A citation-based method for searching scientific literature

Marie Bengtsson, Sten Andréasson, Gert Andersson. Clin Neurophysiol 2005
Times Cited: 8







List of co-cited articles
22 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


The topography of visual evoked response properties across the visual field.
H A Baseler, E E Sutter, S A Klein, T Carney. Electroencephalogr Clin Neurophysiol 1994
246
75



Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene.
Lotta Gränse, Ingar Bergstrand, Dawn Thiselton, Vesna Ponjavic, Anders Heijl, Marcela Votruba, Sten Andréasson. Ophthalmic Genet 2003
20
37


Normative ranges and specificity of the multifocal VEP.
Brad Fortune, Xian Zhang, Donald C Hood, Shaban Demirel, Chris A Johnson. Doc Ophthalmol 2004
48
37

Quantifying the benefits of additional channels of multifocal VEP recording.
Donald C Hood, Xian Zhang, Jenny E Hong, Candice S Chen. Doc Ophthalmol 2002
77
37

Determining abnormal interocular latencies of multifocal visual evoked potentials.
Donald C Hood, Xian Zhang, Christopher Rodarte, E Bo Yang, Nitin Ohri, Brad Fortune, Chris A Johnson. Doc Ophthalmol 2004
26
37


Clinical application of the multifocal VEPs.
Y Betsuin, Y Mashima, H Ohde, R Inoue, Y Oguchi. Curr Eye Res 2001
36
25

Receiver-operating characteristic analysis of multifocal VEPs to diagnose and quantify glaucomatous functional damage.
Makoto Nakamura, Kumiko Ishikawa, Takayuki Nagai, Akira Negi. Doc Ophthalmol 2011
7
28

Improving the quality of multifocal visual evoked potential results by calculating multiple virtual channels.
Babac A E Mazinani, Till D Waberski, Andreas W A Weinberger, Peter Walter, Gernot F Roessler. Jpn J Ophthalmol 2011
3
66

A signal-to-noise analysis of multifocal VEP responses: an objective definition for poor records.
Xian Zhang, Donald C Hood, Candice S Chen, Jenny E Hong. Doc Ophthalmol 2002
64
25


Reproducibility of multifocal VEP latency using different stimulus presentations.
Prema Sriram, Alexander Klistorner, Hemamalini Arvind, Stuart L Graham. Doc Ophthalmol 2012
9
25

Determining abnormal latencies of multifocal visual evoked potentials: a monocular analysis.
Donald C Hood, Nitin Ohri, E Bo Yang, Christopher Rodarte, Xian Zhang, Brad Fortune, Chris A Johnson. Doc Ophthalmol 2004
36
25

Multifocal VEP and OCT in optic neuritis: a topographical study of the structure-function relationship.
Alexander Klistorner, H Arvind, T Nguyen, R Garrick, M Paine, S Graham, J O'Day, C Yiannikas. Doc Ophthalmol 2009
58
25

Correlation between full-field and multifocal VEPs in optic neuritis.
Alexander Klistorner, Clare Fraser, Raymond Garrick, Stuart Graham, Hemamalini Arvind. Doc Ophthalmol 2008
54
25

Multifocal VEP (mfVEP) reveals abnormal neuronal delays in diabetes.
Brian E Wolff, Marcus A Bearse, Marilyn E Schneck, Shirin Barez, Anthony J Adams. Doc Ophthalmol 2010
26
25


Gaussian wavelet transform and classifier to reliably estimate latency of multifocal visual evoked potentials (mfVEP).
Johnson Thie, Prema Sriram, Alexander Klistorner, Stuart L Graham. Vision Res 2012
7
28

Improved measurement of intersession latency in mfVEPs.
L De Santiago, A Fernández, R Blanco, C Pérez-Rico, J M Rodríguez-Ascariz, R Barea, J M Miguel-Jiménez, C Amo, E M Sánchez-Morla, L Boquete. Doc Ophthalmol 2014
5
40

Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium.
A D Marmorstein, L Y Marmorstein, M Rayborn, X Wang, J G Hollyfield, K Petrukhin. Proc Natl Acad Sci U S A 2000
314
12



CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
Susanne Kohl, Balazs Varsanyi, Gesine Abadin Antunes, Britta Baumann, Carel B Hoyng, Herbert Jägle, Thomas Rosenberg, Ulrich Kellner, Birgit Lorenz, Roberto Salati,[...]. Eur J Hum Genet 2005
167
12

