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: 1141



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: 406




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
1

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
1

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
6

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
1

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
0

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
2

Genome-wide copy number variation-, validation- and screening study implicates a new copy number polymorphism associated with suicide attempts in major depressive disorder.
Shitao Rao, Mai Shi, Xinyu Han, Marco Ho Bun Lam, Wai Tong Chien, Keying Zhou, Guangming Liu, Yun Kwok Wing, Hon-Cheong So, Mary Miu Yee Waye. Gene 2020
0

The role of rare compound heterozygous events in autism spectrum disorder.
Bochao Danae Lin, Fabrice Colas, Isaac J Nijman, Jelena Medic, William Brands, Jeremy R Parr, Kristel R van Eijk, Sabine M Klauck, Andreas G Chiocchetti, Christine M Freitag,[...]. Transl Psychiatry 2020
0