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Does CSR affect the cost of equity capital: Empirical evidence from the targeted poverty alleviation of listed companies in China

PloS one, 2020-02, Vol.15 (2), p.e0227952-e0227952

2020

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Next-generation sequencing reveals heterogeneous genetic alterations in key signaling pathways of mismatch repair deficient colorectal carcinomas

Modern pathology, 2020-12, Vol.33 (12), p.2591-2601

2020

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Clinical and genomic features of Chinese lung cancer patients with germline mutations

Nature communications, 2022-03, Vol.13 (1), p.1268-1268, Article 1268

2022

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Circulating tumor DNA analysis depicts subclonal architecture and genomic evolution of small cell lung cancer

Nature communications, 2018-08, Vol.9 (1), p.3114-8, Article 3114

2018

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Association between monocyte-lymphocyte ratio and all-cause and cardiovascular mortality in patients with chronic kidney diseases: A data analysis from national health and nutrition examination survey (NHANES) 2003-2010

Renal failure, 2024-12, Vol.46 (1), p.2352126-2352126

2024

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Prevalence of recurrent oncogenic fusion in mismatch repair-deficient colorectal carcinoma with hypermethylated MLH1 and wild-type BRAF and KRAS

Modern pathology, 2019-07, Vol.32 (7), p.1053-1064

2019

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Comprehensive carrier genetic test using next-generation deoxyribonucleic acid sequencing in infertile couples wishing to conceive through assisted reproductive technology

Fertility and sterility, 2015-11, Vol.104 (5), p.1286-1293

2015

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Comprehensive analysis of oncogenic fusions in mismatch repair deficient colorectal carcinomas by sequential DNA and RNA next generation sequencing

Journal of translational medicine, 2021-10, Vol.19 (1), p.433-433, Article 433

2021

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Author Correction: Circulating tumor DNA analysis depicts subclonal architecture and genomic evolution of small cell lung cancer

Nature communications, 2019-01, Vol.10 (1), p.552-552, Article 552

2019

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Utilizing machine learning for early screening of thyroid nodules: a dual-center cross-sectional study in China

Frontiers in endocrinology (Lausanne), 2024-06, Vol.15, p.1385167

2024

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Maximum Somatic Allele Frequency-Adjusted Blood-Based Tumor Mutational Burden Predicts the Efficacy of Immune Checkpoint Inhibitors in Advanced Non-Small Cell Lung Cancer

Cancers, 2022-11, Vol.14 (22), p.5649

2022

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Construction and Validation of a Platinum Sensitivity Predictive Model With Multiple Genomic Variations for Epithelial Ovarian Cancer

Frontiers in oncology, 2021-09, Vol.11, p.725264-725264

2021

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Circulating Tumor DNA: Less Invasive, More Representative Method to Unveil the Genomic Landscape of Newly Diagnosed Multiple Myeloma Than Bone Marrow Aspirates

Cancers, 2022-10, Vol.14 (19), p.4914

2022

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Newborn hearing concurrent genetic screening for hearing impairment—A clinical practice in 58,397 neonates in Tianjin, China

International journal of pediatric otorhinolaryngology, 2013-12, Vol.77 (12), p.1929-1935

2013

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Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss

PloS one, 2014-08, Vol.9 (8), p.e103133-e103133

2014

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A novel germline ARMC5 mutation in a patient with bilateral macronodular adrenal hyperplasia: a case report

BMC medical genetics, 2018-03, Vol.19 (1), p.49-49, Article 49

2018

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Genomic Alterations and MYD88MUT Variant Mapping in Patients with Diffuse Large B-Cell Lymphoma and Response to Ibrutinib

Targeted oncology, 2020-04, Vol.15 (2), p.221-230

2020

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Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patients

Endocrine Connections, 2018-12, Vol.7 (12), p.1217-1225

2018

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Detection of inherited mutations for hereditary cancer using target enrichment and next generation sequencing

