Kinship Solutions for Partially Observed Multiphenotype Data

Autor Elliott, Lloyd T.
Vydáno v J Comput Biol (2020)

Estimating Genetic Similarity Matrices Using Phylogenies

Autor Wang, Shijia, Ge, Shufei, Colijn, Caroline, Biller, Priscila, Wang, Liangliang, Elliott, Lloyd T.
Vydáno v J Comput Biol (2021)

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

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

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

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

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

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

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

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

Directed functional connectivity using dynamic graphical models

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

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

Autor 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.
Vydáno v Nat Neurosci (2019)

The UK Biobank resource with deep phenotyping and genomic data

Autor 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
Vydáno v Nature (2018)

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

Autor 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
Vydáno v Stroke (2020)