A citation-based method for searching scientific literature

Lisa A Cannon-Albright, Craig C Teerlink, Jeffrey Stevens, Angela K Snow, Bryony A Thompson, Russell Bell, Kim N Nguyen, Nykole R Sargent, Wendy K Kohlmann, Deborah W Neklason, Sean V Tavtigian. Mol Genet Genomic Med 2020
Times Cited: 2







List of co-cited articles
articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
50

UCSF Chimera--a visualization system for exploratory research and analysis.
Eric F Pettersen, Thomas D Goddard, Conrad C Huang, Gregory S Couch, Daniel M Greenblatt, Elaine C Meng, Thomas E Ferrin. J Comput Chem 2004
50

Prognostic relevance of DNA copy number changes in colorectal cancer.
George Poulogiannis, Koichi Ichimura, Rifat A Hamoudi, Feijun Luo, Suet Y Leung, Siu T Yuen, David J Harrison, Andrew H Wyllie, Mark J Arends. J Pathol 2010
40
50


Genotype harmonizer: automatic strand alignment and format conversion for genotype data integration.
Patrick Deelen, Marc Jan Bonder, K Joeri van der Velde, Harm-Jan Westra, Erwin Winder, Dennis Hendriksen, Lude Franke, Morris A Swertz. BMC Res Notes 2014
64
50

Identification and genomic analysis of pedigrees with exceptional longevity identifies candidate rare variants.
Justin B Miller, Elizabeth Ward, Lyndsay A Staley, Jeffrey Stevens, Craig C Teerlink, Justina P Tavana, Matthew Cloward, Madeline Page, Louisa Dayton, Lisa A Cannon-Albright,[...]. Neurobiol Dis 2020
4
50

Fast and accurate long-range phasing in a UK Biobank cohort.
Po-Ru Loh, Pier Francesco Palamara, Alkes L Price. Nat Genet 2016
156
50

Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus.
A Kamb, D Shattuck-Eidens, R Eeles, Q Liu, N A Gruis, W Ding, C Hussey, T Tran, Y Miki, J Weaver-Feldhaus. Nat Genet 1994
532
50

Proteomic analysis reveals that MAEL, a component of nuage, interacts with stress granule proteins in cancer cells.
Liqin Yuan, Yuzhong Xiao, Qiuzhi Zhou, Dongmei Yuan, Baiping Wu, Gannong Chen, Jianlin Zhou. Oncol Rep 2014
16
50

A reference panel of 64,976 haplotypes for genotype imputation.
Shane McCarthy, Sayantan Das, Warren Kretzschmar, Olivier Delaneau, Andrew R Wood, Alexander Teumer, Hyun Min Kang, Christian Fuchsberger, Petr Danecek, Kevin Sharp,[...]. Nat Genet 2016
50



Discovery of biclonal origin and a novel oncogene SLC12A5 in colon cancer by single-cell sequencing.
Chang Yu, Jun Yu, Xiaotian Yao, William K K Wu, Youyong Lu, Senwei Tang, Xiangchun Li, Li Bao, Xiaoxing Li, Yong Hou,[...]. Cell Res 2014
89
50

Significant evidence of linkage for a gene predisposing to colorectal cancer and multiple primary cancers on 22q11.
Craig Teerlink, Quentin Nelson, Randall Burt, Lisa Cannon-Albright. Clin Transl Gastroenterol 2014
4
50

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
50

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age.
Cathie Sudlow, John Gallacher, Naomi Allen, Valerie Beral, Paul Burton, John Danesh, Paul Downey, Paul Elliott, Jane Green, Martin Landray,[...]. PLoS Med 2015
50

FlashPCA2: principal component analysis of Biobank-scale genotype datasets.
Gad Abraham, Yixuan Qiu, Michael Inouye. Bioinformatics 2017
121
50

A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposis.
Bryony A Thompson, Angela K Snow, Cathryn Koptiuch, Wendy K Kohlmann, Ryan Mooney, Sara Johnson, Chad D Huff, Yao Yu, Craig C Teerlink, Bing-Jian Feng,[...]. Clin Genet 2020
12
50


The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds.
S V Tavtigian, J Simard, J Rommens, F Couch, D Shattuck-Eidens, S Neuhausen, S Merajver, S Thorlacius, K Offit, D Stoppa-Lyonnet,[...]. Nat Genet 1996
676
50

RNA-binding proteins and post-transcriptional gene regulation.
Tina Glisovic, Jennifer L Bachorik, Jeongsik Yong, Gideon Dreyfuss. FEBS Lett 2008
872
50

Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.
Devanshi Patel, Jesse Mez, Badri N Vardarajan, Lyndsay Staley, Jaeyoon Chung, Xiaoling Zhang, John J Farrell, Michael J Rynkiewicz, Lisa A Cannon-Albright, Craig C Teerlink,[...]. JAMA Netw Open 2019
37
50

Next-generation genotype imputation service and methods.
Sayantan Das, Lukas Forer, Sebastian Schönherr, Carlo Sidore, Adam E Locke, Alan Kwong, Scott I Vrieze, Emily Y Chew, Shawn Levy, Matt McGue,[...]. Nat Genet 2016
50

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
Fredrick R Schumacher, Ali Amin Al Olama, Sonja I Berndt, Sara Benlloch, Mahbubl Ahmed, Edward J Saunders, Tokhir Dadaev, Daniel Leongamornlert, Ezequiel Anokian, Clara Cieza-Borrella,[...]. Nat Genet 2018
357
50

