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2
Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia 미리보기

학술저널

issue
American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 180(3)
Author
Harold, Denise
Connolly, Siobhan
Riley, Brien P
Kendler, Kenneth S
McCarthy, Shane E
McCombie, William R
Richards, Alex
Owen, Michael J
O'Donovan, Michael C
Walters, James
Donnelly, Peter
Bates, Lesley
Barroso, Ines
Blackwell, Jenefer M
Bramon, Elvira
Brown, Matthew A
Casas, Juan P
Corvin, Aiden
Deloukas, Panos
Duncanson, Audrey
Jankowski, Janusz
Markus, Hugh S
Mathew, Christopher G
Palmer, Colin NA
Plomin, Robert
Rautanen, Anna
Sawcer, Stephen J
Trembath, Richard C
Viswanathan, Ananth C
Wood, Nicholas W
Spencer, Chris CA
Band, Gavin
Bellenguez, Céline
Freeman, Colin
Hellenthal, Garrett
Giannoulatou, Eleni
Hopkins, Lucinda
Pirinen, Matti
Pearson, Richard
Strange, Amy
Su, Zhan
Vukcevic, Damjan
Langford, Cordelia
Hunt, Sarah E
Edkins, Sarah
Gwilliam, Rhian
Blackburn, Hannah
Bumpstead, Suzannah J
Dronov, Serge
Gillman, Matthew
Gray, Emma
Hammond, Naomi
Jayakumar, Alagurevathi
McCann, Owen T
Liddle, Jennifer
Potter, Simon C
Ravindrarajah, Radhi
Ricketts, Michelle
Waller, Matthew
Weston, Paul
Widaa, Sara
Whittaker, Pamela
Ripke, Stephan
Neale, Benjamin M
Walters, James TR
Farh, Kai‐How
Holmans, Peter A
Lee, Phil
Bulik‐Sullivan, Brendan
Collier, David A
Huang, Hailiang
Pers, Tune H
Agartz, Ingrid
Agerbo, Esben
Albus, Margot
Alexander, Madeline
Amin, Farooq
Bacanu, Silviu A
Begemann, Martin
Belliveau, Richard A
Bene, Judit
Bergen, Sarah E
Bevilacqua, Elizabeth
Bigdeli, Tim B
Black, Donald W
Bruggeman, Richard
Buccola, Nancy G
Buckner, Randy L
Byerley, William
Cahn, Wiepke
Cai, Guiqing
Campion, Dominique
Cantor, Rita M
Carr, Vaughan J
Carrera, Noa
Catts, Stanley V
Chambert, Kimberley D
Chan, Raymond CK
Chan, Ronald YL
DB Label
Database : eScholarship
원문보기
Open Access (eScholarship) 
5
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 미리보기

학술저널

issue
Nature. 476(7359)
Author
International Multiple Sclerosis Genetics Consortium
Wellcome Trust Case Control Consortium 2
Sawcer, Stephen
Hellenthal, Garrett
Pirinen, Matti
Spencer, Chris CA
Patsopoulos, Nikolaos A
Moutsianas, Loukas
Dilthey, Alexander
Su, Zhan
Freeman, Colin
Hunt, Sarah E
Edkins, Sarah
Gray, Emma
Booth, David R
Potter, Simon C
Goris, An
Band, Gavin
Oturai, Annette Bang
Strange, Amy
Saarela, Janna
Bellenguez, Céline
Fontaine, Bertrand
Gillman, Matthew
Hemmer, Bernhard
Gwilliam, Rhian
Zipp, Frauke
Jayakumar, Alagurevathi
Martin, Roland
Leslie, Stephen
Hawkins, Stanley
Giannoulatou, Eleni
D'alfonso, Sandra
Blackburn, Hannah
Martinelli Boneschi, Filippo
Liddle, Jennifer
Harbo, Hanne F
Perez, Marc L
Spurkland, Anne
Waller, Matthew J
Mycko, Marcin P
Ricketts, Michelle
Comabella, Manuel
Hammond, Naomi
Kockum, Ingrid
McCann, Owen T
Ban, Maria
Whittaker, Pamela
Kemppinen, Anu
Weston, Paul
Hawkins, Clive
Widaa, Sara
Zajicek, John
Dronov, Serge
Robertson, Neil
Bumpstead, Suzannah J
Barcellos, Lisa F
Ravindrarajah, Rathi
Abraham, Roby
Alfredsson, Lars
Ardlie, Kristin
Aubin, Cristin
Baker, Amie
Baker, Katharine
Baranzini, Sergio E
Bergamaschi, Laura
Bergamaschi, Roberto
Bernstein, Allan
Berthele, Achim
Boggild, Mike
Bradfield, Jonathan P
Brassat, David
Broadley, Simon A
Buck, Dorothea
Butzkueven, Helmut
Capra, Ruggero
Carroll, William M
Cavalla, Paola
Celius, Elisabeth G
Cepok, Sabine
Chiavacci, Rosetta
Clerget-Darpoux, Françoise
Clysters, Katleen
Comi, Giancarlo
Cossburn, Mark
Cournu-Rebeix, Isabelle
Cox, Mathew B
Cozen, Wendy
Cree, Bruce AC
Cross, Anne H
Cusi, Daniele
Daly, Mark J
Davis, Emma
de Bakker, Paul IW
Debouverie, Marc
D'hooghe, Marie Beatrice
Dixon, Katherine
Dobosi, Rita
Dubois, Bénédicte
Ellinghaus, David
DB Label
Database : eScholarship
원문보기
Open Access (eScholarship) 
6
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis 미리보기

