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Phelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoring.
Not available
S-EPMC4362650
|
biostudies-literature
Cite
Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.
Not available
S-EPMC4673986
|
biostudies-literature
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Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women.
Not available
S-EPMC5785705
|
biostudies-literature
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A genome-wide scan for common alleles affecting risk for autism.
Not available
S-EPMC2947401
|
biostudies-literature
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Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p.
Not available
S-EPMC9649437
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biostudies-literature
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A genome-wide linkage and association scan reveals novel loci for autism.
Not available
S-EPMC2772655
|
biostudies-literature
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Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.
Not available
S-EPMC7034316
|
biostudies-literature
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Convergent genetic and expression data implicate immunity in Alzheimer's disease.
Not available
S-EPMC4672734
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biostudies-literature
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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Not available
S-EPMC5737772
|
biostudies-literature
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Distinct genetic liability profiles define clinically relevant patient strata across common diseases.
Not available
S-EPMC11217418
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biostudies-literature
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