研飞ivySCI

研飞客户端支持数万种期刊查询，助你在阅读和写作中随时了解期刊动态

Genetic Testing and Molecular Biomarkers

短名	Genet. Test. Mol. Biomarkers.
Journal Impact	1.02
国际分区	GENETICS & HEREDITY(Q4)
期刊索引	SCI Q4中科院 4 区

ISSN	1945-0257, 1945-0265
h-index	53
国内分区	生物学(4区)生物学遗传学(4区)

《Genetic Testing and Molecular Biomarkers》是一本领先的同行评审期刊，涵盖人类基因检测的各个方面，包括分子生物标志物。该期刊为新技术的发展提供了一个重要的论坛，探讨了基因检测在临床决策中的应用，以及其伦理、法律、社会和经济方面的问题。此外，它还关注有效遗传咨询的相关议题。期刊的内容涉及基因测试的开发、执行和结果解释，服务于研究人员、临床医生和科学家。主要覆盖领域包括：- 整个生命周期的诊断 - 风险评估 - 个体和夫妇的携带者检测 - 人群基因检测的新方法和新仪器 - 分子、生化和细胞遗传学检测的结果 - 遗传咨询。

期刊主页投稿网址

阅读文献时，研飞即可帮你快速了解期刊，查询影响因子与分区，智能高亮期刊预警！

涉及主题	生物遗传学医学化学生物化学基因内科学基因型病理等位基因数学统计内分泌学单核苷酸多态性社会学心理学免疫学环境卫生人口学
出版信息	出版商: Mary Ann Liebert Inc.，出版周期: Bimonthly，期刊类型: journal
基本数据	创刊年份: 2009，原创研究文献占比: 93.75%，自引率:0.00%， Gold OA占比: 4.21%
平均审稿周期	网友分享经验：平均1.0个月
平均录用比例	网友分享经验：容易

期刊引文格式

这些示例是对学术期刊文章的引用，以及它们应该如何出现在您的参考文献中。

并非所有期刊都按卷和期组织其已发表的文章，因此这些字段是可选的。有些电子期刊不提供页面范围，而是列出文章标识符。在这种情况下，使用文章标识符而不是页面范围是安全的。

只有1位作者的期刊

有2位作者的期刊

有3位作者的期刊

有5位以上作者的期刊

书籍引用格式

以下是创作和编辑的书籍的参考文献的示例。

学位论文引用格式

网页引用格式

这些示例是对网页的引用，以及它们应该如何出现在您的参考文献中。

专利引用格式

手工熬夜修改参考文献？研飞自动匹配期刊，一键轻松成稿，支持 Word/WPS

点击下方按钮，免费开启试用！

Evaluation of Multigene Methylation for Blood-Based Detection of Colorectal Cancer

2024-9-23

Human Leukocyte Antigen-G Gene Polymorphism in Peninsular Malaysia: A Preliminary Report

2024-9-16

Relationship Between IL-10 Single Nucleotide Polymorphisms (rs1800871, rs1800872, and rs1800896) and the Severity of COVID-19

2024-9-10

Association Study of 3-untranslated region Haplotype of Human leukocyte antigen-G Gene with Lupus

2024-9-1

Kawasaki Disease: An update on Genetics and Pathophysiology

2024-8-26

A C->T Variation in 3′-Untranslated Region Elevates MED12 Protein Level in Breast Cancer That Relates to Better Prognosis

2024-8-22

Influence of TPMT and NUDT15 Genetic Polymorphisms on Mercaptopurine Pharmacokinetics in Healthy Volunteers

2024-8-1

Genomic Landscape of Osteosarcoma of Bone in an Older-Aged Patient Population and Analysis of Possible Etiologies Based on Molecular Signature

2024-7-25

Mannose-Binding Lectin Gene Variants as Disease Susceptibility Biomarkers in Rheumatoid Arthritis

2024-7-18

METTL5: A Potential Biomarker for Nonsmall Cell Lung Cancer That Promotes Cancer Cell Proliferation by Interacting with IGF2BP3

2024-7-18

Targeted Next-Generation Sequencing Analysis Reveals a Novel Genetic Variant in MYO6 Gene in an Indian Family with Postlingual Nonsyndromic Hearing Loss

2024-7-17

HFE and Non-HFE Hereditary Hemochromatosis Based on Screening of 854 Individuals: 12 Years of an Iranian Experience

