A citation-based method for searching scientific literature

Andy Dahl, Noah Zaitlen. Annu Rev Genomics Hum Genet 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores.
Julie Lecarpentier, Valentina Silvestri, Karoline B Kuchenbaecker, Daniel Barrowdale, Joe Dennis, Lesley McGuffog, Penny Soucy, Goska Leslie, Piera Rizzolo, Anna Sara Navazio,[...]. J Clin Oncol 2017
70
100

Reevaluation of SNP heritability in complex human traits.
Doug Speed, Na Cai, Michael R Johnson, Sergey Nejentsev, David J Balding. Nat Genet 2017
175
100

A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis.
Dan Zhou, Yi Jiang, Xue Zhong, Nancy J Cox, Chunyu Liu, Eric R Gamazon. Nat Genet 2020
8
100

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
802
100

Development of a large-scale de-identified DNA biobank to enable personalized medicine.
D M Roden, J M Pulley, M A Basford, G R Bernard, E W Clayton, J R Balser, D R Masys. Clin Pharmacol Ther 2008
532
100

Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection.
Steven Gazal, Hilary K Finucane, Nicholas A Furlotte, Po-Ru Loh, Pier Francesco Palamara, Xuanyao Liu, Armin Schoech, Brendan Bulik-Sullivan, Benjamin M Neale, Alexander Gusev,[...]. Nat Genet 2017
113
100

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
Lea K Davis, Dongmei Yu, Clare L Keenan, Eric R Gamazon, Anuar I Konkashbaev, Eske M Derks, Benjamin M Neale, Jian Yang, S Hong Lee, Patrick Evans,[...]. PLoS Genet 2013
146
100

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study.
Line Olsen, Thomas Sparsø, Shantel M Weinsheimer, Marcelo Bertalan Quintanilha Dos Santos, Wiktor Mazin, Anders Rosengren, Xabier Calle Sanchez, Louise K Hoeffding, Henriette Schmock, Marie Baekvad-Hansen,[...]. Lancet Psychiatry 2018
38
100

GCTA: a tool for genome-wide complex trait analysis.
Jian Yang, S Hong Lee, Michael E Goddard, Peter M Visscher. Am J Hum Genet 2011
100


Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.
Jamie E Craig, Xikun Han, Ayub Qassim, Mark Hassall, Jessica N Cooke Bailey, Tyler G Kinzy, Anthony P Khawaja, Jiyuan An, Henry Marshall, Puya Gharahkhani,[...]. Nat Genet 2020
47
100

Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types.
Joshua N Sampson, William A Wheeler, Meredith Yeager, Orestis Panagiotou, Zhaoming Wang, Sonja I Berndt, Qing Lan, Christian C Abnet, Laufey T Amundadottir, Jonine D Figueroa,[...]. J Natl Cancer Inst 2015
90
100



A gene-based association method for mapping traits using reference transcriptome data.
Eric R Gamazon, Heather E Wheeler, Kaanan P Shah, Sahar V Mozaffari, Keston Aquino-Michaels, Robert J Carroll, Anne E Eyler, Joshua C Denny, Dan L Nicolae, Nancy J Cox,[...]. Nat Genet 2015
581
100

Ubiquitous polygenicity of human complex traits: genome-wide analysis of 49 traits in Koreans.
Jian Yang, Taeheon Lee, Jaemin Kim, Myeong-Chan Cho, Bok-Ghee Han, Jong-Young Lee, Hyun-Jeong Lee, Seoae Cho, Heebal Kim. PLoS Genet 2013
48
100

Genome-wide association study of Tourette's syndrome.
J M Scharf, D Yu, C A Mathews, B M Neale, S E Stewart, J A Fagerness, P Evans, E Gamazon, C K Edlund, S K Service,[...]. Mol Psychiatry 2013
106
100

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.
Dongmei Yu, Carol A Mathews, Jeremiah M Scharf, Benjamin M Neale, Lea K Davis, Eric R Gamazon, Eske M Derks, Patrick Evans, Christopher K Edlund, Jacquelyn Crane,[...]. Am J Psychiatry 2015
77
100

