Highly conserved gene order and numerous novel repetitive elements in genomic regions linked to wing pattern variation in Heliconius butterflies

por Papa, Riccardo, Morrison, Clayton M, Walters, James R, Counterman, Brian A, Chen, Rui, Halder, Georg, Ferguson, Laura, Chamberlain, Nicola, ffrench-Constant, Richard, Kapan, Durrell D, Jiggins, Chris D, Reed, Robert D, McMillan, William O
Publicado 2008

Strong patterns of intraspecific variation and local adaptation in Great Basin plants revealed through a review of 75 years of experiments

por Baughman, Owen W., Agneray, Alison C., Forister, Matthew L., Kilkenny, Francis F., Espeland, Erin K., Fiegener, Rob, Horning, Matthew E., Johnson, Richard C., Kaye, Thomas N., Ott, Jeff, St. Clair, John Bradley, Leger, Elizabeth A.
Publicado 2019

Leveraging Ethnic Group Incidence Variation to Investigate Genetic Susceptibility to Glioma: A Novel Candidate SNP Approach

por Jacobs, Daniel I., Walsh, Kyle M., Wrensch, Margaret, Wiencke, John, Jenkins, Robert, Houlston, Richard S., Bondy, Melissa, Simon, Matthias, Sanson, Marc, Gousias, Konstantinos, Schramm, Johannes, Labussière, Marianne, Di Stefano, Anna Luisa, Wichmann, H.-Erich, Müller-Nurasyid, Martina, Schreiber, Stefan, Franke, Andre, Moebus, Susanne, Eisele, Lewin, Dewan, Andrew T., Dubrow, Robert
Publicado 2012

Complement Factor H-Related Protein 3 Serum Levels Are Low Compared to Factor H and Mainly Determined by Gene Copy Number Variation in CFHR3

por Pouw, Richard B., Brouwer, Mieke C., Geissler, Judy, van Herpen, Laurens V., Zeerleder, Sacha S., Wuillemin, Walter A., Wouters, Diana, Kuijpers, Taco W.
Publicado 2016

Proteomics Unveils Post-Mortem Changes in Beef Muscle Proteins and Provides Insight into Variations in Meat Quality Traits of Crossbred Young Steers and Heifers Raised in Feedlot

por Severino, Mariane, Gagaoua, Mohammed, Baldassini, Welder, Ribeiro, Richard, Torrecilhas, Juliana, Pereira, Guilherme, Curi, Rogério, Chardulo, Luis Artur, Padilha, Pedro, Neto, Otávio Machado
Publicado 2022

Epigenetic Variation May Compensate for Decreased Genetic Variation with Introductions: A Case Study Using House Sparrows (Passer domesticus) on Two Continents

por Schrey, Aaron W., Coon, Courtney A. C., Grispo, Michael T., Awad, Mohammed, Imboma, Titus, McCoy, Earl D., Mushinsky, Henry R., Richards, Christina L., Martin, Lynn B.
Publicado 2012

Assessing structural variation in a personal genome—towards a human reference diploid genome

por English, Adam C, Salerno, William J, Hampton, Oliver A, Gonzaga-Jauregui, Claudia, Ambreth, Shruthi, Ritter, Deborah I, Beck, Christine R, Davis, Caleb F, Dahdouli, Mahmoud, Ma, Singer, Carroll, Andrew, Veeraraghavan, Narayanan, Bruestle, Jeremy, Drees, Becky, Hastie, Alex, Lam, Ernest T, White, Simon, Mishra, Pamela, Wang, Min, Han, Yi, Zhang, Feng, Stankiewicz, Pawel, Wheeler, David A, Reid, Jeffrey G, Muzny, Donna M, Rogers, Jeffrey, Sabo, Aniko, Worley, Kim C, Lupski, James R, Boerwinkle, Eric, Gibbs, Richard A
Publicado 2015

