| Year | Citation | Score | |||
|---|---|---|---|---|---|
| 2024 | Lim SY, Tan AH, Foo JN, Tan YJ, Chew EG, Annuar AA, Closas AMD, Pajo A, Lim JL, Tay YW, Nadhirah A, Hor JW, Toh TS, Lit LC, Zulkefli J, et al. Loss-of-function SMPD1 gene variant in Progressive Supranuclear Palsy-Richardson Syndrome patients of Chinese ancestry. Journal of Movement Disorders. PMID 38291878 DOI: 10.14802/jmd.24009 | 0.3 | |||
| 2023 | Kim JJ, Vitale D, Otani DV, Lian MM, Heilbron K, Iwaki H, Lake J, Solsberg CW, Leonard H, Makarious MB, Tan EK, Singleton AB, Bandres-Ciga S, Noyce AJ, Blauwendraat C, ... ... Foo JN, et al. Multi-ancestry genome-wide association meta-analysis of Parkinson's disease. Nature Genetics. PMID 38155330 DOI: 10.1038/s41588-023-01584-8 | 0.311 | |||
| 2023 | Li M, Wang YN, Wang L, Meah WY, Shi DC, Heng KK, Wang L, Khor CC, Bei JX, Cheng CY, Aung T, Liao YH, Chen QK, Gu JR, Kong YZ, ... ... Foo JN, et al. Genome-Wide Association Analysis of Protein-Coding Variants in IgA Nephropathy. Journal of the American Society of Nephrology : Jasn. PMID 37787447 DOI: 10.1681/ASN.0000000000000222 | 0.347 | |||
| 2023 | Tan YJ, Yong ACW, Foo JN, Lian MM, Lim WK, Dominguez J, Fong ZH, Narasimhalu K, Chiew HJ, Ng KP, Ting SKS, Kandiah N, Ng ASL. C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort. Annals of Clinical and Translational Neurology. PMID 36799407 DOI: 10.1002/acn3.51744 | 0.328 | |||
| 2023 | Pan H, Liu Z, Ma J, Li Y, Zhao Y, Zhou X, Xiang Y, Wang Y, Zhou X, He R, Xie Y, Zhou Q, Yuan K, Xu Q, Sun Q, ... ... Foo JN, et al. Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population. Npj Parkinson's Disease. 9: 22. PMID 36759515 DOI: 10.1038/s41531-023-00456-6 | 0.328 | |||
| 2021 | Dominguez J, Yu JT, Tan YJ, Ng A, De Guzman MF, Natividad B, Daroy ML, Cano J, Yu J, Lian MM, Zeng L, Lim WK, Foo JN, Ng ASL. Novel Optineurin Frameshift Insertion in a Family With Frontotemporal Dementia and Parkinsonism Without Amyotrophic Lateral Sclerosis. Frontiers in Neurology. 12: 645913. PMID 34093394 DOI: 10.3389/fneur.2021.645913 | 0.303 | |||
| 2020 | Li M, Wang L, Shi DC, Foo JN, Zhong Z, Khor CC, Lanzani C, Citterio L, Salvi E, Yin PR, Bei JX, Wang L, Liao YH, Chen J, Chen QK, et al. Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA Nephropathy. Journal of the American Society of Nephrology : Jasn. PMID 32912934 DOI: 10.1681/Asn.2019080799 | 0.371 | |||
| 2019 | Wu D, Dou J, Chai X, Bellis C, Wilm A, Shih CC, Soon WWJ, Bertin N, Lin CB, Khor CC, DeGiorgio M, Cheng S, Bao L, Karnani N, Hwang WYK, ... ... Foo JN, et al. Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore. Cell. 179: 736-749.e15. PMID 31626772 DOI: 10.1016/J.Cell.2019.09.019 | 0.339 | |||
| 2018 | Kausar M, Siddiqi S, Yaqoob M, Mansoor S, Makitie O, Mir A, Khor CC, Foo JN, Anees M. Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta. Journal of Biomedical Science. 25: 82. PMID 30447692 DOI: 10.1186/s12929-018-0481-x | 0.323 | |||
| 2018 | Chew EGY, Liany H, Tan LCS, Au WL, Prakash KM, Annuar AA, Chan AYY, Lim SY, Mok V, Chung SJ, Song K, Liu J, Foo JN, Tan EK. Evaluation of novel Parkinson's disease candidate genes in the Chinese population. Neurobiology of Aging. PMID 30337193 DOI: 10.1016/J.Neurobiolaging.2018.09.013 | 0.305 | |||
| 2018 | Ng AS, Tan YJ, Yi Z, Tandiono M, Chew E, Dominguez J, Macas M, Ng E, Hameed S, Ting S, Tan EK, Foo JN, Kandiah N. Targeted exome sequencing reveals homozygous TREM2 R47C mutation presenting with behavioral variant frontotemporal dementia without bone involvement. Neurobiology of Aging. PMID 29748150 DOI: 10.1016/j.neurobiolaging.2018.04.003 | 0.338 | |||
| 2017 | Ajmal M, Mir A, Wahid S, Khor CC, Foo JN, Siddiqi S, Kauser M, Malik SA, Nasir M. 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. Bmc Medical Genetics. 18: 148. PMID 29237407 DOI: 10.1186/s12881-017-0506-4 | 0.307 | |||
| 2017 | Aung T, Ozaki M, Lee MC, Schlötzer-Schrehardt U, Thorleifsson G, Mizoguchi T, Igo RP, Haripriya A, Williams SE, Astakhov YS, Orr AC, Burdon KP, Nakano S, Mori K, Abu-Amero K, ... ... Foo JN, et al. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. Nature Genetics. PMID 28553957 DOI: 10.1038/Ng.3875 | 0.351 | |||
| 2015 | Yin X, Low HQ, Wang L, Li Y, Ellinghaus E, Han J, Estivill X, Sun L, Zuo X, Shen C, Zhu C, Zhang A, Sanchez F, Padyukov L, Catanese JJ, ... ... Foo JN, et al. Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. Nature Communications. 6: 6916. PMID 25903422 DOI: 10.1038/Ncomms7916 | 0.312 | |||
| 2015 | Li Z, Allingham RR, Nakano M, Jia L, Chen Y, Ikeda Y, Mani B, Chen LJ, Kee C, Garway-Heath DF, Sripriya S, Fuse N, Abu-Amero KK, Huang C, Namburi P, ... ... Foo JN, et al. A common variant near TGFBR3 is associated with primary open angle glaucoma. Human Molecular Genetics. 24: 3880-92. PMID 25861811 DOI: 10.1093/Hmg/Ddv128 | 0.309 | |||
| 2015 | Aung T, Ozaki M, Mizoguchi T, Allingham RR, Li Z, Haripriya A, Nakano S, Uebe S, Harder JM, Chan AS, Lee MC, Burdon KP, Astakhov YS, Abu-Amero KK, Zenteno JC, ... ... Foo JN, et al. A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nature Genetics. 47: 387-92. PMID 25706626 DOI: 10.1038/Ng.3226 | 0.343 | |||
