Posts classified under: Visual Neurosciences

Michael Gorin, M.D., Ph.D.

Biography

Michael B. Gorin, MD, PhD, is the currently the first recipient of the Harold and Pauline Price Chair in Ophthalmology and Professor of Ophthalmology in the Retina and Vision Science Divisions in the Department of Ophthalmology at the David Geffen School of Medicine ? UCLA and Jules Stein Eye Institute. He also holds an appointment in the Vision Research Division at the Jules Stein Eye Institute. Dr. Gorin obtained his medical and doctor of philosophy degrees from the University of Pennsylvania at Philadelphia and completed his internship at the Center for Health Sciences at the University of California at Los Angeles (UCLA). He stayed on at UCLA for postdoctoral research fellowship and ophthalmology residency training at the Jules Stein Eye Institute, and then finished a clinical fellowship in Medical Retina and Genetics at Moorfields Eye Hospital in London, England. Dr. Gorin returned to UCLA from the University of Pittsburgh, where he served as Assistant Vice Chancellor for Strategic Initiatives for the six graduate health sciences schools. He joined the Pittsburgh campus in 1990, rising to the rank of Professor in the Department of Ophthalmology in the School of Medicine and the Department of Human Genetics in the Graduate School of Public Health and serving as interim chair for both departments. He was founding director of the Center for Human Genetics and a founding senior associate of the Center for Biomedical Informatics at the University. Throughout his 16 years in Pittsburgh, he has provided clinical care on a regular basis in medical retina particularly in the fields of hereditary disorders, retinal diagnostics, drug-related ocular toxicity, and ophthalmic genetics. During 2005-2007, he was named one of the top physicians in the United States by Castle Connolly Medical Ltd. As a full-time faculty member at the Jules Stein Eye Institute, Dr. Gorin divides his time between patient care for diseases of the retina, research into the genetics of inherited eye disorders and training young ophthalmologists and medical students.

Publications

A selected list of publications:

