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The gene spectrum of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Guangdong province, China

Gene, 2018-12, Vol.678, p.312-317

2018

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NSUN2 gene rs13181449 C>T polymorphism reduces neuroblastoma risk

Gene, 2023-02, Vol.854, p.147120-147120, Article 147120

2023

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Associations between PTPN2 gene polymorphisms and psoriasis in Northeastern China

Gene, 2019-01, Vol.681, p.73-79

2019

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A rare homozygous mutation in the YARS2 gene presents with hypertrophic cardiomyopathy, lactic acidosis and anemia in a Chinese infant

Gene, 2024-07, Vol.914, p.148379, Article 148379

2024

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Third-generation sequencing: A novel tool detects complex variants in the α-thalassemia gene

Gene, 2022-05, Vol.822, p.146332-146332, Article 146332

2022

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Compound heterozygous UGT1A128 and UGT1A16 or single homozygous UGT1A128 are major genotypes associated with Gilbert’s syndrome in Chinese Han people

Gene, 2021-05, Vol.781, p.145526-145526, Article 145526

2021

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Prognostic significance of SOCS3 and its biological function in colorectal cancer

Gene, 2017-09, Vol.627, p.114-122

2017

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Genetic variations in ABCA1/G1 associated with plasma lipid levels and risk of ischemic stroke

Gene, 2022-05, Vol.823, p.146343-146343, Article 146343

2022

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Genetic variants in the regulation region of TLR4 reduce the gastric cancer susceptibility

Gene, 2021-01, Vol.767, p.145181-145181, Article 145181

2021

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SMAD3 rs36221701 T>C polymorphism impacts COPD susceptibility in the Kashi population

Gene, 2022-01, Vol.808, p.145970-145970, Article 145970

2022

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Novel heterozygous mutations in the otogelin-like (OTOGL) gene in a child with bilateral mild nonsyndromic sensorineural hearing loss

Gene, 2022-01, Vol.808, p.146000-146000, Article 146000

2022

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A genetic analysis identifies haplotype at adiponectin locus: Association with the metabolic health and obesity phenotypes

Gene, 2021-06, Vol.784, p.145593, Article 145593

2021

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Gene-gene interactions and associations of six hypertension related single nucleotide polymorphisms with obesity risk in a Chinese children population

Gene, 2018-12, Vol.679, p.320-327

2018

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Assessment of interleukin 6 gene polymorphisms with rheumatoid arthritis

Gene, 2021-01, Vol.765, p.145070-145070, Article 145070

2021

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Association of UCP1 polymorphisms with type 2 diabetes mellitus and their interaction with physical activity and sedentary behavior

Gene, 2020-05, Vol.739, p.144497-144497, Article 144497

2020

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Interactive associations of the INAFM2 rs67839313 variant and egg consumption with type 2 diabetes mellitus and fasting blood glucose in a Chinese population: A family-based study

Gene, 2021-02, Vol.770, p.145357-145357, Article 145357

2021

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The ATM rs189037 G>A polymorphism is associated with the risk and prognosis of gastric cancer in Chinese individuals: A case–control study

Gene, 2020-05, Vol.741, p.144578-144578, Article 144578

2020

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Genetic variation at the interleukin-18 locus is associated with wheat-dependent exercise-induced anaphylaxis in the Han Chinese population

Gene, 2020-05, Vol.737, p.144462-144462, Article 144462

2020

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Long non-coding RNA DILC promotes the progression of gallbladder carcinoma

Gene, 2019-04, Vol.694, p.102-110

2019

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Characterization of germline mutations in familial lung cancer from the Chinese population

Gene, 2018-01, Vol.641, p.94-104

2018

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The association of rs710886 in lncRNA PCAT1 with bladder cancer risk in a Chinese population

Gene, 2017-09, Vol.627, p.226-232

2017

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A novel mutation of GATA4 (K300T) associated with familial atrial septal defect

Gene, 2016-01, Vol.575 (2), p.473-477

2016

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Association between polymorphisms in ABO gene and stroke patients with small artery occlusion in southern Chinese Han population

Gene, 2021-02, Vol.769, p.145211-145211, Article 145211

2021

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Vitamin D binding protein polymorphisms influence susceptibility to hepatitis C virus infection in a high-risk Chinese population

Gene, 2018-12, Vol.679, p.405-411

2018

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Genetic diversity and haplotypic structure of Chinese Kazak ethnic group revealed by 19 STRs on the X chromosome

Gene, 2017-02, Vol.600, p.64-69

2017

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The gene spectrum of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Guangdong province, China

NSUN2 gene rs13181449 C>T polymorphism reduces neuroblastoma risk

Associations between PTPN2 gene polymorphisms and psoriasis in Northeastern China

A rare homozygous mutation in the YARS2 gene presents with hypertrophic cardiomyopathy, lactic acidosis and anemia in a Chinese infant

Third-generation sequencing: A novel tool detects complex variants in the α-thalassemia gene

Compound heterozygous UGT1A128 and UGT1A16 or single homozygous UGT1A128 are major genotypes associated with Gilbert’s syndrome in Chinese Han people

Prognostic significance of SOCS3 and its biological function in colorectal cancer

Genetic variations in ABCA1/G1 associated with plasma lipid levels and risk of ischemic stroke

Genetic variants in the regulation region of TLR4 reduce the gastric cancer susceptibility

SMAD3 rs36221701 T>C polymorphism impacts COPD susceptibility in the Kashi population

Novel heterozygous mutations in the otogelin-like (OTOGL) gene in a child with bilateral mild nonsyndromic sensorineural hearing loss

A genetic analysis identifies haplotype at adiponectin locus: Association with the metabolic health and obesity phenotypes

Gene-gene interactions and associations of six hypertension related single nucleotide polymorphisms with obesity risk in a Chinese children population

Assessment of interleukin 6 gene polymorphisms with rheumatoid arthritis

Association of UCP1 polymorphisms with type 2 diabetes mellitus and their interaction with physical activity and sedentary behavior

Interactive associations of the INAFM2 rs67839313 variant and egg consumption with type 2 diabetes mellitus and fasting blood glucose in a Chinese population: A family-based study

The ATM rs189037 G>A polymorphism is associated with the risk and prognosis of gastric cancer in Chinese individuals: A case–control study

Genetic variation at the interleukin-18 locus is associated with wheat-dependent exercise-induced anaphylaxis in the Han Chinese population

Long non-coding RNA DILC promotes the progression of gallbladder carcinoma

Characterization of germline mutations in familial lung cancer from the Chinese population

The association of rs710886 in lncRNA PCAT1 with bladder cancer risk in a Chinese population

A novel mutation of GATA4 (K300T) associated with familial atrial septal defect

Association between polymorphisms in ABO gene and stroke patients with small artery occlusion in southern Chinese Han population

Vitamin D binding protein polymorphisms influence susceptibility to hepatitis C virus infection in a high-risk Chinese population

Genetic diversity and haplotypic structure of Chinese Kazak ethnic group revealed by 19 STRs on the X chromosome

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