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: 77



Paweł Stankiewicz, James R Lupski. Annu Rev Med 2010
Times Cited: 670




List of shared articles



Times cited

Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith-Magenis syndrome with evident peripheral neuropathy.
Bo Yuan, Juanita Neira, Shen Gu, Tamar Harel, Pengfei Liu, Ignacio Briceño, Sarah H Elsea, Alberto Gómez, Lorraine Potocki, James R Lupski. Hum Genet 2016
2

Characterizing polymorphic inversions in human genomes by single-cell sequencing.
Ashley D Sanders, Mark Hills, David Porubský, Victor Guryev, Ester Falconer, Peter M Lansdorp. Genome Res 2016
37


Genome-wide analyses of LINE-LINE-mediated nonallelic homologous recombination.
Michał Startek, Przemyslaw Szafranski, Tomasz Gambin, Ian M Campbell, Patricia Hixson, Chad A Shaw, Paweł Stankiewicz, Anna Gambin. Nucleic Acids Res 2015
45

Human Structural Variation: Mechanisms of Chromosome Rearrangements.
Brooke Weckselblatt, M Katharine Rudd. Trends Genet 2015
91

Genome architecture and its roles in human copy number variation.
Lu Chen, Weichen Zhou, Ling Zhang, Feng Zhang. Genomics Inform 2014
12


Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders.
Trenell J Mosley, H Richard Johnston, David J Cutler, Michael E Zwick, Jennifer G Mulle. BMC Med Genomics 2021
0

Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes.
Kacie N Riley, Lisa M Catalano, John A Bernat, Stacie D Adams, Donna M Martin, Seema R Lalani, Ankita Patel, Rachel D Burnside, Jeffrey W Innis, M Katharine Rudd. Am J Med Genet A 2015
23

Approaches for identifying germ cell mutagens: Report of the 2013 IWGT workshop on germ cell assays(☆).
Carole L Yauk, Marilyn J Aardema, Jan van Benthem, Jack B Bishop, Kerry L Dearfield, David M DeMarini, Yuri E Dubrova, Masamitsu Honma, James R Lupski, Francesco Marchetti,[...]. Mutat Res Genet Toxicol Environ Mutagen 2015
44

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

Mechanisms of germ line genome instability.
Seoyoung Kim, Shaun E Peterson, Maria Jasin, Scott Keeney. Semin Cell Dev Biol 2016
25

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
40

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
5

Mechanisms for the Generation of Two Quadruplications Associated with Split-Hand Malformation.
Shen Gu, Jennifer E Posey, Bo Yuan, Claudia M B Carvalho, H M Luk, Kelly Erikson, Ivan F M Lo, Gordon K C Leung, Curtis R Pickering, Brian H Y Chung,[...]. Hum Mutat 2016
12