Ortube Maria Carolina, Kiderman Alexander, Eydelman Yakov, Yu Fei, Aguilar Nelson, Nusinowitz Steven, Gorin Michael B   Comparative regional pupillography as a noninvasive biosensor screening method for diabetic retinopathy Investigative ophthalmology & visual science, 2013; 54(1): 9-18.
Fritsche Lars G, Chen Wei, Schu Matthew, Yaspan Brian L, Yu Yi, Thorleifsson Gudmar, Zack Donald J, Arakawa Satoshi, Cipriani Valentina, Ripke Stephan, Igo Robert P, Buitendijk Gabriëlle H S, Sim Xueling, Weeks Daniel E, Guymer Robyn H, Merriam Joanna E, Francis Peter J, Hannum Gregory, Agarwal Anita, Armbrecht Ana Maria, Audo Isabelle, Aung Tin, Barile Gaetano R, Benchaboune Mustapha, Bird Alan C, Bishop Paul N, Branham Kari E, Brooks Matthew, Brucker Alexander J, Cade William H, Cain Melinda S, Campochiaro Peter A, Chan Chi-Chao, Cheng Ching-Yu, Chew Emily Y, Chin Kimberly A, Chowers Itay, Clayton David G, Cojocaru Radu, Conley Yvette P, Cornes Belinda K, Daly Mark J, Dhillon Baljean, Edwards Albert O, Evangelou Evangelos, Fagerness Jesen, Ferreyra Henry A, Friedman James S, Geirsdottir Asbjorg, George Ronnie J, Gieger Christian, Gupta Neel, Hagstrom Stephanie A, Harding Simon P, Haritoglou Christos, Heckenlively John R, Holz Frank G, Hughes Guy, Ioannidis John P A, Ishibashi Tatsuro, Joseph Peronne, Jun Gyungah, Kamatani Yoichiro, Katsanis Nicholas, N Keilhauer Claudia, Khan Jane C, Kim Ivana K, Kiyohara Yutaka, Klein Barbara E K, Klein Ronald, Kovach Jaclyn L, Kozak Igor, Lee Clara J, Lee Kristine E, Lichtner Peter, Lotery Andrew J, Meitinger Thomas, Mitchell Paul, Mohand-Saïd Saddek, Moore Anthony T, Morgan Denise J, Morrison Margaux A, Myers Chelsea E, Naj Adam C, Nakamura Yusuke, Okada Yukinori, Orlin Anton, Ortube M Carolina, Othman Mohammad I, Pappas Chris, Park Kyu Hyung, Pauer Gayle J T, Peachey Neal S, Poch Olivier, Priya Rinki Ratna, Reynolds Robyn, Richardson Andrea J, Ripp Raymond, Rudolph Guenther, Ryu Euijung, Sahel José-Alain, Schaumberg Debra A, Scholl Hendrik P N, Schwartz Stephen G, Scott William K, Shahid Humma, Sigurdsson Haraldur, Silvestri Giuliana, Sivakumaran Theru A, Smith R Theodore, Sobrin Lucia, Souied Eric H, Stambolian Dwight E, Stefansson Hreinn, Sturgill-Short Gwen M, Takahashi Atsushi, Tosakulwong Nirubol, Truitt Barbara J, Tsironi Evangelia E, Uitterlinden André G, van Duijn Cornelia M, Vijaya Lingam, Vingerling Johannes R, Vithana Eranga N, Webster Andrew R, Wichmann H-Erich, Winkler Thomas W, Wong Tien Y, Wright Alan F, Zelenika Diana, Zhang Ming, Zhao Ling, Zhang Kang, Klein Michael L, Hageman Gregory S, Lathrop G Mark, Stefansson Kari, Allikmets Rando, Baird Paul N, Gorin Michael B, Wang Jie Jin, Klaver Caroline C W, Seddon Johanna M, Pericak-Vance Margaret A, Iyengar Sudha K, Yates John R W, Swaroop Anand, Weber Bernhard H F, Kubo Michiaki, Deangelis Margaret M, Léveillard Thierry, Thorsteinsdottir Unnur, Haines Jonathan L, Farrer Lindsay A, Heid Iris M, Abecasis Gonçalo R, Abecasis Gonçalo R   Seven new loci associated with age-related macular degeneration Nature genetics, 2013; 45(4): 433-9, 439e1-2.
Sofat Reecha, Casas Juan P, Webster Andrew R, Bird Alan C, Mann Samantha S, Yates John R W, Moore Anthony T, Sepp Tiina, Cipriani Valentina, Bunce Catey, Khan Jane C, Shahid Humma, Swaroop Anand, Abecasis Gonçalo, Branham Kari E H, Zareparsi Sepideh, Bergen Arthur A, Klaver Caroline C W, Baas Dominique C, Zhang Kang, Chen Yuhong, Gibbs Daniel, Weber Bernhard H F, Keilhauer Claudia N, Fritsche Lars G, Lotery Andrew, Cree Angela J, Griffiths Helen L, Bhattacharya Shomi S, Chen Li L, Jenkins Sharon A, Peto Tunde, Lathrop Mark, Leveillard Thierry, Gorin Michael B, Weeks Daniel E, Ortube Maria Carolina, Ferrell Robert E, Jakobsdottir Johanna, Conley Yvette P, Rahu Mati, Seland Johan H, Soubrane Gisele, Topouzis Fotis, Vioque Jesus, Tomazzoli Laura, Young Ian, Whittaker John, Chakravarthy Usha, de Jong Paulus T V M, Smeeth Liam, Fletcher Astrid, Hingorani Aroon D   Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype International journal of epidemiology, 2012; 41(1): 250-62.
Webb Tom R, Parfitt David A, Gardner Jessica C, Martinez Ariadna, Bevilacqua Dalila, Davidson Alice E, Zito Ilaria, Thiselton Dawn L, Ressa Jacob H C, Apergi Marina, Schwarz Nele, Kanuga Naheed, Michaelides Michel, Cheetham Michael E, Gorin Michael B, Hardcastle Alison J   Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23) Human molecular genetics, 2012; 21(16): 3647-54.
Matynia Anna, Parikh Sachin, Chen Bryan, Kim Paul, McNeill David S, Nusinowitz Steven, Evans Christopher, Gorin Michael B   Intrinsically photosensitive retinal ganglion cells are the primary but not exclusive circuit for light aversion Experimental eye research, 2012; 105(11 Pt B): 60-9.
Strom Samuel P, Gao Yong-Qing, Martinez Ariadna, Ortube Carolina, Chen Zugen, Nelson Stanley F, Nusinowitz Steven, Farber Deborah B, Gorin Michael B   Molecular diagnosis of putative Stargardt Disease probands by exome sequencing BMC medical genetics, 2012; 13(16): 67.
Chiu Chung-Jung, Conley Yvette P, Gorin Michael B, Gensler Gary, Lai Chao-Qiang, Shang Fu, Taylor Allen   Associations between genetic polymorphisms of insulin-like growth factor axis genes and risk for age-related macular degeneration Investigative ophthalmology & visual science, 2011; 52(12): 9099-107.
Spencer Kylee L, Olson Lana M, Schnetz-Boutaud Nathalie, Gallins Paul, Wang Gaofeng, Scott William K, Agarwal Anita, Jakobsdottir Johanna, Conley Yvette, Weeks Daniel E, Gorin Michael B, Pericak-Vance Margaret A, Haines Jonathan L   Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility Investigative ophthalmology & visual science, 2011; 52(3): 1748-54.
McKay Gareth J, Patterson Chris C, Chakravarthy Usha, Dasari Shilpa, Klaver Caroline C, Vingerling Johannes R, Ho Lintje, de Jong Paulus T V M, Fletcher Astrid E, Young Ian S, Seland Johan H, Rahu Mati, Soubrane Gisele, Tomazzoli Laura, Topouzis Fotis, Vioque Jesus, Hingorani Aroon D, Sofat Reecha, Dean Michael, Sawitzke Julie, Seddon Johanna M, Peter Inga, Webster Andrew R, Moore Anthony T, Yates John R W, Cipriani Valentina, Fritsche Lars G, Weber Bernhard H F, Keilhauer Claudia N, Lotery Andrew J, Ennis Sarah, Klein Michael L, Francis Peter J, Stambolian Dwight, Orlin Anton, Gorin Michael B, Weeks Daniel E, Kuo Chia-Ling, Swaroop Anand, Othman Mohammad, Kanda Atsuhiro, Chen Wei, Abecasis Goncalo R, Wright Alan F, Hayward Caroline, Baird Paul N, Guymer Robyn H, Attia John, Thakkinstian Ammarin, Silvestri Giuliana   Evidence of association of APOE with age-related macular degeneration: a pooled analysis of 15 studies Human mutation, 2011; 32(12): 1407-16.
