8q24 clear cell renal cell carcinoma germline variant is associated with VHL mutation status and clinical aggressiveness

por Eckel-Passow, Jeanette E., Yan, Huihuang, Kosel, Matthew L., Serie, Daniel, Decker, Paul A., Jenkins, Robert B., Costello, Brian, Leibovich, Bradley, Ho, Thai H., Parker, Alexander
Publicado 2020

Variants in PPP2R2B and IGF2BP3 are associated with higher tau deposition

por Ramanan, Vijay K, Wang, Xuewei, Przybelski, Scott A, Raghavan, Sheelakumari, Heckman, Michael G, Batzler, Anthony, Kosel, Matthew L, Hohman, Timothy J, Knopman, David S, Graff-Radford, Jonathan, Lowe, Val J, Mielke, Michelle M, Jack, Clifford R, Petersen, Ronald C, Ross, Owen A, Vemuri, Prashanthi
Publicado 2020

Risk of Ovarian Cancer and Inherited Variants in Relapse-Associated Genes

por Peedicayil, Abraham, Vierkant, Robert A., Hartmann, Lynn C., Fridley, Brooke L., Fredericksen, Zachary S., White, Kristin L., Elliott, Elaine A., Phelan, Catherine M., Tsai, Ya-Yu, Berchuck, Andrew, Iversen, Edwin S., Couch, Fergus J., Peethamabaran, Prema, Larson, Melissa C., Kalli, Kimberly R., Kosel, Matthew L., Shridhar, Vijayalakshmi, Rider, David N., Liebow, Mark, Cunningham, Julie M., Schildkraut, Joellen M., Sellers, Thomas A., Goode, Ellen L.
Publicado 2010

Variants in the CDKN2B and RTEL1 regions are associated with high grade glioma susceptibility

por Wrensch, Margaret, Jenkins, Robert B., Chang, Jeffrey S., Yeh, Ru-Fang, Xiao, Yuanyuan, Ballman, Karla V., Berger, Mitchel, Buckner, Jan C., Chang, Susan, Decker, Paul A., Giannini, Caterina, Halder, Chandralekha, Kollmeyer, Thomas M., Kosel, Matthew L., LaChance, Daniel H., McCoy, Lucie, O’Neill, Brian, Patoka, Joe, Pico, Alexander R., Prados, Michael, Quesenberry, Charles, Rice, Terri, Rynearson, Amanda, Smirnov, Ivan, Tihan, Tarik, Wiemels, Joe, Yang, Ping, Wiencke, John K.
Publicado 2009

Inherited variation in immune genes and pathways and glioblastoma risk

por Schwartzbaum, Judith A., Xiao, Yuanyuan, Liu, Yanhong, Tsavachidis, Spyros, Berger, Mitchel S., Bondy, Melissa L., Chang, Jeffrey S., Chang, Susan M., Decker, Paul A., Ding, Bo, Hepworth, Sarah J., Houlston, Richard S., Hosking, Fay J., Jenkins, Robert B., Kosel, Matthew L., McCoy, Lucie S., McKinney, Patricia A., Muir, Kenneth, Patoka, Joe S., Prados, Michael, Rice, Terri, Robertson, Lindsay B., Schoemaker, Minouk J., Shete, Sanjay, Swerdlow, Anthony J., Wiemels, Joe L., Wiencke, John K., Yang, Ping, Wrensch, Margaret R.
Publicado 2010

Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk

por Walsh, Kyle M., Codd, Veryan, Smirnov, Ivan V., Rice, Terri, Decker, Paul A., Hansen, Helen M., Kollmeyer, Thomas, Kosel, Matthew L., Molinaro, Annette M., McCoy, Lucie S., Bracci, Paige M., Cabriga, Belinda S., Pekmezci, Melike, Zheng, Shichun, Wiemels, Joseph L., Pico, Alexander R., Tihan, Tarik, Berger, Mitchell S., Chang, Susan M., Prados, Michael D., Lachance, Daniel H., O’Neill, Brian P., Sicotte, Hugues, Eckel-Passow, Jeanette E., van der Harst, Pim, Wiencke, John K., Samani, Nilesh J., Jenkins, Robert B., Wrensch, Margaret R.
Publicado 2014

Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation

por Adlam, David, Berrandou, Takiy-Eddine, Georges, Adrien, Nelson, Christopher P., Giannoulatou, Eleni, Henry, Joséphine, Ma, Lijiang, Blencowe, Montgomery, Turley, Tamiel N., Yang, Min-Lee, Chopade, Sandesh, Finan, Chris, Braund, Peter S., Sadeg-Sayoud, Ines, Iismaa, Siiri E., Kosel, Matthew L., Zhou, Xiang, Hamby, Stephen E., Cheng, Jenny, Liu, Lu, Tarr, Ingrid, Muller, David W. M., d’Escamard, Valentina, King, Annette, Brunham, Liam R., Baranowska-Clarke, Ania A., Debette, Stéphanie, Amouyel, Philippe, Olin, Jeffrey W., Patil, Snehal, Hesselson, Stephanie E., Junday, Keerat, Kanoni, Stavroula, Aragam, Krishna G., Butterworth, Adam S., Tweet, Marysia S., Gulati, Rajiv, Combaret, Nicolas, Kadian-Dodov, Daniella, Kalman, Jonathan M., Fatkin, Diane, Hingorani, Aroon D., Saw, Jacqueline, Webb, Tom R., Hayes, Sharonne N., Yang, Xia, Ganesh, Santhi K., Olson, Timothy M., Kovacic, Jason C., Graham, Robert M., Samani, Nilesh J., Bouatia-Naji, Nabila
Publicado 2023

Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study

por Hu, Yao, Graff, Mariaelisa, Haessler, Jeffrey, Buyske, Steven, Bien, Stephanie A., Tao, Ran, Highland, Heather M., Nishimura, Katherine K., Zubair, Niha, Lu, Yingchang, Verbanck, Marie, Hilliard, Austin T., Klarin, Derek, Damrauer, Scott M., Ho, Yuk-Lam, Wilson, Peter W. F., Chang, Kyong-Mi, Tsao, Philip S., Cho, Kelly, O’Donnell, Christopher J., Assimes, Themistocles L., Petty, Lauren E., Below, Jennifer E., Dikilitas, Ozan, Schaid, Daniel J., Kosel, Matthew L., Kullo, Iftikhar J., Rasmussen-Torvik, Laura J., Jarvik, Gail P., Feng, Qiping, Wei, Wei-Qi, Larson, Eric B., Mentch, Frank D., Almoguera, Berta, Sleiman, Patrick M., Raffield, Laura M., Correa, Adolfo, Martin, Lisa W., Daviglus, Martha, Matise, Tara C., Ambite, Jose Luis, Carlson, Christopher S., Do, Ron, Loos, Ruth J. F., Wilkens, Lynne R., Le Marchand, Loic, Haiman, Chris, Stram, Daniel O., Hindorff, Lucia A., North, Kari E., Kooperberg, Charles, Cheng, Iona, Peters, Ulrike
Publicado 2020