A Pleistocene legacy structures variation in modern seagrass ecosystems

por Duffy, J. Emmett, Stachowicz, John J., Reynolds, Pamela L., Hovel, Kevin A., Jahnke, Marlene, Sotka, Erik E., Boström, Christoffer, Boyer, Katharyn E., Cusson, Mathieu, Eklöf, Johan, Engelen, Aschwin H., Eriksson, Britas Klemens, Fodrie, F. Joel, Griffin, John N., Hereu, Clara M., Hori, Masakazu, Hughes, A. Randall, Ivanov, Mikhail V., Jorgensen, Pablo, Kruschel, Claudia, Lee, Kun-Seop, Lefcheck, Jonathan S., Moksnes, Per-Olav, Nakaoka, Masahiro, O’Connor, Mary I., O’Connor, Nessa E., Orth, Robert J., Peterson, Bradley J., Reiss, Henning, Reiss, Katrin, Richardson, J. Paul, Rossi, Francesca, Ruesink, Jennifer L., Schultz, Stewart T., Thormar, Jonas, Tomas, Fiona, Unsworth, Richard, Voigt, Erin, Whalen, Matthew A., Ziegler, Shelby L., Olsen, Jeanine L.
Publicado 2022

Allelic Variation on Murine Chromosome 11 Modifies Host Inflammatory Responses and Resistance to Bacillus anthracis

por Terra, Jill K., France, Bryan, Cote, Christopher K., Jenkins, Amy, Bozue, Joel A., Welkos, Susan L., Bhargava, Ragini, Ho, Chi-Lee, Mehrabian, Margarete, Pan, Calvin, Lusis, Aldons J., Davis, Richard C., LeVine, Steven M., Bradley, Kenneth A.
Publicado 2011

Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization

por Marioni, John C, Thorne, Natalie P, Valsesia, Armand, Fitzgerald, Tomas, Redon, Richard, Fiegler, Heike, Andrews, T Daniel, Stranger, Barbara E, Lynch, Andrew G, Dermitzakis, Emmanouil T, Carter, Nigel P, Tavaré, Simon, Hurles, Matthew E
Publicado 2007

Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood

por Davies, Matthew N, Volta, Manuela, Pidsley, Ruth, Lunnon, Katie, Dixit, Abhishek, Lovestone, Simon, Coarfa, Cristian, Harris, R Alan, Milosavljevic, Aleksandar, Troakes, Claire, Al-Sarraj, Safa, Dobson, Richard, Schalkwyk, Leonard C, Mill, Jonathan
Publicado 2012

Analysis of Copy Number Variation in Alzheimer’s Disease in a Cohort of Clinically Characterized and Neuropathologically Verified Individuals

por Swaminathan, Shanker, Huentelman, Matthew J., Corneveaux, Jason J., Myers, Amanda J., Faber, Kelley M., Foroud, Tatiana, Mayeux, Richard, Shen, Li, Kim, Sungeun, Turk, Mari, Hardy, John, Reiman, Eric M., Saykin, Andrew J.
Publicado 2012

Multi-ancestry phenome-wide association of complement component 4 variation with psychiatric and brain phenotypes in youth

por Hernandez, Leanna M., Kim, Minsoo, Zhang, Pan, Bethlehem, Richard A. I., Hoftman, Gil, Loughnan, Robert, Smith, Diana, Bookheimer, Susan Y., Fan, Chun Chieh, Bearden, Carrie E., Thompson, Wesley K., Gandal, Michael J.
Publicado 2023

206. Variations in the frequency and impact of polymicrobial cultures in adults with invasive Group B Streptococcal (GBS) infection at the US Veterans Health Administration

por Briggs, Janet, Wilson, Brigid, Zappernick, Taissa, Banks, Richard, Baechle2; Sunah Song, Daniel, Jump, Robin L, Perez, Federico
Publicado 2019