Wittes Janet, Gorin Michael B, Mayne Susan T, McCarthy Cynthia S, Sternberg Paul, Wall Michael   Letter from the DSMC regarding a clinical trial of lutein in patients with retinitis pigmentosa Archives of ophthalmology, 2011; 129(5): 675; author reply 675-6.
Choi Daniel Y, Ortube Maria Carolina, McCannel Colin A, Sarraf David, Hubschman Jean-Pierre, McCannel Tara A, Gorin Michael B   Sustained elevated intraocular pressures after intravitreal injection of bevacizumab, ranibizumab, and pegaptanib Retina (Philadelphia, Pa.), 2011; 31(6): 1028-35.
Charles Bashira A, Conley Yvette P, Chen Guanjie, Miller Rachel G, Dorman Janice S, Gorin Michael B, Ferrell Robert E, Sereika Susan M, Rotimi Charles N, Orchard Trevor J   Variants of the adenosine A(2A) receptor gene are protective against proliferative diabetic retinopathy in patients with type 1 diabetes Ophthalmic research, 2011; 46(1): 1-8.
McKay Gareth J, Silvestri Giuliana, Chakravarthy Usha, Dasari Shilpa, Fritsche Lars G, Weber Bernhard H, Keilhauer Claudia N, Klein Michael L, Francis Peter J, Klaver Caroline C, Vingerling Johannes R, Ho Lintje, De Jong Paulus T D V, Dean Michael, Sawitzke Julie, Baird Paul N, Guymer Robyn H, Stambolian Dwight, Orlin Anton, Seddon Johanna M, Peter Inga, Wright Alan F, Hayward Caroline, Lotery Andrew J, Ennis Sarah, Gorin Michael B, Weeks Daniel E, Kuo Chia-Ling, Hingorani Aroon D, Sofat Reecha, Cipriani Valentina, Swaroop Anand, Othman Mohammad, Kanda Atsuhiro, Chen Wei, Abecasis Goncalo R, Yates John R, Webster Andrew R, Moore Anthony T, Seland Johan H, Rahu Mati, Soubrane Gisele, Tomazzoli Laura, Topouzis Fotis, Vioque Jesus, Young Ian S, Fletcher Astrid E, Patterson Chris C   Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people American journal of epidemiology, 2011; 173(12): 1357-64.
Chen Wei, Stambolian Dwight, Edwards Albert O, Branham Kari E, Othman Mohammad, Jakobsdottir Johanna, Tosakulwong Nirubol, Pericak-Vance Margaret A, Campochiaro Peter A, Klein Michael L, Tan Perciliz L, Conley Yvette P, Kanda Atsuhiro, Kopplin Laura, Li Yanming, Augustaitis Katherine J, Karoukis Athanasios J, Scott William K, Agarwal Anita, Kovach Jaclyn L, Schwartz Stephen G, Postel Eric A, Brooks Matthew, Baratz Keith H, Brown William L, Brown William L, Brucker Alexander J, Orlin Anton, Brown Gary, Ho Allen, Regillo Carl, Donoso Larry, Tian Lifeng, Kaderli Brian, Hadley Dexter, Hagstrom Stephanie A, Peachey Neal S, Klein Ronald, Klein Barbara E K, Gotoh Norimoto, Yamashiro Kenji, Ferris Iii Frederick, Fagerness Jesen A, Reynolds Robyn, Farrer Lindsay A, Kim Ivana K, Miller Joan W, Cortón Marta, Carracedo Angel, Sanchez-Salorio Manuel, Pugh Elizabeth W, Doheny Kimberly F, Brion Maria, Deangelis Margaret M, Weeks Daniel E, Zack Donald J, Chew Emily Y, Heckenlively John R, Yoshimura Nagahisa, Iyengar Sudha K, Francis Peter J, Katsanis Nicholas, Seddon Johanna M, Haines Jonathan L, Gorin Michael B, Abecasis Gonçalo R, Swaroop Anand   Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration Proceedings of the National Academy of Sciences of the United States of America, 2010; 107(16): 7401-6.
Aldave Anthony J, Rosenwasser George O D, Yellore Vivek S, Papp Jeanette C, Sobel Eric M, Pham Michele N, Chen Michael C, Dandekar Sugandha, Sripracha Ram, Rayner Sylvia A, Sassani Joseph W, Gorin Michael B   Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC Investigative ophthalmology & visual science, 2010; 51(8): 4006-12.
Reddy Shantan, Gorin Michael B, McCannel Tara A, Tsui Irena, Straatsma Bradley R   Novel KRIT1/CCM1 mutation in a patient with retinal cavernous hemangioma and cerebral cavernous malformation Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie, 2010; 248(9): 1359-61.
Tosha Chinatsu, Gorin Michael B, Nusinowitz Steven   Test-retest reliability and inter-ocular symmetry of multi-focal electroretinography in Stargardt disease Current eye research, 2010; 35(1): 63-72.
Aldave Anthony J, Yellore Vivek S, Vo Rosalind C, Kamal Khairidzan M, Rayner Sylvia A, Plaisier Christopher L, Chen Michael C, Damani Mausam R, Pham Michele N, Gorin Michael B, Sobel Eric, Papp Jeanette   Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval Cornea, 2009; 28(7): 801-7.
Jakobsdottir Johanna, Gorin Michael B, Conley Yvette P, Ferrell Robert E, Weeks Daniel E   Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers PLoS genetics, 2009; 5(2): e1000337.
Hosseini Shahla M, Biglan Minhnoi W, Larkby Cynthia, Brooks Maria M, Gorin Michael B, Day Nancy L   Trait anxiety in pregnant women predicts offspring birth outcomes Paediatric and perinatal epidemiology, 2009; 23(6): 557-66.
Thiels Edda, Hoffman Eric K, Gorin Michael B   A reliable behavioral assay for the assessment of sustained photophobia in mice Current eye research, 2008; 33(5): 483-91.
Jakobsdottir Johanna, Conley Yvette P, Weeks Daniel E, Ferrell Robert E, Gorin Michael B   C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genes PloS one, 2008; 3(5): e2199.
Gorin Michael B   A clinician’s view of the molecular genetics of age-related maculopathy Archives of ophthalmology, 2007; 125(1): 21-9.
Ghajarnia Mehdi, Gorin Michael B   Acetazolamide in the treatment of X-linked retinoschisis maculopathy Archives of ophthalmology, 2007; 125(4): 571-3.
Tikellis Gabriella, Sun Cong, Gorin Michael B, Klein Ronald, Klein Barbara E K, Larsen Emily K Marino, Siscovick David S, Hubbard Larry D, Wong Tien Y   Apolipoprotein e gene and age-related maculopathy in older individuals: the cardiovascular health study Archives of ophthalmology, 2007; 125(1): 68-73.
Young Tara A, Burgess Barry L, Rao Nagesh P, Gorin Michael B, Straatsma Bradley R   High-density genome array is superior to fluorescence in-situ hybridization analysis of monosomy 3 in choroidal melanoma fine needle aspiration biopsy Molecular vision, 2007; 13(1): 2328-33.
