GPCards: An integrated database of genotype–phenotype correlations in human genetic diseases-Reference-Cited by-同舟云学术

GPCards: An integrated database of genotype–phenotype correlations in human genetic diseases

Published:2021 Issue: Volume:19 Page:1603-1611
ISSN:2001-0370
Container-title:Computational and Structural Biotechnology Journal
language:en
Short-container-title:Computational and Structural Biotechnology Journal

Author:

Li Bin,Wang Zheng,Chen Qian,Li Kuokuo,Wang Xiaomeng,Wang Yijing,Zeng Qian,Han Ying,Lu Bin,Zhao Yuwen^ORCID,Zhang Rui,Jiang Li,Pan Hongxu,Luo Tengfei,Zhang Yi,Fang Zhenghuan,Xiao Xuewen,Zhou Xun,Wang Rui,Zhou Lu,Wang Yige,Yuan Zhenhua,Xia Lu,Guo Jifeng,Tang Beisha,Xia Kun,Zhao Guihu,Li Jinchen

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Computer Science Applications,Genetics,Biochemistry,Structural Biology,Biophysics,Biotechnology

Reference80 articles.

1. Toward clinical implementation of next-generation sequencing-based genetic testing in rare diseases: where are we?;Liu;Trends Genet,2019

2. Advancements in next-generation sequencing;Levy;Annu Rev Genomics Hum Genet,2016

3. NGS technologies as a turning point in rare disease research, diagnosis and treatment;Fernandez-Marmiesse;Curr Med Chem,2018

4. A comprehensive global genotype-phenotype database for rare diseases;Trujillano;Mol Genet Genomic Med,2017

5. Next-generation sequencing approach for the diagnosis of human diseases: open challenges and new opportunities;Di Resta;EJIFCC,2018

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. From uncertain to certain—how to proceed with variants of uncertain significance;Middle East Fertility Society Journal;2024-08-16

2. Genetic Transformer: An Innovative Large Language Model Driven Approach for Rapid and Accurate Identification of Causative Variants in Rare Genetic Diseases;2024-07-19

3. Prevalence of comorbidities in individuals with neurodevelopmental disorders from the aggregated phenomics data of 51,227 pediatric individuals;Nature Medicine;2024-05-14

4. Bioinformatics Databases and Tools for Analysis of Multi-omics;Multi-Omics Analysis of the Human Microbiome;2024

5. PhenomAD-NDD: the Phenomics Aggregation Database of comorbidities in 51,227 pediatric individuals with NeuroDevelopmental Disorders;2023-11-30