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Paul Sieving

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Kari E H Branham; Matthew Brumm; Maria Laura Ciccarelli; Jacque L Duncan; Gerald A Fishman; John R Heckenlively; Alessandro Iannaccone; Samuel G Jacobson; K Thiran Jayasundera; Barbara Jennings; Athanasios J Karoukis; Richard A Lewis; Mohammad Othman; Sharon B Schwartz; Paul Sieving; Niamh B Stover; sten andreasson; Pelin Atmaca Sonmez; Jean Bennett; David Birch; Karmen M Trzupek; Richard G Weleber; Dianna Wheaton; Beverly M Yashar; Anand Swaroop
Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease.
Muhammad Asif Naeem; Saima Riazuddin; Sheikh Riazuddin; Shahbaz Ali; Radha Ayyagari; Venkata R M Chavali; J Fielding Hejtmancik; Tayyab Husnain; Muhammad Iqbal; Shaheen N Khan; Paul Sieving; Sheikh Amer Riazuddin
GNAT1 associated with autosomal recessive congenital stationary night blindness.
Kristen Bowles; Ronald A Bush; Catherine Cukras; Yuri Sergeev; Amy Turriff; Susan Vitale; Paul Sieving
X-linked retinoschisis: RS1 mutation severity and age affect the ERG phenotype in a cohort of 68 affected male subjects.

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All Publications

2012: Kari E H Branham; Matthew Brumm; Maria Laura Ciccarelli; Jacque L Duncan; Gerald A Fishman; John R Heckenlively; Alessandro Iannaccone; Samuel G Jacobson; K Thiran Jayasundera; Barbara Jennings; Athanasios J Karoukis; Richard A Lewis; Mohammad Othman; Sharon B Schwartz; Paul Sieving; Niamh B Stover; sten andreasson; Pelin Atmaca Sonmez; Jean Bennett; David Birch; Karmen M Trzupek; Richard G Weleber; Dianna Wheaton; Beverly M Yashar; Anand Swaroop
Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease.
Investigative ophthalmology & visual science 2012;53(13):8232-7.
2012: Muhammad Asif Naeem; Saima Riazuddin; Sheikh Riazuddin; Shahbaz Ali; Radha Ayyagari; Venkata R M Chavali; J Fielding Hejtmancik; Tayyab Husnain; Muhammad Iqbal; Shaheen N Khan; Paul Sieving; Sheikh Amer Riazuddin
GNAT1 associated with autosomal recessive congenital stationary night blindness.
Investigative ophthalmology & visual science 2012;53(3):1353-61.
2011: Kristen Bowles; Ronald A Bush; Catherine Cukras; Yuri Sergeev; Amy Turriff; Susan Vitale; Paul Sieving
X-linked retinoschisis: RS1 mutation severity and age affect the ERG phenotype in a cohort of 68 affected male subjects.
Investigative ophthalmology & visual science 2011;52(12):9250-6.
2010: Camasamudram Vijayasarathy; Ruifang Sui; Yong Zeng; Guoxing Yang; Fei Xu; Rafael C Caruso; Richard A Lewis; Lucia Ziccardi; Paul Sieving
Molecular mechanisms leading to null-protein product from retinoschisin (RS1) signal-sequence mutants in X-linked retinoschisis (XLRS) disease.
Human mutation 2010;31(11):1251-60.
2010: Sheikh Amer Riazuddin; Amber Shahzadi; Christina Zeitz; Zubair M Ahmed; Radha Ayyagari; Venkata R M Chavali; Virgilio G Ponferrada; Isabelle Audo; Christelle Michiels; Marie-Elise Lancelot; Idrees A Nasir; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Xiaodong Jiao; Ian M MacDonald; Sheikh Riazuddin; Paul Sieving; Nicholas Katsanis; J Fielding Hejtmancik
A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.
American journal of human genetics 2010;87(4):523-31.
2010: Lin Li; Naoki Nakaya; Venkata R M Chavali; Zhiwei Ma; Xiaodong Jiao; Paul Sieving; Sheikh Riazuddin; Stanislav I Tomarev; Radha Ayyagari; Sheikh Amer Riazuddin; J Fielding Hejtmancik
A mutation in ZNF513, a putative regulator of photoreceptor development, causes autosomal-recessive retinitis pigmentosa.
American journal of human genetics 2010;87(3):400-9.
2010: Sten Kjellström; Camasamudram Vijayasarathy; Vesna Ponjavic; Paul Sieving; Sten Andréasson
Long-term 12 year follow-up of X-linked congenital retinoschisis.
Ophthalmic genetics 2010;31(3):114-25.
2010: Svetlana Kotova; Camasamudram Vijayasarathy; Emilios K Dimitriadis; Laertis Ikonomou; Howard Jaffe; Paul Sieving
Retinoschisin (RS1) interacts with negatively charged lipid bilayers in the presence of Ca2+: an atomic force microscopy study.
Biochemistry 2010;49(33):7023-32.
2010: Amber Shahzadi; Sheikh Amer Riazuddin; Shahbaz Ali; David Li; Shaheen N Khan; Tayyab Husnain; Javed Akram; Paul Sieving; J Fielding Hejtmancik; Sheikh Riazuddin
Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family.
The British journal of ophthalmology 2010;94(8):1094-9.
2010: Dorit Raz-Prag; William N Grimes; Robert Fariss; Camasamudram Vijayasarathy; Maria M Campos; Ronald A Bush; Jeffrey S Diamond; Paul Sieving
Probing potassium channel function in vivo by intracellular delivery of antibodies in a rat model of retinal neurodegeneration.
Proceedings of the National Academy of Sciences of the United States of America 2010;107(28):12710-5.
2010: Sheikh Amer Riazuddin; Muhammad Iqbal; Yue Wang; Tomohiro Masuda; Yuhng Chen; Sara Bowne; Lori S Sullivan; Naushin H Waseem; Shomi Bhattacharya; Stephen P Daiger; Kang Zhang; Shaheen N Khan; Sheikh Riazuddin; J Fielding Hejtmancik; Paul Sieving; Donald J Zack; Nicholas Katsanis
A splice-site mutation in a retina-specific exon of BBS8 causes nonsyndromic retinitis pigmentosa.
American journal of human genetics 2010;86(5):805-12.
