A citation-based method for searching scientific literature

Camille Laberthonnière, Frédérique Magdinier, Jérôme D Robin. Cells 2019
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Molecular combing reveals allelic combinations in facioscapulohumeral dystrophy.
Karine Nguyen, Pierre Walrafen, Rafaëlle Bernard, Shahram Attarian, Charlène Chaix, Catherine Vovan, Emilie Renard, Nathalie Dufrane, Jean Pouget, Anne Vannier,[...]. Ann Neurol 2011
27
28

Replication timing of human telomeres is chromosome arm-specific, influenced by subtelomeric structures and connected to nuclear localization.
Nausica Arnoult, Caroline Schluth-Bolard, Anne Letessier, Irena Drascovic, Rachida Bouarich-Bourimi, Judith Campisi, Sahn-Ho Kim, Amina Boussouar, Alexandre Ottaviani, Frédérique Magdinier,[...]. PLoS Genet 2010
69
28

A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy.
Daphne S Cabianca, Valentina Casa, Beatrice Bodega, Alexandros Xynos, Enrico Ginelli, Yujiro Tanaka, Davide Gabellini. Cell 2012
243
28

Alignment and sensitive detection of DNA by a moving interface.
A Bensimon, A Simon, A Chiffaudel, V Croquette, F Heslot, D Bensimon. Science 1994
449
28

A unifying genetic model for facioscapulohumeral muscular dystrophy.
Richard J L F Lemmers, Patrick J van der Vliet, Rinse Klooster, Sabrina Sacconi, Pilar Camaño, Johannes G Dauwerse, Lauren Snider, Kirsten R Straasheijm, Gert Jan van Ommen, George W Padberg,[...]. Science 2010
418
28

Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy.
Richard J L F Lemmers, Marielle Wohlgemuth, Kristiaan J van der Gaag, Patrick J van der Vliet, Corrie M M van Teijlingen, Peter de Knijff, George W Padberg, Rune R Frants, Silvere M van der Maarel. Am J Hum Genet 2007
141
28

Telomeric position effect: from the yeast paradigm to human pathologies?
Alexandre Ottaviani, Eric Gilson, Frédérique Magdinier. Biochimie 2008
97
28

Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere.
Richard J L F Lemmers, Peggy de Kievit, Lodewijk Sandkuijl, George W Padberg, Gert-Jan B van Ommen, Rune R Frants, Silvère M van der Maarel. Nat Genet 2002
175
28

Telomeres and telomerase: three decades of progress.
Jerry W Shay, Woodring E Wright. Nat Rev Genet 2019
155
28

Base excision repair.
Hans E Krokan, Magnar Bjørås. Cold Spring Harb Perspect Biol 2013
470
28

Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral muscular dystrophy.
Isabella Scionti, Francesca Greco, Giulia Ricci, Monica Govi, Patricia Arashiro, Liliana Vercelli, Angela Berardinelli, Corrado Angelini, Giovanni Antonini, Michelangelo Cao,[...]. Am J Hum Genet 2012
67
14

CRISPR-CAS9 D10A nickase target-specific fluorescent labeling of double strand DNA for whole genome mapping and structural variation analysis.
Jennifer McCaffrey, Justin Sibert, Bin Zhang, Yonggang Zhang, Wenhui Hu, Harold Riethman, Ming Xiao. Nucleic Acids Res 2016
28
14

D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detection.
R J L F Lemmers, M Osborn, T Haaf, M Rogers, R R Frants, G W Padberg, D N Cooper, S M van der Maarel, M Upadhyaya. Neurology 2003
50
14

High-throughput single-molecule telomere characterization.
Jennifer McCaffrey, Eleanor Young, Katy Lassahn, Justin Sibert, Steven Pastor, Harold Riethman, Ming Xiao. Genome Res 2017
20
14

Regulation of the Human Telomerase Gene TERT by Telomere Position Effect-Over Long Distances (TPE-OLD): Implications for Aging and Cancer.
Wanil Kim, Andrew T Ludlow, Jaewon Min, Jerome D Robin, Guido Stadler, Ilgen Mender, Tsung-Po Lai, Ning Zhang, Woodring E Wright, Jerry W Shay. PLoS Biol 2016
74
14

