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Baojian Fan, Ph.D., M.D.

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Biography
Southeast University, Nanjing, ChinaM.D.07/1993Preventive Medicine
Southeast University, Nanjing, ChinaMaster of Medicine07/1997Epidemiology
The Chinese University of Hong Kong, Hong KongPh.D.07/2004Ophthalmology
Centre for Disease Control and Prevention, Pukou District, Nanjing, ChinaResident08/1994Infectious disease
The Chinese University of Hong Kong, Hong KongPostdoctoral Fellow01/2006Ophthalmology
The University of Hong Kong, Hong KongPostdoctoral Fellow01/2007Biochemistry
Harvard Medical School, Boston, MASenior Research Fellow12/2011Ophthalmology
1997
National Scientific and Technological Achievements
1998
First Prize Winner of Scientific and Technological Progress
2000
Outstanding Poster Award
2002
Postgraduate Student Grants for Overseas Academic Activities
2003
Postgraduate Student Grants for Overseas Academic Activities
2005
AFV Young Researcher of the Year
2005
Contract-end Merit Award
2009
Winner of the Poster Contest

Overview
Dr. Fan has dedicated his academic career to understanding the genetic basis of glaucoma and other eye disorders. He has fellowship training in Ophthalmology and in Statistical Genetics. He is experienced in analyzing large-scale genetic data, especially on next-generation sequencing, genome-wide association study and phenome-wide association study. His research has yielded 126 publications, which have been cited in 2,609 publications (h-index: 30).

Dr. Fan is primarily interested in gene mapping for Mendelian diseases (e.g., pigment dispersion syndrome) and complex diseases (e.g., adult-onset glaucoma). He is also interested in analysis of gene-gene and gene-environment interactions in complex diseases.

Research
The research activities and funding listed below are automatically derived from NIH ExPORTER and other sources, which might result in incorrect or missing items. Faculty can login to make corrections and additions.
  1. 530606 (FAN, BAOJIAN) Sep 1, 2017 - Aug 31, 2018
    Massachusetts Lions Eye Research Fund
    Gene discovery for pigmentary glaucoma
    Role: PI
  2. R01EY027129 (WIGGS, JANEY L) Sep 9, 2016 - Aug 31, 2019
    NIH/NEI
    INDO US Study of Ocular Quantitative Traits Related to Glaucoma
    Role: Co-Investigator
  3. (WIGGS, JANEY L.) Sep 1, 2014 - Aug 31, 2015
    Massachusetts Lions Eye Research Fund
    Ocular Genomics Institute (OGI): Vision Exome Sequencing Project: Developing a rare sequence variant database for visual disorders.
    Role: Co-PI
  4. G2014107 (FAN, BAOJIAN) Jul 1, 2014 - Jun 30, 2017
    BrightFocus Foundation
    Discovery of PDS/PG genes by exome sequencing
    Role: PI
  5. R01EY020928 (WIGGS, JANEY L) Sep 1, 2011 - Aug 31, 2021
    NIH/NEI
    Genetic and Environmental Risk Factors for Exfoliation Syndrome and Glaucoma
    Role: Co-Investigator

Bibliographic
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
  1. Lahola-Chomiak AA, Footz T, Nguyen-Phuoc K, Neil GJ, Fan B, Allen KF, Greenfield DS, Parrish RK, Linkroum K, Pasquale LR, Leonhardt RM, Ritch R, Javadiyan S, Craig JE, Allison WT, Lehmann OJ, Walter MA, Wiggs JL. Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma. Hum Mol Genet. 2019 04 15; 28(8):1298-1311. PMID: 30561643.
    Citations:    Fields:    
  2. Pasquale LR, Kang JH, Fan B, Levkovitch-Verbin H, Wiggs JL. LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome. J Glaucoma. 2018 07; 27 Suppl 1:S20-S23. PMID: 29965898.