| 2015 | Cheng CY, Yamashiro K, Chen LJ, Ahn J, Huang L, Huang L, Cheung CM, Miyake M, Cackett PD, Yeo IY, Laude A, Mathur R, Pang J, Sim KS, Koh AH, ... ... Foo JN, et al. New loci and coding variants confer risk for age-related macular degeneration in East Asians. Nature Communications. 6: 6063. PMID 25629512 DOI: 10.1038/Ncomms7063 | 0.33 | |||
| 2014 | Siddiqi S, Foo JN, Vu A, Azim S, Silver DL, Mansoor A, Tay SK, Abbasi S, Hashmi AH, Janjua J, Khalid S, Tai ES, Yeo GW, Khor CC. 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. Plos One. 9: e113258. PMID 25474699 DOI: 10.1371/Journal.Pone.0113258 | 0.336 | |||
| 2014 | Liu H, Li Y, Hung KKH, Wang N, Wang C, Chen X, Sheng D, Fu X, See K, Foo JN, Low H, Liany H, Irwan ID, Liu J, Yang B, et al. Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria Plos One. 9. PMID 24498303 DOI: 10.1371/Journal.Pone.0087250 | 0.339 | |||
| 2013 | Wu YR, Foo JN, Tan LC, Chen CM, Prakash KM, Chen YC, Bei JX, Au WL, Chang CW, Wong TY, Liu JJ, Zhao Y, Tan EK. Identification of a novel risk variant in the FUS gene in essential tremor. Neurology. 81: 541-4. PMID 23825177 DOI: 10.1212/Wnl.0B013E31829E700C | 0.344 | |||
| 2013 | Ting SK, Chong MS, Kandiah N, Hameed S, Tan L, Au WL, Prakash KM, Pavanni R, Lee TS, Foo JN, Bei JX, Yu XQ, Liu JJ, Zhao Y, Lee WL, et al. Absence of A673T amyloid-β precursor protein variant in Alzheimer's disease and other neurological diseases. Neurobiology of Aging. 34: 2441.e7-8. PMID 23652020 DOI: 10.1016/j.neurobiolaging.2013.04.012 | 0.306 | |||
| 2012 | Skibola CF, Conde L, Foo JN, Riby J, Humphreys K, Sillé FC, Darabi H, Sanchez S, Hjalgrim H, Liu J, Bracci PM, Smedby KE. A meta-analysis of genome-wide association studies of follicular lymphoma. Bmc Genomics. 13: 516. PMID 23025665 DOI: 10.1186/1471-2164-13-516 | 0.355 | |||
| 2012 | Li Y, Low HQ, Foo JN, Darabi H, EinarsdÏŒttir K, Humphreys K, Spurdle A, Easton DF, Thompson DJ, Dunning AM, Pharoah PD, Czene K, Chia KS, Hall P, et al. Genetic variants in ER cofactor genes and endometrial cancer risk. Plos One. 7: e42445. PMID 22876322 DOI: 10.1371/journal.pone.0042445 | 0.312 | |||
| 2010 | Petersen KF, Dufour S, Hariri A, Nelson-Williams C, Foo JN, Zhang XM, Dziura J, Lifton RP, Shulman GI. Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease. The New England Journal of Medicine. 362: 1082-9. PMID 20335584 DOI: 10.1056/Nejmoa0907295 | 0.379 | |||
| 2009 | Lowe JK, Maller JB, Pe'er I, Neale BM, Salit J, Kenny EE, Shea JL, Burkhardt R, Smith JG, Ji W, Noel M, Foo JN, Blundell ML, Skilling V, Garcia L, et al. Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. Plos Genetics. 5: e1000365. PMID 19197348 DOI: 10.1371/Journal.Pgen.1000365 | 0.479 | |||
| 2008 | Ji W, Foo JN, O'Roak BJ, Zhao H, Larson MG, Simon DB, Newton-Cheh C, State MW, Levy D, Lifton RP. Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nature Genetics. 40: 592-9. PMID 18391953 DOI: 10.1038/Ng.118 | 0.432 | |||
| Low-probability matches (unlikely to be authored by this person) | |||||
| 2014 | Tan LC, Methawasin K, Teng EW, Ng AR, Seah SH, Au WL, Liu JJ, Foo JN, Zhao Y, Tan EK. Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutations. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 21: 674-8. PMID 23551744 DOI: 10.1111/ene.12142 | 0.298 | |||
| 2020 | Foo JN, Chew EGY, Chung SJ, Peng R, Blauwendraat C, Nalls MA, Mok KY, Satake W, Toda T, Chao Y, Tan LCS, Tandiono M, Lian MM, Ng EY, Prakash KM, et al. Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study. Jama Neurology. PMID 32310270 DOI: 10.1001/Jamaneurol.2020.0428 | 0.296 | |||
| 2017 | Chourabi M, Liew MS, Lim S, H'mida-Ben Brahim D, Boussofara L, Dai L, Wong PM, Foo JN, Sriha B, Robinson KS, Denil S, Common JE, Mamaï O, Ben Khalifa Y, Bollen M, et al. ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis. The Journal of Investigative Dermatology. PMID 28964717 DOI: 10.1016/J.Jid.2017.08.045 | 0.292 | |||
| 2016 | Ai Z, Li M, Liu W, Foo JN, Mansouri O, Yin P, Zhou Q, Tang X, Dong X, Feng S, Xu R, Zhong Z, Chen J, Wan J, Lou T, et al. Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction. Science Translational Medicine. 8: 345ra88. PMID 27358498 DOI: 10.1126/scitranslmed.aaf2106 | 0.291 | |||
| 2014 | Li Y, Foo JN, Liany H, Low HQ, Liu J. Combined linkage and family-based association analysis improves candidate gene detection in Genetic Analysis Workshop 18 simulation data. Bmc Proceedings. 8: S29. PMID 25519379 DOI: 10.1186/1753-6561-8-S1-S29 | 0.29 | |||
| 2020 | Ali G, Awan NB, Idrees S, Khawaja AW, Foo JN, Khor CC, Chang CH, Chew EG, Kiani FR, Jelani M. Identification of a recurrent nonsense mutation in HR gene responsible for atrichia with papular lesions in two Kashmiri families. The Journal of Gene Medicine. e3167. PMID 32020700 DOI: 10.1002/jgm.3167 | 0.289 | |||
