Dr. Fann, Cathy S.-J. 's publons link picture Dr. Fann, Cathy S.-J. 's Personal Homepage

范盛娟博士

研究員
  • 02-27899144 (Lab) (Room No: 100)
  • 02-27823047 (Fax)

Specialty:
  • Genetic Statistics
  • Genetic Epidemiology

Education and Positions:
  • Division of Biostatistics, Department of Preventive Medicine and Environmental Health,
    Ph.D. University of Iowa, Iowa City, Iowa, US


本實驗室主要研究方向是發展新的統計方法與軟體為致病基因定位,及尋找族群之間在演化上及遺傳上的差異。目前研究方向為:


1. 應用統計方法與分析工具尋找複雜性疾病相關之致病基因。目前研究包含偏頭痛,老年痴呆症,氣喘,躁鬱症,代謝症候群等疾病。


2. 發展新的稀少變異基因之統計方法,並探討其在複雜性疾病中所扮演的角色和導致不同族群中的差異。


3.應用機械學習及深度學習的方法於多基因風險評分之可行性。


4. 大型生物基因資料庫之分析研究。

Our Team
Team photo

期刊 145 專書 2

  1. Cheng YW, Liao YC, Chen CH, Chung CP, Fann CSJ, Chang CC, Lee YC, Tang SC. Contribution of the APOE Genotype to Cognitive Impairment in Individuals With NOTCH3 Cysteine-Altering Variants. Journal of the American Heart Association e032689, e032689 (2023-11) [JCR] [WOS]
  2. Lee CT, Tsai WH, Chang CC, Chen PC, Fann CS, Chang HK, Liu SY, Wu MZ, Chiu PC, Hsu WM, Yang WS, Lai LP, Tsai WY, Yang SB, Chen PL. Genotype-phenotype correlation in Taiwanese children with diazoxide-unresponsive congenital hyperinsulinism. Frontiers in Endocrinology 14:1283907., 14:1283907. (2023-11) [JCR] [WOS]
  3. Winsvold BS, Harder AVE, Ran C, Chalmer MA, Dalmasso MC, Ferkingstad E, Tripathi KP, Bacchelli E, Børte S, Fourier C, Petersen AS, Vijfhuizen LS, Magnusson SH, O\'Connor E, Bjornsdottir G, Häppölä P, Wang YF, Callesen I, Kelderman T, Gallardo VJ, de Boer I, Olofsgård FJ, Heinze K, Lund N, Thomas LF, Hsu CL, Pirinen M, Hautakangas H, Ribasés M, Guerzoni S, Sivakumar P, Yip J, Heinze A, Küçükali F, Ostrowski SR, Pedersen OB, Kristoffersen ES, Martinsen AE, Artigas MS, Lagrata S, Cainazzo MM, Adebimpe J, Quinn O, Göbel C, Cirkel A, Volk AE, Heilmann-Heimbach S, Skogholt AH, Gabrielsen ME, Wilbrink LA, Danno D, Mehta D, Guðbjartsson DF; HUNT All-In Headache, The International Headache Genetics Consortium, DBDS Genomic Consortium; Rosendaal FR, Willems van Dijk K, Fronczek R, Wagner M, Scherer M, Göbel H, Sleegers K, Sveinsson OA, Pani L, Zoli M, Ramos-Quiroga JA, Dardiotis E, Steinberg A, Riedel-Heller S, Sjöstrand C, Thorgeirsson TE, Stefansson H, Southgate L, Trembath RC, Vandrovcova J, Noordam R, Paemeleire K, Stefansson K, Fann CS, Waldenlind E, Tronvik E, Jensen RH, Chen SP, Houlden H, Terwindt GM, Kubisch C, Maestrini E, Vikelis M, Pozo-Rosich P, Belin AC, Manjit Matharu, Arn M J M van den Maagdenberg, Thomas F Hansen, Alfredo Ramirez, John-Anker Zwart; International Consortium for Cluster Headache Genetics. Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor. Annals of Neurology 2023-07, 07-24 (2023-07) [JCR] [WOS]
  4. Chen TH, Hsu HC, You JF, Lai CC, Tsou YK, Hsu CL, Fann CSJ, Chien RN, Chang ML. Extracellular Nicotinamide Phosphoribosyltransferase as a Surrogate Marker of Prominent Malignant Potential in Colonic Polyps: A 2-Year Prospective Study. Cancers. 15(6):1702., 1702-1702 (2023-03) [JCR] [WOS]
  5. Lian IB, Sie JJ, Chang CC, Fann CSJ, Huang CH. Effects of insomnia and non-vasomotor menopausal symptoms on coronary heart disease risk: a mendelian randomization study. Heliyon. 9(2):e13569, e13569-e13569 (2023-02) [JCR] [WOS]
  6. Chen SP, Hsu CL, Wang YF, Yang FC, Chen TH, Huang JH, Pan LH, Fuh JL, Chang HC, Lee YL, Chang HC, Lee KH, Chang YC, Fann CS*, Wang SJ. Genome-wide analyses identify novel risk loci for cluster headache in Han Chinese residing in Taiwan. J Headache Pain. 23(1), 147 (2022-11-21) [JCR] [WOS]
  7. Lee CJ, Chen TH, Lim AMW, Chang CC, Sie JJ, Chen PL, Chang SW, Wu SJ, Hsu CL, Hsieh AR, Yang WS, Fann CSJ* Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes Commun Biol. 5(1), 1175 (2022-11-03) [JCR] [WOS]
  8. Geevimaan K, Guo JY, Shen CN, Jiang JK, Fann CSJ, Hwang MJ, Shui JW, Lin HT, Wang MJ, Shih HC, Li AF, Chang SC, Yang SH, Chen JY. Patient-Derived Organoid Serves as a Platform for Personalized Chemotherapy in Advanced Colorectal Cancer Patients. Front Oncol. 12, 883437 (2022-06-01) [JCR] [WOS]
  9. Jiang YJ, Fann CS, Fuh JL, Chung MY, Huang HY, Chu KC, Wang YF, Hsu CL, Kao LS, Chen SP, Wang SJ. Genome-wide analysis identified novel susceptible genes of restless legs syndrome in migraineurs. J Headache Pain 23(1), 39-39 (2022-03) [JCR] [WOS]
  10. Tsao YC, Wang SJ, Hsu CL, Wang YF, Fuh JL, Chen SP, Fann CS. Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population. Cephalalgia. 42(3), 229-238 (2022-03) [JCR] [WOS]

- 博士後研究 -
LO, YEN-LI
羅彥俐
- 研究助理 -
Chang, Chien-Ching
張倩青
Hsu	, Chia-Lin
徐佳琳
Wu, Shang-Jung
吳尚容
Lim, Evan Unit
林耘逸
CHEN, SYUE PU
陳學蒲
- 學生 -
SIE, JIA-JYUN
謝佳峻
LIM, Aylwin Ming Wee
林明葳
- 訪問學人 -
Chen, Ting-Huei
陳亭卉
- 昔日夥伴 -
Lee, CJ
李加榮
tom, thomas
湯金諺