A citation-based method for searching scientific literature

Matilda A Haas, Harriet Teare, Megan Prictor, Gabi Ceregra, Miranda E Vidgen, David Bunker, Jane Kaye, Tiffany Boughtwood. Eur J Hum Genet 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Chromosomes in the genomic age. Preserving cytogenomic competence of diagnostic genome laboratories.
Ron Hochstenbach, Thomas Liehr, Rosalind J Hastings. Eur J Hum Genet 2021
5
100

Reflections on dynamic consent in biomedical research: the story so far.
Harriet J A Teare, Megan Prictor, Jane Kaye. Eur J Hum Genet 2021
3
100

A human case of GIMAP6 deficiency: a novel primary immune deficiency.
Bella Shadur, Nathalie Asherie, Shlomit Kfir-Erenfeld, Taly Dubnikov, Adeeb NaserEddin, Yael Dinur Schejter, Orly Elpeleg, Hagar Mor-Shaked, Polina Stepensky. Eur J Hum Genet 2021
3
100

Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome.
Amanda Brignell, Conway Gu, Alison Holm, Bronwyn Carrigg, Daisy A Sheppard, David J Amor, Angela T Morgan. Eur J Hum Genet 2021
3
100

Pathogenic variants causing ABL1 malformation syndrome cluster in a myristoyl-binding pocket and increase tyrosine kinase activity.
Alexander J M Blakes, Emily Gaul, Wayne Lam, Nora Shannon, Karen M Knapp, Louise S Bicknell, Meremaihi R Jackson, Emma M Wade, Stephen Robertson, Susan M White,[...]. Eur J Hum Genet 2021
1
100

Long-read trio sequencing of individuals with unsolved intellectual disability.
Marc Pauper, Erdi Kucuk, Aaron M Wenger, Shreyasee Chakraborty, Primo Baybayan, Michael Kwint, Bart van der Sanden, Marcel R Nelen, Ronny Derks, Han G Brunner,[...]. Eur J Hum Genet 2021
2
100

Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype.
Meena Balasubramanian, Alexander J M Dingemans, Shadi Albaba, Ruth Richardson, Thabo M Yates, Helen Cox, Sofia Douzgou, Ruth Armstrong, Francis H Sansbury, Katherine B Burke,[...]. Eur J Hum Genet 2021
1
100

Whole-exome sequencing of Finnish patients with vascular cognitive impairment.
Saana Mönkäre, Liina Kuuluvainen, Celia Kun-Rodrigues, Susana Carmona, Johanna Schleutker, Jose Bras, Minna Pöyhönen, Rita Guerreiro, Liisa Myllykangas. 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.