Eye Movement Patterns in Response to Anti-Binge Drinking Messages

Por Yzer, Marco, Han, Jiyoung, Choi, Kelvin
Publicado no Health Commun (2017)

New BEST1 mutations in autosomal recessive bestrophinopathy

Por Allikmets, Rando, Fung, Adrian, Yzer, Suzanne, Allikmets, Rando
Publicado no Retina (2015)

On the Conceptual Ambiguity Surrounding Perceived Message Effectiveness

Por Yzer, Marco, LoRusso, Susan, Nagler, Rebekah H.
Publicado no Health Commun (2015)

The Effectiveness of Gateway Communications in Anti-Marijuana Campaigns

Por YZER, MARCO C., CAPPELLA, JOSEPH N., FISHBEIN, MARTIN, HORNIK, ROBERT, AHERN, R. KIRKLAND
Publicado em 2003

Affective Antecedents of the Perceived Effectiveness of Antidrug Advertisements: An Analysis of Adolescents’ Momentary and Retrospective Evaluations

Por Yzer, Marco C., Vohs, Kathleen D., Luciana, Monica, Cuthbert, Bruce N., MacDonald, Angus W.
Publicado em 2011

Abnormality in the External Limiting Membrane in early Stargardt Disease

Por Burke, Tomas R., Yzer, Suzanne, Zernant, Jana, Smith, R. Theodore, Tsang, Stephen H., Allikmets, Rando
Publicado em 2012

The Role of Distal Variables in Behavior Change: Effects of Adolescents’ Risk for Marijuana Use on Intention to Use Marijuana()

Por Yzer, Marco C., Cappella, Joseph N., Fishbein, Martin, Hornik, Robert, Sayeed, Sarah, Ahern, R. Kirkland
Publicado em 2006

Concurrent idiopathic macular telangiectasia type 2 and central serous chorioretinopathy

Por Matet, Alexandre, Yzer, Suzanne, Chew, Emily Y., Daruich, Alejandra, Behar-Cohen, Francine, Spaide, Richard F.
Publicado no Retina (2018)

Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype

Por Tsang, Stephen H., Burke, Tomas, Oll, Maris, Yzer, Suzanne, Lee, Winston, Xie, Yajing (Angela), Allikmets, Rando
Publicado em 2014

Disruption of the human cone photoreceptor mosaic from a defect in NR2E3 transcription factor function in young adults

Por Park, Sung Pyo, Hong, In Hwan, Tsang, Stephen H., Lee, Winston, Horowitz, Jason, Yzer, Suzanne, Allikmets, Rando, Chang, Stanley
Publicado no Graefes Arch Clin Exp Ophthalmol (2013)

Reticular Pseudodrusen in Early Age-Related Macular Degeneration Are Associated With Choroidal Thinning

Por Garg, Aakriti, Oll, Maris, Yzer, Suzanne, Chang, Stanley, Barile, Gaetano R., Merriam, John C., Tsang, Stephen H., Bearelly, Srilaxmi
Publicado em 2013

Associations Between β-Peripapillary Atrophy and Reticular Pseudodrusen in Early Age-Related Macular Degeneration

Por Garg, Aakriti, Blumberg, Dana M., Al-Aswad, Lama A., Oll, Maris, Yzer, Suzanne, Forbes, Max, Allikmets, Rando L., Bearelly, Srilaxmi
Publicado no Invest Ophthalmol Vis Sci (2017)

Expanded Clinical Spectrum of Enhanced S-Cone Syndrome

Por Yzer, Suzanne, Barbazetto, Irene, Allikmets, Rando, van Schooneveld, Mary J., Bergen, Arthur, Tsang, Stephen H., Jacobson, Samuel G., Yannuzzi, Lawrence A.
Publicado no JAMA Ophthalmol (2013)

A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

Por Yzer, S, van den Born, L I, Schuil, J, Kroes, H, van Genderen, M M, Boonstra, F, van den Helm, B, Brunner, H, Koenekoop, R, Cremers, F
Publicado em 2003

NEW BEST1 MUTATIONS IN AUTOSOMAL RECESSIVE BESTROPHINOPATHY

Por FUNG, ADRIAN T., YZER, SUZANNE, GOLDBERG, NAOMI, WANG, HAO, NISSEN, MICHAEL, GIOVANNINI, ALFONSO, MERRIAM, JOANNA E., BUKANOVA, ELENA N., CAI, CAROLYN, YANNUZZI, LAWRENCE A., TSANG, STEPHEN H., ALLIKMETS, RANDO
Publicado no Retina (2015)

Ocular and extra-ocular features of patients with Leber congenital amaurosis and mutations in CEP290

Por Yzer, Suzanne, den Hollander, Anneke I., Lopez, Irma, Pott, Jan-Willem R., de Faber, Jan Tjeerd H.N., Cremers, Frans P.M., Koenekoop, Robert K., van den Born, L. Ingeborgh
Publicado em 2012

Neovascular age-related macular degeneration without drusen in the fellow eye: clinical spectrum and therapeutic outcome

Por Chung, Wing H, van Dijk, Elon H C, Mohabati, Danial, Dijkman, Greet, Yzer, Suzanne, de Jong, Eiko K, Fauser, Sascha, Schlingemann, Reinier O, Hoyng, Carel B, Boon, Camiel J F
Publicado no Clin Ophthalmol (2016)

Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

Por den Hollander, Anneke I., Koenekoop, Robert K., Yzer, Suzanne, Lopez, Irma, Arends, Maarten L., Voesenek, Krysta E. J., Zonneveld, Marijke N., Strom, Tim M., Meitinger, Thomas, Brunner, Han G., Hoyng, Carel B., van den Born, L. Ingeborgh, Rohrschneider, Klaus, Cremers, Frans P. M.
Publicado em 2006

Cadherin 5 is Regulated by Corticosteroids and Associated with Central Serous Chorioretinopathy

Por Schubert, Carl, Pryds, Anders, Zeng, Shemin, Xie, Yajing, Freund, K Bailey, Spaide, Richard F, Merriam, John C, Barbazetto, Irene, Slakter, Jason S, Chang, Stanley, Munch, Inger C, Drack, Arlene V, Hernandez, Jasmine, Yzer, Suzanne, Merriam, Joanna E, Linneberg, Allan, Larsen, Michael, Yannuzzi, Lawrence A, Mullins, Robert F, Allikmets, Rando
Publicado em 2014

Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis

Por Bainbridge, J.W.B., Mehat, M.S., Sundaram, V., Robbie, S.J., Barker, S.E., Ripamonti, C., Georgiadis, A., Mowat, F.M., Beattie, S.G., Gardner, P.J., Feathers, K.L., Luong, V.A., Yzer, S., Balaggan, K., Viswanathan, A., de Ravel, T.J.L., Casteels, I., Holder, G.E., Tyler, N., Fitzke, F.W., Weleber, R.G., Nardini, M., Moore, A.T., Thompson, D.A., Petersen-Jones, S.M., Michaelides, M., van den Born, L.I., Stockman, A., Smith, A.J., Rubin, G., Ali, R.R.
Publicado no N Engl J Med (2015)