2010: Shagufta Naz; Sheikh Amer Riazuddin; Lin Li; Mariam Shahid; Samra Kousar; Paul Sieving; J Fielding Hejtmancik; Sheikh Riazuddin
A novel locus for autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family maps to chromosome 2p.
American journal of ophthalmology 2010;149(5):861-6.
2010: D M Wu; Babak Behnam; Pelin Atmaca Sonmez; Paul Sieving; Kari E H Branham; Mohammad I Othman; Anand Swaroop; Stephen P Daiger; John R Heckenlively
Long-term follow-up of a family with dominant X-linked retinitis pigmentosa.
Eye (London, England) 2010;24(5):764-74.
2010: Y V Sergeev; R C Caruso; M R Meltzer; N Smaoui; I M MacDonald; Paul Sieving
Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisis.
Human molecular genetics 2010;19(7):1302-13.
2010: Paul Sieving
At the frontier of vision research: the National Eye Institute celebrates 40 years.
American journal of ophthalmology 2010;149(2):179-81.
2009: Camasamudram Vijayasarathy; Lucia Ziccardi; Yong Zeng; Nizar Smaoui; Rafael C Caruso; Paul Sieving
Null retinoschisin-protein expression from an RS1 c354del1-ins18 mutation causing progressive and severe XLRS in a cross-sectional family study.
Investigative ophthalmology & visual science 2009;50(11):5375-83.
2009: Gabriel Luna; Sten Kjellstrom; Mark R Verardo; Geoffrey P Lewis; Jiyun Byun; Paul Sieving; Steven K Fisher
The effects of transient retinal detachment on cavity size and glial and neural remodeling in a mouse model of X-linked retinoschisis.
Investigative ophthalmology & visual science 2009;50(8):3977-84.
2009: Dorit Raz-Prag; Yong Zeng; Paul Sieving; Ronald A Bush
Photoreceptor protection by adeno-associated virus-mediated LEDGF expression in the RCS rat model of retinal degeneration: probing the mechanism.
Investigative ophthalmology & visual science 2009;50(8):3897-906.
2009: T K Park; Z Wu; Sten Kjellstrom; Yong Zeng; Ronald A Bush; Paul Sieving; P Colosi
Intravitreal delivery of AAV8 retinoschisin results in cell type-specific gene expression and retinal rescue in the Rs1-KO mouse.
Gene therapy 2009;16(7):916-26.
2009: Masatoshi Haruta; Ronald A Bush; Sten Kjellstrom; Camasamudram Vijayasarathy; Yong Zeng; Yun-Zheng Le; Paul Sieving
Depleting Rac1 in mouse rod photoreceptors protects them from photo-oxidative stress without affecting their structure or function.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(23):9397-402.
2008: Alexander M Dizhoor; Michael L Woodruff; Elena V Olshevskaya; Marianne C Cilluffo; M Carter Cornwall; Paul Sieving; Gordon L Fain
Night blindness and the mechanism of constitutive signaling of mutant G90D rhodopsin.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2008;28(45):11662-72.
2008: Yuichiro Takada; Camasamudram Vijayasarathy; Yong Zeng; Sten Kjellstrom; Ronald A Bush; Paul Sieving
Synaptic pathology in retinoschisis knockout (Rs1-/y) mouse retina and modification by rAAV-Rs1 gene delivery.
Investigative ophthalmology & visual science 2008;49(8):3677-86.
2008: Brian P Brooks; Ian M Macdonald; Santa J Tumminia; Nizar Smaoui; Delphine Blain; Ajaina A Nezhuvingal; Paul Sieving
Genomics in the era of molecular ophthalmology: reflections on the National Ophthalmic Disease Genotyping Network (eyeGENE).
Archives of ophthalmology 2008;126(3):424-5.
2008: Zubair M Ahmed; Sten Kjellstrom; Ricky J L Haywood-Watson; Ronald A Bush; Lori L Hampton; James F Battey; Saima Riazuddin; Gregory Frolenkov; Paul Sieving; Thomas B Friedman
Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration.
Molecular vision 2008;14():2227-36.
2008: Camasamudram Vijayasarathy; Yuichiro Takada; Yong Zeng; Ronald A Bush; Paul Sieving
Organization and molecular interactions of retinoschisin in photoreceptors.
Advances in experimental medicine and biology 2008;613():291-7.
2008: Shigeki Machida; Dorit Raz-Prag; Robert Fariss; Paul Sieving; Ronald A Bush
Photopic ERG negative response from amacrine cell signaling in RCS rat retinal degeneration.
Investigative ophthalmology & visual science 2008;49(1):442-52.
2007: Ian M MacDonald; Brian P Brooks; Paul Sieving
Eyeing a new network.
Science (New York, N.Y.) 2007;318(5853):1068.
2007: Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; Sheikh Amer Riazuddin; Zahoor Ahmad; Raphael Caruso; Ian MacDonald; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene.
Human genetics 2007;122(3-4):293-9.
2007: Michael L Woodruff; Elena V Olshevskaya; Andrey B Savchenko; Igor V Peshenko; Ronald Barrett; Ronald A Bush; Paul Sieving; Gordon L Fain; Alexander M Dizhoor
Constitutive excitation by Gly90Asp rhodopsin rescues rods from degeneration caused by elevated production of cGMP in the dark.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2007;27(33):8805-15.
2007: Naheed W Khan; Bernd Wissinger; Susanne Kohl; Paul Sieving
CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated function.
Investigative ophthalmology & visual science 2007;48(8):3864-71.
2007: Sten Kjellstrom; Ronald A Bush; Yong Zeng; Yuichiro Takada; Paul Sieving
Retinoschisin gene therapy and natural history in the Rs1h-KO mouse: long-term rescue from retinal degeneration.
Investigative ophthalmology & visual science 2007;48(8):3837-45.
2007: Ian M MacDonald; Yves Sauvé; Paul Sieving
Preventing blindness in retinal disease: ciliary neurotrophic factor intraocular implants.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie 2007;42(3):399-402.
2007: Camasamudram Vijayasarathy; Yuichiro Takada; Yong Zeng; Ronald A Bush; Paul Sieving
Retinoschisin is a peripheral membrane protein with affinity for anionic phospholipids and affected by divalent cations.
Investigative ophthalmology & visual science 2007;48(3):991-1000.
2007: Paul Sieving; Francis S Collins
Genetic ophthalmology and the era of clinical care.
JAMA : the journal of the American Medical Association 2007;297(7):733-6.
