A citation-based method for searching scientific literature

A Helbling-Leclerc, X Zhang, H Topaloglu, C Cruaud, F Tesson, J Weissenbach, F M Tomé, K Schwartz, M Fardeau, K Tryggvason. Nat Genet 1995
Times Cited: 515







List of co-cited articles
1036 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations.
Fatemeh Geranmayeh, Emma Clement, Lucy H Feng, Caroline Sewry, Judith Pagan, Rachael Mein, Stephen Abbs, Louise Brueton, Anne-Marie Childs, Heinz Jungbluth,[...]. Neuromuscul Disord 2010
100
22



The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review.
K J Jones, G Morgan, H Johnston, V Tobias, R A Ouvrier, I Wilkinson, K N North. J Med Genet 2001
104
17

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix.
O Ibraghimov-Beskrovnaya, J M Ervasti, C J Leveille, C A Slaughter, S W Sernett, K P Campbell. Nature 1992
16

Laminin-111 protein therapy reduces muscle pathology and improves viability of a mouse model of merosin-deficient congenital muscular dystrophy.
Jachinta E Rooney, Jolie R Knapp, Bradley L Hodges, Ryan D Wuebbles, Dean J Burkin. Am J Pathol 2012
69
23

Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy.
Y Miyagoe, K Hanaoka, I Nonaka, M Hayasaka, Y Nabeshima, K Arahata, Y Nabeshima, S Takeda. FEBS Lett 1997
204
16

Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies.
Kinga I Gawlik, Madeleine Durbeej. Skelet Muscle 2011
72
20

Congenital muscular dystrophy with merosin deficiency.
F M Tomé, T Evangelista, A Leclerc, Y Sunada, E Manole, B Estournet, A Barois, K P Campbell, M Fardeau. C R Acad Sci III 1994
405
14

Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy.
P H Vachon, H Xu, L Liu, F Loechel, Y Hayashi, K Arahata, J C Reed, U M Wewer, E Engvall. J Clin Invest 1997
171
14

LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients.
J Oliveira, R Santos, I Soares-Silva, P Jorge, E Vieira, M E Oliveira, A Moreira, T Coelho, J C Ferreira, M J Fonseca,[...]. Clin Genet 2008
36
38

The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy.
Thomas E Hall, Robert J Bryson-Richardson, Silke Berger, Arie S Jacoby, Nicholas J Cole, Georgina E Hollway, Joachim Berger, Peter D Currie. Proc Natl Acad Sci U S A 2007
127
13



Omigapil ameliorates the pathology of muscle dystrophy caused by laminin-alpha2 deficiency.
Michael Erb, Sarina Meinen, Patrizia Barzaghi, Lazar T Sumanovski, Isabelle Courdier-Früh, Markus A Rüegg, Thomas Meier. J Pharmacol Exp Ther 2009
64
20

Laminin-211 in skeletal muscle function.
Johan Holmberg, Madeleine Durbeej. Cell Adh Migr 2013
77
16

A simplified laminin nomenclature.
Monique Aumailley, Leena Bruckner-Tuderman, William G Carter, Rainer Deutzmann, David Edgar, Peter Ekblom, Jürgen Engel, Eva Engvall, Erhard Hohenester, Jonathan C R Jones,[...]. Matrix Biol 2005
580
13

Diagnostic approach to the congenital muscular dystrophies.
Carsten G Bönnemann, Ching H Wang, Susana Quijano-Roy, Nicolas Deconinck, Enrico Bertini, Ana Ferreiro, Francesco Muntoni, Caroline Sewry, Christophe Béroud, Katherine D Mathews,[...]. Neuromuscul Disord 2014
181
13

Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models.
W Kuang, H Xu, P H Vachon, L Liu, F Loechel, U M Wewer, E Engvall. J Clin Invest 1998
152
12

Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A.
Virginie Carmignac, Martina Svensson, Zandra Körner, Linda Elowsson, Cintia Matsumura, Kinga I Gawlik, Valerie Allamand, Madeleine Durbeej. Hum Mol Genet 2011
91
13

Merosin, a tissue-specific basement membrane protein, is a laminin-like protein.
K Ehrig, I Leivo, W S Argraves, E Ruoslahti, E Engvall. Proc Natl Acad Sci U S A 1990
389
12

An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.
J Moll, P Barzaghi, S Lin, G Bezakova, H Lochmüller, E Engvall, U Müller, M A Ruegg. Nature 2001
176
12

Laminin alpha1 chain reduces muscular dystrophy in laminin alpha2 chain deficient mice.
Kinga Gawlik, Yuko Miyagoe-Suzuki, Peter Ekblom, Shin'ichi Takeda, Madeleine Durbeej. Hum Mol Genet 2004
102
12


