Apparent bias toward long gene misregulation in MeCP2 syndromes disappears after controlling for baseline variations
Ayush T. Raman(National Institutes of Health), Zhandong Liu(Baylor College of Medicine)
Cited by 44
Related Papers
Complement C3aR Inactivation Attenuates Tau Pathology and Reverses an Immune Network Deregulated in Tauopathy Models and Alzheimer’s Disease
|Neuron|2018|525
A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases
|Cell|2014|396
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome
|The American Journal of Human Genetics|2017|223
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females
|The American Journal of Human Genetics|2021|90