Familial cancer, 2015-03, Vol.14 (1), p.9-18

2015

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Novel genotype–phenotype correlations in five Chinese families with Von Hippel–Lindau disease

Endocrine Connections, 2018-07, Vol.7 (7), p.870-878

2018

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The role of fintech, natural resources and trade policy uncertainty towards SDGs in China: New insights from nonlinear approach

Resources policy, 2024-04, Vol.91, p.104889, Article 104889

2024

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Design and development of a high temperature stable sweet protein base on monellin

Process biochemistry (1991), 2020-02, Vol.89, p.29-36

2020

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Abstract 1896: The genomic features of Chinese cancer patients harboring HLA LOH

Cancer research (Chicago, Ill.), 2021-07, Vol.81 (13_Supplement), p.1896-1896

2021

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Dephosphorylation of CatC at Ser-18 improves salt and oxidative tolerance via promoting its tetramerization in rice

Plant science (Limerick), 2023-04, Vol.329, p.111597-111597, Article 111597

2023

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Characteristics of T-cell receptor repertoire between lung cancer patients and healthy people

Journal of clinical oncology, 2019-05, Vol.37 (15_suppl), p.e20728-e20728

2019

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Does CSR affect the cost of equity capital: Empirical evidence from the targeted poverty alleviation of listed companies in China

Next-generation sequencing reveals heterogeneous genetic alterations in key signaling pathways of mismatch repair deficient colorectal carcinomas

Clinical and genomic features of Chinese lung cancer patients with germline mutations

Circulating tumor DNA analysis depicts subclonal architecture and genomic evolution of small cell lung cancer

Association between monocyte-lymphocyte ratio and all-cause and cardiovascular mortality in patients with chronic kidney diseases: A data analysis from national health and nutrition examination survey (NHANES) 2003-2010

Prevalence of recurrent oncogenic fusion in mismatch repair-deficient colorectal carcinoma with hypermethylated MLH1 and wild-type BRAF and KRAS

Comprehensive carrier genetic test using next-generation deoxyribonucleic acid sequencing in infertile couples wishing to conceive through assisted reproductive technology

Comprehensive analysis of oncogenic fusions in mismatch repair deficient colorectal carcinomas by sequential DNA and RNA next generation sequencing

Author Correction: Circulating tumor DNA analysis depicts subclonal architecture and genomic evolution of small cell lung cancer

Utilizing machine learning for early screening of thyroid nodules: a dual-center cross-sectional study in China

Maximum Somatic Allele Frequency-Adjusted Blood-Based Tumor Mutational Burden Predicts the Efficacy of Immune Checkpoint Inhibitors in Advanced Non-Small Cell Lung Cancer

Construction and Validation of a Platinum Sensitivity Predictive Model With Multiple Genomic Variations for Epithelial Ovarian Cancer

Circulating Tumor DNA: Less Invasive, More Representative Method to Unveil the Genomic Landscape of Newly Diagnosed Multiple Myeloma Than Bone Marrow Aspirates

Newborn hearing concurrent genetic screening for hearing impairment—A clinical practice in 58,397 neonates in Tianjin, China

Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss

A novel germline ARMC5 mutation in a patient with bilateral macronodular adrenal hyperplasia: a case report

Genomic Alterations and MYD88MUT Variant Mapping in Patients with Diffuse Large B-Cell Lymphoma and Response to Ibrutinib

Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patients

Detection of inherited mutations for hereditary cancer using target enrichment and next generation sequencing

Novel genotype–phenotype correlations in five Chinese families with Von Hippel–Lindau disease

The role of fintech, natural resources and trade policy uncertainty towards SDGs in China: New insights from nonlinear approach

Design and development of a high temperature stable sweet protein base on monellin

Abstract 1896: The genomic features of Chinese cancer patients harboring HLA LOH

Dephosphorylation of CatC at Ser-18 improves salt and oxidative tolerance via promoting its tetramerization in rice

Characteristics of T-cell receptor repertoire between lung cancer patients and healthy people

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