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Nigel Williams

Cardiff University

87H指数
635论文数
4.9W被引数
收录论文 294
发表时间
Penetrance of neurodevelopmental copy number variants is associated with variations in cortical morphology神经发育性拷贝数变异的穿透性与皮层形态变异相关
err2025-05-23
err0
PREAI
errAna I. Silva; Ida E. Sønderby; George Kirov; Abdel Abdellaoui; Ingrid Agartz; David Ames; Nicola J. Armstrong; Eric Artiges; Tobias Banaschewski; Anne S. Bassett; Carrie E. Bearden; John Blangero; Rune Boen; Dorret I. Boomsma; Robin Bülow; Nancy J. Butcher; Vince Calhoun; Linda E. Campbell; Eva W.C. Chow; Simone Ciufolini; Michael C. Craig; Benedicto Crespo-Farroco; Adam C. Cunningham; Shareefa Dalvie; Eileen Daly; Paola Dazzan; Eco J.C. de Geus; Greig I. de Zubicaray; Joanne L. Doherty; Gary Donohoe; Mark Drakesmith; Thomas Espeseth; Vincent Frouin; Hugh Garavan; David C. Glahn; Naomi J. Goodrich-Hunsaker; Penny A. Gowland; Hans J. Grabe; Antoine Grigis; Maria Gudbrandsen; Boris A. Gutman; Jan Haavik; Asta K. Håberg; Jeremy Hall; Andreas Heinz; Sarah Hohmann; Jouke-Jan Hottenga; Sébastien Jacquemont; Neda Jahanshad; Rachel K. Jonas; Derek K. Jones; Erik G. Jönsson; Sanne Koops; Kuldeep Kumar; Stephanie Le Hellard; Herve Lemaitre; Jingyu Liu; Astri J. Lundervold; Jean-Luc Martinot; Karen A. Mather; Donna M. McDonald-McGinn; Katie L. McMahon; Allan F. McRae; Sarah E. Medland; Clara A. Moreau; Kieran C. Murphy; Declan Murphy; Robin M. Murray; Frauke Nees; Michael J. Owen; Marie-Laure Paillère Martinot; Diimitri Papadopoulos Orfanos; Tomas Paus; Luise Poustka; Tiago Reis Marques; David R. Roalf; Perminder S. Sachdev; Freda Scheffler; J. Eric Schmitt; Gunter Schumann; Vidar M. Steen; Dan J. Stein; Lachlan T. Strike; Alexander Teumer; Anbupalam Thalamuthu; Sophia I. Thomopoulos; Diana Tordesillas-Gutiérrez; Julian N. Trollor; Anne Uhlmann; Ariana Vajdi; Dennis van ’t Ent; Therese van Amelsvoort; Marianne B.M. van den Bree; Dennis van der Meer; Javier Vázquez-Bourgon; Julio E. Villalón-Reina; Uwe Völker; Henry Völzke; Jacob A.S. Vorstman; Lars T. Westlye; Nigel Williams; Katharina Wittfeld; Margaret J. Wright; Paul M. Thompson; Ole A. Andreassen; David E.J. Linden
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Genome-wide determinants of mortality and motor progression in Parkinson's disease帕金森病死亡率和运动进展的全基因组决定因素
err2024-06-07
err0
errOAAI
errTan, Manuela M. X.; Lawton, Michael A.; Pollard, Miriam I.; Brown, Emmeline; Real, Raquel; Carrasco, Alejandro Martinez; Bekadar, Samir; Jabbari, Edwin; Reynolds, Regina H.; Iwaki, Hirotaka; Blauwendraat, Cornelis; Kanavou, Sofia; Hubbard, Leon; Malek, Naveed; Grosset, Katherine A.; Bajaj, Nin; Barker, Roger A.; Burn, David J.; Bresner, Catherine; Foltynie, Thomas; Wood, Nicholas W.; Williams-Gray, Caroline H.; Andreassen, Ole A.; Toft, Mathias; Elbaz, Alexis; Artaud, Fanny; Brice, Alexis; Corvol, Jean-Christophe; Aasly, Jan; Farrer, Matthew J.; Nalls, Michael A.; Singleton, Andrew B.; Williams, Nigel M.; Ben-Shlomo, Yoav; Hardy, John; Hu, Michele T. M.; Grosset, Donald G.; Shoai, Maryam; Pihlstrom, Lasse; Morris, Huw R.
