Exome Analysis of Two Limb-Girdle Muscular Dystrophy Families: Mutations Identified and Challenges Encountered

by McDonald K.K., Stajich J., Blach C., Ashley-Koch A.E., Hauser M.A.
Published 2019

Screening of the seed region of MIR184 in Keratoconus patients from Saudi Arabia

by Abu-Amero, K.K, Helwa, I, Al-Muammar, A, Strickland, S, Hauser, M.A, Allingham, R.R, Liu, Y
Published 2020

Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population

by Abu-Amero, K.K, Helwa, I, Al-Muammar, A, Strickland, S, Hauser, M.A, Allingham, R.R, Liu, Y
Published 2020

Serotonin transporter gene polymorphisms and brain function during emotional distraction from cognitive processing in posttraumatic stress disorder

by Morey, R.A, Hariri, A.R, Gold, A.L, Hauser, M.A, Munger, H.J, Dolcos, F, McCarthy, G
Published 2020

An examination of the association between 5-HTTLPR, combat exposure, and PTSD diagnosis among U.S. Veterans

by Liu Y., Garrett M.E., Dennis M.F., Green K.T., Ashley-Koch A.E., Hauser M.A., Beckham J.C., Kimbrel N.A.
Published 2019

Spink2 modulates apoptotic susceptibility and is a candidate gene in the Rgcs1 QTL that affects retinal ganglion cell death after optic nerve damage

by Dietz J.A., Maes M.E., Huang S., Yandell B.S., Schlamp C.L., Montgomery A.D., Allingham R.R., Hauser M.A., Nickells R.W.
Published 2019

Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls

by Morey, R.A, Davis, S.L, Garrett, M.E, Haswell, C.C, Marx, C.E, Beckham, J.C, McCarthy, G, Hauser, M.A, Ashley-Koch, A.E
Published 2020

Mitochondrial DNA polymorphism A4917G is independently associated with age-related macular degeneration

by Canter J.A., Olson L.M., Spencer K., Schnetz-Boutaud N., Anderson B., Hauser M.A., Schmidt S., Postel E.A., Agarwal A., Pericak-Vance M.A., Sternberg Jr. P., Haines J.L.
Published 2019

Genome-Wide linkage scan for primary open angle glaucoma: Influences of ancestry and age at diagnosis

by Crooks K.R., Allingham R.R., Qin X., Liu Y., Gibson J.R., Santiago-Turla C., Larocque-Abramson K.R., Del Bono E., Challa P., Herndon L.W., Akafo S., Wiggs J.L., Schmidt S., Hauser M.A.
Published 2019

Replication of tcf4 through association and linkage studies in late-onset fuchs endothelial corneal dystrophy

by Li Y.-J., Minear M.A., Rimmler J., Zhao B., Balajonda E., Hauser M.A., Allingham R.R., Eghrari A.O., Riazuddin S.A., Katsanis N., Gottsch J.D., Gregory S.G., Klintworth G.K., Afshari N.A.
Published 2019

Characterization of the poly-t variant in the tomm40 gene in diverse populations

by Linnertz C., Saunders A.M., Lutz M.W., Crenshaw D.M., Grossman I., Burns D.K., Whitfield K.E., Hauser M.A., McCarthy J.J., Ulmer M., Allingham R., Welsh-Bohmer K.A., Roses A.D., Chiba-Falek O.
Published 2019

GALC deletions increase the risk of primary Open-Angle Glaucoma: The role of mendelian variants in complex disease

by Liu Y., Gibson J., Wheeler J., Kwee L.C., Santiago-Turla C.M., Akafo S.K., Lichter P.R., Gaasterland D.E., Moroi S.E., Challa P., Herndon L.W., Girkin C.A., Budenz D.L., Richards J.E., Allingham R.R., Hauser M.A.
Published 2019

