Results 201 to 210 of about 337,686 (261)

Shared genetics between ADHD and reading/language abilities: Genome‐wide correlations, stratified enrichment, cross‐trait association, and mendelian randomization

JCPP Advances, EarlyView.
Abstract Background Attention‐deficit/hyperactivity disorder (ADHD) and language/reading difficulties frequently co‐occur. The extent of shared genetic architecture remains incompletely defined. We investigated genome‐wide overlap between ADHD and four core skills: word reading, nonword reading, spelling, and phoneme awareness.
Jinzhu Zhao, Shi Huang, Wei Liu, Feng Wang, Hong Qian, Xiaolin Hu   +5 more
wiley   +1 more source

Genetic composition of Kazakh horses of Zhabe type evaluated by SNP genotyping. [PDF]

Heliyon
Pozharskiy A, Beishova I, Nametov A, Shamshidin A, Ulyanova T, Kovalchuk A, Ulyanov V, Shamekova M, Bekova G, Gritsenko D.   +9 more
europepmc   +1 more source

Targeted genome-wide SNP genotyping in feral horses using non-invasive fecal swabs. [PDF]

Conserv Genet Resour, 2022
Gavriliuc S, Reza S, Jeong C, Getachew F, McLoughlin PD, Poissant J.   +5 more
europepmc   +1 more source

Multivariate genetic analyses test for the presence of a general ‘n’ factor underlying neurodevelopmental conditions

JCPP Advances, EarlyView.
Abstract Background Neurodevelopmental conditions often emerge early in life and have substantial genetic influences. There are significant genetic correlations between neurodevelopmental conditions, such as between autism spectrum disorder (Autism) and attention deficit‐hyperactivity disorder (ADHD), and they are listed together in diagnostic manuals.
Morgan James Morgan, Margherita Malanchini, Elise B. Robinson, Angelica Ronald   +3 more
wiley   +1 more source

Shared genetic and molecular architecture between neurodevelopmental disorders and type 1 diabetes

Journal of Intelligent Medicine, EarlyView.
Abstract Epidemiological and clinical studies have suggested possible associations between type 1 diabetes (T1D) and neurodevelopmental disorders (NDDs), but these relationships remain inconsistent across disorders and populations. To clarify whether such mixed findings, we investigated the genetic architecture linking T1D with autism spectrum disorder
Jingxuan Zhang, Zhentao Zhou, Lirong Zhu, Wei Liu   +3 more
wiley   +1 more source

Development of SNP genotyping assays for heading date in rice. [PDF]

Breed Sci
Kitazawa N, Shomura A, Mizubayashi T, Ando T, Hayashi N, Yabe S, Matsubara K, Ebana K, Yamanouchi U, Fukuoka S.   +9 more
europepmc   +1 more source

The Swedish Arctic Fox Project: 40 years of research in ecology and conservation

The Journal of Wildlife Management, EarlyView.
The 4 central research themes in The Swedish Arctic Fox Project and key deliverables for practical conservation achieved over 4 decades. Abstract The scientific community widely recognizes the value of long‐term studies, especially those with individual‐level resolution; however, maintaining a consecutive data series is associated with multiple ...
Anders Angerbjörn, Julie Bommerlund, Christopher A. Cockerill, Love Dalén, Bodil Elmhagen, Rasmus Erlandsson, Malin Hasselgren, Peter Hellström, Malin Larm, Karin Norén, Magnus Tannerfeldt, Johan Wallén   +11 more
wiley   +1 more source

Optimization of Whole-Genome Resequencing Depth for High-Throughput SNP Genotyping in Litopenaeus vannamei. [PDF]

Int J Mol Sci
Lin P, Yu Y, Bao Z, Li F.
europepmc   +1 more source

Effect of COMT and UGT1A Variants on Clinical Response to Opicapone in Parkinson's Disease

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Parkinson's disease (PD) is the second most common neurodegenerative disease. Symptomatic treatment is based on dopaminergic replacement. With disease progression, the initial benefit of levodopa becomes inconsistent, and motor complications emerge.
Elena Ojeda‐Lepe, Sergio García‐Díaz, Laura Muñoz‐Delgado, Miguel Martín‐Bórnez, Silvia Jesús, Dolores Buiza‐Rueda, Marta Bonilla‐Toribio, Rafael Díaz‐Belloso, Daniel Macías‐García, Astrid Adarmes‐Gómez, Antonio Luque‐Ambrosiani, Rocío Pineda‐Sánchez, Lorena Clavijo‐Jiménez, Fátima Carrillo‐García, Pilar Gómez‐Garre, Pablo Mir   +15 more
wiley   +1 more source

Genetic diversity and population structure in Ethiopian mustard (Brassica carinata A. Braun) revealed by high-density DArTSeq SNP genotyping. [PDF]

BMC Genomics
Ambaw YD, Abitea AG, Olango TM.
europepmc   +1 more source