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Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns.
Not available
S-EPMC6559955
|
biostudies-literature
Cite
Identifying the Common Genetic Basis of Antidepressant Response.
Not available
S-EPMC9117153
|
biostudies-literature
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Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data.
Not available
S-EPMC4392068
|
biostudies-literature
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Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data.
Not available
S-EPMC6848993
|
biostudies-literature
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CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Not available
S-EPMC6218476
|
biostudies-literature
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Variation in Initial U.S. Hospital Responses to the Coronavirus Disease 2019 Pandemic.
Not available
S-EPMC8217146
|
biostudies-literature
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Organization of Outpatient Care After COVID-19 Hospitalization.
Not available
S-EPMC8801392
|
biostudies-literature
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Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects.
Not available
S-EPMC5392243
|
biostudies-literature
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Effect of Vitamin C, Thiamine, and Hydrocortisone on Ventilator- and Vasopressor-Free Days in Patients With Sepsis: The VICTAS Randomized Clinical Trial.
Not available
S-EPMC7903252
|
biostudies-literature
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Large-scale discovery of novel genetic causes of developmental disorders.
Not available
S-EPMC5955210
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biostudies-literature
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