| 2013 | Tan EK, Foo JN, Tan L, Au WL, Prakash KM, Ng E, Ikram MK, Wong TY, Liu JJ, Zhao Y. SLC1A2 variant associated with essential tremor but not Parkinson disease in Chinese subjects. Neurology. 80: 1618-9. PMID 23596072 DOI: 10.1212/WNL.0b013e31828f1903 | 0.288 | |||
| 2016 | Pigors M, Common J, Wong C, Malik S, Scott C, Foo J, Liu J, Margolis D, van Heel D, Baurecht H, Rodriguez E, Weidinger S, O’Toole E, Simpson M, Kelsell D. 380 Exome sequencing and rare variant analysis reveals multiple filaggrin mutations in Bangladeshi atopic eczema families and novel risk genes Journal of Investigative Dermatology. 136: S67. DOI: 10.1016/J.Jid.2016.02.413 | 0.288 | |||
| 2020 | Hayat A, Hussain S, Bilal M, Kausar M, Almuzzaini B, Abbas S, Tanveer A, Khan A, Siddiqi S, Foo JN, Ahmad F, Khan F, Khan B, Anees M, Mäkitie O, et al. Biallelic variants in four genes underlying recessive osteogenesis imperfecta. European Journal of Medical Genetics. 103954. PMID 32413570 DOI: 10.1016/j.ejmg.2020.103954 | 0.282 | |||
| 2014 | Skibola CF, Berndt SI, Cerhan JR, Wang Z, Vijai J, Conde L, Bakker Pd, Wang SS, Vajdic CM, Birmann BM, Slager SL, McKay J, Bracci PM, Nieters A, Lan Q, ... ... Foo JN, et al. Abstract 5072: Meta-analysis of genome-wide association studies identifies novel susceptibility loci for follicular lymphoma Cancer Research. 74: 5072-5072. DOI: 10.1158/1538-7445.Am2014-5072 | 0.28 | |||
| 2018 | Sun Y, Hong L, Yang B, Wang C, Foo JN, Bao F, Irwanto A, Yu G, Fu X, Wang Z, You J, Liu J, Zhou G, Liu J, Zhang F. Investigation of the Predisposing Factor of Pemphigus and its clinical subtype through a Genome-wide association and next generation sequence analysis. Journal of the European Academy of Dermatology and Venereology : Jeadv. PMID 30169916 DOI: 10.1111/jdv.15227 | 0.278 | |||
| 2011 | Smedby KE, Foo JN, Skibola CF, Darabi H, Conde L, Hjalgrim H, Kumar V, Chang ET, Rothman N, Cerhan JR, Brooks-Wilson AR, Rehnberg E, Irwan ID, Ryder LP, Brown PN, et al. GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma. Plos Genetics. 7: e1001378. PMID 21533074 DOI: 10.1371/Journal.Pgen.1001378 | 0.277 | |||
| 2021 | Naito T, Satake W, Ogawa K, Suzuki K, Hirata J, Foo JN, Tan EK, Toda T, Okada Y. Trans-Ethnic Fine-Mapping of the Major Histocompatibility Complex Region Linked to Parkinson's Disease. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33973677 DOI: 10.1002/mds.28583 | 0.276 | |||
| 2012 | Foo JN, Liu JJ, Tan EK. Whole-genome and whole-exome sequencing in neurological diseases. Nature Reviews. Neurology. 8: 508-17. PMID 22847385 DOI: 10.1038/nrneurol.2012.148 | 0.275 | |||
| 2013 | Foo JN, Smedby KE, Akers NK, Berglund M, Irwan ID, Jia X, Li Y, Conde L, Darabi H, Bracci PM, Melbye M, Adami HO, Glimelius B, Khor CC, Hjalgrim H, et al. Coding variants at hexa-allelic amino acid 13 of HLA-DRB1 explain independent SNP associations with follicular lymphoma risk. American Journal of Human Genetics. 93: 167-72. PMID 23791106 DOI: 10.1016/j.ajhg.2013.05.020 | 0.275 | |||
| 2016 | Cui Q, Feng QS, Mo HY, Sun J, Xia YF, Zhang H, Foo JN, Guo YM, Chen LZ, Li M, Liu WS, Xu M, Zhou G, He F, Yu X, et al. An Extended Genome-Wide Association Study Identifies Novel Susceptibility Loci for Nasopharyngeal Carcinoma. Human Molecular Genetics. PMID 27436580 DOI: 10.1093/hmg/ddw200 | 0.273 | |||
| 2016 | Seco CZ, Castells-Nobau A, Joo SH, Schraders M, Foo JN, van der Voet M, Velan SS, Nijhof B, Oostrik J, de Vrieze E, Katana R, Mansoor A, Huynen M, Szklarczyk R, Oti M, et al. A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy. Disease Models & Mechanisms. PMID 28067622 DOI: 10.1242/Dmm.026476 | 0.272 | |||
| 2014 | Wong LP, Lai JK, Saw WY, Ong RT, Cheng AY, Pillai NE, Liu X, Xu W, Chen P, Foo JN, Tan LW, Koo SH, Soong R, Wenk MR, Lim WY, et al. Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencing. Plos Genetics. 10: e1004377. PMID 24832686 DOI: 10.1371/journal.pgen.1004377 | 0.271 | |||
| 2019 | Kausar M, Chew EGY, Ullah H, Anees M, Khor CC, Foo JN, Makitie O, Siddiqi S. A Novel Homozygous Frameshift Variant in Causes Spondyloocular Syndrome in a Consanguineous Pakistani Family. Frontiers in Genetics. 10: 144. PMID 30891060 DOI: 10.3389/fgene.2019.00144 | 0.269 | |||
| 2014 | Foo JN, Tan LC, Liany H, Koh TH, Irwan ID, Ng YY, Ahmad-Annuar A, Au WL, Aung T, Chan AY, Chong SA, Chung SJ, Jung Y, Khor CC, Kim J, et al. Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations. Human Molecular Genetics. 23: 3891-7. PMID 24565865 DOI: 10.1093/Hmg/Ddu086 | 0.266 | |||
| 2016 | Oh SH, Baek J, Liany H, Foo JN, Kim KM, Yang SC, Liu J, Song K. A Synonymous Variant in IL10RA Affects RNA Splicing in Pediatric Patients with Refractory Inflammatory Bowel Disease. Journal of Crohn's & Colitis. PMID 27177777 DOI: 10.1093/ecco-jcc/jjw102 | 0.265 | |||
| 2015 | Foo JN, Chung SJ, Tan LC, Liany H, Ryu HS, Hong M, Koh TH, Irwan ID, Au WL, Prakash KM, Aung T, Cheng CY, Chong SA, Khor CC, Lee J, et al. Linking a genome-wide association study signal to a LRRK2 coding variant in Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 26687033 DOI: 10.1002/Mds.26495 | 0.264 | |||