    Citations:    Fields:    
  3. Wiggs JL, Kang JH, Fan B, Levkovitch-Verbin H, Pasquale LR. A Role for Clusterin in Exfoliation Syndrome and Exfoliation Glaucoma? J Glaucoma. 2018 07; 27 Suppl 1:S61-S66. PMID: 29965900.
    Citations:    Fields:    
  4. Fan BJ, Chen X, Sondhi N, Sharmila PF, Soumittra N, Sripriya S, Sacikala S, Asokan R, Friedman DS, Pasquale LR, Gao XR, Vijaya L, Cooke Bailey J, Vitart V, MacGregor S, Hammond CJ, Khor CC, Haines JL, George R, Wiggs JL. Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus. Invest Ophthalmol Vis Sci. 2018 05 01; 59(6):2495-2502. PMID: 29847655.
    Citations: 1     Fields:    
  5. Zhao J, Chen W, Huang X, Peng S, Zhu T, Deng Z, Liang P, Chang H, Fan BJ. Serum Th1 and Th17 related cytokines and autoantibodies in patients with Posner-Schlossman syndrome. PLoS One. 2017; 12(4):e0175519. PMID: 28384257.
    Citations: 1     Fields:    Translation:HumansCells
  6. Fan BJ, Pasquale LR. International Glaucoma Review. New genetic loci associated with primary angle closure glaucoma. 2017; 18-1.
  7. Gao X, Nannini DR, Corrao K, Torres M, Chen YI, Fan BJ, Wiggs JL, Taylor KD, Gauderman WJ, Rotter JI, Varma R. Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos. Hum Mol Genet. 2016 11 15; 25(22):5035-5045. PMID: 28171582.
    Citations: 5     Fields:    Translation:Humans
  8. Chen X, Chen Y, Wiggs JL, Pasquale LR, Sun X, Fan BJ. Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma. PLoS One. 2016; 11(6):e0157093. PMID: 27272641.
    Citations: 1     Fields:    Translation:Humans
  9. Chen X, Chen Y, Fan BJ, Xia M, Wang L, Sun X. Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma. Mol Vis. 2016; 22:528-35. PMID: 27293371.
    Citations: 2     Fields:    Translation:Humans
  10. Fan BJ, Pasquale LR, Kang JH, Levkovitch-Verbin H, Haines JL, Wiggs JL. Association of clusterin (CLU) variants and exfoliation syndrome: An analysis in two Caucasian studies and a meta-analysis. Exp Eye Res. 2015 Oct; 139:115-22. PMID: 26272660.
    Citations: 1     Fields:    Translation:Humans
  11. Zhao J, Zhu T, Chen W, Fan BJ, He L, Yang B, Deng Z. Human Leukocyte Antigens-B and -C Loci Associated with Posner-Schlossman Syndrome in a Southern Chinese Population. PLoS One. 2015; 10(7):e0132179. PMID: 26161794.
    Citations: 1     Fields:    Translation:Humans
  12. Fan BJ. Inherited optic neuropathies: genetics and new directions for diagnosis and therapy. CML – Ophthalmology. 2014; 3(24):73-80. View Publication.
  13. Wiggs JL, Hewitt AW, Fan BJ, Wang DY, Figueiredo Sena DR, O'Brien C, Realini A, Craig JE, Dimasi DP, Mackey DA, Haines JL, Pasquale LR. The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in caucasians with primary open angle glaucoma. PLoS One. 2012; 7(9):e45613. PMID: 23049825.
    Citations: 8     Fields:    Translation:Humans
  14. Chen LJ, Tam PO, Leung DY, Fan AH, Zhang M, Tham CC, Chiang SW, Fan BJ, Wang N, Pang CP. SNP rs1533428 at 2p16.3 as a marker for late-onset primary open-angle glaucoma. Mol Vis. 2012; 18:1629-39. PMID: 22773901.
