1.     Neruban K, M Georgiou, W B Bainbridge, M Bertelsen, M Larsen, C Ayuso, HV Tran, F Munier, A Kalitzeos, M Michaelides   Retinal structure in RPE65-associated Leber congenital amaurosis. IOVS, 2020 accepted

2.     Palmowski-Wolfe A, Stingl K, Habibi I, Schorderet D, Tran HV       Correction: Novel PDE6B Mutation Presenting with Retinitis Pigmentosa - A Case Series of Three Patients. Klin Monbl Augenheilkd. 2019 Feb 15.

3.     Escher P, Passarin O, Munier FL, Tran VH, Vaclavik V. Variability in clinical phenotypes of PRPF8-linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions. Ophthalmic Genet. 2018 Jan-Feb;39(1):80-86.

4.     Romdhane K, Vaclavik V, Schorderet DF, Munier FL, Viet Tran. CRX-linked macular dystrophy with intrafamilial variable expressivity. Ophthalmic Genet. 2018 Oct;39(5):637-641.

5.     C.Dysli, S. Wolf, H.V. Tran, et al. Autofluorescence lifetimes in patients with choroideremia identify photoreceptors in areas with retinal pigment epithelium atrophy. Invest Ophthalmol Vis Sci. 2016 Dec 1;57(15):6714-6721

6.     A. Daruich, A. Moulin, H.V. Tran, Marie-Claire Gaillard, Francis L. Subfoveal nodule in Coats disease: towards an updated classification predicting visual prognosis. Retina, 2016 Dec 23. doi: 10.1097

7.     Bedoni N, Haer-Wigman L, Vaclavik V, Tran VH, et al. Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertility. Hum Mol Genet. 2016 Aug 22. pii: ddw282. [Epub ahead of print]

8.     Escher P, Vaclavik V, Munier FL, Tran HV Presence of a Triple Concentric Autofluorescence Ring in NR2E3-p.G56R-Linked Autosomal Dominant Retinitis Pigmentosa (ADRP). Invest Ophthalmol Vis Sci. 2016 Apr 1;57(4):2001-2.

9.     H. Viet Tran, E.Moret, V. Vaclavik, F. Marcelli, M. Abitbol, F.L. Munier, D.F. Schorderet. Swiss dominant Stargardt family caused by a recurrent mutation in the ELOVL4 gene. Klin Monatsbl Augenheilkd. 2016 Apr;233(4):475-7.

10.  A. Daruich, A. Matet, C. Bergin, H. V. Tran, et al. Extramacular Fibrosis in Coats’ Disease. Retina, 2016 Oct;36(10):2022-8.

11.  Tran HV, Ambresin A, Pournaras J-A, Sabani I, Wolfensberger TJ. Posterior sub-tenon triamcinolone injection for chronic macular oedema associated with non-ischemic branch or central retinal vein occlusion. Ophthalmol. Open J. 2015; 1(1): 9-14.

12.  Tran HV, von Alpen D, Guex N, Venturini G, Munier FL, Schorderet DF, Haider NB, Escher P. Differential dimerization of variants linked to enhanced S-cone sensitivity syndrome (ESCS) located in the NR2E3 ligand-binding domain. Hum Mutat. 2015 Jun;36(6):599-610. Epub 2015 Apr 27.

13.  Tan MH, Mackay DS, Cowing J, Tran HV, Smith AJ, Wright GA, Dev-Borman A, Henderson RH, Moradi P, Russell-Eggitt I, MacLaren RE, Robson AG, Cheetham ME, Thompson DA, Webster AR, Michaelides M, Ali RR, Moore AT. Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy. PLoS One. 2012;7(3):e32330.

14.  Hoai V. Tran, Pascal Escher, Veronika Vaclavik, et al. Autofluorescence Study In NR2E3 p.G56R-linked Autosomal Dominant Retinitis Pigmentosa In A Single Kindred.   Invest Ophthalmol Vis Sci. 2012 Jul 13;53(8):4754-64

‍15.  V Vaclavik, HV Tran, MC Gaillard, D Schorderet, FL Munier. Pattern dystrophy with high Intrafamilial variability associated with the Y141C mutation in the Peripherin/RDS gene and a successful treatment of subfoveal CNV related to multifocal pattern type with anti-VEGF (ranibizumab) intravitreal injections. Retina. 2012 Oct;32(9):1942-9.

‍16.   Tan MH, Vanakker OM, Tran HV, Robson AG, Lai-Cheong JE, Groves R, Holder GE, Moore AT. Angioid streaks with severe macular dysfunction and generalised retinal involvement due to a homozygous duplication in the ABCC6 gene.Eye (Lond). 2012 Jan 20. doi: 10.1038/eye.2011.344.

17.   H. Viet Tran, Schorderet D, Zografos L, Munier F. Risk Assessment of Sporadic Retinoblastoma Transmission Using a Molecular Algorithm. Ophthalmic Genet. Ophthalmic Genet. 2012 Mar;33(1):6-11.

18.   H.Viet Tran, S. Eperon, Y. Guex-Crosier. Eotaxin-1 (CCL11) Remains Up-Regulated in Tears of Patients with Contact Lens Papillary Conjunctivitis Over A 2-years Follow-Up Klin Monatsbl Augenheilkd. 2011 Apr;228:326-9.

19.   Andrei S., Tran H.V., Beknazar E., Guex-Crosier Y.Therapeutic strategies for non-endemic Onchocerciasis: A case report and update of the literature. Klin Monatsbl Augenheilkd. 2011 Apr;228:372-3.

