Genetic studies in intellectual disability and related disorders

By L. Vissers, C. Gilissen, J. Veltman. Nature reviews genetics, 2015

695 citations recorded by the source corpus.

Subfields: Genetics

View Paper: https://www.semanticscholar.org/paper/928a764528335b8a821c0df5089c90dcbd779298

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In Genetics

1. Nick V. Grishin
2. Lisa N. Kinch
3. Zbyszek Otwinowski
4. Jimin Pei

Citations in the corpus

• Mutation severity spectrum of rare alleles in the human genome is predictive of disease type (2019, background): “Association of rare and de novo mutations to common and rare diseases could be unveiled through familial or trio studies that are facilitated by genome or exome sequencing nowadays [16, 17].”