Volume 140, Issue 5

Search all Human Genetics articles

May 2021

Special Topic on The Human Microbiome and Genetic Disease

Issue Editor:

Huiying Zhao

11 articles in this issue

The human microbiome and genetic disease: towards the integration of metagenomic and multi-omics data
Huiying Zhao
Editorial 30 March 2021 Pages: 701 - 702
Part of 2 collections:

The human microbiome and genetic disease

The human microbiome and genetic disease
Gut microbiota in inflammatory bowel diseases: moving from basic science to clinical applications
Valerie Collij
Marjolein A. Y. Klaassen
Arnau Vich Vila
Perspective Open access 28 August 2020 Pages: 703 - 708
Part of 2 collections:

The human microbiome and genetic disease

The human microbiome and genetic disease
The role of the gut microbiome in graft fibrosis after pediatric liver transplantation
Tian Qin
Jingyuan Fu
Henkjan J. Verkade
Review Open access 13 September 2020 Pages: 709 - 724
Part of 2 collections:

The human microbiome and genetic disease

The human microbiome and genetic disease
The microbiome, genetics, and gastrointestinal neoplasms: the evolving field of molecular pathological epidemiology to analyze the tumor–immune–microbiome interaction
Kosuke Mima
Keisuke Kosumi
Shuji Ogino
Review 12 November 2020 Pages: 725 - 746
Part of 2 collections:

The human microbiome and genetic disease

The human microbiome and genetic disease
The relationship between the gut microbiome and host gene expression: a review
Robert G. Nichols
Emily R. Davenport
Review Open access 22 November 2020 Pages: 747 - 760
Part of 2 collections:

The human microbiome and genetic disease

The human microbiome and genetic disease
Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia
Ting Guo
Chao-Feng Tu
Hong Luo
Original Investigation 03 January 2021 Pages: 761 - 773
Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier
Jesper Eisfeldt
Maria Pettersson
Anna Lindstrand
Original Investigation Open access 14 December 2020 Pages: 775 - 790
Loss of PIGK function causes severe infantile encephalopathy and extensive neuronal apoptosis
Xin Chen
Wu Yin
Lingqian Wu
Original Investigation 04 January 2021 Pages: 791 - 803
Missense3D-DB web catalogue: an atom-based analysis and repository of 4M human protein-coding genetic variants
Tarun Khanna
Gordon Hanna
Alessia David
Original Investigation Open access 27 January 2021 Pages: 805 - 812
RET compound inheritance in Chinese patients with Hirschsprung disease: lack of penetrance from insufficient gene dysfunction
Qian Jiang
Yang Wang
Long Li
Original Investigation 12 January 2021 Pages: 813 - 825
Alternative splicing in normal and pathological human placentas is correlated to genetic variants
Camino S. M. Ruano
Clara Apicella
Daniel Vaiman
Original Investigation Open access 12 January 2021 Pages: 827 - 848

Volume 140, Issue 5

The human microbiome and genetic disease: towards the integration of metagenomic and multi-omics data

Gut microbiota in inflammatory bowel diseases: moving from basic science to clinical applications

The role of the gut microbiome in graft fibrosis after pediatric liver transplantation

The microbiome, genetics, and gastrointestinal neoplasms: the evolving field of molecular pathological epidemiology to analyze the tumor–immune–microbiome interaction

The relationship between the gut microbiome and host gene expression: a review

Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia

Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier

Loss of PIGK function causes severe infantile encephalopathy and extensive neuronal apoptosis

Missense3D-DB web catalogue: an atom-based analysis and repository of 4M human protein-coding genetic variants

RET compound inheritance in Chinese patients with Hirschsprung disease: lack of penetrance from insufficient gene dysfunction

Alternative splicing in normal and pathological human placentas is correlated to genetic variants

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