Thomas George, Grassi Michael A, Lee John R, Edwards Albert O, Gorin Michael B, Klein Ronald, Casavant Thomas L, Scheetz Todd E, Stone Edwin M, Williams Andrew B   IDOCS: intelligent distributed ontology consensus system–the use of machine learning in retinal drusen phenotyping Investigative ophthalmology & visual science, 2007; 48(5): 2278-84.
Yellore Vivek S, Khan M Ali, Bourla Nirit, Rayner Sylvia A, Chen Michael C, Sonmez Baris, Momi Rominder S, Sampat Kapil M, Gorin Michael B, Aldave Anthony J   Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy Molecular vision, 2007; 13(5): 1777-82.
Finn, D. A. Beadles-Bohling, A. S. Beckley, E. H. Ford, M. M. Gililland, K. R. Gorin-Meyer, R. E. Wiren, K. M.   A new look at the 5alpha-reductase inhibitor finasteride CNS Drug Rev, 2006; 12(1): 53-76.
Demirci F Yesim K, Rigatti Brian W, Mah Tammy S, Gorin Michael B   A novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa and Coats’-like exudative vasculopathy American journal of ophthalmology, 2006; 141(1): 208-10.
Conley Yvette P, Jakobsdottir Johanna, Mah Tammy, Weeks Daniel E, Klein Ronald, Kuller Lewis, Ferrell Robert E, Gorin Michael B   CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses Human molecular genetics, 2006; 15(21): 3206-18.
Demirci F Yesim K, Chang Min-Hwang, Mah Tammy S, Romero Michael F, Gorin Michael B   Proximal renal tubular acidosis and ocular pathology: a novel missense mutation in the gene (SLC4A4) for sodium bicarbonate cotransporter protein (NBCe1) Molecular vision, 2006; 12(21): 324-30.
Gorin Michael B   A new vision for age-related macular degeneration European journal of human genetics : EJHG, 2005; 13(7): 793-4.
Conley Yvette P, Thalamuthu Anbupalam, Jakobsdottir Johanna, Weeks Daniel E, Mah Tammy, Ferrell Robert E, Gorin Michael B   Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy Human molecular genetics, 2005; 14(14): 1991-2002.
Demirci F Yesim K, Gupta Nisha, Radak Amy L, Rigatti Brian W, Mah Tammy S, Milam Ann H, Gorin Michael B   Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15 American journal of ophthalmology, 2005; 139(2): 386-8.
Gorin Michael B, Costantino Joseph P, Kulacoglu Destan N, Demirci F Yesim K, Wickerham D Lawrence, Fisher Bernard, Wolmark Norman   Is tamoxifen a risk factor for retinal vaso-occlusive disease? Retina (Philadelphia, Pa.), 2005; 25(4): 523-6.
Fisher Sheila A, Abecasis Goncalo R, Yashar Beverly M, Zareparsi Sepideh, Swaroop Anand, Iyengar Sudha K, Klein Barbara E K, Klein Ronald, Lee Kristine E, Majewski Jacek, Schultz Dennis W, Klein Michael L, Seddon Johanna M, Santangelo Susan L, Weeks Daniel E, Conley Yvette P, Mah Tammy S, Schmidt Silke, Haines Jonathan L, Pericak-Vance Margaret A, Gorin Michael B, Schulz Heidi L, Pardi Fabio, Lewis Cathryn M, Weber Bernhard H F   Meta-analysis of genome scans of age-related macular degeneration Human molecular genetics, 2005; 14(15): 2257-64.
Jakobsdottir Johanna, Conley Yvette P, Weeks Daniel E, Mah Tammy S, Ferrell Robert E, Gorin Michael B   Susceptibility genes for age-related maculopathy on chromosome 10q26 American journal of human genetics, 2005; 77(3): 389-407.
Gorin Michael B   The coming of age for age-related macular degeneration genetics Ophthalmic genetics, 2005; 26(2): 57-9.
Demirci F Yesim K, Rigatti Brian W, Mah Tammy S, Gorin Michael B   A novel compound heterozygous mutation in the cellular retinaldehyde-binding protein gene (RLBP1) in a patient with retinitis punctata albescens American journal of ophthalmology, 2004; 138(1): 171-3.
Demirci F Yesim K, Radak Amy L, Rigatti Brian W, Mah Tammy S, Gorin Michael B   A presumed missense mutation of RPGR causes abnormal RNA splicing with exon skipping American journal of ophthalmology, 2004; 138(3): 504-5.
Weeks Daniel E, Conley Yvette P, Tsai Hui-Ju, Mah Tammy S, Schmidt Silke, Postel Eric A, Agarwal Anita, Haines Jonathan L, Pericak-Vance Margaret A, Rosenfeld Philip J, Paul T Otis, Eller Andrew W, Morse Lawrence S, Dailey J P, Ferrell Robert E, Gorin Michael B   Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regions American journal of human genetics, 2004; 75(2): 174-89.
Schmidt Silke, Scott William K, Postel Eric A, Agarwal Anita, Hauser Elizabeth R, De La Paz Monica A, Gilbert John R, Weeks Daniel E, Gorin Michael B, Haines Jonathan L, Pericak-Vance Margaret A   Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12 BMC genetics, 2004; 5(3): 18.
Jalkanen, R. Demirci, F. Y. Tyynismaa, H. Bech-Hansen, T. Meindl, A. Peippo, M. Mantyjarvi, M. Gorin, M. B. Alitalo, T.   A new genetic locus for X linked progressive cone-rod dystrophy J Med Genet, 2003; 40(6): 418-23.
Telmer Cheryl A, Retchless Adam C, Kinsey Ashley D, Conley Yvette, Rigatti Brian, Gorin Michael B, Jarvik Jonathan W, Retchless Adam R   Detection and assignment of mutations and minihaplotypes in human DNA using peptide mass signature genotyping (PMSG): application to the human RDS/peripherin gene Genome research, 2003; 13(8): 1944-51.
Demirci, F. Y. Ramser, J. White, N. J. Rigatti, B. W. Meindl, A. Lewis, K. F. Wen, G. Gorin, M. B.   Refinement of the physical location and the genomic characterization of the CRSP2 (EXLM1) gene on Xp11.4 DNA Seq, 2003; 14(2): 123-7.
Conley, Y. P. Gorin, M. B.   The genetics of age-related macular degeneration Medsurg Nurs, 2003; 12(4): 238-41, 259.
Schmidt, S. Klaver, C. Saunders, A. Postel, E. De La Paz, M. Agarwal, A. Small, K. Udar, N. Ong, J. Chalukya, M. Nesburn, A. Kenney, C. Domurath, R. Hogan, M. Mah, T. Conley, Y. Ferrell, R. Weeks, D. de Jong, P. T. van Duijn, C. Haines, J. Pericak-Vance, M. Gorin, M.   A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathy Ophthalmic Genet, 2002; 23(4): 209-23.
Weeks, D. E. Conley, Y. P. Ferrell, R. E. Mah, T. S. Gorin, M. B.   A tale of two genotypes: consistency between two high-throughput genotyping centers Genome Res, 2002; 12(3): 430-5.
Gordon, Y. J. Mann, R. K. Mah, T. S. Gorin, M. B.   Fluorescein-potentiated argon laser therapy improves symptoms and appearance of corneal neovascularization Cornea, 2002; 21(8): 770-3.
