Articoli con mandati relativi all'accesso pubblico - Michael P. EpsteinUlteriori informazioni
TotaleNIHVAMRCNHMRCWellcomeDFGGatesGovernment of SpainHHMICIHRNIHRSNSFFWONSFAHANSERCAcademy of FinlandAlzheimers's UKBHFNRFEuropean CommissionBMBFPCORIMichael J Fox FoundationFRQSGenome CanadaHRBBreast Cancer Now, UKCancer Research UKFNRState of CalifoniaUK Research & InnovationTUBITAKAutism Speaks Inc, USAJDRFLeducq Foundation, USAMedical Research Future Fund, Australia
Non disponibili pubblicamente: 3
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes
SW Curtis, JC Carlson, TH Beaty, JC Murray, SM Weinberg, ML Marazita, ...
Human genetics 142 (10), 1531-1541, 2023
Mandati: US National Institutes of Health
Familial aggregation of seizure outcomes in four familial epilepsy cohorts
CA Ellis, D Tu, KL Oliver, HC Mefford, WA Hauser, J Buchhalter, ...
Epilepsia, 2024
Mandati: National Health and Medical Research Council, Australia
The role of copy number variants in the genetic architecture of common familial epilepsies
Epi4K Consortium, EP Almanza Fuerte, J Nguyen, M Mehaffey, A Sulovari, ...
Epilepsia 65 (3), 792-804, 2024
Mandati: Howard Hughes Medical Institute
Disponibili pubblicamente: 125
Association of FKBP5 polymorphisms and childhood abuse with risk of posttraumatic stress disorder symptoms in adults
EB Binder, RG Bradley, W Liu, MP Epstein, TC Deveau, KB Mercer, ...
Jama 299 (11), 1291-1305, 2008
Mandati: Howard Hughes Medical Institute
De novo mutations in epileptic encephalopathies
Nature 501 (7466), 217-221, 2013
Mandati: US National Institutes of Health
Powerful SNP-set analysis for case-control genome-wide association studies
MC Wu, P Kraft, MP Epstein, DM Taylor, SJ Chanock, DJ Hunter, X Lin
The American Journal of Human Genetics 86 (6), 929-942, 2010
Mandati: US National Institutes of Health
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies
S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ...
The American Journal of Human Genetics 95 (4), 360-370, 2014
Mandati: US National Institutes of Health
De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies
S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ...
American journal of human genetics 95 (4), 360-370, 2014
Mandati: US National Institutes of Health
Testing in microbiome-profiling studies with MiRKAT, the microbiome regression-based kernel association test
N Zhao, J Chen, IM Carroll, T Ringel-Kulka, MP Epstein, H Zhou, JJ Zhou, ...
The American Journal of Human Genetics 96 (5), 797-807, 2015
Mandati: US National Institutes of Health
De novo mutations in SLC1A2 and CACNA1A are important causes of epileptic encephalopathies
CT Myers, JM McMahon, AL Schneider, S Petrovski, AS Allen, GL Carvill, ...
The American Journal of Human Genetics 99 (2), 287-298, 2016
Mandati: US National Institutes of Health
Accounting for population stratification in DNA methylation studies
RT Barfield, LM Almli, V Kilaru, AK Smith, KB Mercer, R Duncan, ...
Genetic epidemiology 38 (3), 231-241, 2014
Mandati: US National Institutes of Health
Integrating human brain proteomes with genome-wide association data implicates new proteins in Alzheimer’s disease pathogenesis
AP Wingo, Y Liu, ES Gerasimov, J Gockley, BA Logsdon, DM Duong, ...
Nature genetics 53 (2), 143-146, 2021
Mandati: US National Institutes of Health, US Department of Veterans Affairs …
Pilot study of dietary phosphorus restriction and phosphorus binders to target fibroblast growth factor 23 in patients with chronic kidney disease
T Isakova, OM Gutiérrez, K Smith, M Epstein, LK Keating, H Jüppner, ...
Nephrology Dialysis Transplantation 26 (2), 584-591, 2011
Mandati: US National Institutes of Health
Ultra-rare genetic variation in common epilepsies: a case-control sequencing study
AS Allen, ST Bellows, SF Berkovic, J Bridgers, R Burgess, G Cavalleri, ...
The Lancet Neurology 16 (2), 135-143, 2017
Mandati: US National Institutes of Health, UK Medical Research Council
Tracking evolution of aromatase inhibitor resistance with circulating tumour DNA analysis in metastatic breast cancer
C Fribbens, IG Murillas, M Beaney, S Hrebien, B O’Leary, L Kilburn, ...
Annals of Oncology 29 (1), 145-153, 2018
Mandati: Breast Cancer Now, UK, Cancer Research UK, UK Medical Research Council …
Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice
LA Papale, B Beyer, JM Jones, LM Sharkey, S Tufik, M Epstein, VA Letts, ...
Human molecular genetics 18 (9), 1633-1641, 2009
Mandati: US National Institutes of Health
Brain proteome-wide association study implicates novel proteins in depression pathogenesis
TS Wingo, Y Liu, ES Gerasimov, J Gockley, BA Logsdon, DM Duong, ...
Nature neuroscience 24 (6), 810-817, 2021
Mandati: US National Institutes of Health, US Department of Veterans Affairs …
Genetic contributors to risk of schizophrenia in the presence of a 22q11. 2 deletion
I Cleynen, W Engchuan, MS Hestand, T Heung, AM Holleman, ...
Molecular psychiatry 26 (8), 4496-4510, 2021
Mandati: Swiss National Science Foundation, US National Institutes of Health …
Fibroblast growth factor 23 in patients undergoing peritoneal dialysis
T Isakova, H Xie, A Barchi-Chung, G Vargas, N Sowden, J Houston, ...
Clinical Journal of the American Society of Nephrology 6 (11), 2688-2695, 2011
Mandati: US National Institutes of Health
SNP set association analysis for familial data
ED Schifano, MP Epstein, LF Bielak, MA Jhun, SLR Kardia, PA Peyser, ...
Genetic epidemiology 36 (8), 797-810, 2012
Mandati: US National Institutes of Health
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