A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Human methylenetetrahydrofolate reductase: isolation of cDNA mapping and mutation identification.
P Goyette, J S Sumner, R Milos, A M Duncan, D S Rosenblatt, R G Matthews, R Rozen. Nat Genet 1994
110
37




An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
T M Strom, G Nyakatura, E Apfelstedt-Sylla, H Hellebrand, B Lorenz, B H Weber, K Wutz, N Gutwillinger, K Rüther, B Drescher,[...]. Nat Genet 1998
347
25

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
N T Bech-Hansen, M J Naylor, T A Maybaum, R L Sparkes, B Koop, D G Birch, A A Bergen, C F Prinsen, R C Polomeno, A Gal,[...]. Nat Genet 2000
239
25

[Analysis of the human electroretinogram].
G SCHUBERT, H BORNSCHEIN. Ophthalmologica 1952
227
23

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
N T Bech-Hansen, M J Naylor, T A Maybaum, W G Pearce, B Koop, G A Fishman, M Mets, M A Musarella, K M Boycott. Nat Genet 1998
371
23

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
352
21

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase.
P Frosst, H J Blom, R Milos, P Goyette, C A Sheppard, R G Matthews, G J Boers, M den Heijer, L A Kluijtmans, L P van den Heuvel. Nat Genet 1995
19

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
C M Pusch, C Zeitz, O Brandau, K Pesch, H Achatz, S Feil, C Scharfe, J Maurer, F K Jacobi, A Pinckers,[...]. Nat Genet 2000
186
19

Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.
Christina Zeitz, Barbara Kloeckener-Gruissem, Ursula Forster, Susanne Kohl, István Magyar, Bernd Wissinger, Gábor Mátyás, François-Xavier Borruat, Daniel F Schorderet, Eberhart Zrenner,[...]. Am J Hum Genet 2006
122
19

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.
Thaddeus P Dryja, Terri L McGee, Eliot L Berson, Gerald A Fishman, Michael A Sandberg, Kenneth R Alexander, Deborah J Derlacki, Aruna S Rajagopalan. Proc Natl Acad Sci U S A 2005
168
19

TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
Isabelle Audo, Susanne Kohl, Bart P Leroy, Francis L Munier, Xavier Guillonneau, Saddek Mohand-Saïd, Kinga Bujakowska, Emeline F Nandrot, Birgit Lorenz, Markus Preising,[...]. Am J Hum Genet 2009
163
19

A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.
S Amer Riazuddin, Amber Shahzadi, Christina Zeitz, Zubair M Ahmed, Radha Ayyagari, Venkata R M Chavali, Virgilio G Ponferrada, Isabelle Audo, Christelle Michiels, Marie-Elise Lancelot,[...]. Am J Hum Genet 2010
50
22


Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness.
S Yamamoto, K C Sippel, E L Berson, T P Dryja. Nat Genet 1997
189
17

Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
Christina Zeitz, Maria van Genderen, John Neidhardt, Ulrich F O Luhmann, Frank Hoeben, Ursula Forster, Katharina Wycisk, Gábor Mátyás, Carel B Hoyng, Frans Riemslag,[...]. Invest Ophthalmol Vis Sci 2005
108
17

Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.
Maria M van Genderen, Mieke M C Bijveld, Yvonne B Claassen, Ralph J Florijn, Jillian N Pearring, Francoise M Meire, Maureen A McCall, Frans C C Riemslag, Ronald G Gregg, Arthur A B Bergen,[...]. Am J Hum Genet 2009
148
17

Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.
Zheng Li, Panagiotis I Sergouniotis, Michel Michaelides, Donna S Mackay, Genevieve A Wright, Sophie Devery, Anthony T Moore, Graham E Holder, Anthony G Robson, Andrew R Webster. Am J Hum Genet 2009
127
16


A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness.
N al-Jandal, G J Farrar, A S Kiang, M M Humphries, N Bannon, J B Findlay, P Humphries, P F Kenna. Hum Mutat 1999
67
14

Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.
P A Sieving, J E Richards, F Naarendorp, E L Bingham, K Scott, M Alpern. Proc Natl Acad Sci U S A 1995
135
14


Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy.
Katharina Agnes Wycisk, Christina Zeitz, Silke Feil, Mariana Wittmer, Ursula Forster, John Neidhardt, Bernd Wissinger, Eberhart Zrenner, Robert Wilke, Susanne Kohl,[...]. Am J Hum Genet 2006
105
12

Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.
Christina Zeitz, Samuel G Jacobson, Christian P Hamel, Kinga Bujakowska, Marion Neuillé, Elise Orhan, Xavier Zanlonghi, Marie-Elise Lancelot, Christelle Michiels, Sharon B Schwartz,[...]. Am J Hum Genet 2013
89
12

Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.
Isabelle Audo, Kinga Bujakowska, Elise Orhan, Charlotte M Poloschek, Sabine Defoort-Dhellemmes, Isabelle Drumare, Susanne Kohl, Tien D Luu, Odile Lecompte, Eberhart Zrenner,[...]. Am J Hum Genet 2012
89
12

GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.
Neal S Peachey, Thomas A Ray, Ralph Florijn, Lucy B Rowe, Trijntje Sjoerdsma, Susana Contreras-Alcantara, Kenkichi Baba, Gianluca Tosini, Nikita Pozdeyev, P Michael Iuvone,[...]. Am J Hum Genet 2012
94
12



Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase.
C Bowes, T Li, M Danciger, L C Baxter, M L Applebury, D B Farber. Nature 1990
683
10

Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking.
Christina Zeitz, Ursula Forster, John Neidhardt, Silke Feil, Stefan Kälin, Dorothee Leifert, Peter J Flor, Wolfgang Berger. Hum Mutat 2007
48
12

GNAT1 associated with autosomal recessive congenital stationary night blindness.
Muhammad Asif Naeem, Venkata R M Chavali, Shahbaz Ali, Muhammad Iqbal, Saima Riazuddin, Shaheen N Khan, Tayyab Husnain, Paul A Sieving, Radha Ayyagari, Sheikh Riazuddin,[...]. Invest Ophthalmol Vis Sci 2012
44
13

Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase.
S H Huang, S J Pittler, X Huang, L Oliveira, E L Berson, T P Dryja. Nat Genet 1995
209
8

Identification and functional characterization of a novel rhodopsin mutation associated with autosomal dominant CSNB.
Christina Zeitz, Alecia K Gross, Dorothee Leifert, Barbara Kloeckener-Gruissem, Suzanne D McAlear, Johannes Lemke, John Neidhardt, Wolfgang Berger. Invest Ophthalmol Vis Sci 2008
42
11

ISCEV Standard for full-field clinical electroretinography (2008 update).
M F Marmor, A B Fulton, G E Holder, Y Miyake, M Brigell, M Bach. Doc Ophthalmol 2009
767
8

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa.
P J Rosenfeld, G S Cowley, T L McGee, M A Sandberg, E L Berson, T P Dryja. Nat Genet 1992
338
7


Autosomal dominant stationary night-blindness. A large family rediscovered.
T Rosenberg, M Haim, Y Piczenik, S E Simonsen. Acta Ophthalmol (Copenh) 1991
19
21

Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis.
I Perrault, J M Rozet, P Calvas, S Gerber, A Camuzat, H Dollfus, S Châtelin, E Souied, I Ghazi, C Leowski,[...]. Nat Genet 1996
372
7


Retinal degeneration in mice lacking the gamma subunit of the rod cGMP phosphodiesterase.
S H Tsang, P Gouras, C K Yamashita, H Kjeldbye, J Fisher, D B Farber, S P Goff. Science 1996
148
7

Avoiding recomputation in linkage analysis.
A A Schäffer, S K Gupta, K Shriram, R W Cottingham. Hum Hered 1994
653
7

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
802
7





TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade.
Chieko Koike, Takehisa Obara, Yoshitsugu Uriu, Tomohiro Numata, Rikako Sanuki, Kentarou Miyata, Toshiyuki Koyasu, Shinji Ueno, Kazuo Funabiki, Akiko Tani,[...]. Proc Natl Acad Sci U S A 2010
200
7



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.