학술저널

issue
Nature. 476(7359)
Author
Sawcer, Stephen
Hellenthal, Garrett
Pirinen, Matti
Spencer, Chris CA
Patsopoulos, Nikolaos A
Moutsianas, Loukas
Dilthey, Alexander
Su, Zhan
Freeman, Colin
Hunt, Sarah E
Edkins, Sarah
Gray, Emma
Booth, David R
Potter, Simon C
Goris, An
Band, Gavin
Oturai, Annette Bang
Strange, Amy
Saarela, Janna
Bellenguez, Celine
Fontaine, Bertrand
Gillman, Matthew
Hemmer, Bernhard
Gwilliam, Rhian
Zipp, Frauke
Jayakumar, Alagurevathi
Martin, Roland
Leslie, Stephen
Hawkins, Stanley
Giannoulatou, Eleni
D'alfonso, Sandra
Blackburn, Hannah
Boneschi, Filippo Martinelli
Liddle, Jennifer
Harbo, Hanne F
Perez, Marc L
Spurkland, Anne
Waller, Matthew J
Mycko, Marcin P
Ricketts, Michelle
Comabella, Manuel
Hammond, Naomi
Kockum, Ingrid
McCann, Owen T
Ban, Maria
Whittaker, Pamela
Kemppinen, Anu
Weston, Paul
Hawkins, Clive
Widaa, Sara
Zajicek, John
Dronov, Serge
Robertson, Neil
Bumpstead, Suzannah J
Barcellos, Lisa F
Ravindrarajah, Rathi
Abraham, Roby
Alfredsson, Lars
Ardlie, Kristin
Aubin, Cristin
Baker, Amie
Baker, Katharine
Baranzini, Sergio E
Bergamaschi, Laura
Bergamaschi, Roberto
Bernstein, Allan
Berthele, Achim
Boggild, Mike
Bradfield, Jonathan P
Brassat, David
Broadley, Simon A
Buck, Dorothea
Butzkueven, Helmut
Capra, Ruggero
Carroll, William M
Cavalla, Paola
Celius, Elisabeth G
Cepok, Sabine
Chiavacci, Rosetta
Clerget-Darpoux, Francoise
Clysters, Katleen
Comi, Giancarlo
Cossburn, Mark
Cournu-Rebeix, Isabelle
Cox, Mathew B
Cozen, Wendy
Cree, Bruce AC
Cross, Anne H
Cusi, Daniele
Daly, Mark J
Davis, Emma
de Bakker, Paul IW
Debouverie, Marc
D'hooghe, Marie Beatrice
Dixon, Katherine
Dobosi, Rita
Dubois, Benedicte
Ellinghaus, David
Elovaara, Irina
Esposito, Federica
DB Label
Database : eScholarship
원문보기
Open Access (eScholarship) 
7
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinsonʼs disease with a sexual dimorphism 미리보기

