robert K.;
Fishman, Gerald A.;
Paul Yang;
Yumei Li;
Pennesi, Mark E.;
Rui Chen

Publication type:

Article

The source altitude, electric current, and intrinsic brightness of terrestrial gamma ray flashes.

Published in:

Geophysical Research Letters, 2014, v. 41, n. 23, p. 8586, doi. 10.1002/2014GL062196

By:

Cummer, Steven A.;
Briggs, Michael S.;
Dwyer, Joseph R.;
Xiong, Shaolin;
Connaughton, Valerie;
Fishman, Gerald J.;
Lu, Gaopeng;
Lyu, Fanchao;
Solanki, Rahulkumar

Publication type:

Article

The lightning-TGF relationship on microsecond timescales.

Published in:

Geophysical Research Letters, 2011, v. 38, n. 14, p. n/a, doi. 10.1029/2011GL048099

By:

Cummer, Steven A.;
Lu, Gaopeng;
Briggs, Michael S.;
Connaughton, Valerie;
Xiong, Shaolin;
Fishman, Gerald J.;
Dwyer, Joseph R.

Publication type:

Article

Electron-positron beams from terrestrial lightning observed with Fermi GBM.

Published in:

Geophysical Research Letters, 2011, v. 38, n. 2, p. n/a, doi. 10.1029/2010GL046259

By:

Briggs, Michael S.;
Connaughton, Valerie;
Wilson-Hodge, Colleen;
Preece, Robert D.;
Fishman, Gerald J.;
Kippen, R. Marc;
Bhat, P. N.;
Paciesas, William S.;
Chaplin, Vandiver L.;
Meegan, Charles A.;
von Kienlin, Andreas;
Greiner, Jochen;
Dwyer, Joesph R.;
Smith, David M.

Publication type:

Article

Chorioretinal Lesions in a Case of Melanoma-Associated Retinopathy Treated With Pembrolizumab.

Published in:

2016

By:

Roberts, Philipp;
Fishman, Gerald A.;
Joshi, Komal;
Jampol, Lee M.

Publication type:

journal article

Visual Acuity Changes in Patients With Leber Congenital Amaurosis and Mutations in CEP290.

Published in:

JAMA Ophthalmology, 2013, v. 131, n. 2, p. 178, doi. 10.1001/2013.jamaophthalmol.354

By:

McAnany, J. Jason;
Genead, Mohamed A.;
Walia, Saloni;
Drack, Arlene V.;
Stone, Edwin M.;
Koenekoop, Robert K.;
Traboulsi, Elias I.;
Smith, Alison;
Weleber, Richard G.;
Jacobson, Samuel G.;
Fishman, Gerald A.

Publication type:

Article

Spontaneous Regression of Choroidal Neovascularization in a Patient with Pattern Dystrophy.

Published in:

Case Reports in Ophthalmological Medicine, 2016, p. 1, doi. 10.1155/2016/9685290

By:

Anastasakis, Anastasios;
Goleni, Flamur;
Livir-Rallatos, Gerasimos;
Livir-Rallatos, Charalampos;
Zafirakis, Panagiotis;
Allen Fishman, Gerald

Publication type:

Article

Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration.

Published in:

Nature Genetics, 2012, v. 44, n. 9, p. 1035, doi. 10.1038/ng.2356

By:

Koenekoop, Robert K;
Wang, Hui;
Majewski, Jacek;
Wang, Xia;
Lopez, Irma;
Ren, Huanan;
Chen, Yiyun;
Li, Yumei;
Fishman, Gerald A;
Genead, Mohammed;
Schwartzentruber, Jeremy;
Solanki, Naimesh;
Traboulsi, Elias I;
Cheng, Jingliang;
Logan, Clare V;
McKibbin, Martin;
Hayward, Bruce E;
Parry, David A;
Johnson, Colin A;
Nageeb, Mohammed

Publication type:

Article

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 127, doi. 10.1038/72777

By:

Haider, Neena B.;
Jacobson, Samuel G.;
Cideciyan, Artur V.;
Swiderski, Ruth;
Streb, Luan M.;
Searby, Charles;
Beck, Gretel;
Hockey, Robin;
Hanna, David B.;
Gorman, Susan;
Duhl, David;
Carmi, Rivka;
Bennett, Jean;
Weleber, Richard G.;
Fishman, Gerald A.;
Wright, Alan F.;
Stone, Edwin M.;
Sheffield, Val C.

