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: 1151



Stefano Colella, Christopher Yau, Jennifer M Taylor, Ghazala Mirza, Helen Butler, Penny Clouston, Anne S Bassett, Anneke Seller, Christopher C Holmes, Jiannis Ragoussis. Nucleic Acids Res 2007
Times Cited: 407




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

Alterations in nicotinic receptor alpha5 subunit gene differentially impact early and later stages of cocaine addiction: a translational study in transgenic rats and patients.
Benoît Forget, Romain Icick, Jonathan Robert, Caroline Correia, Marie S Prevost, Marc Gielen, Pierre-Jean Corringer, Frank Bellivier, Florence Vorspan, Morgane Besson,[...]. Prog Neurobiol 2021
3

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

Functional characterization of Copy Number Variations regions in Djallonké sheep.
Félix Goyache, Iván Fernández, Arnaud Stephan R Tapsoba, Amadou Traoré, Nuria A Menéndez-Arias, Isabel Álvarez. J Anim Breed Genet 2021
0

Culture Variabilities of Human iPSC-Derived Cerebral Organoids Are a Major Issue for the Modelling of Phenotypes Observed in Alzheimer's Disease.
Damián Hernández, Louise A Rooney, Maciej Daniszewski, Lerna Gulluyan, Helena H Liang, Anthony L Cook, Alex W Hewitt, Alice Pébay. Stem Cell Rev Rep 2021
2

The copy number variation and stroke (CaNVAS) risk and outcome study.
John W Cole, Taiwo Adigun, Rufus Akinyemi, Onoja Matthew Akpa, Steven Bell, Bowang Chen, Jordi Jimenez Conde, Uxue Lazcano Dobao, Israel Fernandez, Myriam Fornage,[...]. PLoS One 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

Single cell eQTL analysis identifies cell type-specific genetic control of gene expression in fibroblasts and reprogrammed induced pluripotent stem cells.
Drew Neavin, Quan Nguyen, Maciej S Daniszewski, Helena H Liang, Han Sheng Chiu, Yong Kiat Wee, Anne Senabouth, Samuel W Lukowski, Duncan E Crombie, Grace E Lidgerwood,[...]. Genome Biol 2021
2

Genome-wide CNV investigation suggests a role for cadherin, Wnt, and p53 pathways in primary open-angle glaucoma.
Valeria Lo Faro, Jacoline B Ten Brink, Harold Snieder, Nomdo M Jansonius, Arthur A Bergen. BMC Genomics 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


Critical evaluation of copy number variant calling methods using DNA methylation.
Varun Kilaru, Anna K Knight, Seyma Katrinli, Dawayland Cobb, Adriana Lori, Charles F Gillespie, Adam X Maihofer, Caroline M Nievergelt, Anne L Dunlop, Karen N Conneely,[...]. Genet Epidemiol 2020
0

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.
Yun Rose Li, Joseph T Glessner, Bradley P Coe, Jin Li, Maede Mohebnasab, Xiao Chang, John Connolly, Charlly Kao, Zhi Wei, Jonathan Bradfield,[...]. Nat Commun 2020
9

Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates.
Jae Hoon Sul, Susan K Service, Alden Y Huang, Vasily Ramensky, Sun-Goo Hwang, Terri M Teshiba, YoungJun Park, Anil P S Ori, Zhongyang Zhang, Niamh Mullins,[...]. Transl Psychiatry 2020
5


Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy.
Hayley S Mountford, Dorothy V M Bishop, Paul A Thompson, Nuala H Simpson, Dianne F Newbury. Am J Med Genet C Semin Med Genet 2020
2

Recurrent Rare Copy Number Variants Increase Risk for Esotropia.
Mary C Whitman, Silvio Alessandro Di Gioia, Wai-Man Chan, Alon Gelber, Brandon M Pratt, Jessica L Bell, Thomas E Collins, James A Knowles, Christopher Armoskus, Michele Pato,[...]. Invest Ophthalmol Vis Sci 2020
0

Estimating the effects of copy-number variants on intelligence using hierarchical Bayesian models.
Lai Jiang, Guillaume Huguet, Catherine Schramm, Antonio Ciampi, Antoine Main, Claudine Passo, Martineau Jean-Louis, Maude Auger, Gunter Schumann, David Porteous,[...]. Genet Epidemiol 2020
1

Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes.
Peter A Perrino, Lidiya Talbot, Rose Kirkland, Amanda Hill, Amanda R Rendall, Hayley S Mountford, Jenny Taylor, Alexzandrea N Buscarello, Nayana Lahiri, Anand Saggar,[...]. Commun Biol 2020
4