A citation-based method for searching scientific literature

Oliver Pain, Alexandra C Gillett, Jehannine C Austin, Lasse Folkersen, Cathryn M Lewis. Eur J Hum Genet 2022
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


The Young Geneticists Network and the ESHG-Young committee, a forward-looking international community.
Florence Riccardi, Ruta Marcinkute, Celia Azevedo Soares, Patricia Stefana Calapod, Juliana Miranda Cerqueira, Elena Avram, Can Ding. Eur J Hum Genet 2022
1
100

Establishing the phenotypic spectrum of ZTTK syndrome by analysis of 52 individuals with variants in SON.
Alexander J M Dingemans, Kim M G Truijen, Jung-Hyun Kim, Zahide Alaçam, Laurence Faivre, Kathleen M Collins, Erica H Gerkes, Mieke van Haelst, Ingrid M B H van de Laar, Kristin Lindstrom,[...]. Eur J Hum Genet 2022
4
33

Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update.
Anthony McGuigan, James Whitworth, Avgi Andreou, Timothy Hearn, Marc Tischkowitz, Eamonn R Maher. Eur J Hum Genet 2022
3
33

Polygenic risk modeling for prediction of epithelial ovarian cancer risk.
Eileen O Dareng, Jonathan P Tyrer, Daniel R Barnes, Michelle R Jones, Xin Yang, Katja K H Aben, Muriel A Adank, Simona Agata, Irene L Andrulis, Hoda Anton-Culver,[...]. Eur J Hum Genet 2022
3
33

Bi-allelic SMO variants in hypothalamic hamartoma: a recessive cause of Pallister-Hall syndrome.
Timothy E Green, Mareike Schimmel, Susanna Schubert, Johannes R Lemke, Mark F Bennett, Michael S Hildebrand, Samuel F Berkovic. Eur J Hum Genet 2022
3
33

Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies.
Julian Schröter, Bernt Popp, Heiko Brennenstuhl, Jan H Döring, Stephany H Donze, Emilia K Bijlsma, Arie van Haeringen, Dagmar Huhle, Leonie Jestaedt, Andreas Merkenschlager,[...]. Eur J Hum Genet 2022
2
50

Natural history of NF1 c.2970_2972del p.(Met992del): confirmation of a low risk of complications in a longitudinal study.
Claire Forde, Emma Burkitt-Wright, Peter D Turnpenny, Eric Haan, John Ealing, Sahar Mansour, Muriel Holder, Nayana Lahiri, Abhijit Dixit, Annie Procter,[...]. Eur J Hum Genet 2022
1
100

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.
Haoyu Zhang, Thomas U Ahearn, Julie Lecarpentier, Daniel Barnes, Jonathan Beesley, Guanghao Qi, Xia Jiang, Tracy A O'Mara, Ni Zhao, Manjeet K Bolla,[...]. Nat Genet 2020
82
33

Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention.
Michael Inouye, Gad Abraham, Christopher P Nelson, Angela M Wood, Michael J Sweeting, Frank Dudbridge, Florence Y Lai, Stephen Kaptoge, Marta Brozynska, Tingting Wang,[...]. J Am Coll Cardiol 2018
278
33

The role of polygenic risk and susceptibility genes in breast cancer over the course of life.
Nina Mars, Elisabeth Widén, Sini Kerminen, Tuomo Meretoja, Matti Pirinen, Pietro Della Briotta Parolo, Priit Palta, Aarno Palotie, Jaakko Kaprio, Heikki Joensuu,[...]. Nat Commun 2020
23
33

Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.
Alicia R Martin, Christopher R Gignoux, Raymond K Walters, Genevieve L Wojcik, Benjamin M Neale, Simon Gravel, Mark J Daly, Carlos D Bustamante, Eimear E Kenny. Am J Hum Genet 2017
519
33

Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases.
Scott C Ritchie, Samuel A Lambert, Matthew Arnold, Shu Mei Teo, Sol Lim, Petar Scepanovic, Jonathan Marten, Sohail Zahid, Mark Chaffin, Yingying Liu,[...]. Nat Metab 2021
6
33

Complex Trait Prediction from Genome Data: Contrasting EBV in Livestock to PRS in Humans: Genomic Prediction.
Naomi R Wray, Kathryn E Kemper, Benjamin J Hayes, Michael E Goddard, Peter M Visscher. Genetics 2019
45
33

Reduced signal for polygenic adaptation of height in UK Biobank.
Jeremy J Berg, Arbel Harpak, Nasa Sinnott-Armstrong, Anja Moltke Joergensen, Hakhamanesh Mostafavi, Yair Field, Evan August Boyle, Xinjun Zhang, Fernando Racimo, Jonathan K Pritchard,[...]. Elife 2019
145
33


