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Jia Nee Foo, Ph.D. - Publications

Affiliations: 
2009 Yale University, New Haven, CT 
Area:
Genetics
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26 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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
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