Second-generation PLINK: rising to the challenge of larger and richer datasets.
Christopher C Chang, Carson C Chow, Laurent Cam Tellier, Shashaank Vattikuti, Shaun M Purcell, James J Lee. Gigascience 2015
100

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
Amit V Khera, Mark Chaffin, Krishna G Aragam, Mary E Haas, Carolina Roselli, Seung Hoan Choi, Pradeep Natarajan, Eric S Lander, Steven A Lubitz, Patrick T Ellinor,[...]. Nat Genet 2018
744
100

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, Carl Baker, Laura Vives, Tiffany H Vu, Neil Shafer, Raphael Bernier, Giovanni B Ferrero, Margherita Silengo,[...]. PLoS Genet 2011
204
100

Testing for an unusual distribution of rare variants.
Benjamin M Neale, Manuel A Rivas, Benjamin F Voight, David Altshuler, Bernie Devlin, Marju Orho-Melander, Sekar Kathiresan, Shaun M Purcell, Kathryn Roeder, Mark J Daly. PLoS Genet 2011
412
100

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
S Hong Lee, Stephan Ripke, Benjamin M Neale, Stephen V Faraone, Shaun M Purcell, Roy H Perlis, Bryan J Mowry, Anita Thapar, Michael E Goddard, John S Witte,[...]. Nat Genet 2013
100

Common SNPs explain a large proportion of the heritability for human height.
Jian Yang, Beben Benyamin, Brian P McEvoy, Scott Gordon, Anjali K Henders, Dale R Nyholt, Pamela A Madden, Andrew C Heath, Nicholas G Martin, Grant W Montgomery,[...]. Nat Genet 2010
100

Most genetic risk for autism resides with common variation.
Trent Gaugler, Lambertus Klei, Stephan J Sanders, Corneliu A Bodea, Arthur P Goldberg, Ann B Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert,[...]. Nat Genet 2014
537
100

Exploiting the GTEx resources to decipher the mechanisms at GWAS loci.
Alvaro N Barbeira, Rodrigo Bonazzola, Eric R Gamazon, Yanyu Liang, YoSon Park, Sarah Kim-Hellmuth, Gao Wang, Zhuoxun Jiang, Dan Zhou, Farhad Hormozdiari,[...]. Genome Biol 2021
12
100

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.
Lauren M McGrath, Dongmei Yu, Christian Marshall, Lea K Davis, Bhooma Thiruvahindrapuram, Bingbin Li, Carolina Cappi, Gloria Gerber, Aaron Wolf, Frederick A Schroeder,[...]. J Am Acad Child Adolesc Psychiatry 2014
70
100

Association of BRCA1 and BRCA2 mutations with survival, chemotherapy sensitivity, and gene mutator phenotype in patients with ovarian cancer.
Da Yang, Sofia Khan, Yan Sun, Kenneth Hess, Ilya Shmulevich, Anil K Sood, Wei Zhang. JAMA 2011
336
100

Explaining additional genetic variation in complex traits.
Matthew R Robinson, Naomi R Wray, Peter M Visscher. Trends Genet 2014
86
100

Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders.
M T Oetjens, M A Kelly, A C Sturm, C L Martin, D H Ledbetter. Nat Commun 2019
28
100


Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers.
Karoline B Kuchenbaecker, Lesley McGuffog, Daniel Barrowdale, Andrew Lee, Penny Soucy, Joe Dennis, Susan M Domchek, Mark Robson, Amanda B Spurdle, Susan J Ramus,[...]. J Natl Cancer Inst 2017
112
100

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale. Nat Genet 2015
100

CNVs in neuropsychiatric disorders.
George Kirov. Hum Mol Genet 2015
77
100


Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening.
Tianyuan Lu, Sirui Zhou, Haoyu Wu, Vincenzo Forgetta, Celia M T Greenwood, J Brent Richards. Genet Med 2021
3
100

Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.
J P Szatkiewicz, B M Neale, C O'Dushlaine, M Fromer, J I Goldstein, J L Moran, K Chambert, A Kähler, P K E Magnusson, C M Hultman,[...]. Mol Psychiatry 2013
21
100

Genome-wide association study of obsessive-compulsive disorder.
S E Stewart, D Yu, J M Scharf, B M Neale, J A Fagerness, C A Mathews, P D Arnold, P D Evans, E R Gamazon, L K Davis,[...]. Mol Psychiatry 2013
173
100

Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
Sarah E Bergen, Alexander Ploner, Daniel Howrigan, Michael C O'Donovan, Jordan W Smoller, Patrick F Sullivan, Jonathan Sebat, Benjamin Neale, Kenneth S Kendler. Am J Psychiatry 2019
41
100

A polygenic burden of rare disruptive mutations in schizophrenia.
Shaun M Purcell, Jennifer L Moran, Menachem Fromer, Douglas Ruderfer, Nadia Solovieff, Panos Roussos, Colm O'Dushlaine, Kimberly Chambert, Sarah E Bergen, Anna Kähler,[...]. Nature 2014
875
100

Exchangeable models of complex inherited diseases.
Montgomery Slatkin. Genetics 2008
29
100

Additive genetic variation in schizophrenia risk is shared by populations of African and European descent.
Teresa R de Candia, S Hong Lee, Jian Yang, Brian L Browning, Pablo V Gejman, Douglas F Levinson, Bryan J Mowry, John K Hewitt, Michael E Goddard, Michael C O'Donovan,[...]. Am J Hum Genet 2013
56
100

Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions.
Akl C Fahed, Minxian Wang, Julian R Homburger, Aniruddh P Patel, Alexander G Bick, Cynthia L Neben, Carmen Lai, Deanna Brockman, Anthony Philippakis, Patrick T Ellinor,[...]. Nat Commun 2020
42
100

A framework for the interpretation of de novo mutation in human disease.
Kaitlin E Samocha, Elise B Robinson, Stephan J Sanders, Christine Stevens, Aniko Sabo, Lauren M McGrath, Jack A Kosmicki, Karola Rehnström, Swapan Mallick, Andrew Kirby,[...]. Nat Genet 2014
511
100

A better coefficient of determination for genetic profile analysis.
Sang Hong Lee, Michael E Goddard, Naomi R Wray, Peter M Visscher. Genet Epidemiol 2012
105
100

Signatures of negative selection in the genetic architecture of human complex traits.
Jian Zeng, Ronald de Vlaming, Yang Wu, Matthew R Robinson, Luke R Lloyd-Jones, Loic Yengo, Chloe X Yap, Angli Xue, Julia Sidorenko, Allan F McRae,[...]. Nat Genet 2018
89
100

Familial Risk and Heritability of Cancer Among Twins in Nordic Countries.
Lorelei A Mucci, Jacob B Hjelmborg, Jennifer R Harris, Kamila Czene, David J Havelick, Thomas Scheike, Rebecca E Graff, Klaus Holst, Sören Möller, Robert H Unger,[...]. JAMA 2016
296
100

Common genetic variants, acting additively, are a major source of risk for autism.
Lambertus Klei, Stephan J Sanders, Michael T Murtha, Vanessa Hus, Jennifer K Lowe, A Jeremy Willsey, Daniel Moreno-De-Luca, Timothy W Yu, Eric Fombonne, Daniel Geschwind,[...]. Mol Autism 2012
248
100

Autism spectrum disorder severity reflects the average contribution of de novo and familial influences.
Elise B Robinson, Kaitlin E Samocha, Jack A Kosmicki, Lauren McGrath, Benjamin M Neale, Roy H Perlis, Mark J Daly. Proc Natl Acad Sci U S A 2014
75
100

Rare and common variants: twenty arguments.
Greg Gibson. Nat Rev Genet 2012
675
100


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.