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Human Genetics and Genomics Advances

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Evolving with you

Introducing Human Genetics and Genomics Advances

Cover image volume 3, Issue 3

14 July 2022

Volume 3, Issue 3

Table of Contents

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Abstract Image

Article

The genetic architecture of Alzheimer disease risk in the Ohio and Indiana Amish

Osterman et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100114

Article

Improving polygenic prediction with genetically inferred ancestry

Naret et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100109

Article

Translating principles of precision medicine into speech-language pathology: Clinical trial of a proactive speech and language intervention for infants with classic galactosemia

Peter et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100119

Latest Content

Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3

Nair et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100122

A probable cis-acting genetic modifier of Huntington disease frequent in individuals with African ancestry

Dawson et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100130

Prevalence, parameters, and pathogenic mechanisms for splice-altering acceptor variants that disrupt the AG exclusion zone

Bryen et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100125

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A Mendelian randomization-based exploration of red blood cell distribution width and mean corpuscular volume with risk of hemorrhagic strokes

Liu et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100135

Assessing Vietnamese American patient perspectives on population genetic testing in primary care: a community engaged approach

Lemke et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100134

Developmental genomics of congenital limb malformations: further indication of allelic series in association with gene dosage effects that contribute to the variability of phenotypes

Duan et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100132

Omics-informed CNV calls reduce false positive rate and improve power for CNV-trait associations

Lepamets et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100133

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An LDLR missense variant poses high risk of familial hypercholesterolemia in 30% of Greenlanders and offers potential of early cardiovascular disease intervention

Jørsboe et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100118

Polynomial Mendelian randomization reveals non-linear causal effects for obesity-related traits

Sulc et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100124

The genetic architecture of Alzheimer disease risk in the Ohio and Indiana Amish

Osterman et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100114

Improving polygenic prediction with genetically inferred ancestry

Naret et al.

DOI: https://doi.org/10.1016/j.xhgg.2022.100109

Human Genetics and Genomics Advances2666-2477 (online)

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