Original Research

Published on 02 May 2022

Pan-Cancer Study of SHC-Adaptor Protein 1 (SHC1) as a Diagnostic, Prognostic and Immunological Biomarker in Human Cancer

in Human and Medical Genomics

Jianlin Chen
Gan Gao
Limin Li
Junping Ding
Xianhua Chen
Jianfei Lei
Haihua Long
Lihua Wu
Xin Long
Lian He

Frontiers in Genetics

doi 10.3389/fgene.2022.817118

5,232 views
14 citations

Original Research

Published on 29 Apr 2022

Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in Newborns

in Human and Medical Genomics

Jiale Xiang
Hongfu Zhang
Xiangzhong Sun
Junqing Zhang
Zhenpeng Xu
Jun Sun
Zhiyu Peng

Frontiers in Genetics

doi 10.3389/fgene.2022.883617

2,910 views
3 citations

Brief Research Report

Published on 28 Apr 2022

Pinpointing the Geographic Origin of 165-Year-Old Human Skeletal Remains Found in Punjab, India: Evidence From Mitochondrial DNA and Stable Isotope Analysis

in Human and Medical Genomics

J.S. Sehrawat
Shailesh Agrawal
Deeksha Sankhyan
Monika Singh
Sachin Kumar
Satya Prakash
Richa Rajpal
Gyaneshwer Chaubey
Kumarasamy Thangaraj
Niraj Rai

Frontiers in Genetics

doi 10.3389/fgene.2022.813934

14,627 views
5 citations

Brief Research Report

Published on 27 Apr 2022

A View on Genomic Medicine Activities in Africa: Implications for Policy

in Human and Medical Genomics

C. Victor Jongeneel
Maritha J. Kotze
Archana Bhaw-Luximon
Faisal M. Fadlelmola
Yasmina J. Fakim
Yosr Hamdi
Samar Kamal Kassim
Judit Kumuthini
Victoria Nembaware
Fouzia Radouani

Frontiers in Genetics

doi 10.3389/fgene.2022.769919

4,332 views
17 citations

Original Research

Published on 27 Apr 2022

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

in Human and Medical Genomics

Brittan Armstrong
Kurt D. Christensen
Casie A. Genetti
Richard B. Parad
Jill Oliver Robinson
Carrie L. Blout Zawatsky
Bethany Zettler
Alan H. Beggs
Ingrid A. Holm
Robert C. Green

Frontiers in Genetics

doi 10.3389/fgene.2022.867371

5,960 views
35 citations

Case Report

Published on 27 Apr 2022

Case Report: A Novel Homozygous Frameshift Mutation of the SKIV2L Gene in a Trichohepatoenteric Syndrome Patient Presenting With Short Stature, Premature Ovarian Failure, and Osteoporosis

in Human and Medical Genomics

Minyi Yang
Yu Jiang
Xinyu Shao

Frontiers in Genetics

doi 10.3389/fgene.2022.879899

2,251 views
4 citations

Original Research

Published on 27 Apr 2022

Incomplete Penetrance of Population-Based Genetic Screening Results in Electronic Health Record

in Human and Medical Genomics

Gai Elhanan
Daniel Kiser
Iva Neveux
Shaun Dabe
Alexandre Bolze
William J. Metcalf
James T. Lu
Joseph J. Grzymski

Frontiers in Genetics

doi 10.3389/fgene.2022.866169

3,493 views
6 citations

Review

Published on 26 Apr 2022

Molecular Mechanisms of Isolated Polycystic Liver Diseases

in Human and Medical Genomics

Ziqi Yu
Xiang Shen
Chong Hu
Jun Zeng
Aiyao Wang
Jianyong Chen

Frontiers in Genetics

doi 10.3389/fgene.2022.846877

3,260 views
4 citations

Original Research

Published on 26 Apr 2022

Assessing the Potential Prognostic and Immunological Role of TK1 in Prostate Cancer

in Human and Medical Genomics

Hui Xie
Linpei Guo
Zhun Wang
Shuanghe Peng
Qianwang Ma
Zhao Yang
Zhiqun Shang
Yuanjie Niu

Frontiers in Genetics

doi 10.3389/fgene.2022.778850

4,878 views
9 citations

Original Research

Published on 26 Apr 2022

Characterization of the Ferroptosis-Related Genes for Prognosis and Immune Infiltration in Low-Grade Glioma

in Human and Medical Genomics

Xiuwei Yan
Hang Ji
Zhihui Liu
Shuai Ma
Jiawei Dong
Xiaoyan Jiang
Xueyan Hu
Fang Wang
Hongtao Zhao
Jiaqi Jin

