A citation-based method for searching scientific literature

Kate Wolfe, Andrew McQuillin, Viola Alesi, Elise Boudry Labis, Peter Cutajar, Bruno Dallapiccola, Maria Lisa Dentici, Anne Dieux-Coeslier, Benedicte Duban-Bedu, Tina Duelund Hjortshøj, Himanshu Goel, Sara Loddo, Deborah Morrogh, Anne-Laure Mosca-Boidron, Antonio Novelli, Laurence Olivier-Faivre, Jennifer Parker, Michael J Parker, Christine Patch, Anna L Pelling, Thomas Smol, Zeynep Tümer, Olivier Vanakker, Arie van Haeringen, Clémence Vanlerberghe, Andre Strydom, David Skuse, Nick Bass. Am J Med Genet B Neuropsychiatr Genet 2018
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Masahiro Kanai, Masato Akiyama, Atsushi Takahashi, Nana Matoba, Yukihide Momozawa, Masashi Ikeda, Nakao Iwata, Shiro Ikegawa, Makoto Hirata, Koichi Matsuda,[...]. Nat Genet 2018
212
16

Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development.
Richard S Smith, Connor J Kenny, Vijay Ganesh, Ahram Jang, Rebeca Borges-Monroy, Jennifer N Partlow, R Sean Hill, Taehwan Shin, Allen Y Chen, Ryan N Doan,[...]. Neuron 2018
52
16


The Matchmaker Exchange: a platform for rare disease gene discovery.
Anthony A Philippakis, Danielle R Azzariti, Sergi Beltran, Anthony J Brookes, Catherine A Brownstein, Michael Brudno, Han G Brunner, Orion J Buske, Knox Carey, Cassie Doll,[...]. Hum Mutat 2015
224
16

Dynamic expression of genes associated with schizophrenia and bipolar disorder across development.
Nicholas E Clifton, Eilís Hannon, Janet C Harwood, Arianna Di Florio, Kerrie L Thomas, Peter A Holmans, James T R Walters, Michael C O'Donovan, Michael J Owen, Andrew J Pocklington,[...]. Transl Psychiatry 2019
9
16

A novel small-subunit processome assembly intermediate that contains the U3 snoRNP, nucleolin, RRP5, and DBP4.
Amy Jane Turner, Andrew Alexander Knox, José-Luis Prieto, Brian McStay, Nicholas James Watkins. Mol Cell Biol 2009
49
16

CAPN1 mutations are associated with a syndrome of combined spasticity and ataxia.
Vera Tadic, Christine Klein, Frauke Hinrichs, Alexander Münchau, Katja Lohmann, Norbert Brüggemann. J Neurol 2017
13
16


Hereditary spastic paraparesis and psychosis.
P McMonagle, M Hutchinson, B Lawlor. Eur J Neurol 2006
10
16

An overview of pre-ribosomal RNA processing in eukaryotes.
Anthony K Henras, Célia Plisson-Chastang, Marie-Françoise O'Donohue, Anirban Chakraborty, Pierre-Emmanuel Gleizes. Wiley Interdiscip Rev RNA 2015
275
16

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
Santhi K Ganesh, Neil A Zakai, Frank J A van Rooij, Nicole Soranzo, Albert V Smith, Michael A Nalls, Ming-Huei Chen, Anna Kottgen, Nicole L Glazer, Abbas Dehghan,[...]. Nat Genet 2009
266
16

Deletion of the Capn1 Gene Results in Alterations in Signaling Pathways Related to Alzheimer's Disease, Protein Quality Control and Synaptic Plasticity in Mouse Brain.
Wenyue Su, Qian Zhou, Yubin Wang, Athar Chishti, Qingshun Q Li, Sujay Dayal, Shayan Shiehzadegan, Ariel Cheng, Clare Moore, Xiaoning Bi,[...]. Front Genet 2020
3
33

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Ryan K C Yuen, Daniele Merico, Matt Bookman, Jennifer L Howe, Bhooma Thiruvahindrapuram, Rohan V Patel, Joe Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang,[...]. Nat Neurosci 2017
332
16

GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
Jin Li, Joseph T Glessner, Haitao Zhang, Cuiping Hou, Zhi Wei, Jonathan P Bradfield, Frank D Mentch, Yiran Guo, Cecilia Kim, Qianghua Xia,[...]. Hum Mol Genet 2013
65
16

SPG76: An extremely rare hereditary spastic paraplegia with a new expanding complicated phenotype.
P V S Souza, L H L Silva, B M L Badia, I B Farias, W B V R Pinto, A S B Oliveira. Rev Neurol (Paris) 2019
3
33

Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder.
Chih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang. Taiwan J Obstet Gynecol 2017
1
100


Cognitive profile in a large French cohort of adults with Prader-Willi syndrome: differences between genotypes.
P Copet, J Jauregi, V Laurier, V Ehlinger, C Arnaud, A-M Cobo, C Molinas, M Tauber, D Thuilleaux. J Intellect Disabil Res 2010
41
16

Morphological differences in the mirror neuron system in Williams syndrome.
Rowena Ng, Timothy T Brown, Matthew Erhart, Anna M Järvinen, Julie R Korenberg, Ursula Bellugi, Eric Halgren. Soc Neurosci 2016
4
25

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
806
16

Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): a cross-sectional and longitudinal study.
Marie Schaer, Martin Debbané, Meritxell Bach Cuadra, Marie-Christine Ottet, Bronwyn Glaser, Jean-Philippe Thiran, Stephan Eliez. Schizophr Res 2009
85
16


Performance on the Kaufman Brief Intelligence Test-2 by Children With Williams Syndrome.
C Holley Pitts, Carolyn B Mervis. Am J Intellect Dev Disabil 2016
8
16