Genome-wide analysis of high-risk primary brain cancer pedigrees identifies PDXDC1 as a candidate brain cancer predisposition gene.
Lisa A Cannon-Albright, James M Farnham, Jeffrey Stevens, Craig C Teerlink, Cheryl A Palmer, Kerry Rowe, Melissa H Cessna, Deborah T Blumenthal. Neuro Oncol 2021
3
50


Finding the missing heritability of complex diseases.
Teri A Manolio, Francis S Collins, Nancy J Cox, David B Goldstein, Lucia A Hindorff, David J Hunter, Mark I McCarthy, Erin M Ramos, Lon R Cardon, Aravinda Chakravarti,[...]. Nature 2009
50

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.
Alexandre Bureau, Samuel G Younkin, Margaret M Parker, Joan E Bailey-Wilson, Mary L Marazita, Jeffrey C Murray, Elisabeth Mangold, Hasan Albacha-Hejazi, Terri H Beaty, Ingo Ruczinski. Bioinformatics 2014
21
50

Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience.
Perry G Ridge, Celeste M Karch, Simon Hsu, Ivan Arano, Craig C Teerlink, Mark T W Ebbert, Josue D Gonzalez Murcia, James M Farnham, Anna R Damato, Mariet Allen,[...]. Genome Med 2017
41
50

A candidate prostate cancer susceptibility gene at chromosome 17p.
S V Tavtigian, J Simard, D H Teng, V Abtin, M Baumgard, A Beck, N J Camp, A R Carillo, Y Chen, P Dayananth,[...]. Nat Genet 2001
430
50


A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.
Y Miki, J Swensen, D Shattuck-Eidens, P A Futreal, K Harshman, S Tavtigian, Q Liu, C Cochran, L M Bennett, W Ding. Science 1994
50

Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.
Elad Ziv, Eric Dean, Donglei Hu, Alessandro Martino, Daniel Serie, Karen Curtin, Daniele Campa, Blake Aftab, Paige Bracci, Gabriele Buda,[...]. Nat Commun 2015
29
50

Discovery of common and rare genetic risk variants for colorectal cancer.
Jeroen R Huyghe, Stephanie A Bien, Tabitha A Harrison, Hyun Min Kang, Sai Chen, Stephanie L Schmit, David V Conti, Conghui Qu, Jihyoun Jeon, Christopher K Edlund,[...]. Nat Genet 2019
208
50

A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma.
Craig C Teerlink, Chad Huff, Jeff Stevens, Yao Yu, Sheri L Holmen, Mark R Silvis, Kirby Trombetti, Hua Zhao, Douglas Grossman, James M Farnham,[...]. J Natl Cancer Inst 2018
23
50

Identifying a high fraction of the human genome to be under selective constraint using GERP++.
Eugene V Davydov, David L Goode, Marina Sirota, Gregory M Cooper, Arend Sidow, Serafim Batzoglou. PLoS Comput Biol 2010
990
50


Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis.
Kristina Allen-Brady, Benjamin D Horne, Alka Malhotra, Craig Teerlink, Nicola J Camp, Alun Thomas. BMC Proc 2007
11
50

A robust multipoint linkage statistic (tlod) for mapping complex trait loci.
V Abkevich, N J Camp, A Gutin, J M Farnham, L Cannon-Albright, A Thomas. Genet Epidemiol 2001
23
50

Unipro UGENE: a unified bioinformatics toolkit.
Konstantin Okonechnikov, Olga Golosova, Mikhail Fursov. Bioinformatics 2012
50

The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
50

A role for the MEGF6 gene in predisposition to osteoporosis.
Craig C Teerlink, Michael J Jurynec, Rolando Hernandez, Jeff Stevens, Dana C Hughes, Cherie P Brunker, Kerry Rowe, David J Grunwald, Julio C Facelli, Lisa A Cannon-Albright. Ann Hum Genet 2021
6
50


BRCA Mutations in Prostate Cancer: Prognostic and Predictive Implications.
Carlo Messina, Carlo Cattrini, Davide Soldato, Giacomo Vallome, Orazio Caffo, Elena Castro, David Olmos, Francesco Boccardo, Elisa Zanardi. J Oncol 2020
31
50

Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries.
Hyuna Sung, Jacques Ferlay, Rebecca L Siegel, Mathieu Laversanne, Isabelle Soerjomataram, Ahmedin Jemal, Freddie Bray. CA Cancer J Clin 2021
50

Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
Matthew B Yurgelun, Brian Allen, Rajesh R Kaldate, Karla R Bowles, Thaddeus Judkins, Praveen Kaushik, Benjamin B Roa, Richard J Wenstrup, Anne-Renee Hartman, Sapna Syngal. Gastroenterology 2015
167
50


Persistent double strand break accumulation does not precede cell death in an Olaparib-sensitive BRCA-deficient colorectal cancer cell model.
Natalia Soledad Paviolo, María Belén de la Vega, María Florencia Pansa, Iris Alejandra García, Nicolás Luis Calzetta, Gastón Soria, Vanesa Gottifredi. Genet Mol Biol 2019
5
50

Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
Matthew B Yurgelun, Matthew H Kulke, Charles S Fuchs, Brian A Allen, Hajime Uno, Jason L Hornick, Chinedu I Ukaegbu, Lauren K Brais, Philip G McNamara, Robert J Mayer,[...]. J Clin Oncol 2017
240
50

Mechanism, specificity, and function of FANCD2-FANCI ubiquitination and deubiquitination.
Kimon Lemonidis, Connor Arkinson, Martin L Rennie, Helen Walden. FEBS J 2022
10
50


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.