Frontiers in Genetics

doi 10.3389/fgene.2022.880864

3,140 views
1 citation

Original Research

Published on 26 Apr 2022

A Polygenic Score for Type 2 Diabetes Improves Risk Stratification Beyond Current Clinical Screening Factors in an Ancestrally Diverse Sample

in Human and Medical Genomics

James R. Ashenhurst
Olga V. Sazonova
Olivia Svrchek
Stacey Detweiler
Ryosuke Kita
Liz Babalola
Matthew McIntyre
Stella Aslibekyan
Pierre Fontanillas
Suyash Shringarpure

Frontiers in Genetics

doi 10.3389/fgene.2022.871260

7,486 views
12 citations

Original Research

Published on 26 Apr 2022

Novel Prognostic Signature for Acute Myeloid Leukemia: Bioinformatics Analysis of Combined CNV-Driven and Ferroptosis-Related Genes

in Human and Medical Genomics

Chunjiao Han
Jiafeng Zheng
Fangfang Li
Wei Guo
Chunquan Cai

Frontiers in Genetics

doi 10.3389/fgene.2022.849437

5,308 views
11 citations

Mini Review

Published on 26 Apr 2022

Organoids as Model Systems to Investigate Circadian Clock-Related Diseases and Treatments

in Human and Medical Genomics

Suengwon Lee
Christian I. Hong

Frontiers in Genetics

doi 10.3389/fgene.2022.874288

5,314 views
2 citations

Perspective

Published on 26 Apr 2022

Reaching for Precision Healthcare in Finland via Use of Genomic Data

in Human and Medical Genomics

Tiina Wahlfors
Birgit Simell
Kati Kristiansson
Sirpa Soini
Terhi Kilpi
Marina Erhola
Markus Perola

Frontiers in Genetics

doi 10.3389/fgene.2022.877891

2,910 views
2 citations

Original Research

Published on 25 Apr 2022

Pathway-Based Analysis Revealed the Role of Keap1-Nrf2 Pathway and PI3K-Akt Pathway in Chinese Esophageal Squamous Cell Carcinoma Patients With Definitive Chemoradiotherapy

in Human and Medical Genomics

Honghai Dai
Yanjun Wei
Yunxia Liu
Jingwen Liu
Ruoying Yu
Junli Zhang
Jiaohui Pang
Yang Shao
Qiang Li
Zhe Yang

Frontiers in Genetics

doi 10.3389/fgene.2021.799663

3,240 views
3 citations

Original Research

Published on 25 Apr 2022

Primary Care Implementation of Genomic Population Health Screening Using a Large Gene Sequencing Panel

in Human and Medical Genomics

Robert S. Wildin
Christine A. Giummo
Aaron W. Reiter
Thomas C. Peterson
Debra G. B. Leonard

Frontiers in Genetics

doi 10.3389/fgene.2022.867334

3,839 views
5 citations

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Articles

Pan-Cancer Study of SHC-Adaptor Protein 1 (SHC1) as a Diagnostic, Prognostic and Immunological Biomarker in Human Cancer

Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in Newborns

Pinpointing the Geographic Origin of 165-Year-Old Human Skeletal Remains Found in Punjab, India: Evidence From Mitochondrial DNA and Stable Isotope Analysis

A View on Genomic Medicine Activities in Africa: Implications for Policy

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

Case Report: A Novel Homozygous Frameshift Mutation of the SKIV2L Gene in a Trichohepatoenteric Syndrome Patient Presenting With Short Stature, Premature Ovarian Failure, and Osteoporosis

Incomplete Penetrance of Population-Based Genetic Screening Results in Electronic Health Record

Molecular Mechanisms of Isolated Polycystic Liver Diseases

Assessing the Potential Prognostic and Immunological Role of TK1 in Prostate Cancer

Characterization of the Ferroptosis-Related Genes for Prognosis and Immune Infiltration in Low-Grade Glioma

A Polygenic Score for Type 2 Diabetes Improves Risk Stratification Beyond Current Clinical Screening Factors in an Ancestrally Diverse Sample

Novel Prognostic Signature for Acute Myeloid Leukemia: Bioinformatics Analysis of Combined CNV-Driven and Ferroptosis-Related Genes

Organoids as Model Systems to Investigate Circadian Clock-Related Diseases and Treatments

Reaching for Precision Healthcare in Finland via Use of Genomic Data

Pathway-Based Analysis Revealed the Role of Keap1-Nrf2 Pathway and PI3K-Akt Pathway in Chinese Esophageal Squamous Cell Carcinoma Patients With Definitive Chemoradiotherapy

Primary Care Implementation of Genomic Population Health Screening Using a Large Gene Sequencing Panel