Demirci F Yesim K, Rigatti Brian W, Wen Gaiping, Radak Amy L, Mah Tammy S, Baic Corrine L, Traboulsi Elias I, Alitalo Tiina, Ramser Juliane, Gorin Michael B   X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15 American journal of human genetics, 2002; 70(4): 1049-53.
Ayyagari, R. Demirci, F. Y. Liu, J. Bingham, E. L. Stringham, H. Kakuk, L. E. Boehnke, M. Gorin, M. B. Richards, J. E. Sieving, P. A.   X-linked recessive atrophic macular degeneration from RPGR mutation Genomics, 2002; 80(2): 166-71.
Weeks, D. E. Conley, Y. P. Tsai, H. J. Mah, T. S. Rosenfeld, P. J. Paul, T. O. Eller, A. W. Morse, L. S. Dailey, J. P. Ferrell, R. E. Gorin, M. B.   Age-related maculopathy: an expanded genome-wide scan with evidence of susceptibility loci within the 1q31 and 17q25 regions Am J Ophthalmol, 2001; 132(5): 682-92.
Milam, A. H. De Castro, E. B. Smith, J. E. Tang, W. X. John, S. K. Gorin, M. B. Stone, E. M. Aguirre, G. D. Jacobson, S. G.   Concentric retinitis pigmentosa: clinicopathologic correlations Exp Eye Res, 2001; 73(4): 493-508.
Weeks, D. E. Conley, Y. P. Mah, T. S. Paul, T. O. Morse, L. Ngo-Chang, J. Dailey, J. P. Ferrell, R. E. Gorin, M. B.   A full genome scan for age-related maculopathy Hum Mol Genet, 2000; 9(9): 1329-49.
Conley, Y. P. Erturk, D. Keverline, A. Mah, T. S. Keravala, A. Barnes, L. R. Bruchis, A. Hess, J. F. FitzGerald, P. G. Weeks, D. E. Ferrell, R. E. Gorin, M. B.   A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2 Am J Hum Genet, 2000; 66(4): 1426-31.
Kniazeva, M. Traboulsi, E. I. Yu, Z. Stefko, S. T. Gorin, M. B. Shugart, Y. Y. O’Connell, J. R. Blaschak, C. J. Cutting, G. Han, M. Zhang, K.   A new locus for dominant drusen and macular degeneration maps to chromosome 6q14 Am J Ophthalmol, 2000; 130(2): 197-202.
Stefko, S. T. Zhang, K. Gorin, M. B. Traboulsi, E. I.   Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration Am J Ophthalmol, 2000; 130(2): 203-8.
Hardcastle, A. J. Thiselton, D. L. Zito, I. Ebenezer, N. Mah, T. S. Gorin, M. B. Bhattacharya, S. S.   Evidence for a new locus for X-linked retinitis pigmentosa (RP23) Invest Ophthalmol Vis Sci, 2000; 41(8): 2080-6.
Pieke-Dahl, S. Moller, C. G. Kelley, P. M. Astuto, L. M. Cremers, C. W. Gorin, M. B. Kimberling, W. J.   Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q J Med Genet, 2000; 37(4): 256-62.
Astuto, L. M. Weston, M. D. Carney, C. A. Hoover, D. M. Cremers, C. W. Wagenaar, M. Moller, C. Smith, R. J. Pieke-Dahl, S. Greenberg, J. Ramesar, R. Jacobson, S. G. Ayuso, C. Heckenlively, J. R. Tamayo, M. Gorin, M. B. Reardon, W. Kimberling, W. J.   Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I Am J Hum Genet, 2000; 67(6): 1569-74.
Feng, L. Rigatti, B. W. Novak, E. K. Gorin, M. B. Swank, R. T.   Genomic structure of the mouse Ap3b1 gene in normal and pearl mice Genomics, 2000; 69(3): 370-9.
Zito, I. Gorin, M. B. Plant, C. Bird, A. C. Bhattacharya, S. S. Hardcastle, A. J.   Novel mutations of the RPGR gene in RP3 families Hum Mutat, 2000; 15(4): 386.
Zhen, L. Jiang, S. Feng, L. Bright, N. A. Peden, A. A. Seymour, A. B. Novak, E. K. Elliott, R. Gorin, M. B. Robinson, M. S. Swank, R. T.   Abnormal expression and subcellular distribution of subunit proteins of the AP-3 adaptor complex lead to platelet storage pool deficiency in the pearl mouse Blood, 1999; 94(1): 146-55.
Zito, I. Thiselton, D. L. Gorin, M. B. Stout, J. T. Plant, C. Bird, A. C. Bhattacharya, S. S. Hardcastle, A. J.   Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus Hum Genet, 1999; 105(1-2): 57-62.
Feng, L. Seymour, A. B. Jiang, S. To, A. Peden, A. A. Novak, E. K. Zhen, L. Rusiniak, M. E. Eicher, E. M. Robinson, M. S. Gorin, M. B. Swank, R. T.   The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness Hum Mol Genet, 1999; 8(2): 323-30.
Gorin, M. B. Breitner, J. C. De Jong, P. T. Hageman, G. S. Klaver, C. C. Kuehn, M. H. Seddon, J. M.   The genetics of age-related macular degeneration Mol Vis, 1999; 5(number): 29.
Keverline, M. R. Mah, T. S. Keverline, P. O. Gorin, M. B.   A practice-based survey of familial age-related maculopathy Ophthalmic Genet, 1998; 19(1): 19-26.
Seymour, A. B. Dash-Modi, A. O’Connell, J. R. Shaffer-Gordon, M. Mah, T. S. Stefko, S. T. Nagaraja, R. Brown, J. Kimura, A. E. Ferrell, R. E. Gorin, M. B.   Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3 Am J Hum Genet, 1998; 62(1): 122-9.
Gorin, M. B. Day, R. Costantino, J. P. Fisher, B. Redmond, C. K. Wickerham, L. Gomolin, J. E. Margolese, R. G. Mathen, M. K. Bowman, D. M. Kaufman, D. I. Dimitrov, N. V. Singerman, L. J. Bornstein, R. Wolmark, N.   Long-term tamoxifen citrate use and potential ocular toxicity Am J Ophthalmol, 1998; 125(4): 493-501.
Andersen, J. S. Pralea, A. M. DelBono, E. A. Haines, J. L. Gorin, M. B. Schuman, J. S. Mattox, C. G. Wiggs, J. L.   A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36 Arch Ophthalmol, 1997; 115(3): 384-8.
Nwokoro, N. A. Korytkowski, M. T. Rose, S. Gorin, M. B. Penles Stadler, M. Witchel, S. F. Mulvihill, J. J.   Spectrum of malignancy and premalignancy in Carney syndrome Am J Med Genet, 1997; 73(4): 369-77.
Seymour, A. B. Yanak, B. L. O’Brien, E. P. Rusiniak, M. E. Novak, E. K. Pinto, L. H. Swank, R. T. Gorin, M. B.   An integrated genetic map of the pearl locus of mouse chromosome 13 Genome Res, 1996; 6(6): 538-44.
Weston, M. D. Kelley, P. M. Overbeck, L. D. Wagenaar, M. Orten, D. J. Hasson, T. Chen, Z. Y. Corey, D. Mooseker, M. Sumegi, J. Cremers, C. Moller, C. Jacobson, S. G. Gorin, M. B. Kimberling, W. J.   Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients Am J Hum Genet, 1996; 59(5): 1074-83.
Xu, H. P. Yanak, B. L. Wigler, M. H. Gorin, M. B.   New polymorphic markers in the vicinity of the pearl locus on mouse chromosome 13 Mamm Genome, 1996; 7(1): 16-9.
Nayfield, S. G. Gorin, M. B.   Tamoxifen-associated eye disease. A review J Clin Oncol, 1996; 14(3): 1018-26.
Gorin, M. B. Jackson, K. E. Ferrell, R. E. Sheffield, V. C. Jacobson, S. G. Gass, J. D. Mitchell, E. Stone, E. M.   A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration Ophthalmology, 1995; 102(2): 246-55.
Day, R. Gorin, M. B. Eller, A. W.   Prevalence of lens changes in Ukrainian children residing around Chernobyl Health Phys, 1995; 68(5): 632-42.
Parker, L. S. Gorin, M. B.   Preventive ethics in the management of ophthalmic genetic disorders Semin Ophthalmol, 1995; 10(4): 331-43.
