PubRank

A M Payne

Author PubWeight™ 39.43‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Nat Genet 2000 2.85
2 Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12). Nat Genet 1999 2.75
3 Prevalence of AIPL1 mutations in inherited retinal degenerative disease. Mol Genet Metab 2000 2.07
4 Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy. Hum Mol Genet 1998 1.84
5 A mutation in NRL is associated with autosomal dominant retinitis pigmentosa. Nat Genet 1999 1.79
6 GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy. Mol Cell 1998 1.38
7 Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1. Arch Ophthalmol 2001 1.24
8 A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13. Invest Ophthalmol Vis Sci 2000 1.23
9 Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1. Arch Ophthalmol 2001 1.22
10 A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32. Am J Hum Genet 1998 1.15
11 Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies. J Med Genet 2001 1.11
12 Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families. Arch Ophthalmol 1999 1.02
13 Coccidia-induced mucogenesis promotes the onset of necrotic enteritis by supporting Clostridium perfringens growth. Vet Immunol Immunopathol 2007 0.99
14 Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin. Am J Hum Genet 1999 0.99
15 Spectrum of mutations in USH2A in British patients with Usher syndrome type II. Exp Eye Res 2001 0.98
16 Preventive medicine at the Yale School of Medicine, 1950-1965. Milbank Mem Fund Q 1967 0.97
17 Familial cavernous hemangioma: An expanding ocular spectrum. Arch Ophthalmol 2000 0.95
18 Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24. Invest Ophthalmol Vis Sci 2000 0.95
19 Founder effect, seen in the British population, of the 172 peripherin/RDS mutation-and further refinement of genetic positioning of the peripherin/RDS gene. Am J Hum Genet 1998 0.94
20 Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online. Hum Mutat 1999 0.93
21 Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32. Br J Ophthalmol 1999 0.91
22 The Scope and Methods of Epidemiology. Am J Public Health Nations Health 1962 0.91
23 Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreous. Invest Ophthalmol Vis Sci 2001 0.90
24 Comparison of CO(2) stunning with manual electrical stunning (50 Hz) of pigs on carcass and meat quality. Meat Sci 2002 0.82
25 Oral immunization against poliomyelitis. Bull World Health Organ 1960 0.82
26 Approaches to communicable disease control. WHO Chron 1968 0.80
27 A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family. Invest Ophthalmol Vis Sci 2001 0.80
28 Halothane genotype, pre-slaughter handling and stunning method all influence pork quality. Meat Sci 2000 0.79
29 Social stress and cardiovascular disease. The limitations of limitation. Milbank Mem Fund Q 1967 0.79
30 NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies. Eur J Hum Genet 2000 0.78
31 Extragenic suppressors of the nimX2(cdc2) mutation of Aspergillus nidulans affect nuclear division, septation and conidiation. Genetics 2000 0.77
32 Insulin-like growth factor 1, but not growth hormone, has in vitro proliferative effects on neonatal foreskin fibroblasts without affecting 5-alpha-reductase or androgen receptor activity. J Androl 1993 0.77
33 Further refinement of the Usher 2A locus at 1q41. J Med Genet 1998 0.77
34 The effect of macrophage conditioned media on Leydig cell function. Ann Clin Lab Sci 1994 0.77
35 Molecular genetic study of autosomal dominant retinitis pigmentosa in Lithuanian patients. Hum Hered 1999 0.77
36 The medical school and international health. Yale J Biol Med 1967 0.75
37 Innovation out of unity. Milbank Mem Fund Q 1965 0.75
38 Macrophage conditioned media affects steroid hormone production by placental cultures. Ann Clin Lab Sci 1995 0.75
39 Specialized or integrated services in the control of communicable diseases. Bull Int Union Tuberc 1968 0.75
40 Acute infectious respiratory diseases. Newer knowledge as it affects our concepts of future control. Arch Environ Health 1967 0.75
41 Foreword. Yale J Biol Med 1963 0.75
42 [Some principles of epidemiology]. Bol Oficina Sanit Panam 1965 0.75
43 Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r) J Med Genet 2000 0.75
44 The environmental determinants of community well-being. Jpn J Med Sci Biol 1968 0.75