Kuang Lin
Kuang Lin
Verified email at ndph.ox.ac.uk
Cited by
Cited by
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
S Ripke, C O'Dushlaine, K Chambert, JL Moran, AK Kähler, S Akterin, ...
Nature genetics 45 (10), 1150, 2013
A simple and fast secondary structure prediction method using hidden neural networks
K Lin, VA Simossis, WR Taylor, J Heringa
Bioinformatics 21 (2), 152-159, 2005
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ...
Nature genetics 48 (9), 1043-1048, 2016
Association between telomere length and risk of cancer and non-neoplastic diseases: a Mendelian randomization study
PC Haycock, S Burgess, A Nounu, J Zheng, GN Okoli, J Bowden, ...
JAMA oncology 3 (5), 636-651, 2017
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ...
Cell 173 (7), 1705-1715. e16, 2018
Clusterin regulates β-amyloid toxicity via Dickkopf-1-driven induction of the wnt–PCP–JNK pathway
R Killick, EM Ribe, R Al-Shawi, B Malik, C Hooper, C Fernandes, ...
Molecular psychiatry 19 (1), 88-98, 2014
Common variant at 16p11. 2 conferring risk of psychosis
S Steinberg, S de Jong, M Mattheisen, J Costas, D Demontis, S Jamain, ...
Molecular psychiatry 19 (1), 108-114, 2014
Protein knots: a tangled problem
WR Taylor, K Lin
Nature 421 (6918), 25-25, 2003
A genome-wide association meta-analysis identifies a novel locus at 17q11. 2 associated with sporadic amyotrophic lateral sclerosis
I Fogh, A Ratti, C Gellera, K Lin, C Tiloca, V Moskvina, L Corrado, ...
Human molecular genetics 23 (8), 2220-2231, 2014
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect
A Ratti, L Corrado, B Castellotti, R Del Bo, I Fogh, C Cereda, C Tiloca, ...
Neurobiology of aging 33 (10), 2528. e7-2528. e14, 2012
Genomic analyses from non-invasive prenatal testing reveal genetic associations, patterns of viral infections, and Chinese population history
S Liu, S Huang, F Chen, L Zhao, Y Yuan, SS Francis, L Fang, Z Li, L Lin, ...
Cell 175 (2), 347-359. e14, 2018
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
N Shrine, AL Guyatt, AM Erzurumluoglu, VE Jackson, BD Hobbs, ...
Nature genetics 51 (3), 481-493, 2019
Adherence to healthy lifestyle and cardiovascular diseases in the Chinese population
J Lv, C Yu, Y Guo, Z Bian, L Yang, Y Chen, X Tang, W Zhang, Y Qian, ...
Journal of the American college of cardiology 69 (9), 1116-1125, 2017
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia
RL McLaughlin, D Schijven, W Van Rheenen, KR Van Eijk, M O’Brien, ...
Nature communications 8 (1), 1-12, 2017
Age-specific association between blood pressure and vascular and non-vascular chronic diseases in 0· 5 million adults in China: a prospective cohort study
B Lacey, S Lewington, R Clarke, XL Kong, Y Chen, Y Guo, L Yang, ...
The Lancet Global Health 6 (6), e641-e649, 2018
Non‐junctional human desmoglein 3 acts as an upstream regulator of Src in E‐cadherin adhesion, a pathway possibly involved in the pathogenesis of pemphigus vulgaris
SM Tsang, L Brown, K Lin, L Liu, K Piper, EA O'Toole, R Grose, IR Hart, ...
The Journal of pathology 227 (1), 81-93, 2012
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis
I Fogh, K Lin, C Tiloca, J Rooney, C Gellera, FP Diekstra, A Ratti, ...
JAMA neurology 73 (7), 812-820, 2016
A knot or not a knot? SETting the record ‘straight’on proteins
WR Taylor, B Xiao, SJ Gamblin, K Lin
Computational biology and chemistry 27 (1), 11-15, 2003
The role of ABCA1 gene sequence variants on risk of Alzheimer's disease
MK Lupton, P Proitsi, K Lin, G Hamilton, M Daniilidou, M Tsolaki, ...
Journal of Alzheimer's Disease 38 (4), 897-906, 2014
A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains
S Ranlund, S Calafato, JH Thygesen, K Lin, W Cahn, B Crespo‐Facorro, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 …, 2018
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