A citation-based method for searching scientific literature

Antonella Carsana, Giulia Frisso, Maria Roberta Tremolaterra, Elisabetta Ricci, Domenico De Rasmo, Francesco Salvatore. J Mol Diagn 2007
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


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
903
30

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
23

Prenatal diagnosis of inherited diseases: 20 years' experience of an Italian Regional Reference Centre.
Giuseppe Maria Maruotti, Giulia Frisso, Giuseppe Calcagno, Giuliana Fortunato, Giuseppe Castaldo, Pasquale Martinelli, Lucia Sacchetti, Francesco Salvatore. Clin Chem Lab Med 2013
17
23

DNA sequence capture and next-generation sequencing for the molecular diagnosis of genetic cardiomyopathies.
Valeria D'Argenio, Giulia Frisso, Vincenza Precone, Angelo Boccia, Antonella Fienga, Giuseppe Pacileo, Giuseppe Limongelli, Giovanni Paolella, Raffaele Calabrò, Francesco Salvatore. J Mol Diagn 2014
32
23

A 15-year molecular analysis of DMD/BMD: genetic features in a large cohort
Antonella Carsana, Giulia Frisso, Mariano Intrieri, Maria Roberta Tremolaterra, Giovanni Savarese, Giovanni Scapagnini, Gabriella Esposito, Lucio Santoro, Francesco Salvatore. Front Biosci (Elite Ed) 2010
12
25

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
23

Normal pregnancy after preimplantation DNA diagnosis of a dystrophin gene deletion.
J Liu, W Lissens, C Van Broeckhoven, A Löfgren, M Camus, I Liebaers, A Van Steirteghem. Prenat Diagn 1995
49
15

Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCR.
Mira Malcov, Dalit Ben-Yosef, Tamar Schwartz, Nava Mey-Raz, Foad Azem, Joseph B Lessing, Ami Amit, Yuval Yaron. Prenat Diagn 2005
16
15

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
384
15

Proof of principle and first cases using preimplantation genetic haplotyping--a paradigm shift for embryo diagnosis.
Pamela J Renwick, Jane Trussler, Elham Ostad-Saffari, Hiva Fassihi, Cheryl Black, Peter Braude, Caroline Mackie Ogilvie, Stephen Abbs. Reprod Biomed Online 2006
90
15

Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene.
S Abbs, R G Roberts, C G Mathew, D R Bentley, M Bobrow. Genomics 1990
88
15

Specific detection of deleted and non-deleted dystrophin exons together with gender assignment in preimplantation genetic diagnosis of Duchenne muscular dystrophy.
A Girardet, S Hamamah, H Déchaud, T Anahory, C Coubes, B Hédon, J Demaille, M Claustres. Mol Hum Reprod 2003
15
15

Regional genomic instability predisposes to complex dystrophin gene rearrangements.
Junko Oshima, Daniel B Magner, Jennifer A Lee, Amy M Breman, Eric S Schmitt, Lisa D White, Carol A Crowe, Michelle Merrill, Parul Jayakar, Aparna Rajadhyaksha,[...]. Hum Genet 2009
33
15


Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.
Henriett Pikó, Viktor Vancsó, Bálint Nagy, Zoltán Bán, Agnes Herczegfalvi, Veronika Karcagi. Neuromuscul Disord 2009
23
15

Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction.
A H Beggs, M Koenig, F M Boyce, L M Kunkel. Hum Genet 1990
616
15


Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approach.
A H Ligon, C D Kashork, C S Richards, L G Shaffer. Eur J Hum Genet 2000
21
15

Recurrence risk due to germ line mosaicism: Duchenne and Becker muscular dystrophy.
A T J M Helderman-van den Enden, R de Jong, J T den Dunnen, J J Houwing-Duistermaat, A L J Kneppers, H B Ginjaar, M H Breuning, E Bakker. Clin Genet 2009
48
15

High frequency of de novo deletions in Mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling.
M A Alcántara, M T Villarreal, V Del Castillo, G Gutiérrez, Y Saldaña, I Maulen, R Lee, M Macías, L Orozco. Clin Genet 1999
16
15

Analysis of dystrophin gene deletions indicates that the hinge III region of the protein correlates with disease severity.
A Carsana, G Frisso, M R Tremolaterra, R Lanzillo, D F Vitale, L Santoro, F Salvatore. Ann Hum Genet 2005
37
15

Direct detection of exon deletions/duplications in female carriers of and male patients with Duchenne/Becker muscular dystrophy.
Giulia Frisso, Antonella Carsana, Nadia Tinto, Giuseppe Calcagno, Francesco Salvatore, Lucia Sacchetti. Clin Chem 2004
14
15

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms.
P R Clemens, R G Fenwick, J S Chamberlain, R A Gibbs, M de Andrade, R Chakraborty, C T Caskey. Am J Hum Genet 1991
208
15


Dystrophin and mutations: one gene, several proteins, multiple phenotypes.
Francesco Muntoni, Silvia Torelli, Alessandra Ferlini. Lancet Neurol 2003
580
15

