Genetic determinism and the overprotection of human subjects

Pre-conception 25-hydroxyvitamin D (25(OH)D) and fecundability.

Human reproduction (Oxford, England)·2019

A Population-Based Study of Effects of Genetic Loci on Orofacial Clefts.

Journal of dental research·2017

Offspring birthweight by gestational age and parental cardiovascular mortality: a population-based cohort study.

BJOG : an international journal of obstetrics and gynaecology·2017

Ultrasound prediction of perinatal outcome: the unrecognised value of sibling data.

BJOG : an international journal of obstetrics and gynaecology·2014

Length of human pregnancy and contributors to its natural variation.

Human reproduction (Oxford, England)·2013

Association between inhibited binding of folic acid to folate receptor alpha in maternal serum and folate-related birth defects in Norway.

Human reproduction (Oxford, England)·2011

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

Nature genetics·2026

Multiancestry genome-wide association and multiomics analyses elucidate spatiocellular features of multiple sclerosis genetics.

Nature genetics·2026

Scalable, generalizable and uncertainty-aware integration of spatial multiomics across diverse modalities and platforms with SCIGMA.

Nature genetics·2026

Spatiotemporal lineage tracing reveals the dynamic spatial architecture of tumor growth and metastasis.

Nature genetics·2026

A single-cell atlas of multiple myeloma defines malignant archetypes and proliferative states.

Nature genetics·2026

Mechanisms and functional implications of long-range enhancer-dependent gene regulation.

Nature genetics·2026

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Research (Washington, D.C.)·2026

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Clinical case reports·2026

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Journal of human genetics·2026

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Psychiatric genetics·2026

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Frontiers in genetics·2026

Related Experiment Videos

Genetic determinism and the overprotection of human subjects

Related Concept Videos

Pre-conception 25-hydroxyvitamin D (25(OH)D) and fecundability.

A Population-Based Study of Effects of Genetic Loci on Orofacial Clefts.

Offspring birthweight by gestational age and parental cardiovascular mortality: a population-based cohort study.

Ultrasound prediction of perinatal outcome: the unrecognised value of sibling data.

Length of human pregnancy and contributors to its natural variation.

Association between inhibited binding of folic acid to folate receptor alpha in maternal serum and folate-related birth defects in Norway.

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

Multiancestry genome-wide association and multiomics analyses elucidate spatiocellular features of multiple sclerosis genetics.

Scalable, generalizable and uncertainty-aware integration of spatial multiomics across diverse modalities and platforms with SCIGMA.

Spatiotemporal lineage tracing reveals the dynamic spatial architecture of tumor growth and metastasis.

A single-cell atlas of multiple myeloma defines malignant archetypes and proliferative states.

Mechanisms and functional implications of long-range enhancer-dependent gene regulation.

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Related Experiment Videos

Genetic determinism and the overprotection of human subjects

Related Concept Videos

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