| 2016 | Li Z, Xia Y, Feng LN, Chen JR, Li HM, Cui J, Cai QQ, Sim KS, Nairismägi ML, Laurensia Y, Meah WY, Liu WS, Guo YM, Chen LZ, Feng QS, ... ... Foo JN, et al. Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study. The Lancet. Oncology. PMID 27470079 DOI: 10.1016/S1470-2045(16)30148-6 | 0.262 | |||
| 2023 | Zaka A, Yousaf M, Shahzad S, Rao HZ, Foo JN, Siddiqi S. Structural and functional insights into a novel homozygous missense pathogenic variant in identified in consanguineous Pakistani family. Journal of Biomolecular Structure & Dynamics. 1-12. PMID 37345548 DOI: 10.1080/07391102.2023.2224889 | 0.262 | |||
| 2022 | Ravindran E, Ullah N, Mani S, Chew EGY, Tandiono M, Foo JN, Khor CC, Kaindl AM, Siddiqi S. Case report: Expanding the phenotype of mutations from increased intracranial aneurysm risk to a neurodevelopmental disease. Frontiers in Neurology. 13: 1017654. PMID 36341116 DOI: 10.3389/fneur.2022.1017654 | 0.261 | |||
| 2021 | Brolin K, Bandres-Ciga S, Leonard H, Makarious MB, Blauwendraat C, Mata IF, Foo JN, Pihlstrøm L, Swanberg M, Gan-Or Z, Tan MM. RIC3 variants are not associated with Parkinson's disease in large European, Latin American, or East Asian cohorts. Neurobiology of Aging. PMID 34538707 DOI: 10.1016/j.neurobiolaging.2021.08.009 | 0.258 | |||
| 2013 | Wong LP, Ong RT, Poh WT, Liu X, Chen P, Li R, Lam KK, Pillai NE, Sim KS, Xu H, Sim NL, Teo SM, Foo JN, Tan LW, Lim Y, et al. Deep whole-genome sequencing of 100 southeast Asian Malays. American Journal of Human Genetics. 92: 52-66. PMID 23290073 DOI: 10.1016/J.Ajhg.2012.12.005 | 0.256 | |||
| 2015 | Li M, Foo JN, Wang JQ, Low HQ, Tang XQ, Toh KY, Yin PR, Khor CC, Goh YF, Irwan ID, Xu RC, Andiappan AK, Bei JX, Rotzschke O, Chen MH, et al. Identification of new susceptibility loci for IgA nephropathy in Han Chinese. Nature Communications. 6: 7270. PMID 26028593 DOI: 10.1038/Ncomms8270 | 0.255 | |||
| 2018 | Foo JN, Tan LC, Au WL, Prakash KM, Liu J, Tan EK. No Association of DNM3 with age of onset in Asian Parkinson's disease. European Journal of Neurology. PMID 30133089 DOI: 10.1111/ene.13785 | 0.255 | |||
| 2015 | Chao YX, Ng EY, Foo JN, Liu J, Zhao Y, Tan EK. Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease. Neurogenetics. 16: 241-2. PMID 25791756 DOI: 10.1007/s10048-015-0443-3 | 0.254 | |||
| 2016 | Khor CC, Do T, Jia H, Nakano M, George R, Abu-Amero K, Duvesh R, Chen LJ, Li Z, Nongpiur ME, Perera SA, Qiao C, Wong HT, Sakai H, Barbosa de Melo M, ... ... Foo JN, et al. Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma. Nature Genetics. PMID 27064256 DOI: 10.1038/Ng.3540 | 0.254 | |||
| 2013 | Foo JN, Liany H, Bei JX, Yu XQ, Liu J, Au WL, Prakash KM, Tan LC, Tan EK. Rare lysosomal enzyme gene SMPD1 variant (p.R591C) associates with Parkinson's disease. Neurobiology of Aging. 34: 2890.e13-5. PMID 23871123 DOI: 10.1016/j.neurobiolaging.2013.06.010 | 0.253 | |||
| 2019 | Foo JN, Xia Y. Polycystic kidney disease: new knowledge and future promises. Current Opinion in Genetics & Development. 56: 69-75. PMID 31476629 DOI: 10.1016/j.gde.2019.06.007 | 0.249 | |||
| 2015 | Foo JN, Zhao Y, Liu J, Tan EK. Nonsynonymous variants in MC1R are rare in Chinese Parkinson disease cases. Annals of Neurology. 78: 152-3. PMID 25894970 DOI: 10.1002/ana.24419 | 0.247 | |||
| 2014 | Skibola CF, Berndt SI, Vijai J, Conde L, Wang Z, Yeager M, de Bakker PI, Birmann BM, Vajdic CM, Foo JN, Bracci PM, Vermeulen RC, Slager SL, de Sanjose S, Wang SS, et al. Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region. American Journal of Human Genetics. 95: 462-71. PMID 25279986 DOI: 10.1016/J.Ajhg.2014.09.004 | 0.245 | |||
| 2010 | Wang Y, Fu W, Xie F, Wang Y, Chu X, Wang H, Shen M, Wang Y, Wang Y, Sun W, Lei R, Yang L, Wu H, Foo J, Liu J, et al. Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population. Journal of Human Genetics. 55: 490-4. PMID 20485444 DOI: 10.1038/Jhg.2010.53 | 0.243 | |||
| 2017 | Ma D, Foo JN, Yulin Ng E, Zhao Y, Liu JJ, Tan EK. Screening for TMEM230 mutations in young-onset Parkinson's disease. Neurobiology of Aging. PMID 28709721 DOI: 10.1016/j.neurobiolaging.2017.06.011 | 0.24 | |||
| 2018 | Ma D, Ng S, Setiawan F, Foo J, Ng E, Zhao Y, Liu J, Tan E. Screening for TMEM230 mutations in young onset Parkinson’s disease Parkinsonism & Related Disorders. 46: e70. DOI: 10.1016/J.PARKRELDIS.2017.11.239 | 0.239 | |||
| 2014 | Dunstan SJ, Hue NT, Han B, Li Z, Tram TT, Sim KS, Parry CM, Chinh NT, Vinh H, Lan NP, Thieu NT, Vinh PV, Koirala S, Dongol S, Arjyal A, ... ... Foo JN, et al. Variation at HLA-DRB1 is associated with resistance to enteric fever. Nature Genetics. 46: 1333-6. PMID 25383971 DOI: 10.1038/Ng.3143 | 0.239 | |||
| 2013 | Tayebi N, Ke T, Foo JN, Friedlander Y, Liu J, Heng CK. Association of single nucleotide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean population Clinical Biochemistry. 46: 755-759. PMID 23337689 DOI: 10.1016/j.clinbiochem.2013.01.004 | 0.238 | |||
