Burden Test | List of Frontiers open access articles

Original Research

Published on 15 Jun 2021

Revisiting an Expression Dataset of Discordant Inflammatory Bowel Disease Twin Pairs Using a Mutation Burden Test Reveals CYP2C18 as a Novel Marker

in Computational Genomics

Juan Du
Jie Yin
Haojie Du
Jiawei Zhang

Frontiers in Genetics

doi 10.3389/fgene.2021.680125

4,409 views
10 citations

Original Research

Published on 15 Sep 2020

Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences

in Genetics of Common and Rare Diseases

Roozbeh Manshaei
Daniele Merico
Miriam S. Reuter
Worrawat Engchuan
Bahareh A. Mojarad
Rajiv Chaturvedi
Tracy Heung
Giovanna Pellecchia
Mehdi Zarrei
Thomas Nalpathamkalam

Frontiers in Genetics

doi 10.3389/fgene.2020.00957

11,752 views
37 citations

Original Research

Published on 15 Jun 2022

The Involvement of ALPK3 in Hypertrophic Cardiomyopathy in East Asia

in Gene and Cell Therapy

Jiaqi Dai
Ke Li
Man Huang
Yang Sun
Hao Liu
Zongzhe Li
Peng Chen
Hong Wang
Dongyang Wu
Yanghui Chen

Frontiers in Medicine

doi 10.3389/fmed.2022.915649

5,051 views
14 citations

Original Research

Published on 02 Jul 2021

Bronchopulmonary Dysplasia Predicted by Developing a Machine Learning Model of Genetic and Clinical Information

in Genetics of Common and Rare Diseases

Dan Dai
Huiyao Chen
Xinran Dong
Jinglong Chen
Mei Mei
Yulan Lu
Lin Yang
Bingbing Wu
Yun Cao
Jin Wang

Frontiers in Genetics

doi 10.3389/fgene.2021.689071

6,635 views
47 citations

Original Research

Published on 07 Mar 2023

Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders

in Neurogenomics

Hosneara Akter
Muhammad Mizanur Rahman
Shaoli Sarker
Mohammed Basiruzzaman
Md. Mazharul Islam
Md. Atikur Rahaman
Md. Ashiquir Rahaman
Tamannyat Binte Eshaque
Nushrat Jahan Dity
Shouvik Sarker

Frontiers in Genetics

doi 10.3389/fgene.2023.955631

12,263 views
16 citations

Original Research

Published on 13 Sep 2023

Rare variants in complement system genes associate with endothelial damage after pediatric allogeneic hematopoietic stem cell transplantation

in Alloimmunity and Transplantation

Lilli Leimi
Jessica R. Koski
Outi Kilpivaara
Kim Vettenranta
A. Inkeri Lokki
Seppo Meri

Frontiers in Immunology

doi 10.3389/fimmu.2023.1249958

3,540 views
4 citations

Articles

Revisiting an Expression Dataset of Discordant Inflammatory Bowel Disease Twin Pairs Using a Mutation Burden Test Reveals CYP2C18 as a Novel Marker

Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences

The Involvement of ALPK3 in Hypertrophic Cardiomyopathy in East Asia

Bronchopulmonary Dysplasia Predicted by Developing a Machine Learning Model of Genetic and Clinical Information

Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders

Rare variants in complement system genes associate with endothelial damage after pediatric allogeneic hematopoietic stem cell transplantation