A citation-based method for searching scientific literature

Piotr Dittwald, Tomasz Gambin, Przemyslaw Szafranski, Jian Li, Stephen Amato, Michael Y Divon, Lisa Ximena Rodríguez Rojas, Lindsay E Elton, Daryl A Scott, Christian P Schaaf, Wilfredo Torres-Martinez, Abby K Stevens, Jill A Rosenfeld, Satish Agadi, David Francis, Sung-Hae L Kang, Amy Breman, Seema R Lalani, Carlos A Bacino, Weimin Bi, Aleksandar Milosavljevic, Arthur L Beaudet, Ankita Patel, Chad A Shaw, James R Lupski, Anna Gambin, Sau Wai Cheung, Pawel Stankiewicz. Genome Res 2013
Times Cited: 78



Andrew J Sharp, Devin P Locke, Sean D McGrath, Ze Cheng, Jeffrey A Bailey, Rhea U Vallente, Lisa M Pertz, Royden A Clark, Stuart Schwartz, Rick Segraves, Vanessa V Oseroff, Donna G Albertson, Daniel Pinkel, Evan E Eichler. Am J Hum Genet 2005
Times Cited: 662




List of shared articles



Times cited

An exploratory study of predisposing genetic factors for DiGeorge/velocardiofacial syndrome.
Laia Vergés, Francesca Vidal, Esther Geán, Alexandra Alemany-Schmidt, Maria Oliver-Bonet, Joan Blanco. Sci Rep 2017
5

Mechanisms underlying structural variant formation in genomic disorders.
Claudia M B Carvalho, James R Lupski. Nat Rev Genet 2016
274


Genome architecture and its roles in human copy number variation.
Lu Chen, Weichen Zhou, Ling Zhang, Feng Zhang. Genomics Inform 2014
13


Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delays.
Andrey Shuvarikov, Ian M Campbell, Piotr Dittwald, Nicholas J Neill, Martin G Bialer, Christine Moore, Patricia G Wheeler, Stephanie E Wallace, Mark C Hannibal, Michael F Murray,[...]. Hum Mutat 2013
29

Predicting human genes susceptible to genomic instability associated with Alu/Alu-mediated rearrangements.
Xiaofei Song, Christine R Beck, Renqian Du, Ian M Campbell, Zeynep Coban-Akdemir, Shen Gu, Amy M Breman, Pawel Stankiewicz, Grzegorz Ira, Chad A Shaw,[...]. Genome Res 2018
34

Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination.
Ian M Campbell, Tomasz Gambin, Piotr Dittwald, Christine R Beck, Andrey Shuvarikov, Patricia Hixson, Ankita Patel, Anna Gambin, Chad A Shaw, Jill A Rosenfeld,[...]. BMC Biol 2014
41

Consideration of the haplotype diversity at nonallelic homologous recombination hotspots improves the precision of rearrangement breakpoint identification.
Morten Hillmer, Anna Summerer, Victor-Felix Mautner, Josef Högel, David N Cooper, Hildegard Kehrer-Sawatzki. Hum Mutat 2017
7