受强制性开放获取政策约束的文章 - Wouter van Rheenen了解详情
无法在其他位置公开访问的文章：6 篇
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UNC13A is a modifier of survival in amyotrophic lateral sclerosis
FP Diekstra, PWJ van Vught, W van Rheenen, M Koppers, RJ Pasterkamp, ...
Neurobiology of aging 33 (3), 630. e3-630. e8, 2012
强制性开放获取政策： Research Foundation (Flanders)
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Risk in relatives, heritability, SNP-based heritability, and genetic correlations in psychiatric disorders: a review
BML Baselmans, L Yengo, W van Rheenen, NR Wray
Biological Psychiatry 89 (1), 11-19, 2021
强制性开放获取政策： National Health and Medical Research Council, Australia, Netherlands …
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Associations between lifestyle and amyotrophic lateral sclerosis stratified by C9orf72 genotype: a longitudinal, population-based, case-control study
HJ Westeneng, K van Veenhuijzen, RA van der Spek, S Peters, AE Visser, ...
The Lancet Neurology 20 (5), 373-384, 2021
强制性开放获取政策： European Commission
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Large-scale screening in sporadic amyotrophic lateral sclerosis identifies genetic modifiers in C9orf72 repeat carriers
AM Dekker, M Seelen, PTC van Doormaal, W van Rheenen, RJP Bothof, ...
Neurobiology of aging 39, 220. e9-220. e15, 2016
强制性开放获取政策： European Commission, Netherlands Organisation for Health Research and …
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H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis
W van Rheenen, FP Diekstra, PTC van Doormaal, M Seelen, K Kenna, ...
Neurobiology of Aging 34 (5), 1517. e5-1517. e7, 2013
强制性开放获取政策： Motor Neurone Disease Association, UK, UK Medical Research Council, Wellcome …
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Diagnosing primary lateral sclerosis: a clinico-pathological study
EMJ de Boer, BS de Vries, W Van Hecke, A Mühlebner, KL Vincken, ...
Journal of neurology 272 (1), 1-12, 2025
强制性开放获取政策： European Commission, Netherlands Organisation for Health Research and …
可在其他位置公开访问的文章：71 篇
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A reference panel of 64,976 haplotypes for genotype imputation
Nature genetics 48 (10), 1279-1283, 2016
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
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Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1267-1288, 2018
强制性开放获取政策： US National Institutes of Health, US Department of Veterans Affairs, Howard …
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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
强制性开放获取政策： US National Institutes of Health, UK Economic and Social Research Council …
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Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model
HJ Westeneng, TPA Debray, AE Visser, RPA van Eijk, JPK Rooney, ...
The Lancet Neurology 17 (5), 423-433, 2018
强制性开放获取政策： Health Research Board, Ireland, Science Foundation Ireland, Motor Neurone …
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Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
BN Smith, N Ticozzi, C Fallini, AS Gkazi, S Topp, KP Kenna, EL Scotter, ...
Neuron 84 (2), 324-331, 2014
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
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Genetic correlations of polygenic disease traits: from theory to practice
W Van Rheenen, WJ Peyrot, AJ Schork, SH Lee, NR Wray
Nature Reviews Genetics 20 (10), 567-581, 2019
强制性开放获取政策： National Health and Medical Research Council, Australia, Netherlands …
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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
W Van Rheenen, RAA Van Der Spek, MK Bakker, JJFA Van Vugt, PJ Hop, ...
Nature genetics 53 (12), 1636-1648, 2021
强制性开放获取政策： US National Institutes of Health, Motor Neurone Disease Association, UK, UK …
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NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
KP Kenna, PTC Van Doormaal, AM Dekker, N Ticozzi, BJ Kenna, ...
Nature genetics 48 (9), 1037-1042, 2016
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, National …
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Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
MK Bakker, RAA van der Spek, W van Rheenen, S Morel, R Bourcier, ...
Nature genetics 52 (12), 1303-1313, 2020
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research, 国 …
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Population genetic differentiation of height and body mass index across Europe
MR Robinson, G Hemani, C Medina-Gomez, M Mezzavilla, T Esko, ...
Nature genetics 47 (11), 1357-1362, 2015
强制性开放获取政策： US National Institutes of Health, Australian Research Council, National …
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Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
MA Van Es, HJ Schelhaas, PWJ Van Vught, N Ticozzi, PM Andersen, ...
Annals of neurology 70 (6), 964-973, 2011
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders), Fondazione …
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The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease
CM Lill, A Rengmark, L Pihlstrøm, I Fogh, A Shatunov, PM Sleiman, ...
Alzheimer's & Dementia 11 (12), 1407-1416, 2015
强制性开放获取政策： US National Institutes of Health, UK Medical Research Council, Wellcome …
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Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases
N de Klein, EA Tsai, M Vochteloo, D Baird, Y Huang, CY Chen, ...
Nature genetics 55 (3), 377-388, 2023
强制性开放获取政策： UK Medical Research Council, European Commission, Netherlands Organisation …
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A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
C Akimoto, AE Volk, M van Blitterswijk, M Van den Broeck, CS Leblond, ...
Journal of medical genetics 51 (6), 419-424, 2014
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders), Swedish …
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