Last Posted: Mar 28, 2020
- Epigenetic Therapeutics for Cardiovascular Disease- Writing, Erasing, Reading, and Maybe Forgetting
J Plutzky, JAMA, March 27, 2020 - Re-evaluating the first-tier status of fragile X testing in neurodevelopmental disorders.
Borch Lauren A et al. Genetics in medicine : official journal of the American College of Medical Genetics 2020 Mar - Genetic counsellors in a multidisciplinary model of clinical genetics and hereditary cancer.
López-Fernández Adrià et al. Medicina clinica 2020 Mar - Perceived utility of biological testing for autism spectrum disorder is associated with child and family functioning.
Yusuf Afiqah et al. Research in developmental disabilities 2020 Feb 100103605 - Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use.
Husson Thomas et al. Translational psychiatry 2020 Feb 10(1) 77 - Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways.
Aldosary Mazhor et al. Omics : a journal of integrative biology 2020 Feb - Identification of newborns at risk for autism using electronic medical records and machine learning.
Rahman Rayees et al. European psychiatry : the journal of the Association of European Psychiatrists 2020 Feb 63(1) e22 - Towards the automatic detection of social biomarkers in autism spectrum disorder: introducing the simulated interaction task (SIT)
H Drimalla et al, NPJ Digital Medicine, February 27, 2020 - Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy.
Backenroth Daniel et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 21(6) 1390-1399 - Utility of a ready-to-use PCR system for neuroendocrine tumor diagnosis.
Kidd Mark et al. PloS one 2019 14(6) e0218592
.png)
No hay comentarios:
Publicar un comentario