Prenatal molecular diagnosis of inherited neuromuscular diseases: Duchenne/Becker muscular dystrophy, myotonic dystrophy type 1 and spinal muscular atrophy.
Gabriella Esposito, Raffaella Ruggiero, Maria Savarese, Giovanni Savarese, Maria Roberta Tremolaterra, Francesco Salvatore, Antonella Carsana. Clin Chem Lab Med 2013
12
16

Prevalence and clinical significance of red flags in patients with hypertrophic cardiomyopathy.
Giuseppe Limongelli, Emanuele Monda, Stefania Tramonte, Felice Gragnano, Daniele Masarone, Giulia Frisso, Augusto Esposito, Rita Gravino, Ernesto Ammendola, Gemma Salerno,[...]. Int J Cardiol 2020
19
15

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria.
Frank I Marcus, William J McKenna, Duane Sherrill, Cristina Basso, Barbara Bauce, David A Bluemke, Hugh Calkins, Domenico Corrado, Moniek G P J Cox, James P Daubert,[...]. Eur Heart J 2010
729
15

Trends in sudden cardiovascular death in young competitive athletes after implementation of a preparticipation screening program.
Domenico Corrado, Cristina Basso, Andrea Pavei, Pierantonio Michieli, Maurizio Schiavon, Gaetano Thiene. JAMA 2006
892
15

Genetic analysis in a family affected by sick sinus syndrome may reduce the sudden death risk in a young aspiring competitive athlete.
Nicola Detta, Giulia Frisso, Giuseppe Limongelli, Michele Marzullo, Raffaele Calabrò, Francesco Salvatore. Int J Cardiol 2014
16
15

Does sports activity enhance the risk of sudden death in adolescents and young adults?
Domenico Corrado, Cristina Basso, Giulio Rizzoli, Maurizio Schiavon, Gaetano Thiene. J Am Coll Cardiol 2003
738
15

HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.
Silvia G Priori, Arthur A Wilde, Minoru Horie, Yongkeun Cho, Elijah R Behr, Charles Berul, Nico Blom, Josep Brugada, Chern-En Chiang, Heikki Huikuri,[...]. Heart Rhythm 2013
15

A child cohort study from southern Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy.
G Frisso, G Limongelli, G Pacileo, A Del Giudice, L Forgione, P Calabrò, M Iacomino, N Detta, L M Di Fonzo, V Maddaloni,[...]. Clin Genet 2009
27
15

Comprehensive human genome amplification using multiple displacement amplification.
Frank B Dean, Seiyu Hosono, Linhua Fang, Xiaohong Wu, A Fawad Faruqi, Patricia Bray-Ward, Zhenyu Sun, Qiuling Zong, Yuefen Du, Jing Du,[...]. Proc Natl Acad Sci U S A 2002
921
7



Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification.
A H Handyside, E H Kontogianni, K Hardy, R M Winston. Nature 1990
954
7

Genetics of Duchenne muscular dystrophy.
R G Worton, M W Thompson. Annu Rev Genet 1988
107
7

The role of muscle biopsy in analysis of the dystrophin gene in Duchenne muscular dystrophy: experience of a national referral centre.
Sylvie Tuffery-Giraud, Céline Saquet, Sylvie Chambert, Bernard Echenne, Jean Marie Cuisset, François Rivier, Mireille Cossée, Christophe Philippe, Nicole Monnier, Eric Bieth,[...]. Neuromuscul Disord 2004
31
7

Well-devised quantification analysis for duplication mutation of Duchenne muscular dystrophy aimed at preimplantation genetic diagnosis.
Akira Nakabayashi, Kou Sueoka, Hiroto Tajima, Kenji Sato, Yoshiaki Sakamoto, Shingo Katou, Yasunori Yoshimura. J Assist Reprod Genet 2007
4
25

Efficient strategies for preimplantation genetic diagnosis of spinal muscular atrophy.
Anne Girardet, Céline Fernandez, Mireille Claustres. Fertil Steril 2008
15
7



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
205
7


Preimplantation diagnosis and HLA typing for haemoglobin disorders.
A Kuliev, S Rechitsky, O Verlinsky, I Tur-Kaspa, G Kalakoutis, M Angastiniotis, Y Verlinsky. Reprod Biomed Online 2005
50
7


Strategies and clinical outcome of 250 cycles of Preimplantation Genetic Diagnosis for single gene disorders.
F Fiorentino, A Biricik, A Nuccitelli, R De Palma, S Kahraman, M Iacobelli, V Trengia, D Caserta, M A Bonu, A Borini,[...]. Hum Reprod 2006
66
7

Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typing.
A Girardet, M S McPeek, E P Leeflang, F Munier, N Arnheim, M Claustres, F Pellestor. Am J Hum Genet 2000
9
11

First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markers.
A Girardet, S Hamamah, T Anahory, H Déchaud, P Sarda, B Hédon, J Demaille, M Claustres. Mol Hum Reprod 2003
34
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.