A citation-based method for searching scientific literature

Philip M Boone, Bo Yuan, Ian M Campbell, Jennifer C Scull, Marjorie A Withers, Brett C Baggett, Christine R Beck, Christine J Shaw, Pawel Stankiewicz, Paolo Moretti, Wendy E Goodwin, Nichole Hein, John K Fink, Moon-Woo Seong, Soo Hyun Seo, Sung Sup Park, Izabela D Karbassi, Sat Dev Batish, Andrés Ordóñez-Ugalde, Beatriz Quintáns, María-Jesús Sobrido, Susanne Stemmler, James R Lupski. Am J Hum Genet 2014
Times Cited: 60



Pengfei Liu, Melanie Lacaria, Feng Zhang, Marjorie Withers, P J Hastings, James R Lupski. Am J Hum Genet 2011
Times Cited: 74




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

Complex genomic rearrangements at the PLP1 locus include triplication and quadruplication.
Christine R Beck, Claudia M B Carvalho, Linda Banser, Tomasz Gambin, Danielle Stubbolo, Bo Yuan, Karen Sperle, Suzanne M McCahan, Marco Henneke, Pavel Seeman,[...]. PLoS Genet 2015
41

Mechanisms underlying structural variant formation in genomic disorders.
Claudia M B Carvalho, James R Lupski. Nat Rev Genet 2016
275

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

PacBio-LITS: a large-insert targeted sequencing method for characterization of human disease-associated chromosomal structural variations.
Min Wang, Christine R Beck, Adam C English, Qingchang Meng, Christian Buhay, Yi Han, Harsha V Doddapaneni, Fuli Yu, Eric Boerwinkle, James R Lupski,[...]. BMC Genomics 2015
39


Decoding NF1 Intragenic Copy-Number Variations.
Meng-Chang Hsiao, Arkadiusz Piotrowski, Tom Callens, Chuanhua Fu, Katharina Wimmer, Kathleen B M Claes, Ludwine Messiaen. Am J Hum Genet 2015
14

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

The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy.
Davut Pehlivan, Christine R Beck, Yuji Okamoto, Tamar Harel, Zeynep H C Akdemir, Shalini N Jhangiani, Marjorie A Withers, Meryem Tuba Goksungur, Claudia M B Carvalho, Dirk Czesnik,[...]. Genet Med 2016
13