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List of works by Jia Nee Foo

2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

scientific article

A Novel Homozygous Frameshift Variant in XYLT2 Causes Spondyloocular Syndrome in a Consanguineous Pakistani Family

scientific article published on 05 March 2019

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

scientific article published on 13 May 2016

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

scientific article

A common variant near TGFBR3 is associated with primary open angle glaucoma.

scientific article published on 10 April 2015

A comprehensive evaluation of the role of genetic variation in follicular lymphoma survival

scientific article

A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy ⬇️

scientific article published on December 25, 2011

A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy

scientific article published on 15 December 2016

A meta-analysis of genome-wide association studies of follicular lymphoma

scientific article

A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias.

scientific article

A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri families

scientific article published on 05 August 2019

Absence of A673T amyloid-β precursor protein variant in Alzheimer's disease and other neurological diseases.

scientific article published on 4 May 2013

Abstract 5072: Meta-analysis of genome-wide association studies identifies novel susceptibility loci for follicular lymphoma

An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma

scientific article published on 19 July 2016

Analysis of EIF4G1 in Parkinson's disease among Asians

scientific article published on 23 October 2012

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

scientific article published on 23 February 2014

Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants

scientific article published on 19 October 2017

CHCHD2 and Parkinson's disease

scholarly article by Jia Nee Foo et al published 1 July 2015 in Lancet Neurology

Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutations

scientific article published on 29 March 2013

Coding variants at hexa-allelic amino acid 13 of HLA-DRB1 explain independent SNP associations with follicular lymphoma risk

scientific article published on 20 June 2013

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

scientific article

Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

scientific article published on 28 April 2019

Corrigendum: New loci and coding variants confer risk for age-related macular degeneration in East Asians

scientific article published on 30 March 2015

Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

scientific article published in June 2015

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

scientific article

ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis.

scientific article published on 27 September 2017

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

article

GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers

scientific journal article

GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma

scientific article

Generation of Human PSC-Derived Kidney Organoids with Patterned Nephron Segments and a De Novo Vascular Network

scientific article published on 11 July 2019

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

scientific article

Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study.

scientific article published on 25 July 2016

Genetic variants in ER cofactor genes and endometrial cancer risk

scientific article

Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae

scientific article

Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma

scientific article

Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region

scientific article published in October 2014

Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population

scientific article

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

scientific article published on 03 February 2014

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

scientific article published on 23 April 2015

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

scientific article

ITPKB and ZNF184 are associated with Parkinson's disease risk in East Asians

scientific article published on 02 February 2019

Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family

scientific article published on 13 December 2017

Identification of a recurrent nonsense mutation in HR gene responsible for atrichia with papular lesions in two Kashmiri families

scientific article published on 05 February 2020

Identification of new susceptibility loci for IgA nephropathy in Han Chinese.

scientific article published on June 2015

Identifying genes in Parkinson disease: state of the art

scientific article published on 01 May 2018

Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencing

scientific article

Investigation of the predisposing factor of pemphigus and its clinical subtype through a genome-wide association and next generation sequence analysis

scientific article published on 19 September 2018

Large 3-Mb deletions at 22q11.2 locus in Parkinson's disease and schizophrenia

scientific article published on 27 October 2016

Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore

scientific article published on 1 October 2019

Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size

scientific article

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

scientific article published on 21 December 2015

Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction.

scientific article published on June 2016

Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease

scientific article published on 20 March 2015

New loci and coding variants confer risk for age-related macular degeneration in East Asians

scientific article

Next-generation sequencing diagnostics for neurological diseases/disorders: from a clinical perspective ⬇️

scientific article published on March 23, 2013

No association of DNM3 with age of onset in Asian Parkinson's disease

scientific article published on 14 September 2018

Nonsynonymous variants in MC1R are rare in Chinese Parkinson disease cases

scientific article published on 25 May 2015

Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

scientific article published on 17 November 2018

Parkinson's disease GWAS-linked Park16 carriers show greater motor progression

scientific article published on 27 February 2019

Phenotypic bases of NOTCH2NLC GGC expansion positive Neuronal Intranuclear Inclusion Disease (NIID) in a South East Asian cohort

scientific article published on 30 June 2020

Polycystic kidney disease: new knowledge and future promises

scientific article published on 01 June 2019

Possible Interaction Between Cigarette Smoking and HLA-DRB1 Variation in the Risk of Follicular Lymphoma

scientific article published on 28 March 2017

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

scientific article

Screening for TMEM230 mutations in young-onset Parkinson's disease.

scientific article published on 24 June 2017

Systematic evaluation of CRISPR-Cas systems reveals design principles for genome editing in human cells.

scientific article published on 29 May 2018

Targeted exome sequencing reveals homozygous TREM2 R47C mutation presenting with behavioral variant frontotemporal dementia without bone involvement

scientific article published on 16 April 2018

Targeted next-generation sequencing to diagnose disorders of HDL cholesterol.

scientific article

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

article

Validation of GWAS Loci for Atopic Dermatitis in a Singapore Chinese Population

article

Variation at HLA-DRB1 is associated with resistance to enteric fever

scientific article

Whole-genome and whole-exome sequencing in neurological diseases.

scientific article published on 31 July 2012

X chromosome-wide association study of follicular lymphoma

scientific article published on 25 June 2013

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