Evaluating the spatial and temporal variations of aquatic weeds (Biomass) on Lower Volta River using multi-sensor Landsat Images and machine learning

por Nyamekye, Clement, Ofosu, Samuel Anim, Arthur, Richard, Osei, Gabriel, Appiah, Linda Boamah, Kwofie, Samuel, Ghansah, Benjamin, Bryniok, Dieter
Publicado 2021

Population health needs as predictors of variations in NHS practice payments: a cross-sectional study of English general practices in 2013–2014 and 2014–2015

por Levene, Louis S, Baker, Richard, Wilson, Andrew, Walker, Nicola, Boomla, Kambiz, Bankart, M John G
Publicado 2017

Biodiversity of pig breeds from China and Europe estimated from pooled DNA samples: differences in microsatellite variation between two areas of domestication

por Megens, Hendrik-Jan, Crooijmans, Richard PMA, Cristobal, Magali San, Hui, Xiao, Li, Ning, Groenen, Martien AM
Publicado 2008

Detection of Marker-Free Precision Genome Editing and Genetic Variation through the Capture of Genomic Signatures

por Billon, Pierre, Nambiar, Tarun S., Hayward, Samuel B., Zafra, Maria P., Schatoff, Emma M., Oshima, Koichi, Dunbar, Andrew, Breinig, Marco, Park, Young C., Ryu, Han S., Tschaharganeh, Darjus F., Levine, Ross L., Baer, Richard, Ferrando, Adolfo, Dow, Lukas E., Ciccia, Alberto
Publicado 2020

Seasonal variations of patients presenting dyspnea to emergency departments in Europe: Results from the EURODEM Study

por KARAMERCAN, Mehmet Akif, DÜNDAR, Zerrin Defne, ERGİN, Mehmet, VAN MEER, Oene, BODY, Richard, HARJOLA, Veli-Pekka, VERSCHUREN, Franck, CHRIST, Michael, GOLEA, Adela, CAPSEC, Jean, BARLETTA, Cinzia, GARCIA-CASTRILLO, Luis, ALTUNCI, Yusuf Ali, KATIRCI, Yavuz, KELLY, Anne-Maree, LARIBI, Said
Publicado 2020

Variation in Responses of Fishes across Multiple Reserves within a Network of Marine Protected Areas in Temperate Waters

por Starr, Richard M., Wendt, Dean E., Barnes, Cheryl L., Marks, Corina I., Malone, Dan, Waltz, Grant, Schmidt, Katherine T., Chiu, Jennifer, Launer, Andrea L., Hall, Nathan C., Yochum, Noëlle
Publicado 2015

Inhibin Alpha-Subunit (INHA) Expression in Adrenocortical Cancer Is Linked to Genetic and Epigenetic INHA Promoter Variation

por Hofland, Johannes, Steenbergen, Jacobie, Voorsluijs, Jacoba M., Verbiest, Michael M. P. J., de Krijger, Ronald R., Hofland, Leo J., de Herder, Wouter W., Uitterlinden, Andre G., Feelders, Richard A., de Jong, Frank H.
Publicado 2014

European sea bass genome and its variation provide insights into adaptation to euryhalinity and speciation

por Tine, Mbaye, Kuhl, Heiner, Gagnaire, Pierre-Alexandre, Louro, Bruno, Desmarais, Erick, Martins, Rute S.T., Hecht, Jochen, Knaust, Florian, Belkhir, Khalid, Klages, Sven, Dieterich, Roland, Stueber, Kurt, Piferrer, Francesc, Guinand, Bruno, Bierne, Nicolas, Volckaert, Filip A. M., Bargelloni, Luca, Power, Deborah M., Bonhomme, François, Canario, Adelino V. M., Reinhardt, Richard
Publicado 2014

The genetic variation in the R1a clade among the Ashkenazi Levites’ Y chromosome

por Behar, Doron M., Saag, Lauri, Karmin, Monika, Gover, Meir G., Wexler, Jeffrey D., Sanchez, Luisa Fernanda, Greenspan, Elliott, Kushniarevich, Alena, Davydenko, Oleg, Sahakyan, Hovhannes, Yepiskoposyan, Levon, Boattini, Alessio, Sarno, Stefania, Pagani, Luca, Carmi, Shai, Tzur, Shay, Metspalu, Ene, Bormans, Concetta, Skorecki, Karl, Metspalu, Mait, Rootsi, Siiri, Villems, Richard
Publicado 2017