A high-density genome-wide association screen of sporadic als in US veterans

by Kwee L.C., Liu Y., Haynes C., Gibson J.R., Stone A., Schichman S.A., Kamel F., Nelson L.M., Topol B., van Den Eeden S.K., Tanner C.M., Cudkowicz M.E., Grasso D.L., Lawson R., Muralidhar S., Oddone E.Z., Schmidt S., Hauser M.A.
Published 2019

Discovery and Functional Annotation of SIX6 Variants in Primary Open-Angle Glaucoma

by Ulmer Carnes M., Liu Y.P., Allingham R.R., Whigham B.T., Havens S., Garrett M.E., Qiao C., Katsanis N., Wiggs J.L., Pasquale L.R., Ashley-Koch A., Oh E.C., Hauser M.A., Brilliant M., Budenz D.L., Chin H.R., Cooke Bailey J., Fingert J., Friedman D.S., Gaasterland D., Gaasterland T., Haines J., Hauser M.A., Kang J.H., Lee R.K., Lichter P.R., Liu Y., Loomis S., McCarty C.E., Moroi S.E., Pasquale L.R., Pericak-Vance M., Realini A., Richards J.E., Schuman J.S., Scott W.K., Singh K., Sit A., Vollrath D., Weinreb R.N., Wiggs J.L., Wollstein G., Yaspan B.L., Zack D., Zhang K.
Published 2019

Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma

by Wiggs J.L., Yaspan B.L., Hauser M.A., Kang J.H., Allingham R.R., Olson L.M., Abdrabou W., Fan B.J., Wang D.Y., Brodeur W., Budenz D.L., Caprioli J., Crenshaw A., Crooks K., DelBono E., Doheny K.F., Friedman D.S., Gaasterland D., Gaasterland T., Laurie C., Lee R.K., Lichter P.R., Loomis S., Liu Y., Medeiros F.A., McCarty C., Mirel D., Moroi S.E., Musch D.C., Realini A., Rozsa F.W., Schuman J.S., Scott K., Singh K., Stein J.D., Trager E.H., VanVeldhuisen P., Vollrath D., Wollstein G., Yoneyama S., Zhang K., Weinreb R.N., Ernst J., Kellis M., Masuda T., Zack D., Richards J.E., Pericak-Vance M., Pasquale L.R., Haines J.L.
Published 2019

ABCC5, a Gene That Influences the Anterior Chamber Depth, Is Associated with Primary Angle Closure Glaucoma

by Nongpiur M.E., Khor C.C., Jia H., Cornes B.K., Chen L.-J., Qiao C., Nair K.S., Cheng C.-Y., Xu L., George R., Tan D., Abu-Amero K., Perera S.A., Ozaki M., Mizoguchi T., Kurimoto Y., Low S., Tajudin L.-S.A., Ho C.-L., Tham C.C.Y., Soto I., Chew P.T.K., Wong H.-T., Shantha B., Kuroda M., Osman E.A., Tang G., Fan S., Meng H., Wang H., Feng B., Yong V.H.K., Ting S.M.L., Li Y., Wang Y.-X., Li Z., Lavanya R., Wu R.-Y., Zheng Y.-F., Su D.H., Loon S.-C., Allingham R.R., Hauser M.A., Soumittra N., Ramprasad V.L., Waseem N., Yaakub A., Chia K.-S., Kumaramanickavel G., Wong T.T., How A.C., Chau T.N.B., Simmons C.P., Bei J.-X., Zeng Y.-X., Bhattacharya S.S., Zhang M., Tan D.T., Teo Y.-Y., Al-Obeidan S.A., Hon D.N., Tai E.-S., Saw S.-M., Foster P.J., Vijaya L., Jonas J.B., Wong T.-Y., John S.W.M., Pang C.-P., Vithana E.N., Wang N., Aung T.
Published 2018

Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma

by Vithana, E.N., Khor, C.-C., Qiao, C., Nongpiur, M.E., George, R., Chen, L.-J., Do, T., Abu-Amero, K., Huang, C.K., Low, S., Tajudin, L.-S.A., Perera, S.A., Cheng, C.-Y., Xu, L., Jia, H., Ho, C.-L., Sim, K.S., Wu, R.-Y., Tham, C.C.Y., Chew, P.T.K., Su, D.H., Oen, F.T., Sarangapani, S., Soumittra, N., Osman, E.A., Wong, H.-T., Tang, G., Fan, S., Meng, H., Huong, D.T.L., Wang, H., Feng, B., Baskaran, M., Shantha, B., Ramprasad, V.L., Kumaramanickavel, G., Iyengar, S.K., How, A.C., Lee, K.Y., Sivakumaran, T.A., Yong, V.H.K., Ting, S.M.L., Li, Y., Wang, Y.-X., Tay, W.-T., Sim, X., Lavanya, R., Cornes, B.K., Zheng, Y.-F., Wong, T.T., Loon, S.-C., Yong, V.K.Y., Waseem, N., Yaakub, A., Chia, K.-S., Rand Allingham, R., Hauser, M.A., Lam, D.S.C., Hibberd, M.L., Bhattacharya, S.S., Zhang, M., Teo, Y.Y., Tan, D.T., Jonas, J.B., Tai, E.-S., Saw, S.-M., Hon, D.N., Al-Obeidan, S.A., Liu, J., Chau, T.N.B., Simmons, C.P., Bei, J.-X., Zeng, Y.-X., Foster, P.J., Vijaya, L., Wong, T.-Y., Pang, C.-P., Wang, N., Aung, T.
Published 2014

Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology

by Springelkamp, Henriet, Mishra, Aniket, Hysi, Pirro G., Gharahkhani, Puyo, Hohn, Rene, Khor, Chiea Chuen, Cooke, Bailey Jessica N., Luo Xiaoyan, Ramdas, Wishal D., Vithana, Eranga Nishanthie, Koh, Victor, Yazar, Seyhan, Xu, Liang, Forward, H., Kearns, L.S., Amin, N., Iglesias, A.I., Sim, K.-S., van Leeuwen, E.M., Demirkan, A., van der Lee, S., Loon, Seng-Chee, Rivadeneira, F., Nag, A., Sanfilippo, P.G., Schillert, A., de Jong, P.T.V.M., Oostra, B.A., Uitterlinden, A.G., Hofman, A., Zhou, T., Burdon, K.P., Spector, T.D., Lackner, K.J., Saw, Seang-Mei, Vingerling, J.R., Teo,Yik-Ying, Pasquale L.R., Wolfs, R.C.W., Lemij, H.G., Tai, E.-Shyong, Jonas, J.B., Cheng, Ching-Yu, Aung, Tin, Jansonius, N.M., Klaver, C.C.W., Craig, J.E., Young, T.L., Haines, J.L., Macgregor, S., Mackey, D.A., Pfeiffer, N., Wong, Tien Yin, Wiggs, J.L., Hewitt, A.W., van Duijn, C.M., Hammond, C.J., Allingham, R.R., Brilliant, M.H., Budenz, D.L., Bailey, J.N.C., Christen, W.G., Fingert, J., Gaasterland, D., Gaasterland, T., Hauser, M.A., Kang, J.H., Kraft, P., Lee, R.K., Lichter, P.A., Liu, Y., Loomis, S.J., Moroi, S.E., Pericak-Vance, M.A., Realini, A., Richards, J.E., Schuman, J.S., Scott, W.K., Singh, K., Sit, A.J., Vollrath, D., Weinreb, R.N., Wollstein, G., Zack, D.J., Zhang, K.
Published 2016