Laminin-deficient muscular dystrophy: Molecular pathogenesis and structural repair strategies.
Peter D Yurchenco, Karen K McKee, Judith R Reinhard, Markus A Rüegg. Matrix Biol 2018
48
22


Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of alpha-dystroglycan.
Renzhi Han, Motoi Kanagawa, Takako Yoshida-Moriguchi, Erik P Rader, Rainer A Ng, Daniel E Michele, David E Muirhead, Stefan Kunz, Steven A Moore, Susan T Iannaccone,[...]. Proc Natl Acad Sci U S A 2009
104
10


Pathology is alleviated by doxycycline in a laminin-alpha2-null model of congenital muscular dystrophy.
Mahasweta Girgenrath, Mary Lou Beermann, Vivek K Vishnudas, Sachiko Homma, Jeffrey Boone Miller. Ann Neurol 2009
63
15

Inhibition of apoptosis improves outcome in a model of congenital muscular dystrophy.
Mahasweta Girgenrath, Janice A Dominov, Christine A Kostek, Jeffrey Boone Miller. J Clin Invest 2004
97
10

Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice.
Virginie Carmignac, Ronan Quéré, Madeleine Durbeej. Hum Mol Genet 2011
48
20

Laminin alpha1 chain mediated reduction of laminin alpha2 chain deficient muscular dystrophy involves integrin alpha7beta1 and dystroglycan.
Kinga I Gawlik, Ulrike Mayer, Kristina Blomberg, Arnoud Sonnenberg, Peter Ekblom, Madeleine Durbeej. FEBS Lett 2006
46
21

The congenital muscular dystrophies in 2004: a century of exciting progress.
Francesco Muntoni, Thomas Voit. Neuromuscul Disord 2004
164
10

Laminin-111 restores regenerative capacity in a mouse model for alpha7 integrin congenital myopathy.
Jachinta E Rooney, Praveen B Gurpur, Zipora Yablonka-Reuveni, Dean J Burkin. Am J Pathol 2009
56
17

Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging.
J Philpot, F Cowan, J Pennock, C Sewry, V Dubowitz, G Bydder, F Muntoni. Neuromuscul Disord 1999
86
11

Epistatic dissection of laminin-receptor interactions in dystrophic zebrafish muscle.
Tamar E Sztal, Carmen Sonntag, Thomas E Hall, Peter D Currie. Hum Mol Genet 2012
38
26


Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients.
H Xiong, D Tan, S Wang, S Song, H Yang, K Gao, A Liu, H Jiao, B Mao, J Ding,[...]. Clin Genet 2015
33
30

Mutations in the integrin alpha7 gene cause congenital myopathy.
Y K Hayashi, F L Chou, E Engvall, M Ogawa, C Matsuda, S Hirabayashi, K Yokochi, B L Ziober, R H Kramer, S J Kaufman,[...]. Nat Genet 1998
275
10

Apoptosis inhibitors and mini-agrin have additive benefits in congenital muscular dystrophy mice.
Sarina Meinen, Shuo Lin, Raphael Thurnherr, Michael Erb, Thomas Meier, Markus A Rüegg. EMBO Mol Med 2011
36
25

Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy.
M L Mostacciuolo, M Miorin, F Martinello, C Angelini, P Perini, C P Trevisan. Hum Genet 1996
75
12


The ever-expanding spectrum of congenital muscular dystrophies.
Eugenio Mercuri, Francesco Muntoni. Ann Neurol 2012
64
14

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.
V Nigro, E de Sá Moreira, G Piluso, M Vainzof, A Belsito, L Politano, A A Puca, M R Passos-Bueno, M Zatz. Nat Genet 1996
350
9

Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle.
K Matsumura, J M Ervasti, K Ohlendieck, S D Kahl, K P Campbell. Nature 1992
451
9

A dystroglycan mutation associated with limb-girdle muscular dystrophy.
Yuji Hara, Burcu Balci-Hayta, Takako Yoshida-Moriguchi, Motoi Kanagawa, Daniel Beltrán-Valero de Bernabé, Hülya Gündeşli, Tobias Willer, Jakob S Satz, Robert W Crawford, Steven J Burden,[...]. N Engl J Med 2011
170
9

Absence of integrin alpha 7 causes a novel form of muscular dystrophy.
U Mayer, G Saher, R Fässler, A Bornemann, F Echtermeyer, H von der Mark, N Miosge, E Pöschl, K von der Mark. Nat Genet 1997
348
9

Altered expression of the alpha7beta1 integrin in human and murine muscular dystrophies.
B L Hodges, Y K Hayashi, I Nonaka, W Wang, K Arahata, S J Kaufman. J Cell Sci 1997
152
8


Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.
V Straub, J A Rafael, J S Chamberlain, K P Campbell. J Cell Biol 1997
401
8


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.