A citation-based method for searching scientific literature

Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig, Hoda Abdel-Hamid, Patricia Bader, Elizabeth McCracken, Dmitriy Niyazov, Kathleen Leppig, Heidi Thiese, Marybeth Hummel, Nora Alexander, Jerome Gorski, Jennifer Kussmann, Vandana Shashi, Krys Johnson, Catherine Rehder, Blake C Ballif, Lisa G Shaffer, Evan E Eichler. Nat Genet 2011
Times Cited: 778



Feng Zhang, Wenli Gu, Matthew E Hurles, James R Lupski. Annu Rev Genomics Hum Genet 2009
Times Cited: 667




List of shared articles



Times cited

Clinical Utility of Next-Generation Sequencing for Developmental Disorders in the Rehabilitation Department: Experiences from a Single Chinese Center.
Yun Liu, Xiaomei Liu, Dongdong Qin, Yiming Zhao, Xuanlan Cao, Xiaoli Deng, Yu Cheng, Fuping Liu, Fang Yang, Tiesong Zhang,[...]. J Mol Neurosci 2021
0

Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents.
Dinka Smajlagić, Ksenia Lavrichenko, Siren Berland, Øyvind Helgeland, Gun Peggy Knudsen, Marc Vaudel, Jan Haavik, Per Morten Knappskog, Pål Rasmus Njølstad, Gunnar Houge,[...]. Eur J Hum Genet 2021
2

Usefulness of copy number variant detection following monogenic disease exclusion in prenatal diagnosis.
Panlai Shi, Yanjie Xia, Qianqian Li, Xiangdong Kong. J Obstet Gynaecol Res 2021
0


Drosophila models of pathogenic copy-number variant genes show global and non-neuronal defects during development.
Tanzeen Yusuff, Matthew Jensen, Sneha Yennawar, Lucilla Pizzo, Siddharth Karthikeyan, Dagny J Gould, Avik Sarker, Erika Gedvilaite, Yurika Matsui, Janani Iyer,[...]. PLoS Genet 2020
2

Identification of copy number variation and population analysis of the sacred lotus (Nelumbo nucifera).
Qing Zhang, Xueting Zhang, Jing Liu, Chaoyi Mao, Sha Chen, Yujun Zhang, Liang Leng. Biosci Biotechnol Biochem 2020
0

7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient with Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability.
Francesco Paduano, Emma Colao, Sara Loddo, Valeria Orlando, Francesco Trapasso, Antonio Novelli, Nicola Perrotti, Rodolfo Iuliano. Genes (Basel) 2020
0