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Genotype-phenotype correlation in PRKN-associated Parkinson's disease
err2024-03-29
err10
errOAAI
errMenon, Poornima Jayadev; Sambin, Sara; Criniere-Boizet, Baptiste; Courtin, Thomas; Tesson, Christelle; Casse, Fanny; Ferrien, Melanie; Mariani, Louise-Laure; Carvalho, Stephanie; Lejeune, Francois-Xavier; Rebbah, Sana; Martet, Gaspard; Houot, Marion; Lanore, Aymeric; Mangone, Graziella; Roze, Emmanuel; Vidailhet, Marie; Aasly, Jan; Gan Or, Ziv; Yu, Eric; Dauvilliers, Yves; Zimprich, Alexander; Tomantschger, Volker; Pirker, Walter; Alvarez, Ignacio; Pastor, Pau; Di Fonzo, Alessio; Bhatia, Kailash P.; Magrinelli, Francesca; Houlden, Henry; Real, Raquel; Quattrone, Andrea; Limousin, Patricia; Korlipara, Prasad; Foltynie, Thomas; Grosset, Donald; Williams, Nigel; Narendra, Derek; Lin, Hsin-Pin; Jovanovic, Carna; Svetel, Marina; Lynch, Timothy; Gallagher, Amy; Vandenberghe, Wim; Gasser, Thomas; Brockmann, Kathrin; Morris, Huw R.; Borsche, Max; Klein, Christine; Corti, Olga; Brice, Alexis; Lesage, Suzanne; Corvol, Jean Christophe
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Genome-wide Analysis of Motor Progression in Parkinson Disease
err2023-10-01
err2
errOAAI
errCarrasco, Alejandro Martinez; Real, Raquel; Lawton, Michael; Reynolds, Regina Hertfelder; Tan, Manuela; Wu, Lesley; Williams, Nigel; Carroll, Camille; Corvol, Jean-Christophe; Hu, Michele; Grosset, Donald; Hardy, John; Ryten, Mina; Ben-Shlomo, Yoav; Shoai, Maryam; Morris, Huw R.
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Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease
err2023-08-31
err3
errOAAI
errMartinez-Carrasco, Alejandro; Real, Raquel; Lawton, Michael; Iwaki, Hirotaka; Tan, Manuela M. X.; Wu, Lesley; Williams, Nigel M.; Carroll, Camille; Hu, Michele T. M.; Grosset, Donald G.; Hardy, John; Ryten, Mina; Foltynie, Tom; Ben-Shlomo, Yoav; Shoai, Maryam; Morris, Huw R.
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Th1 Cells Alter the Inflammatory Signature of IL-6 by Channeling STAT Transcription Factors to Alu-like Retroelements
err2023-06-05
err2
errOAAI
errMillrine, David; Figueras, Ana Cardus; Fernandez, Javier Uceda; Andrews, Robert; Szomolay, Barbara; Cossins, Benjamin C.; Rice, Christopher M.; Li, Jasmine; Tyrrell, Victoria J.; McLeod, Louise; Holmans, Peter; O'Donnell, Valerie B.; Taylor, Philip R.; Turner, Stephen J.; Jenkins, Brendan J.; Jones, Gareth W.; Topley, Nicholas; Williams, Nigel M.; Jones, Simon A.
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The sink splash zone
err2023-05-01
err8
PREAI
errGarvey, M. I.; Williams, N.; Gardiner, A.; Ruston, C.; Wilkinson, M. A. C.; Kiernan, M.; Walker, J. T.; Holden, E.
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Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia罕见的编码变体作为22 q11.2缺失的风险修饰语暗示了综合征型精神分裂症的产后皮质发育
err2023-03-03
err3
PREAI
errLin, Jhih-Rong; Zhao, Yingjie; Jabalameli, M. Reza; Nguyen, Nha; Mitra, Joydeep; Swillen, Ann; Vorstman, Jacob A. S.; Chow, Eva W. C.; van den Bree, Marianne; Emanuel, Beverly S.; Vermeesch, Joris R.; Owen, Michael J.; Williams, Nigel M.; Bassett, Anne S.; McDonald-McGinn, Donna M.; Gur, Raquel E.; Bearden, Carrie E.; Morrow, Bernice E.; Lachman, Herbert M.; Zhang, Zhengdong D.
