Kinship Solutions for Partially Observed Multiphenotype Data

von Elliott, Lloyd T.
Veröffentlicht in J Comput Biol (2020)

Estimating Genetic Similarity Matrices Using Phylogenies

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

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

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

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

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

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

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

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

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

Directed functional connectivity using dynamic graphical models

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

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

von 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.
Veröffentlicht in Nat Neurosci (2019)

The UK Biobank resource with deep phenotyping and genomic data

von 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
Veröffentlicht in Nature (2018)

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

von 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
Veröffentlicht in Stroke (2020)