Gorin, M. B. To, A. C. Narfstrom, K.   Sequence analysis and exclusion of phosducin as the gene for the recessive retinal degeneration of the Abyssinian cat Biochim Biophys Acta, 1995; 1260(3): 323-7.
Gorin, M. B.   The interplay of genetics and surgery in ophthalmic care Semin Ophthalmol, 1995; 10(4): 303-17.
Gorin, M. B. Paul, T. O. Rader, D. J.   Angioid streaks associated with abetalipoproteinemia Ophthalmic Genet, 1994; 15(3-4): 151-9.
Hong, H. K. Ferrell, R. E. Gorin, M. B.   Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1) Am J Hum Genet, 1994; 55(6): 1173-81.
Brown, D. L. Gorin, M. B. Weeks, D. E.   Efficient strategies for genomic searching using the affected-pedigree-member method of linkage analysis Am J Hum Genet, 1994; 54(3): 544-52.
Donahue, S. P. Wenger, S. L. Steele, M. W. Gorin, M. B.   Broad-spectrum Mobius syndrome associated with a 1;11 chromosome translocation Ophthalmic Paediatr Genet, 1993; 14(1): 17-21.
Pieke Dahl, S. Kimberling, W. J. Gorin, M. B. Weston, M. D. Furman, J. M. Pikus, A. Moller, C.   Genetic heterogeneity of Usher syndrome type II J Med Genet, 1993; 30(10): 843-8.
Rikke, B. A. Pinto, L. H. Gorin, M. B. Hardies, S. C.   Mus spretus-specific LINE-1 DNA probes applied to the cloning of the murine pearl locus Genomics, 1993; 15(2): 291-6.
Sigman, D. S. Chen, C. H. Gorin, M. B.   Sequence-specific scission of DNA by RNAs linked to a chemical nuclease Nature, 1993; 363(6428): 474-5.
Chen, C. B. Gorin, M. B. Sigman, D. S.   Sequence-specific scission of DNA by the chemical nuclease activity of 1,10-phenanthroline-copper(I) targeted by RNA Proc Natl Acad Sci U S A, 1993; 90(9): 4206-10.
Gorin, M. B. Snyder, S. To, A. Narfstrom, K. Curtis, R.   The cat RDS transcript: candidate gene analysis and phylogenetic sequence analysis Mamm Genome, 1993; 4(9): 544-8.
Filling-Katz, M. R. Fink, J. K. Gorin, M. B. Caruso, R. Carl, J. B. Fitzgibbon, E. J. Barton, N. W. Katz, N. N.   Ophthalmologic manifestations of type B Niemann-Pick diseases Metab Pediatr Syst Ophthalmol, 1992; 15(1-3): 16-20.
Glenn, G. M. Linehan, W. M. Hosoe, S. Latif, F. Yao, M. Choyke, P. Gorin, M. B. Chew, E. Olfield, E. Manolatos, C. et al.,   Screening for von Hippel-Lindau disease by DNA polymorphism analysis JAMA, 1992; 267(9): 1226-31.
Filling-Katz, M. R. Choyke, P. L. Oldfield, E. Charnas, L. Patronas, N. J. Glenn, G. M. Gorin, M. B. Morgan, J. K. Linehan, W. M. Seizinger, B. R. et al.,   Central nervous system involvement in Von Hippel-Lindau disease Neurology, 1991; 41(1): 41-6.
Glenn, G. M. Daniel, L. N. Choyke, P. Linehan, W. M. Oldfield, E. Gorin, M. B. Hosoe, S. Latif, F. Weiss, G. Walther, M. et al.,   Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus Hum Genet, 1991; 87(2): 207-10.
Hosoe, S. Brauch, H. Latif, F. Glenn, G. Daniel, L. Bale, S. Choyke, P. Gorin, M. Oldfield, E. Berman, A. et al.,   Localization of the von Hippel-Lindau disease gene to a small region of chromosome 3 Genomics, 1990; 8(4): 634-40.
Choyke, P. L. Filling-Katz, M. R. Shawker, T. H. Gorin, M. B. Travis, W. D. Chang, R. Seizinger, B. R. Dwyer, A. J. Linehan, W. M.   von Hippel-Lindau disease: radiologic screening for visceral manifestations Radiology, 1990; 174(3 Pt 1): 815-20.
Gibbons, I. Gorin, M. Yassinzadeh, Z. Peterson, P. Besemer, D. Dillon, K. Burd, T. Hillman, R. Smoluk, G. Cobb, M.   Patient-side immunoassay system with a single-use cartridge for measuring analytes in blood Clin Chem, 1989; 35(9): 1869-73.
Filling-Katz, M. R. Choyke, P. L. Patronas, N. J. Gorin, M. B. Barba, D. Chang, R. Doppman, J. L. Seizinger, B. Oldfield, E. H.   Radiologic screening for von Hippel-Lindau disease: the role of Gd-DTPA enhanced MR imaging of the CNS J Comput Assist Tomogr, 1989; 13(5): 743-55.
Arden, G. B. Gorin, M. B. Polkinghorne, P. J. Jay, M. Bird, A. C.   Detection of the carrier state of X-linked retinoschisis Am J Ophthalmol, 1988; 105(6): 590-5.
Barrett, D. J. Sparkes, R. S. Gorin, M. B. Bhat, S. P. Spence, M. A. Marazita, M. L. Bateman, J. B.   Genetic linkage analysis of autosomal dominant congenital cataracts with lens-specific DNA probes and polymorphic phenotypic markers Ophthalmology, 1988; 95(4): 538-44.
Hogg, D. Gorin, M. B. Heinzmann, C. Zollman, S. Mohandas, T. Klisak, I. Sparkes, R. S. Breitman, M. Tsui, L. C. Horwitz, J.   Nucleotide sequence for the cDNA of the bovine beta B2 crystallin and assignment of the orthologous human locus to chromosome 22 Curr Eye Res, 1987; 6(11): 1335-42.
Sparkes, R. S. Mohandas, T. Heinzmann, C. Gorin, M. B. Zollman, S. Horwitz, J.   Assignment of a human beta-crystallin gene to 17cen-q23 Hum Genet, 1986; 74(2): 133-6.
Sparkes, R. S. Mohandas, T. Heinzmann, C. Gorin, M. B. Horwitz, J. Law, M. L. Jones, C. A. Bateman, J. B.   The gene for the major intrinsic protein (MIP) of the ocular lens is assigned to human chromosome 12cen-q14 Invest Ophthalmol Vis Sci, 1986; 27(9): 1351-4.
Gorin, M. B. Horwitz, J.   Cloning and characterization of a cow beta crystallin cDNA Curr Eye Res, 1984; 3(7): 939-48.
Gorin, M. B. Yancey, S. B. Cline, J. Revel, J. P. Horwitz, J.   The major intrinsic protein (MIP) of the bovine lens fiber membrane: characterization and structure based on cDNA cloning Cell, 1984; 39(1): 49-59.
Gorin, M. B. Cooper, D. L. Eiferman, F. van de Rijn, P. Tilghman, S. M.   The evolution of alpha-fetoprotein and albumin. I. A comparison of the primary amino acid sequences of mammalian alpha-fetoprotein and albumin J Biol Chem, 1981; 256(4): 1954-9.
Kioussis, D. Eiferman, F. van de Rijn, P. Gorin, M. B. Ingram, R. S. Tilghman, S. M.   The evolution of alpha-fetoprotein and albumin. II. The structures of the alpha-fetoprotein and albumin genes in the mouse J Biol Chem, 1981; 256(4): 1960-7.
Gorin, M. B. Tilghman, S. M.   Structure of the alpha-fetoprotein gene in the mouse Proc Natl Acad Sci U S A, 1980; 77(3): 1351-5.
Tilghman, S. M. Kioussis, D. Gorin, M. B. Ruiz, J. P. Ingram, R. S.   The presence of intervening sequences in the alpha-fetoprotein gene of the mouse J Biol Chem, 1979; 254(15): 7393-9.
Hansch, C. Nakamoto, K. Gorin, M. Denisevich, P. Garret, E. R. Heman-Ackah, S. M. Won, C. H.   Structure-activity relationship of chloramphenicols J Med Chem, 1973; 16(8): 917-22.