| 2013 | Foo JN, Liu J, Tan EK. Next-generation sequencing diagnostics for neurological diseases/disorders: from a clinical perspective. Human Genetics. 132: 721-34. PMID 23525706 DOI: 10.1007/s00439-013-1287-2 | 0.237 | |||
| 2019 | Chew EGY, Tan LCS, Au WL, Prakash KM, Liu J, Foo JN, Tan EK. ITPKB and ZNF184 are associated with Parkinson's disease risk in East Asians. Neurobiology of Aging. PMID 30814023 DOI: 10.1016/j.neurobiolaging.2019.01.026 | 0.236 | |||
| 2021 | Ali G, Sadia, Foo JN, Nasir A, Chang CH, Chew EG, Latif Z, Azeem Z, Ain-Ul-Batool S, Kazmi SAR, Awan NB, Khan AH, Rehman FU, Khalid M, Wali A, et al. Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in in a Kashmiri Family with Bardet-Biedl Syndrome. Biomed Research International. 2021: 6626015. PMID 33688495 DOI: 10.1155/2021/6626015 | 0.234 | |||
| 2022 | Tay KY, Wu KX, Chioh FWJ, Autio MI, Pek NMQ, Narmada BC, Tan SH, Low AF, Lian MM, Chew EGY, Lau HH, Kao SL, Teo AKK, Foo JN, Foo RSY, et al. Trans-interaction of risk loci 6p24.1 and 10q11.21 is associated with endothelial damage in coronary artery disease. Atherosclerosis. 362: 11-22. PMID 36435092 DOI: 10.1016/j.atherosclerosis.2022.10.012 | 0.233 | |||
| 2017 | Liu H, Wang Z, Li Y, Yu G, Fu X, Wang C, Liu W, Yu Y, Bao F, Irwanto A, Liu J, Chu T, Andiappan AK, Maurer-Stroh S, Limviphuvadh V, ... ... Foo JN, et al. Genome-wide Analysis of Protein-Coding Variants in Leprosy. The Journal of Investigative Dermatology. PMID 28842327 DOI: 10.1016/J.Jid.2017.08.004 | 0.233 | |||
| 2020 | Chao YX, Lee B, Ng EY, Lian MM, Chew EGY, Tandiono M, Li Z, Khor CC, Kumar P, Tan LCS, Foo JN, Tan EK. Association analysis of PSAP variants in Parkinson's disease patients. Brain : a Journal of Neurology. PMID 33221828 DOI: 10.1093/brain/awaa358 | 0.231 | |||
| 2014 | Foo JN, Liany H, Tan LC, Au WL, Prakash KM, Liu J, Tan EK. DNAJ mutations are rare in Chinese Parkinson's disease patients and controls. Neurobiology of Aging. 35: 935.e1-2. PMID 24126164 DOI: 10.1016/j.neurobiolaging.2013.09.018 | 0.23 | |||
| 2013 | Lu Y, Vitart V, Burdon KP, Khor CC, Bykhovskaya Y, Mirshahi A, Hewitt AW, Koehn D, Hysi PG, Ramdas WD, Zeller T, Vithana EN, Cornes BK, Tay WT, Tai ES, ... ... Foo JN, et al. Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nature Genetics. 45: 155-63. PMID 23291589 DOI: 10.1038/Ng.2506 | 0.228 | |||
| 2016 | Foo JN, Tan LC, Irwan ID, Au WL, Low HQ, Prakash KM, Ahmad-Annuar A, Bei J, Chan AY, Chen CM, Chen YC, Chung SJ, Deng H, Lim SY, Mok V, et al. Genome-wide association study of Parkinson's disease in East Asians. Human Molecular Genetics. PMID 28011712 DOI: 10.1093/Hmg/Ddw379 | 0.228 | |||
| 2015 | Sadananda SN, Foo JN, Toh MT, Cermakova L, Trigueros-Motos L, Chan T, Liany H, Collins J, Germai S, Singaraja RR, Hayden MR, Francis GA, Frohlich J, Khor CC, Brunham LR. Targeted Next-Generation Sequencing to Diagnose Disorders of HDL Cholesterol. Journal of Lipid Research. PMID 26255038 DOI: 10.1194/Jlr.P058891 | 0.226 | |||
| 2021 | Sia MW, Foo JN, Saffari SE, Wong AS, Khor CC, Yuan JM, Tan EK, Koh WP, Tan LC. Polygenic Risk Scores in a Prospective Parkinson's Disease Cohort. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 34402545 DOI: 10.1002/mds.28761 | 0.223 | |||
| 2013 | Xin Lee JJ, En Tan GS, Tan CH, Pan S, Khor CC, Liu J, Foo JN, Tan SY, Ng SB, Tao M, Lim ST, Tang T. Prognostic Significance Of rs6773853 Susceptibility Locus In B-Cell Non-Hodgkin’s Lymphoma Blood. 122: 4249-4249. DOI: 10.1182/BLOOD.V122.21.4249.4249 | 0.22 | |||
| 2019 | Idrees S, Foo JN, Khor CC, Jelani M, Ghazanfar A. A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri families. The Journal of Gene Medicine. e3113. PMID 31310406 DOI: 10.1002/jgm.3113 | 0.215 | |||
| 2021 | Chen Z, Tan YJ, Lian MM, Tandiono M, Foo JN, Lim WK, Kandiah N, Tan EK, Ng ASL. High Diagnostic Utility Incorporating a Targeted Neurodegeneration Gene Panel With MRI Brain Diagnostic Algorithms in Patients With Young-Onset Cognitive Impairment With Leukodystrophy. Frontiers in Neurology. 12: 631407. PMID 33597917 DOI: 10.3389/fneur.2021.631407 | 0.215 | |||
| 2023 | Lim SY, Dy Closas AMF, Tan AH, Lim JL, Tan YJ, Vijayanathan Y, Tay YW, Abdul Khalid RB, Ng WK, Kanesalingam R, Martinez-Martin P, Ahmad Annuar A, Lit LC, Foo JN, Lim WK, et al. New insights from a multi-ethnic Asian progressive supranuclear palsy cohort. Parkinsonism & Related Disorders. 108: 105296. PMID 36682278 DOI: 10.1016/j.parkreldis.2023.105296 | 0.213 | |||
| 2015 | Foo JN, Liu J, Yu XQ. GWAS reveal novel IgA nephropathy risk loci. Oncotarget. PMID 26119152 | 0.21 | |||
| 2012 | Yu XQ, Li M, Zhang H, Low HQ, Wei X, Wang JQ, Sun LD, Sim KS, Li Y, Foo JN, Wang W, Li ZJ, Yin XY, Tang XQ, Fan L, et al. A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy. Nature Genetics. 44: 178-82. PMID 22197929 DOI: 10.1038/ng.1047 | 0.203 | |||
