Jia Nee Foo

8.9k total citations · 2 hit papers
71 papers, 2.1k citations indexed

About

Jia Nee Foo is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Jia Nee Foo has authored 71 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 26 papers in Genetics and 20 papers in Neurology. Recurrent topics in Jia Nee Foo's work include Parkinson's Disease Mechanisms and Treatments (16 papers), Neurological diseases and metabolism (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Jia Nee Foo is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (16 papers), Neurological diseases and metabolism (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Jia Nee Foo collaborates with scholars based in Singapore, United States and Pakistan. Jia Nee Foo's co-authors include Richard P. Lifton, Jianjun Liu, David B. Simon, Christopher Newton‐Cheh, Daniel Levy, Weizhen Ji, Martin G. Larson, Matthew W. State, Brian J. O’Roak and Hongyu Zhao and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Jia Nee Foo

68 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

2008 543 citations Jia Nee Foo et al. profile →
Generation of Human PSC-Derived Kidney Organoids with Patterned Nephron Segments and a De Novo Vascular Network

2019 253 citations Jian Hui Low, Pin Li et al. Cell stem cell profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Jia Nee Foo Singapore	20	896	559	335	304	264	71	2.1k
Elisabeth Graf Germany	25	1.2k 1.4×	411 0.7×	340 1.0×	292 1.0×	136 0.5×	45	2.8k
Jing‐Ping Lin United States	21	788 0.9×	263 0.5×	134 0.4×	191 0.6×	137 0.5×	52	2.1k
Annette Hammes Germany	19	1.2k 1.4×	445 0.8×	190 0.6×	61 0.2×	230 0.9×	33	2.1k
George E. Farmer United States	17	957 1.1×	206 0.4×	133 0.4×	136 0.4×	299 1.1×	41	2.2k
Tetsuya Ueba Japan	23	662 0.7×	194 0.3×	93 0.3×	293 1.0×	478 1.8×	112	1.8k
Annie Laquerrière France	32	1.4k 1.5×	584 1.0×	84 0.3×	343 1.1×	248 0.9×	109	3.3k
Elisabetta Gazzerro Italy	28	2.4k 2.6×	418 0.7×	216 0.6×	272 0.9×	42 0.2×	52	3.5k
Antônio Marcondes Lerário United States	30	1.2k 1.4×	769 1.4×	1.1k 3.1×	118 0.4×	160 0.6×	139	3.3k
Colm O’Brien Ireland	39	1.6k 1.8×	183 0.3×	71 0.2×	431 1.4×	217 0.8×	153	4.8k
Göknur Haliloğlu Türkiye	23	922 1.0×	259 0.5×	75 0.2×	110 0.4×	210 0.8×	116	1.7k

Countries citing papers authored by Jia Nee Foo

Since Specialization

Citations

This map shows the geographic impact of Jia Nee Foo's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jia Nee Foo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jia Nee Foo more than expected).

Fields of papers citing papers by Jia Nee Foo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jia Nee Foo. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jia Nee Foo. The network helps show where Jia Nee Foo may publish in the future.

Co-authorship network of co-authors of Jia Nee Foo

This figure shows the co-authorship network connecting the top 25 collaborators of Jia Nee Foo. A scholar is included among the top collaborators of Jia Nee Foo based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jia Nee Foo. Jia Nee Foo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Lim, Kah‐Leong, et al.. (2024). Synaptic Vesicle Glycoprotein 2C: a role in Parkinson’s disease. Frontiers in Cellular Neuroscience. 18. 1437144–1437144. 1 indexed citations

Lim, Shen‐Yang, Ai Huey Tan, Jia Nee Foo, et al.. (2024). Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry. Journal of Movement Disorders. 17(2). 213–217. 3 indexed citations

Tan, Yi Jayne, Jia Nee Foo, Michelle Mulan Lian, et al.. (2023). C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort. Annals of Clinical and Translational Neurology. 10(4). 568–578. 4 indexed citations

Zheng, Xiaofeng, Xin Yi Yeo, Sneha Muralidharan, et al.. (2022). 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. 119(11). e2113074119–e2113074119. 27 indexed citations

