A citation-based method for searching scientific literature

Julia Vogt, Kathrin Bengesser, Kathleen B M Claes, Katharina Wimmer, Victor-Felix Mautner, Rick van Minkelen, Eric Legius, Hilde Brems, Meena Upadhyaya, Josef Högel, Conxi Lazaro, Thorsten Rosenbaum, Simone Bammert, Ludwine Messiaen, David N Cooper, Hildegard Kehrer-Sawatzki. Genome Biol 2014
Times Cited: 37







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



Times Cited
  Times     Co-cited
Similarity


The non-autonomous retrotransposon SVA is trans-mobilized by the human LINE-1 protein machinery.
Julija Raiz, Annette Damert, Sergiu Chira, Ulrike Held, Sabine Klawitter, Matthias Hamdorf, Johannes Löwer, Wolf H Strätling, Roswitha Löwer, Gerald G Schumann. Nucleic Acids Res 2012
132
32

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
32

Roles for retrotransposon insertions in human disease.
Dustin C Hancks, Haig H Kazazian. Mob DNA 2016
275
32

Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1).
Ludwine Messiaen, Julia Vogt, Kathrin Bengesser, Chuanhua Fu, Fady Mikhail, Eduard Serra, Carles Garcia-Linares, David N Cooper, Conxi Lazaro, Hildegard Kehrer-Sawatzki. Hum Mutat 2011
79
29

SVA elements: a hominid-specific retroposon family.
Hui Wang, Jinchuan Xing, Deepak Grover, Dale J Hedges, Kyudong Han, Jerilyn A Walker, Mark A Batzer. J Mol Biol 2005
216
29

Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder.
Julia Vogt, Tanja Mussotter, Kathrin Bengesser, Kathleen Claes, Josef Högel, Nadia Chuzhanova, Chuanhua Fu, Jenneke van den Ende, Victor-Felix Mautner, David N Cooper,[...]. Hum Mutat 2012
21
47

NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype.
Eric Pasmant, Audrey Sabbagh, Gill Spurlock, Ingrid Laurendeau, Elisa Grillo, Marie-José Hamel, Ludovic Martin, Sébastien Barbarot, Bruno Leheup, Diana Rodriguez,[...]. Hum Mutat 2010
145
27

Retrotransposition of marked SVA elements by human L1s in cultured cells.
Dustin C Hancks, John L Goodier, Prabhat K Mandal, Ling E Cheung, Haig H Kazazian. Hum Mol Genet 2011
133
27

The impact of retrotransposons on human genome evolution.
Richard Cordaux, Mark A Batzer. Nat Rev Genet 2009
950
27

Exon-trapping mediated by the human retrotransposon SVA.
Dustin C Hancks, Adam D Ewing, Jesse E Chen, Katsushi Tokunaga, Haig H Kazazian. Genome Res 2009
73
27

Emerging genotype-phenotype relationships in patients with large NF1 deletions.
Hildegard Kehrer-Sawatzki, Victor-Felix Mautner, David N Cooper. Hum Genet 2017
103
27

High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 gene.
H Kehrer-Sawatzki, L Kluwe, C Sandig, M Kohn, K Wimmer, U Krammer, A Peyrl, D E Jenne, I Hansmann, V-F Mautner. Am J Hum Genet 2004
101
24

A novel third type of recurrent NF1 microdeletion mediated by nonallelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2.
Kathrin Bengesser, David N Cooper, Katharina Steinmann, Lan Kluwe, Nadia A Chuzhanova, Katharina Wimmer, Marcos Tatagiba, Sigrid Tinschert, Victor-Felix Mautner, Hildegard Kehrer-Sawatzki. Hum Mutat 2010
34
26

Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions.
V-F Mautner, L Kluwe, R E Friedrich, A C Roehl, S Bammert, J Högel, H Spöri, D N Cooper, H Kehrer-Sawatzki. J Med Genet 2010
104
24

Screening 500 unselected neurofibromatosis 1 patients for deletions of the NF1 gene.
Lan Kluwe, Reiner Siebert, Stefan Gesk, Reinhard E Friedrich, Sigrid Tinschert, Hildegard Kehrer-Sawatzki, Victor-F Mautner. Hum Mutat 2004
121
24

