Report of the committee on human gene mapping by recombinant DNA techniques

Evidence for HTR1A and LHPP as interacting genetic risk factors in major depression.

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Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis.

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Variants in Apaf-1 segregating with major depression promote apoptosome function.

Molecular psychiatry·2005

Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation.

Journal of medical genetics·2004

Identification of a common variant in the lipoprotein lipase gene in a large Utah kindred ascertained for coronary heart disease: the -93G/D9N variant predisposes to low HDL-C/high triglycerides.

Clinical genetics·2001

A candidate prostate cancer susceptibility gene at chromosome 17p.

Nature genetics·2001

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Birth defects original article series·1996

Multisite neural tube closure in humans.

Birth defects original article series·1996

Comprehensive analysis of non-synonymous single-nucleotide polymorphism of human TSC1 and TSC2 genes: An in silico approach.

PloS one·2026

Genome-wide candidate signatures of divergent selection between broody Silkie and White Leghorn chickens revealed by high-density SNP genotyping.

British poultry science·2026

Successful radiofrequency catheter ablation of right-sided focal atrial tachycardia in a patient with Holt-Oram syndrome: a case report.

Frontiers in cardiovascular medicine·2026

SNP genotyping in Pseudotsuga menziesii and Pinus radiata using targeted genotyping-by-sequencing (GBS): improved Bayesian SNP calling using a beta-binomial distribution and other optimized input parameters.

BMC genomics·2026

Causal Effects of Lipoproteins and Lipids on Atrial Fibrillation: A Mendelian Randomization Study.

Lipids·2026

Dissecting the shared genetic architecture and biological mechanisms linking sleep traits and suicide attempts: from variants to genes.

Molecular psychiatry·2026

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Report of the committee on human gene mapping by recombinant DNA techniques

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Evidence for HTR1A and LHPP as interacting genetic risk factors in major depression.

Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis.

Variants in Apaf-1 segregating with major depression promote apoptosome function.

Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation.

Identification of a common variant in the lipoprotein lipase gene in a large Utah kindred ascertained for coronary heart disease: the -93G/D9N variant predisposes to low HDL-C/high triglycerides.

A candidate prostate cancer susceptibility gene at chromosome 17p.

Limb anomalies from evolutionary, developmental, and genetic perspectives.

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Genome-wide candidate signatures of divergent selection between broody Silkie and White Leghorn chickens revealed by high-density SNP genotyping.

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SNP genotyping in Pseudotsuga menziesii and Pinus radiata using targeted genotyping-by-sequencing (GBS): improved Bayesian SNP calling using a beta-binomial distribution and other optimized input parameters.

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Report of the committee on human gene mapping by recombinant DNA techniques

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