GSTM1 null and NAT2 slow acetylation genotypes, smoking intensity and bladder cancer risk: results from the New England bladder cancer study and NAT2 meta-analysis

Por Moore, L.E., Baris, D.R., Figueroa, J.D., Garcia-Closas, M., Karagas, M.R., Schwenn, M.R., Johnson, A.T., Lubin, J.H., Hein, D.W., Dagnall, C.L., Colt, J.S., Kida, M., Jones, M.A., Schned, A.R., Cherala, S.S., Chanock, S.J., Cantor, K.P., Silverman, D.T., Rothman, N.
Publicado em 2011

A new statistic and its power to infer membership and phenotype in a genome-wide association study using genotype frequencies

Por Jacobs, Kevin B., Yeager, Meredith, Wacholder, Sholom, Craig, David, Kraft, Peter, Hunter, David J., Paschal, Justin, Manolio, Teri A., Tucker, Margaret, Hoover, Robert N., Thomas, Gilles D., Chanock, Stephen J., Chatterjee, Nilanjan
Publicado em 2009

Association between the gut microbiome and atherosclerosis

Por Barrington, William T., Lusis, Aldons J.
Publicado no Nat Rev Cardiol (2017)

Comparative analysis of ear-hole closure identifies epimorphic regeneration as a discrete trait in mammals

Por Gawriluk, Thomas R., Simkin, Jennifer, Thompson, Katherine L., Biswas, Shishir K., Clare-Salzler, Zak, Kimani, John M., Kiama, Stephen G., Smith, Jeramiah J., Ezenwa, Vanessa O., Seifert, Ashley W.
Publicado no Nat Commun (2016)

Application and analysis of debris-flow early warning system in Wenchuan earthquake-affected area

Por D. L. Liu, S. J. Zhang, H. J. Yang, L. Q. Zhao, Y. H. Jiang, D. Tang, X. P. Leng
Publicado em 2016-02-01

Evaluation of the Procleix Ultrio Plus ID NAT assay for detection of HIV 1, HBV and HCV in blood donors

Por Makroo, Raj Nath, Chowdhry, Mohit, Bhatia, Aakanksha, Antony, Minimol
Publicado no Asian J Transfus Sci (2015)

Homological scaffolds of brain functional networks

Por Petri, G., Expert, P., Turkheimer, F., Carhart-Harris, R., Nutt, D., Hellyer, P. J., Vaccarino, F.
Publicado no J R Soc Interface (2014)

Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer

Por Lesseur, Corina, Diergaarde, Brenda, Olshan, Andrew F, Wünsch-Filho, Victor, Ness, Andrew R, Liu, Geoffrey, Lacko, Martin, Eluf-Neto, José, Franceschi, Silvia, Lagiou, Pagona, Macfarlane, Gary J, Richiardi, Lorenzo, Boccia, Stefania, Polesel, Jerry, Kjaerheim, Kristina, Zaridze, David, Johansson, Mattias, Menezes, Ana M, Curado, Maria Paula, Robinson, Max, Ahrens, Wolfgang, Canova, Cristina, Znaor, Ariana, Castellsagué, Xavier, Conway, David I, Holcátová, Ivana, Mates, Dana, Vilensky, Marta, Healy, Claire M, Szeszenia-Dąbrowska, Neonila, Fabiánová, Eleonóra, Lissowska, Jolanta, Grandis, Jennifer R, Weissler, Mark C, Tajara, Eloiza H, Nunes, Fabio D, de Carvalho, Marcos B, Thomas, Steve, Hung, Rayjean J, Peters, Wilbert H M, Herrero, Rolando, Cadoni, Gabriella, Bueno-de-Mesquita, H Bas, Steffen, Annika, Agudo, Antonio, Shangina, Oxana, Xiao, Xiangjun, Gaborieau, Valérie, Chabrier, Amélie, Anantharaman, Devasena, Boffetta, Paolo, Amos, Christopher I, McKay, James D, Brennan, Paul
Publicado no Nat Genet (2016)

Comparative analysis of detecting cervical lymph node metastasis with fine needle aspiration cytology