2007: Katy Downs; David N Zacks; Rafael Caruso; Athanasios J Karoukis; Kari E H Branham; Beverly M Yashar; Mark H Haimann; Karmen M Trzupek; Meira Meltzer; Delphine Blain; Julia E Richards; Richard G Weleber; John R Heckenlively; Paul Sieving; Radha Ayyagari
Molecular testing for hereditary retinal disease as part of clinical care.
Archives of ophthalmology 2007;125(2):252-8.
2006: Rong Wen; Ying Song; Sten Kjellstrom; Atsuhiro Tanikawa; Yun Liu; Yiwen Li; Lian Zhao; Ronald A Bush; Alan M Laties; Paul Sieving
Regulation of rod phototransduction machinery by ciliary neurotrophic factor.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2006;26(52):13523-30.
2006: Camasamudram Vijayasarathy; Mary Ann Gawinowicz; Yong Zeng; Yuichiro Takada; Ronald A Bush; Paul Sieving
Identification and characterization of two mature isoforms of retinoschisin in murine retina.
Biochemical and biophysical research communications 2006;349(1):99-105.
2006: Azamat Aslanukov; Reshma Bhowmick; Mallikarjuna Guruju; John Oswald; Dorit Raz; Ronald A Bush; Paul Sieving; Xinrong Lu; Cheryl B Bock; Paulo A Ferreira
RanBP2 modulates Cox11 and hexokinase I activities and haploinsufficiency of RanBP2 causes deficits in glucose metabolism.
PLoS genetics 2006;2(10):e177.
2006: Vidyullatha Vasireddy; Monica M Jablonski; Md Nawajes A Mandal; Dorit Raz-Prag; Xiaofei F Wang; Lesli Nizol; Alessandro Iannaccone; David C Musch; Ronald A Bush; Norman Salem; Paul Sieving; Radha Ayyagari
Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor degeneration.
Investigative ophthalmology & visual science 2006;47(10):4558-68.
2006: Jonathan L Prenner; Antonio Capone; Stefano Ciaccia; Yuichiro Takada; Paul Sieving; Michael T Trese
Congenital X-linked retinoschisis classification system.
Retina (Philadelphia, Pa.) 2006;26(7 Suppl):S61-4.
2006: Dorit Raz-Prag; Radha Ayyagari; Robert Fariss; Md Nawajes A Mandal; Vidyullatha Vasireddy; Sharon Majchrzak-Hong; Andrea L Webber; Ronald A Bush; Norman Salem; Konstantin Petrukhin; Paul Sieving
Haploinsufficiency is not the key mechanism of pathogenesis in a heterozygous Elovl4 knockout mouse model of STGD3 disease.
Investigative ophthalmology & visual science 2006;47(8):3603-11.
2006: Ricky J L Haywood-Watson; Zubair M Ahmed; Sten Kjellstrom; Ronald A Bush; Yuichiro Takada; Lori L Hampton; James F Battey; Paul Sieving; Thomas B Friedman
Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts.
Investigative ophthalmology & visual science 2006;47(7):3074-84.
2006: Duane F Alexander; Barbara M Alving; James F Battey; Jeremy Berg; Francis S Collins; Anthony Fauci; John Gallin; Patricia A Grady; Richard J Hodes; Sharon H Hrynkow; Thomas R Insel; Jack F Jones; Stephen I Katz; Story C Landis; Ting-Kai Li; Donald A Lindberg; Elizabeth G Nabel; John E Niederhuber; Roderic I Pettigrew; Griffin P Rodgers; John Ruffin; Antonio Scarpa; David A Schwartz; Paul Sieving; Stephen E Straus; Lawrence Tabak; Nora D Volkow
Response to: "Rescuing the NIH before it is too late".
The Journal of clinical investigation 2006;116(6):1462-3.
2006: Paul Sieving; Rafael C Caruso; Weng Tao; Hanna R Coleman; Darby J S Thompson; Keri Fullmer; Ronald A Bush
Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implants.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(10):3896-901.
2006: Sheikh Amer Riazuddin; Fareeha Zulfiqar; Qingjiong Zhang; Wenliang Yao; Shouling Li; Xiaodong Jiao; Amber Shahzadi; MUHAMMAD AMER; Muhammad Iqbal; Tayyab Hussnain; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Mutations in the gene encoding the alpha-subunit of rod phosphodiesterase in consanguineous Pakistani families.
Molecular vision 2006;12():1283-91.
2006: Yuichiro Takada; Robert Fariss; Morten Muller; Ronald A Bush; Elisabeth J Rushing; Paul Sieving
Retinoschisin expression and localization in rodent and human pineal and consequences of mouse RS1 gene knockout.
Molecular vision 2006;12():1108-16.
2005: Debra A Thompson; Andreas R Janecke; Jessica Lange; Kecia L Feathers; Christian A Hübner; Christina L McHenry; David Wayne Stockton; Gabriele Rammesmayer; James R Lupski; Guillermo Antinolo; Carmen Ayuso; Montserrat Baiget; Peter Gouras; John R Heckenlively; Anneke I den Hollander; Samuel G Jacobson; Richard A Lewis; Paul Sieving; Bernd Wissinger; Suzanne Yzer; Eberhart Zrenner; Gerd Utermann; Andreas Gal
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle.
Human molecular genetics 2005;14(24):3865-75.
2005: Paul Sieving
Fostering partnerships: The National Institutes of Health (NIH) Mission.
Retina (Philadelphia, Pa.) 2005;25(8 Suppl):S84-S85.
2005: Paul Sieving
The national eye institute: translational clinical research initiatives on inherited and orphan retinal diseases: personal observations.
Retina (Philadelphia, Pa.) 2005;25(8 Suppl):S8-S9.
2005: Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; Sheikh Amer Riazuddin; Radha Ayyagari; Farooq Sabar; Raphael Caruso; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4.
Human genetics 2005;118(3-4):356-65.
2005: Radha Ayyagari; Md Nawajes A Mandal; Athanasios J Karoukis; Lianchun Chen; Ning C McLaren; Mona Lichter; David T Wong; Peter F Hitchcock; Rafael C Caruso; Sayoko E Moroi; Irene H Maumenee; Paul Sieving
Late-onset macular degeneration and long anterior lens zonules result from a CTRP5 gene mutation.
Investigative ophthalmology & visual science 2005;46(9):3363-71.