Mani, Shyamala, Elaine Guo Yan Chew, Moses Tandiono, et al.. (2022). Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease. Frontiers in Neurology. 13. 1017654–1017654. 2 indexed citations

Wu, Kan Xing, Matias Autio, Nicole Min Qian Pek, et al.. (2022). Trans-interaction of risk loci 6p24.1 and 10q11.21 is associated with endothelial damage in coronary artery disease. Atherosclerosis. 362. 11–22. 2 indexed citations

Ain, Noor Ul, Shahid Hussain, Sadaf Naz, et al.. (2022). Biallelic variants in CHST3 cause Spondyloepiphyseal dysplasia with joint dislocations in three Pakistani kindreds. BMC Musculoskeletal Disorders. 23(1). 818–818. 5 indexed citations

Brolin, Kajsa, Sara Bandrés‐Ciga, Hampton L. Leonard, et al.. (2021). RIC3 variants are not associated with Parkinson's disease in large European, Latin American, or East Asian cohorts. Neurobiology of Aging. 109. 264–268. 2 indexed citations

Dominguez, Jacqueline C., Yi Jayne Tan, Arlene R. Ng, et al.. (2021). Novel Optineurin Frameshift Insertion in a Family With Frontotemporal Dementia and Parkinsonism Without Amyotrophic Lateral Sclerosis. Frontiers in Neurology. 12. 645913–645913. 9 indexed citations

10.

Carollo, Alessandro, Andrea Bonassi, Ilaria Cataldo, et al.. (2021). The relation between oxytocin receptor gene polymorphisms, adult attachment and Instagram sociability: An exploratory analysis. Heliyon. 7(9). e07894–e07894. 10 indexed citations

11.

Chen, Zhiyong, Michelle Mulan Lian, Moses Tandiono, et al.. (2021). 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. 631407–631407. 4 indexed citations

12.

Chen, Zhiyong, Zheyu Xu, Yi Jayne Tan, et al.. (2020). Phenotypic bases of NOTCH2NLC GGC expansion positive neuronal intranuclear inclusion disease in a Southeast Asian cohort. Clinical Genetics. 98(3). 274–281. 29 indexed citations

13.

Chew, Elaine Guo Yan, Louis C.S. Tan, Wing‐Lok Au, et al.. (2019). ITPKB and ZNF184 are associated with Parkinson's disease risk in East Asians. Neurobiology of Aging. 86. 201.e15–201.e17. 7 indexed citations

14.

Foo, Jia Nee & Yun Xia. (2019). Polycystic kidney disease: new knowledge and future promises. Current Opinion in Genetics & Development. 56. 69–75. 4 indexed citations

15.

Low, Jian Hui, Pin Li, Elaine Guo Yan Chew, et al.. (2019). Generation of Human PSC-Derived Kidney Organoids with Patterned Nephron Segments and a De Novo Vascular Network. Cell stem cell. 25(3). 373–387.e9. 253 indexed citations breakdown →

16.

Chew, Elaine Guo Yan, Herty Liany, Louis C.S. Tan, et al.. (2018). Evaluation of novel Parkinson's disease candidate genes in the Chinese population. Neurobiology of Aging. 74. 235.e1–235.e4. 7 indexed citations

17.

Foo, Jia Nee, Johan Askling, Sandra Eloranta, et al.. (2017). Possible Interaction Between Cigarette Smoking and HLA-DRB1 Variation in the Risk of Follicular Lymphoma. American Journal of Epidemiology. 185(8). 681–687. 8 indexed citations

18.

Cui, Qian, Qi-Sheng Feng, Hao-Yuan Mo, et al.. (2016). An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma. Human Molecular Genetics. 25(16). 3626–3634. 30 indexed citations

19.

Foo, Jia Nee, Herty Liany, Jin‐Xin Bei, et al.. (2013). A rare lysosomal enzyme gene SMPD1 variant (p.R591C) associates with Parkinson's disease. Neurobiology of Aging. 34(12). 2890.e13–2890.e15. 71 indexed citations

20.

Wang, Ying, Wenqing Fu, Fang Xie, et al.. (2010). 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(8). 490–494. 19 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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