Medical genetic services in 31 countries: an overview

First Evidence for Mixing-Induced CP Violation in B_{s}^{0}→J/ψϕ(1020) Decays in pp Collisions at sqrt[s]=13 TeV.

Physical review letters·2026

Measurement of D^{0} Meson Photoproduction in Ultraperipheral Heavy Ion Collisions.

Physical review letters·2026

Observation of Coherent ϕ(1020) Meson Photoproduction in Ultraperipheral PbPb Collisions at sqrt[s_{NN}]=5.36 TeV.

Physical review letters·2026

Search for New Physics in Jet Multiplicity Patterns of Multilepton Events at sqrt[s]=13 TeV.

Physical review letters·2025

Search for the Rare Decay D^{0}→μ^{+}μ^{-} in Proton-Proton Collisions at sqrt[s]=13.6 TeV.

Physical review letters·2025

Observation of Λ Hyperon Local Polarization in p-Pb Collisions at sqrt[s_{NN}]=8.16 TeV.

Physical review letters·2025

Holding the story, holding the professional: a pilot study of genetic counselling supervision in Portugal.

European journal of human genetics : EJHG·2026

An episignature informed systematic analysis to ascertain the clinical significance and consequences of CHD8 missense variants.

European journal of human genetics : EJHG·2026

Rapid genomic sequencing in the NICU: Who to test and why.

European journal of human genetics : EJHG·2026

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

European journal of human genetics : EJHG·2026

Patients' and parents' views on how digital tools enable personalized and partnered care in genetics: a qualitative study.

European journal of human genetics : EJHG·2026

To screen or not to screen G6PD deficiency in gNBS: insights from the BabyDetect pilot and current evidence.

European journal of human genetics : EJHG·2026

Nucleation-dependent propagation of Polycomb modifications emerges during the Drosophila maternal to zygotic transition.

eLife·2026

Epigenetic-proteomic network crosstalk at birth across HLA risk groups in type 1 diabetes.

Frontiers in immunology·2026

Polygenic Risk Scores in Cardiovascular Prevention: Clinical Promise, Implementation Challenges, and Genomic Risk Stewardship.

Cureus·2026

ADAMTS18 as a candidate gene linking social stress and depression: a cross-species study in African wild dogs (Lycaon pictus) and humans.

Frontiers in behavioral neuroscience·2026

DNMT1 as an environmental sensor: epigenetic pathways linking environmental exposures, sex hormone signaling, and vulnerability to neurodevelopmental and neurodegenerative diseases.

Frontiers in neurology·2026

Pulmonary Manifestations of Birt-Hogg-Dubé Syndrome: A Single-Centre Retrospective Case Series of Seven Genetically Confirmed Patients.

Journal of clinical medicine·2026

Related Experiment Videos

Medical genetic services in 31 countries: an overview

Related Concept Videos

First Evidence for Mixing-Induced CP Violation in B_{s}^{0}→J/ψϕ(1020) Decays in pp Collisions at sqrt[s]=13 TeV.

Measurement of D^{0} Meson Photoproduction in Ultraperipheral Heavy Ion Collisions.

Observation of Coherent ϕ(1020) Meson Photoproduction in Ultraperipheral PbPb Collisions at sqrt[s_{NN}]=5.36 TeV.

Search for New Physics in Jet Multiplicity Patterns of Multilepton Events at sqrt[s]=13 TeV.

Search for the Rare Decay D^{0}→μ^{+}μ^{-} in Proton-Proton Collisions at sqrt[s]=13.6 TeV.

Observation of Λ Hyperon Local Polarization in p-Pb Collisions at sqrt[s_{NN}]=8.16 TeV.

Holding the story, holding the professional: a pilot study of genetic counselling supervision in Portugal.

An episignature informed systematic analysis to ascertain the clinical significance and consequences of CHD8 missense variants.

Rapid genomic sequencing in the NICU: Who to test and why.

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

Patients' and parents' views on how digital tools enable personalized and partnered care in genetics: a qualitative study.

To screen or not to screen G6PD deficiency in gNBS: insights from the BabyDetect pilot and current evidence.

Nucleation-dependent propagation of Polycomb modifications emerges during the Drosophila maternal to zygotic transition.

Epigenetic-proteomic network crosstalk at birth across HLA risk groups in type 1 diabetes.

Polygenic Risk Scores in Cardiovascular Prevention: Clinical Promise, Implementation Challenges, and Genomic Risk Stewardship.

ADAMTS18 as a candidate gene linking social stress and depression: a cross-species study in African wild dogs (Lycaon pictus) and humans.

DNMT1 as an environmental sensor: epigenetic pathways linking environmental exposures, sex hormone signaling, and vulnerability to neurodevelopmental and neurodegenerative diseases.

Pulmonary Manifestations of Birt-Hogg-Dubé Syndrome: A Single-Centre Retrospective Case Series of Seven Genetically Confirmed Patients.

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Medical genetic services in 31 countries: an overview

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