2005: Md Nawajes A Mandal; John R Heckenlively; Tracy Burch; Lianchun Chen; Vidyullatha Vasireddy; Robert K Koenekoop; Paul Sieving; Radha Ayyagari
Sequencing arrays for screening multiple genes associated with early-onset human retinal degenerations on a high-throughput platform.
Investigative ophthalmology & visual science 2005;46(9):3355-62.
2005: Joseph A Brzezinski; Nadean L Brown; Atsuhiro Tanikawa; Ronald A Bush; Paul Sieving; Martha Hotz Vitaterna; Joseph S Takahashi; Thomas M Glaser
Loss of circadian photoentrainment and abnormal retinal electrophysiology in Math5 mutant mice.
Investigative ophthalmology & visual science 2005;46(7):2540-51.
2005: Sheikh Amer Riazuddin; Fareeha Zulfiqar; Qingjiong Zhang; Yuri V Sergeev; Zaheeruddin A Qazi; Tayyab Husnain; Raphael Caruso; Sheikh Riazuddin; Paul Sieving; J Fielding Hejtmancik
Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
Investigative ophthalmology & visual science 2005;46(7):2264-70.
2005: Susanne Kohl; Balazs Varsanyi; Gesine Abadin Antunes; Britta Baumann; Carel B Hoyng; Herbert Jägle; Thomas Rosenberg; Ulrich Kellner; Birgit Lorenz; Roberto Salati; Bernhard Jurklies; Ágnes Farkas; sten andreasson; Richard G Weleber; Samuel G Jacobson; Günther Rudolph; Claudio Castellan; Hélène Dollfus; Eric Legius; Mario Anastasi; Pierre Bitoun; Dorit Lev; Paul Sieving; Francis L Munier; Eberhart Zrenner; Lindsay T Sharpe; Frans P M Cremers; Bernd Wissinger
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
European journal of human genetics : EJHG 2005;13(3):302-8.
2005: Qingjiong Zhang; Fareeha Zulfiqar; Sheikh Amer Riazuddin; Xueshan Xiao; Afshan Yasmeen; Peter K Rogan; Raphael Caruso; Paul Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.
Molecular vision 2005;11():977-85.
2005: Vidyullatha Vasireddy; Camasamudram Vijayasarathy; Jibiao Huang; Xiaofei F Wang; Monica M Jablonski; Howard R Petty; Paul Sieving; Radha Ayyagari
Stargardt-like macular dystrophy protein ELOVL4 exerts a dominant negative effect by recruiting wild-type protein into aggresomes.
Molecular vision 2005;11():665-76.
2005: Naheed W Khan; Mineo Kondo; Kelaginamane T Hiriyanna; Jeffrey A Jamison; Ronald A Bush; Paul Sieving
Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Genetic Night Blindness.
Journal of neurophysiology 2005;93(1):481-92.
2004: Yuichiro Takada; Robert Fariss; Atsuhiro Tanikawa; Yong Zeng; Deborah A Carper; Ronald Bush; Paul Sieving
A retinal neuronal developmental wave of retinoschisin expression begins in ganglion cells during layer formation.
Investigative ophthalmology & visual science 2004;45(9):3302-12.
2004: Yong Zeng; Yuichiro Takada; Sten Kjellstrom; Kelaginamane T Hiriyanna; Atsuhiro Tanikawa; Eric F Wawrousek; Nizar Smaoui; Rafael Caruso; Ronald A Bush; Paul Sieving
RS-1 Gene Delivery to an Adult Rs1h Knockout Mouse Model Restores ERG b-Wave with Reversal of the Electronegative Waveform of X-Linked Retinoschisis.
Investigative ophthalmology & visual science 2004;45(9):3279-85.
2004: Ronald A Bush; Bo Lei; Weng Tao; Dorit Raz; Chi-Chao Chan; Terry A Cox; Maria Santos-Muffley; Paul Sieving
Encapsulated cell-based intraocular delivery of ciliary neurotrophic factor in normal rabbit: dose-dependent effects on ERG and retinal histology.
Investigative ophthalmology & visual science 2004;45(7):2420-30.
2004: Paul Sieving
Healthy Vision Month--May 2004: focus is on diabetic retinopathy.
Optometry (St. Louis, Mo.) 2004;75(5):271-3.
2004: Thomas R Insel; Nora D Volkow; Story C Landis; Ting-Kai Li; James F Battey; Paul Sieving
Limits to growth: why neuroscience needs large-scale science.
Nature neuroscience 2004;7(5):426-7.
2004: Christina L McHenry; Yuhui Liu; Wei Feng; Anita R Nair; Kecia L Feathers; Xiaoling Ding; Andreas Gal; Douglas Vollrath; Paul Sieving; Debra A Thompson
MERTK arginine-844-cysteine in a patient with severe rod-cone dystrophy: loss of mutant protein function in transfected cells.
Investigative ophthalmology & visual science 2004;45(5):1456-63.
2004: Md Nawajes A Mandal; Rajesh Ambasudhan; Paul W Wong; Philip J Gage; Paul Sieving; Radha Ayyagari
Characterization of mouse orthologue of ELOVL4: genomic organization and spatial and temporal expression.
Genomics 2004;83(4):626-35.
2004: Rajesh Ambasudhan; XiaoFei Wang; Monica M Jablonski; Debra A Thompson; Pamela S Lagali; Paul W Wong; Paul Sieving; Radha Ayyagari
Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein.
Genomics 2004;83(4):615-25.
2004: Goncalo Abecasis; Beverly M Yashar; Yu Zhao; Noor M Ghiasvand; Sepideh Zareparsi; Kari E H Branham; Adam C Reddick; Edward H Trager; Shigeo Yoshida; John Bahling; Elena Filippova; Susan G Elner; Mark W Johnson; Andrew K Vine; Paul Sieving; Samuel G Jacobson; Julia E Richards; Anand Swaroop
Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease.
American journal of human genetics 2004;74(3):482-94.
2003: Zubair M Ahmed; Sheikh Amer Riazuddin; Jamil Ahmad; Steven L Bernstein; Yan Guo; Muhammad F Sabar; Paul Sieving; Sheikh Riazuddin; Andrew J Griffith; Thomas B Friedman; Inna A Belyantseva; Edward R Wilcox
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23.
Human molecular genetics 2003;12(24):3215-23.
2003: Sayoko E Moroi; Kurt K Lark; Paul Sieving; Kouros Nouri-Mahdavi; Ursula Schlötzer-Schrehardt; Gregory J Katz; Robert Ritch
Long anterior zonules and pigment dispersion.