Por Shakeel, Mohammed Kamran, Daniel, Mariappan Jonathan, Srinivasan, Subramaniam Vasudevan, Koliyan, Ramadoss, Kumar, Jimsha Vannathan
Publicado no J Nat Sci Biol Med (2015)

A novel, primate-specific, brain isoform of KCNH2 impacts cortical physiology, cognition, neuronal repolarization and risk for schizophrenia

Por Huffaker, Stephen J., Chen, Jingshan, Nicodemus, Kristin K., Sambataro, Fabio, Yang, Feng, Mattay, Venkata, Lipska, Barbara K., Hyde, Thomas M., Song, Jian, Rujescu, Daniel, Giegling, Ina, Mayilyan, Karine, Proust, Morgan J., Soghoyan, Armen, Caforio, Grazia, Callicott, Joseph H., Bertolino, Alessandro, Meyer-Lindenberg, Andreas, Chang, Jay, Ji, Yuanyuan, Egan, Michael F., Goldberg, Terry E., Kleinman, Joel E., Lu, Bai, Weinberger, Daniel R.
Publicado em 2009

Comparative study of frequency of micronuclei in normal, potentially malignant diseases and oral squamous cell carcinoma

Por Sangle, Varsha Ajit, Bijjaragi, Shobha, Shah, Nishat, Kangane, Suresh, Ghule, Hrishikesh M., Rani, SR Ashwini
Publicado no J Nat Sci Biol Med (2016)

Hair Dye Use and Risk of Bladder Cancer in the New England Bladder Cancer Study

Por Koutros, Stella, Silverman, Debra T., Baris, Dalsu, Zahm, Shelia Hoar, Morton, Lindsay M., Colt, Joanne S., Hein, David W., Moore, Lee E., Johnson, Alison, Schwenn, Molly, Cherala, Sai, Schned, Alan, Doll, Mark A., Rothman, Nathaniel, Karagas, Margaret R.
Publicado em 2011

Case-Control Studies of Gene-Environment Interaction: Bayesian Design and Analysis

Por Mukherjee, Bhramar, Ahn, Jaeil, Gruber, Stephen B., Ghosh, Malay, Chatterjee, Nilanjan
Publicado em 2010

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

Por Springelkamp, Henriët., Höhn, René, Mishra, Aniket, Hysi, Pirro G., Khor, Chiea-Chuen, Loomis, Stephanie J., Bailey, Jessica N. Cooke, Gibson, Jane, Thorleifsson, Gudmar, Janssen, Sarah F., Luo, Xiaoyan, Ramdas, Wishal D., Vithana, Eranga, Nongpiur, Monisha E., Montgomery, Grant W., Xu, Liang, Mountain, Jenny E., Gharahkhani, Puya, Lu, Yi, Amin, Najaf, Karssen, Lennart C., Sim, Kar-Seng, van Leeuwen, Elisabeth M., Iglesias, Adriana I., Verhoeven, Virginie J. M., Hauser, Michael A., Loon, Seng-Chee, Despriet, Dominiek D. G., Nag, Abhishek, Venturini, Cristina, Sanfilippo, Paul G., Schillert, Arne, Kang, Jae H., Landers, John, Jonasson, Fridbert, Cree, Angela J., van Koolwijk, Leonieke M. E., Rivadeneira, Fernando, Souzeau, Emmanuelle, Jonsson, Vesteinn, Menon, Geeta, Weinreb, Robert N., de Jong, Paulus T. V. M., Oostra, Ben A., Uitterlinden, André G., Hofman, Albert, Ennis, Sarah, Thorsteinsdottir, Unnur, Burdon, Kathryn P., Spector, Timothy D., Mirshahi, Alireza, Saw, Seang-Mei, Vingerling, Johannes R., Teo, Yik-Ying, Haines, Jonathan L., Wolfs, Roger C. W., Lemij, Hans G., Tai, E-Shyong, Jansonius, Nomdo M., Jonas, Jost B., Cheng, Ching-Yu, Aung, Tin, Viswanathan, Ananth C., Klaver, Caroline C. W., Craig, Jamie E., Macgregor, Stuart, Mackey, David A., Lotery, Andrew J., Stefansson, Kari, Bergen, Arthur A. B., Young, Terri L., Wiggs, Janey L., Pfeiffer, Norbert, Wong, Tien-Yin, Pasquale, Louis R., Hewitt, Alex W., van Duijn, Cornelia M., Hammond, Christopher J.
Publicado em 2014

Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance

Por Patel, Kashyap A., Kettunen, Jarno, Laakso, Markku, Stančáková, Alena, Laver, Thomas W., Colclough, Kevin, Johnson, Matthew B., Abramowicz, Marc, Groop, Leif, Miettinen, Päivi J., Shepherd, Maggie H., Flanagan, Sarah E., Ellard, Sian, Inagaki, Nobuya, Hattersley, Andrew T., Tuomi, Tiinamaija, Cnop, Miriam, Weedon, Michael N.
Publicado no Nat Commun (2017)

Incidental finding of two rare developmental anomalies: Fusion and dilaceration: A case report and literature review

Por Sultan, Nishat
Publicado no J Nat Sci Biol Med (2015)

Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis

Por Zengini, Eleni, Hatzikotoulas, Konstantinos, Tachmazidou, Ioanna, Steinberg, Julia, Hartwig, Fernando P., Southam, Lorraine, Hackinger, Sophie, Boer, Cindy G., Styrkarsdottir, Unnur, Gilly, Arthur, Suveges, Daniel, Killian, Britt, Ingvarsson, Thorvaldur, Jonsson, Helgi, Babis, George C., McCaskie, Andrew, Uitterlinden, Andre G., van Meurs, Joyce B. J., Thorsteinsdottir, Unnur, Stefansson, Kari, Smith, George Davey, Wilkinson, Jeremy M., Zeggini, Eleftheria
Publicado no Nat Genet (2018)

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

Por Capasso, Mario, Devoto, Marcella, Hou, Cuiping, Asgharzadeh, Shahab, Glessner, Joseph T., Attiyeh, Edward F., Mosse, Yael P., Kim, Cecilia, Diskin, Sharon J., Cole, Kristina A., Bosse, Kristopher, Diamond, Maura, Laudenslager, Marci, Winter, Cynthia, Bradfield, Jonathan P., Scott, Richard H., Jagannathan, Jayanti, Garris, Maria, McConville, Carmel, London, Wendy B., Seeger, Robert C., Grant, Struan F. A., Li, Hongzhe, Rahman, Nazneen, Rappaport, Eric, Hakonarson, Hakon, Maris, John M.
Publicado em 2009

Exploring the genetic architecture of inflammatory bowel disease by whole genome sequencing identifies association at ADCY7

Por Luo, Yang, de Lange, Katrina M., Jostins, Luke, Moutsianas, Loukas, Randall, Joshua, Kennedy, Nicholas A., Lamb, Christopher A., McCarthy, Shane, Ahmad, Tariq, Edwards, Cathryn, Serra, Eva Goncalves, Hart, Ailsa, Hawkey, Chris, Mansfield, John C., Mowat, Craig, Newman, William G., Nichols, Sam, Pollard, Martin, Satsangi, Jack, Simmons, Alison, Tremelling, Mark, Uhlig, Holm, Wilson, David C., Lee, James C., Prescott, Natalie J., Lees, Charlie W., Mathew, Christopher G., Parkes, Miles, Barrett, Jeffrey C., Anderson, Carl A.
Publicado no Nat Genet (2017)

The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions

Por Bolouri, Hamid, Farrar, Jason E, Triche, Timothy, Ries, Rhonda E, Lim, Emilia L, Alonzo, Todd A, Ma, Yussanne, Moore, Richard, Mungall, Andrew J, Marra, Marco A, Zhang, Jinghui, Ma, Xiaotu, Liu, Yu, Liu, Yanling, Auvil, Jaime M Guidry, Davidsen, Tanja M, Gesuwan, Patee, Hermida, Leandro C, Salhia, Bodour, Capone, Stephen, Ramsingh, Giridharan, Zwaan, Christian Michel, Noort, Sanne, Piccolo, Stephen R, Kolb, E Anders, Gamis, Alan S, Smith, Malcolm A, Gerhard, Daniela S, Meshinchi, Soheil
Publicado no Nat Med (2017)