Results 81 to 90 of about 228 (131)

Transcriptional subtyping explains phenotypic variability in genetic subtypes of autism spectrum disorder. [PDF]

Dev Psychopathol, 2020
Trinh S, Arnett A, Kurtz-Nelson E, Beighley J, Picoto M, Bernier R.   +5 more
europepmc   +1 more source

Spatiotemporal dynamics of ethylene biosynthesis shape infection and nodule initiation in Medicago truncatula. [PDF]

Plant Cell
Müller S, Stegmann T, Adema K, Holmer R, van Seters A, van Velzen R, Kulikova O, Wijsman T, Klein J, Fernandez-Moreno JP, Stepanova AN, Alonso JM, Franssen H, Larrainzar E, van Zeijl A, Kohlen W.   +15 more
europepmc   +1 more source

Genomic Exploration of Essential Hypertension in African-Brazilian Quilombo Populations: A Comprehensive Approach With Pedigree Analysis and Family-Based Association Studies. [PDF]

J Am Heart Assoc
Borges VM, Horimoto ARVR, Wijsman EM, Kimura L, Nunes K, Nato AQ, Mingroni-Netto RC.   +6 more
europepmc   +1 more source

Stress Accelerates Depressive-Like Behaviors through Increase of Notch2 Expression in N141I Mutation Presenilin-2 Transgenic Mice. [PDF]

Biomol Ther (Seoul)
Yoo SS, Gu SM, Nam KT, Choi JS, Lee YS, Yeo IJ, Yu JE, Kim S, Lee DW, Ham HJ, Chang JY, Yun J, Son DJ, Han SB, Hong JT.   +14 more
europepmc   +1 more source

Enhancing physical activity in older type 2 diabetic adults through remote patient monitoring: a pre-post study in Taiwan. [PDF]

PeerJ
Lin CF, Chang HM, Hsu CY, Yang CT, Lin SY.   +4 more
europepmc   +1 more source

CWAS-Plus: estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data. [PDF]

Brief Bioinform
Kim Y, Jeong M, Koh IG, Kim C, Lee H, Kim JH, Yurko R, Kim IB, Park J, Werling DM, Sanders SJ, An JY.   +11 more
europepmc   +1 more source

Genetic Analysis Workshop 19: methods and strategies for analyzing human sequence and gene expression data in extended families and unrelated individuals. [PDF]

BMC Proc, 2016
Engelman CD, Greenwood CM, Bailey JN, Cantor RM, Kent JW, König IR, Bermejo JL, Melton PE, Santorico SA, Schillert A, Wijsman EM, MacCluer JW, Almasy L.   +12 more
europepmc   +1 more source

De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types. [PDF]

Mol Autism, 2020
Chen S, Wang J, Cicek E, Roeder K, Yu H, Devlin B.   +5 more
europepmc   +1 more source

Structural models of genome-wide covariance identify multiple common dimensions in autism. [PDF]

Nat Commun
de Hoyos L, Barendse MT, Schlag F, van Donkelaar MMJ, Verhoef E, Shapland CY, Klassmann A, Buitelaar J, Verhulst B, Fisher SE, Rai D, St Pourcain B.   +11 more
europepmc   +1 more source

Structural models of genome-wide covariance identify multiple common dimensions in autism

, 2022
de Hoyos L, Barendse MT, Schlag F, van Donkelaar MM, Verhoef E, Shapland CY, Klassmann A, Buitelaar J, Verhulst B, Fisher SE, Rai D, Pourcain BS.   +11 more
europepmc   +1 more source