American journal of ophthalmology 2003;136(6):1176-8.
2003: Lisa A Schimmenti; Glenda S Manligas; Paul Sieving
Optic nerve dysplasia and renal insufficiency in a family with a novel PAX2 mutation, Arg115X: further ophthalmologic delineation of the renal-coloboma syndrome.
Ophthalmic genetics 2003;24(4):191-202.
2003: Thomas K M Lee; Kerry E McTaggart; Paul Sieving; John R Heckenlively; Alex V Levin; Jacquie Greenberg; Richard G Weleber; Patrick Y Tong; Edward F Anhalt; Berkley R Powell; Ian M MacDonald
Clinical diagnoses that overlap with choroideremia.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie 2003;38(5):364-72; quiz 372.
2003: Roxana A Radu; Nathan L Mata; Steven Nusinowitz; Xinran Liu; Paul Sieving; Gabriel H Travis
Treatment with isotretinoin inhibits lipofuscin accumulation in a mouse model of recessive Stargardt's macular degeneration.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(8):4742-7.
2003: Carlo Rivolta; Radha Ayyagari; Paul Sieving; Eliot L Berson; Thaddeus P Dryja
Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis.
Molecular vision 2003;9():49-51.
2003: Ceren Acar; Alan J Mears; Beverly M Yashar; Anjali S Maheshwary; sten andreasson; Alfonso Baldi; Paul Sieving; Alessandro Iannaccone; Maria A Musarella; Samuel G Jacobson; Anand Swaroop
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene.
Molecular vision 2003;9():14-7.
2002: Radha Ayyagari; F Yesim Demirci; Jiafan Liu; Eve L Bingham; Heather M Stringham; Laura E Kakuk; Michael Boehnke; Michael B Gorin; Julia E Richards; Paul Sieving
X-linked recessive atrophic macular degeneration from RPGR mutation.
Genomics 2002;80(2):166-71.
2002: Mineo Kondo; Paul Sieving
Post-photoreceptoral activity dominates primate photopic 32-Hz ERG for sine-, square-, and pulsed stimuli.
Investigative ophthalmology & visual science 2002;43(7):2500-7.
2002: Debra K Breuer; Beverly M Yashar; Elena Filippova; Suja Hiriyanna; Robert H Lyons Jr; Alan J Mears; Bersabell Asaye; Ceren Acar; Raf Vervoort; Alan F Wright; Maria A Musarella; Patricia Wheeler; Ian MacDonald; Alessandro Iannaccone; David Birch; Dennis R Hoffman; Gerald A Fishman; John R Heckenlively; Samuel G Jacobson; Paul Sieving; Anand Swaroop
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa.
American journal of human genetics 2002;70(6):1545-54.
2002: Valerie Traverso; Ronald A Bush; Paul Sieving; Dusanka Deretic
Retinal cAMP levels during the progression of retinal degeneration in rhodopsin P23H and S334ter transgenic rats.
Investigative ophthalmology & visual science 2002;43(5):1655-61.
2002: Joost Felius; Debra A Thompson; Naheed W Khan; Eve L Bingham; Jeffrey A Jamison; Jennifer A Kemp; Paul Sieving
Clinical course and visual function in a family with mutations in the RPE65 gene.
Archives of ophthalmology 2002;120(1):55-61.
2001: Radha Ayyagari; Kang Zhang; Amy Hutchinson; Z Yu; Anand Swaroop; Laura E Kakuk; J M Seddon; Paul S Bernstein; R A Lewis; Jaana Tammur; Zhenglin Yang; Yingying Li; H Zhang; Beverly M Yashar; Jiafan Liu; Konstantin Petrukhin; Paul Sieving; Rando Allikmets
Evaluation of the ELOVL4 gene in patients with age-related macular degeneration.
Ophthalmic genetics 2001;22(4):233-9.
2001: Naheed W Khan; Jeffrey A Jamison; J A Kemp; Paul Sieving
Analysis of photoreceptor function and inner retinal activity in juvenile X-linked retinoschisis.
Vision research 2001;41(28):3931-42.
2001: Alan J Mears; Mineo Kondo; Prabodh K Swain; Y Takada; Ronald A Bush; Thomas L Saunders; Paul Sieving; Anand Swaroop
Nrl is required for rod photoreceptor development.
Nature genetics 2001;29(4):447-52.
2001: David V Weinberg; Paul Sieving; Eve L Bingham; Lee M Jampol; Marilyn B Mets
Bietti crystalline retinopathy and juvenile retinoschisis in a family with a novel RS1 mutation.
Archives of ophthalmology 2001;119(11):1719-21.
2001: Paul Sieving; M L Fowler; Ronald A Bush; S Machida; Peter D Calvert; Daniel G Green; Clint L Makino; C L McHenry
Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell loss.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2001;21(15):5449-60.
2001: Paul Sieving
Fifteen years of work: the COMS outcomes for medium-sized choroidal melanoma.
Archives of ophthalmology 2001;119(7):1067-8.
2001: Debra A Thompson; Yun Li; Christina L McHenry; T J Carlson; X Ding; Paul Sieving; E Apfelstedt-Sylla; Andreas Gal
Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy.
Nature genetics 2001;28(2):123-4.
2001: Jeffrey A Jamison; Ronald A Bush; Bo Lei; Paul Sieving
Characterization of the rod photoresponse isolated from the dark-adapted primate ERG.
Visual neuroscience 2001;18(3):445-55.
2001: Marian Humphries; S Kiang; Niamh McNally; M A Donovan; Paul Sieving; Ronald A Bush; S Machida; Thomas G Cotter; AH Hobson; J Farrar; Peter Humphries; Paul F Kenna
Comparative structural and functional analysis of photoreceptor neurons of Rho-/- mice reveal increased survival on C57BL/6J in comparison to 129Sv genetic background.
Visual neuroscience 2001;18(3):437-43.
2001: S Machida; P Chaudhry; T Shinohara; Dhirendra P Singh; Venkat N Reddy; Leo T Chylack; Paul Sieving; Ronald A Bush
Lens epithelium-derived growth factor promotes photoreceptor survival in light-damaged and RCS rats.
Investigative ophthalmology & visual science 2001;42(5):1087-95.
