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



Claudia M B Carvalho, James R Lupski. Nat Rev Genet 2016
Times Cited: 268




List of shared articles



Times cited

Fatal perinatal mitochondrial cardiac failure caused by recurrent de novo duplications in the ATAD3 locus.
Ann E Frazier, Alison G Compton, Yoshihito Kishita, Daniella H Hock, AnneMarie E Welch, Sumudu S C Amarasekera, Rocio Rius, Luke E Formosa, Atsuko Imai-Okazaki, David Francis,[...]. Med (N Y) 2021
4


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


Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes.
Tamar Harel, Wan Hee Yoon, Caterina Garone, Shen Gu, Zeynep Coban-Akdemir, Mohammad K Eldomery, Jennifer E Posey, Shalini N Jhangiani, Jill A Rosenfeld, Megan T Cho,[...]. Am J Hum Genet 2016
83

Major influence of repetitive elements on disease-associated copy number variants (CNVs).
Ana R Cardoso, Manuela Oliveira, Antonio Amorim, Luisa Azevedo. Hum Genomics 2016
10

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


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
32

Multi-invasions Are Recombination Byproducts that Induce Chromosomal Rearrangements.
Aurèle Piazza, William Douglass Wright, Wolf-Dietrich Heyer. Cell 2017
50

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