A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity



New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy.
Elena Martín-Hernández, María Elena Rodríguez-García, Ana Camacho, Antoni Matilla-Dueñas, María Teresa García-Silva, Pilar Quijada-Fraile, Marc Corral-Juan, Pilar Tejada-Palacios, Rogelio Simón de Las Heras, Joaquín Arenas,[...]. Neurogenetics 2016
22
100

Disruption of the Zdhhc9 intellectual disability gene leads to behavioural abnormalities in a mouse model.
Marianna Kouskou, David M Thomson, Ros R Brett, Lee Wheeler, Rothwelle J Tate, Judith A Pratt, Luke H Chamberlain. Exp Neurol 2018
4
100

Analysis copy number variation of Chinese children in early-onset epileptic encephalopathies with unknown cause.
Y Ma, C Chen, Y Wang, L Wu, F He, C Chen, C Zhang, X Deng, L Yang, Y Chen,[...]. Clin Genet 2016
8
100

Self-Concept in Mothers of Educable Mentally Retarded Children.
Zahra Aliakbarzadeh-Arani. Nurs Midwifery Stud 2016
1
100

Simultaneous use of sensory stimulation and motor exercise improves the manual skills of educable children with mental retardation at preprimary and primary school levels.
Raheleh Mollajani, Seyed Saeid Taghavi, Agha Fatemeh Hosseini, Mona Farhadi, Mana Jameie, Melika Jameie, Seyed Behnamedin Jameie. Med J Islam Repub Iran 2019
1
100

DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies.
Jianling Ji, Hane Lee, Bob Argiropoulos, Naghmeh Dorrani, John Mann, Julian A Martinez-Agosto, Natalia Gomez-Ospina, Natalie Gallant, Jonathan A Bernstein, Louanne Hudgins,[...]. Eur J Hum Genet 2015
54
100

GeneMatcher aids in the identification of a new malformation syndrome with intellectual disability, unique facial dysmorphisms, and skeletal and connective tissue abnormalities caused by de novo variants in HNRNPK.
P Y Billie Au, Jing You, Oana Caluseriu, Jeremy Schwartzentruber, Jacek Majewski, Francois P Bernier, Marcia Ferguson, David Valle, Jillian S Parboosingh, Nara Sobreira,[...]. Hum Mutat 2015
40
100




Differences in the clinical presentation of Trisomy 21 with and without autism.
C A Molloy, D S Murray, A Kinsman, H Castillo, T Mitchell, F J Hickey, B Patterson. J Intellect Disabil Res 2009
52
100


Genetic studies in intellectual disability and related disorders.
Lisenka E L M Vissers, Christian Gilissen, Joris A Veltman. Nat Rev Genet 2016
311
100

Potential oligogenic disease of mental retardation, short stature, spastic paraparesis, and osteopetrosis.
Abdulaziz Alsemari, Mohanned Alsuhaibani, Rawabi Alhathlool, Bayan Mamdouh Ali. Appl Clin Genet 2018
1
100

Prevalence of cerebral palsy in children < 10 years of age in R.S. Pura town of Jammu and Kashmir.
Sunil Kumar Raina, Sushil Razdan, Renu Nanda. J Trop Pediatr 2011
8
100

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.
Gurdeep S Sagoo, Adam S Butterworth, Simon Sanderson, Charles Shaw-Smith, Julian P T Higgins, Hilary Burton. Genet Med 2009
146
100

The genetic basis of non-syndromic intellectual disability: a review.
Liana Kaufman, Muhammad Ayub, John B Vincent. J Neurodev Disord 2010
129
100

A clinical approach to developmental delay and intellectual disability.
Pradeep Vasudevan, Mohnish Suri. Clin Med (Lond) 2017
21
100

Hyperphosphatasia with mental retardation syndrome, expanded phenotype of PIGL related disorders.
Ruqaiah Altassan, Stephanie Fox, Chantal Poulin, Daniela Buhas. Mol Genet Metab Rep 2018
4
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.