    Citations: 8     Fields:    Translation:HumansCells
  15. Wiggs JL, Yaspan BL, Hauser MA, Kang JH, Allingham RR, Olson LM, Abdrabou W, Fan BJ, Wang DY, Brodeur W, Budenz DL, Caprioli J, Crenshaw A, Crooks K, Delbono E, Doheny KF, Friedman DS, Gaasterland D, Gaasterland T, Laurie C, Lee RK, Lichter PR, Loomis S, Liu Y, Medeiros FA, McCarty C, Mirel D, Moroi SE, Musch DC, Realini A, Rozsa FW, Schuman JS, Scott K, Singh K, Stein JD, Trager EH, Vanveldhuisen P, Vollrath D, Wollstein G, Yoneyama S, Zhang K, Weinreb RN, Ernst J, Kellis M, Masuda T, Zack D, Richards JE, Pericak-Vance M, Pasquale LR, Haines JL. Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. PLoS Genet. 2012; 8(4):e1002654. PMID: 22570617.
    Citations: 99     Fields:    Translation:HumansCells
  16. Fan BJ, Pasquale LR, Rhee D, Li T, Haines JL, Wiggs JL. LOXL1 promoter haplotypes are associated with exfoliation syndrome in a U.S. Caucasian population. Invest Ophthalmol Vis Sci. 2011 Apr; 52(5):2372-8. PMID: 21212179.
    Citations: 20     Fields:    Translation:HumansCells
  17. Fan BJ, Wang DY, Pasquale LR, Haines JL, Wiggs JL. Genetic variants associated with optic nerve vertical cup-to-disc ratio are risk factors for primary open angle glaucoma in a US Caucasian population. Invest Ophthalmol Vis Sci. 2011 Mar 28; 52(3):1788-92. PMID: 21398277.
    Citations: 39     Fields:    Translation:HumansCells
  18. Fan BJ, Pasquale LR. Copy number variations on chromosome 12q14 in patients with normal tension glaucoma. International Glaucoma Review. 2011; 13(2).
  19. Desronvil T, Logan-Wyatt D, Abdrabou W, Triana M, Jones R, Taheri S, Del Bono E, Pasquale LR, Olivier M, Haines JL, Fan BJ, Wiggs JL. Distribution of COL8A2 and COL8A1 gene variants in Caucasian primary open angle glaucoma patients with thin central corneal thickness. Mol Vis. 2010 Oct 29; 16:2185-91. PMID: 21139683.
    Citations: 16     Fields:    Translation:HumansAnimalsCells
  20. Fan BJ, Wiggs JL. Glaucoma: genes, phenotypes, and new directions for therapy. J Clin Invest. 2010 Sep; 120(9):3064-72. PMID: 20811162.
    Citations: 46     Fields:    Translation:Humans
  21. Fan BJ, Figuieredo Sena DR, Pasquale LR, Grosskreutz CL, Rhee DJ, Chen TC, Delbono EA, Haines JL, Wiggs JL. Lack of association of polymorphisms in elastin with pseudoexfoliation syndrome and glaucoma. J Glaucoma. 2010 Sep; 19(7):432-6. PMID: 20051886.
    Citations: 1     Fields:    Translation:Humans
  22. Fan BJ, Liu K, Wang DY, Tham CC, Tam PO, Lam DS, Pang CP. Association of polymorphisms of tumor necrosis factor and tumor protein p53 with primary open-angle glaucoma. Invest Ophthalmol Vis Sci. 2010 Aug; 51(8):4110-6. PMID: 20357201.
    Citations: 27     Fields:    Translation:Humans
  23. Ng TK, Lam CY, Lam DS, Chiang SW, Tam PO, Wang DY, Fan BJ, Yam GH, Fan DS, Pang CP. AC and AG dinucleotide repeats in the PAX6 P1 promoter are associated with high myopia. Mol Vis. 2009 Nov 05; 15:2239-48. PMID: 19907666.
    Citations: 17     Fields:    Translation:HumansCells
  24. Kang JH, Wiggs JL, Rosner BA, Hankinson SE, Abdrabou W, Fan BJ, Haines J, Pasquale LR. Endothelial nitric oxide synthase gene variants and primary open-angle glaucoma: interactions with sex and postmenopausal hormone use. Invest Ophthalmol Vis Sci. 2010 Feb; 51(2):971-9. PMID: 19815736.