Analysis of crossover breakpoints yields new insights into the nature of the gene conversion events associated with large NF1 deletions mediated by nonallelic homologous recombination.
Kathrin Bengesser, Julia Vogt, Tanja Mussotter, Victor-Felix Mautner, Ludwine Messiaen, David N Cooper, Hildegard Kehrer-Sawatzki. Hum Mutat 2014
15
60

Hot L1s account for the bulk of retrotransposition in the human population.
Brook Brouha, Joshua Schustak, Richard M Badge, Sheila Lutz-Prigge, Alexander H Farley, John V Moran, Haig H Kazazian. Proc Natl Acad Sci U S A 2003
659
24

The NF1 gene contains hotspots for L1 endonuclease-dependent de novo insertion.
Katharina Wimmer, Tom Callens, Annekatrin Wernstedt, Ludwine Messiaen. PLoS Genet 2011
58
24

DNA repair mediated by endonuclease-independent LINE-1 retrotransposition.
Tammy A Morrish, Nicolas Gilbert, Jeremy S Myers, Bethaney J Vincent, Thomas D Stamato, Guillermo E Taccioli, Mark A Batzer, John V Moran. Nat Genet 2002
314
24

Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletions.
Angelika C Roehl, Julia Vogt, Tanja Mussotter, Antje N Zickler, Helene Spöti, Josef Högel, Nadia A Chuzhanova, Katharina Wimmer, Lan Kluwe, Victor-Felix Mautner,[...]. Hum Mutat 2010
28
28

Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion.
Thomas De Raedt, Matthew Stephens, Ine Heyns, Hilde Brems, Daisy Thijs, Ludwine Messiaen, Karen Stephens, Conxi Lazaro, Katharina Wimmer, Hildegard Kehrer-Sawatzki,[...]. Nat Genet 2006
67
21

Characterization of the nonallelic homologous recombination hotspot PRS3 associated with type-3 NF1 deletions.
Antje M Zickler, Stephanie Hampp, Ludwine Messiaen, Kathrin Bengesser, Tanja Mussotter, Angelika C Roehl, Katharina Wimmer, Victor-Felix Mautner, Lan Kluwe, Meena Upadhyaya,[...]. Hum Mutat 2012
19
42

Unequal meiotic crossover: a frequent cause of NF1 microdeletions.
C López Correa, H Brems, C Lázaro, P Marynen, E Legius. Am J Hum Genet 2000
78
21

LINE-mediated retrotransposition of marked Alu sequences.
Marie Dewannieux, Cécile Esnault, Thierry Heidmann. Nat Genet 2003
683
21


SVA retrotransposons: Evolution and genetic instability.
Dustin C Hancks, Haig H Kazazian. Semin Cancer Biol 2010
89
21

Somatic retrotransposition alters the genetic landscape of the human brain.
J Kenneth Baillie, Mark W Barnett, Kyle R Upton, Daniel J Gerhardt, Todd A Richmond, Fioravante De Sapio, Paul M Brennan, Patrizia Rizzu, Sarah Smith, Mark Fell,[...]. Nature 2011
441
21

Active human retrotransposons: variation and disease.
Dustin C Hancks, Haig H Kazazian. Curr Opin Genet Dev 2012
373
21

Landscape of somatic retrotransposition in human cancers.
Eunjung Lee, Rebecca Iskow, Lixing Yang, Omer Gokcumen, Psalm Haseley, Lovelace J Luquette, Jens G Lohr, Christopher C Harris, Li Ding, Richard K Wilson,[...]. Science 2012
458
21

Endogenous retrotransposition activates oncogenic pathways in hepatocellular carcinoma.
Ruchi Shukla, Kyle R Upton, Martin Muñoz-Lopez, Daniel J Gerhardt, Malcolm E Fisher, Thu Nguyen, Paul M Brennan, J Kenneth Baillie, Agnese Collino, Serena Ghisletti,[...]. Cell 2013
251
21

Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man.
H H Kazazian, C Wong, H Youssoufian, A F Scott, D G Phillips, S E Antonarakis. Nature 1988
648
21

