A citation-based method for searching scientific literature

Feng Zhang, Pavel Seeman, Pengfei Liu, Marian A J Weterman, Claudia Gonzaga-Jauregui, Charles F Towne, Sat Dev Batish, Els De Vriendt, Peter De Jonghe, Bernd Rautenstrauss, Klaus-Henning Krause, Mehrdad Khajavi, Jan Posadka, Antoon Vandenberghe, Francesc Palau, Lionel Van Maldergem, Frank Baas, Vincent Timmerman, James R Lupski. Am J Hum Genet 2010
Times Cited: 90







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



Times Cited
  Times     Co-cited
Similarity


The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans.
Feng Zhang, Mehrdad Khajavi, Anne M Connolly, Charles F Towne, Sat Dev Batish, James R Lupski. Nat Genet 2009
298
40

DNA duplication associated with Charcot-Marie-Tooth disease type 1A.
J R Lupski, R M de Oca-Luna, S Slaugenhaupt, L Pentao, V Guzzetta, B J Trask, O Saucedo-Cardenas, D F Barker, J M Killian, C A Garcia,[...]. Cell 1991
37



Copy number variation upstream of PMP22 in Charcot-Marie-Tooth disease.
Marian A J Weterman, Fred van Ruissen, Marit de Wissel, Lou Bordewijk, Johnny P A Samijn, W Ludo van der Pol, Farid Meggouh, Frank Baas. Eur J Hum Genet 2010
36
61

DNA deletion associated with hereditary neuropathy with liability to pressure palsies.
P F Chance, M K Alderson, K A Leppig, M W Lensch, N Matsunami, B Smith, P D Swanson, S J Odelberg, C M Disteche, T D Bird. Cell 1993
675
23

Mechanisms of change in gene copy number.
P J Hastings, James R Lupski, Susan M Rosenberg, Grzegorz Ira. Nat Rev Genet 2009
723
21

Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching.
Claudia M B Carvalho, Feng Zhang, Pengfei Liu, Ankita Patel, Trilochan Sahoo, Carlos A Bacino, Chad Shaw, Sandra Peacock, Amber Pursley, Y Jane Tavyev,[...]. Hum Mol Genet 2009
141
21

Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
Lisenka E L M Vissers, Samarth S Bhatt, Irene M Janssen, Zhilian Xia, Seema R Lalani, Rolph Pfundt, Katarzyna Derwinska, Bert B A de Vries, Christian Gilissen, Alexander Hoischen,[...]. Hum Mol Genet 2009
119
20


Mutation spectrum revealed by breakpoint sequencing of human germline CNVs.
Donald F Conrad, Christine Bird, Ben Blackburne, Sarah Lindsay, Lira Mamanova, Charles Lee, Daniel J Turner, Matthew E Hurles. Nat Genet 2010
175
17

Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome.
Claudia M B Carvalho, Melissa B Ramocki, Davut Pehlivan, Luis M Franco, Claudia Gonzaga-Jauregui, Ping Fang, Alanna McCall, Eniko Karman Pivnick, Stacy Hines-Dowell, Laurie H Seaver,[...]. Nat Genet 2011
126
17

Mechanisms for human genomic rearrangements.
Wenli Gu, Feng Zhang, James R Lupski. Pathogenetics 2008
375
16

Genome architecture, rearrangements and genomic disorders.
Paweł Stankiewicz, James R Lupski. Trends Genet 2002
627
16

Complex human chromosomal and genomic rearrangements.
Feng Zhang, Claudia M B Carvalho, James R Lupski. Trends Genet 2009
182
14

Structural variation in the human genome and its role in disease.
Paweł Stankiewicz, James R Lupski. Annu Rev Med 2010
675
14

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A.
P I Patel, B B Roa, A A Welcher, R Schoener-Scott, B J Trask, L Pentao, G J Snipes, C A Garcia, U Francke, E M Shooter,[...]. Nat Genet 1992
480
14

Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
13

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group.
P Raeymaekers, V Timmerman, E Nelis, P De Jonghe, J E Hoogendijk, F Baas, D F Barker, J J Martin, M De Visser, P A Bolhuis. Neuromuscul Disord 1991
426
13

Origins and functional impact of copy number variation in the human genome.
Donald F Conrad, Dalila Pinto, Richard Redon, Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T Daniel Andrews, Chris Barnes, Peter Campbell,[...]. Nature 2010
12

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders.
Daniel J Turner, Marcos Miretti, Diana Rajan, Heike Fiegler, Nigel P Carter, Martyn L Blayney, Stephan Beck, Matthew E Hurles. Nat Genet 2008
214
12

Copy number variation in human health, disease, and evolution.
Feng Zhang, Wenli Gu, Matthew E Hurles, James R Lupski. Annu Rev Genomics Hum Genet 2009
697
12

Mapping copy number variation by population-scale genome sequencing.
Ryan E Mills, Klaudia Walter, Chip Stewart, Robert E Handsaker, Ken Chen, Can Alkan, Alexej Abyzov, Seungtai Chris Yoon, Kai Ye, R Keira Cheetham,[...]. Nature 2011
707
12

Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease.
Jia Huang, Xingyao Wu, Gladys Montenegro, Justin Price, Gaofeng Wang, Jeffery M Vance, Michael E Shy, Stephan Züchner. J Neurol 2010
20
50

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
11

Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease.
Edith Passage, Jean Chrétien Norreel, Pauline Noack-Fraissignes, Véronique Sanguedolce, Josette Pizant, Xavier Thirion, Andrée Robaglia-Schlupp, Jean François Pellissier, Michel Fontés. Nat Med 2004
237
11