    Citations: 47     Fields:    Translation:Humans
  25. Fan BJ, Wang DY, Cheng CY, Ko WC, Lam SC, Pang CP. Different WDR36 mutation pattern in Chinese patients with primary open-angle glaucoma. Mol Vis. 2009; 15:646-53. PMID: 19347049.
    Citations: 13     Fields:    Translation:Humans
  26. Fan BJ, Chen T, Grosskreutz C, Pasquale L, Rhee D, DelBono E, Haines JL, Wiggs JL. Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma. Mol Vis. 2008; 14:2484-91. PMID: 19112534.
    Citations: 12     Fields:    Translation:Humans
  27. Li H, Louey JW, Choy KW, Liu DT, Chan WM, Chan YM, Fung NS, Fan BJ, Baum L, Chan JC, Lam DS, Pang CP. EDN1 Lys198Asn is associated with diabetic retinopathy in type 2 diabetes. Mol Vis. 2008 Sep 15; 14:1698-704. PMID: 18806884.
    Citations: 9     Fields:    Translation:Humans
  28. Fan BJ, Wang DY, Tham CC, Lam DS, Pang CP. Gene expression profiles of human trabecular meshwork cells induced by triamcinolone and dexamethasone. Invest Ophthalmol Vis Sci. 2008 May; 49(5):1886-97. PMID: 18436822.
    Citations: 24     Fields:    Translation:HumansCells
  29. Song YQ, Ho DW, Karppinen J, Kao PY, Fan BJ, Luk KD, Yip SP, Leong JC, Cheah KS, Sham P, Chan D, Cheung KM. Association between promoter -1607 polymorphism of MMP1 and lumbar disc disease in Southern Chinese. BMC Med Genet. 2008 Apr 28; 9:38. PMID: 18439317.
    Citations: 12     Fields:    Translation:HumansCells
  30. Lam CY, Tam PO, Fan DS, Fan BJ, Wang DY, Lee CW, Pang CP, Lam DS. A genome-wide scan maps a novel high myopia locus to 5p15. Invest Ophthalmol Vis Sci. 2008 Sep; 49(9):3768-78. PMID: 18421076.
    Citations: 33     Fields:    Translation:HumansCells
  31. Fan BJ, Pasquale L, Grosskreutz CL, Rhee D, Chen T, DeAngelis MM, Kim I, del Bono E, Miller JW, Li T, Haines JL, Wiggs JL. DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity. BMC Med Genet. 2008 Feb 06; 9:5. PMID: 18254956.
    Citations: 53     Fields:    Translation:HumansCells
  32. Wang DY, Fan BJ, Yam GY, Lam DS, Pang CP. The cytotoxic and stress responses of human trabecular meshwork cells treated with triamcinolone acetonide. Mol Vis. 2008 Jan 22; 14:105-13. PMID: 18253094.
    Citations: 3     Fields:    Translation:HumansCells
  33. Fan BJ, Wiggs JL. DNA sequence variants in LOXL1 and pseudoexfoliation glaucoma. US Ophthalmic Review. 2008; 3:18-20. View Publication.
  34. Fan BJ, Ko WC, Wang DY, Canlas O, Ritch R, Lam DS, Pang CP. Fine mapping of new glaucoma locus GLC1M and exclusion of neuregulin 2 as the causative gene. Mol Vis. 2007 May 23; 13:779-84. PMID: 17563728.
    Citations: 10     Fields:    Translation:HumansCells
  35. Wang DY, Fan BJ, Chua JK, Tam PO, Leung CK, Lam DS, Pang CP. A genome-wide scan maps a novel juvenile-onset primary open-angle glaucoma locus to 15q. Invest Ophthalmol Vis Sci. 2006 Dec; 47(12):5315-21. PMID: 17122119.