2024-7-9

Association of ACTN4 Gene Mutation with Primary Nephrotic Syndrome in Children in Guangxi Autonomous Region, China

2024-7-1

The Association between Obesity Susceptibility and Polymorphisms of MC4R, SH2B1, and NEGR1 in Tibetans

2024-7-1

The Evaluation of the Genetic Variation Types of the Uridine Diphosphate Glucuronosyl Transferase 1A1 Gene by Next-Generation Sequencing and Their Effects on Bilirubin Levels in Obese Children

2024-6-25

High Frequency of Ancestral Haplotype A of Fatty Acid Desaturase Genes in the Yakut Population

2024-6-11

Identification of a Homozygous Mutation of CCDC40 in a Chinese Infertile Man with MMAF and PCD-like Phenotypes

2024-6-5

The 3′UTR Polymorphisms in the NLRP3 Gene Associated with the Risk of COPD and Their Putative Effects on the microRNA Mechanism

2024-5-17

Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome

2024-5-9

Aberrant Super-Enhancer Landscape in Enzalutamide-Resistant Prostate Cancer Cells

2024-5-9

Genetic Polymorphism of Interleukin-6 in Asymptomatic and ICU-Admitted COVID-19 Patients in Sulaymaniyah Province, Kurdistan Region of Iraq

2024-5-9

MTHFR 677C>T and 1298A>C Variants in Mothers of Infants with Down Syndrome from Western Mexico

2024-5-8

TP53-Mutated Myelodysplastic Syndrome: A Diagnostic Approach in Different Clinical Settings

2024-5-6

Association of Matrix Metalloproteinase-2 (MMP-2) and MMP-9 Promoter Variants, Their Serum Levels, and Activities with Aortic Valve Calcification (AVC) in a Population from Western Iran

2024-5-6

Association Study of Pleural Mesothelioma and Oncogenic Simian Virus 40 in the Crocidolite-Contaminated Area of Dayao County, Yunnan Province, Southwest China

2024-4-18

YKL-40 Knockdown Decreases Oxidative Stress Damage in Ovarian Granulosa Cells

2024-4-18

The Phenotypic Spectrum of Desanto–Shinawi Syndrome: A Comparative Report of the First Reported Case in Turkey

2024-4-13

VEGF-2578C/A, -460T/C Polymorphisms and Gastrointestinal Tract Cancer Risk: An Updated Meta-Analysis

2024-4-10

Expanding the Genetic Spectrum of AGXT Gene Variants in Egyptian Patients with Primary Hyperoxaluria Type I

2024-4-1

EGR3 Polymorphism Is a Potential Susceptibility Factor of Schizophrenia Risk in a Chinese Population

2024-4-1

The Association Between the 5-Hydroxytryptamine Receptor 2A Gene Variants rs6311 and rs6313 and Obstructive Sleep Apnea in the Iranian Kurdish Population

2024-4-1

Carrier Screening and Diagnosis for Spinal Muscular Atrophy Using Droplet Digital PCR Versus MLPA: Analytical Validation and Early Test Outcome

2024-3-27

Association Between Hashimoto's Thyroiditis and Rheumatoid Arthritis: A Bidirectional Mendelian Randomization Study

2024-3-20

Analysis of ceRNA Network and Identification of Potential Treatment Target and Biomarkers of Endothelial Cell Injury in Sepsis

2024-3-19

miR-107 and miR-126 and Risk of Breast Cancer: A Case–Control Study

2024-3-15

Ferroptosis-Related Genes Are Associated with Radioresistance and Immune Suppression in Head and Neck Cancer

2024-3-13

Association of TIMP2 418 G/C and MMP Gene Polymorphism with Risk of Urinary Cancers: Systematic Review and Meta-analysis

2024-3-13

Association of Tenascin-C Gene Polymorphisms with Risk of Acute Coronary Syndrome in South Indian Population: A Case−Control Genetic Association Study

2024-3-12

Identification of Coding Variants in 10q22.1 Associated with Vitiligo in the Chinese Han Population

2024-3-1

Correction to: The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis, by Hao Shen, et al. Genet Test Mol Biomarkers 2024; (vol. 28, no. 1; 33–38); doi: 10.1089/gtmb.2023.0307

2024-2-28

A New Era for Genetic Testing and Molecular Biomarkers

2024-2-15

Inflammatory Bowel Disease and Skin Cancer: A Two-Sample Mendelian Randomization Analysis

