[HTML][HTML] Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan

B Franke, G Michelini, P Asherson… - European …, 2018 - Elsevier
Attention-deficit/hyperactivity disorder (ADHD) is highly heritable and the most common
neurodevelopmental disorder in childhood. In recent decades, it has been appreciated that …

Molecular genetic testing and the future of clinical genomics

SH Katsanis, N Katsanis - Nature Reviews Genetics, 2013 - nature.com
Genomic technologies are reaching the point of being able to detect genetic variation in
patients at high accuracy and reduced cost, offering the promise of fundamentally altering …

Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

J O'Rawe, T Jiang, G Sun, Y Wu, W Wang, J Hu… - Genome medicine, 2013 - Springer
Background To facilitate the clinical implementation of genomic medicine by next-generation
sequencing, it will be critically important to obtain accurate and consistent variant calls on …

Moving towards causality in attention-deficit hyperactivity disorder: overview of neural and genetic mechanisms

EF Gallo, J Posner - The Lancet Psychiatry, 2016 - thelancet.com
Attention-deficit hyperactivity disorder (ADHD) is a neurodevelopmental disorder
characterised by developmentally inappropriate levels of inattention and hyperactivity or …

[图书][B] Neurobiology of attention

L Itti, G Rees, JK Tsotsos - 2005 - books.google.com
A key property of neural processing in higher mammals is the ability to focus resources by
selectively directing attention to relevant perceptions, thoughts or actions. Research into …

The molecular genetic architecture of attention deficit hyperactivity disorder

Z Hawi, TDR Cummins, J Tong, B Johnson, R Lau… - Molecular …, 2015 - nature.com
Attention deficit hyperactivity disorder (ADHD) is a common childhood behavioral condition
which affects 2–10% of school age children worldwide. Although the underlying molecular …

Exome sequencing: dual role as a discovery and diagnostic tool

CS Ku, DN Cooper, C Polychronakos… - Annals of …, 2012 - Wiley Online Library
Recent developments in high‐throughput sequence capture methods and next‐generation
sequencing technologies have now made exome sequencing a viable approach to …

Molecular genetic studies of ADHD and its candidate genes: a review

Z Li, S Chang, L Zhang, L Gao, J Wang - Psychiatry research, 2014 - Elsevier
Attention-deficit/hyperactivity disorder (ADHD) is a common childhood-onset psychiatric
disorder with high heritability. In recent years, numerous molecular genetic studies have …

Next‐generation sequencing: ready for the clinics?

AN Desai, A Jere - Clinical genetics, 2012 - Wiley Online Library
Desai AN, Jere A. Next‐generation sequencing: ready for the clinics? Next‐generation
sequencing (NGS) has transformed genomic research by decreasing the cost of sequencing …

The Wilms Tumor Gene, Wt1, Is Critical for Mouse Spermatogenesis via Regulation of Sertoli Cell Polarity and Is Associated with Non-Obstructive Azoospermia in …

XN Wang, ZS Li, Y Ren, T Jiang, YQ Wang… - PLoS …, 2013 - journals.plos.org
Azoospermia is one of the major reproductive disorders which cause male infertility in
humans; however, the etiology of this disease is largely unknown. In the present study, six …