Of mice, men, and the genome

The utility of spectral karyotyping in the cytogenetic analysis of newly diagnosed pediatric acute lymphoblastic leukemia.

Leukemia·2002

[Chapters in the history of psychiatry in Israel and its surroundings: B). The Asfouriyeh hospital for the insane in Lebanon].

Harefuah·2001

Preponderance of thiopurine S-methyltransferase deficiency and heterozygosity among patients intolerant to mercaptopurine or azathioprine.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology·2001

The erroneous diagnosis of malingering in a military setting.

Military medicine·1996

[Misdiagnosis and labeling in psychiatry and their consequences: Part II].

Harefuah·1995

[Consequences of misdiagnosis and labeling in psychiatry].

Harefuah·1995

Bayesian inference of lineage trees by joint analysis of single-cell multimodal lineage-tracing data with BiLinT.

Genome research·2026

Nuclear mitochondrial sequences in great ape Telomere-to-Telomere genomes.

Genome research·2026

A biobank-scale method for learning modulators of gene-environment interaction underlying human complex traits from multiple environmental exposures.

Genome research·2026

Characterizing intra- and intertumor heterogeneity in ovarian high-grade serous carcinoma subtypes using single-cell and spatial transcriptomics.

Genome research·2026

Private information leakage from polygenic risk scores.

Genome research·2026

Massively parallel characterization of adolescent idiopathic scoliosis risk variants.

Genome research·2026

Wilson disease associated with a novel variant in the ATP7B gene.

Frontiers in neurology·2026

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Scientific reports·2026

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Journal of genetics and genomics = Yi chuan xue bao·2026

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Clinica chimica acta; international journal of clinical chemistry·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

The Journal of heredity·2026

Related Experiment Videos

Of mice, men, and the genome

Related Concept Videos

The utility of spectral karyotyping in the cytogenetic analysis of newly diagnosed pediatric acute lymphoblastic leukemia.

[Chapters in the history of psychiatry in Israel and its surroundings: B). The Asfouriyeh hospital for the insane in Lebanon].

Preponderance of thiopurine S-methyltransferase deficiency and heterozygosity among patients intolerant to mercaptopurine or azathioprine.

The erroneous diagnosis of malingering in a military setting.

[Misdiagnosis and labeling in psychiatry and their consequences: Part II].

[Consequences of misdiagnosis and labeling in psychiatry].

Bayesian inference of lineage trees by joint analysis of single-cell multimodal lineage-tracing data with BiLinT.

Nuclear mitochondrial sequences in great ape Telomere-to-Telomere genomes.

A biobank-scale method for learning modulators of gene-environment interaction underlying human complex traits from multiple environmental exposures.

Characterizing intra- and intertumor heterogeneity in ovarian high-grade serous carcinoma subtypes using single-cell and spatial transcriptomics.

Private information leakage from polygenic risk scores.

Massively parallel characterization of adolescent idiopathic scoliosis risk variants.

Wilson disease associated with a novel variant in the ATP7B gene.

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

Related Experiment Videos

Of mice, men, and the genome

Related Concept Videos

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