In vivo evaluation of a regenerative approach to nasal dorsum augmentation with a polycaprolactone-based implant

by Wiggenhauser, Paul S., Balmayor, Elizabeth R., Rotter, Nicole, Schantz, Jan Thorsten
Published 2019

Unconventional modes in lasers with spatially varying gain and loss

by Rotter, S., Türeci, H. E., Ge, Li, Chong, Yidong, Stone, A. Douglas
Published 2013

Challenges in elucidating the genetics of diabetic retinopathy

by Kuo, J.Z., Wong, T.Y., Rotter, J.I., Wiggs, J.L.
Published 2014

Breaking of PT-symmetry in bounded and unbounded scattering systems

by Ambichl, Philipp, Makris, Konstantinos G., Ge, Li, Chong, Yidong, Stone, A. Douglas, Rotter, Stefan
Published 2014

Reconfigurable symmetry-broken laser in a symmetric microcavity

by Cao, Q.-T., Liu, R., Wang, H., Lu, Y.-K., Qiu, C.-W., Rotter, S., Gong, Q., Xiao, Y.-F.
Published 2021

Revisiting food security in 2021: An overview of the past year

by Serge Savary, Stephen Waddington, Sonia Akter, Conny J. M. Almekinders, Jody Harris, Lise Korsten, Reimund P. Rötter, Goedele Van den Broeck
Published 2022

Chronic kidney disease and cardiovascular risk: Epidemiology, mechanisms, and prevention

by Gansevoort, R.T., Correa-Rotter, R., Hemmelgarn, B.R., Jafar, T.H., Heerspink, H.J.L., Mann, J.F., Matsushita, K., Wen, C.P.
Published 2016

Associations of candidate genes to age-related macular degeneration among racial/ethnic groups in the multi-ethnic study of atherosclerosis

by Klein, R., Li, X., Kuo, J.Z., Klein, B.E.K., Cotch, M.F., Wong, T.Y., Taylor, K.D., Rotter, J.I.
Published 2014

Personalized medicine in ophthalmology: From pharmacogenetic biomarkers to therapeutic and dosage optimization

by Ong, F.S, Kuo, J.Z, Wu, W.-C, Cheng, C.-Y, Blackwell, W.-L.B, Taylor, B.L, Grody, W.W, Rotter, J.I, Lai, C.-C, Wong, T.Y
Published 2020

No association of 9p21 with arterial elasticity and retinal microvascular findings

by Folsom, A.R., Pankow, J.S., Li, X., Duprez, D.A., Jacobs, D.R., Klein, R., Klein, B., Tang, W., Wong, T.Y., Cotch, M.F., Taylor, K.D., Rich, S.S., Hall, J.L., Post, W.S., Rotter, J.I.
Published 2014

The Association of Estrogen Receptor-β Gene Variation with Salt-Sensitive Blood Pressure

by Worapaka Manosroi, Jia Wei Tan, Chevon M. Rariy, Bei Sun, Mark O. Goodarzi, Aditi R. Saxena, Jonathan S. Williams, Luminita H. Pojoga, Jessica Lasky-Su, Jinrui Cui, Xiuqing Guo, Kent D. Taylor, Yii Der I. Chen, Anny H. Xiang, Willa A. Hsueh, Leslie J. Raffel, Thomas A. Buchanan, Jerome I. Rotter, Gordon H. Williams, Ellen W. Seely
Published 2018

The Association of Estrogen Receptor-β Gene Variation With Salt-Sensitive Blood Pressure

by Worapaka Manosroi, Jia Wei Tan, Chevon M. Rariy, Bei Sun, Mark O. Goodarzi, Aditi R. Saxena, Jonathan S. Williams, Luminita H. Pojoga, Jessica Lasky-Su, Jinrui Cui, Xiuqing Guo, Kent D. Taylor, Yii Der I. Chen, Anny H. Xiang, Willa A. Hsueh, Leslie J. Raffel, Thomas A. Buchanan, Jerome I. Rotter, Gordon H. Williams, Ellen W. Seely
Published 2018

Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: The candidate gene association resource (CARe)

by Sobrin, L., Green, T., Sim, X., Jensen, R.A., Shyong Tai, E., Tay, W.T., Wang, J.J., Mitchell, P., Sandholm, N., Liu, Y., Hietala, K., Iyengar, S.K., Brooks, M., Buraczynska, M., van Zuydam, N., Smith, A.V., Gudnason, V., Doney, A.S.F., Morris, A.D., Leese, G.P., Palmer, C.N.A., Swaroop, A., Taylor Jr., H.A., Wilson, J.G., Penman, A., Chen, C.J., Groop, P.-H., Saw, S.-M., Aung, T., Klein, B.E., Rotter, J.I., Siscovick, D.S., Cotch, M.F., Klein, R., Daly, M.J., Wong, T.Y.
Published 2014

Microbial exposure during early human development primes fetal immune cells

by Mishra, Archita, Lai, Ghee Chuan, Yao, Leong Jing, Aung, Thet Tun, Shental, Noam, Rotter-Maskowitz, Aviva, Shepherdson, Edwin, Singh, Gurmit Singh Naranjan, Pai, Rhea, Shanti, Adhika, Wong, Regina Men Men, Lee, Andrea, Khyriem, Costerwell, Dutertre, Charles Antoine, Chakarov, Svetoslav, Srinivasan, K. G., Shadan, Nurhidaya Binte, Zhang, Xiao-Meng, Khalilnezhad, Shabnam, Cottier, Fabien, Tan, Alrina Shin Min, Low, Gillian, Chen, Phyllis, Fan, Yiping, Hor, Pei Xiang, Lee, Avery Khoo May, Choolani, Mahesh, Vermijlen, David, Sharma, Ankur, Fuks, Garold, Straussman, Ravid, Pavelka, Norman, Malleret, Benoit, McGovern, Naomi, Albani, Salvatore, Chan, Jerry Kok Yen, Ginhoux, Florent
Published 2022

Insights into the Genetic Architecture of Early Stage Age-Related Macular Degeneration: A Genome-Wide Association Study Meta-Analysis

by Holliday, E.G., Smith, A.V., Cornes, B.K., Buitendijk, G.H.S., Jensen, R.A., Sim, X., Aspelund, T., Aung, T., Baird, P.N., Boerwinkle, E., Cheng, C.Y., van Duijn, C.M., Eiriksdottir, G., Gudnason, V., Harris, T., Hewitt, A.W., Inouye, M., Jonasson, F., Klein, B.E.K., Launer, L., Li, X., Liew, G., Lumley, T., McElduff, P., McKnight, B., Mitchell, P., Psaty, B.M., Rochtchina, E., Rotter, J.I., Scott, R.J., Tay, W., Taylor, K., Teo, Y.Y., Uitterlinden, A.G., Viswanathan, A., Xie, S., Vingerling, J.R., Klaver, C.C.W., Tai, E.S., Siscovick, D., Klein, R., Cotch, M.F., Wong, T.Y., Attia, J., Wang, J.J.
Published 2014

A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes

by Meng W., Shah K.P., Pollack S., Toppila I., Hebert H.L., McCarthy M.I., Groop L., Ahlqvist E., Lyssenko V., Agardh E., Daniell M., Kaidonis G., Craig J.E., Mitchell P., Liew G., Kifley A., Wang J.J., Christiansen M.W., Jensen R.A., Penman A., Hancock H.A., Chen C.J., Correa A., Kuo J.Z., Li X., Chen Y.-D.I., Rotter J.I., Klein R., Klein B., Wong T.Y., Morris A.D., Doney A.S.F., Colhoun H.M., Price A.L., Burdon K.P., Groop P.-H., Sandholm N., Grassi M.A., Sobrin L., Palmer C.N.A., Wellcome Trust Case Control Consortium 2 (WTCCC2), Surrogate markers for Micro- and Macro-vascular hard endpoints for Innovative diabetes Tools (SUMMIT) study group
Published 2019