Publication type:

Article

Loss-of-function mutations in a calcium-channel α<sub>1</sub>-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 264, doi. 10.1038/947

By:

Bech-Hansen, N. Torben;
Naylor, Margaret J.;
Maybaum, Tracy A.;
Pearce, William G.;
Koop, Ben;
Fishman, Gerald A.;
Mets, Marilyn;
Musarella, Maria A.;
Boycott, Kym M.

Publication type:

Article

Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt disease.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 14, p. 1293, doi. 10.1093/hmg/ddab122

By:

Lee, Winston;
Zernant, Jana;
Nagasaki, Takayuki;
Molday, Laurie L;
Su, Pei-Yin;
Fishman, Gerald A;
Tsang, Stephen H;
Molday, Robert S;
Allikmets, Rando

Publication type:

Article

Multimodal Imaging of Photoreceptor Structure in Choroideremia.

Published in:

PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0167526

By:

Sun, Lynn W.;
Johnson, Ryan D.;
Williams, Vesper;
Summerfelt, Phyllis;
Dubra, Alfredo;
Weinberg, David V.;
Stepien, Kimberly E.;
Fishman, Gerald A.;
Carroll, Joseph

Publication type:

Article

Gamma Ray Observations of the Crab Pulsar-Past, Present, Future.

Published in:

Annals of the New York Academy of Sciences, 1992, v. 655, n. 1, p. 309, doi. 10.1111/j.1749-6632.1992.tb17079.x

By:

FISHMAN, GERALD J.

Publication type:

Article

Retinal Histopathology in Eyes from a Patient with Stargardt disease caused by Compound Heterozygous ABCA4 Mutations.

Published in:

Ophthalmic Genetics, 2016, v. 37, n. 2, p. 150, doi. 10.3109/13816810.2014.958861

By:

Bonilha, Vera L.;
Rayborn, Mary E.;
Bell, Brent A.;
Marino, Meghan J.;
Fishman, Gerald A.;
Hollyfield, Joe G.

Publication type:

Article

Whole Exome Sequencing Identifies an Adult-Onset Case of Methylmalonic Aciduria and Homocystinuria Type C (cblC) with Non-Syndromic Bull’s Eye Maculopathy.

Published in:

Ophthalmic Genetics, 2015, v. 36, n. 3, p. 270, doi. 10.3109/13816810.2015.1010736

By:

Collison, Frederick T.;
Xie, Yajing (Angela);
Gambin, Tomasz;
Jhangiani, Shalini;
Muzny, Donna;
Gibbs, Richard;
Lupski, James R.;
Fishman, Gerald A.;
Allikmets, Rando

Publication type:

Article

Resolution of Mid-Peripheral Schisis in X-Linked Retinoschisis with the Use of Dorzolamide.

Published in:

Ophthalmic Genetics, 2014, v. 35, n. 2, p. 125, doi. 10.3109/13816810.2013.779383

By:

Collison, Frederick T.;
Genead, Mohamed A.;
Fishman, Gerald A.;
Stone, Edwin M.

Publication type:

Article

The Prevalence of Macular Cysts in Patients with Clinical Cone-Rod Dystrophy Determined by Spectral-Domain Optical Coherence Tomography.

Published in:

Ophthalmic Genetics, 2014, v. 35, n. 1, p. 47, doi. 10.3109/13816810.2013.804095

By:

Salvatore, Serena;
Genead, Mohamed A.;
Fishman, Gerald A.

Publication type:

Article

Electroretinographic Findings in a Patient with Congenital Stationary Night Blindness Due to a Novel NYX Mutation.

Published in:

Ophthalmic Genetics, 2013, v. 34, n. 3, p. 167, doi. 10.3109/13816810.2012.743570

By:

McAnany, J. Jason;
Alexander, Kenneth R.;
Kumar, Nalin M.;
Ying, Hongyu;
Anastasakis, Anastasios;
Fishman, Gerald A.

