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Editorial: Celebration of DNA Day

Hereditas, 2024-05, Vol.161 (1), p.16-16, Article 16

2024

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Haplotype function score improves biological interpretation and cross-ancestry polygenic prediction of human complex traits

eLife, 2024-04, Vol.12

2024

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Proteogenomic characterization identifies clinically relevant subgroups of intrahepatic cholangiocarcinoma

Cancer cell, 2022-01, Vol.40 (1), p.70-87.e15

2022

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Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia

Nature genetics, 2017-11, Vol.49 (11), p.1576-1583

2017

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Oxidation modification of chitosan-based mesoporous carbon by soft template method and the adsorption and release properties of hydroxycamptothecin

Scientific reports, 2020-09, Vol.10 (1), p.15772-15772, Article 15772

2020

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MiRNAs of peripheral blood as the biomarker of schizophrenia

Hereditas, 2017-08, Vol.155 (1), p.9-9, Article 9

2017

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Identification of recurrent USP48 and BRAF mutations in Cushing’s disease

Nature communications, 2018-08, Vol.9 (1), p.3171-9, Article 3171

2018

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The centenary of Hereditas - almost a fairytale

Hereditas, 2020-11, Vol.157 (1), p.1-45, Article 45

2020

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Preparation of ultramicroporous volume carbon using high-speed ball-milling and its selective adsorption of CH4 in low-concentration coalbed methane

Journal of materials science, 2022-04, Vol.57 (13), p.6914-6928

2022

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Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3

Nature genetics, 2011-01, Vol.43 (1), p.55-59

2011

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DNA origami-based shape IDs for single-molecule nanomechanical genotyping

Nature communications, 2017-04, Vol.8 (1), p.14738-7, Article 14738

2017

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Identification of SHANK2 Pathogenic Variants in a Chinese Uygur Population with Schizophrenia

Journal of molecular neuroscience, 2021, Vol.71 (1), p.1-8

2021

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Whole‐exome sequencing of oral mucosal melanoma reveals mutational profile and therapeutic targets

The Journal of pathology, 2018-03, Vol.244 (3), p.358-366

2018

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Genetic variants associated with phenytoin-related severe cutaneous adverse reactions

JAMA : the journal of the American Medical Association, 2014-08, Vol.312 (5), p.525

2014

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A genome-wide association study identifies new susceptibility loci for non-cardia gastric cancer at 3q13.31 and 5p13.1

Nature genetics, 2011-12, Vol.43 (12), p.1215-1218

2011

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Identification of loci associated with schizophrenia by genome-wide association and follow-up

Nature genetics, 2008-09, Vol.40 (9), p.1053-1055

2008

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One-Step Synthesis of Nitrogen-Doped Hydrophilic Mesoporous Carbons from Chitosan-Based Triconstituent System for Drug Release

Nanoscale research letters, 2019-07, Vol.14 (1), p.259-12, Article 259

2019

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Performance comparison of four types of target enrichment baits for exome DNA sequencing

Hereditas, 2021-02, Vol.158 (1), p.10-12, Article 10

2021

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Correction to: Performance comparison of four types of target enrichment baits for exome DNA sequencing

Hereditas, 2023-09, Vol.160 (1), p.1-35, Article 35

2023

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A regulatory variant at 19p13.3 is associated with primary biliary cholangitis risk and ARID3A expression

Nature communications, 2023-03, Vol.14 (1), p.1732-1732, Article 1732

2023

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The role of gut microbiota in chronic restraint stress-induced cognitive deficits in mice

BMC microbiology, 2024-08, Vol.24 (1), p.289-12, Article 289

2024

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Transversus Thoracis Muscle Plane Block in Paediatric Patients Who Underwent Minimally Invasive Closure of Transthoracic Ventricular Septal Defect: A Retrospective Study

Pain research & management, 2023, Vol.2023, p.3488552-7

2023

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CACNA1C, schizophrenia and major depressive disorder in the Han Chinese population

British journal of psychiatry, 2014-01, Vol.204 (1), p.36-39

2014

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Editorial: Celebration of DNA Day

Haplotype function score improves biological interpretation and cross-ancestry polygenic prediction of human complex traits

Proteogenomic characterization identifies clinically relevant subgroups of intrahepatic cholangiocarcinoma

Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia

Oxidation modification of chitosan-based mesoporous carbon by soft template method and the adsorption and release properties of hydroxycamptothecin

MiRNAs of peripheral blood as the biomarker of schizophrenia

Identification of recurrent USP48 and BRAF mutations in Cushing’s disease

The centenary of Hereditas - almost a fairytale

Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome

Preparation of ultramicroporous volume carbon using high-speed ball-milling and its selective adsorption of CH4 in low-concentration coalbed methane

Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3

DNA origami-based shape IDs for single-molecule nanomechanical genotyping

Identification of SHANK2 Pathogenic Variants in a Chinese Uygur Population with Schizophrenia

Whole‐exome sequencing of oral mucosal melanoma reveals mutational profile and therapeutic targets

Genetic variants associated with phenytoin-related severe cutaneous adverse reactions

A genome-wide association study identifies new susceptibility loci for non-cardia gastric cancer at 3q13.31 and 5p13.1

Identification of loci associated with schizophrenia by genome-wide association and follow-up

One-Step Synthesis of Nitrogen-Doped Hydrophilic Mesoporous Carbons from Chitosan-Based Triconstituent System for Drug Release

Performance comparison of four types of target enrichment baits for exome DNA sequencing

A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese

Correction to: Performance comparison of four types of target enrichment baits for exome DNA sequencing

A regulatory variant at 19p13.3 is associated with primary biliary cholangitis risk and ARID3A expression

The role of gut microbiota in chronic restraint stress-induced cognitive deficits in mice

Transversus Thoracis Muscle Plane Block in Paediatric Patients Who Underwent Minimally Invasive Closure of Transthoracic Ventricular Septal Defect: A Retrospective Study

CACNA1C, schizophrenia and major depressive disorder in the Han Chinese population

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