A citation-based method for searching scientific literature

Andy W Pang, Jeffrey R MacDonald, Dalila Pinto, John Wei, Muhammad A Rafiq, Donald F Conrad, Hansoo Park, Matthew E Hurles, Charles Lee, J Craig Venter, Ewen F Kirkness, Samuel Levy, Lars Feuk, Stephen W Scherer. Genome Biol 2010
Times Cited: 182



Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall, Anthony Leotta, Deepa Pai, Ray Zhang, Yoon-Ha Lee, James Hicks, Sarah J Spence, Annette T Lee, Kaija Puura, Terho Lehtimäki, David Ledbetter, Peter K Gregersen, Joel Bregman, James S Sutcliffe, Vaidehi Jobanputra, Wendy Chung, Dorothy Warburton, Mary-Claire King, David Skuse, Daniel H Geschwind, T Conrad Gilliam, Kenny Ye, Michael Wigler. Science 2007
Times Cited: 1798




List of shared articles



Times cited

Robust Benchmark Structural Variant Calls of An Asian Using the State-of-art Long Fragment Sequencing Technologies.
Xiao Du, Lili Li, Fan Liang, Sanyang Liu, Wenxin Zhang, Shuai Sun, Yuhui Sun, Fei Fan, Linying Wang, Xinming Liang,[...]. Genomics Proteomics Bioinformatics 2021
1

Discovery of genomic variation across a generation.
Brett Trost, Livia O Loureiro, Stephen W Scherer. Hum Mol Genet 2021
1

Structural variation in the sequencing era.
Steve S Ho, Alexander E Urban, Ryan E Mills. Nat Rev Genet 2020
67

A robust benchmark for detection of germline large deletions and insertions.
Justin M Zook, Nancy F Hansen, Nathan D Olson, Lesley Chapman, James C Mullikin, Chunlin Xiao, Stephen Sherry, Sergey Koren, Adam M Phillippy, Paul C Boutros,[...]. Nat Biotechnol 2020
44

Genetic Risk Profiling in Parkinson's Disease and Utilizing Genetics to Gain Insight into Disease-Related Biological Pathways.
Ashley Hall, Sara Bandres-Ciga, Monica Diez-Fairen, John P Quinn, Kimberley J Billingsley. Int J Mol Sci 2020
6

Identifying structural variants using linked-read sequencing data.
Rebecca Elyanow, Hsin-Ta Wu, Benjamin J Raphael. Bioinformatics 2018
32

Characteristics of de novo structural changes in the human genome.
Wigard P Kloosterman, Laurent C Francioli, Fereydoun Hormozdiari, Tobias Marschall, Jayne Y Hehir-Kwa, Abdel Abdellaoui, Eric-Wubbo Lameijer, Matthijs H Moed, Vyacheslav Koval, Ivo Renkens,[...]. Genome Res 2015
67

Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms.
Alexej Abyzov, Shantao Li, Daniel Rhee Kim, Marghoob Mohiyuddin, Adrian M Stütz, Nicholas F Parrish, Xinmeng Jasmine Mu, Wyatt Clark, Ken Chen, Matthew Hurles,[...]. Nat Commun 2015
54

Detection of Genomic Structural Variants from Next-Generation Sequencing Data.
Lorenzo Tattini, Romina D'Aurizio, Alberto Magi. Front Bioeng Biotechnol 2015
132

Family-Based Benchmarking of Copy Number Variation Detection Software.
Marcel Elie Nutsua, Annegret Fischer, Almut Nebel, Sylvia Hofmann, Stefan Schreiber, Michael Krawczak, Michael Nothnagel. PLoS One 2015
5

Copy number variations in the genome of the Qatari population.
Khalid A Fakhro, Noha A Yousri, Juan L Rodriguez-Flores, Amal Robay, Michelle R Staudt, Francisco Agosto-Perez, Jacqueline Salit, Joel A Malek, Karsten Suhre, Amin Jayyousi,[...]. BMC Genomics 2015
5

Rare autosomal copy number variations in early-onset familial Alzheimer's disease.
B V Hooli, Z M Kovacs-Vajna, K Mullin, M A Blumenthal, M Mattheisen, C Zhang, C Lange, G Mohapatra, L Bertram, R E Tanzi. Mol Psychiatry 2014
49

Copy number variation distribution in six monozygotic twin pairs discordant for schizophrenia.
Christina A Castellani, Zain Awamleh, Melkaye G Melka, Richard L O'Reilly, Shiva M Singh. Twin Res Hum Genet 2014
25

Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts.
John J Connolly, Joseph T Glessner, Berta Almoguera, David R Crosslin, Gail P Jarvik, Patrick M Sleiman, Hakon Hakonarson. Front Genet 2014
8

Biological relevance of CNV calling methods using familial relatedness including monozygotic twins.
Christina A Castellani, Melkaye G Melka, Andrea E Wishart, M Elizabeth O Locke, Zain Awamleh, Richard L O'Reilly, Shiva M Singh. BMC Bioinformatics 2014
11

Etiology of autism spectrum disorder: a genomics perspective.
John J Connolly, Hakon Hakonarson. Curr Psychiatry Rep 2014
8