Xiangdong Kong

The First Affiliated Hospital of Zhengzhou University

H指数:22

被引数:1,521

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Broadening horizons: Pathogenesis and therapeutics of renal ciliopathies

拓宽视野：肾纤毛病的发病机制与治疗学

Journal of Cell Communication and Signaling

IF3.9

2026-09-300

OAAI

Whole exome sequencing: a new era in prenatal diagnostics

全外显子组测序：产前诊断的新纪元

Journal of Translational Medicine

IF7.5

2026-02-260

OAAI

MLDP-AS: an optimized next-generation sequencing assay for enhanced detection of technically challenging variants in expanded carrier screening

MLDP-AS：一种优化型下一代测序检测方法，用于增强扩展性携带者筛查中技术挑战性变异的检测

Journal of Translational Medicine

IF7.5

2026-02-140

OAAI

Whole-Genome Sequencing for the Prenatal Evaluation of Fetal Structural Anomalies: A prospective multicenter study

全基因组测序在产前评估胎儿结构异常中的应用：一项前瞻性多中心研究

American Journal of Obstetrics and Gynecology

IF8.4

2025-08-250

PRE

Clinical application of whole exome sequencing (WES) in the genetic diagnosis of 768 Chinese patients with bilateral hearing loss

768例双侧听力损失中国患者中全外显子组测序（WES）在遗传诊断中的临床应用

European Journal of Human Genetics

IF4.6

2025-06-210

PRE

Chromosome-scale assembly and analysis of yellow Camellia ( Camellia limonia) genome reveal plant adaptation mechanism and flavonoid biosynthesis in karst region

黄茶 (Camellia limonia) 基因组的染色体规模组装和分析揭示喀斯特地区植物适应机制和类黄酮生物合成

GLOBAL ECOLOGY AND CONSERVATION

IF3.4

2024-12-010

OAAI

Fundamentals and Challenges of Ligand Modification in Heterogeneous Electrocatalysis

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

IF16.9

2024-11-140

PRE

Accurate prenatal diagnosis of facioscapulohumeral muscular dystrophy 1 using nanopore sequencing

JOURNAL OF MEDICAL GENETICS

IF3.7

2024-10-260

PRE

Atomic Defects Engineering Boosts Urea Synthesis toward Carbon Dioxide and Nitrate Coelectroreduction

原子缺陷工程促进尿素合成向二氧化碳和硝酸盐共还原

NANO LETTERS

IF9.1

2024-09-090

PRE

Detection of genomic variants by genome sequencing in foetuses with central nervous system abnormalities

ANNALS OF MEDICINE

IF4.3

2024-09-061

OAAI

Molecular findings in patients for whole exome sequencing and mitochondrial genome assessment

全外显子组测序和线粒体基因组评估患者的分子发现

CLINICA CHIMICA ACTA

IF2.9

2024-07-011

PRE

The uncertainty of copy number variants: pregnancy decisions and clinical follow-up

AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY

IF8.4

2023-08-017

PRE

Utility of trio-based prenatal exome sequencing incorporating splice-site and mitochondrial genome assessment in pregnancies with fetal ultrasound anomalies: prospective cohort study

ULTRASOUND IN OBSTETRICS & GYNECOLOGY

IF6.3

2022-12-015

PRE

Genetic analysis of 55 cases with fetal skeletal dysplasia

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2022-11-095

OAAI

Investigation of the genetic etiology in male infertility with apparently balanced chromosomal structural rearrangements by genome sequencing

ASIAN JOURNAL OF ANDROLOGY

IF2.7

2022-05-019

OAAI

Genetic Surveillance of Five SARS-CoV-2 Clinical Samples in Henan Province Using Nanopore Sequencing

FRONTIERS IN IMMUNOLOGY

IF5.9

2022-04-046

OAAI

Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China

性染色体非整倍体无创产前检测在华中地区的临床应用

FRONTIERS IN MEDICINE

IF3

2022-01-2612

OAAI

Molecular analysis and novel variation identification of Chinese pedigrees with mucopolysaccharidosis using targeted next-generation sequencing

CLINICA CHIMICA ACTA

IF2.9

2022-01-013

PRE

Genetic analysis by targeted next-generation sequencing and novel variation identification of maple syrup urine disease in Chinese Han population (vol 11, 18939, 2021)

SCIENTIFIC REPORTS

IF3.9

2021-10-200

OAAI

A Novel Five-Gene Signature for Prognosis Prediction in Hepatocellular Carcinoma

一种新的预测肝细胞癌预后的五基因标记

FRONTIERS IN ONCOLOGY

IF3.3

2021-07-1618

OAAI

Xiangdong Kong

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