5'-Transducing SVA retrotransposon groups spread efficiently throughout the human genome.
Annette Damert, Julija Raiz, Axel V Horn, Johannes Löwer, Hui Wang, Jinchuan Xing, Mark A Batzer, Roswitha Löwer, Gerald G Schumann. Genome Res 2009
81
21


Recombination hotspot in NF1 microdeletion patients.
C López-Correa, M Dorschner, H Brems, C Lázaro, M Clementi, M Upadhyaya, D Dooijes, U Moog, H Kehrer-Sawatzki, J L Rutkowski,[...]. Hum Mol Genet 2001
138
21

Fine mapping of meiotic NAHR-associated crossovers causing large NF1 deletions.
Morten Hillmer, David Wagner, Anna Summerer, Michaela Daiber, Victor-Felix Mautner, Ludwine Messiaen, David N Cooper, Hildegard Kehrer-Sawatzki. Hum Mol Genet 2016
12
66

Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions.
D E Jenne, S Tinschert, H Reimann, W Lasinger, G Thiel, H Hameister, H Kehrer-Sawatzki. Am J Hum Genet 2001
99
21

NF1 microdeletion breakpoints are clustered at flanking repetitive sequences.
M O Dorschner, V P Sybert, M Weaver, B A Pletcher, K Stephens. Hum Mol Genet 2000
147
21

Genomic context of paralogous recombination hotspots mediating recurrent NF1 region microdeletion.
Stephen H Forbes, Michael O Dorschner, Rosalynda Le, Karen Stephens. Genes Chromosomes Cancer 2004
32
21

Reverse transcriptase encoded by a human transposable element.
S L Mathias, A F Scott, H H Kazazian, J D Boeke, A Gabriel. Science 1991
562
18

Genomic deletions created upon LINE-1 retrotransposition.
Nicolas Gilbert, Sheila Lutz-Prigge, John V Moran. Cell 2002
339
18

LINE-1 retrotransposition activity in human genomes.
Christine R Beck, Pamela Collier, Catriona Macfarlane, Maika Malig, Jeffrey M Kidd, Evan E Eichler, Richard M Badge, John V Moran. Cell 2010
367
18

Multiple fates of L1 retrotransposition intermediates in cultured human cells.
Nicolas Gilbert, Sheila Lutz, Tammy A Morrish, John V Moran. Mol Cell Biol 2005
194
18

Human LINE retrotransposons generate processed pseudogenes.
C Esnault, J Maestre, T Heidmann. Nat Genet 2000
574
18

LINE-1 elements in structural variation and disease.
Christine R Beck, José Luis Garcia-Perez, Richard M Badge, John V Moran. Annu Rev Genomics Hum Genet 2011
323
18

Disruption of the APC gene by a retrotransposal insertion of L1 sequence in a colon cancer.
Y Miki, I Nishisho, A Horii, Y Miyoshi, J Utsunomiya, K W Kinzler, B Vogelstein, Y Nakamura. Cancer Res 1992
407
18

SVA elements are nonautonomous retrotransposons that cause disease in humans.
Eric M Ostertag, John L Goodier, Yue Zhang, Haig H Kazazian. Am J Hum Genet 2003
222
18

L1 retrotransposition in human neural progenitor cells.
Nicole G Coufal, José L Garcia-Perez, Grace E Peng, Gene W Yeo, Yangling Mu, Michael T Lovci, Maria Morell, K Sue O'Shea, John V Moran, Fred H Gage. Nature 2009
527
18

Natural mutagenesis of human genomes by endogenous retrotransposons.
Rebecca C Iskow, Michael T McCabe, Ryan E Mills, Spencer Torene, W Stephen Pittard, Andrew F Neuwald, Erwin G Van Meir, Paula M Vertino, Scott E Devine. Cell 2010
396
18

Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition.
Alysson R Muotri, Vi T Chu, Maria C N Marchetto, Wei Deng, John V Moran, Fred H Gage. Nature 2005
603
18

Deletion of entire HLA-A gene accompanied by an insertion of a retrotransposon.
M Takasu, R Hayashi, E Maruya, M Ota, K Imura, K Kougo, C Kobayashi, H Saji, Y Ishikawa, T Asai,[...]. Tissue Antigens 2007
30
23


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.