2024-2-15

Upregulation of Long Noncoding RNA PCAT1 in Iranian Patients with Colorectal Cancer and Its Performance as a Potential Diagnostic Biomarker

2024-2-1

Association of Interleukin-17A and Interleukin-17F Gene Polymorphisms with Atopic Dermatitis in Chinese Children

2024-2-1

Vitamin D Receptor Polymorphisms in a Spanish Cohort of Parkinson's Disease Patients

2024-2-1

Identification and Analysis of Gene Biomarkers for Ovarian Cancer

2024-2-1

Profiling of Long Non-Coding RNAs in Auricular Cartilage of Patients with Isolated Microtia

2024-2-1

Toward the Future: Perspectives on the Impacts of Genetic Testing and Biomarkers on Advancing Health Care

2024-1-1

Determination of the Relationship Between the Development and Recurrence of Subacute Thyroiditis and Human Leukocyte Antigen Subtypes

2024-1-1

EGLN1: A Biomarker of Poor Prognosis of Cervical Cancer and a Target of Treatment

2024-1-1

帮你贴心管理全部的文献
研飞ivySCI，高效的论文管理

投稿经验分享

分享我的经验，帮你走得更远

研飞客户端支持数万种期刊查询，助你在阅读和写作中随时了解期刊动态

Genetic Testing and Molecular Biomarkers

阅读文献时，研飞即可帮你快速了解期刊，查询影响因子与分区，智能高亮期刊预警！

期刊引文格式

只有1位作者的期刊

有2位作者的期刊

有3位作者的期刊

有5位以上作者的期刊

书籍引用格式

学位论文引用格式

网页引用格式

专利引用格式

手工熬夜修改参考文献？研飞自动匹配期刊，一键轻松成稿，支持 Word/WPS

最新文章

Evaluation of Multigene Methylation for Blood-Based Detection of Colorectal Cancer

Human Leukocyte Antigen-G Gene Polymorphism in Peninsular Malaysia: A Preliminary Report

Relationship Between IL-10 Single Nucleotide Polymorphisms (rs1800871, rs1800872, and rs1800896) and the Severity of COVID-19

Association Study of 3-untranslated region Haplotype of Human leukocyte antigen-G Gene with Lupus

Kawasaki Disease: An update on Genetics and Pathophysiology

A C-&gt;T Variation in 3′-Untranslated Region Elevates MED12 Protein Level in Breast Cancer That Relates to Better Prognosis

Influence of TPMT and NUDT15 Genetic Polymorphisms on Mercaptopurine Pharmacokinetics in Healthy Volunteers

Genomic Landscape of Osteosarcoma of Bone in an Older-Aged Patient Population and Analysis of Possible Etiologies Based on Molecular Signature

Mannose-Binding Lectin Gene Variants as Disease Susceptibility Biomarkers in Rheumatoid Arthritis

METTL5: A Potential Biomarker for Nonsmall Cell Lung Cancer That Promotes Cancer Cell Proliferation by Interacting with IGF2BP3

Targeted Next-Generation Sequencing Analysis Reveals a Novel Genetic Variant in <i>MYO6</i> Gene in an Indian Family with Postlingual Nonsyndromic Hearing Loss

<i>HFE</i> and Non-<i>HFE</i> Hereditary Hemochromatosis Based on Screening of 854 Individuals: 12 Years of an Iranian Experience

Association of <i>ACTN4</i> Gene Mutation with Primary Nephrotic Syndrome in Children in Guangxi Autonomous Region, China

The Association between Obesity Susceptibility and Polymorphisms of MC4R, SH2B1, and NEGR1 in Tibetans

The Evaluation of the Genetic Variation Types of the <i>Uridine Diphosphate Glucuronosyl Transferase 1A1</i> Gene by Next-Generation Sequencing and Their Effects on Bilirubin Levels in Obese Children

High Frequency of Ancestral Haplotype A of Fatty Acid Desaturase Genes in the Yakut Population

Identification of a Homozygous Mutation of CCDC40 in a Chinese Infertile Man with MMAF and PCD-like Phenotypes

The 3′UTR Polymorphisms in the <i>NLRP3</i> Gene Associated with the Risk of COPD and Their Putative Effects on the microRNA Mechanism

Novel <i>WFS1</i> Variants in Two Moroccan Families with Wolfram Syndrome

Aberrant Super-Enhancer Landscape in Enzalutamide-Resistant Prostate Cancer Cells