Cardiovascular risk management in patients with coronary heart disease in primary care: variation across countries and practices. An observational study based on quality indicators

por van Lieshout, Jan, Grol, Richard, Campbell, Stephen, Falcoff, Hector, Capell, Eva Frigola, Glehr, Mathias, Goldfracht, Margalit, Kumpusalo, Esko, Künzi, Beat, Ludt, Sabine, Petek, Davorina, Vanderstighelen, Veerle, Wensing, Michel
Publicado 2012

Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin’s Lymphoma

por Frampton, Matthew, da Silva Filho, Miguel Inacio, Broderick, Peter, Thomsen, Hauke, Försti, Asta, Vijayakrishnan, Jayaram, Cooke, Rosie, Enciso-Mora, Victor, Hoffmann, Per, Nöthen, Markus M, Lloyd, Amy, Holroyd, Amy, Eisele, Lewin, Jöckel, Karl-Heinz, Ponader, Sabine, von Strandmann, Elke Pogge, Lightfoot, Tracy, Roman, Eve, Lake, Annette, Montgomery, Dorothy, Jarrett, Ruth F, Swerdlow, Anthony J, Engert, Andreas, Hemminki, Kari, Houlston, Richard S
Publicado 2013

A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS

por Gelfman, Sahar, Dugger, Sarah, de Araujo Martins Moreno, Cristiane, Ren, Zhong, Wolock, Charles J., Shneider, Neil A., Phatnani, Hemali, Cirulli, Elizabeth T., Lasseigne, Brittany N., Harris, Tim, Maniatis, Tom, Rouleau, Guy A., Brown, Robert H., Gitler, Aaron D., Myers, Richard M., Petrovski, Slavé, Allen, Andrew, Goldstein, David B., Harms, Matthew B.
Publicado 2019

Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience

por Miller, Cecelia R., Lee, Kristy, Pfau, Ruthann B., Reshmi, Shalini C., Corsmeier, Donald J., Hashimoto, Sayaka, Dave-Wala, Ashita, Jayaraman, Vijayakumar, Koboldt, Daniel, Matthews, Theodora, Mouhlas, Danielle, Stein, Maggie, McKinney, Aimee, Grossman, Tom, Kelly, Benjamin J., White, Peter, Magrini, Vincent, Wilson, Richard K., Mardis, Elaine R., Cottrell, Catherine E.
Publicado 2020

Towards Genetic Dissection of Skeletal Class III Malocclusion: A Review of Genetic Variations Underlying the Phenotype in Humans and Future Directions

por Zohud, Osayd, Lone, Iqbal M., Midlej, Kareem, Obaida, Awadi, Masarwa, Samir, Schröder, Agnes, Küchler, Erika C., Nashef, Aysar, Kassem, Firas, Reiser, Vadim, Chaushu, Gavriel, Mott, Richard, Krohn, Sebastian, Kirschneck, Christian, Proff, Peter, Watted, Nezar, Iraqi, Fuad A.
Publicado 2023

Weed germinable seedbanks of rice–wheat systems in the Eastern Indo‐Gangetic Plains: Do tillage and edaphic factors explain community variation?

por Lowry, Carolyn J., Brainard, Daniel C., Kumar, Virender, Smith, Richard G., Singh, Madhulika, Kumar, Pankaj, Kumar, Ajay, Kumar, Vipin, Joon, Rajiv K., Jat, Raj K., Poonia, Shishpal, Malik, Ram K., McDonald, Andrew
Publicado 2021

High-resolution genetic mapping reveals cis-regulatory and copy number variation in loci associated with cytochrome P450-mediated detoxification in a generalist arthropod pest

por Fotoukkiaii, Seyedeh Masoumeh, Wybouw, Nicky, Kurlovs, Andre H., Tsakireli, Dimitra, Pergantis, Spiros A., Clark, Richard M., Vontas, John, Van Leeuwen, Thomas
Publicado 2021

