Artikel dengan mandat akses publik - Patrick MayPelajari lebih lanjut
KeseluruhanFNRNIHDFGEuropean CommissionMRCBMBFWellcomeMichael J Fox FoundationNIHRFWOParkinson's UKGovernment of SpainGovernment of ItalySNSFNHMRCSwedish Research CouncilHelmholtzAcademy of FinlandANRParkinson's Foundation, USADOEDoDSFIZonMwNSFFWFCIHRNRFNWOCancer Research UKCanada First Research Excellence FundFRQSINSERMAlzheimers's UKRCNResearch Grants Council, Hong KongASAPAutism Speaks Inc, USAFAPESPGatesVAUSDAHHMIFNRSGenome CanadaNSERCEMBLVolkswagen FoundationHRBRannisBBSRCBHFMotor Neurone Disease Association, UKDoris Duke Charitable FoundationSCLKWFBusiness FinlandUK Research & InnovationTUBITAKPancreatic Cancer, UKSusan G. Komen
Tidak tersedia di mana pun: 5
De novo mutations in HCN1 cause early infantile epileptic encephalopathy
C Nava, C Dalle, A Rastetter, P Striano, CGF de Kovel, R Nabbout, ...
Nature Genetics, 2014
Mandat: Research Foundation (Flanders), National Institute of Health and Medical …
An integrative approach towards completing genome-scale metabolic networks
N Christian, P May, S Kempa, T Handorf, O Ebenhöh
Molecular BioSystems 5 (12), 1889-1903, 2009
Mandat: German Research Foundation
Machine learning-based identification and characterization of 15 novel pathogenic SUOX missense mutations
AT Kaczmarek, N Bahlmann, B Thaqi, P May, G Schwarz
Molecular Genetics and Metabolism 134 (1-2), 188-194, 2021
Mandat: Luxembourg National Research Fund
Association of body mass index and parkinson disease: A bidirectional mendelian randomization study
C Domenighetti, PE Sugier, A Ashok Kumar Sreelatha, C Schulte, ...
Neurology 103 (3), e209620, 2024
Mandat: UK Medical Research Council
CNV-ClinViewer
M Macnee, E Pérez-Palma, T Brünger, C Klöckner, K Platzer, A Stefanski, ...
Bioinformatics 39 (5), 2023
Mandat: German Research Foundation, Federal Ministry of Education and Research, Germany
Tersedia di suatu tempat: 179
Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state
S Smajić, CA Prada-Medina, Z Landoulsi, J Ghelfi, S Delcambre, ...
Brain 145 (3), 964-978, 2022
Mandat: US National Institutes of Health, German Research Foundation, Alzheimers's …
Birth mode is associated with earliest strain-conferred gut microbiome functions and immunostimulatory potential
L Wampach, A Heintz-Buschart, JV Fritz, J Ramiro-Garcia, J Habier, ...
Nature communications 9 (1), 5091, 2018
Mandat: Luxembourg National Research Fund
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
R Chia, MS Sabir, S Bandres-Ciga, S Saez-Atienzar, RH Reynolds, ...
Nature genetics 53 (3), 294-303, 2021
Mandat: US National Institutes of Health, UK Medical Research Council, Wellcome Trust
The phenotypic spectrum of SCN8A encephalopathy
J Larsen, GL Carvill, E Gardella, G Kluger, G Schmiedel, N Barisic, ...
Neurology 84 (5), 480-489, 2015
Mandat: US National Institutes of Health, National Health and Medical Research …
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy
S Syrbe, UBS Hedrich, E Riesch, T Djémié, S Müller, RS Møller, B Maher, ...
Nature genetics 47 (4), 393-399, 2015
Mandat: US National Institutes of Health, Research Foundation (Flanders), German …
De novo variants in neurodevelopmental disorders with epilepsy
HO Heyne, T Singh, H Stamberger, RA Jamra, H Caglayan, D Craiu, ...
Nature genetics 50 (7), 1048-1053, 2018
Mandat: Research Foundation (Flanders), German Research Foundation, UK Medical …
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
E Collaborative, YCA Feng, DP Howrigan, LE Abbott, K Tashman, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
Mandat: US National Institutes of Health, UK Medical Research Council, National …
A cross-disorder dosage sensitivity map of the human genome
RL Collins, JT Glessner, E Porcu, M Lepamets, R Brandon, C Lauricella, ...
Cell 185 (16), 3041-3055. e25, 2022
Mandat: US National Science Foundation, Swiss National Science Foundation, US …
Parkinson’s disease-associated alterations of the gut microbiome predict disease-relevant changes in metabolic functions
F Baldini, J Hertel, E Sandt, CC Thinnes, L Neuberger-Castillo, L Pavelka, ...
BMC biology 18, 1-21, 2020
Mandat: UK Medical Research Council, Parkinson's UK, European Commission, Luxembourg …
Systems genomics evaluation of the SH-SY5Y neuroblastoma cell line as a model for Parkinson’s disease
A Krishna, M Biryukov, C Trefois, PMA Antony, R Hussong, J Lin, ...
BMC genomics 15, 1-21, 2014
Mandat: US National Institutes of Health, German Research Foundation
A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51
N Ameziane, P May, A Haitjema, HJ Van De Vrugt, ...
Nature communications 6 (1), 1-11, 2015
Mandat: US National Institutes of Health, Netherlands Organisation for Scientific …
The effects of carbon dioxide and temperature on microRNA expression in Arabidopsis development
P May, W Liao, Y Wu, B Shuai, W Richard McCombie, MQ Zhang, QA Liu
Nature communications 4 (1), 2145, 2013
Mandat: US National Institutes of Health
CHD2 variants are a risk factor for photosensitivity in epilepsy
EC Galizia, CT Myers, C Leu, CGF De Kovel, T Afrikanova, ...
Brain 138 (5), 1198-1208, 2015
Mandat: US National Institutes of Health, National Health and Medical Research …
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
C Blauwendraat, F Faghri, L Pihlstrom, JT Geiger, A Elbaz, S Lesage, ...
Neurobiology of Aging, 2017
Mandat: US National Institutes of Health, UK Medical Research Council, Parkinson's …
Genomic Sequence Diversity and Population Structure of Saccharomyces cerevisiae Assessed by RAD-seq
GA Cromie, KE Hyma, CL Ludlow, C Garmendia-Torres, TL Gilbert, P May, ...
G3: Genes, Genomes, Genetics 3 (12), 2163-2171, 2013
Mandat: US National Institutes of Health
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