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Microduplications of 16p11.2 are associated with schizophrenia.
Not available
S-EPMC2951180
|
biostudies-literature
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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.
Not available
S-EPMC4380508
|
biostudies-literature
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Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Not available
S-EPMC11646479
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biostudies-literature
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Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Not available
S-EPMC9980234
|
biostudies-literature
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Evaluation of appendicitis risk prediction models in adults with suspected appendicitis.
Not available
S-EPMC6972511
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biostudies-literature
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Extended pharmacological thromboprophylaxis and clinically relevant venous thromboembolism after major abdominal and pelvic surgery: international, prospective, propensity score-weighted cohort study.
Not available
S-EPMC11894929
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biostudies-literature
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SARS-CoV-2 vaccination modelling for safe surgery to save lives: data from an international prospective cohort study.
Not available
S-EPMC7995808
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biostudies-literature
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Timing of surgery following SARS-CoV-2 infection: an international prospective cohort study.
Not available
S-EPMC8206995
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biostudies-literature
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SARS-CoV-2 infection and venous thromboembolism after surgery: an international prospective cohort study.
Not available
S-EPMC8652887
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biostudies-literature
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Empagliflozin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial.
Not available
S-EPMC10957483
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biostudies-literature
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