Genome-Wide Association Study of Retinopathy in Individuals without Diabetes

by Jensen, R.A., Sim, X., Li, X., Cotch, M.F., Ikram, M.K., Holliday, E.G., Eiriksdottir, G., Harris, T.B., Jonasson, F., Klein, B.E.K., Launer, L.J., Smith, A.V., Boerwinkle, E., Cheung, N., Hewitt, A.W., Liew, G., Mitchell, P., Wang, J.J., Attia, J., Scott, R., Glazer, N.L., Lumley, T., McKnight, B., Psaty, B.M., Taylor, K., Hofman, A., de Jong, P.T.V.M., Rivadeneira, F., Uitterlinden, A.G., Tay, W.-T., Teo, Y.Y., Seielstad, M., Liu, J., Cheng, C.-Y., Saw, S.-M., Aung, T., Ganesh, S.K., O'Donnell, C.J., Nalls, M.A., Wiggins, K.L., Kuo, J.Z., van Duijn, C.M., Gudnason, V., Klein, R., Siscovick, D.S., Rotter, J.I., Tai, E.S., Vingerling, J., Wong, T.Y.
Published 2014

Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: A meta-analysis

by Thomson, G., Valdes, A.M., Noble, J.A., Kockum, I., Grote, M.N., Najman, J., Erlich, H.A., Cucca, F., Pugliese, A., Steenkiste, A., Dorman, J.S., Caillat-Zucman, S., Hermann, R., Ilonen, J., Lambert, A.P., Bingley, P.J., Gillespie, K.M., Lernmark, Å., Sanjeevi, C.B., Rønningen, K.S., Undlien, D.E., Thorsby, E., Petrone, A., Buzzetti, R., Koeleman, B.P.C., Roep, B.O., Saruhan-Direskeneli, G., Uyar, F.A., Günoz, H., Gorodezky, C., Alaez, C., Boehm, B.O., Mlynarski, W., Ikegami, H., Berrino, M., Fasano, M.E., Dametto, E., Israel, S., Brautbar, C., Santiago-Cortes, A., Frazer De Llado, T., She, J.-X., Bugawan, T.L., Rotter, J.I., Raffel, L., Zeidler, A., Leyva-Cobian, F., Hawkins, B.R., Chan, S.H., Castano, L., Pociot, F., Nerup, J.
Published 2014

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

by Jakobsdottir J., van der Lee S.J., Bis J.C., Chouraki V., Li-Kroeger D., Yamamoto S., Grove M.L., Naj A., Vronskaya M., Salazar J.L., DeStefano A.L., Brody J.A., Smith A.V., Amin N., Sims R., Ibrahim-Verbaas C.A., Choi S.-H., Satizabal C.L., Lopez O.L., Beiser A., Ikram M.A., Garcia M.E., Hayward C., Varga T.V., Ripatti S., Franks P.W., Hallmans G., Rolandsson O., Jansson J.-H., Porteous D.J., Salomaa V., Eiriksdottir G., Rice K.M., Bellen H.J., Levy D., Uitterlinden A.G., Emilsson V., Rotter J.I., Aspelund T., O?Donnell C.J., Fitzpatrick A.L., Launer L.J., Hofman A., Wang L.-S., Williams J., Schellenberg G.D., Boerwinkle E., Psaty B.M., Seshadri S.
Published 2019

Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci

by Simpson C.L., Wojciechowski R., Oexle K., Murgia F., Portas L., Li X., Virginie J.M.V., Vitart V., Schache M., Mohsen Hosseini S., Hysi P.G., Raffel L.J., Cotch M.F., Chew E., Klein B.E.K., Klein R., Wong T.Y., Van Duijn C.M., Mitchell P., Saw S.M., Fossarello M., Wang J.J., Polašek O., Campbell H., Rudan I., Oostra B.A., Uitterlinden A.G., Hofman A., Rivadeneira F., Amin N., Karssen L.C., Vingerling J.R., Döring A., Bettecken T., Bencic G., Gieger C., Wichmann H.-E., Wilson J.F., Venturini C., Fleck B., Cumberland P.M., Rahi J.S., Hammond C.J., Hayward C., Wright A.F., Paterson A.D., Baird P.N., Klaver C.C.W., Rotter J.I., Pirastu M., Meitinger T., Bailey-Wilson J.E., Stambolian D.
Published 2018