    Citations: 27     Fields:    Translation:HumansCells
  36. Lam CY, Fan BJ, Wang DY, Tam PO, Yung Tham CC, Leung DY, Ping Fan DS, Chiu Lam DS, Pang CP. Association of apolipoprotein E polymorphisms with normal tension glaucoma in a Chinese population. J Glaucoma. 2006 Jun; 15(3):218-22. PMID: 16778644.
    Citations: 15     Fields:    Translation:Humans
  37. Yao HY, Cheng CY, Fan BJ, Tam OS, Tham CY, Wang DY, Lam SC, Pang CP. [Polymorphisms of myocilin and optineurin in primary open angle glaucoma patients]. Zhonghua Yi Xue Za Zhi. 2006 Feb 28; 86(8):554-9. PMID: 16681888.
    Citations: 6     Fields:    Translation:Humans
  38. Pang CP, Fan BJ, Canlas O, Wang DY, Dubois S, Tam PO, Lam DS, Raymond V, Ritch R. A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q. Mol Vis. 2006 Feb 14; 12:85-92. PMID: 16518310.
    Citations: 27     Fields:    Translation:HumansCells
  39. Fan BJ, Tam PO, Choy KW, Wang DY, Lam DS, Pang CP. Molecular diagnostics of genetic eye diseases. Clin Biochem. 2006 Mar; 39(3):231-9. PMID: 16412407.
    Citations: 6     Fields:    Translation:Humans
  40. Fan BJ, Leung DY, Wang DY, Gobeil S, Raymond V, Tam PO, Lam DS, Pang CP. Novel myocilin mutation in a Chinese family with juvenile-onset open-angle glaucoma. Arch Ophthalmol. 2006 Jan; 124(1):102-6. PMID: 16401791.
    Citations: 11     Fields:    Translation:HumansAnimalsCells
  41. Fan BJ, Wang DY, Lam DS, Pang CP. Gene mapping for primary open angle glaucoma. Clin Biochem. 2006 Mar; 39(3):249-58. PMID: 16332362.
    Citations: 74     Fields:    Translation:Humans
  42. Fan BJ, Wang DY, Fan DS, Tam PO, Lam DS, Tham CC, Lam CY, Lau TC, Pang CP. SNPs and interaction analyses of myocilin, optineurin, and apolipoprotein E in primary open angle glaucoma patients. Mol Vis. 2005 Aug 29; 11:625-31. PMID: 16148883.
    Citations: 36     Fields:    Translation:Humans
  43. Wang DY, Fan BJ, Chan WM, Tam OS, Chiang WY, Lam SC, Pang CP. [Digenic association of RHO and RP1 genes with retinitis pigmentosa among Chinese population in Hong Kong]. Zhonghua Yi Xue Za Zhi. 2005 Jun 22; 85(23):1613-7. PMID: 16185528.
    Citations: 1     Fields:    Translation:Humans
  44. Wang DY, Fan BJ, Wu XQ, Chan WM, Lam SC, Pang CP. [Recent progress in molecular genetics and gene therapy for retinitis pigmentosa]. Zhonghua Yan Ke Za Zhi. 2005 Feb; 41(2):188-92. PMID: 15840355.
    Citations:    Fields:    Translation:Humans
  45. Wang DY, Chan WM, Tam PO, Baum L, Lam DS, Chong KK, Fan BJ, Pang CP. Gene mutations in retinitis pigmentosa and their clinical implications. Clin Chim Acta. 2005 Jan; 351(1-2):5-16. PMID: 15563868.
    Citations: 24     Fields:    Translation:Humans
  46. Wang DY, Fan BJ, Canlas O, Tam PO, Ritch R, Lam DS, Fan DS, Pang CP. Absence of myocilin and optineurin mutations in a large Philippine family with juvenile onset primary open angle glaucoma. Mol Vis. 2004 Nov 09; 10:851-6. PMID: 15547491.
    Citations: 15     Fields:    Translation:HumansCells
  47. Fan BJ, Leung YF, Pang CP, Fan DS, Wang DY, Tong WC, Tam PO, Chua JK, Lau TC, Lam DS. Polymorphisms in the myocilin promoter unrelated to the risk and severity of primary open-angle glaucoma. J Glaucoma. 2004 Oct; 13(5):377-84. PMID: 15354075.