Association between Common Germline Genetic Variation in 94 Candidate Genes or Regions and Risks of Invasive Epithelial Ovarian Cancer

por Quaye, Lydia, Tyrer, Jonathan, Ramus, Susan J., Song, Honglin, Wozniak, Eva, DiCioccio, Richard A., McGuire, Valerie, Høgdall, Estrid, Høgdall, Claus, Blaakaer, Jan, Goode, Ellen L., Schildkraut, Joellen M., Easton, Douglas F., Krüger-Kjaer, Susanne, Whittemore, Alice S., Gayther, Simon A., Pharoah, Paul D. P.
Publicado 2009

Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk

por Bettens, Karolien, Brouwers, Nathalie, Engelborghs, Sebastiaan, Lambert, Jean-Charles, Rogaeva, Ekaterina, Vandenberghe, Rik, Le Bastard, Nathalie, Pasquier, Florence, Vermeulen, Steven, Van Dongen, Jasper, Mattheijssens, Maria, Peeters, Karin, Mayeux, Richard, St George-Hyslop, Peter, Amouyel, Philippe, De Deyn, Peter P, Sleegers, Kristel, Van Broeckhoven, Christine
Publicado 2012

Identifying Extrinsic versus Intrinsic Drivers of Variation in Cell Behavior in Human iPSC Lines from Healthy Donors

por Vigilante, Alessandra, Laddach, Anna, Moens, Nathalie, Meleckyte, Ruta, Leha, Andreas, Ghahramani, Arsham, Culley, Oliver J., Kathuria, Annie, Hurling, Chloe, Vickers, Alice, Wiseman, Erika, Tewary, Mukul, Zandstra, Peter W., Durbin, Richard, Fraternali, Franca, Stegle, Oliver, Birney, Ewan, Luscombe, Nicholas M., Danovi, Davide, Watt, Fiona M.
Publicado 2019

PPARα L162V underlies variation in serum triglycerides and subcutaneous fat volume in young males

por Uthurralt, Julieta, Gordish-Dressman, Heather, Bradbury, Meg, Tesi-Rocha, Carolina, Devaney, Joseph, Harmon, Brennan, Reeves, Erica K, Brandoli, Cinzia, Hansen, Barbara C, Seip, Richard L, Thompson, Paul D, Price, Thomas B, Angelopoulos, Theodore J, Clarkson, Priscilla M, Moyna, Niall M, Pescatello, Linda S, Visich, Paul S, Zoeller, Robert F, Gordon, Paul M, Hoffman, Eric P
Publicado 2007

Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma

por Johnson, David C., Weinhold, Niels, Mitchell, Jonathan S., Chen, Bowang, Kaiser, Martin, Begum, Dil B., Hillengass, Jens, Bertsch, Uta, Gregory, Walter A., Cairns, David, Jackson, Graham H., Försti, Asta, Nickel, Jolanta, Hoffmann, Per, Nöethen, Markus M., Stephens, Owen W., Barlogie, Bart, Davis, Faith E., Hemminki, Kari, Goldschmidt, Hartmut, Houlston, Richard S., Morgan, Gareth J.
Publicado 2016

Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk

por Ajore, Ram, Niroula, Abhishek, Pertesi, Maroulio, Cafaro, Caterina, Thodberg, Malte, Went, Molly, Bao, Erik L., Duran-Lozano, Laura, Lopez de Lapuente Portilla, Aitzkoa, Olafsdottir, Thorunn, Ugidos-Damboriena, Nerea, Magnusson, Olafur, Samur, Mehmet, Lareau, Caleb A., Halldorsson, Gisli H., Thorleifsson, Gudmar, Norddahl, Gudmundur L., Gunnarsdottir, Kristbjorg, Försti, Asta, Goldschmidt, Hartmut, Hemminki, Kari, van Rhee, Frits, Kimber, Scott, Sperling, Adam S., Kaiser, Martin, Anderson, Kenneth, Jonsdottir, Ingileif, Munshi, Nikhil, Rafnar, Thorunn, Waage, Anders, Weinhold, Niels, Thorsteinsdottir, Unnur, Sankaran, Vijay G., Stefansson, Kari, Houlston, Richard, Nilsson, Björn
Publicado 2022