| 2023 | Saffie-Awad P, Elsayed I, Sanyaolu AO, Crea PW, Schumacher Schuh AF, Levine KS, Vitale D, Korestky MJ, Kim J, Leal TP, Periñan MT, Dey S, Noyce AJ, Reyes-Palomares A, Rodriguez-Losada N, ... Foo JN, et al. Evaluating the performance of polygenic risk profiling across diverse ancestry populations in Parkinson's disease. Medrxiv : the Preprint Server For Health Sciences. PMID 38076954 DOI: 10.1101/2023.11.28.23299090 | 0.202 | |||
| 2020 | Bonassi A, Cataldo I, Gabrieli G, Foo JN, Lepri B, Esposito G. Oxytocin Receptor Gene Polymorphisms and Early Parental Bonding Interact in Shaping Instagram Social Behavior. International Journal of Environmental Research and Public Health. 17. PMID 33022913 DOI: 10.3390/ijerph17197232 | 0.199 | |||
| 2018 | Chew EG, Foo JN, Tan EK. Identifying genes in Parkinson disease: state of the art. The Medical Journal of Australia. 208: 381-382. PMID 29764346 DOI: 10.5694/mja17.01254 | 0.199 | |||
| 2012 | Andiappan AK, Foo JN, Choy MW, Chen H, Common JE, Tang MB, van Bever HP, Giam YC, Suri BK, Ramani A, Nilkanth PP, Lane EB, Wang de Y, Chew FT, Liu J. Validation of GWAS loci for atopic dermatitis in a Singapore Chinese population. The Journal of Investigative Dermatology. 132: 1505-7. PMID 22318392 DOI: 10.1038/jid.2011.471 | 0.196 | |||
| 2013 | Zhao Y, Ho P, Prakash KM, Foo JN, Liu JJ, Au WL, Tan LC, Tan EK. Analysis of EIF4G1 in Parkinson's disease among Asians. Neurobiology of Aging. 34: 1311.e5-6. PMID 23092605 DOI: 10.1016/j.neurobiolaging.2012.09.003 | 0.196 | |||
| 2013 | Tan DE, Foo JN, Bei JX, Chang J, Peng R, Zheng X, Wei L, Huang Y, Lim WY, Li J, Cui Q, Chew SH, Ebstein RP, Kuperan P, Lim ST, et al. Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population. Nature Genetics. 45: 804-7. PMID 23749188 DOI: 10.1038/ng.2666 | 0.194 | |||
| 2017 | Wong XFCC, Denil SLIJ, Foo JN, Chen H, Ling Tay AS, Haines RL, Tang MBY, McLean WHI, Sandilands A, Smith FJD, Lane EB, Liu J, Common JEA. Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants. The Journal of Allergy and Clinical Immunology. PMID 29056476 DOI: 10.1016/j.jaci.2017.10.001 | 0.193 | |||
| 2020 | Chen Z, Xu Z, Cheng Q, Tan YJ, Ong HL, Zhao Y, Lim WK, Teo JX, Foo JN, Lee HY, Tan JMM, Hang L, Yu WY, Ting SKS, Tan EK, et al. Phenotypic bases of NOTCH2NLC GGC expansion positive Neuronal Intranuclear Inclusion Disease (NIID) in a South East Asian cohort. Clinical Genetics. PMID 32602554 DOI: 10.1111/cge.13802 | 0.191 | |||
| 2011 | Low HQ, Chen CP, Kasiman K, Thalamuthu A, Ng SS, Foo JN, Chang HM, Wong MC, Tai ES, Liu J. A comprehensive association analysis of homocysteine metabolic pathway genes in Singaporean Chinese with ischemic stroke. Plos One. 6: e24757. PMID 21935458 DOI: 10.1371/journal.pone.0024757 | 0.189 | |||
| 2012 | Li S, Qian J, Yang Y, Zhao W, Dai J, Bei JX, Foo JN, McLaren PJ, Li Z, Yang J, Shen F, Liu L, Yang J, Li S, Pan S, et al. GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers. Plos Genetics. 8: e1002791. PMID 22807686 DOI: 10.1371/Journal.Pgen.1002791 | 0.189 | |||
| 2021 | Cataldo I, Bonassi A, Lepri B, Foo JN, Setoh P, Esposito G. Recalled Parental Bonding Interacts with Oxytocin Receptor Gene Polymorphism in Modulating Anxiety and Avoidance in Adult Relationships. Brain Sciences. 11. PMID 33919740 DOI: 10.3390/brainsci11040496 | 0.187 | |||
| 2023 | Le Guen Y, Luo G, Ambati A, Damotte V, Jansen I, Yu E, Nicolas A, de Rojas I, Peixoto Leal T, Miyashita A, Bellenguez C, Lian MM, Parveen K, Morizono T, Park H, ... ... Foo JN, et al. Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by subtypes. Proceedings of the National Academy of Sciences of the United States of America. 120: e2302720120. PMID 37643212 DOI: 10.1073/pnas.2302720120 | 0.187 | |||
| 2022 | Kausar M, Ain NU, Hayat F, Fatima H, Azim S, Ullah H, Mushtaq M, Khalid S, Hussain S, Naz S, Janjua J, Amjad SB, Baig RM, Makitie O, Qamar R, ... ... Foo JN, et al. Biallelic variants in CHST3 cause Spondyloepiphyseal dysplasia with joint dislocations in three Pakistani kindreds. Bmc Musculoskeletal Disorders. 23: 818. PMID 36042462 DOI: 10.1186/s12891-022-05719-6 | 0.183 | |||
| 2013 | Li J, Foo JN, Schoof N, Varghese JS, Fernandez-Navarro P, Gierach GL, Quek ST, Hartman M, Nord S, Kristensen VN, Pollán M, Figueroa JD, Thompson DJ, Li Y, Khor CC, et al. Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size. Journal of Medical Genetics. 50: 666-73. PMID 23825393 DOI: 10.1136/jmedgenet-2013-101708 | 0.181 | |||
| 2017 | Haycock PC, Burgess S, Nounu A, Zheng J, Okoli GN, Bowden J, Wade KH, Timpson NJ, Evans DM, Willeit P, Aviv A, Gaunt TR, Hemani G, Mangino M, ... ... Foo JN, et al. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study. Jama Oncology. PMID 28241208 DOI: 10.1001/Jamaoncol.2016.5945 | 0.176 | |||
| 2019 | Deng X, Xiao B, Allen JC, Ng E, Foo JN, Lo YL, Tan LCS, Tan EK. Parkinson's disease GWAS-linked Park16 carriers show greater motor progression. Journal of Medical Genetics. PMID 30814270 DOI: 10.1136/jmedgenet-2018-105661 | 0.173 | |||
