A citation-based method for searching scientific literature

Rosie O'Shea, Nicole M Rankin, Maira Kentwell, Margaret Gleeson, Katherine M Tucker, Heather Hampel, Natalie Taylor, Sarah Lewis. Eur J Hum Genet 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


A comparison of genotyping arrays.
Joost A M Verlouw, Eva Clemens, Jard H de Vries, Oliver Zolk, Annemieke J M H Verkerk, Antoinette Am Zehnhoff-Dinnesen, Carolina Medina-Gomez, Claudia Lanvers-Kaminsky, Fernando Rivadeneira, Thorsten Langer,[...]. Eur J Hum Genet 2021
4
100

A systematic review assessing the existence of pneumothorax-only variants of FLCN. Implications for lifelong surveillance of renal tumours.
Kenki Matsumoto, Derek Lim, Paul D Pharoah, Eamonn R Maher, Stefan J Marciniak. Eur J Hum Genet 2021
3
100

TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility.
Aafke Engwerda, Erika K S M Leenders, Barbara Frentz, Paulien A Terhal, Katharina L√∂hner, Bert B A de Vries, Trijnie Dijkhuizen, Yvonne J Vos, Tuula Rinne, Maarten P van den Berg,[...]. Eur J Hum Genet 2021
4
100

The genetic structure of Norway.
Morten Mattingsdal, S Sunna Ebenesersd√≥ttir, Kristjan H S Moore, Ole A Andreassen, Thomas F Hansen, Thomas Werge, Ingrid Kockum, Tomas Olsson, Lars Alfredsson, Agnar Helgason,[...]. Eur J Hum Genet 2021
3
100

SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect.
Alisdair McNeill, Emanuela Iovino, Luke Mansard, Christel Vache, David Baux, Emma Bedoukian, Helen Cox, John Dean, David Goudie, Ajith Kumar,[...]. Brain 2020
16
100

Identifying challenges in neurofibromatosis: a modified Delphi procedure.
Britt A E Dhaenens, Rosalie E Ferner, Annette Bakker, Marco Nievo, D Gareth Evans, Pierre Wolkenstein, Cornelia Potratz, Scott R Plotkin, Guenter Heimann, Eric Legius,[...]. Eur J Hum Genet 2021
1
100

Deletion in COL4A2 is associated with a three-generation variable phenotype: from fetal to adult manifestations.
Moran Hausman-Kedem, Liat Ben-Sira, Debora Kidron, Shay Ben-Shachar, Rachel Straussberg, Daphna Marom, Penina Ponger, Anat Bar-Shira, Gustavo Malinger, Aviva Fattal-Valevski. Eur J Hum Genet 2021
1
100

Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability.
Natja Haag, Ene-Choo Tan, Matthias Begemann, Lars Buschmann, Florian Kraft, Petra Holschbach, Angeline H M Lai, Maggie Brett, Ganeshwaran H Mochida, Stephanie DiTroia,[...]. Eur J Hum Genet 2021
3
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.