A citation-based method for searching scientific literature

Nadieh A Jansen, Ruth O Braden, Siddharth Srivastava, Erin F Otness, Gaetan Lesca, Massimiliano Rossi, Mathilde Nizon, Raphael A Bernier, ChloĆ© Quelin, Arie van Haeringen, Tjitske Kleefstra, Maggie M K Wong, Sandra Whalen, Simon E Fisher, Angela T Morgan, Bregje W van Bon. Eur J Hum Genet 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates.
Beatrice Spedicati, Massimiliano Cocca, Roberto Palmisano, Flavio Faletra, Caterina Barbieri, Margherita Francescatto, Massimo Mezzavilla, Anna Morgan, Giulia Pelliccione, Paolo Gasparini,[...]. Eur J Hum Genet 2021
1
100

Regional heritability mapping identifies several novel loci (STAT4, ULK4, and KCNH5) for primary biliary cholangitis in the Japanese population.
Olivier Gervais, Kazuko Ueno, Yosuke Kawai, Yuki Hitomi, Yoshihiro Aiba, Mayumi Ueta, Minoru Nakamura, Katsushi Tokunaga, Masao Nagasaki. Eur J Hum Genet 2021
1
100

Germline variants in UNC13D and AP3B1 are enriched in COVID-19 patients experiencing severe cytokine storms.
Hui Luo, Dan Liu, Wenbing Liu, Gaoxiang Wang, Liting Chen, Yang Cao, Jia Wei, Min Xiao, Xin Liu, Gang Huang,[...]. Eur J Hum Genet 2021
1
100

Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer.
Rabea Wagener, Julia Taeubner, Carolin Walter, Layal Yasin, Deya Alzoubi, Christoph Bartenhagen, Andishe Attarbaschi, Carl-Friedrich Classen, Udo Kontny, Julia Hauer,[...]. Eur J Hum Genet 2021
1
100

Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formation.
Lance P Doucette, Nicole C L Noel, Yi Zhai, Manlong Xu, Oana Caluseriu, Stephanie C Hoang, Alina J Radziwon, Ian M MacDonald. Eur J Hum Genet 2021
1
100

Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria.
Judy Savige, Helen Storey, Elizabeth Watson, Jens Michael Hertz, Constantinos Deltas, Alessandra Renieri, Francesca Mari, Pascale Hilbert, Pavlina Plevova, Peter Byers,[...]. Eur J Hum Genet 2021
1
100

Deletion of the last two exons of FGF10 in a family with LADD syndrome and pulmonary acinar hypoplasia.
Emma M Wade, Padmini Parthasarathy, Jingyi Mi, Tim Morgan, Bernd Wollnik, Stephen P Robertson, Tim Cundy. Eur J Hum Genet 2021
1
100

Parent clinical trial priorities for fragile X syndrome: a best-worst scaling.
Erin Turbitt, Celeste D'Amanda, Sarah Hyman, Jayne Dixon Weber, John F P Bridges, Holly L Peay, Barbara B Biesecker. Eur J Hum Genet 2021
1
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.