A citation-based method for searching scientific literature

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, Carlos A Bacino, Luis Daniel Campos-Acevedo, Mauricio R Delgado, Debra Freedenberg, Adolfo Garnica, Theresa A Grebe, Dolores Hernández-Almaguer, LaDonna Immken, Seema R Lalani, Scott D McLean, Hope Northrup, Fernando Scaglia, Lane Strathearn, Pamela Trapane, Sung-Hae L Kang, Ankita Patel, Sau Wai Cheung, P J Hastings, Paweł Stankiewicz, James R Lupski, Weimin Bi. Cell 2011
Times Cited: 278



Ryan L Collins, Harrison Brand, Claire E Redin, Carrie Hanscom, Caroline Antolik, Matthew R Stone, Joseph T Glessner, Tamara Mason, Giulia Pregno, Naghmeh Dorrani, Giorgia Mandrile, Daniela Giachino, Danielle Perrin, Cole Walsh, Michelle Cipicchio, Maura Costello, Alexei Stortchevoi, Joon-Yong An, Benjamin B Currall, Catarina M Seabra, Ashok Ragavendran, Lauren Margolin, Julian A Martinez-Agosto, Diane Lucente, Brynn Levy, Stephan J Sanders, Ronald J Wapner, Fabiola Quintero-Rivera, Wigard Kloosterman, Michael E Talkowski. Genome Biol 2017
Times Cited: 84




List of shared articles



Times cited

Deciphering the complexity of simple chromosomal insertions by genome sequencing.
Zirui Dong, Matthew Hoi Kin Chau, Yanyan Zhang, Peng Dai, Xiaofan Zhu, Tak Yeung Leung, Xiangdong Kong, Yvonne K Kwok, Paweł Stankiewicz, Sau Wai Cheung,[...]. Hum Genet 2021
2

Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier.
Jesper Eisfeldt, Maria Pettersson, Anna Petri, Daniel Nilsson, Lars Feuk, Anna Lindstrand. Hum Genet 2021
0

Chromoanagenesis, the mechanisms of a genomic chaos.
F Pellestor, J B Gaillard, A Schneider, J Puechberty, V Gatinois. Semin Cell Dev Biol 2021
3

Chromothripsis-Explosion in Genetic Science.
Mariia Shorokhova, Nikolay Nikolsky, Tatiana Grinchuk. Cells 2021
1

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
1


Chromoanasynthesis as a cause of Jacobsen syndrome.
Sarah Anzick, Audrey Thurm, Sandra Burkett, Daniel Velez, Elena Cho, Colby Chlebowski, Kimmo Virtaneva, Daniel Bruno, Clare B Martin, David M Lang,[...]. Am J Med Genet A 2020
2

Prenatal Diagnosis of a De Novo Partial Trisomy 6q and Partial Monosomy 18p Associated with Cephalocele: A Case Report.
A Karaman, B Karaman, A Çetinkaya, S Karaman, O Demirci. Balkan J Med Genet 2020
0


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
25

The Iceberg under Water: Unexplored Complexity of Chromoanagenesis in Congenital Disorders.
Cinthya J Zepeda-Mendoza, Cynthia C Morton. Am J Hum Genet 2019
16

On the Complexity of Mechanisms and Consequences of Chromothripsis: An Update.
Alla S Koltsova, Anna A Pendina, Olga A Efimova, Olga G Chiryaeva, Tatyana V Kuznetzova, Vladislav S Baranov. Front Genet 2019
25

Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cells.
Atsushi Hattori, Kohji Okamura, Yumiko Terada, Rika Tanaka, Yuko Katoh-Fukui, Yoichi Matsubara, Keiko Matsubara, Masayo Kagami, Reiko Horikawa, Maki Fukami. BMC Med Genomics 2019
5

Failure of NIPT to detect constitutional chromoanasynthesis involving chromosome 21 in a case of fetal hydrops-A case report.
Kathleen Bone, Melissa Jean MacPherson, Judy Chernos, Julie Lauzon. Clin Case Rep 2019
1


Identifying simultaneous rearrangements in cancer genomes.
Layla Oesper, Simone Dantas, Benjamin J Raphael. Bioinformatics 2018
1

Very short DNA segments can be detected and handled by the repair machinery during germline chromothriptic chromosome reassembly.
Zuzana Slamova, Lusine Nazaryan-Petersen, Mana M Mehrjouy, Jana Drabova, Miroslava Hancarova, Tatana Marikova, Drahuse Novotna, Marketa Vlckova, Zdenka Vlckova, Mads Bak,[...]. Hum Mutat 2018
15

The Genomic Characteristics and Origin of Chromothripsis.
Alessio Marcozzi, Franck Pellestor, Wigard P Kloosterman. Methods Mol Biol 2018
10

Mutational game changer: Chromothripsis and its emerging relevance to cancer.
Monique Nicole Helena Luijten, Jeannie Xue Ting Lee, Karen Carmelina Crasta. Mutat Res Rev Mutat Res 2018
31

Stable transmission of an unbalanced chromosome 21 derived from chromoanasynthesis in a patient with a SYNGAP1 likely pathogenic variant.
Peter J B Sabatini, Resham Ejaz, Dimitri J Stavropoulos, Roberto Mendoza-Londono, Ann M Joseph-George. Mol Cytogenet 2018
5


Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization.
Lusine Nazaryan-Petersen, Jesper Eisfeldt, Maria Pettersson, Johanna Lundin, Daniel Nilsson, Josephine Wincent, Agne Lieden, Lovisa Lovmar, Jesper Ottosson, Jelena Gacic,[...]. PLoS Genet 2018
19

Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing.
Alba Sanchis-Juan, Jonathan Stephens, Courtney E French, Nicholas Gleadall, Karyn Mégy, Christopher Penkett, Olga Shamardina, Kathleen Stirrups, Isabelle Delon, Eleanor Dewhurst,[...]. Genome Med 2018
39