Finite-sample properties of family-based association tests

Measurement of the high-energy gamma-ray emission from the Moon with the Fermi Large Area Telescope.

Physical review. D. (2016)·2020

Observation of inverse Compton emission from a long γ-ray burst.

Nature·2019

Differential cannibalism and population dynamics in a host-parasitoid system.

Oecologia·2017

Suppression of Emittance Growth Using a Shaped Cold Atom Electron and Ion Source.

Physical review letters·2016

Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.

International journal of epidemiology·2015

Classification of neurological abnormalities in children with congenital melanocytic naevus syndrome identifies magnetic resonance imaging as the best predictor of clinical outcome.

The British journal of dermatology·2015

Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk.

American journal of human genetics·2026

Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditions.

American journal of human genetics·2026

RNA splicing evidence enables robust classification of BRCA1 exon 18 variants: Results from the ENIGMA consortium.

American journal of human genetics·2026

Distinct mutational landscapes for germline and somatic cancer variants in forty tumor suppressor genes.

American journal of human genetics·2026

Shared genetic basis and structure of syndromic and normal facial variation.

American journal of human genetics·2026

The Gabriella Miller Kids First Data Resource for genomic research in pediatric cancer and congenital anomalies.

American journal of human genetics·2026

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Science (New York, N.Y.)·2026

Related Experiment Videos

Finite-sample properties of family-based association tests

Related Concept Videos

Measurement of the high-energy gamma-ray emission from the Moon with the Fermi Large Area Telescope.

Observation of inverse Compton emission from a long γ-ray burst.

Differential cannibalism and population dynamics in a host-parasitoid system.

Suppression of Emittance Growth Using a Shaped Cold Atom Electron and Ion Source.

Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.

Classification of neurological abnormalities in children with congenital melanocytic naevus syndrome identifies magnetic resonance imaging as the best predictor of clinical outcome.

Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk.

Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditions.

RNA splicing evidence enables robust classification of BRCA1 exon 18 variants: Results from the ENIGMA consortium.

Distinct mutational landscapes for germline and somatic cancer variants in forty tumor suppressor genes.

Shared genetic basis and structure of syndromic and normal facial variation.

The Gabriella Miller Kids First Data Resource for genomic research in pediatric cancer and congenital anomalies.

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Related Experiment Videos

Finite-sample properties of family-based association tests

Related Concept Videos

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