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Polygenic scores via penalized regression on summary statistics

Genetic epidemiology, 2017-09, Vol.41 (6), p.469-480

2017

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Interactive effect of nitrogen addition and throughfall reduction decreases soil aggregate stability through reducing biological binding agents

Forest ecology and management, 2019-08, Vol.445, p.13-19

2019

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Identification of long non-protein coding RNAs in chicken skeletal muscle using next generation sequencing

Genomics (San Diego, Calif.), 2012-05, Vol.99 (5), p.292-298

2012

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Co-occurring protein phosphorylation are functionally associated

PLoS computational biology, 2017-05, Vol.13 (5), p.e1005502-e1005502

2017

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Phase separation as a possible mechanism for dosage sensitivity

Genome Biology, 2024-01, Vol.25 (1), p.17-27, Article 17

2024

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Nitrogen addition decreases soil aggregation but enhances soil organic carbon stability in a temperate forest

Geoderma, 2022-11, Vol.426, p.116112, Article 116112

2022

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Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

Nature genetics, 2011-06, Vol.43 (6), p.531-538

2011

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Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes

Genetics in medicine, 2020-12, Vol.22 (12), p.2020-2028

2020

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Environmental Regulation, Promotion Pressure of Officials, and Enterprise Environmental Protection Investment

Frontiers in public health, 2021-08, Vol.9, p.724351-724351

2021

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A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population

Neurobiology of aging, 2018-08, Vol.68, p.160.e1-160.e7

2018

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Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches

Journal of human genetics, 2014-11, Vol.59 (11), p.599-607

2014

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Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Genome medicine, 2021-06, Vol.13 (1), p.106-1, Article 106

2021

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Soil water response to rainfall in a dune-interdune landscape in Horqin Sand Land, northern China

Soil and water research, 2019-01, Vol.14 (4), p.229-239

2019

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Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density

Frontiers in genetics, 2018-08, Vol.9, p.267-267

2018

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A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family

Clinica chimica acta, 2012-07, Vol.413 (13-14), p.1049-1052

2012

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Identification and Characterization of Human snoRNA Core Promoters

Genomics (San Diego, Calif.), 2010-07, Vol.96 (1), p.50-56

2010

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Polymorphisms at 16p13 are associated with systemic lupus erythematosus in the Chinese population

Journal of medical genetics, 2011-01, Vol.48 (1), p.69-72

2011

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Recent ultra-rare inherited variants implicate new autism candidate risk genes

Nature genetics, 2021-08, Vol.53 (8), p.1125-1134

2021

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A rare variant at the KYNU gene is associated with kynureninase activity and essential hypertension in the Han Chinese population

Circulation. Cardiovascular genetics, 2011-12, Vol.4 (6), p.687

2011

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A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway

Molecular human reproduction, 2016-09, Vol.22 (9), p.669-678

2016

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Systematic Characterization and Prediction of Post-Translational Modification Cross-Talk

Molecular & cellular proteomics, 2015-03, Vol.14 (3), p.761-770

2015

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Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations

American journal of human genetics, 2013-09, Vol.93 (3), p.545-554

2013

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Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Genome medicine, 2021-05, Vol.13 (1), p.80-18, Article 80

2021

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Polygenic scores via penalized regression on summary statistics

Interactive effect of nitrogen addition and throughfall reduction decreases soil aggregate stability through reducing biological binding agents

Identification of long non-protein coding RNAs in chicken skeletal muscle using next generation sequencing

Co-occurring protein phosphorylation are functionally associated

Phase separation as a possible mechanism for dosage sensitivity

Nitrogen addition decreases soil aggregation but enhances soil organic carbon stability in a temperate forest

De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes

Environmental Regulation, Promotion Pressure of Officials, and Enterprise Environmental Protection Investment

A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population

Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches

Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Soil water response to rainfall in a dune-interdune landscape in Horqin Sand Land, northern China

Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family

Identification and Characterization of Human snoRNA Core Promoters

Polymorphisms at 16p13 are associated with systemic lupus erythematosus in the Chinese population

Recent ultra-rare inherited variants implicate new autism candidate risk genes

A rare variant at the KYNU gene is associated with kynureninase activity and essential hypertension in the Han Chinese population

A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway

Systematic Characterization and Prediction of Post-Translational Modification Cross-Talk

Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations

Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene

Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

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