A citation-based method for searching scientific literature

Reza Asadollahi, Beatrice Oneda, Pascal Joset, Silvia Azzarello-Burri, Deborah Bartholdi, Katharina Steindl, Marie Vincent, Joana Cobilanschi, Heinrich Sticht, Rosa Baldinger, Regina Reissmann, Irene Sudholt, Christian T Thiel, Arif B Ekici, AndrĂ© Reis, Emilia K Bijlsma, Joris Andrieux, Anne Dieux, David FitzPatrick, Susanne Ritter, Alessandra Baumer, Beatrice Latal, Barbara Plecko, Oskar G Jenni, Anita Rauch. J Med Genet 2014
Times Cited: 57



Ni Huang, Insuk Lee, Edward M Marcotte, Matthew E Hurles. PLoS Genet 2010
Times Cited: 414




List of shared articles



Times cited

CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens.
Binbin Wang, Taoyun Ji, Xueya Zhou, Jing Wang, Xi Wang, Jingmin Wang, Dingliang Zhu, Xuejun Zhang, Pak Chung Sham, Xuegong Zhang,[...]. Sci Rep 2016
9

5p deletions: Current knowledge and future directions.
Joanne M Nguyen, Krista J Qualmann, Rebecca Okashah, AmySue Reilly, Mikhail F Alexeyev, Dennis J Campbell. Am J Med Genet C Semin Med Genet 2015
38

Integrated small copy number variations and epigenome maps of disorders of sex development.
Ina E Amarillo, Isabelle Nievera, Andrew Hagan, Vishwa Huchthagowder, Jennifer Heeley, Abby Hollander, Joel Koenig, Paul Austin, Ting Wang. Hum Genome Var 2016
9

Understanding Language from a Genomic Perspective.
Sarah A Graham, Simon E Fisher. Annu Rev Genet 2015
47

Clinical relevance of small copy-number variants in chromosomal microarray clinical testing.
Dana Hollenbeck, Crescenda L Williams, Kathryn Drazba, Maria Descartes, Bruce R Korf, S Lane Rutledge, Edward J Lose, Nathaniel H Robin, Andrew J Carroll, Fady M Mikhail. Genet Med 2017
12