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Identification of a possible proteomic biomarker in Parkinson's disease: discovery and replication in blood, brain and cerebrospinal fluid
err2022-12-28
err15
errOAAI
errWinchester, Laura; Barber, Imelda; Lawton, Michael; Ash, Jessica; Liu, Benjamine; Evetts, Samuel; Hopkins-Jones, Lucinda; Lewis, Suppalak; Bresner, Catherine; Malpartida, Ana Belen; Williams, Nigel; Gentlemen, Steve; Wade-Martins, Richard; Ryan, Brent; Holgado-Nevado, Alejo; Hu, Michele; Ben-Shlomo, Yoav; Grosset, Donald; Lovestone, Simon
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Association between the LRP1B and APOE loci and the development of Parkinson's disease dementiaLRP1B和APOE基因位点与帕金森病痴呆发病的关系
errBRAIN
IF11.7
err2022-11-09
err25
errOAAI
errReal, Raquel; Martinez-Carrasco, Alejandro; Reynolds, Regina H.; Lawton, Michael A.; Tan, Manuela M. X.; Shoai, Maryam; Corvol, Jean-Christophe; Ryten, Mina; Bresner, Catherine; Hubbard, Leon; Brice, Alexis; Lesage, Suzanne; Faouzi, Johann; Elbaz, Alexis; Artaud, Fanny; Williams, Nigel; Hu, Michele T. M.; Ben-Shlomo, Yoav; Grosset, Donald G.; Hardy, John; Morris, Huw R.
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Genetics of validated Parkinson's disease subtypes in the Oxford Discovery and Tracking Parkinson's cohorts牛津发现和跟踪帕金森队列中经过验证的帕金森病亚型的遗传学
err2022-06-22
err9
errOAAI
errLawton, Michael; Tan, Manuela M. X.; Ben-Shlomo, Yoav; Baig, Fahd; Barber, Thomas; Klein, Johannes C.; Evetts, Samuel G.; Millin, Stephanie; Malek, Naveed; Grosset, Katherine; Barker, Roger A.; Williams, Nigel; Burn, David J.; Foltynie, Thomas; Morris, Huw R.; Wood, Nicholas; Grosset, Donald G.; Hu, Michele Tao-Ming
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Combining biomarkers for prognostic modelling of Parkinson's disease帕金森病预后建模的生物标志物组合
err2022-05-16
err17
errOAAI
errVijiaratnam, Nirosen; Lawton, Michael; Heslegrave, Amanda J.; Guo, Tong; Tan, Manuela; Jabbari, Edwin; Real, Raquel; Woodside, John; Grosset, Katherine; Chelban, Viorica; Athauda, Dilan; Girges, Christine; Barker, Roger A.; Hardy, John; Wood, Nicholas; Houlden, Henry; Williams, Nigel; Ben-Shlomo, Yoav; Zetterberg, Henrik; Grosset, Donald G.; Foltynie, Thomas; Morris, Huw R.
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Psychopathology in adults with copy number variants
err2022-02-11
err4
errOAAI
errAdams, Rachael L.; Baird, Alister; Smith, Jacqueline; Williams, Nigel; van den Bree, Marianne B. M.; Linden, David E. J.; Owen, Michael J.; Hall, Jeremy; Linden, Stefanie C.
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PROTEIN CODING TANDEM REPEAT IN TCERG1 MODIFIES HUNTINGTON'S DISEASE ONSET
err2021-09-05
err0
PREAI
errLobanov, Sergey; McAllister, Branduff; McDade-Kumar, Mia; Lee, Jong-Min; MacDonald, Marcy; Gusella, James; Ryten, Mina; Williams, Nigel; Holmans, Peter; Massey, Thomas; Jones, Lesley
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CSF-resident CD4+ T-cells display a distinct gene expression profile with relevance to immune surveillance and multiple sclerosis
err2021-07-13
err9
errOAAI
errHrastelj, James; Andrews, Robert; Loveless, Samantha; Morgan, Joanne; Bishop, Stefan Mark; Bray, Nicholas J.; Williams, Nigel M.; Robertson, Neil P.
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Explaining the missing heritability of psychiatric disorders
err2021-05-18
err20
errOAAI
errOwen, Michael J.; Williams, Nigel M.
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Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease
err2021-05-11
err53
errOAAI
errMcAllister, Branduff; Gusella, James F.; Landwehrmeyer, G. Bernhard; Lee, Jong-Min; MacDonald, Marcy E.; Orth, Michael; Rosser, Anne E.; Williams, Nigel M.; Holmans, Peter; Jones, Lesley; Massey, Thomas H.
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The psychiatric phenotypes of 1q21 distal deletion and duplication
err2021-02-04
err13
errOAAI
errLinden, Stefanie C.; Watson, Cameron J.; Smith, Jacqueline; Chawner, Samuel J. R. A.; Lancaster, Thomas M.; Evans, Ffion; Williams, Nigel; Skuse, David; Raymond, F. Lucy; Hall, Jeremy; Owen, Michael J.; Linden, David E. J.; Green-Snyder, LeeAnne; Chung, Wendy K.; Maillard, Anne M.; Jacquemont, Sebastien; van den Bree, Marianne B. M.
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