    Citations: 3     Fields:    Translation:HumansCells
  48. Fan BJ, Leung YF, Wang N, Lam SC, Liu Y, Tam OS, Pang CP. Genetic and environmental risk factors for primary open-angle glaucoma. Chin Med J (Engl). 2004 May; 117(5):706-10. PMID: 15161538.
    Citations: 23     Fields:    Translation:Humans
  49. Fan BJ, Leung YF, Pang CP, Baum L, Tam OS, Wang N, Lam SC. [Single nucleotide polymorphisms of the myocilin gene in primary open-angle glaucoma patients]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Feb; 21(1):70-3. PMID: 14767915.
    Citations: 6     Fields:    Translation:HumansCells
  50. Leung YF, Tam PO, Lee WS, Lam DS, Yam HF, Fan BJ, Tham CC, Chua JK, Pang CP. The dual role of dexamethasone on anti-inflammation and outflow resistance demonstrated in cultured human trabecular meshwork cells. Mol Vis. 2003 Sep 05; 9:425-39. PMID: 12963864.
    Citations: 15     Fields:    Translation:HumansCells
  51. Leung YF, Fan BJ, Lam DS, Lee WS, Tam PO, Chua JK, Tham CC, Lai JS, Fan DS, Pang CP. Different optineurin mutation pattern in primary open-angle glaucoma. Invest Ophthalmol Vis Sci. 2003 Sep; 44(9):3880-4. PMID: 12939304.
    Citations: 36     Fields:    Translation:Humans
  52. Lam DS, Lee WS, Leung YF, Tam PO, Fan DS, Fan BJ, Pang CP. TGFbeta-induced factor: a candidate gene for high myopia. Invest Ophthalmol Vis Sci. 2003 Mar; 44(3):1012-5. PMID: 12601022.
    Citations: 19     Fields:    Translation:HumansCells
  53. Fan BJ, Leung YF. Beginning microarray data analysis: A biologist's guide to analysis of DNA microarray data. J Cell Sci. 2003; 116:1649-50. View Publication.
  54. Pang CP, Leung YF, Fan B, Baum L, Tong WC, Lee WS, Chua JK, Fan DS, Liu Y, Lam DS. TIGR/MYOC gene sequence alterations in individuals with and without primary open-angle glaucoma. Invest Ophthalmol Vis Sci. 2002 Oct; 43(10):3231-5. PMID: 12356829.
    Citations: 32     Fields:    Translation:HumansCells
  55. Wang N, Peng Z, Fan B, Liu Y, Dong X, Liang X, Luan J. [Case control study on the risk factors of primary open angle glaucoma in China]. Zhonghua Liu Xing Bing Xue Za Zhi. 2002 Aug; 23(4):293-6. PMID: 12411077.
    Citations: 3     Fields:    Translation:Humans
  56. Fan B, Liang X, Peng Z, Dong X, Liu Y, Luan J, Wang N. [Study on single nucleotide polymorphism of TIGR gene in primary open-angle glaucoma patients]. Zhonghua Yi Xue Za Zhi. 2002 Jun 10; 82(11):743-7. PMID: 12126543.
    Citations: 2     Fields:    Translation:HumansCells
  57. Lu Y, Chen DC, Li Q, Xuan GW, Fan BJ, Zhao JW, Wang N. [Antibacterial effect of niaoluqing oral liquid on clinical drug-resistant strains and different serotype strains of Ureaplasma urealyticum in vitro]. Zhonghua Nan Ke Xue. 2002; 8(2):152-4. PMID: 12479037.
    Citations:    Fields:    Translation:HumansCells
  58. Yam HF, Pang CP, Fan DS, Fan BJ, Yu EY, Lam DS. Growth factor changes in ex vivo expansion of human limbal epithelial cells on human amniotic membrane. Cornea. 2002 Jan; 21(1):101-5. PMID: 11805517.
    Citations: 2     Fields:    Translation:HumansCells
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.