| 2014 | Baecklund F, Foo JN, Bracci P, Darabi H, Karlsson R, Hjalgrim H, Rosenquist R, Adami HO, Glimelius B, Melbye M, Conde L, Liu J, Humphreys K, Skibola CF, Smedby KE. A comprehensive evaluation of the role of genetic variation in follicular lymphoma survival. Bmc Medical Genetics. 15: 113. PMID 25294155 DOI: 10.1186/s12881-014-0113-6 | 0.171 | |||
| 2015 | Aung T, Ozaki M, Mizoguchi T, Allingham RR, Li Z, Haripriya A, Nakano S, Uebe S, Harder JM, Chan AS, Lee MC, Burdon KP, Astakhov YS, Abu-Amero KK, Zenteno JC, ... ... Foo JN, et al. Corrigendum: A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nature Genetics. 47: 689. PMID 26018902 DOI: 10.1038/Ng0615-689C | 0.171 | |||
| 2022 | Neoh MJY, Setoh P, Bizzego A, Tandiono M, Foo JN, Lee A, Bornstein MH, Esposito G. Gene-Environment Interactions in Face Categorization: Oxytocin Receptor Genotype x Childcare Experience Shortens Reaction Time. Frontiers in Psychology. 13: 873676. PMID 35756198 DOI: 10.3389/fpsyg.2022.873676 | 0.166 | |||
| 2021 | Carollo A, Bonassi A, Cataldo I, Gabrieli G, Tandiono M, Foo JN, Lepri B, Esposito G. The relation between oxytocin receptor gene polymorphisms, adult attachment and Instagram sociability: An exploratory analysis. Heliyon. 7: e07894. PMID 34611556 DOI: 10.1016/j.heliyon.2021.e07894 | 0.163 | |||
| 2020 | Ng AS, Lim WK, Xu Z, Ong HL, Tan YJ, Sim WY, Ng EY, Teo JX, Foo JN, Lim TC, Yu WY, Chan LL, Lee HY, Chen Z, Lim EW, et al. NOTCH2NLC GGC repeat expansions are associated with sporadic essential tremor: Variable disease expressivity on long-term follow-up. Annals of Neurology. PMID 32495371 DOI: 10.1002/ana.25803 | 0.156 | |||
| 2017 | Baecklund F, Foo JN, Askling J, Eloranta S, Glimelius I, Liu J, Hjalgrim H, Rosenquist R, Padyukov L, Smedby KE. Possible Interaction Between Cigarette Smoking and HLA-DRB1 Variation in the Risk of Follicular Lymphoma. American Journal of Epidemiology. 1-7. PMID 28369180 DOI: 10.1093/aje/kww118 | 0.156 | |||
| 2019 | Kausar M, Siddiqi S, Yaqoob M, Mansoor S, Makitie O, Mir A, Khor CC, Foo JN, Anees M. Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta. Journal of Biomedical Science. 26: 31. PMID 31030663 DOI: 10.1186/s12929-019-0525-x | 0.155 | |||
| 2020 | Bonassi A, Cataldo I, Gabrieli G, Foo JN, Lepri B, Esposito G. P.677 Serotonin transporter gene polymorphisms and confidence in adult relationships affect the number of followed people on Instagram European Neuropsychopharmacology. 40: S385-S386. DOI: 10.1016/j.euroneuro.2020.09.500 | 0.154 | |||
| 2020 | Cataldo I, Neoh MJ, Chew WF, Foo JN, Lepri B, Esposito G. Oxytocin receptor gene and parental bonding modulate prefrontal responses to cries: a NIRS Study. Scientific Reports. 10: 8588. PMID 32444796 DOI: 10.1038/s41598-020-65582-0 | 0.152 | |||
| 2019 | Low JH, Li P, Chew EGY, Zhou B, Suzuki K, Zhang T, Lian MM, Liu M, Aizawa E, Rodriguez Esteban C, Yong KSM, Chen Q, Campistol JM, Fang M, Khor CC, ... Foo JN, et al. Generation of Human PSC-Derived Kidney Organoids with Patterned Nephron Segments and a De Novo Vascular Network. Cell Stem Cell. PMID 31303547 DOI: 10.1016/j.stem.2019.06.009 | 0.148 | |||
| 2013 | Zheng X, Bei JX, Xu H, Lee J, Chong SA, Sim K, Liany H, Shyong TE, Liu T, Foo JN, Irwan ID, Teo YY, Liu J. The association between rare large duplication of 16p11.2 and schizophrenia in the Singaporean Chinese population. Schizophrenia Research. 146: 368-9. PMID 23510594 DOI: 10.1016/j.schres.2013.02.029 | 0.148 | |||
| 2022 | Bonassi A, Cataldo I, Gabrieli G, Tandiono M, Foo JN, Lepri B, Esposito G. The Interaction between Serotonin Transporter Allelic Variation and Maternal Care Modulates Instagram Sociability in a Sample of Singaporean Users. International Journal of Environmental Research and Public Health. 19. PMID 35564743 DOI: 10.3390/ijerph19095348 | 0.143 | |||
| 2023 | Murray A, Gough G, Cindrić A, Vučković F, Koschut D, Borelli V, Petrović DJ, Bekavac A, Plećaš A, Hribljan V, Brunmeir R, Jurić J, Pučić-Baković M, Slana A, Deriš H, ... ... Foo JN, et al. Dose imbalance of DYRK1A kinase causes systemic progeroid status in Down syndrome by increasing the un-repaired DNA damage and reducing LaminB1 levels. Ebiomedicine. 104692. PMID 37451904 DOI: 10.1016/j.ebiom.2023.104692 | 0.14 | |||
| 2021 | Li Z, Wang Z, Lee MC, Zenkel M, Peh E, Ozaki M, Topouzis F, Nakano S, Chan A, Chen S, Williams SEI, Orr A, Nakano M, Kobakhidze N, ... ... Foo JN, et al. Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye. Jama. 325: 753-764. PMID 33620406 DOI: 10.1001/jama.2021.0507 | 0.136 | |||
| 2020 | Alić I, Goh PA, Murray A, Portelius E, Gkanatsiou E, Gough G, Mok KY, Koschut D, Brunmeir R, Yeap YJ, O'Brien NL, Groet J, Shao X, Havlicek S, Dunn NR, ... ... Foo JN, et al. Patient-specific Alzheimer-like pathology in trisomy 21 cerebral organoids reveals BACE2 as a gene dose-sensitive AD suppressor in human brain. Molecular Psychiatry. PMID 32647257 DOI: 10.1038/S41380-020-0806-5 | 0.134 | |||
| 2015 | Foo JN, Liu J, Tan EK. CHCHD2 and Parkinson's disease. The Lancet. Neurology. 14: 681-2. PMID 26067114 DOI: 10.1016/S1474-4422(15)00098-8 | 0.134 | |||
