A citation-based method for searching scientific literature

Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
Times Cited: 1148



Dalila Pinto, Katayoon Darvishi, Xinghua Shi, Diana Rajan, Diane Rigler, Tom Fitzgerald, Anath C Lionel, Bhooma Thiruvahindrapuram, Jeffrey R Macdonald, Ryan Mills, Aparna Prasad, Kristin Noonan, Susan Gribble, Elena Prigmore, Patricia K Donahoe, Richard S Smith, Ji Hyeon Park, Matthew E Hurles, Nigel P Carter, Charles Lee, Stephen W Scherer, Lars Feuk. Nat Biotechnol 2011
Times Cited: 289




List of shared articles



Times cited

DeepCNV: a deep learning approach for authenticating copy number variations.
Joseph T Glessner, Xiurui Hou, Cheng Zhong, Jie Zhang, Munir Khan, Fabian Brand, Peter Krawitz, Patrick M A Sleiman, Hakon Hakonarson, Zhi Wei. Brief Bioinform 2021
0

A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa.
Lilia Romdhane, Nessrine Mezzi, Hamza Dallali, Olfa Messaoud, Jingxuan Shan, Khalid A Fakhro, Rym Kefi, Lotfi Chouchane, Sonia Abdelhak. NPJ Genom Med 2021
0

Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.
Ida E Sønderby, Christopher R K Ching, Sophia I Thomopoulos, Dennis van der Meer, Daqiang Sun, Julio E Villalon-Reina, Ingrid Agartz, Katrin Amunts, Celso Arango, Nicola J Armstrong,[...]. Hum Brain Mapp 2021
0

Genome-wide copy number variations in a large cohort of bantu African children.
Feyza Yilmaz, Megan Null, David Astling, Hung-Chun Yu, Joanne Cole, Stephanie A Santorico, Benedikt Hallgrimsson, Mange Manyama, Richard A Spritz, Audrey E Hendricks,[...]. BMC Med Genomics 2021
0

SeeCiTe: a method to assess CNV calls from SNP arrays using trio data.
Ksenia Lavrichenko, Øyvind Helgeland, Pål R Njølstad, Inge Jonassen, Stefan Johansson. Bioinformatics 2021
0

Copy number variation-based gene set analysis reveals cytokine signalling pathways associated with psychiatric comorbidity in patients with inflammatory bowel disease.
Svetlana Frenkel, Charles N Bernstein, Michael Sargent, Wenxin Jiang, Qin Kuang, Wei Xu, Pingzhao Hu. Genomics 2020
3

Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN Mutations.
Lamis Yehia, Marilyn Seyfi, Lisa-Marie Niestroj, Roshan Padmanabhan, Ying Ni, Thomas W Frazier, Dennis Lal, Charis Eng. JAMA Netw Open 2020
2


CNV Radar: an improved method for somatic copy number alteration characterization in oncology.
David Soong, Jeran Stratford, Herve Avet-Loiseau, Nizar Bahlis, Faith Davies, Angela Dispenzieri, A Kate Sasser, Jordan M Schecter, Ming Qi, Chad Brown,[...]. BMC Bioinformatics 2020
2