학술저널

issue
Journal of Neurology, Neurosurgery & Psychiatry. Jun 01, 2013 84(6):666-673
Author
Klebe, Stephan
Golmard, Jean-Louis
Nalls, Michael A
Saad, Mohamad
Singleton, Andrew B
Bras, Jose M
Hardy, John
Simon-Sanchez, Javier
Heutink, Peter
Kuhlenbäumer, Gregor
Charfi, Rim
Klein, Christine
Hagenah, Johann
Gasser, Thomas
Wurster, Isabel
Lesage, Suzanne
Lorenz, Delia
Deuschl, Günther
Durif, Franck
Pollak, Pierre
Damier, Philippe
Tison, François
Durr, Alexandra
Amouyel, Philippe
Lambert, Jean-Charles
Tzourio, Christophe
Maubaret, Cécilia
Charbonnier-Beaupel, Fanny
Tahiri, Khadija
Vidailhet, Marie
Martinez, Maria
Brice, Alexis
Corvol, Jean-Christophe
Agid, Y
Anheim, M
Bonnet, A-M
Borg, M
Brice, A.
Broussolle, E
Corvol, J-C
Damier, Ph.
Destée, A.
Durr, A
Durif, F
Klebe, S
Lohmann, E
Martinez, M
Penet, C
Pollak, P
Krack, P
Rascol, O
Tison, F
Tranchant, C
Vérin, M
Viallet, F
Plagnol, Vincent
Bras, Jose M
Hernandez, Dena G
Sharma, Manu
Sheerin, Una-Marie
Saad, Mohamad
Simón-Sánchez, Javier
Schulte, Claudia
Lesage, Suzanne
Sveinbjörnsdóttir, Sigurlaug
Amouyel, Philippe
Arepalli, Sampath
Band, Gavin
Barker, Roger A
Bellinguez, Céline
Ben-Shlomo, Yoav
Berendse, Henk W
Berg, Daniela
Bhatia, Kailash
de Bie, Rob MA
Biffi, Alessandro
Bloem, Bas
Bochdanovits, Zoltan
Bonin, Michael
Brockmann, Kathrin
Brooks, Janet
Burn, David J
Charlesworth, Gavin
Chen, Honglei
Chinnery, Patrick F
Chong, Sean
Clarke, Carl E
Cookson, Mark R
Cooper, J Mark
Corvol, Jean Christophe
Counsell, Carl
Damier, Philippe
Dartigues, Jean-François
Deloukas, Panos
Dexter, David T
van Dijk, Karin D
Dillman, Allissa
Durif, Frank
Edkins, Sarah
Evans, Jonathan R
Foltynie, Thomas
Freeman, Colin
Gao, Jianjun
Gardner, Michelle
Gibbs, Raphael
Goate, Alison
Gray, Emma
Guerreiro, Rita
Gústafsson, Ómar
Harris, Clare
Hellenthal, Garrett
van Hilten, Jacobus J
Hofman, Albert
Hollenbeck, Albert
Holton, Janice
Hu, Michele
Huang, Xuemei
Huber, Heiko
Hudson, Gavin
Hunt, Sarah E
Huttenlocher, Johanna
Illig, Thomas
Jónsson, Pálmi V
Langford, Cordelia
Lees, Andrew
Lichtner, Peter
Limousin, Patricia
Lopez, Grisel
Lorenz, Delia
McNeill, Alisdair
Moorby, Catriona
Morris, Huw
Morrison, Karen E
Mudanohwo, Ese
OʼSullivan, Sean S
Pearson, Justin
Pearson, Richard
Perlmutter, Joel S
Pétursson, Hjörvar
Pirinen, Matti
Pollak, Pierre
Post, Bart
Potter, Simon
Ravina, Bernard
Revesz, Tamas
Riess, Olaf
Rivadeneira, Fernando
Rizzu, Patrizia
Ryten, Mina
Sawcer, Stephen
Schapira, Anthony
Scheffer, Hans
Shaw, Karen
Shoulson, Ira
Sidransky, Ellen
de Silva, Rohan
Smith, Colin
Spencer, Chris CA
Stefánsson, Hreinn
Steinberg, Stacy
Stockton, Joanna D
Strange, Amy
Su, Zhan
Talbot, Kevin
Tanner, Carlie M
Tashakkori-Ghanbaria, Avazeh
Tison, François
Trabzuni, Daniah
Traynor, Bryan J
Uitterlinden, G
Vandrovcova, Jana
Velseboer, Daan
Vidailhet, Marie
Vukcevic, Damjan
Walker, Robert
van de Warrenburg, Bart
Weale, Michael E
Wickremaratchi, Mirdhu
Williams, Nigel
Williams-Gray, Caroline H
Winder-Rhodes, Sophie
Martinez, Maria
Donnelly, Peter
Hardy, John
Heutink, Peter
Brice, Alexis
Gasser, Thomas
Wood, Nicholas W
Singleton, Andrew B
DB Label
Database : Journals@OVID
원문보기
등재 - SCOPUS  조회 - Impact Factor (JCR)  등재 - Web of Science (SCIE) 
8
Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease 미리보기

