Related Experiment Videos
Dissecting the genetic contribution to coronary heart disease
American Journal of Human Genetics
|December 1, 1991
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Relative influence of heritability, environment and genetics on serum sclerostin.
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2013
Localization of a major susceptibility locus influencing preterm birth.
Molecular human reproduction·2013
Genetic analysis of serum osteocalcin and bone mineral in multigenerational Afro-Caribbean families.
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2011
Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes.
Molecular psychiatry·2011
Genetic analysis of vertebral trabecular bone density and cross-sectional area in older men.
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2010
The Gabriella Miller Kids First Data Resource for genomic research in pediatric cancer and congenital anomalies.
American journal of human genetics·2026
Shared inheritance reveals landscape of somatic and germline cancer risk in TP53.
American journal of human genetics·2026
Examining gaps in institutional policies for clinical genomic data sharing: A cross-jurisdictional study.
American journal of human genetics·2026
Anthropometric and cardio-metabolic trait variation and genetic associations in sub-Saharan Africa.
American journal of human genetics·2026
Systematic and proactive evaluation of AIRE missense variant effects.
American journal of human genetics·2026
Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.
American journal of human genetics·2026
QTL mapping.
Genetics·2026
Genetic Insights Into Retinitis Pigmentosa: A De Novo RPGR Mutation in an Iranian-Azeri Family.
Case reports in ophthalmological medicine·2026
Altered thalamo-prefrontal synchrony dynamics during spatial working memory task performance in a SETD1A loss-of-function mouse model of schizophrenia predisposition.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology·2026
Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.
Italian journal of pediatrics·2026