H. Liany

发表

DruID: Personalized Drug Recommendations by Integrating Multiple Biomedical Databases for Cancer

Herty Liany, Vaibhav Rajan, Anand Jeyasekharan, 2021, bioRxiv.

Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy

Y. Okada, H. Liany, Jianjun Liu, 2015, Nature Genetics.

HLA-B*13:01 and the dapsone hypersensitivity syndrome.

P. D. de Bakker, J. Wang, H. Liany, 2013, The New England journal of medicine.

DNAJ mutations are rare in Chinese Parkinson's disease patients and controls

H. Liany, Jianjun Liu, W. Au, 2014, Neurobiology of Aging.

ASTER: A Method to Predict Clinically Actionable Synthetic Lethal Interactions

H. Liany, A. Jeyasekharan, Vaibhav Rajan, 2020, bioRxiv.

Impaired Development of Neural‐Crest Cell‐Derived Organs and Intellectual Disability Caused by MED13L Haploinsufficiency

H. Liany, A. Hillmer, K. H. Utami, 2014, Human mutation.

Combined linkage and family-based association analysis improves candidate gene detection in Genetic Analysis Workshop 18 simulation data

H. Liany, H. Low, Yi Li, 2014, BMC Proceedings.

Analysis of POFUT1 Gene Mutation in a Chinese Family with Dowling-Degos Disease

H. Liany, Jianjun Liu, Yi Yu, 2014, PloS one.

An association study of TOLL and CARD with leprosy susceptibility in Chinese population

H. Liany, Jianjun Liu, A. Irwanto, 2013, Human molecular genetics.

A Synonymous Variant in IL10RA Affects RNA Splicing in Paediatric Patients with Refractory Inflammatory Bowel Disease.

H. Liany, Jianjun Liu, K. Song, 2016, Journal of Crohn's & colitis.

Targeted next-generation sequencing to diagnose disorders of HDL cholesterol patient-oriented and epidemiological research

G. Francis, M. Hayden, H. Liany, 2020 .

A rare lysosomal enzyme gene SMPD1 variant (p.R591C) associates with Parkinson's disease

H. Liany, Jianjun Liu, W. Au, 2013, Neurobiology of Aging.

MultiDCoX: Multi-factor analysis of differential co-expression

Karuturi R. Krishna Murthy, Jagath C. Rajapakse, Herty Liany, 2017, BMC Bioinformatics.

MultiDCoX: Multi-factor analysis of differential co-expression

Jagath C. Rajapakse, Herty Liany, R. Krishna Murthy Karuturi, 2017, BMC Bioinformatics.

Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations.

T. Wong, E. Tai, H. Liany, 2014, Human molecular genetics.

Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility

X. Estivill, M. Weichenthal, A. Bowcock, 2015, Nature Communications.

Genome-Wide Analysis of Protein-Coding Variants in Leprosy.

H. Liany, Chaolong Wang, S. Maurer-Stroh, 2017, The Journal of investigative dermatology.

Genome-Wide Linkage, Exome Sequencing and Functional Analyses Identify ABCB6 as the Pathogenic Gene of Dyschromatosis Universalis Hereditaria

H. Liany, Hong Liu, Yongxiang Yu, 2014, PloS one.

Targeted next-generation sequencing to diagnose disorders of HDL cholesterol[S]

G. Francis, M. Hayden, H. Liany, 2015, Journal of Lipid Research.

Integrative Analysis Identifies Key Molecular Signatures Underlying Neurodevelopmental Deficits in Fragile X Syndrome

M. Mann, H. Liany, Qiyu Chen, 2019, Biological Psychiatry.

Discovery of a novel genetic susceptibility locus on X chromosome for systemic lupus erythematosus

Liangdan Sun, X. Zuo, Xuejun Zhang, 2015, Arthritis Research & Therapy.

Evaluation of novel Parkinson's disease candidate genes in the Chinese population

H. Liany, Jianjun Liu, V. Mok, 2019, Neurobiology of Aging.

Title Discovery of a novel genetic susceptibility locus on Xchromosome for systemic lupus erythematosus

Liangdan Sun, X. Zuo, Xuejun Zhang, 2015 .

Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes.

X. F. C. C. Wong, M. Tang, J. Common, 2018, The Journal of investigative dermatology.

Linking a genome‐wide association study signal to a LRRK2 coding variant in Parkinson's disease

T. Wong, E. Tai, H. Liany, 2016, Movement disorders : official journal of the Movement Disorder Society.

Predicting Synthetic Lethal Interactions using Heterogeneous Data Sources.

Vaibhav Rajan, Herty Liany, Anand Jeyasekharan, 2019, Bioinformatics.

Predicting Synthetic Lethal Interactions using Heterogeneous Data Sources

Herty Liany, Vaibhav Rajan, Anand D. Jeyasekharan, 2019, bioRxiv.

Mining Pathway Associations from Networks of Mutual Exclusivity Interactions

Vaibhav Rajan, Yu Lin, Anand D. Jeyasekharan, 2020, bioRxiv.

Linking a genome‐wide association study signal to a LRRK2 coding variant in Parkinson's disease

E. Tai, H. Liany, Jianjun Liu, 2016, Movement disorders : official journal of the Movement Disorder Society.

The association between rare large duplication of 16p11.2 and schizophrenia in the Singaporean Chinese population

Y. Teo, H. Liany, Jianjun Liu, 2013, Schizophrenia Research.

Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy

Y. Okada, H. Liany, A. Irwanto, 2015, Nature Genetics.

Genome-Wide Analysis of Protein-Coding Variants in Leprosy.

H. Liany, Chaolong Wang, S. Maurer-Stroh, 2017, The Journal of investigative dermatology.

ASTER: A Method to Predict Clinically Relevant Synthetic Lethal Genetic Interactions

Dachuan Huang, C. Ong, H. Liany, 2024, IEEE Journal of Biomedical and Health Informatics.

ASTER: A Method to Predict Clinically Actionable Synthetic Lethal Genetic Interactions

H. Liany, Vaibhav Rajan, Anand D. Jeyasekharan, 2021 .