학술저널

issue
NPJ GENOMIC MEDICINE; MAY 4 2016, 3 p16008 6p.
Author
Robinson, Philip C.
Leo, Paul J.
Pointon, Jennifer J.
Harris, Jessica
Cremin, Katie
Bradbury, Linda A.
Stebbings, Simon
Harrison, Andrew A.
Duncan, Emma L.
Evans, David M.
Wordsworth, Paul B.
Brown, Matthew A.
Donnelly, Peter
Barroso, Ines
Blackwell, Jenefer M.
Bramon, Elvira
Casas, Juan P.
Corvin, Aiden
Deloukas, Panos
Duncanson, Audrey
Jankowski, Janusz
Markus, Hugh S.
Mathew, Christopher G.
Palmer, Colin Na
Plomin, Robert
Rautanen, Anna
Sawcer, Stephen J.
Trembath, Richard C.
Viswanathan, Ananth C.
Wood, Nicholas W.
Spencer, Chris Ca
Band, Gavin
Bellenguez, Celine
Freeman, Colin
Hellenthal, Garrett
Giannoulatou, Eleni
Pirinen, Matti
Pearson, Richard
Strange, Amy
Su, Zhan
Vukcevic, Damjan
Langford, Cordelia
Hunt, Sarah E.
Edkins, Sarah
Gwilliam, Rhian
Blackburn, Hannah
Bumpstead, Suzannah J.
Dronov, Serge
Gillman, Matthew
Gray, Emma
Hammond, Naomi
Jayakumar, Alagurevathi
McCann, Owen T.
Liddle, Jennifer
Potter, Simon C.
Ravindrarajah, Radhi
Ricketts, Michelle
Waller, Matthew
Weston, Paul
Widaa, Sara
Whittaker, Pamela
Spencer, Chris C. A.
McCloskey, Eugene
Eisman, John
Jones, Graeme
Nicholson, Geoff
Eastell, Richard
Sambrook, Philip
Prince, Richard
Dennison, Elaine
Reid, Ian
Wark, John
Australian Osteoporosis Genetics C
Wellcome Trust Case Control Cons
DB Label
Database : Science Citation Index Expanded
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등재 - SCOPUS  조회 - Impact Factor (JCR)  등재 - Web of Science 
9
Scanning the human genome for signals of selection 미리보기

학술저널

issue
Current Opinion in Genetics & Development. Dec2006, Vol. 16 Issue 6, p624-629. 6p.
Author
McVean, Gil1 mcvean@stats.ox.ac.uk
Spencer, Chris CA1
DB Label
Database : Academic Search Complete
원문보기
Full Text (ScienceDirect)  등재 - SCOPUS  조회 - Impact Factor (JCR)  등재 - Web of Science (SCIE) 
10
Interferon lambda 4 impacts the genetic diversity of hepatitis C virus. 미리보기

학술저널

issue
ELife [Elife] 2019 Sep 03; Vol. 8. Date of Electronic Publication: 2019 Sep 03.
Author
Ansari MA; Wellcome Centre Human Genetics, University of Oxford, Oxford, United Kingdom.
Aranday-Cortes E; MRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, Glasgow, United Kingdom.
Ip CL; Wellcome Centre Human Genetics, University of Oxford, Oxford, United Kingdom.
da Silva Filipe A; MRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, Glasgow, United Kingdom.
Lau SH; MRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, Glasgow, United Kingdom.
Bamford C; MRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, Glasgow, United Kingdom.
Bonsall D; Nuffield Department of Medicine and the Oxford NIHR BRC, University of Oxford, Oxford, United Kingdom.
Trebes A; Wellcome Centre Human Genetics, University of Oxford, Oxford, United Kingdom.
Piazza P; Wellcome Centre Human Genetics, University of Oxford, Oxford, United Kingdom.
Sreenu V; MRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, Glasgow, United Kingdom.
Cowton VM; MRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, Glasgow, United Kingdom.
Hudson E; Nuffield Department of Medicine and the Oxford NIHR BRC, University of Oxford, Oxford, United Kingdom.
Bowden R; Wellcome Centre Human Genetics, University of Oxford, Oxford, United Kingdom.
Patel AH; MRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, Glasgow, United Kingdom.
Foster GR; Blizard Institute, Queen Mary University, London, United Kingdom.
Irving WL; National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and University of Nottingham, Nottingham, United Kingdom.
Agarwal K; Institute of Liver Studies, King's College Hospital, London, United Kingdom.
Thomson EC; MRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, Glasgow, United Kingdom.
Simmonds P; Nuffield Department of Medicine and the Oxford NIHR BRC, University of Oxford, Oxford, United Kingdom.
Klenerman P; Nuffield Department of Medicine and the Oxford NIHR BRC, University of Oxford, Oxford, United Kingdom.
Holmes C; Department of Statistics, University of Oxford, Oxford, United Kingdom.
Barnes E; Nuffield Department of Medicine and the Oxford NIHR BRC, University of Oxford, Oxford, United Kingdom.
Spencer CC; Wellcome Centre Human Genetics, University of Oxford, Oxford, United Kingdom.
McLauchlan J; MRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, Glasgow, United Kingdom.
Pedergnana V; Wellcome Centre Human Genetics, University of Oxford, Oxford, United Kingdom.; Laboratoire MIVEGEC (UMR CNRS 5290, IRD, UM), Montpellier, France.
DB Label
Database : MEDLINE
원문보기
Open Access (PubMed Central)  등재 - SCOPUS  조회 - Impact Factor (JCR)  등재 - Web of Science (SCIE) 
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