PubRank

E I Traboulsi

Author PubWeight™ 62.62‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Ocular pathology in congenital heart disease. Eye (Lond) 2005 1.96
2 Prevalence and importance of pigmented ocular fundus lesions in Gardner's syndrome. N Engl J Med 1987 1.76
3 Dominant inheritance of optic pits. Am J Ophthalmol 1997 1.74
4 A comparative histologic study of the fibrillin microfibrillar system in the lens capsule of normal subjects and subjects with Marfan syndrome. Invest Ophthalmol Vis Sci 1998 1.71
5 A third locus (GLC1D) for adult-onset primary open-angle glaucoma maps to the 8q23 region. Am J Ophthalmol 1998 1.50
6 Immunohistochemical localization of fibrillin in human ocular tissues. Relevance to the Marfan syndrome. Arch Ophthalmol 1995 1.44
7 Visual prognosis in autosomal dominant optic atrophy (Kjer type). Am J Ophthalmol 1993 1.38
8 Comparison of clinical characteristics of familial and sporadic acquired accommodative esotropia. J AAPOS 2001 1.36
9 Update on the molecular genetics of retinitis pigmentosa. Ophthalmic Genet 2001 1.17
10 The natural history of Leber's congenital amaurosis. Age-related findings in 35 patients. Ophthalmology 1992 1.10
11 Oral erythromycin treatment for childhood blepharokeratitis. J AAPOS 2000 1.10
12 Glaucoma in the Marfan syndrome. Trans Am Ophthalmol Soc 1992 1.09
13 Ophthalmologic manifestations of X-linked childhood adrenoleukodystrophy. Ophthalmology 1987 1.09
14 Horizontal gaze palsy with progressive scoliosis can result from compound heterozygous mutations in ROBO3. J Med Genet 2006 1.08
15 Ocular malformations, moyamoya disease, and midline cranial defects: a distinct syndrome. Am J Ophthalmol 1999 1.07
16 Value of combined phenotypic markers in identifying inheritance of familial adenomatous polyposis. Gut 1991 1.07
17 An Arg311Gln NR2E3 mutation in a family with classic Goldmann-Favre syndrome. Br J Ophthalmol 2005 1.03
18 A family with the Bardet-Biedl syndrome and diabetes mellitus. Arch Ophthalmol 1989 0.98
19 Bilateral melanosis of the iris. Am J Ophthalmol 1987 0.96
20 Neovascular glaucoma and ischemia. J Clin Neuroophthalmol 1986 0.96
21 Optic nerve head swelling and optic atrophy in the systemic mucopolysaccharidoses. Ophthalmology 1990 0.96
22 APC gene mutations and extraintestinal phenotype of familial adenomatous polyposis. Gut 1997 0.95
23 A histopathologic study of the pigmented fundus lesions in familial adenomatous polyposis. Retina 1992 0.93
24 The ocular findings in Kniest dysplasia. Am J Ophthalmol 1985 0.93
25 Waardenburg's recessive anophthalmia syndrome. Ophthalmic Paediatr Genet 1984 0.92
26 Aniridia, atypical iris defects, optic pit and the morning glory disc anomaly in a family. Ophthalmic Paediatr Genet 1986 0.91
27 Periocular pigmentation in the Peutz-Jeghers syndrome. Am J Ophthalmol 1986 0.91
28 Mapping a new genetic locus for X linked retinitis pigmentosa to Xq28. J Med Genet 2006 0.89
29 A new locus for dominant drusen and macular degeneration maps to chromosome 6q14. Am J Ophthalmol 2000 0.87
30 Hepatoblastoma, pigmented ocular fundus lesions and jaw lesions in Gardner syndrome. Am J Med Genet 1988 0.86
31 A family with a syndrome of ectopia lentis, spontaneous filtering blebs, and craniofacial dysmorphism. Ophthalmic Genet 1995 0.86
