A citation-based method for searching scientific literature

A H Beggs, M Koenig, F M Boyce, L M Kunkel. Hum Genet 1990
Times Cited: 617







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



Times Cited
  Times     Co-cited
Similarity


Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification.
J S Chamberlain, R A Gibbs, J E Ranier, P N Nguyen, C T Caskey. Nucleic Acids Res 1988
884
43

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus.
A P Monaco, C J Bertelson, S Liechti-Gallati, H Moser, L M Kunkel. Genomics 1988
906
43


Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule.
Annemieke Aartsma-Rus, Judith C T Van Deutekom, Ivo F Fokkema, Gert-Jan B Van Ommen, Johan T Den Dunnen. Muscle Nerve 2006
390
31

Dystrophin and mutations: one gene, several proteins, multiple phenotypes.
Francesco Muntoni, Silvia Torelli, Alessandra Ferlini. Lancet Neurol 2003
591
29



Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification.
Jan P Schouten, Cathal J McElgunn, Raymond Waaijer, Danny Zwijnenburg, Filip Diepvens, Gerard Pals. Nucleic Acids Res 2002
25


Deletion and duplication screening in the DMD gene using MLPA.
Tanja Lalic, Rolf H A M Vossen, Jordy Coffa, Jan P Schouten, Marija Guc-Scekic, Danijela Radivojevic, Marina Djurisic, Martÿn H Breuning, Stefan J White, Johan T den Dunnen. Eur J Hum Genet 2005
122
24


Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.
J T Den Dunnen, P M Grootscholten, E Bakker, L A Blonden, H B Ginjaar, M C Wapenaar, H M van Paassen, C van Broeckhoven, P L Pearson, G J van Ommen. Am J Hum Genet 1989
456
22

Rapid direct sequence analysis of the dystrophin gene.
Kevin M Flanigan, Andrew von Niederhausern, Diane M Dunn, Jonathan Alder, Jerry R Mendell, Robert B Weiss. Am J Hum Genet 2003
135
19

Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.
Daniela del Gaudio, Yaping Yang, Barbara A Boggs, Eric S Schmitt, Jennifer A Lee, Trilochan Sahoo, Hoang T Pham, Joanna Wiszniewska, A Craig Chinault, Arthur L Beaudet,[...]. Hum Mutat 2008
68
27

Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase.
Sylvie Tuffery-Giraud, Christophe Béroud, France Leturcq, Rabah Ben Yaou, Dalil Hamroun, Laurence Michel-Calemard, Marie-Pierre Moizard, Rafaëlle Bernard, Mireille Cossée, Pierre Boisseau,[...]. Hum Mutat 2009
209
19


Microarray-based mutation detection in the dystrophin gene.
Madhuri R Hegde, Ephrem L H Chin, Jennifer G Mulle, David T Okou, Stephen T Warren, Michael E Zwick. Hum Mutat 2008
76
23

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
M Koenig, A H Beggs, M Moyer, S Scherpf, K Heindrich, T Bettecken, G Meng, C R Müller, M Lindlöf, H Kaariainen,[...]. Am J Hum Genet 1989
802
18

Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center.
Yasuhiro Takeshima, Mariko Yagi, Yo Okizuka, Hiroyuki Awano, Zhujun Zhang, Yumiko Yamauchi, Hisahide Nishio, Masafumi Matsuo. J Hum Genet 2010
145
17

Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridization.
Stefan White, Margot Kalf, Qiang Liu, Michel Villerius, Dieuwke Engelsma, Marjolein Kriek, Ellen Vollebregt, Bert Bakker, Gert-Jan B van Ommen, Martijn H Breuning,[...]. Am J Hum Genet 2002
142
16

Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.
Katharine Bushby, Richard Finkel, David J Birnkrant, Laura E Case, Paula R Clemens, Linda Cripe, Ajay Kaul, Kathi Kinnett, Craig McDonald, Shree Pandya,[...]. Lancet Neurol 2010
16

Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.
Kevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, Payam Soltanzadeh, Eduard Gappmaier, Michael T Howard, Jacinda B Sampson, Jerry R Mendell, Cheryl Wall, Wendy M King,[...]. Hum Mutat 2009
189
16


Duplications in the DMD gene.
S J White, A Aartsma-Rus, K M Flanigan, R B Weiss, A L J Kneppers, T Lalic, A A M Janson, H B Ginjaar, M H Breuning, J T den Dunnen. Hum Mutat 2006
98
15

Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA).
Valentina Gatta, Oronzo Scarciolla, Anna Rita Gaspari, Chiara Palka, Maria Vittoria De Angelis, Antonio Di Muzio, Paolo Guanciali-Franchi, Giuseppe Calabrese, Antonino Uncini, Liborio Stuppia. Hum Genet 2005
82
18

Local dystrophin restoration with antisense oligonucleotide PRO051.
Judith C van Deutekom, Anneke A Janson, Ieke B Ginjaar, Wendy S Frankhuizen, Annemieke Aartsma-Rus, Mattie Bremmer-Bout, Johan T den Dunnen, Klaas Koop, Anneke J van der Kooi, Nathalie M Goemans,[...]. N Engl J Med 2007
595
13

