Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes

door Hutcheson, Holli B, Olson, Lana M, Bradford, Yuki, Folstein, Susan E, Santangelo, Susan L, Sutcliffe, James S, Haines, Jonathan L
Gepubliceerd in 2004

Localization of age-related macular degeneration-associated ARMS2 in cytosol, not mitochondria

door Wang, Gaofeng, Spencer, Kylee L., Court, Brenda L., Olson, Lana M., Scott, William K., Haines, Jonathan L., Pericak-Vance, Margaret A.
Gepubliceerd in 2009

Screening for UGT1A1 Genotype in Study A5257 Would Have Markedly Reduced Premature Discontinuation of Atazanavir for Hyperbilirubinemia

door Vardhanabhuti, Saran, Ribaudo, Heather J., Landovitz, Raphael J., Ofotokun, Ighovwerha, Lennox, Jeffrey L., Currier, Judith S., Olson, Lana M., Haas, David W.
Gepubliceerd in Open Forum Infect Dis (2015)

Mapping of the Disease Locus and Identification of ADAMTS10 As a Candidate Gene in a Canine Model of Primary Open Angle Glaucoma

door Kuchtey, John, Olson, Lana M., Rinkoski, Tommy, MacKay, Edward O., Iverson, T. M., Gelatt, Kirk N., Haines, Jonathan L., Kuchtey, Rachel W.
Gepubliceerd in 2011

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

door McCauley, Jacob L, Li, Chun, Jiang, Lan, Olson, Lana M, Crockett, Genea, Gainer, Kimberly, Folstein, Susan E, Haines, Jonathan L, Sutcliffe, James S
Gepubliceerd in 2005

C3 R102G polymorphism increases risk of age-related macular degeneration

door Spencer, Kylee L., Olson, Lana M., Anderson, Brent M., Schnetz-Boutaud, Nathalie, Scott, William K., Gallins, Paul, Agarwal, Anita, Postel, Eric A., Pericak-Vance, Margaret A., Haines, Jonathan L.
Gepubliceerd in 2008

Feasibility of High-Throughput Genome-Wide Genotyping using DNA from Stored Buccal Cell Samples

door Loomis, Stephanie J., Olson, Lana M., Pasquale, Louis R., Wiggs, Janey, Mirel, Daniel, Crenshaw, Andrew, Parkin, Melissa, Rahhal, Brandon, Tetreault, Stephanie, Kraft, Peter, Tworoger, Shelley S., Haines, Jonathan L., Kang, Jae H.
Gepubliceerd in 2010

Mitochondrial DNA Polymorphism A4917G Is Independently Associated with Age-Related Macular Degeneration

door Canter, Jeffrey A., Olson, Lana M., Spencer, Kylee, Schnetz-Boutaud, Nathalie, Anderson, Brent, Hauser, Michael A., Schmidt, Silke, Postel, Eric A., Agarwal, Anita, Pericak-Vance, Margaret A., Sternberg, Paul, Haines, Jonathan L.
Gepubliceerd in 2008

Dissection of Chromosome 16p12 Linkage Peak Suggests a Possible Role for CACNG3 Variants in Age-Related Macular Degeneration Susceptibility

door 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.
Gepubliceerd in 2011

Using Genetic Variation and Environmental Risk Factor Data to Identify Individuals at High Risk for Age-Related Macular Degeneration

door Spencer, Kylee L., Olson, Lana M., Schnetz-Boutaud, Nathalie, Gallins, Paul, Agarwal, Anita, Iannaccone, Alessandro, Kritchevsky, Stephen B., Garcia, Melissa, Nalls, Michael A., Newman, Anne B., Scott, William K., Pericak-Vance, Margaret A., Haines, Jonathan L.
Gepubliceerd in 2011

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA

door Wiggs, Janey L., Hee Kang, Jae, Yaspan, Brian L., Mirel, Daniel B., Laurie, Cathy, Crenshaw, Andrew, Brodeur, Wendy, Gogarten, Stephanie, Olson, Lana M., Abdrabou, Wael, DelBono, Elizabeth, Loomis, Stephanie, Haines, Jonathan L., Pasquale, Louis R.
Gepubliceerd in 2011

Mechanistic Phenotypes: An Aggregative Phenotyping Strategy to Identify Disease Mechanisms Using GWAS Data

door Mosley, Jonathan D., Van Driest, Sara L., Larkin, Emma K., Weeke, Peter E., Witte, John S., Wells, Quinn S., Karnes, Jason H., Guo, Yan, Bastarache, Lisa, Olson, Lana M., McCarty, Catherine A., Pacheco, Jennifer A., Jarvik, Gail P., Carrell, David S., Larson, Eric B., Crosslin, David R., Kullo, Iftikhar J., Tromp, Gerard, Kuivaniemi, Helena, Carey, David J., Ritchie, Marylyn D., Denny, Josh C., Roden, Dan M.
Gepubliceerd in 2013

Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy

door Van Driest, Sara L., McGregor, Tracy L., Velez Edwards, Digna R., Saville, Ben R., Kitchner, Terrie E., Hebbring, Scott J., Brilliant, Murray, Jouni, Hayan, Kullo, Iftikhar J., Creech, C. Buddy, Kannankeril, Prince J., Vear, Susan I., Brothers, Kyle B., Bowton, Erica A., Shaffer, Christian M., Patel, Neelam, Delaney, Jessica T., Bradford, Yuki, Wilson, Sarah, Olson, Lana M., Crawford, Dana C., Potts, Amy L., Ho, Richard H., Roden, Dan M., Denny, Josh C.
Gepubliceerd in PLoS One (2015)

Rare Variants in RTEL1 Are Associated with Familial Interstitial Pneumonia

door Cogan, Joy D., Kropski, Jonathan A., Zhao, Min, Mitchell, Daphne B., Rives, Lynette, Markin, Cheryl, Garnett, Errine T., Montgomery, Keri H., Mason, Wendi R., McKean, David F., Powers, Julia, Murphy, Elissa, Olson, Lana M., Choi, Leena, Cheng, Dong-Sheng, Blue, Elizabeth Marchani, Young, Lisa R., Lancaster, Lisa H., Steele, Mark P., Brown, Kevin K., Schwarz, Marvin I., Fingerlin, Tasha E., Schwartz, David A., Lawson, William E., Loyd, James E., Zhao, Zhongming, Phillips, John A., Blackwell, Timothy S.
Gepubliceerd in Am J Respir Crit Care Med (2015)

Pitfalls of Merging GWAS Data: Lessons Learned in the eMERGE Network and Quality Control Procedures to Maintain High Data Quality

door Zuvich, Rebecca L., Armstrong, Loren L., Bielinski, Suzette J., Bradford, Yuki, Carlson, Christopher S., Crawford, Dana C., Crenshaw, Andrew T., de Andrade, Mariza, Doheny, Kimberly F., Haines, Jonathan L., Hayes, M. Geoffrey, Jarvik, Gail P., Jiang, Lan, Kullo, Iftikhar J., Li, Rongling, Ling, Hua, Manolio, Teri A., Matsumoto, Martha E., McCarty, Catherine A., McDavid, Andrew N., Mirel, Daniel B., Olson, Lana M., Paschall, Justin E., Pugh, Elizabeth W., Rasmussen, Luke V., Rasmussen-Torvik, Laura J., Turner, Stephen D., Wilke, Russell A., Ritchie, Marylyn D.
Gepubliceerd in 2011

The NEIGHBOR Consortium Primary Open Angle Glaucoma Genome-wide Association Study: Rationale, Study design and Clinical variables

door Wiggs, Janey L, Hauser, Michael A, Abdrabou, Wael, Allingham, R Rand, Budenz, Donald L, DelBono, Elizabeth, Friedman, David S, Kang, Jae H, Gaasterland, Douglas, Gaasterland, Terry, Lee, Richard K, Lichter, Paul R, Loomis, Stephanie, Liu, Yutao, McCarty, Cathy, Medeiros, Felipe A, Moroi, Sayoko E, Olson, Lana M, Realini, Anthony, Richards, Julia E, Rozsa, Frank W, Schuman, Joel S, Singh, Kuldev, Stein, Joshua D, Vollrath, Douglas, Weinreb, Robert N, Wollstein, Gadi, Yaspan, Brian L, Yoneyama, Sachiko, Zack, Don, Zhang, Kang, Pericak-Vance, Margaret, Pasquale, Louis R, Haines, Jonathan L
Gepubliceerd in 2013

CDKN2B-AS1 Genotype – Glaucoma Feature Correlations in Primary Open-Angle Glaucoma Patients from the United States

door Pasquale, Louis R., Loomis, Stephanie J., Kang, Jae H., Yaspan, Brian L., Abdrabou, Wael, Budenz, Donald L., Chen, Teresa C., DelBono, Elizabeth, Friedman, David S., Gaasterland, Douglas, Gaasterland, Terry, Grosskreutz, Cynthia L., Lee, Richard K., Lichter, Paul R., Liu, Yutao, McCarty, Catherine A., Moroi, Sayoko E., Olson, Lana M., Realini, Tony, Rhee, Douglas J., Schuman, Joel S., Singh, Kuldev, Vollrath, Douglas, Wollstein, Gadi, Zack, Donald J., Allingham, R. Rand, Pericak-Vance, Margaret A., Weinreb, Robert N., Zhang, Kang, Hauser, Michael A., Richards, Julia E., Haines, Jonathan L., Wiggs, Janey L.
Gepubliceerd in 2012

Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma

door Wiggs, Janey L., Yaspan, Brian L., Hauser, Michael A., Kang, Jae H., Allingham, R. Rand, Olson, Lana M., Abdrabou, Wael, Fan, Bao J., Wang, Dan Y., Brodeur, Wendy, Budenz, Donald L., Caprioli, Joseph, Crenshaw, Andrew, Crooks, Kristy, DelBono, Elizabeth, Doheny, Kimberly F., Friedman, David S., Gaasterland, Douglas, Gaasterland, Terry, Laurie, Cathy, Lee, Richard K., Lichter, Paul R., Loomis, Stephanie, Liu, Yutao, Medeiros, Felipe A., McCarty, Cathy, Mirel, Daniel, Moroi, Sayoko E., Musch, David C., Realini, Anthony, Rozsa, Frank W., Schuman, Joel S., Scott, Kathleen, Singh, Kuldev, Stein, Joshua D., Trager, Edward H., VanVeldhuisen, Paul, Vollrath, Douglas, Wollstein, Gadi, Yoneyama, Sachiko, Zhang, Kang, Weinreb, Robert N., Ernst, Jason, Kellis, Manolis, Masuda, Tomohiro, Zack, Don, Richards, Julia E., Pericak-Vance, Margaret, Pasquale, Louis R., Haines, Jonathan L.
Gepubliceerd in 2012

Identification of a Rare Coding Variant in Complement 3 Associated with Age-related Macular Degeneration

door Zhan, Xiaowei, Larson, David E., Wang, Chaolong, Koboldt, Daniel C., Sergeev, Yuri V., Fulton, Robert S., Fulton, Lucinda L., Fronick, Catrina C., Branham, Kari E., Bragg-Gresham, Jennifer, Jun, Goo, Hu, Youna, Kang, Hyun Min, Liu, Dajiang, Othman, Mohammad, Brooks, Matthew, Ratnapriya, Rinki, Boleda, Alexis, Grassmann, Felix, von Strachwitz, Claudia, Olson, Lana M., Buitendijk, Gabriëlle H.S., Hofman, Albert, van Duijn, Cornelia M., Cipriani, Valentina, Moore, Anthony T., Shahid, Humma, Jiang, Yingda, Conley, Yvette P., Morgan, Denise J., Kim, Ivana K., Johnson, Matthew P., Cantsilieris, Stuart, Richardson, Andrea J., Guymer, Robyn H., Luo, Hongrong, Ouyang, Hong, Licht, Christoph, Pluthero, Fred G., Zhang, Mindy M., Zhang, Kang, Baird, Paul N., Blangero, John, Klein, Michael L., Farrer, Lindsay A., DeAngelis, Margaret M., Weeks, Daniel E., Gorin, Michael B., Yates, John R.W., Klaver, Caroline C.W., Pericak-Vance, Margaret A., Haines, Jonathan L., Weber, Bernhard H.F., Wilson, Richard K., Heckenlively, John R., Chew, Emily Y., Stambolian, Dwight, Mardis, Elaine R., Swaroop, Anand, Abecasis, Goncalo R.
Gepubliceerd in 2013

Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration

door Ratnapriya, Rinki, Zhan, Xiaowei, Fariss, Robert N., Branham, Kari E., Zipprer, David, Chakarova, Christina F., Sergeev, Yuri V., Campos, Maria M., Othman, Mohammad, Friedman, James S., Maminishkis, Arvydas, Waseem, Naushin H., Brooks, Matthew, Rajasimha, Harsha K., Edwards, Albert O., Lotery, Andrew, Klein, Barbara E., Truitt, Barbara J., Li, Bingshan, Schaumberg, Debra A., Morgan, Denise J., Morrison, Margaux A., Souied, Eric, Tsironi, Evangelia E., Grassmann, Felix, Fishman, Gerald A., Silvestri, Giuliana, Scholl, Hendrik P.N., Kim, Ivana K., Ramke, Jacqueline, Tuo, Jingsheng, Merriam, Joanna E., Merriam, John C., Park, Kyu Hyung, Olson, Lana M., Farrer, Lindsay A., Johnson, Matthew P., Peachey, Neal S., Lathrop, Mark, Baron, Robert V., Igo, Robert P., Klein, Ronald, Hagstrom, Stephanie A., Kamatani, Yoichiro, Martin, Tammy M., Jiang, Yingda, Conley, Yvette, Sahel, Jose-Alan, Zack, Donald J., Chan, Chi-Chao, Pericak-Vance, Margaret A., Jacobson, Samuel G., Gorin, Michael B., Klein, Michael L., Allikmets, Rando, Iyengar, Sudha K., Weber, Bernhard H., Haines, Jonathan L., Léveillard, Thierry, Deangelis, Margaret M., Stambolian, Dwight, Weeks, Daniel E., Bhattacharya, Shomi S., Chew, Emily Y., Heckenlively, John R., Abecasis, Gonçalo R., Swaroop, Anand
Gepubliceerd in 2014