32 Screening relatives of patients with familial chronic open angle glaucoma. Ophthalmology 2000 0.85
33 Confirmation of the autosomal recessive syndrome of ectopia lentis and distinctive craniofacial appearance. Am J Med Genet 2001 0.85
34 Melanocytoma of the ciliary body: presentation of four cases and review of nineteen reports. Surv Ophthalmol 1985 0.84
35 Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration. Am J Ophthalmol 2000 0.84
36 Crystalline retinopathy. Ann Ophthalmol 1987 0.84
37 Microcephaly, colobomatous microphthalmia, short stature, and severe psychomotor retardation in two male cousins: a new MCA/MR syndrome? Am J Med Genet 1999 0.83
38 Keratoconus after penetrating keratoplasty. Ophthalmic Surg 1990 0.83
39 Visual outcome after surgery for Peters' anomaly. Ophthalmic Genet 1994 0.82
40 Progression of retinopathy in olivopontocerebellar atrophy with retinal degeneration. Arch Ophthalmol 1992 0.82
41 Extraocular muscle aplasia in Moebius syndrome. J Pediatr Ophthalmol Strabismus 1986 0.81
42 Dominant radial drusen and Arg345Trp EFEMP1 mutation. Am J Ophthalmol 2001 0.81
43 The genetics of strabismus. Am Orthopt J 2001 0.80
44 Bilateral microphthalmia with cyst, facial clefts, and limb anomalies: a new syndrome with features of Waardenburg syndrome, cerebro-oculo-nasal syndrome, and craniotelencephalic dysplasia. Am J Med Genet A 2003 0.80
45 Anterior segment malformations in 18q- (de Grouchy) syndrome. Ophthalmic Paediatr Genet 1993 0.79
46 Retinal pigment epithelium tear as a cause of vitreous hemorrhage. Ann Ophthalmol 1985 0.79
47 Duane's retraction syndrome in the fetal alcohol syndrome. Am J Ophthalmol 1990 0.79
48 The retinopathy of primary hyperoxaluria. Retina 1985 0.79
49 Strabismus in the Marfan syndrome. Am J Ophthalmol 1994 0.78
50 Spondylometaphyseal dysplasia with cone-rod dystrophy. Ophthalmic Genet 2010 0.78
51 Familial posterior lenticonus and microcornea. Arch Ophthalmol 1992 0.77
52 Corneal opacities in Gaucher disease. Am J Ophthalmol 1998 0.76
53 Familial adenomatous polyposis. Dis Colon Rectum 1989 0.76
54 Hereditary pigmented paravenous chorioretinal atrophy. Arch Ophthalmol 1986 0.76
55 Ocular findings in partial trisomy 3q. A case report and review of the literature. Ophthalmic Paediatr Genet 1988 0.76
56 A patient with de Morsier and Duane syndromes. J AAPOS 2000 0.76
57 Pigmented fundus lesions in a preterm infant with familial adenomatous polyposis. Arch Ophthalmol 1993 0.76
58 Anterior transposition of the inferior oblique muscle as the initial treatment of a snapped inferior rectus muscle. J AAPOS 2001 0.76
59 Dominant syndrome with isolated cryptophthalmos and ocular anomalies. Am J Med Genet 1992 0.76
60 Idiopathic macular hypoplasia: a report of four cases and refinement of the phenotype of so-called ateliotic macula. Eur J Ophthalmol 2006 0.76
61 Coats' disease and central nervous system venous malformation. Ophthalmic Genet 1996 0.75
62 Ocular findings in the candidiasis-endocrinopathy syndrome. Am J Ophthalmol 1985 0.75
63 Bread crumb-flecked retinopathy. Retina 1993 0.75
64 Congenital third nerve palsy, moyamoya disease and optic nerve head staphyloma. Br J Ophthalmol 2005 0.75
65 To lump or to split? Ophthalmic Paediatr Genet 1993 0.75
