A citation-based method for searching scientific literature

Feng Zhang, Claudia M B Carvalho, James R Lupski. Trends Genet 2009
Times Cited: 182



Wigard P Kloosterman, Victor Guryev, Mark van Roosmalen, Karen J Duran, Ewart de Bruijn, Saskia C M Bakker, Tom Letteboer, Bernadette van Nesselrooij, Ron Hochstenbach, Martin Poot, Edwin Cuppen. Hum Mol Genet 2011
Times Cited: 204




List of shared articles



Times cited

Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses.
Darine Villela, Patricia C Mazzonetto, Michele P Migliavacca, Eduardo Perrone, Gustavo Guida, Maria Fernanda G Milanezi, Alexander A L Jorge, Lucilene A Ribeiro-Bicudo, Fernando Kok, Francine Campagnari,[...]. Am J Med Genet A 2021
0

A 14q distal chromoanagenesis elucidated by whole genome sequencing.
Flavie Ader, Solveig Heide, Pauline Marzin, Alexandra Afenjar, Flavie Diguet, Sandra Chantot Bastaraud, Pierre-Antoine Rollat-Farnier, Damien Sanlaville, Marie-France Portnoï, Jean-Pierre Siffroi,[...]. Eur J Med Genet 2020
2

Structural variant identification and characterization.
Parithi Balachandran, Christine R Beck. Chromosome Res 2020
4


Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2.
Christine R Beck, Claudia M B Carvalho, Zeynep C Akdemir, Fritz J Sedlazeck, Xiaofei Song, Qingchang Meng, Jianhong Hu, Harsha Doddapaneni, Zechen Chong, Edward S Chen,[...]. Cell 2019
29

Flanking complex copy number variants in the same family formed through unequal crossing-over during meiosis.
Maria Pettersson, Jesper Eisfeldt, Elisabeth Syk Lundberg, Johanna Lundin, Anna Lindstrand. Mutat Res 2018
6

Catastrophic cellular events leading to complex chromosomal rearrangements in the germline.
M Fukami, H Shima, E Suzuki, T Ogata, K Matsubara, T Kamimaki. Clin Genet 2017
25

A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences.
Natalia Trpchevska, Ivanka Dimova, Tatyana Arabadji, Tanya Milachich, Svetlana Angelova, Magdalena Dimitrova, Mariela Hristova-Savova, Petya Andreeva, Tania Timeva, Atanas Shterev. J Assist Reprod Genet 2017
6

A de novo complex chromosome rearrangement associated with multisystematic abnormalities, a case report.
Chan Tian, Dan Li, Ping Liu, Liping Jiao, Xuefeng Gao, Jie Qiao. Mol Cytogenet 2017
2

Error-Prone Repair of DNA Double-Strand Breaks.
Kasey Rodgers, Mitch McVey. J Cell Physiol 2016
168

Complex chromosomal rearrangement involving five chromosomes: deciphering genomic imbalances in an apparently balanced chromosomal translocation.
Kausik Mandal, Meenal Agarwal, Vijay R Boggula, Siddaramappa J Patil, Shubha R Phadke. Clin Dysmorphol 2016
0

Mechanisms for Complex Chromosomal Insertions.
Shen Gu, Przemyslaw Szafranski, Zeynep Coban Akdemir, Bo Yuan, Mitchell L Cooper, Maria A Magriñá, Carlos A Bacino, Seema R Lalani, Amy M Breman, Janice L Smith,[...]. PLoS Genet 2016
29

A decade of structural variants: description, history and methods to detect structural variation.
Geòrgia Escaramís, Elisa Docampo, Raquel Rabionet. Brief Funct Genomics 2015
46

Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies.
Bruno Faulin Gamba, Antônio Richieri-Costa, Silvia Costa, Carla Rosenberg, Lucilene Arilho Ribeiro-Bicudo. Mol Genet Genomics 2015
11

Nine de novo duplications affecting both maternal and paternal chromosomes and an inherited 15q11.2 deletion, in a patient with developmental delay.
Marwan K Tayeh, Tracy Rocco, Todd Ackley, Leslie Ernst, Thomas Glover, Jeffrey W Innis. Clin Case Rep 2015
1

Human Structural Variation: Mechanisms of Chromosome Rearrangements.
Brooke Weckselblatt, M Katharine Rudd. Trends Genet 2015
95

Chromothripsis: A New Mechanism for Rapid Karyotype Evolution.
Mitchell L Leibowitz, Cheng-Zhong Zhang, David Pellman. Annu Rev Genet 2015
102

Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome.
Évelin Aline Zanardo, Flavia Balbo Piazzon, Roberta Lelis Dutra, Alexandre Torchio Dias, Marília Moreira Montenegro, Gil Monteiro Novo-Filho, Thaís Virgínia Moura Machado Costa, Amom Mendes Nascimento, Chong Ae Kim, Leslie Domenici Kulikowski. Mol Genet Genomics 2014
9

Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms.
Ankit Malhotra, Michael Lindberg, Gregory G Faust, Mitchell L Leibowitz, Royden A Clark, Ryan M Layer, Aaron R Quinlan, Ira M Hall. Genome Res 2013
122

Chromothripsis in congenital disorders and cancer: similarities and differences.
Wigard P Kloosterman, Edwin Cuppen. Curr Opin Cell Biol 2013
63

Mechanisms for Structural Variation in the Human Genome.
Benjamin B Currall, C Chiang, Michael E Talkowski, Cynthia C Morton. Curr Genet Med Rep 2013
15

Chromothripsis and beyond: rapid genome evolution from complex chromosomal rearrangements.
Cheng-Zhong Zhang, Mitchell L Leibowitz, David Pellman. Genes Dev 2013
156