2001: Paul Sieving; P Chaudhry; Mineo Kondo; M Provenzano; D Wu; T J Carlson; Ronald A Bush; Debra A Thompson
Inhibition of the visual cycle in vivo by 13-cis retinoic acid protects from light damage and provides a mechanism for night blindness in isotretinoin therapy.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(4):1835-40.
2001: Kang Zhang; MF Kniazeva; Min Han; W Li; Z Yu; Zhenglin Yang; Yingying Li; Michael Metzker; Rando Allikmets; Donald J Zack; Laura E Kakuk; Pamela S Lagali; Paul W Wong; Ian M MacDonald; Paul Sieving; David Figueroa; Christopher P Austin; Robert Gould; Radha Ayyagari; Konstantin Petrukhin
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy.
Nature genetics 2001;27(1):89-93.
2001: Mineo Kondo; Paul Sieving
Primate photopic sine-wave flicker ERG: vector modeling analysis of component origins using glutamate analogs.
Investigative ophthalmology & visual science 2001;42(1):305-12.
2000: Debra A Thompson; P Gyürüs; L L Fleischer; Eve L Bingham; Christina L McHenry; E Apfelstedt-Sylla; E Zrenner; B Lorenz; Julia E Richards; Samuel G Jacobson; Paul Sieving; Andreas Gal
Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.
Investigative ophthalmology & visual science 2000;41(13):4293-9.
2000: Alan J Mears; Suja Hiriyanna; Raf Vervoort; Beverly M Yashar; L Gieser; S Fahrner; Stephen P Daiger; John R Heckenlively; Paul Sieving; Alan F Wright; Anand Swaroop
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15.
American journal of human genetics 2000;67(4):1000-3.
2000: S Machida; Mineo Kondo; Jeffrey A Jamison; Naheed W Khan; L T Kononen; T Sugawara; Ronald A Bush; Paul Sieving
P23H rhodopsin transgenic rat: correlation of retinal function with histopathology.
Investigative ophthalmology & visual science 2000;41(10):3200-9.
2000: Susanne Kohl; Britta Baumann; Martina Broghammer; Herbert Jägle; Paul Sieving; Ulrich Kellner; R Spegal; M Anastasi; Eberhart Zrenner; Lindsay T Sharpe; Bernd Wissinger
Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.
Human molecular genetics 2000;9(14):2107-16.
2000: Ronald A Bush; L Kononen; S Machida; Paul Sieving
The effect of calcium channel blocker diltiazem on photoreceptor degeneration in the rhodopsin Pro213His rat.
Investigative ophthalmology & visual science 2000;41(9):2697-701.
2000: L C Eksandh; Vesna Ponjavic; Radha Ayyagari; Eve L Bingham; Kelaginamane T Hiriyanna; Sten Andréasson; Berndt Ehinger; Paul Sieving
Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene.
Archives of ophthalmology 2000;118(8):1098-104.
2000: Radha Ayyagari; Laura E Kakuk; Eve L Bingham; J J Szczesny; J Kemp; Y Toda; Joost Felius; Paul Sieving
Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy.
Human genetics 2000;107(1):75-82.
2000: T Sugawara; Paul Sieving; Ronald A Bush
Quantitative relationship of the scotopic and photopic ERG to photoreceptor cell loss in light damaged rats.
Experimental eye research 2000;70(5):693-705.
2000: C J Hrach; Mark W Johnson; Adam S Hassan; Bo Lei; Paul Sieving; Victor M Elner
Retinal toxicity of commercial intravitreal tissue plasminogen activator solution in cat eyes.
Archives of ophthalmology 2000;118(5):659-63.
2000: Radha Ayyagari; IB Griesinger; Eve L Bingham; K K Lark; Sayoko E Moroi; Paul Sieving
Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene.
Archives of ophthalmology 2000;118(1):85-92.
2000: Bo Lei; Ronald A Bush; Ann H Milam; Paul Sieving
Human melanoma-associated retinopathy (MAR) antibodies alter the retinal ON-response of the monkey ERG in vivo.
Investigative ophthalmology & visual science 2000;41(1):262-6.
2000: IB Griesinger; Paul Sieving; Radha Ayyagari
Autosomal dominant macular atrophy at 6q14 excludes CORD7 and MCDR1/PBCRA loci.
Investigative ophthalmology & visual science 2000;41(1):248-55.
1999: Paul Sieving; Eve L Bingham; J Kemp; Julia E Richards; Kelaginamane T Hiriyanna
Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave.
American journal of ophthalmology 1999;128(2):179-84.
1999: Radha Ayyagari; Laura E Kakuk; CL Coats; Eve L Bingham; Y Toda; Joost Felius; Paul Sieving
Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene.
Molecular vision 1999;5():13.
1999: Niamh McNally; Paul F Kenna; Marian Humphries; AH Hobson; Naheed W Khan; Ronald A Bush; Paul Sieving; Peter Humphries; G Jane Farrar
Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgene.
Human molecular genetics 1999;8(7):1309-12.
1999: G M Caldwell; Laura E Kakuk; IB Griesinger; S A Simpson; Norma J Nowak; Kent W Small; Irene H Maumenee; Philip J Rosenfeld; Paul Sieving; TB Shows; Radha Ayyagari
Bestrophin gene mutations in patients with Best vitelliform macular dystrophy.
Genomics 1999;58(1):98-101.
1999: R Mendoza-Londono; Kelaginamane T Hiriyanna; Eve L Bingham; F Rodriguez; Barkur S Shastry; A Rodriguez; Paul Sieving; M L Tamayo
A Colombian family with X-linked juvenile retinoschisis with three affected females finding of a frameshift mutation.
Ophthalmic genetics 1999;20(1):37-43.
1999: K Toda; Ronald A Bush; Peter Humphries; Paul Sieving
The electroretinogram of the rhodopsin knockout mouse.
Visual neuroscience 1999;16(2):391-8.
1999: Alan J Mears; L Gieser; Denise Yan; C Chen; S Fahrner; Suja Hiriyanna; Ricardo Fujita; Samuel G Jacobson; Paul Sieving; Anand Swaroop
Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosa.
American journal of human genetics 1999;64(3):897-900.
1999: SM Walpole; K T Hiriyana; A Nicolaou; E L Bingham; J Durham; Mark Vaudin; Mark T Ross; J R W Yates; Paul Sieving; Dorothy Trump
Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22.
Genomics 1999;55(3):275-83.
1999: Anand Swaroop; Q L Wang; W Wu; J Cook; CL Coats; Siqun Xu; Shiming Chen; Donald J Zack; Paul Sieving
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function.
