![Haplotype Diversity and Linkage Disequilibrium at Human G6PD: Recent Origin of Alleles That Confer Malarial Resistance | Science Haplotype Diversity and Linkage Disequilibrium at Human G6PD: Recent Origin of Alleles That Confer Malarial Resistance | Science](https://www.science.org/cms/10.1126/science.1061573/asset/ba5040a5-089e-435e-b8be-a534e3779a11/assets/graphic/se2719485001.jpeg)
Haplotype Diversity and Linkage Disequilibrium at Human G6PD: Recent Origin of Alleles That Confer Malarial Resistance | Science
![JPM | Free Full-Text | Targeted RNAseq Improves Clinical Diagnosis of Very Early-Onset Pediatric Immune Dysregulation JPM | Free Full-Text | Targeted RNAseq Improves Clinical Diagnosis of Very Early-Onset Pediatric Immune Dysregulation](https://pub.mdpi-res.com/jpm/jpm-12-00919/article_deploy/html/images/jpm-12-00919-g003.png?1654070461)
JPM | Free Full-Text | Targeted RNAseq Improves Clinical Diagnosis of Very Early-Onset Pediatric Immune Dysregulation
![A coding mutation within the first exon of the human MD-2 gene results in decreased lipopolysaccharide-induced signaling | Genes & Immunity A coding mutation within the first exon of the human MD-2 gene results in decreased lipopolysaccharide-induced signaling | Genes & Immunity](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsj.gene.6364068/MediaObjects/41435_2004_Article_BF6364068_Fig1_HTML.jpg)
A coding mutation within the first exon of the human MD-2 gene results in decreased lipopolysaccharide-induced signaling | Genes & Immunity
![Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles - ScienceDirect Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0002929718302039-gr1.jpg)
Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles - ScienceDirect
![JPM | Free Full-Text | Targeted RNAseq Improves Clinical Diagnosis of Very Early-Onset Pediatric Immune Dysregulation JPM | Free Full-Text | Targeted RNAseq Improves Clinical Diagnosis of Very Early-Onset Pediatric Immune Dysregulation](https://pub.mdpi-res.com/jpm/jpm-12-00919/article_deploy/html/images/jpm-12-00919-g004.png?1654070458)
JPM | Free Full-Text | Targeted RNAseq Improves Clinical Diagnosis of Very Early-Onset Pediatric Immune Dysregulation
![eQTL Catalogue: a compendium of uniformly processed human gene expression and splicing QTLs | bioRxiv eQTL Catalogue: a compendium of uniformly processed human gene expression and splicing QTLs | bioRxiv](https://www.biorxiv.org/content/biorxiv/early/2021/01/09/2020.01.29.924266/F1.large.jpg)
eQTL Catalogue: a compendium of uniformly processed human gene expression and splicing QTLs | bioRxiv
![Structural Basis of Huntingtin Fibril Polymorphism Revealed by Cryogenic Electron Microscopy of Exon 1 HTT Fibrils | Journal of the American Chemical Society Structural Basis of Huntingtin Fibril Polymorphism Revealed by Cryogenic Electron Microscopy of Exon 1 HTT Fibrils | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.2c00509/asset/images/large/ja2c00509_0006.jpeg)
Structural Basis of Huntingtin Fibril Polymorphism Revealed by Cryogenic Electron Microscopy of Exon 1 HTT Fibrils | Journal of the American Chemical Society
![Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis | Translational Psychiatry Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis | Translational Psychiatry](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41398-022-02014-9/MediaObjects/41398_2022_2014_Fig1_HTML.png)