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



Mehdi Zarrei, Jeffrey R MacDonald, Daniele Merico, Stephen W Scherer. Nat Rev Genet 2015
Times Cited: 357




List of shared articles



Times cited



Genome-wide detection of CNV regions and their potential association with growth and fatness traits in Duroc pigs.
Yibin Qiu, Rongrong Ding, Zhanwei Zhuang, Jie Wu, Ming Yang, Shenping Zhou, Yong Ye, Qian Geng, Zheng Xu, Sixiu Huang,[...]. BMC Genomics 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

Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.
Chloe X Yap, Gail A Alvares, Anjali K Henders, Tian Lin, Leanne Wallace, Alaina Farrelly, Tiana McLaren, Jolene Berry, Anna A E Vinkhuyzen, Maciej Trzaskowski,[...]. Mol Autism 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

Detection of copy number variants in African goats using whole genome sequence data.
Wilson Nandolo, Gábor Mészáros, Maria Wurzinger, Liveness J Banda, Timothy N Gondwe, Henry A Mulindwa, Helen N Nakimbugwe, Emily L Clark, M Jennifer Woodward-Greene, Mei Liu,[...]. BMC Genomics 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
3

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

Population-wide copy number variation calling using variant call format files from 6,898 individuals.
Grace Png, Daniel Suveges, Young-Chan Park, Klaudia Walter, Kousik Kundu, Ioanna Ntalla, Emmanouil Tsafantakis, Maria Karaleftheri, George Dedoussis, Eleftheria Zeggini,[...]. Genet Epidemiol 2020
0

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

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

Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases.
Maria Yamasaki, Takashi Makino, Seik-Soon Khor, Hiromi Toyoda, Taku Miyagawa, Xiaoxi Liu, Hitoshi Kuwabara, Yukiko Kano, Takafumi Shimada, Toshiro Sugiyama,[...]. BMC Med Genomics 2020
2

Large Copy-Number Variants in UK Biobank Caused by Clonal Hematopoiesis May Confound Penetrance Estimates.
Marcus Tuke, Jessica Tyrrell, Katherine S Ruth, Robin N Beaumont, Andrew R Wood, Anna Murray, Timothy M Frayling, Michael N Weedon, Caroline F Wright. Am J Hum Genet 2020
1

Population Structure, and Selection Signatures Underlying High-Altitude Adaptation Inferred From Genome-Wide Copy Number Variations in Chinese Indigenous Cattle.
Yaran Zhang, Yan Hu, Xiuge Wang, Qiang Jiang, Han Zhao, Jinpeng Wang, Zhihua Ju, Liguo Yang, Yaping Gao, Xiaochao Wei,[...]. Front Genet 2020
3

Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.
Lisa-Marie Niestroj, Eduardo Perez-Palma, Daniel P Howrigan, Yadi Zhou, Feixiong Cheng, Elmo Saarentaus, Peter Nürnberg, Remi Stevelink, Mark J Daly, Aarno Palotie,[...]. Brain 2020
3