Kinship Solutions for Partially Observed Multiphenotype Data

by Elliott, Lloyd T.
Published in J Comput Biol (2020)

Estimating Genetic Similarity Matrices Using Phylogenies

by Wang, Shijia, Ge, Shufei, Colijn, Caroline, Biller, Priscila, Wang, Liangliang, Elliott, Lloyd T.
Published in J Comput Biol (2021)

Probing principles of large‐scale object representation: Category preference and location encoding

by Cichy, Radoslaw Martin, Sterzer, Philipp, Heinzle, Jakob, Elliott, Lloyd T., Ramirez, Fernando, Haynes, John‐Dylan
Published in Hum Brain Mapp (2012)

An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank

by Smith, Stephen M, Douaud, Gwenaëlle, Chen, Winfield, Hanayik, Taylor, Alfaro-Almagro, Fidel, Sharp, Kevin, Elliott, Lloyd T
Published in Nat Neurosci (2021)

Genome-wide association studies of brain imaging phenotypes in UK Biobank

by Elliott, Lloyd T., Sharp, Kevin, Alfaro-Almagro, Fidel, Shi, Sinan, Miller, Karla L., Douaud, Gwenaëlle, Marchini, Jonathan, Smith, Stephen M.
Published in Nature (2018)

Brain aging comprises many modes of structural and functional change with distinct genetic and biophysical associations

by Smith, Stephen M, Elliott, Lloyd T, Alfaro-Almagro, Fidel, McCarthy, Paul, Nichols, Thomas E, Douaud, Gwenaëlle, Miller, Karla L
Published in eLife (2020)

Directed functional connectivity using dynamic graphical models

by Schwab, Simon, Harbord, Ruth, Zerbi, Valerio, Elliott, Lloyd, Afyouni, Soroosh, Smith, Jim Q., Woolrich, Mark W., Smith, Stephen M., Nichols, Thomas E.
Published in Neuroimage (2018)

The spatial correspondence and genetic influence of inter-hemispheric connectivity with white matter microstructure

by Mollink, Jeroen, Smith, Stephen M., Elliott, Lloyd T., Kleinnijenhuis, Michiel, Hiemstra, Marlies, Alfaro-Almagro, Fidel, Marchini, Jonathan, van Cappellen van Walsum, Anne-Marie, Jbabdi, Saad, Miller, Karla L.
Published in Nat Neurosci (2019)

The UK Biobank resource with deep phenotyping and genomic data

by Bycroft, Clare, Freeman, Colin, Petkova, Desislava, Band, Gavin, Elliott, Lloyd T., Sharp, Kevin, Motyer, Allan, Vukcevic, Damjan, Delaneau, Olivier, O’Connell, Jared, Cortes, Adrian, Welsh, Samantha, Young, Alan, Effingham, Mark, McVean, Gil, Leslie, Stephen, Allen, Naomi, Donnelly, Peter, Marchini, Jonathan
Published in Nature (2018)

Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities

by Armstrong, Nicola J, Mather, Karen A, Sargurupremraj, Muralidharan, Knol, Maria J, Malik, Rainer, Satizabal, Claudia L, Yanek, Lisa R, Wen, Wei, Gudnason, Vilmundur G, Dueker, Nicole D, Elliott, Lloyd T, Hofer, Edith, Bis, Joshua, Jahanshad, Neda, Li, Shuo, Logue, Mark A, Luciano, Michelle, Scholz, Markus, Smith, Albert V, Trompet, Stella S, Vojinovic, Dina, Xia, Rui, Alfaro-Almagro, Fidel, Ames, David, Amin, Najaf, Amouyel, Philippe, Beiser, Alexa S, Brodaty, Henry, Deary, Ian J, Fennema-Notestine, Christine, Gampawar, Piyush G, Gottesman, Rebecca, Griffanti, Ludovica, Jnr, Clifford R Jack, Jenkinson, Mark, Jiang, Jiyang, Kral, Brian G, Kwok, John B, Lampe, Leonie, Liewald, David CM, Maillard, Pauline, Marchini, Jonathan, Bastin, Mark E, Mazoyer, Bernard, Pirpamer, Lukas, Romero, José Rafael, Roshchupkin, Gennady V, Schofield, Peter R, Schroeter, Matthias L, Stott, David J, Thalamuthu, Anbupalam, Trollor, Julian, Tzourio, Christophe, van der Grond, Jeroen, Vernooij, Meike W, Witte, Veronica A, Wright, Margaret J, Yang, Qiong, Morris, Zoe, Siggurdsson, Siggi, Psaty, Bruce, Villringer, Arno, Schmidt, Helena, Haberg, Asta K, van Duijn, Cornelia M, Jukema, J Wouter, Dichgans, Martin, Sacco, Ralph L, Wright, Clinton B, Kremen, William S, Becker, Lewis C, Thompson, Paul M, Mosley, Thomas H, Wardlaw, Joanna M, Ikram, M Arfan, Adams, Hieab HH, Seshadri, Sudha, Sachdev, Perminder S, Smith, Stephen M, Launer, Lenore, Longstreth, William, DeCarli, Charles, Schmidt, Reinhold, Fornage, Myriam, Debette, Stephanie, Nyquist, Paul A
Published in Stroke (2020)