Human molecular genetics 1999;8(2):299-305.
1999: Paul Sieving; Beverly M Yashar; Radha Ayyagari
Juvenile retinoschisis: a model for molecular diagnostic testing of X-linked ophthalmic disease.
Transactions of the American Ophthalmological Society 1999;97():451-64; discussion 464-9.
1999: Kelaginamane T Hiriyanna; Eve L Bingham; Beverly M Yashar; Radha Ayyagari; Gerald A Fishman; Kent W Small; David V Weinberg; Richard G Weleber; R A Lewis; sten andreasson; Julia E Richards; Paul Sieving
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change.
Human mutation 1999;14(5):423-7.
1998: T Sugawara; Paul Sieving; P M Iuvone; Ronald A Bush
The melatonin antagonist luzindole protects retinal photoreceptors from light damage in the rat.
Investigative ophthalmology & visual science 1998;39(12):2458-65.
1998: Paul Sieving; E B Arnold; Jeffrey A Jamison; A Liepa; CL Coats
Submicrovolt flicker electroretinogram: cycle-by-cycle recording of multiple harmonics with statistical estimation of measurement uncertainty.
Investigative ophthalmology & visual science 1998;39(8):1462-9.
1998: Jeffrey W Innis; Paul Sieving; P McMillan; Robert A Weatherly
Apparently new syndrome of sensorineural hearing loss, retinal pigment epithelium lesions, and discolored teeth.
American journal of medical genetics 1998;75(1):13-7.
1997: Prabodh K Swain; Shiming Chen; Q L Wang; Louisa M Affatigato; CL Coats; K D Brady; Gerald A Fishman; Samuel G Jacobson; Anand Swaroop; E Stone; Paul Sieving; Donald J Zack
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration.
Neuron 1997;19(6):1329-36.
1997: Monika Buraczynska; W Wu; Ricardo Fujita; Kinga Buraczynska; E Phelps; Sten Andréasson; J Bennett; David G Birch; Gerald A Fishman; Dennis R Hoffman; George Inana; Samuel G Jacobson; Maria A Musarella; Paul Sieving; Anand Swaroop
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa.
American journal of human genetics 1997;61(6):1287-92.
1997: Qais A Farjo; A Jackson; S Pieke-Dahl; K Scott; William J Kimberling; Paul Sieving; Julia E Richards; Anand Swaroop
Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degeneration.
Genomics 1997;45(2):395-401.
1997: S H Kim; Ronald A Bush; Paul Sieving
Increased phase lag of the fundamental harmonic component of the 30 Hz flicker ERG in Schubert-Bornschein complete type CSNB.
Vision research 1997;37(17):2471-5.
1997: Ricardo Fujita; Monika Buraczynska; L Gieser; W Wu; P Forsythe; Magnus Abrahamson; Samuel G Jacobson; Paul Sieving; Sten Andréasson; Anand Swaroop
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families.
American journal of human genetics 1997;61(3):571-80.
1997: Marian Humphries; D Rancourt; G Jane Farrar; Paul F Kenna; M Hazel; Ronald A Bush; Paul Sieving; D M Sheils; Niamh McNally; P Creighton; A Erven; A Boros; Karoly Gulya; Mario R Capecchi; Peter Humphries
Retinopathy induced in mice by targeted disruption of the rhodopsin gene.
Nature genetics 1997;15(2):216-9.
1996: H Pawar; Eve L Bingham; Kelaginamane T Hiriyanna; M Segal; Julia E Richards; Paul Sieving
X-linked juvenile retinoschisis: localization between (DXS1195, DXS418) and AFM291wf5 on a single YAC.
Human heredity 1996;46(6):329-35.
1996: F Naarendorp; K S Rice; Paul Sieving
Summation of rod and S cone signals at threshold in human observers.
Vision research 1996;36(17):2681-8.
1996: Y C Hou; Julia E Richards; Eve L Bingham; H Pawar; K Scott; M Segal; Kathryn L Lunetta; Michael Boehnke; Paul Sieving
Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American family.
Human heredity 1996;46(4):211-20.
1996: Ricardo Fujita; E Bingham; P Forsythe; C McHenry; V Aita; B A Navia; K Dry; M Segal; M Devoto; G Bruns; Alan F Wright; J Ott; Paul Sieving; Anand Swaroop
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.
American journal of human genetics 1996;59(1):152-8.
1996: Ronald A Bush; Paul Sieving
Inner retinal contributions to the primate photopic fast flicker electroretinogram.
Journal of the Optical Society of America. A, Optics, image science, and vision 1996;13(3):557-65.
1996: Paul Sieving; S Boskovich; Eve L Bingham; H Pawar
Sorsby's fundus dystrophy in a family with a Ser-181-CVS mutation in the TIMP-3 gene: poor outcome after laser photocoagulation.
Transactions of the American Ophthalmological Society 1996;94():275-94; discussion 295-7.
1995: Ricardo Fujita; M Blumberg; Douglas R Anderson; P Forsythe; C McHenry; Denise Yan; TL Yang-Feng; Paul Sieving; Anand Swaroop
A polymorphic trinucleotide repeat at DXS8170 in the critical region of X-linked retinitis pigmentosa locus RP3 at Xp21.1.
Molecular vision 1995;1():3.
1995: Paul Sieving
Diagnostic issues with inherited retinal and macular dystrophies.
Seminars in ophthalmology 1995;10(4):279-94.
1995: Ronald A Bush; K W Hawks; Paul Sieving
Preservation of inner retinal responses in the aged Royal College of Surgeons rat. Evidence against glutamate excitotoxicity in photoreceptor degeneration.
Investigative ophthalmology & visual science 1995;36(10):2054-62.
1995: H Pawar; Eve L Bingham; Kathryn L Lunetta; M Segal; Julia E Richards; Michael Boehnke; Paul Sieving
Refined genetic mapping of juvenile X-linked retinoschisis.
Human heredity 1995;45(4):206-10.
1995: Julia E Richards; Kathleen M Scott; Paul Sieving
Disruption of conserved rhodopsin disulfide bond by Cys187Tyr mutation causes early and severe autosomal dominant retinitis pigmentosa.
Ophthalmology 1995;102(4):669-77.
1995: L J Frishman; Paul Sieving
Evidence for two sites of adaptation affecting the dark-adapted ERG of cats and primates.
