New mechanisms for genetic disease and nontraditional modes of inheritance

Preservation of erniettomorph fossils in clay-rich siliciclastic deposits from the Ediacaran Wood Canyon Formation, Nevada.

Interface focus·2020

The early history of Pallister-Hall syndrome-Buried treasure of a sort.

Gene·2016

Biliglobulin: a new look at IgA.

Immunology today·2014

Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype.

Clinical genetics·2013

Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability.

Clinical genetics·2012

Absence of binding of alpha-bungarotoxin and cobra neurotoxin to central acetylcholine receptors - an autoradiographic study.

Neuroscience letters·2009

Reducing Restraint Use in the Pediatric Agitated Patient: A Review of Approaches and Best Practices.

Advances in pediatrics·2026

Pain Management in Pediatric Patients with Sickle Cell Disease.

Advances in pediatrics·2026

Updates in Adolescent Contraception.

Advances in pediatrics·2026

Climate Stewardship in the Clinical Setting.

Advances in pediatrics·2026

Management of Foreign Bodies: Beads, Coins, and Magnets.

Advances in pediatrics·2026

Approach to a Child with Gait Disturbances.

Advances in pediatrics·2026

Beyond in silico prediction: multi-omics to identify a pathogenic deep intronic HNRNPK variant in Au-Kline syndrome.

Journal of human genetics·2026

Phenotypes of Hereditary Diseases Associated With Rauch-Steindl Syndrome.

Human mutation·2026

Multi-omics Mendelian Randomization Prioritizes Neutrophil Extracellular Trap-related Genes Associated with Atrial Fibrillation Risk.

Endocrine, metabolic & immune disorders drug targets·2026

Developmental and cellular vulnerabilities underlie genetic architecture of schizophrenia.

Molecular psychiatry·2026

Methodological frameworks to probe histone acetylation-driven circuit plasticity in SYNGAP1-associated neurodevelopmental disorders.

Methods in enzymology·2026

Exploring the genetic spectrum of parkinsonism in Brazil.

Parkinsonism & related disorders·2026

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New mechanisms for genetic disease and nontraditional modes of inheritance

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Preservation of erniettomorph fossils in clay-rich siliciclastic deposits from the Ediacaran Wood Canyon Formation, Nevada.

The early history of Pallister-Hall syndrome-Buried treasure of a sort.

Biliglobulin: a new look at IgA.

Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype.

Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability.

Absence of binding of alpha-bungarotoxin and cobra neurotoxin to central acetylcholine receptors - an autoradiographic study.

Reducing Restraint Use in the Pediatric Agitated Patient: A Review of Approaches and Best Practices.

Pain Management in Pediatric Patients with Sickle Cell Disease.

Updates in Adolescent Contraception.

Climate Stewardship in the Clinical Setting.

Management of Foreign Bodies: Beads, Coins, and Magnets.

Approach to a Child with Gait Disturbances.

Beyond in silico prediction: multi-omics to identify a pathogenic deep intronic HNRNPK variant in Au-Kline syndrome.

Phenotypes of Hereditary Diseases Associated With Rauch-Steindl Syndrome.

Multi-omics Mendelian Randomization Prioritizes Neutrophil Extracellular Trap-related Genes Associated with Atrial Fibrillation Risk.

Developmental and cellular vulnerabilities underlie genetic architecture of schizophrenia.

Methodological frameworks to probe histone acetylation-driven circuit plasticity in SYNGAP1-associated neurodevelopmental disorders.

Exploring the genetic spectrum of parkinsonism in Brazil.

Related Experiment Videos

New mechanisms for genetic disease and nontraditional modes of inheritance

Related Concept Videos

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