Zili Liu, Ph.D.

Publications

  1. Yang, Xing. Zili, Liu. (2026). Vision Research. Quantifying Stereokinetic depth: Divergence across methods despite robust within-subject precision
  2. Rong, Liu. Yifeng, Zhou. Zili, Liu. (2026). Vision ResearchDepth-dependent noise interference reveals scene-structure constraints on contour completion
  3. Karjack, S., Yu, A., Liu, Z. (2025). Facilitation Beyond Suppression: Enhanced Direction Discrimination After Bidirectional Motion Adaptation. ScienceDirect. Facilitation beyond suppression: Enhanced direction discrimination after bidirectional motion adaptation – ScienceDirect
  4. Yeh, M.S., Li, T., Huang, J., and Liu, Z. (2024). Comparing conventional and action video game training in visual perceptual learning. Sci Rep 14, 27864. https://doi.org/10.1038/s41598-024-71987-y
  5. Cui L, Lo S, and Liu Z (2023). The Use of Visualizations to Improve Bayesian Reasoning: A Literature Review, Vision; 7(1(17)): 1–15.
  6. Willey C and Liu Z (2022). Re-assessing the Role of Culture on the Visual Orientation Perception of the Rod and Frame Test, PLoS ONE; 17(10): e0276393.
  7. Yu Z, Zhang R, Silva A, Xing Y, Thompson B, and Liu Z (2022). Motion opponency at the middle temporal cortex: preserved motion information and the effect of perceptual learning, European Journal of Neuroscience, 2022; 1–12.
  8. Deeb, A-R., Silva, A.E., and Liu, Z (2022). Causality Modulates Perception of Apparent Motion Stimuli, Vision Research; 210(December): 1–6. 2
  9. Huang J, Yu A, Zhou Y, and Liu Z (2021). Deciphering Human Decision Rules in Motion Discrimination, Attention, Perception, & Psychophysics, 2021.
  10. Waz S C and Liu Z (2021). Evidence for strictly monocular processing in visual motion opponency and Glass pattern perception Vision Research, 186: 103—111.
  11. Karjack S, Erlikhman G, and Liu Z (2021). Reduced Direction Discrimination Sensitivity in Visual Motion Adaptation, and the Role of Perceptual Learning Vision Research, 185: 111-122.
  12. Silva A, Thompson B, and Liu Z (2021). Motion opponency examined throughout visual cortex with multivariate pattern analysis of fMRI data. Human Brain Mapping, 42: 5-13.
  13. Lee A L F, Liu Z, and Lu H (2020). Parts beget parts: Bootstrapping hierarchical object representations through visual statistical learning, Cognition, 2020, (104515) 1 – 14.
  14. Cui L and Liu Z (2020). Synergy between Research on Ensemble Perception, Data Visualization, and Statistics Education: A Tutorial Review Attention, Perception, & Psychophysics, 83 (Special Issue on Ensemble Perception): 1290–1311.
  15. Erlikhman G, Singh G, Ghose T, and Liu Z (2019). The effect of perceptual contour orientation uncertainty on the tilt aftereffect. Vision Research, 158, 126–134.
  16. Silva A and Liu Z (2018). Spatial proximity modulates the strength of motion opponent suppression elicited by locally paired dot displays. Vision Research, 144, 1—8.
  17. Xing Y and Liu Z (2018). A Preference for Minimal Deformation Constrains the Perceived Depth of a Stereokinetic Stimulus. Vision Research, 153: 53–59.
  18. Zavagno D, Daneyko O, and Liu Z (2018). The influence of physical illumination on lightness perception in simultaneous contrast displays. i-Perception; 9(4): 1–22.
  19. Ren Na R, Bi T, Tjan BS, Liu Z, and Fang F (2018). Effect of Task Difficulty on Blood[1]Oxygen-Level-Dependent Signal: a Functional Magnetic Resonance Imaging Study in a Motion Discrimination Task. PLOS ONE. doi.org/10.1371/journal.pone.0199440
  20. Willey C and Liu Z (2018). Limited generalization with varied, as compared to specific, practice in short-term motor learning. Acta Psychologica 182, 39–45.
  21. Zhou ZW, Liu Z, Clavagnier S, Reynaud A, Hou F (2017). Visual plasticity in adults. Neural Plasticity. doi.org/10.1155/2017/8469580.
  22. Lu H, Tjan BS, and Liu Z (2017). Human efficiency in detecting and discriminating biological motion. Journal of Vision, 17(6), 1–14.
  23. Willey C and Liu Z (2018). Long-term motor learning: effects of varied and specific practice. Vision Research, 152, 10-16.
  24. Huang J, Liang J, Zhou Y, and Liu Z (2017). Transfer in motion discrimination learning was no greater in double training than in single training. Journal of Vision, vol.17, doi:10.1167/17.6.7
  25. Thompson B, Deblieck C, Wu AD, Iacoboni M, Liu Z (2016). Psychophysical and rTMS evi[1]dence for the presence of motion opponency in human V5. Brain Stimulation (doi:10.1016/j.brs.2016.05.012).
  26. Chang J, Zhou Y, and Liu Z (2016). Limited top-down influence from recognition to same[1]different matching of Chinese characters. PLoS ONE, 11(6): e0156517. doi:10.1371/journal.pone.0156517.
  27. Liu Z, Yang X, and Intraub H (2016). Boundary extension: insights from Signal Detection Theory, Journal of Vision, 16(8):7, 1–10.
  28. Liang J, Zhou Y, and Liu Z (2016). Examining the standard model of Signal Detection Theory in motion discrimination, Journal of Vision, Special Issue on Perceptual Learning, 16, 9. doi:10.1167/16.7.9
  29. Liang J, Zhou Y, Fahle M, and Liu Z (2015). Specificity of motion discrimination learning even with double training and staircase, Journal of Vision, Special Issue on Perceptual Learning, 15(3), 1–10. 3
  30. Liang J, Zhou Y, Fahle M, and Liu Z (2015). Limited transfer of long-term motion perceptual learning with double training, Journal of Vision, Special Issue on Perceptual Learning, 15(1), 1–9.
  31. Silva A and Liu Z (2015). Opponent backgrounds reduce discrimination sensitivity to com[1]peting motions: effects of different vertical motions on horizontal motion perception, Vision Research, 113, 55–64.
  32. Chen N, Bi T, Zhou T, Li S, Liu Z, and Fang F (2015). Sharpened cortical tuning and enhanced cortico-cortical communication contribute to the long-term neural mechanisms of visual motion perceptual learning, Neural Image, 115: 17 – 29.
  33. Ghose T and Liu Z (2013). Generalization between canonical and non-canonical views in object recognition, Journal of Vision, 2013; 13(1): 1–15.
  34. Thompson B, Tjan B S, and Liu Z (2013). Perceptual Learning of Motion Direction Discrimi[1]nation with Suppressed and Unsuppressed MT in Humans: An fMRI Study, PLoS ONE, 8(1): 1 – 14.
  35. Wang X, Zhou Y, and Liu Z (2013). Transfer in motion perceptual learning depends on the difficulty of the training task, Journal of Vision, 2013; 13((7):5): 1 – 9.
  36. Huang X, Lu H, Zhou Y, and Liu Z (2011). General and specific perceptual learning in radial speed discrimination, Journal of Vision, 11(4): 7, 1 – 11.
  37. Lu H and Liu Z (2009) When a never-seen but less-occluded image is better recognized: Evi[1]dence from same-different matching experiments and a model, Journal of Vision, 9(4): 4, 1 – 12.
  38. Lu H and Liu Z. (2008). When a never-seen but less-occluded image is better recognized: Evidence from old—new memory experiments, Journal of Vision, 8(7): 31, 1 – 9.
  39. Zhou J, Gotch C, Zhou Y, and Liu Z (2008). Perceiving an object in its context – is the context cultural or perceptual? Journal of Vision, 8(12):2, 1 — 5.
  40. Zhou J, Tjan B S, Zhou Y, and Liu Z (2008). Better discrimination for illusory than for occluded perceptual completions, Journal of Vision, 8(7): 26, 1 – 17.
  41. Huang X, Lu H, Tjan B S, Zhou Y, and Liu Z (2007). Motion perceptual learning: when only task-relevant information is learned, Journal of Vision 7(10): 14, 1—10.
  42. Lu H and Liu Z (2006). Computing dynamic classification images from correlation maps, Journal of Vision (Special Issue on Classification Images), 6. 475 – 483.
  43. Lu H, Zavagno D, and Liu Z (2006). The glare effect does not give rise to a longer lasting afterimage, Perception, 35, 701—707.
  44. Rokers B, Yuille A, and Liu Z (2006). The perceived motion of a stereokinetic stimulus, Vision Research, 46, 2575 – 2387.
  45. Thompson B and Liu Z (2006). Learning motion discrimination with suppressed and unsup[1]pressed MT, Vision Research, 4, 2110—2121.
  46. Lu H, Tjan B S, and Liu Z (2006). Shape recognition alters stereoscopic depth discrimination, Journal of Vision, 6, 75-86.
  47. Hou F, Lu H, Zhou Y, and Liu Z (2006). Amodal completion impairs stereo acuity discrimi[1]nation, Vision Research, 46, 2061 – 2068.
  48. Tjan B S and Liu Z (2005). Symmetry impedes symmetry discrimination, Journal of Vision, 5, 888 – 900.
  49. Lu H, Qian N, and Liu Z (2004). Learning motion discrimination with suppressed MT, Vision Research, 44, 1817-1825.
  50. Rokers B and Liu Z (2004). On the minimal relative motion principle – lateral displacement of a contracting bar, Journal of Mathematical Psychology, 48, 292—295. 4
  51. Liu Z (2004). On the principle of minimal relative motion – the oscillating tilted bar, Journal of Mathematical Psychology, 28. 196 – 198.
  52. Liu Z (2003). On the principle of minimal speed difference – the bar, the circle with a lot, and the ellipse, Journal of Vision, 3, 625 — 629.
  53. Liu Z and Kersten D (2003). 3D symmetric shapes are discriminated more efficiently than asymmetric ones, Journal of Optical Society of America, Special Issue on Bayesian and Sta[1]tistical Approaches to Vision, 20, 1331—1340.
  54. Matthews N, Liu Z, and Qian N (2001). The effect of orientation learning on contrast sensi[1]tivity, Vision Research, 41, 463 — 471.
  55. Liu Z and Weinshall D (2000). Mechanisms of generalization in perceptual learning, Vision Research, 40, 97- 109.
  56. Liu Z (1999). Perceptual learning in motion discrimination that generalizes across motion directions, Proceedings of National Academy of Sciences, 96, 11085 —11087.
  57. Liu Z, Jacobs D W, and Basri R (1999). The role of convexity in perceptual completion – beyond good continuation, Vision Research, 39, 4244 — 4257.
  58. Matthews N, Liu Z, Geesaman B J, and Qian N (1999). Perceptual learning on orientation and direction discrimination, Vision Research, 39: 3692 — 3701.
  59. Liu Z, Kersten D, and Knill D C (1999). Dissociating stimulus information from internal representation —- a case study in object recognition, Vision Research, 39, 603 – 612.
  60. Liu Z and Kersten D (1998). 2D observers for human 3D object recognition? Vision Research, Special issue on Models of Recognition, 3 2507 – 2519.
  61. Liu Z and Vaina L (1998). Simultaneous learning of motion discrimination in two directions, Cognitive Brain Research, 6, 347 – 349.
  62. Liu Z (1996). Viewpoint-dependency in object representation and recognition, Spatial Vision, Special Issue on Perceptual Learning & Adaptation in Man & Machine, 9: 491 — 521.
  63. Liu Z, Knill D C, and Kersten D (1995). Object classification for human and ideal Observers, Vision Research, 35, 549 – 568.
  64. Liu Z, Wang X, and Zhang S W (1992). An electronic network for edge detection using DOC operator function, Acta Automatica Sinica, 18, 239 – 243.
  65. Zhang S W, Wang X, Liu Z, and Srinivasan M V (1990). Visual tracking of moving targets by freely flying honeybees. Visual Neuroscience, 4, 379 – 386.