Publication type:

Article

Structural and Functional Measures of Inner Retinal Integrity Following Visual Acuity Improvement in a Patient with Hereditary Motor and Sensory Neuropathy Type VI.

Published in:

Ophthalmic Genetics, 2011, v. 32, n. 3, p. 188, doi. 10.3109/13816810.2011.587859

By:

Gowrisankaran, Sowjanya;
Anastasakis, Anastasios;
Fishman, Gerald A.;
Alexander, Kenneth R.

Publication type:

Article

Retinal Nerve Fiber Thickness Measurements In Choroideremia Patients With Spectral-Domain Optical Coherence Tomography.

Published in:

Ophthalmic Genetics, 2011, v. 32, n. 2, p. 101, doi. 10.3109/13816810.2010.544364

By:

Genead, Mohamed A.;
McAnany, J. Jason;
Fishman, Gerald A.

Publication type:

Article

Microperimetry and OCT findings in female carriers of choroideremia.

Published in:

Ophthalmic Genetics, 2010, v. 31, n. 4, p. 235, doi. 10.3109/13816810.2010.518578

By:

Thobani, Azzrah;
Anastasakis, Anastasios;
Fishman, Gerald A.

Publication type:

Article

Historical evolution in the understanding of Stargardt macular dystrophy.

Published in:

Ophthalmic Genetics, 2010, v. 31, n. 4, p. 183, doi. 10.3109/13816810.2010.499887

By:

Fishman, Gerald Allen

Publication type:

Article

Spectral-Domain Optical Coherence Tomography and Fundus Autofluorescence Characteristics in Patients with Fundus Albipunctatus and Retinitis Punctata Albescens.

Published in:

Ophthalmic Genetics, 2010, v. 31, n. 2, p. 66, doi. 10.3109/13816810903584971

By:

Genead, Mohamed A.;
Fishman, Gerald A.;
Lindeman, Martin

Publication type:

Article

Retinal pathology of a patient with Goldmann-Favre Syndrome.

Published in:

Ophthalmic Genetics, 2009, v. 30, n. 4, p. 172, doi. 10.3109/13816810903176765

By:

Bonilha, Vera L.;
Fishman, Gerald A.;
Rayborn, Mary E.;
Hollyfield, Joe G.

Publication type:

Article

Natural History of Phenotypic Changes in Stargardt Macular Dystrophy.

Published in:

Ophthalmic Genetics, 2009, v. 30, n. 2, p. 63, doi. 10.1080/13816810802695550

By:

Walia, Saloni;
Fishman, Gerald A.

Publication type:

Article

Flecked-Retina Syndromes.

Published in:

Ophthalmic Genetics, 2009, v. 30, n. 2, p. 69, doi. 10.1080/13816810802654516

By:

Walia, Saloni;
Fishman, Gerald A.;
Kapur, Rashmi

Publication type:

Article

John Dalton: Though in Error, He Still Influenced Our Understanding of Congenital Color Deficiency.

Published in:

Ophthalmic Genetics, 2008, v. 29, n. 4, p. 162, doi. 10.1080/13816810802251446

By:

Fishman, Gerald A.

Publication type:

Article

Retinal Dysfunction in Carriers of Bardet-Biedl Syndrome.

Published in:

Ophthalmic Genetics, 2007, v. 28, n. 3, p. 163, doi. 10.1080/13816810701537440

By:

Kim, Linda S.;
Fishman, Gerald A.;
Seiple, William H.;
Szlyk, Janet P.;
Stone, Edwin M.

Publication type:

Article

Abnormal Distribution of Red/Green Cone Opsins in a Patient with an Autosomal Dominant Cone Dystrophy.

Published in:

Ophthalmic Genetics, 2005, v. 26, n. 2, p. 69, doi. 10.1080/13816810590968041

By:

Bonilha, Vera L.;
Hollyfield, Joe G.;
Grover, Sandeep;
Fishman, Gerald A.

Publication type:

Article

Autoantibodies in Melanoma-Associated Retinopathy Target TRPM1 Cation Channels of Retinal ON Bipolar Cells.