66 Morning glory disc anomaly or optic disc coloboma? Arch Ophthalmol 1994 0.75
67 X-linked microphthalmia syndrome. Am J Med Genet 1990 0.75
68 Retinoblastoma in Lebanon. Ophthalmic Paediatr Genet 1986 0.75
69 Persistent hyperplastic primary vitreous and recessive oculo-dento-osseous dysplasia. Am J Med Genet 1986 0.75
70 Tick infestation of the eyelid. Am J Ophthalmol 1998 0.75
71 Pituitary stalk duplication in association with moya moya disease and bilateral morning glory disc anomaly - broadening the clinical spectrum of midline defects. J Neurol 2008 0.75
72 Spraying topical ophthalmic preparations. Am J Ophthalmol 1984 0.75
73 Ocular findings in a family with Sotos syndrome (cerebral gigantism). Am J Ophthalmol 1995 0.75
74 Occipital cortical infarction complicating respiratory failure. J Clin Neuroophthalmol 1984 0.75
75 Clinical, genetic and histopathologic findings in two siblings with muscle-eye-brain disease. Eur J Ophthalmol 2002 0.75
76 Giant intracavernous carotid aneurysm presenting as isolated sixth nerve palsy in an infant. Br J Ophthalmol 2008 0.75
77 Systemic associations of pigmentary retinopathy. Int Ophthalmol Clin 1991 0.75
78 Failure of subretinal fluid drainage during scleral buckling procedure in high myopia. Ann Ophthalmol 1985 0.75
79 Retinal dystrophy in the cardiofaciocutaneous syndrome. J Pediatr Ophthalmol Strabismus 1993 0.75
80 Vitreous histocytology of primary choroidal malignant melanoma. Ann Ophthalmol 1987 0.75
81 Corneal changes in familial iris coloboma. Ophthalmology 1986 0.75
82 A-pattern esotropia with bilateral inferior oblique muscle overaction. Ann Ophthalmol 1988 0.75
83 The use of a cautery for trimming exposed nylon sutures. Am J Ophthalmol 1983 0.75
84 Coloboma of the lens, optic nerve hypoplasia, and orbital hemangioma--a possible developmental field defect. Ophthalmic Genet 1998 0.75
85 A 14-year old boy with presumed autosomal dominant macular dystrophy causing moderate visual impairment with no discernible progression over several years. J Pediatr Ophthalmol Strabismus 1999 0.75
86 Eighties and nineties have witnessed an explosion of new information on the genetics of human diseases. Ophthalmic Paediatr Genet 1993 0.75
87 Choroidal rupture associated with forceps delivery. Am J Ophthalmol 2000 0.75
88 Histologic study of a torn inferior oblique muscle. J AAPOS 1998 0.75
89 Unilateral megalocornea in lamellar ichthyosis. Ann Ophthalmol 1985 0.75
90 A syndrome with true anophthalmia, hand-foot defects and mental retardation. Ophthalmic Paediatr Genet 1984 0.75
91 Chorioretinal lacuna in the amniotic band syndrome. J Pediatr Ophthalmol Strabismus 1991 0.75
92 Fleck retina in Kjellin's syndrome. Am J Ophthalmol 1985 0.75
93 Practical slit-lamp photography. Ann Ophthalmol 1985 0.75
94 Homonymous hemianopia and systemic lupus erythematosus. J Clin Neuroophthalmol 1985 0.75
95 Pseudomonas aeruginosa ophthalmia neonatorum. Am J Ophthalmol 1984 0.75
96 Eye findings in interstitial deletion of band q12 of chromosome 5. Ophthalmic Paediatr Genet 1984 0.75
97 Caruncular involvement in myelomonocytic leukemia: a case report. Med Pediatr Oncol 1985 0.75
98 Ophthalmologic findings in mucolipidosis III (pseudo-Hurler polydystrophy). Am J Ophthalmol 1986 0.75