CanRisk Tool-A Web Interface for the Prediction of Breast and Ovarian Cancer Risk and the Likelihood of Carrying Genetic Pathogenic Variants.
Tim Carver, Simon Hartley, Andrew Lee, Alex P Cunningham, Stephanie Archer, Chantal Babb de Villiers, Jonathan Roberts, Rod Ruston, Fiona M Walter, Marc Tischkowitz,[...]. Cancer Epidemiol Biomarkers Prev 2021
20
33

The Polygenic Score Catalog as an open database for reproducibility and systematic evaluation.
Samuel A Lambert, Laurent Gil, Simon Jupp, Scott C Ritchie, Yu Xu, Annalisa Buniello, Aoife McMahon, Gad Abraham, Michael Chapman, Helen Parkinson,[...]. Nat Genet 2021
72
33

Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial).
Iftikhar J Kullo, Hayan Jouni, Erin E Austin, Sherry-Ann Brown, Teresa M Kruisselbrink, Iyad N Isseh, Raad A Haddad, Tariq S Marroush, Khader Shameer, Janet E Olson,[...]. Circulation 2016
137
33

Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studies.
Mashaal Sohail, Robert M Maier, Andrea Ganna, Alex Bloemendal, Alicia R Martin, Michael C Turchin, Charleston Wk Chiang, Joel Hirschhorn, Mark J Daly, Nick Patterson,[...]. Elife 2019
142
33

Combined Utility of 25 Disease and Risk Factor Polygenic Risk Scores for Stratifying Risk of All-Cause Mortality.
Allison Meisner, Prosenjit Kundu, Yan Dora Zhang, Lauren V Lan, Sungwon Kim, Disha Ghandwani, Parichoy Pal Choudhury, Sonja I Berndt, Neal D Freedman, Montserrat Garcia-Closas,[...]. Am J Hum Genet 2020
21
33

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
33

Leveraging the electronic health record to implement genomic medicine.
Iftikhar J Kullo, Gail P Jarvik, Teri A Manolio, Marc S Williams, Dan M Roden. Genet Med 2013
38
33


Developing and evaluating polygenic risk prediction models for stratified disease prevention.
Nilanjan Chatterjee, Jianxin Shi, Montserrat García-Closas. Nat Rev Genet 2016
332
33

Impute.me: An Open-Source, Non-profit Tool for Using Data From Direct-to-Consumer Genetic Testing to Calculate and Interpret Polygenic Risk Scores.
Lasse Folkersen, Oliver Pain, Andrés Ingason, Thomas Werge, Cathryn M Lewis, Jehannine Austin. Front Genet 2020
16
33

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.
Nasim Mavaddat, Kyriaki Michailidou, Joe Dennis, Michael Lush, Laura Fachal, Andrew Lee, Jonathan P Tyrer, Ting-Huei Chen, Qin Wang, Manjeet K Bolla,[...]. Am J Hum Genet 2019
328
33

Reliability of self-reported family history of cancer in a large case-control study of lymphoma.
Ellen T Chang, Karin Ekström Smedby, Henrik Hjalgrim, Bengt Glimelius, Hans-Olov Adami. J Natl Cancer Inst 2006
101
33

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar. Nature 2009
33

BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors.
Andrew Lee, Nasim Mavaddat, Amber N Wilcox, Alex P Cunningham, Tim Carver, Simon Hartley, Chantal Babb de Villiers, Angel Izquierdo, Jacques Simard, Marjanka K Schmidt,[...]. Genet Med 2019
183
33

Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.
J Peto, N Collins, R Barfoot, S Seal, W Warren, N Rahman, D F Easton, C Evans, J Deacon, M R Stratton. J Natl Cancer Inst 1999
644
33

Problems with Using Polygenic Scores to Select Embryos.
Patrick Turley, Michelle N Meyer, Nancy Wang, David Cesarini, Evelynn Hammonds, Alicia R Martin, Benjamin M Neale, Heidi L Rehm, Louise Wilkins-Haug, Daniel J Benjamin,[...]. N Engl J Med 2021
25
33

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
142
33

Can epigenetics shine a light on the biological pathways underlying major mental disorders?
Luis Alameda, Giulia Trotta, Harriet Quigley, Victoria Rodriguez, Romayne Gadelrab, Daniella Dwir, Emma Dempster, Chloe C Y Wong, Marta Di Forti. Psychol Med 2022
5
33

Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems.
Amanda B Zheutlin, Jessica Dennis, Richard Karlsson Linnér, Arden Moscati, Nicole Restrepo, Peter Straub, Douglas Ruderfer, Victor M Castro, Chia-Yen Chen, Tian Ge,[...]. Am J Psychiatry 2019
70
33

Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials.
J L Mega, N O Stitziel, J G Smith, D I Chasman, M Caulfield, J J Devlin, F Nordio, C Hyde, C P Cannon, F Sacks,[...]. Lancet 2015
356
33

Novel subgroups of adult-onset diabetes and their association with outcomes: a data-driven cluster analysis of six variables.
Emma Ahlqvist, Petter Storm, Annemari Käräjämäki, Mats Martinell, Mozhgan Dorkhan, Annelie Carlsson, Petter Vikman, Rashmi B Prasad, Dina Mansour Aly, Peter Almgren,[...]. Lancet Diabetes Endocrinol 2018
735
33

Use of multiple polygenic risk scores for distinguishing schizophrenia-spectrum disorder and affective psychosis categories in a first-episode sample; the EU-GEI study.
Victoria Rodriguez, Luis Alameda, Diego Quattrone, Giada Tripoli, Charlotte Gayer-Anderson, Edoardo Spinazzola, Giulia Trotta, Hannah E Jongsma, Simona Stilo, Caterina La Cascia,[...]. Psychol Med 2022
1
100

The power of genetic diversity in genome-wide association studies of lipids.
Sarah E Graham, Shoa L Clarke, Kuan-Han H Wu, Stavroula Kanoni, Greg J M Zajac, Shweta Ramdas, Ida Surakka, Ioanna Ntalla, Sailaja Vedantam, Thomas W Winkler,[...]. Nature 2021
21
33

Multi-polygenic score approach to trait prediction.
E Krapohl, H Patel, S Newhouse, C J Curtis, S von Stumm, P S Dale, D Zabaneh, G Breen, P F O'Reilly, R Plomin. Mol Psychiatry 2018
70
33

Large uncertainty in individual polygenic risk score estimation impacts PRS-based risk stratification.
Yi Ding, Kangcheng Hou, Kathryn S Burch, Sandra Lapinska, Florian Privé, Bjarni Vilhjálmsson, Sriram Sankararaman, Bogdan Pasaniuc. Nat Genet 2022
7
33

The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
524
33

Weighing the risks and benefits of tamoxifen treatment for preventing breast cancer.
M H Gail, J P Costantino, J Bryant, R Croyle, L Freedman, K Helzlsouer, V Vogel. J Natl Cancer Inst 1999
472
33

Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer.
Thomas J Hoffmann, Michael N Passarelli, Rebecca E Graff, Nima C Emami, Lori C Sakoda, Eric Jorgenson, Laurel A Habel, Jun Shan, Dilrini K Ranatunga, Charles P Quesenberry,[...]. Nat Commun 2017
36
33

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
94
33

A roadmap to increase diversity in genomic studies.
Segun Fatumo, Tinashe Chikowore, Ananyo Choudhury, Muhammad Ayub, Alicia R Martin, Karoline Kuchenbaecker. Nat Med 2022
9
33

Evaluation of polygenic prediction methodology within a reference-standardized framework.
Oliver Pain, Kylie P Glanville, Saskia P Hagenaars, Saskia Selzam, Anna E Fürtjes, Héléna A Gaspar, Jonathan R I Coleman, Kaili Rimfeld, Gerome Breen, Robert Plomin,[...]. PLoS Genet 2021
22
33

How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study.
Elisabeth Widén, Nella Junna, Sanni Ruotsalainen, Ida Surakka, Nina Mars, Pietari Ripatti, Juulia J Partanen, Johanna Aro, Pekka Mustonen, Tiinamaija Tuomi,[...]. Circ Genom Precis Med 2022
5
33

A call for training programmes in cardiovascular genomics.
Maya S Safarova, Michael J Ackerman, Iftikhar J Kullo. Nat Rev Cardiol 2021
1
100

Prospective evaluation of a breast-cancer risk model integrating classical risk factors and polygenic risk in 15 cohorts from six countries.
Amber N Hurson, Parichoy Pal Choudhury, Chi Gao, Anika Hüsing, Mikael Eriksson, Min Shi, Michael E Jones, D Gareth R Evans, Roger L Milne, Mia M Gaudet,[...]. Int J Epidemiol 2022
8
33

Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease.
Amit V Khera, Connor A Emdin, Isabel Drake, Pradeep Natarajan, Alexander G Bick, Nancy R Cook, Daniel I Chasman, Usman Baber, Roxana Mehran, Daniel J Rader,[...]. N Engl J Med 2016
565
33


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.