Vision research 1995;35(3):435-42.
1995: Paul Sieving; Julia E Richards; F Naarendorp; Eve L Bingham; K Scott; M Alpern
Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(3):880-4.
1994: Denise Yan; D Wong; K Zheng; D Thiselton; R Fujita; Paul Sieving; S S Bhattacharya; TL Yang-Feng; Julia E Richards; Anand Swaroop
Dinucleotide repeat polymorphism at the DXS977 locus.
Human molecular genetics 1994;3(6):1030.
1994: Paul Sieving; K Murayama; F Naarendorp
Push-pull model of the primate photopic electroretinogram: a role for hyperpolarizing neurons in shaping the b-wave.
Visual neuroscience 1994;11(3):519-32.
1994: Ronald A Bush; Paul Sieving
A proximal retinal component in the primate photopic ERG a-wave.
Investigative ophthalmology & visual science 1994;35(2):635-45.
1994: Paul Sieving
'Unilateral cone dystrophy': ERG changes implicate abnormal signaling by hyperpolarizing bipolar and/or horizontal cells.
Transactions of the American Ophthalmological Society 1994;92():459-71; discussion 471-4.
1993: F Naarendorp; P F Hitchock; Paul Sieving
Dopaminergic modulation of rod pathway signals does not affect the scotopic ERG of cat at dark-adapted threshold.
Journal of neurophysiology 1993;70(4):1681-91.
1993: A M Geller; Paul Sieving
Assessment of foveal cone photoreceptors in Stargardt's macular dystrophy using a small dot detection task.
Vision research 1993;33(11):1509-24.
1993: Paul Sieving
Photopic ON- and OFF-pathway abnormalities in retinal dystrophies.
Transactions of the American Ophthalmological Society 1993;91():701-73.
1992: A M Geller; Paul Sieving; Daniel G Green
Effect on grating identification of sampling with degenerate arrays.
Journal of the Optical Society of America. A, Optics and image science 1992;9(3):472-7.
1991: Julia E Richards; C Y Kuo; Michael Boehnke; Paul Sieving
Rhodopsin Thr58Arg mutation in a family with autosomal dominant retinitis pigmentosa.
Ophthalmology 1991;98(12):1797-805.
1991: S R Sneed; Paul Sieving
Fenestrated sheen macular dystrophy.
American journal of ophthalmology 1991;112(1):1-7.
1991: E L Arrindell; Jonathan D Trobe; Paul Sieving; J L Barnett
Pupillary and electroretinographic abnormalities in a family with neuronal intranuclear hyaline inclusion disease.
Archives of ophthalmology 1991;109(3):373-8.
1991: F Naarendorp; Paul Sieving
The scotopic threshold response of the cat ERG is suppressed selectively by GABA and glycine.
Vision research 1991;31(1):1-15.
1990: S E Rowe; Jonathan D Trobe; Paul Sieving
Idiopathic photoreceptor dysfunction causes unexplained visual acuity loss in later adulthood.
Ophthalmology 1990;97(12):1632-7.
1990: Paul Sieving; E L Bingham; M S Roth; M R Young; Michael Boehnke; C Y Kuo; David Ginsburg
Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes.
American journal of human genetics 1990;47(4):616-21.
1989: Ben Ticho; Paul Sieving
Leber's congenital amaurosis with marbelized fundus and juvenile nephronophthisis.
American journal of ophthalmology 1989;107(4):426-8.
1988: K Wakabayashi; J Gieser; Paul Sieving
Aspartate separation of the scotopic threshold response (STR) from the photoreceptor a-wave of the cat and monkey ERG.
Investigative ophthalmology & visual science 1988;29(11):1615-22.
1988: Paul Sieving; C Nino
Scotopic threshold response (STR) of the human electroretinogram.
Investigative ophthalmology & visual science 1988;29(11):1608-14.
1988: Dennis P Han; Paul Sieving; Mark W Johnson; C L Martonyi
Foveal retinoschisis associated with senile retinoschisis in a woman.
American journal of ophthalmology 1988;106(1):107-9.
1988: L J Frishman; Paul Sieving; RH Steinberg
Contributions to the electroretinogram of currents originating in proximal retina.
Visual neuroscience 1988;1(3):307-15.
1987: Paul Sieving; R H Steinberg
Proximal retinal contribution to the intraretinal 8-Hz pattern ERG of cat.
Journal of neurophysiology 1987;57(1):104-20.
1986: Paul Sieving; L J Frishman; RH Steinberg
Scotopic threshold response of proximal retina in cat.
Journal of neurophysiology 1986;56(4):1049-61.
1986: Paul Sieving; L J Frishman; RH Steinberg
M-wave of proximal retina in cat.
Journal of neurophysiology 1986;56(4):1039-48.
1986: Paul Sieving; J H Niffenegger; E L Berson
Electroretinographic findings in selected pedigrees with choroideremia.
American journal of ophthalmology 1986;101(3):361-7.
1985: Paul Sieving; R H Steinberg
Contribution from proximal retina to intraretinal pattern ERG: the M-wave.
Investigative ophthalmology & visual science 1985;26(11):1642-7.
1984: Paul Sieving; Gerald A Fishman; L M Jampol; D Pugh
Multiple evanescent white dot syndrome. II. Electrophysiology of the photoreceptors during retinal pigment epithelial disease.
Archives of ophthalmology 1984;102(5):675-9.
1984: L M Jampol; Paul Sieving; D Pugh; Gerald A Fishman; H Gilbert
Multiple evanescent white dot syndrome. I. Clinical findings.
Archives of ophthalmology 1984;102(5):671-4.
1984: Paul Sieving; Gerald A Fishman; T Salzano; M F Rabb
Acute macular neuroretinopathy: early receptor potential change suggests photoreceptor pathology.
The British journal of ophthalmology 1984;68(4):229-34.
1983: Paul Sieving; Gerald A Fishman; Kenneth R Alexander; Morton F Goldberg
Early receptor potential measurements in human ocular siderosis.
Archives of ophthalmology 1983;101(11):1716-20.
1978: Paul Sieving; Gerald A Fishman; J M Maggiano
Corneal wick electrode for recording bright flash electroretinograms and early receptor potentials.
Archives of ophthalmology 1978;96(5):899-900.
1978: Paul Sieving; Gerald A Fishman
Refractive errors of retinitis pigmentosa patients.
The British journal of ophthalmology 1978;62(3):163-7.