Theoretic applicability of antisense-mediated exon skipping for Duchenne muscular dystrophy mutations.
Annemieke Aartsma-Rus, Ivo Fokkema, Jan Verschuuren, Ieke Ginjaar, Judith van Deutekom, Gert-Jan van Ommen, Johan T den Dunnen. Hum Mutat 2009
348
13

The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations.
Catherine L Bladen, David Salgado, Soledad Monges, Maria E Foncuberta, Kyriaki Kekou, Konstantina Kosma, Hugh Dawkins, Leanne Lamont, Anna J Roy, Teodora Chamova,[...]. Hum Mutat 2015
293
13

Multiplex ligation-dependent probe amplification identification of deletions and duplications of the Duchenne muscular dystrophy gene in Taiwanese subjects.
Hsiao-Lin Hwa, Yih-Yuan Chang, Chung-Hsiung Chen, Yen-Shi Kao, Yuh-Jyh Jong, Mei-Chyn Chao, Tsang-Ming Ko. J Formos Med Assoc 2007
29
37



A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies.
Matteo Bovolenta, Marcella Neri, Sergio Fini, Marina Fabris, Cecilia Trabanelli, Anna Venturoli, Elena Martoni, Elena Bassi, Pietro Spitali, Simona Brioschi,[...]. BMC Genomics 2008
48
20

Best practice guidelines on molecular diagnostics in Duchenne/Becker muscular dystrophies.
Stephen Abbs, Sylvie Tuffery-Giraud, Egbert Bakker, Alessandra Ferlini, Thomas Sejersen, Clemens R Mueller. Neuromuscul Disord 2010
61
16

Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study.
Sebahattin Cirak, Virginia Arechavala-Gomeza, Michela Guglieri, Lucy Feng, Silvia Torelli, Karen Anthony, Stephen Abbs, Maria Elena Garralda, John Bourke, Dominic J Wells,[...]. Lancet 2011
601
10

Prevalence and incidence of Becker muscular dystrophy.
K M Bushby, M Thambyayah, D Gardner-Medwin. Lancet 1991
120
10

The muscular dystrophies.
Alan E H Emery. Lancet 2002
932
9

Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients.
Aziza Sbiti, Fatiha El Kerch, Abdelaziz Sefiani. J Biomed Biotechnol 2002
18
50

Diagnosis of Duchenne dystrophy by enhanced detection of small mutations.
J R Mendell, C H Buzin, J Feng, J Yan, C Serrano, D S Sangani, C Wall, T W Prior, S S Sommer. Neurology 2001
89
10

Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing.
R R Bennett, J den Dunnen, K F O'Brien, B T Darras, L M Kunkel. BMC Genet 2001
72
12


Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation.
Michelle Eagle, Simon V Baudouin, Colin Chandler, David R Giddings, Robert Bullock, Kate Bushby. Neuromuscul Disord 2002
518
9

Point mutations in the dystrophin gene.
R G Roberts, M Bobrow, D R Bentley. Proc Natl Acad Sci U S A 1992
193
9

Genetic diagnosis of Duchenne and Becker muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform.
Byung Chan Lim, Seungbok Lee, Jong-Yeon Shin, Jong-Il Kim, Hee Hwang, Ki Joong Kim, Yong Seung Hwang, Jeong-Sun Seo, Jong Hee Chae. J Med Genet 2011
65
13

The importance of genetic diagnosis for Duchenne muscular dystrophy.
Annemieke Aartsma-Rus, Ieke B Ginjaar, Kate Bushby. J Med Genet 2016
136
9

Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies.
Tracy L Stockley, Sarah Akber, Natalie Bulgin, Peter N Ray. Genet Test 2006
21
38

Small mutations detected by multiplex ligation-dependent probe amplification of the dystrophin gene.
Yo Okizuka, Yasuhiro Takeshima, Hiroyuki Awano, Zhujun Zhang, Mariko Yagi, Masafumi Matsuo. Genet Test Mol Biomarkers 2009
15
53

Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study.
E M Hoogerwaard, E Bakker, P F Ippel, J C Oosterwijk, D F Majoor-Krakauer, N J Leschot, A J Van Essen, H G Brunner, P A van der Wouw, A A Wilde,[...]. Lancet 1999
146
8


Multiplex real-time PCR for detection of deletions and duplications in dystrophin gene.
Monica Traverso, Mauro Malnati, Carlo Minetti, Stefano Regis, Silvana Tedeschi, Marina Pedemonte, Claudio Bruno, Roberto Biassoni, Federico Zara. Biochem Biophys Res Commun 2006
32
25

Improved molecular diagnosis of dystrophinopathies in an unselected clinical cohort.
K M Dent, D M Dunn, A C von Niederhausern, A T Aoyagi, L Kerr, M B Bromberg, K J Hart, T Tuohy, S White, J T den Dunnen,[...]. Am J Med Genet A 2005
97
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.