Published in:

Journal of Neuroscience, 2011, v. 31, n. 11, p. 3962, doi. 10.1523/JNEUROSCI.6007-10.2011

By:

Dhingra, Anuradha;
Fina, Marie E.;
Neinstein, Adam;
Ramsey, David J.;
Ying Xu;
Fishman, Gerald A.;
Alexander, Kenneth R.;
Haohua Qian;
Peachey, Neal S.;
Gregg, Ronald G.;
Vardi, Noga

Publication type:

Article

Two-color pupillometry in KCNV2 retinopathy.

Published in:

Documenta Ophthalmologica, 2019, v. 139, n. 1, p. 11, doi. 10.1007/s10633-019-09691-w

By:

Collison, Frederick T.;
Park, Jason C.;
Fishman, Gerald A.;
Stone, Edwin M.;
McAnany, J. Jason

Publication type:

Article

Unanticipated prognosis for a patient with type 2 Usher syndrome.

Published in:

Documenta Ophthalmologica, 2019, v. 138, n. 2, p. 161, doi. 10.1007/s10633-019-09677-8

By:

Vezinaw, Chloe M.;
Fishman, Gerald A.;
Chiang, John

Publication type:

Article

Abnormal 8-Hz flicker electroretinograms in carriers of X-linked retinoschisis.

Published in:

Documenta Ophthalmologica, 2016, v. 133, n. 1, p. 61, doi. 10.1007/s10633-016-9551-0

By:

Mcanany, J.;
Park, Jason;
Collison, Frederick;
Fishman, Gerald;
Stone, Edwin

Publication type:

Article

Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

Published in:

Documenta Ophthalmologica, 2016, v. 132, n. 3, p. 157, doi. 10.1007/s10633-016-9535-0

By:

Fishman, Gerald;
Collison, Frederick;
Park, Jason;
McAnany, J.;
Stone, Edwin

Publication type:

Article

Rod and cone contributions to the dark-adapted 15-Hz flicker electroretinogram.

Published in:

Documenta Ophthalmologica, 2015, v. 130, n. 2, p. 111, doi. 10.1007/s10633-015-9480-3

By:

Park, Jason;
Cao, Dingcai;
Collison, Frederick;
Fishman, Gerald;
Jason McAnany, J.

Publication type:

Article

Gamma-Ray Observatory: The next great observatory in space.

Published in:

Mercury, 1990, v. 19, n. 4, p. 98

By:

Neal, Valerie;
Fishman, Gerald

Publication type:

Article

Polymorphisms and rare sequence variants at the ROM1 locus.

Published in:

Human Molecular Genetics, 1993, v. 2, n. 11, p. 1975

By:

Bascom, Roger A.;
Liu, Lin;
Humphries, Peter;
Fishman, Gerald A.;
Murray, Jeffrey C.;
Mcinnes, Roderick R.

Publication type:

Article

Novel frameshift mutations in CRX associated with Leber congenital amaurosis.

Published in:

Human Mutation, 2001, v. 18, n. 6, p. 550, doi. 10.1002/humu.1243

By:

Rivolta, Carlo;
Peck, Naomi E.;
Fulton, Anne B.;
Fishman, Gerald A.;
Berson, Eliot L.;
Dryja, Thaddeus P.

Publication type:

Article

Five novel RPGR mutations in families with X-linked retinitis pigmentosa.

Published in:

Human Mutation, 2001, v. 17, n. 2, p. 151, doi. 10.1002/1098-1004(200102)17:2<151::AID-HUMU7>3.0.CO;2-W

By:

Guevara-Fujita, Maria;
Fahrner, Stacey;
Buraczynska, Kinga;
Cook, Jason;
Wheaton, Dianna;
Cortes, Fanny;
Vicencio, Cesar;
Pena, Marcela;
Fishman, Gerald A.;
Mintz-Hittner, Helen;
Birch, David;
Hoffman, Dennis;
Mears, Alan J.;
Fujita, Ricardo;
Swaroop, Anand

Publication type:

Article

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change.

