Related Experiment Videos
Increased rate of twins among affected sibling pairs with autism
American Journal of Human Genetics
|April 16, 2002
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder.
medRxiv : the preprint server for health sciences·2026
Deleterious coding variation associated with autism is shared across ancestries.
Nature medicine·2026
Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations.
medRxiv : the preprint server for health sciences·2025
Characterization of cornea donors at a tissue center in the city of Medellin, Colombia.
Cell and tissue banking·2023
Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.
American journal of human genetics·2026
Beyond exons: Linking noncoding heritability and polygenicity across complex human traits and disorders.
American journal of human genetics·2026
Phenome- and laboratory-wide meta-analyses of sickle cell trait reveal multi-system disease associations.
American journal of human genetics·2026
Mutation rate heterogeneity biases variant effect prediction and reveals genuine mutational robustness.
American journal of human genetics·2026
A phenotypic paradigm for cerebral palsy genetics.
American journal of human genetics·2026
Androgens mediate sexual dimorphism in Pilarowski-Bjornsson syndrome.
American journal of human genetics·2026
Widespread male-female expression imbalance of X-linked genes across phrynosomatid lizards.
Molecular biology and evolution·2026
Multimodal quantitative MRI finds early brain changes in asymptomatic X-linked adrenoleukodystrophy.
Brain communications·2026
Fatal ascending aortic dissection in a 12-year-old boy with previously undiagnosed Loeys-Dietz syndrome: A molecular autopsy case.
Legal medicine (Tokyo, Japan)·2026
LINE-1 repeats are a defining feature of the Xce.
Proceedings of the National Academy of Sciences of the United States of America·2026