Results 101 to 110 of about 1,649 (150)

The Genus <i>Petunia</i> (Solanaceae): Evolutionary Synthesis and Taxonomic Review. [PDF]

Plants (Basel)
Soares LS, Stehmann JR, Freitas LB.
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

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

Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders. [PDF]

Hum Genet, 2016
Truong DT, Shriberg LD, Smith SD, Chapman KL, Scheer-Cohen AR, DeMille MM, Adams AK, Nato AQ, Wijsman EM, Eicher JD, Gruen JR.   +10 more
europepmc   +1 more source

GIGI: an approach to effective imputation of dense genotypes on large pedigrees. [PDF]

Am J Hum Genet, 2013
Cheung CY, Thompson EA, Wijsman EM.
europepmc   +1 more source