Genetic Polymorphism of Interleukin-6 in Asymptomatic and ICU-Admitted COVID-19 Patients in Sulaymaniyah Province, Kurdistan Region of Iraq

<i>MTHFR</i> 677C&gt;T and 1298A&gt;C Variants in Mothers of Infants with Down Syndrome from Western Mexico

TP53-Mutated Myelodysplastic Syndrome: A Diagnostic Approach in Different Clinical Settings

Association of Matrix Metalloproteinase-2 (MMP-2) and MMP-9 Promoter Variants, Their Serum Levels, and Activities with Aortic Valve Calcification (AVC) in a Population from Western Iran

Association Study of Pleural Mesothelioma and Oncogenic Simian Virus 40 in the Crocidolite-Contaminated Area of Dayao County, Yunnan Province, Southwest China

YKL-40 Knockdown Decreases Oxidative Stress Damage in Ovarian Granulosa Cells

The Phenotypic Spectrum of Desanto–Shinawi Syndrome: A Comparative Report of the First Reported Case in Turkey

<i>VEGF</i>-2578C/A, -460T/C Polymorphisms and Gastrointestinal Tract Cancer Risk: An Updated Meta-Analysis

Expanding the Genetic Spectrum of <i>AGXT</i> Gene Variants in Egyptian Patients with Primary Hyperoxaluria Type I

EGR3 Polymorphism Is a Potential Susceptibility Factor of Schizophrenia Risk in a Chinese Population

The Association Between the 5-Hydroxytryptamine Receptor 2A Gene Variants rs6311 and rs6313 and Obstructive Sleep Apnea in the Iranian Kurdish Population

Carrier Screening and Diagnosis for Spinal Muscular Atrophy Using Droplet Digital PCR Versus MLPA: Analytical Validation and Early Test Outcome

Association Between Hashimoto's Thyroiditis and Rheumatoid Arthritis: A Bidirectional Mendelian Randomization Study

Analysis of ceRNA Network and Identification of Potential Treatment Target and Biomarkers of Endothelial Cell Injury in Sepsis

miR-107 and miR-126 and Risk of Breast Cancer: A Case–Control Study

Ferroptosis-Related Genes Are Associated with Radioresistance and Immune Suppression in Head and Neck Cancer

Association of <i>TIMP2</i> 418 G/C and MMP Gene Polymorphism with Risk of Urinary Cancers: Systematic Review and Meta-analysis

Association of <i>Tenascin-C</i> Gene Polymorphisms with Risk of Acute Coronary Syndrome in South Indian Population: A Case−Control Genetic Association Study

Identification of Coding Variants in 10q22.1 Associated with Vitiligo in the Chinese Han Population

<i>Correction to:</i> The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis, by Hao Shen, et al. <i>Genet Test Mol Biomarkers</i> 2024; (vol. 28, no. 1; 33–38); doi: 10.1089/gtmb.2023.0307

A New Era for Genetic Testing and Molecular Biomarkers

Inflammatory Bowel Disease and Skin Cancer: A Two-Sample Mendelian Randomization Analysis

Upregulation of Long Noncoding RNA PCAT1 in Iranian Patients with Colorectal Cancer and Its Performance as a Potential Diagnostic Biomarker

Association of Interleukin-17A and Interleukin-17F Gene Polymorphisms with Atopic Dermatitis in Chinese Children

Vitamin D Receptor Polymorphisms in a Spanish Cohort of Parkinson's Disease Patients

Identification and Analysis of Gene Biomarkers for Ovarian Cancer

Profiling of Long Non-Coding RNAs in Auricular Cartilage of Patients with Isolated Microtia

Toward the Future: Perspectives on the Impacts of Genetic Testing and Biomarkers on Advancing Health Care

Determination of the Relationship Between the Development and Recurrence of Subacute Thyroiditis and Human Leukocyte Antigen Subtypes

<i>EGLN1:</i> A Biomarker of Poor Prognosis of Cervical Cancer and a Target of Treatment

帮你贴心管理全部的文献研飞ivySCI，高效的论文管理

A C->T Variation in 3′-Untranslated Region Elevates MED12 Protein Level in Breast Cancer That Relates to Better Prognosis

<i>MTHFR</i> 677C>T and 1298A>C Variants in Mothers of Infants with Down Syndrome from Western Mexico

帮你贴心管理全部的文献
研飞ivySCI，高效的论文管理