Foveal cone electroretinograms in retinitis pigmentosa and juvenile maular degeneration.
M A Sandberg, S G Jacobson, E L Berson. Am J Ophthalmol 1979
75
12

Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene.
S Andréasson, V Ponjavic, M Abrahamson, B Ehinger, W Wu, R Fujita, M Buraczynska, A Swaroop. Am J Ophthalmol 1997
45
12

Full-field electroretinograms in patients with the carbohydrate-deficient glycoprotein syndrome.
S Andréasson, G Blennow, B Ehinger, K Strömland. Am J Ophthalmol 1991
27
12

Serum transferrin in patients with retinitis pigmentosa.
S Andréasson, H Stibler, B Ehinger. Acta Ophthalmol (Copenh) 1992
4
25

Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS.
U Ekström, V Ponjavic, M Abrahamson, P Nilsson-Ehle, S Andrëasson, I Stenström, B Ehinger. Ophthalmic Genet 1998
9
12

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.
T P Dryja, T L McGee, E Reichel, L B Hahn, G S Cowley, D W Yandell, M A Sandberg, E L Berson. Nature 1990
807
12

Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene.
Felix K Jacobi, Sten Andréasson, Hana Langrova, Alfons Meindl, Eberhart Zrenner, Eckart Apfelstedt-Sylla, Carsten M Pusch. Graefes Arch Clin Exp Ophthalmol 2002
13
12

Retinitis pigmentosa. The Friedenwald Lecture.
E L Berson. Invest Ophthalmol Vis Sci 1993
521
12

Effect of vitamin A supplementation on rhodopsin mutants threonine-17 --> methionine and proline-347 --> serine in transgenic mice and in cell cultures.
T Li, M A Sandberg, B S Pawlyk, B Rosner, K C Hayes, T P Dryja, E L Berson. Proc Natl Acad Sci U S A 1998
145
12

Standard for clinical electroretinography (2004 update).
Michael F Marmor, Graham E Holder, Mathias W Seeliger, Shuichi Yamamoto. Doc Ophthalmol 2004
378
12

A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-Leu.
V Ponjavic, M Abrahamson, S Andréasson, B Ehinger, G Fex, W Polland. Ophthalmic Genet 1997
12
12

Phenotype of an X-linked retinitis pigmentosa family with a novel splice defect in the RPGR gene.
S Bauer, R Fujita, M Buraczynska, M Abrahamson, B Ehinger, W Wu, T J Falls, S Andréasson, A Swaroop. Invest Ophthalmol Vis Sci 1998
19
12


Full-field electroretinograms in infants with hereditary tapetoretinal degeneration.
S Andréasson, V Ponjavic. Acta Ophthalmol Scand Suppl 1996
6
16

CNGA3 mutations in hereditary cone photoreceptor disorders.
B Wissinger, D Gamer, H Jägle, R Giorda, T Marx, S Mayer, S Tippmann, M Broghammer, B Jurklies, T Rosenberg,[...]. Am J Hum Genet 2001
225
12


Electroretinograms in patients with achromatopsia.
S Andréasson, K Tornqvist. Acta Ophthalmol (Copenh) 1991
37
12


Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families.
R Fujita, M Buraczynska, L Gieser, W Wu, P Forsythe, M Abrahamson, S G Jacobson, P A Sieving, S Andréasson, A Swaroop. Am J Hum Genet 1997
59
12

Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes.
Sten Andréasson, Debra K Breuer, Louise Eksandh, Vesna Ponjavic, Christina Frennesson, Suja Hiriyanna, Elena Filippova, Beverly M Yashar, Anand Swaroop. Ophthalmic Genet 2003
19
12

Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype.
V Ponjavic, S Andréasson, M Abrahamson, B Ehinger, L Gieser, R Fujita, A Swaroop. Ophthalmic Genet 1998
4
25

Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.
Patrik Schatz, Vesna Ponjavic, Sten Andréasson, Terri L McGee, Thaddeus P Dryja, Magnus Abrahamson. Ophthalmic Genet 2005
13
12

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change.
K T Hiriyanna, E L Bingham, B M Yashar, R Ayyagari, G Fishman, K W Small, D V Weinberg, R G Weleber, R A Lewis, S Andreasson,[...]. Hum Mutat 1999
35
12

Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene.
L B Eksandh, V B Ponjavic, P B Munroe, H E Eiberg, P E Uvebrant, B E Ehinger, S E Mole, S Andréasson. Ophthalmic Genet 2000
18
12


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.