| 2020 | Ng ASL, Xu Z, Chen Z, Tan YJ, Lim WK, Ting SKS, Yu WY, Cheng QH, Foo JN, Tan EK, Lim TCC. NOTCH2NLC-linked neuronal intranuclear inclusion body disease and fragile X-associated tremor/ataxia syndrome. Brain : a Journal of Neurology. PMID 32789443 DOI: 10.1093/brain/awaa210 | 0.124 | |||
| 2024 | Liu M, Zhang C, Gong X, Zhang T, Lian MM, Chew EGY, Cardilla A, Suzuki K, Wang H, Yuan Y, Li Y, Naik MY, Wang Y, Zhou B, Soon WZ, ... ... Foo JN, et al. Kidney organoid models reveal cilium-autophagy metabolic axis as a therapeutic target for PKD both in vitro and in vivo. Cell Stem Cell. 31: 52-70.e8. PMID 38181751 DOI: 10.1016/j.stem.2023.12.003 | 0.123 | |||
| 2013 | Zhang FR, Liu H, Irwanto A, Fu XA, Li Y, Yu GQ, Yu YX, Chen MF, Low HQ, Li JH, Bao FF, Foo JN, Bei JX, Jia XM, Liu J, et al. HLA-B*13:01 and the dapsone hypersensitivity syndrome. The New England Journal of Medicine. 369: 1620-8. PMID 24152261 DOI: 10.1056/NEJMoa1213096 | 0.12 | |||
| 2021 | Bonassi A, Carollo A, Cataldo I, Gabrieli G, Tandiono M, Foo JN, Lepri B, Esposito G. Modulation of Instagram Number of Followings by Avoidance in Close Relationships in Young Adults under a Gene x Environment Perspective. International Journal of Environmental Research and Public Health. 18. PMID 34300010 DOI: 10.3390/ijerph18147547 | 0.117 | |||
| 2016 | Foo JN, Lee J, Tan LC, Liu J, Tan EK. Large 3-Mb deletions at 22q11.2 locus in parkinson's disease and schizophrenia. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 27787935 DOI: 10.1002/mds.26822 | 0.109 | |||
| 2013 | Conde L, Foo JN, Riby J, Liu J, Darabi H, Hjalgrim H, Bracci PM, Smedby KE, Skibola CF. X chromosome-wide association study of follicular lymphoma. British Journal of Haematology. 162: 858-62. PMID 23795672 DOI: 10.1111/bjh.12438 | 0.099 | |||
| 2018 | Wang Y, Liu KI, Sutrisnoh NB, Srinivasan H, Zhang J, Li J, Zhang F, Lalith CRJ, Xing H, Shanmugam R, Foo JN, Yeo HT, Ooi KH, Bleckwehl T, Par YYR, et al. Systematic evaluation of CRISPR-Cas systems reveals design principles for genome editing in human cells. Genome Biology. 19: 62. PMID 29843790 DOI: 10.1186/s13059-018-1445-x | 0.099 | |||
| 2022 | Zheng X, Ho QWC, Chua M, Stelmashenko O, Yeo XY, Muralidharan S, Torta F, Chew EGY, Lian MM, Foo JN, Jung S, Wong SH, Tan NS, Tong N, Rutter GA, et al. Destabilization of β Cell FIT2 by saturated fatty acids alter lipid droplet numbers and contribute to ER stress and diabetes. Proceedings of the National Academy of Sciences of the United States of America. 119: e2113074119. PMID 35254894 DOI: 10.1073/pnas.2113074119 | 0.096 | |||
| 2021 | Alić I, Goh PA, Murray A, Portelius E, Gkanatsiou E, Gough G, Mok KY, Koschut D, Brunmeir R, Yeap YJ, O'Brien NL, Groet J, Shao X, Havlicek S, Dunn NR, ... ... Foo JN, et al. Correction: Patient-specific Alzheimer-like pathology in trisomy 21 cerebral organoids reveals BACE2 as a gene dose-sensitive AD suppressor in human brain. Molecular Psychiatry. PMID 34272490 DOI: 10.1038/s41380-021-01206-x | 0.086 | |||
| 2015 | Sadananda S, Foo J, Toh M, Francis G, Frohlich J, Khor C, Brunham L. Molecular diagnosis of abnormalities of HDL cholesterol by targeted next-generation sequencing Atherosclerosis. 241: e117. DOI: 10.1016/J.ATHEROSCLEROSIS.2015.04.407 | 0.085 | |||
| 2015 | Cheng CY, Yamashiro K, Chen LJ, Ahn J, Huang L, Huang L, Cheung CM, Miyake M, Cackett PD, Yeo IY, Laude A, Mathur R, Pang J, Sim KS, Koh AH, ... ... Foo JN, et al. Corrigendum: New loci and coding variants confer risk for age-related macular degeneration in East Asians. Nature Communications. 6: 6817. PMID 25817435 DOI: 10.1038/Ncomms7817 | 0.075 | |||
| 2015 | Brunham L, Sadananda S, Foo J, Frohlich J, Francis G, Khor C. TARGETED NEXT-GENERATION SEQUENCING TO DIAGNOSE ABNORMALITIES OF HDL CHOLESTEROL Canadian Journal of Cardiology. 31: S296. DOI: 10.1016/J.CJCA.2015.07.729 | 0.074 | |||
| 2018 | Ng Y, Common J, Wong C, Bishnoi P, Foo J, Denil S, Venkatesh B, Tohari S, Ng A, Lacina L, Lunny D, Firdaus M, Oh H, Ho M, Giam Y, et al. LB1543 Comprehensive molecular analysis of 61 epidermolysis bullosa families from Singapore and Malaysia Journal of Investigative Dermatology. 138: B13. DOI: 10.1016/J.JID.2018.06.077 | 0.065 | |||
| 2014 | Li J, Lindström LS, Foo JN, Rafiq S, Schmidt MK, Pharoah PD, Michailidou K, Dennis J, Bolla MK, Wang Q, Van 't Veer LJ, Cornelissen S, Rutgers E, Southey MC, Apicella C, et al. 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy. Nature Communications. 5: 4051. PMID 24937182 DOI: 10.1038/Ncomms5051 | 0.037 | |||
| 2021 | Zhang N, Lin J, Lin VPH, Milbreta U, Chin JS, Chew EGY, Lian MM, Foo JN, Zhang K, Wu W, Chew SY. A 3D Fiber-Hydrogel Based Non-Viral Gene Delivery Platform Reveals that microRNAs Promote Axon Regeneration and Enhance Functional Recovery Following Spinal Cord Injury. Advanced Science (Weinheim, Baden-Wurttemberg, Germany). e2100805. PMID 34050637 DOI: 10.1002/advs.202100805 | 0.016 | |||
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