about
Advancing paternal age is associated with deficits in social and exploratory behaviors in the offspring: a mouse model.Regional differences in mitochondrial DNA methylation in human post-mortem brain tissue.Allelic skewing of DNA methylation is widespread across the genome.Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's diseaseEnvironmental risk, Oxytocin Receptor Gene (OXTR) methylation and youth callous-unemotional traits: a 13-year longitudinal study.Methylomic trajectories across human fetal brain development.DNA methylation at the Igf2/H19 imprinting control region is associated with cerebellum mass in outbred miceTissue-specific patterns of allelically-skewed DNA methylation.DNA methylation in interleukin-11 predicts clinical response to antidepressants in GENDEPTranscriptomic changes in the frontal cortex associated with paternal age.Variation in 5-hydroxymethylcytosine across human cortex and cerebellum.Neonatal DNA methylation and early-onset conduct problems: A genome-wide, prospective study.Increased DNA methylation near TREM2 is consistently seen in the superior temporal gyrus in Alzheimer's disease brain.Effects of advanced paternal age on trajectories of social behavior in offspring.Genetic differences in cytochrome P450 enzymes and antidepressant treatment response.Genetic predictors of increase in suicidal ideation during antidepressant treatment in the GENDEP project.Moderation of antidepressant response by the serotonin transporter gene.Interaction between serotonin transporter gene variants and life events predicts response to antidepressants in the GENDEP project.Genetic predictors of response to antidepressants in the GENDEP project.Epigenetics and DNA methylomic profiling in Alzheimer's disease and other neurodegenerative diseases.Advanced paternal age is associated with altered DNA methylation at brain-expressed imprinted loci in inbred mice: implications for neuropsychiatric disease.Blood methylomic signatures of presymptomatic dementia in elderly subjects with type 2 diabetes mellitus.CYP2C19 genotype predicts steady state escitalopram concentration in GENDEP.No association between genetic markers in BDNF gene and lithium prophylaxis in a Greek sampleEpigenetics and Chronic Diseases: An Overview
P50
Q33521226-C1AEB165-3E45-4EDB-A825-87D7822FF5A5Q33634725-EBA27B88-FB10-47F3-8F7C-E2AD39A245A8Q33645884-178FA8D1-18A8-4F05-9FAB-3F64A5619907Q34433837-86EE4F84-BECD-4E41-BBCC-38D1AEA0AE15Q34507551-8B3F3EBC-4013-4495-8BD0-D64D04D575E0Q35157209-5F6B2878-2DA0-4B2B-BEB4-5B205A22710AQ36521372-78FB4C4E-1D98-49A6-9792-4528AECCF07BQ36838971-0827C658-95DD-415F-B425-D935937248BEQ37201357-F9FBBD73-C34C-4884-A1A2-30E72A64932BQ37720547-9479542C-0349-4193-9EDE-3C46F7E855D9Q38524768-F246214A-5CFD-4411-AC26-F2FB5A4B7DBAQ38735767-5D2D6472-CE0E-4092-86AC-A4D460639004Q39492108-64F4E8AE-99BC-4F68-901E-CD456289D877Q41652282-44A52724-BE6A-40B4-BB8E-E6AB2D86D1D8Q45729383-B240B80C-5BBD-4DDF-9C0A-836014FD797EQ45916412-F4A3EC0B-1867-4946-9DCB-4B1314F035E4Q45945437-BF0588DC-36A3-44CF-9869-B7B0F070F490Q46036202-16DFB09D-683E-4EA7-A731-261691DF1841Q46051862-935ACA76-8323-4A89-8DE0-7841094838C1Q47647776-C6A95CB1-F91F-4281-AA90-216DE0E2E846Q48460645-5A89D096-528A-42DC-83A2-1C57817459CEQ49165122-3D759501-82C4-4CF7-9A53-644AEBE5F7CEQ50786670-AEAE1C7B-4CAC-4637-A262-3EB0B7F3BE3DQ56988477-BB7BF966-BE84-4106-BD86-89F07360E447Q60641813-EAE3AA53-2688-46D1-8080-B9E409F56AA2
P50
description
hulumtuese
@sq
researcher
@en
հետազոտող
@hy
name
Rebecca Smith
@ast
Rebecca Smith
@en
Rebecca Smith
@es
Rebecca Smith
@nl
Rebecca Smith
@sl
রেবেকা স্মিথ
@bn
type
label
Rebecca Smith
@ast
Rebecca Smith
@en
Rebecca Smith
@es
Rebecca Smith
@nl
Rebecca Smith
@sl
রেবেকা স্মিথ
@bn
altLabel
R G Smith
@en
Rebecca G Smith
@en
prefLabel
Rebecca Smith
@ast
Rebecca Smith
@en
Rebecca Smith
@es
Rebecca Smith
@nl
Rebecca Smith
@sl
রেবেকা স্মিথ
@bn
P1053
C-1978-2012
P106
P21
P31
P3829
P496
0000-0001-9264-1056