Published in:

Human Mutation, 1999, v. 14, n. 5, p. 423, doi. 10.1002/(SICI)1098-1004(199911)14:5<423::AID-HUMU8>3.0.CO;2-D

By:

Hiriyanna, Kelaginamane T.;
Bingham, Eve L.;
Yashar, Beverly M.;
Ayyagari, Radha;
Fishman, Gerald;
Small, Kent W.;
Weinberg, David V.;
Weleber, Richard G.;
Lewis, Richard A.;
Andreasson, Sten;
Richards, Julia E.;
Sieving, Paul A.

Publication type:

Article

Dealer Options.

Published in:

Journal of Futures Markets, 1981, v. 1, n. 1, p. 535

By:

Fishman, Gerald L.

Publication type:

Article

Interocular Symmetry of Foveal Cone Topography in Congenital Achromatopsia.

Published in:

Current Eye Research, 2020, v. 45, n. 10, p. 1257, doi. 10.1080/02713683.2020.1737138

By:

Litts, Katie M.;
Georgiou, Michalis;
Langlo, Christopher S.;
Patterson, Emily J.;
Mastey, Rebecca R.;
Kalitzeos, Angelos;
Linderman, Rachel E.;
Lam, Byron L.;
Fishman, Gerald A.;
Pennesi, Mark E.;
Kay, Christine N.;
Hauswirth, William W.;
Michaelides, Michel;
Carroll, Joseph

Publication type:

Article

Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease.

Published in:

PLoS Genetics, 2022, v. 18, n. 3, p. 1, doi. 10.1371/journal.pgen.1010129

By:

Zernant, Jana;
Lee, Winston;
Wang, Jun;
Goetz, Kerry;
Ullah, Ehsan;
Nagasaki, Takayuki;
Su, Pei-Yin;
Fishman, Gerald A.;
Tsang, Stephen H.;
Tumminia, Santa J.;
Brooks, Brian P.;
Hufnagel, Robert B.;
Chen, Rui;
Allikmets, Rando

Publication type:

Article

On the association of terrestrial gamma-ray bursts with lightning and implications for sprites.

Published in:

Geophysical Research Letters, 1996, v. 23, n. 9, p. 1017, doi. 10.1029/96GL00746

By:

Inan, Umran S.;
Reising, Steven C.;
Fishman, Gerald J.;
Horack, John M.

Publication type:

Article

Psychological Profiles of Patients with Central Vision Loss.

Published in:

Journal of Visual Impairment & Blindness, 2000, v. 94, n. 12, p. 781, doi. 10.1177/0145482x0009401206

By:

Szlyk, Janet P.;
Becker, Jillian E.;
Fishman, Gerald A.;
Seiple, William

Publication type:

Article

Efficacy of topical dorzolamide for treatment of cystic macular lesions in a patient with enhanced S-cone syndrome.

Published in:

Documenta Ophthalmologica, 2010, v. 121, n. 3, p. 231, doi. 10.1007/s10633-010-9247-9

By:

Genead, Mohamed;
Fishman, Gerald;
McAnany, J.

Publication type:

Article

Macular vitelliform lesion in desferrioxamine-related retinopathy.

Published in:

Documenta Ophthalmologica, 2010, v. 121, n. 2, p. 161, doi. 10.1007/s10633-010-9236-z

By:

Genead, Mohamed A.;
Fishman, Gerald A.;
Anastasakis, Anastasios;
Lindeman, Martin

Publication type:

Article

Fundus white spots and acquired night blindness due to vitamin A deficiency.

Published in:

Documenta Ophthalmologica, 2009, v. 119, n. 3, p. 229, doi. 10.1007/s10633-009-9200-y

By:

Mohamed Genead;
Gerald Fishman;
Martin Lindeman

Publication type:

Article

Diagnosis in a patient with fundus albipunctatus and atypical fundus changes.

Published in:

Documenta Ophthalmologica, 2009, v. 118, n. 3, p. 233, doi. 10.1007/s10633-008-9151-8

By:

Manal Hajali;
Gerald Fishman;
Thaddeus Dryja;
Meredith Sweeney;
Martin Lindeman

Publication type:

Article

Multifocal ERG findings in carriers of X-linked retinoschisis.

Published in:

Documenta Ophthalmologica, 2007, v. 114, n. 1, p. 21, doi. 10.1007/s10633-006-9034-9

By:

Linda Kim;
Gerald Fishman

Publication type:

Article