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

by Lu, Y., Vitart, V., Burdon, K.P., Khor, C.C., Bykhovskaya, Y., Mirshahi, A., Hewitt, A.W., Koehn, D., Hysi, P.G., Ramdas, W.D., Zeller, T., Vithana, E.N., Cornes, B.K., Tay, W.-T., Tai, E.S., Cheng, C.-Y., Liu, J., Foo, J.-N., Saw, S.M., Thorleifsson, G., Stefansson, K., Dimasi, D.P., Mills, R.A., Mountain, J., Ang, W., Hoehn, R., Verhoeven, V.J.M., Grus, F., Wolfs, R., Castagne, R., Lackner, K.J., Springelkamp, H., Yang, J., Jonasson, F., Leung, D.Y.L., Chen, L.J., Tham, C.C.Y., Rudan, I., Vatavuk, Z., Hayward, C., Gibson, J., Cree, A.J., MacLeod, A., Ennis, S., Polasek, O., Campbell, H., Wilson, J.F., Viswanathan, A.C., Fleck, B., Li, X., Siscovick, D., Taylor, K.D., Rotter, J.I., Yazar, S., Ulmer, M., Li, J., Yaspan, B.L., Ozel, A.B., Richards, J.E., Moroi, S.E., Haines, J.L., Kang, J.H., Pasquale, L.R., Allingham, R.R., Ashley-Koch, A., Mitchell, P., Wang, J.J., Wright, A.F., Pennell, C., Spector, T.D., Young, T.L., Klaver, C.C.W., Martin, N.G., Montgomery, G.W., Anderson, M.G., Aung, T., Willoughby, C.E., Wiggs, J.L., Pang, C.P., Thorsteinsdottir, U., Lotery, A.J., Hammond, C.J., Van Duijn, C.M., Hauser, M.A., Rabinowitz, Y.S., Pfeiffer, N., MacKey, D.A., Craig, J.E., MacGregor, S., Wong, T.Y.
Published 2014

Erratum to: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (Nature Communications, (2018), 9, 1, (...

by Iglesias, A.I., Mishra, A., Vitart, V., Bykhovskaya, Y., Höhn, R., Springelkamp, H., Cuellar-Partida, G., Gharahkhani, P., Bailey, J.N.C., Willoughby, C.E., Li, X., Budenz, D.L., Christen, W.G., Fingert, J., Friedman, D.S., Gaasterland, D., Gaasterland, T., Hauser, M.A., Kraft, P., Lee, R.K., Lichter, P.R., Yazar, S., Liu, Y., Loomis, S.J., Moroi, S.E., Pericak-Vance, M.A., Realini, A., Richards, J.E., Schuman, J.S., Scott, W.K., Singh, K., Sit, A.J., Nag, A., Vollrath, D., Weinreb, R.N., Wollstein, G., Zack, D.J., Zhang, K., Uitterlinden, A.G., Vithana, E.N., Foster, P.J., Hysi, P.G., Hewitt, A.W., Khawaja, A.P., Khor, C.C., Pasquale, L.R., Montgomery, G.W., Klaver, C.C.W., Aung, T., Pfeiffer, N., Mackey, D.A., Hammond, C.J., Cheng, C.-Y., Craig, J.E., Polašek, O., Rabinowitz, Y.S., Wiggs, J.L., Burdon, K.P., van Duijn, C.M., MacGregor, S., Siscovick, D., Mitchell, P., Tham, Y.C., Haines, J.L., Kearns, L.S., Hayward, C., Shi, Y., van Leeuwen, E.M., Taylor, K.D., Wang, J.J., Rochtchina, E., Attia, J., Scott, R., Holliday, E.G., Wong, T.Y., Baird, P.N., Xie, J., Inouye, M., Viswanathan, A., Sim, X., Bonnemaijer, P., Rotter, J.I., Martin, N.G., Zeller, T., Mills, R.A., Souzeau, E., Staffieri, S.E., Jonas, J.B., Schmidtmann, I., Boutin, T., Kang, J.H., Lucas, S.E.M., Beutel, M.E., Wilson, J.F., Donnelly, P., Barroso, I., Blackwell, J.M., Bramon, E., Brown, M.A., Casas, J.P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H.S., Mathew, C.G., Palmer, C.N.A., Plomin, R., Rautanen, A., Sawcer, S.J., Trembath, R.C., Wood, N.W., Spencer, C.C.A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Langford, C., Hunt, S.E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S.J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., McCann, O.T., Liddle, J., Potter, S.C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Allingham, R.R., Brilliant, M.H.
Published 2022