Parkinson-associated risk variant in enhancer element produces subtle effect on target gene expression

Por Soldner, Frank, Stelzer, Yonatan, Shivalila, Chikdu S., Abraham, Brian J., Latourelle, Jeanne C., Barrasa, M. Inmaculada, Goldmann, Johanna, Myers, Richard H., Young, Richard A., Jaenisch, Rudolf
Publicado no Nature (2016)

Association mapping in sunflower (Helianthus annuus L.) reveals independent control of apical vs. basal branching

Por Nambeesan, Savithri U, Mandel, Jennifer R, Bowers, John E, Marek, Laura F, Ebert, Daniel, Corbi, Jonathan, Rieseberg, Loren H, Knapp, Steven J, Burke, John M
Publicado no BMC Plant Biol (2015)

Genetic Contributors to Variation in Alcohol Consumption Vary by Race/Ethnicity in a Large Multi-Ethnic Genome-wide Association Study

Por Jorgenson, Eric, Thai, Khanh K., Hoffmann, Thomas J., Sakoda, Lori C., Kvale, Mark N., Banda, Yambazi, Schaefer, Catherine, Risch, Neil, Mertens, Jennifer, Weisner, Constance, Choquet, Hélène
Publicado no Mol Psychiatry (2017)

metaCCA: summary statistics-based multivariate meta-analysis of genome-wide association studies using canonical correlation analysis

Por Cichonska, Anna, Rousu, Juho, Marttinen, Pekka, Kangas, Antti J., Soininen, Pasi, Lehtimäki, Terho, Raitakari, Olli T., Järvelin, Marjo-Riitta, Salomaa, Veikko, Ala-Korpela, Mika, Ripatti, Samuli, Pirinen, Matti
Publicado no Bioinformatics (2016)

Genome-Wide Associations of Gene Expression Variation in Humans

Por Stranger, Barbara E, Forrest, Matthew S, Clark, Andrew G, Minichiello, Mark J, Deutsch, Samuel, Lyle, Robert, Hunt, Sarah, Kahl, Brenda, Antonarakis, Stylianos E, Tavaré, Simon, Deloukas, Panagiotis, Dermitzakis, Emmanouil T
Publicado em 2005

Genome-wide Epigenetic Data Facilitate Understanding of Disease Susceptibility Association Studies

Por Hardison, Ross C.
Publicado em 2012

Genome-wide search for higher order epistasis as modifiers of treatment effects on bone mineral density in childhood cancer survivors

Por Im, Cindy, Ness, Kirsten K., Kaste, Sue C., Chemaitilly, Wassim, Moon, Wonjong, Sapkota, Yadav, Brooke, Russell J., Hudson, Melissa M., Robison, Leslie L., Yasui, Yutaka, Wilson, Carmen L.
Publicado no Eur J Hum Genet (2018)

XPAT: a toolkit to conduct cross-platform association studies with heterogeneous sequencing datasets

Por Yu, Yao, Hu, Hao, Bohlender, Ryan J, Hu, Fulan, Chen, Jiun-Sheng, Holt, Carson, Fowler, Jerry, Guthery, Stephen L, Scheet, Paul, Hildebrandt, Michelle A T, Yandell, Mark, Huff, Chad D
Publicado no Nucleic Acids Res (2018)

Mutations in COQ8B (ADCK4) found in patients with steroid‐resistant nephrotic syndrome alter COQ8B function

Por Vazquez Fonseca, Luis, Doimo, Mara, Calderan, Cristina, Desbats, Maria Andrea, Acosta, Manuel J., Cerqua, Cristina, Cassina, Matteo, Ashraf, Shazia, Hildebrandt, Friedhelm, Sartori, Geppo, Navas, Placido, Trevisson, Eva, Salviati, Leonardo
Publicado no Hum Mutat (2017)

Positively selected enhancer elements endow osteosarcoma cells with metastatic competence

Por Morrow, James J., Bayles, Ian, Funnell, Alister PW, Miller, Tyler E., Saiakhova, Alina, Lizardo, Michael M., Bartels, Cynthia F., Kapteijn, Maaike Y., Hung, Stevephen, Mendoza, Arnulfo, Dhillon, Gursimran, Chee, Daniel R., Myers, Jay T., Allen, Frederick, Gambarotti, Marco, Righi, Alberto, DiFeo, Analisa, Rubin, Brian P., Huang, Alex Y., Meltzer, Paul S., Helman, Lee J., Picci, Piero, Versteeg, Henri, Stamatoyannopolus, John, Khanna, Chand, Scacheri, Peter C.
Publicado no Nat Med (2018)

Maternal Factors Predicting Cognitive and Behavioral Characteristics of Children with Fetal Alcohol Spectrum Disorders

Por May, Philip A., Tabachnick, Barbara G., Gossage, J. Phillip, Kalberg, Wendy O., Marais, Anna-Susan, Robinson, Luther K., Manning, Melanie A., Blankenship, Jason, Buckley, David, Hoyme, H. Eugene, Adnams, Colleen M.
Publicado em 2013

Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

Por van den Berg, Stéphanie M., de Moor, Marleen H. M., Verweij, Karin J. H., Krueger, Robert F., Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K., Derringer, Jaime, Esko, Tõnu, Amin, Najaf, Gordon, Scott D., Hansell, Narelle K., Hart, Amy B., Seppälä, Ilkka, Huffman, Jennifer E., Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abdellaoui, Abdel, Abecasis, Goncalo R., Adkins, Daniel E., Agrawal, Arpana, Allik, Jüri, Appel, Katja, Bigdeli, Timothy B., Busonero, Fabio, Campbell, Harry, Costa, Paul T., Smith, George Davey, Davies, Gail, de Wit, Harriet, Ding, Jun, Engelhardt, Barbara E., Eriksson, Johan G., Fedko, Iryna O., Ferrucci, Luigi, Franke, Barbara, Giegling, Ina, Grucza, Richard, Hartmann, Annette M., Heath, Andrew C., Heinonen, Kati, Henders, Anjali K., Homuth, Georg, Hottenga, Jouke-Jan, Iacono, William G., Janzing, Joost, Jokela, Markus, Karlsson, Robert, Kemp, John P., Kirkpatrick, Matthew G., Latvala, Antti, Lehtimäki, Terho, Liewald, David C., Madden, Pamela A. F., Magri, Chiara, Magnusson, Patrik K. E., Marten, Jonathan, Maschio, Andrea, Mbarek, Hamdi, Medland, Sarah E., Mihailov, Evelin, Milaneschi, Yuri, Montgomery, Grant W., Nauck, Matthias, Nivard, Michel G., Ouwens, Klaasjan G., Palotie, Aarno, Pettersson, Erik, Polasek, Ozren, Qian, Yong, Pulkki-Råback, Laura, Raitakari, Olli T., Realo, Anu, Rose, Richard J., Ruggiero, Daniela, Schmidt, Carsten O., Slutske, Wendy S., Sorice, Rossella, Starr, John M., St Pourcain, Beate, Sutin, Angelina R., Timpson, Nicholas J., Trochet, Holly, Vermeulen, Sita, Vuoksimaa, Eero, Widen, Elisabeth, Wouda, Jasper, Wright, Margaret J., Zgaga, Lina, Porteous, David, Minelli, Alessandra, Palmer, Abraham A., Rujescu, Dan, Ciullo, Marina, Hayward, Caroline, Rudan, Igor, Metspalu, Andres, Kaprio, Jaakko, Deary, Ian J., Räikkönen, Katri, Wilson, James F., Keltikangas-Järvinen, Liisa, Bierut, Laura J., Hettema, John M., Grabe, Hans J., Penninx, Brenda W. J. H., van Duijn, Cornelia M., Evans, David M., Schlessinger, David, Pedersen, Nancy L., Terracciano, Antonio, McGue, Matt, Martin, Nicholas G., Boomsma, Dorret I.
Publicado no Behav Genet (2015)

Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype.

Por Yamaoka, L. H., Welsh-Bohmer, K. A., Hulette, C. M., Gaskell, P. C., Murray, M., Rimmler, J. L., Helms, B. R., Guerra, M., Roses, A. D., Schmechel, D. E., Pericak-Vance, M. A.
Publicado em 1996

A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data

Por Buchanan, Carrie C, Torstenson, Eric S, Bush, William S, Ritchie, Marylyn D
Publicado em 2012

Transcriptomic analysis of wheat near-isogenic lines identifies PM19-A1 and A2 as candidates for a major dormancy QTL

Por Barrero, Jose M., Cavanagh, Colin, Verbyla, Klara L., Tibbits, Josquin F.G., Verbyla, Arunas P., Huang, B. Emma, Rosewarne, Garry M., Stephen, Stuart, Wang, Penghao, Whan, Alex, Rigault, Philippe, Hayden, Matthew J., Gubler, Frank
Publicado no Genome Biol (2015)

Identification of Non-dot/icm Suppressors of the Legionella pneumophila ΔdotL Lethality Phenotype

Por Vincent, Carr D., Buscher, Benjamin A., Friedman, Jonathan R., Williams, Lee Anne, Bardill, Patrick, Vogel, Joseph P.
Publicado em 2006

Exome array analysis identifies novel loci and low-frequency variants for insulin processing and secretion

Por Huyghe, Jeroen R, Jackson, Anne U, Fogarty, Marie P, Buchkovich, Martin L, Stančáková, Alena, Stringham, Heather M, Sim, Xueling, Yang, Lingyao, Fuchsberger, Christian, Cederberg, Henna, Chines, Peter S, Teslovich, Tanya M, Romm, Jane M, Ling, Hua, McMullen, Ivy, Ingersoll, Roxann, Pugh, Elizabeth W, Doheny, Kimberly F, Neale, Benjamin M, Daly, Mark J, Kuusisto, Johanna, Scott, Laura J, Kang, Hyun Min, Collins, Francis S, Abecasis, Gonçalo R, Watanabe, Richard M, Boehnke, Michael, Laakso, Markku, Mohlke, Karen L
Publicado em 2012

Chromosomal assignment of quantitative trait loci influencing baseline circulating total...

Por van Lith, Hein A, Laarakker, Marijke C, Lozeman-van’t Klooster, José G, Ohl, Frauke
Publicado no BMC Res Notes (2015)

RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa

Por Moore, A, Escudier, E, Roger, G, Tamalet, A, Pelosse, B, Marlin, S, Clément, A, Geremek, M, Delaisi, B, Bridoux, A‐M, Coste, A, Witt, M, Duriez, B, Amselem, S
Publicado em 2006

Dissecting genetics of cutaneous miRNA in a mouse model of an autoimmune blistering disease

Por Gupta, Yask, Möller, Steffen, Witte, Mareike, Belheouane, Meriem, Sezin, Tanya, Hirose, Misa, Vorobyev, Artem, Niesar, Felix, Bischof, Julia, Ludwig, Ralf J., Zillikens, Detlef, Sadik, Christian D., Restle, Tobias, Häsler, Robert, Baines, John F., Ibrahim, Saleh M.
Publicado no BMC Genomics (2016)