Deficits in voice and multisensory processing in patients with Prader-Willi syndrome.
Juliette Salles, Kuzma Strelnikov, Mantoulan Carine, Thuilleaux Denise, Virginie Laurier, Catherine Molinas, Maïthé Tauber, Pascal Barone. Neuropsychologia 2016
7
16

Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.
T van Amelsvoort, J Zinkstok, M Figee, E Daly, R Morris, M J Owen, K C Murphy, L De Haan, D H Linszen, B Glaser,[...]. Psychol Med 2008
38
16


Abnormalities in gray matter microstructure in young adults with 22q11.2 deletion syndrome.
Zora Kikinis, Nikos Makris, Valerie J Sydnor, Sylvain Bouix, Ofer Pasternak, Ioana L Coman, Kevin M Antshel, Wanda Fremont, Marek R Kubicki, Martha E Shenton,[...]. Neuroimage Clin 2019
4
25

The relationship between compulsive behaviour and academic achievement across the three genetic subtypes of Prader-Willi syndrome.
J Zarcone, D Napolitano, C Peterson, J Breidbord, S Ferraioli, M Caruso-Anderson, L Holsen, M G Butler, T Thompson. J Intellect Disabil Res 2007
40
16

Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
Samuel J R A Chawner, Michael J Owen, Peter Holmans, F Lucy Raymond, David Skuse, Jeremy Hall, Marianne B M van den Bree. Lancet Psychiatry 2019
34
16

Facial emotion processing in patients with social anxiety disorder and Williams-Beuren syndrome: an fMRI study.
Cynthia Binelli, Armando Muñiz, Susana Subira, Ricard Navines, Laura Blanco-Hinojo, Debora Perez-Garcia, Jose Crippa, Magi Farré, Luis Pérez-Jurado, Jesus Pujol,[...]. J Psychiatry Neurosci 2016
10
16

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion.
M Woodin, P P Wang, D Aleman, D McDonald-McGinn, E Zackai, E Moss. Genet Med 2001
175
16

Language characterization in 16p11.2 deletion and duplication syndromes.
So Hyun Kim, LeeAnne Green-Snyder, Catherine Lord, Somer Bishop, Kyle J Steinman, Raphael Bernier, Ellen Hanson, Robin P Goin-Kochel, Wendy K Chung. Am J Med Genet B Neuropsychiatr Genet 2020
4
25

Clinical implications of copy number variations in autoimmune disorders.
Seon-Hee Yim, Seung-Hyun Jung, Boram Chung, Yeun-Jun Chung. Korean J Intern Med 2015
8
16

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, Carl Baker, Laura Vives, Tiffany H Vu, Neil Shafer, Raphael Bernier, Giovanni B Ferrero, Margherita Silengo,[...]. PLoS Genet 2011
206
16

Cognitive functioning in adults with Williams syndrome.
P Howlin, M Davies, O Udwin. J Child Psychol Psychiatry 1998
98
16

Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults.
K Momma, A Takao, R Matsuoka, Y Imai, A Muto, M Osawa, M Takayama. Genet Med 2001
18
16

Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome.
J Whittington, A Holland, T Webb, J Butler, D Clarke, H Boer. J Intellect Disabil Res 2004
107
16

3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry.
Ming-Chang Chiang, Allan L Reiss, Agatha D Lee, Ursula Bellugi, Albert M Galaburda, Julie R Korenberg, Debra L Mills, Arthur W Toga, Paul M Thompson. Neuroimage 2007
107
16

Copy Number Variation Disorders.
Tamim H Shaikh. Curr Genet Med Rep 2017
10
16

Childhood Executive Functioning Predicts Young Adult Outcomes in 22q11.2 Deletion Syndrome.
Avery B Albert, Tamara Abu-Ramadan, Wendy R Kates, Wanda Fremont, Kevin M Antshel. J Int Neuropsychol Soc 2018
6
16


Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome.
Adam C Cunningham, Sue Delport, Wendy Cumines, Monica Busse, David E J Linden, Jeremy Hall, Michael J Owen, Marianne B M van den Bree. Br J Psychiatry 2018
12
16

A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome.
Stephen R Hooper, Kathleen Curtiss, Kelly Schoch, Matcheri S Keshavan, Andrew Allen, Vandana Shashi. Res Dev Disabil 2013
38
16

A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndrome.
Melanie A Porter, Carol Dobson-Stone, John B J Kwok, Peter R Schofield, William Beckett, May Tassabehji. PLoS One 2012
25
16

Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects.
Miri Carmel, Omer Zarchi, Elena Michaelovsky, Amos Frisch, Miriam Patya, Tamar Green, Doron Gothelf, Abraham Weizman. J Psychiatr Res 2014
13
16

The genetic variability and commonality of neurodevelopmental disease.
Bradley P Coe, Santhosh Girirajan, Evan E Eichler. Am J Med Genet C Semin Med Genet 2012
74
16

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
E M Moss, M L Batshaw, C B Solot, M Gerdes, D M McDonald-McGinn, D A Driscoll, B S Emanuel, E H Zackai, P P Wang. J Pediatr 1999
217
16

The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
Loyse Hippolyte, Anne M Maillard, Borja Rodriguez-Herreros, Aurélie Pain, Sandra Martin-Brevet, Carina Ferrari, Philippe Conus, Aurélien Macé, Nouchine Hadjikhani, Andres Metspalu,[...]. Biol Psychiatry 2016
50
16

Lateral preference in Williams-Beuren syndrome is associated with cognition and language.
D Pérez-García, R Flores, C Brun-Gasca, L A Pérez-Jurado. Eur Child Adolesc Psychiatry 2015
6
16

The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome.
E Hidding, H Swaab, L M J de Sonneville, H van Engeland, J A S Vorstman. Clin Genet 2016
10
16


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.