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication.
V Timmerman, E Nelis, W Van Hul, B W Nieuwenhuijsen, K L Chen, S Wang, K Ben Othman, B Cullen, R J Leach, C O Hanemann. Nat Genet 1992
381
11

Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements.
Pengfei Liu, Ayelet Erez, Sandesh C Sreenath Nagamani, Shweta U Dhar, Katarzyna E Kołodziejska, Avinash V Dharmadhikari, M Lance Cooper, Joanna Wiszniewska, Feng Zhang, Marjorie A Withers,[...]. Cell 2011
282
11

Regulation of the PMP22 gene through an intronic enhancer.
Erin A Jones, Camila Lopez-Anido, Rajini Srinivasan, Courtney Krueger, Li-Wei Chang, Rakesh Nagarajan, John Svaren. J Neurosci 2011
45
22

Genomic disorders ten years on.
James R Lupski. Genome Med 2009
108
10

Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS.
Feng Zhang, Lorraine Potocki, Jacinda B Sampson, Pengfei Liu, Amarilis Sanchez-Valle, Patricia Robbins-Furman, Alicia Delicado Navarro, Patricia G Wheeler, J Edward Spence, Campbell K Brasington,[...]. Am J Hum Genet 2010
66
13

Large-scale copy number polymorphism in the human genome.
Jonathan Sebat, B Lakshmi, Jennifer Troge, Joan Alexander, Janet Young, Pär Lundin, Susanne Månér, Hillary Massa, Megan Walker, Maoyen Chi,[...]. Science 2004
10

Complex gene rearrangements caused by serial replication slippage.
Jian-Min Chen, Nadia Chuzhanova, Peter D Stenson, Claude Férec, David N Cooper. Hum Mutat 2005
77
11


A human genome structural variation sequencing resource reveals insights into mutational mechanisms.
Jeffrey M Kidd, Tina Graves, Tera L Newman, Robert Fulton, Hillary S Hayden, Maika Malig, Joelle Kallicki, Rajinder Kaul, Richard K Wilson, Evan E Eichler. Cell 2010
189
10

Massive genomic rearrangement acquired in a single catastrophic event during cancer development.
Philip J Stephens, Chris D Greenman, Beiyuan Fu, Fengtang Yang, Graham R Bignell, Laura J Mudie, Erin D Pleasance, King Wai Lau, David Beare, Lucy A Stebbings,[...]. Cell 2011
10

Increased LIS1 expression affects human and mouse brain development.
Weimin Bi, Tamar Sapir, Oleg A Shchelochkov, Feng Zhang, Marjorie A Withers, Jill V Hunter, Talia Levy, Vera Shinder, Daniel A Peiffer, Kevin L Gunderson,[...]. Nat Genet 2009
169
10

Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A).
Michael W Sereda, Gerd Meyer zu Hörste, Ueli Suter, Naureen Uzma, Klaus-Armin Nave. Nat Med 2003
203
10

Charcot-Marie-Tooth disease subtypes and genetic testing strategies.
Anita S D Saporta, Stephanie L Sottile, Lindsey J Miller, Shawna M E Feely, Carly E Siskind, Michael E Shy. Ann Neurol 2011
312
10

The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles.
Philip M Boone, Bo Yuan, Ian M Campbell, Jennifer C Scull, Marjorie A Withers, Brett C Baggett, Christine R Beck, Christine J Shaw, Pawel Stankiewicz, Paolo Moretti,[...]. Am J Hum Genet 2014
60
15

Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases.
N Birouk, R Gouider, E Le Guern, M Gugenheim, S Tardieu, T Maisonobe, N Le Forestier, Y Agid, A Brice, P Bouche. Brain 1997
201
8


Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and females.
Ken Inoue, Hitoshi Osaka, Virginia C Thurston, Joe T R Clarke, Akira Yoneyama, Lisa Rosenbarker, Thomas D Bird, M E Hodes, Lisa G Shaffer, James R Lupski. Am J Hum Genet 2002
121
8

On the mechanism of gene amplification induced under stress in Escherichia coli.
Andrew Slack, P C Thornton, Daniel B Magner, Susan M Rosenberg, P J Hastings. PLoS Genet 2006
121
8

Mapping and sequencing of structural variation from eight human genomes.
Jeffrey M Kidd, Gregory M Cooper, William F Donahue, Hillary S Hayden, Nick Sampas, Tina Graves, Nancy Hansen, Brian Teague, Can Alkan, Francesca Antonacci,[...]. Nature 2008
768
8


Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13).
G J Snipes, U Suter, A A Welcher, E M Shooter. J Cell Biol 1992
336
8

A transgenic rat model of Charcot-Marie-Tooth disease.
M Sereda, I Griffiths, A Pühlhofer, H Stewart, M J Rossner, F Zimmerman, J P Magyar, A Schneider, E Hund, H M Meinck,[...]. Neuron 1996
281
8

Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study.
E Nelis, C Van Broeckhoven, P De Jonghe, A Löfgren, A Vandenberghe, P Latour, E Le Guern, A Brice, M L Mostacciuolo, F Schiavon,[...]. Eur J Hum Genet 1996
353
8

Distal enhancers upstream of the Charcot-Marie-Tooth type 1A disease gene PMP22.
Erin A Jones, Megan H Brewer, Rajini Srinivasan, Courtney Krueger, Guannan Sun, Kira N Charney, Sunduz Keles, Anthony Antonellis, John Svaren. Hum Mol Genet 2012
25
32


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.