Telomere length regulates ISG15 expression in human cells.
Zhenjun Lou, Jun Wei, Harold Riethman, Joseph A Baur, Regina Voglauer, Jerry W Shay, Woodring E Wright. Aging (Albany NY) 2009
56
14

Telomere position effect regulates DUX4 in human facioscapulohumeral muscular dystrophy.
Guido Stadler, Fedik Rahimov, Oliver D King, Jennifer C J Chen, Jerome D Robin, Kathryn R Wagner, Jerry W Shay, Charles P Emerson, Woodring E Wright. Nat Struct Mol Biol 2013
59
14

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy.
C Wijmenga, J E Hewitt, L A Sandkuijl, L N Clark, T J Wright, H G Dauwerse, A M Gruter, M H Hofker, P Moerer, R Williamson. Nat Genet 1992
481
14

Somatic mosaicism in FSHD often goes undetected.
Richard J L F Lemmers, Michiel J R van der Wielen, Egbert Bakker, George W Padberg, Rune R Frants, Silvère M van der Maarel. Ann Neurol 2004
47
14

Telomere dynamics in human cells.
Duncan M Baird. Biochimie 2008
41
14

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium.
M Sarfarazi, C Wijmenga, M Upadhyaya, B Weiffenbach, C Hyser, K Mathews, J Murray, J Gilbert, M Pericak-Vance, P Lunt. Am J Hum Genet 1992
113
14

Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy.
Karine Nguyen, Francesca Puppo, Stéphane Roche, Marie-Cécile Gaillard, Charlène Chaix, Arnaud Lagarde, Marjorie Pierret, Catherine Vovan, Sylviane Olschwang, Emmanuelle Salort-Campana,[...]. Hum Mutat 2017
19
14

The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD).
M Upadhyaya, P Lunt, M Sarfarazi, W Broadhead, J Farnham, P S Harper. Am J Hum Genet 1992
38
14

Human telomeric position effect is determined by chromosomal context and telomeric chromatin integrity.
Catherine Elaine Koering, Alessandra Pollice, Maria Pia Zibella, Serge Bauwens, Alain Puisieux, Michele Brunori, Christine Brun, Luis Martins, Laure Sabatier, John F Pulitzer,[...]. EMBO Rep 2002
126
14

Nanopore-based single molecule sequencing of the D4Z4 array responsible for facioscapulohumeral muscular dystrophy.
Satomi Mitsuhashi, So Nakagawa, Mahoko Takahashi Ueda, Tadashi Imanishi, Martin C Frith, Hiroaki Mitsuhashi. Sci Rep 2017
17
14

Telomeric repeat containing RNA and RNA surveillance factors at mammalian chromosome ends.
Claus M Azzalin, Patrick Reichenbach, Lela Khoriauli, Elena Giulotto, Joachim Lingner. Science 2007
799
14

Cis D4Z4 repeat duplications associated with facioscapulohumeral muscular dystrophy type 2.
Richard J L F Lemmers, Patrick J van der Vliet, Jeroen P Vreijling, Don Henderson, Nienke van der Stoep, Nicol Voermans, Baziel van Engelen, Frank Baas, Sabrina Sacconi, Rabi Tawil,[...]. Hum Mol Genet 2018
9
14

Myogenic enhancers regulate expression of the facioscapulohumeral muscular dystrophy-associated DUX4 gene.
Charis L Himeda, Céline Debarnot, Sachiko Homma, Mary Lou Beermann, Jeffrey B Miller, Peter L Jones, Takako I Jones. Mol Cell Biol 2014
39
14

Profiles of neuromuscular diseases. Facioscapulohumeral muscular dystrophy.
D D Kilmer, R T Abresch, M A McCrory, G T Carter, W M Fowler, E R Johnson, C M McDonald. Am J Phys Med Rehabil 1995
79
14

Molecular combing compared to Southern blot for measuring D4Z4 contractions in FSHD.
Jessica Vasale, Fatih Boyar, Michael Jocson, Vladimira Sulcova, Patricia Chan, Khalida Liaquat, Carol Hoffman, Marc Meservey, Isabell Chang, David Tsao,[...]. Neuromuscul Disord 2015
12
14

Worldwide population analysis of the 4q and 10q subtelomeres identifies only four discrete interchromosomal sequence transfers in human evolution.
Richard J L F Lemmers, Patrick J van der Vliet, Kristiaan J van der Gaag, Sofia Zuniga, Rune R Frants, Peter de Knijff, Silvère M van der Maarel. Am J Hum Genet 2010
67
14

