The emergence of genotypic divergence and future precision medicine applications
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Elsevier
Reference140 articles.
1. Clinical and molecular characterisation of Bardet-Biedl syndrome in consanguineous populations: the power of homozygosity mapping;Abu Safieh;J Med Genet,2010
2. In search of triallelism in Bardet-Biedl syndrome;Abu-Safieh;Eur J Hum Genet,2012
3. Potential oligogenic disease of mental retardation, short stature, spastic paraparesis, and osteopetrosis;Alsemari;Appl Clin Genet,2018
4. De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy;Ambrosino;Ann Neurol,2018
5. Interpretation of risk loci from genome-wide association studies of Alzheimer's disease;Andrews;Lancet Neurol,2020
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1. How do stochastic processes and genetic threshold effects explain incomplete penetrance and inform causal disease mechanisms?;Philosophical Transactions of the Royal Society B: Biological Sciences;2024-03-04
2. How do stochastic processes and genetic threshold effects explain incomplete penetrance and inform causal disease mechanisms?;2023-10-06
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