CAPICE: a computational method for Consequence-Agnostic Pathogenicity Interpretation of Clinical Exome variations

por Li, Shuang, van der Velde, K. Joeri, de Ridder, Dick, van Dijk, Aalt D. J., Soudis, Dimitrios, Zwerwer, Leslie R., Deelen, Patrick, Hendriksen, Dennis, Charbon, Bart, van Gijn, Marielle E., Abbott, Kristin, Sikkema-Raddatz, Birgit, van Diemen, Cleo C., Kerstjens-Frederikse, Wilhelmina S., Sinke, Richard J., Swertz, Morris A.
Publicado 2020

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

por Jia, Xiaoming, Goes, Fernando S., Locke, Adam E., Palmer, Duncan, Wang, Weiqing, Cohen-Woods, Sarah, Genovese, Giulio, Jackson, Anne U., Jiang, Chen, Kvale, Mark, Mullins, Niamh, Nguyen, Hoang, Pirooznia, Mehdi, Rivera, Margarita, Ruderfer, Douglas M., Shen, Ling, Thai, Khanh, Zawistowski, Matthew, Zhuang, Yongwen, Abecasis, Gonçalo, Akil, Huda, Bergen, Sarah, Burmeister, Margit, Chapman, Sinéad, DelaBastide, Melissa, Juréus, Anders, Kang, Hyun Min, Kwok, Pui-Yan, Li, Jun Z., Levy, Shawn E., Monson, Eric T., Moran, Jennifer, Sobell, Janet, Watson, Stanley, Willour, Virginia, Zöllner, Sebastian, Adolfsson, Rolf, Blackwood, Douglas, Boehnke, Michael, Breen, Gerome, Corvin, Aiden, Craddock, Nick, DiFlorio, Arianna, Hultman, Christina M., Landen, Mikael, Lewis, Cathryn, McCarroll, Steven A., Richard McCombie, W., McGuffin, Peter, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek, Myers, Richard M., O’Donovan, Michael, Ophoff, Roel, Boks, Marco, Kahn, Rene, Ouwehand, Willem, Owen, Michael, Pato, Carlos, Pato, Michele, Posthuma, Danielle, Potash, James B., Reif, Andreas, Sklar, Pamela, Smoller, Jordan, Sullivan, Patrick F., Vincent, John, Walters, James, Neale, Benjamin, Purcell, Shaun, Risch, Neil, Schaefer, Catherine, Stahl, Eli A., Zandi, Peter P., Scott, Laura J.
Publicado 2021

Quantifying redox-induced Schottky barrier variations in memristive devices via in operando spectromicroscopy with graphene electrodes

por Baeumer, Christoph, Schmitz, Christoph, Marchewka, Astrid, Mueller, David N., Valenta, Richard, Hackl, Johanna, Raab, Nicolas, Rogers, Steven P., Khan, M. Imtiaz, Nemsak, Slavomir, Shim, Moonsub, Menzel, Stephan, Schneider, Claus Michael, Waser, Rainer, Dittmann, Regina
Publicado 2016

Identifying tagging SNPs for African specific genetic variation from the African Diaspora Genome

por Johnston, Henry Richard, Hu, Yi-Juan, Gao, Jingjing, O’Connor, Timothy D., Abecasis, Gonçalo R., Wojcik, Genevieve L, Gignoux, Christopher R., Gourraud, Pierre-Antoine, Lizee, Antoine, Hansen, Mark, Genuario, Rob, Bullis, Dave, Lawley, Cindy, Kenny, Eimear E., Bustamante, Carlos, Beaty, Terri H., Mathias, Rasika A., Barnes, Kathleen C., Qin, Zhaohui S.
Publicado 2017