20.   Beknazar E, Tran HV, Andrei S, Martinez A, Vaudaux J, Guex-Crosier Y. Drug-induced uveitis - panuveitis with Rifabutin. Klin Monatsbl Augenheilkd. 2011 Apr;228:374-5.

21.   A. Codreanu, Ch. Wiaux, H. Viet Tran, S. Roy, A. Mermoud. A Comparative Randomized Clinical and Histological Study between X-Shaped Acrylic and Cylindrical Collagen Implants in Experimental Deep Sclerectomy. Clin Experiment Ophthalmol. 2011 Mar;39(2):135-41.

22.   Mansouri K, Tran HV, Ravinet E, Mermoud A. Comparing deep sclerectomy with collagen implant to the new method of very deep sclerectomy with collagen implant: a single-masked randomized controlled trial. J Glaucoma. 2010 Jan;19(1):24-30.

23.   M.H. Tan, S. Smith, B. Pawlyk, J. Xu, X. Liu, J. Bainbridge, M.Basche, J. Mcintosh, H. Viet Tran, A. Nathwani, T. Li, R.R. Ali. Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors. Hum Mol Gen. 2009 Jun 15;18:2099-114

‍24.   H. Viet Tran, Schorderet DF, Kostic C, Munier FL, Arsenijevic Y. Gene therapy forhereditary eye diseases: where are we? Rev Med Suisse. 2009 Jan 14;5(186):118-23.

25.   H. Viet Tran, A. Schalenbourg, L. Zografos. Bilateral Circumscribed Choroidal Hemangiomas in an Otherwise Healthy Individual. Retinal Cases & Brief Reports. 2007 Summer, 1(2):149-52.

26.   R. Ritch, H. Viet Tran, R.M. Vessani, J.M. Liebmann, C. Tello. Ultrasound Biomicroscopic Assessment of Zonular Appearance in Exfoliation Syndrome. Acta Ophthalmol. 2007 Jun 21-

27.   H. Viet Tran, E.H. Bovey, S. Uffer, L. Zografos. Peripapillary Choroidal Neovascularization Associated with Melnocytoma of the Optic Disc. Graefes Arch Clin Exp Ophthalmol. 2006 Oct;244(10):1367-9.

28.   H. Viet Tran, F.L. Munier. Evanescens white linear flecks and posterior microphtalmos: new feature of a recently established disease. Klin Monatsbl Augenheilkd. 2006 May;223(5):397-9.

29.   H. Viet Tran, C.C. Schnyder, E. Ravinet, Y. Guex-Crosier. Topiramate-induced acute-onset angle-closure glaucoma: a consequence of blood-brain barrier breakdown. Klin Monatsbl Augenheilkd. 2006 May;223(5):425-427.

30.   G. Klainguti, H. Viet Tran, C. Nguyen, J. Strickler. Surgical correction of excylotorsion by tucking only the anterior part of the superior oblique muscle tendon. Klin Monatsbl Augenheilkd. Klin Monatsbl Augenheilkd. 2006 May;223(5):386-9.

31.   Tran HV, Zografos L. Primary choroidal melanoma in phakomatosis pigmentovascularis IIa. Ophthalmology. 2005 Jul;112(7):1232-5.

32.   Ritch R, Liebmann JM, Tran HV. Iridociliary apposition in plateau iris syndrome persists after cataract extraction. Am J Ophthalmol. 2003 Aug;136(2):395; author reply 395-6.

33.   Finger PT, Tran HV, Turbin RE, Perry HD, Abramson DH, Chin K, Della Rocca R, Ritch R. High-frequency ultrasonographic evaluation of conjunctival intraepithelial neoplasia and squamous cell carcinoma. Arch Ophthalmol. 2003 Feb;121(2):168-72.

34.   Tran HV, Ishikawa H, Liebmann JM, Ritch R. A new silicone eyecup for ultrasound biomicroscopy. Ophthalmic Surg Lasers Imaging. 2003 Jan-Feb;34(1):73-5.

35.   Tran HV, Liebmann JM, Ritch R. Iridociliary apposition in plateau iris syndrome persists after cataract extraction. Am J Ophthalmol. 2003 Jan;135(1):40-3.  

36.   Piette S, Canlas OA, Tran HV, Ishikawa H, Liebmann JM, Ritch R. Ultrasound biomicroscopy in uveitis-glaucoma-hyphema syndrome. Am J Ophthalmol. 2002 Jun;133(6):839-41.

37.   C. Tello, H. Viet Tran, J. Liebmann, R. Ritch. Angle closure: classification, concepts, and the role of ultrasound biomicroscopy in diagnosis and treatment. Seminars in Ophthalmology June 2002 Taylor & Francis 17(2):69-78.

38.   HV Tran, RM Vessani, JM Liebmann, R Ritch. Ultrasound Biomicroscopy in the Diagnosis and Management of Cyclodialysis Cleft: Case Report and Review of the Literature. Asian J Ophthalmol 2002;4(3):11-15.


Pascal Escher, Kaspar Schuerch, Martin S. Zinkernagel,  Viet Hoai Tran, Francis Munier   NR2E3-linked retinal degenerations: recessive enhanced S-cone syndrome (ESCS)/Goldmann-Favre syndrome, and dominant retinitis pigmentosa (RP),Practical Genomics for Clinical Ophthalmology, Elsevier 2018

Tran HV, Ishikawa H, Liebmann JM, Ritch R: Rhee DJ. Ultrasound Biomicroscopy in Glaucoma; Color Atlas and Synopsis of Clinical Ophthalmology: Glaucoma, New York, NY: McGraw-Hill. 2002.

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