Articoli con mandati relativi all'accesso pubblico - Margit BurmeisterUlteriori informazioni
TotaleNIHWellcomeMRCNSFCEuropean CommissionNHMRCNIHRBHFCancer Research UKHHMIDFGNWOSwedish Research CouncilBBSRCGovernment of SpainBMBFDoDVAFWFZonMwDOESNSFCIHRMTATelethonNational Centre for the Replacement, Refinement and Reduction of Animals in Research, UKRCNANRGoverno ItalianoUK Research & InnovationNCNRWJFDamon Runyon Cancer Research FoundationNSFUSEDAHAARCGenome CanadaINSERMFORTEAlzheimers's UKVersus Arthritis, UKESRCParkinson's UKWorldwide Cancer Research, UKDoris Duke Charitable FoundationAutism Science Foundation, USAHealth Data Research, UK
Non disponibili pubblicamente: 2
The recurrent mutation in RNF220 also causes hypomyelination in China and is a CpG hot spot
H Yan, T Kubisiak, K Gao, J Xiao, J Wang, Y Zhang, Y Wu, Y Jiang, ...
Brain 145 (12), e122-e124, 2022
Mandati: National Natural Science Foundation of China
817. Neuropeptide Y Genetic Risk Affects Striatal Response to Potential Loss
K Warthen, B Sanford, K Walker, S Black, M Angstadt, C Sripada, R Welsh, ...
Biological Psychiatry 81 (10), S331-S332, 2017
Mandati: US National Institutes of Health
Disponibili pubblicamente: 97
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
Mandati: Swiss National Science Foundation, US National Institutes of Health, US …
The serotonin transporter promoter variant (5-HTTLPR), stress, and depression meta-analysis revisited: evidence of genetic moderation
K Karg, M Burmeister, K Shedden, S Sen
Archives of general psychiatry 68 (5), 444-454, 2011
Mandati: US National Institutes of Health
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Nature genetics 43 (10), 977-983, 2011
Mandati: US National Institutes of Health
Genome-wide association study identifies 30 loci associated with bipolar disorder
EA Stahl, G Breen, AJ Forstner, A McQuillin, S Ripke, V Trubetskoy, ...
Nature genetics 51 (5), 793-803, 2019
Mandati: Swiss National Science Foundation, US National Institutes of Health …
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
Mandati: US National Institutes of Health, Swedish Research Council, UK Medical …
Psychiatric genetics: progress amid controversy
M Burmeister, MG McInnis, S Zöllner
Nature Reviews Genetics 9 (7), 527-540, 2008
Mandati: US National Institutes of Health
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
Psychiatric GWAS Consortium Coordinating Committee
American Journal of Psychiatry 166 (5), 540-556, 2009
Mandati: US National Institutes of Health
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
Mandati: US National Institutes of Health, National Health and Medical Research …
Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression
RC Culverhouse, NL Saccone, AC Horton, Y Ma, KJ Anstey, ...
Molecular psychiatry 23 (1), 133-142, 2018
Mandati: US National Institutes of Health, Australian Research Council, National …
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry
LJ Scott, P Muglia, XQ Kong, W Guan, M Flickinger, R Upmanyu, F Tozzi, ...
Proceedings of the National Academy of Sciences 106 (18), 7501-7506, 2009
Mandati: US National Institutes of Health
Genome-wide association scan for five major dimensions of personality
A Terracciano, S Sanna, M Uda, B Deiana, G Usala, F Busonero, ...
Molecular psychiatry 15 (6), 647-656, 2010
Mandati: US National Institutes of Health
New insights into the genetics of addiction
MD Li, M Burmeister
Nature Reviews Genetics 10 (4), 225-231, 2009
Mandati: US National Institutes of Health
Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delay
M Kim, E Sandford, D Gatica, Y Qiu, X Liu, Y Zheng, BA Schulman, J Xu, ...
elife 5, e12245, 2016
Mandati: US Department of Energy, US National Institutes of Health, Howard Hughes …
Mutations in KCND3 cause spinocerebellar ataxia type 22
YC Lee, A Durr, K Majczenko, YH Huang, YC Liu, CC Lien, PC Tsai, ...
Annals of neurology 72 (6), 859-869, 2012
Mandati: US National Institutes of Health
Impulsiveness and insula activation during reward anticipation are associated with genetic variants in GABRA2 in a family sample enriched for alcoholism
S Villafuerte, MM Heitzeg, S Foley, WY Wendy Yau, K Majczenko, ...
Molecular psychiatry 17 (5), 511-519, 2012
Mandati: US National Institutes of Health
The genetics of the mood disorder spectrum: genome-wide association analyses of more than 185,000 cases and 439,000 controls
JRI Coleman, HA Gaspar, J Bryois, EM Byrne, AJ Forstner, PA Holmans, ...
Biological psychiatry 88 (2), 169-184, 2020
Mandati: US National Institutes of Health, National Health and Medical Research …
Review and consensus on pharmacogenomic testing in psychiatry
CA Bousman, SA Bengesser, KJ Aitchison, AT Amare, H Aschauer, ...
Pharmacopsychiatry 54 (01), 5-17, 2021
Mandati: US National Institutes of Health, European Commission, Federal Ministry of …
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects
E Seong, R Insolera, M Dulovic, EJ Kamsteeg, J Trinh, N Brüggemann, ...
Annals of neurology 83 (6), 1075-1088, 2018
Mandati: US National Institutes of Health, European Commission, Netherlands …
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