Hybridization analysis of D4Z4 repeat arrays linked to FSHD.
Melanie Ehrlich, Kesmic Jackson, Koji Tsumagari, Pilar Camaño, Richard J F L Lemmers. Chromosoma 2007
14
14

Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2.
Richard Jlf Lemmers, Patrick J van der Vliet, Judit Balog, Jelle J Goeman, Wibowo Arindrarto, Yvonne D Krom, Kirsten R Straasheijm, Rashmie D Debipersad, Gizem Özel, Janet Sowden,[...]. Eur J Hum Genet 2018
13
14

Human subtelomeric duplicon structure and organization.
Anthony Ambrosini, Sheila Paul, Sufen Hu, Harold Riethman. Genome Biol 2007
37
14

Human subtelomeric copy number variations.
H Riethman. Cytogenet Genome Res 2008
27
14

Telomere position effect in human cells.
J A Baur, Y Zou, J W Shay, W E Wright. Science 2001
316
14

High-throughput single-molecule mapping links subtelomeric variants and long-range haplotypes with specific telomeres.
Eleanor Young, Steven Pastor, Ramakrishnan Rajagopalan, Jennifer McCaffrey, Justin Sibert, Angel C Y Mak, Pui-Yan Kwok, Harold Riethman, Ming Xiao. Nucleic Acids Res 2017
12
14

Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.
K L Deak, R J L F Lemmers, J M Stajich, R Klooster, R Tawil, R R Frants, M C Speer, S M van der Maarel, J R Gilbert. Neurology 2007
23
14

Single DNA molecule analysis: applications of molecular combing.
Ronald Lebofsky, Aaron Bensimon. Brief Funct Genomic Proteomic 2003
36
14

Extensive allelic variation and ultrashort telomeres in senescent human cells.
Duncan M Baird, Jan Rowson, David Wynford-Thomas, David Kipling. Nat Genet 2003
351
14

Telomere position effect: regulation of gene expression with progressive telomere shortening over long distances.
Jérôme D Robin, Andrew T Ludlow, Kimberly Batten, Frédérique Magdinier, Guido Stadler, Kathyrin R Wagner, Jerry W Shay, Woodring E Wright. Genes Dev 2014
139
14

FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit.
J C van Deutekom, C Wijmenga, E A van Tienhoven, A M Gruter, J E Hewitt, G W Padberg, G J van Ommen, M H Hofker, R R Frants. Hum Mol Genet 1993
364
14

Genomic analysis of human chromosome 10q and 4q telomeres suggests a common origin.
Michel van Geel, Morag C Dickson, Amy F Beck, Daniel J Bolland, Rune R Frants, Silvère M van der Maarel, Pieter J de Jong, Jane E Hewitt. Genomics 2002
91
14

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.
C Wijmenga, R R Frants, O F Brouwer, P Moerer, J L Weber, G W Padberg. Lancet 1990
239
14

Transcription of tandemly repetitive DNA: functional roles.
Maria Assunta Biscotti, Adriana Canapa, Mariko Forconi, Ettore Olmo, Marco Barucca. Chromosome Res 2015
62
14

CENP-B controls centromere formation depending on the chromatin context.
Teruaki Okada, Jun-ichirou Ohzeki, Megumi Nakano, Kinya Yoda, William R Brinkley, Vladimir Larionov, Hiroshi Masumoto. Cell 2007
157
14

Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy.
R Tupler, A Berardinelli, L Barbierato, R Frants, J E Hewitt, G Lanzi, P Maraschio, L Tiepolo. J Med Genet 1996
85
14

Unstable transmission of the RS447 human megasatellite tandem repetitive sequence that contains the USP17 deubiquitinating enzyme gene.
Takeya Okada, Yoichi Gondo, Jun Goto, Ichiro Kanazawa, Shinji Hadano, Joh-E Ikeda. Hum Genet 2002
25
14

An association study between Heme oxygenase-1 genetic variants and Parkinson's disease.
Pedro Ayuso, Carmen Martínez, Pau Pastor, Oswaldo Lorenzo-Betancor, Antonio Luengo, Félix J Jiménez-Jiménez, Hortensia Alonso-Navarro, José A G Agúndez, Elena García-Martín. Front Cell Neurosci 2014
28
14



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.