Stan Schein, M.D., Ph.D.

Faculty Member

Professor
Department of Psychology
College of Life Sciences
University of California, Los Angeles

 

Franz Hall, Room 8522
502 Portola Plaza,
Los Angeles, CA 90095
Mailcode 951563

 

Publications

A selected list of publications:

G Brinkmann, P Goetschalckx, S Schein   Comparing the constructions of Goldberg, Fuller, Caspar, Klug and Coxeter, and a general approach to local symmetry-preserving operations, Proc Roy Soc Lond A , 2017; 2017.0267.

S Schein, AJ Yeh, K Coolsaet, JM Gayed   Decoration of the truncated tetrahedron—an Archimedean polyhedron—to produce a new class of convex equilateral polyhedra with tetrahedral symmetry, Symmetry, 2016; 8: 82-91.
X Zhang, P Ge, X Yu, JM Brannan, G Bi, Q Zhang, S Schein, ZH Zhou   Cryo-EM structure of the mature dengue virus at 3.5-Å resolution, Nature Structural and Molecular Biology, 2012; 20: 105-110.
Wang Zhi, Su Hai-Feng, Tan Yuan-Zhi, Schein Stan, Lin Shui-Chao, Liu Wei, Wang Shu-Ao, Wang Wen-Guang, Tung Chen-Ho, Sun Di, Zheng Lan-Sun   Assembly of silver Trigons into a buckyball-like Ag180 nanocage Proceedings of the National Academy of Sciences of the United States of America, 2017; 114(46): 12132-12137.
Schein Stan, Gayed James Maurice   Fourth class of convex equilateral polyhedron with polyhedral symmetry related to fullerenes and viruses Proceedings of the National Academy of Sciences of the United States of America, 2014; 111(8): 2920-5.
Zhang Xiaokang, Ge Peng, Yu Xuekui, Brannan Jennifer M, Bi Guoqiang, Zhang Qinfen, Schein Stan, Zhou Z Hong   Cryo-EM structure of the mature dengue virus at 3.5-Å resolution Nature structural & molecular biology, 2013; 20(1): 105-10.
Schein S, Ngo IT, Huang TM, Klug K, Sterling P, Herr S   Cone synapses in macaque fovea: I. Two types of non-S cones are distinguished by numbers of contacts with OFF midget bipolar cells Vis Neurosci, 2011; 28(1): 3-16.
Hongrong Liu, Lei Jin, Sok Boon S. Koh, Ivo Atanasov, Stan Schein, Lily Wu, Z. Hong Zhou   Atomic Structure of Human Adenovirus by Cryo-EM Reveals Interactions Among Protein Networks Science, 2010; 329(5995): 1038-1043.
Zhang X, Boyce M, Bhattacharya B, Zhang X, Schein S, Roy P, Zhou ZH   Bluetongue virus coat protein VP2 contains sialic acid-binding domains, and VP5 resembles enveloped virus fusion proteins Proc Natl Acad Sci U S A, 2010; 107(14): 6292-7.
Ge P, Tsao J, Schein S, Green TJ, Luo M, Zhou ZH   Cryo-EM model of the bullet-shaped vesicular stomatitis virus Science, 2010; 327(5966): 689-93.
Schein Stan, Friedrich Tara   A geometric constraint, the head-to-tail exclusion rule, may be the basis for the isolated-pentagon rule in fullerenes with more than 60 vertices Proceedings of the National Academy of Sciences of the United States of America, 2008; 105(49): 19142-7.
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Stan Schein, Michelle Sands-Kidner, Tara Friedrich   The physical basis for the head-to-tail rule that excludes most fullerene cages from self assembly Biophysical J, 2008; 94: 938-957.
Schein, S. Sands-Kidner, M.   A geometric principle may guide self-assembly of fullerene cages from clathrin triskelia and from carbon atoms Biophysical Journal, 2008; 94(3): 958-976.
S Schein, KM Ahmad   Efficiency of synaptic transmission of single-photoreceptor to rod bipolar dendrite, Biophysical J, 2006; 91: 3257-3267.
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S Schein, KM Ahmad   A clockwork hypothesis: Synaptic release by rod photoreceptors must be regular, Biophysical J, 2005; 89: 3931-3949.
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Schein, S. Sterling, P. Ngo, I. T. Huang, T. M. Herr, S.   Evidence that each S cone in macaque fovea drives one narrow-field and several wide-field blue-yellow ganglion cells Journal of Neuroscience, 2004; 24(38): 8366-8378.
Ahmad, K. M. Klug, K. Herr, S. Sterling, P. Schein, S.   Cell density ratios in a foveal patch in macaque retina Visual Neuroscience, 2003; 20(2): 189-209.
AA Sadun, V Carelli, SR Salomao, A Berezovsky, PA Quiros, F Sadun, AM DeNegri, R Andrade, M Moraes, A Passos, P Kjaer, J Pereira, ML Valentino, S Schein, R Belfort   Extensive investigation of a large Brazilian pedigree of 11778/Haplogroup J Leber American Journal of Ophthalmology, 2003; 136(2): 231-238.
S Herr, KJ Klug, P Sterling, S Schein   Inner S-cone bipolar cells provide all of the central elements for S cones in macaque retina, J Comp Neurol, 2003; 457: 185-201.
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K Klug, S Herr, IT Ngo, P Sterling, S Schein   Macaque retina contains an S-cone OFF midget pathway, J Neurosci, 2003; 23: 9881-9887.
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K Migdale, S Herr, K Klug, K Ahmad, K Linberg, P Sterling, S Schein   Two ribbon synaptic units in rod photoreceptors of macaque, human, and cat, J Comp Neurol, 2003; 455: 100-112.
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Herr, S. Klug, K. Sterling, P. Schein, S.   Inner S-cone bipolar cells provide all of the central elements for S cones in macaque retina Journal of Comparative Neurology, 2003; 457(2): 185-201.
Burris, C. Klug, K. Ngo, I. T. Sterling, P. Schein, S.   How Muller glial cells in macaque fovea coat and isolate the synaptic terminals of cone photoreceptors Journal of Comparative Neurology, 2002; 453(1): 100-111.
AA Sadun, V Carelli, SR Salomao, A Berezovsky, P Quiros, F Sadun, AM DeNegri, R Andrade, S Schein, R Belfort   A very large Brazilian pedigree with 11 778 Leber’s hereditary optic, Trans Ant Ophthalmol Soc, 2002; 100: 169-77.
C Burris, K Klug, IT Ngo, P Sterling, S Schein   How Müller glial cells in macaque fovea coat and isolate the synaptic terminals of cone photoreceptors, J Comp Neurol, 2002; 453: 100-11.
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