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An Algorithm to Mine Therapeutic Motifs for Cancer From Networks of Genetic Interactions

IEEE journal of biomedical and health informatics, 2022-06, Vol.26 (6), p.2830-2838

2022

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

IEEE journal of biomedical and health informatics, 2024-03, Vol.28 (3), p.1785-1796

2024

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

Nature genetics, 2015-03, Vol.47 (3), p.267-271

2015

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MultiDCoX: Multi-factor analysis of differential co-expression

BMC bioinformatics, 2017-12, Vol.18 (Suppl 16), p.576-576, Article 576

2017

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Targeted next-generation sequencing to diagnose disorders of HDL cholesterol

Journal of lipid research, 2015-10, Vol.56 (10), p.1993-2001

2015

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

Arthritis research & therapy, 2015-12, Vol.17 (1), p.349-349, Article 349

2015

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Predicting synthetic lethal interactions using heterogeneous data sources

Bioinformatics, 2020-04, Vol.36 (7), p.2209-2216

2020

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Analysis of POFUT1 gene mutation in a Chinese family with Dowling-Degos disease

PloS one, 2014-08, Vol.9 (8), p.e104496

2014

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Single-cell landscape of idiopathic multicentric Castleman disease in identical twins

Blood, 2024-05, Vol.143 (18), p.1837-1844

2024

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

Biological psychiatry (1969), 2020-09, Vol.88 (6), p.500-511

2020

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

Neurobiology of aging, 2013-12, Vol.34 (12), p.2890.e13-2890.e15

2013

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Genome-Wide Analysis of Protein-Coding Variants in Leprosy

Journal of investigative dermatology, 2017-12, Vol.137 (12), p.2544-2551

2017

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

Journal of investigative dermatology, 2018-12, Vol.138 (12), p.2674-2677

2018

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

Journal of Crohn's and colitis, 2016-11, Vol.10 (11), p.1366-1371

2016

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

Human mutation, 2014-11, Vol.35 (11), p.1311-1320

2014

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

Neurobiology of aging, 2019-02, Vol.74, p.235.e1-235.e4

2019

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

Neurobiology of aging, 2014-04, Vol.35 (4), p.935.e1-935.e2

2014

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

Human molecular genetics, 2014-07, Vol.23 (14), p.3891-3897

2014

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Abstract 4458: Single cell landscape of multicentric Castleman disease in identical twins

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.4458-4458

2023

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

Human molecular genetics, 2013-11, Vol.22 (21), p.4430-4437

2013

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

Movement disorders, 2016-04, Vol.31 (4), p.484-487

2016

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

Schizophrenia research, 2013-05, Vol.146 (1), p.368-369

2013

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

BMC proceedings, 2014, Vol.8 (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo), p.S29-S29, Article S29

2014

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An Algorithm to Mine Therapeutic Motifs for Cancer From Networks of Genetic Interactions

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

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

MultiDCoX: Multi-factor analysis of differential co-expression

Targeted next-generation sequencing to diagnose disorders of HDL cholesterol

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

Predicting synthetic lethal interactions using heterogeneous data sources

Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria

Analysis of POFUT1 gene mutation in a Chinese family with Dowling-Degos disease

Single-cell landscape of idiopathic multicentric Castleman disease in identical twins

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

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

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

Genome-Wide Analysis of Protein-Coding Variants in Leprosy

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

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

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

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

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

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

Abstract 4458: Single cell landscape of multicentric Castleman disease in identical twins

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

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

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

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

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