A citation-based method for searching scientific literature

Haiming Yuan, Shaofang Shangguan, Zhengchang Li, Jingsi Luo, Jiasun Su, Ruen Yao, Shun Zhang, Chen Liang, Qian Chen, Zhijie Gao, Yanli Zhu, Shujie Zhang, Wei Li, Weiliang Lu, Yu Zhang, Hua Xie, Fang Liu, Qingming Wang, Yangyang Lin, Liying Liu, Xiuming Wang, Liyang Liang, Jianmin Zhong, Haibo Li, Haiyan Qiu, Huifeng Zhang, Mei Yan, Maimaiti Mireguli, Yanhui Liu, Dan Zhang, Hongying Wang, Haitao Lv, Bobo Xie, Chunrong Gui, Xiaodai Cui, Liping Zou, Jian Wang, James F Gusella, Yiping Shen, Xiaoli Chen. Genet Med 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.
Clyde Francks, Simon E Fisher, Richard K Olson, Bruce F Pennington, Shelley D Smith, John C DeFries, Anthony P Monaco. Psychiatr Genet 2002
46
100

First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.
D Roeske, K U Ludwig, N Neuhoff, J Becker, J Bartling, J Bruder, F F Brockschmidt, A Warnke, H Remschmidt, P Hoffmann,[...]. Mol Psychiatry 2011
66
100

Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability.
Guillaume Huguet, Catherine Schramm, Elise Douard, Petra Tamer, Antoine Main, Pauline Monin, Jade England, Khadije Jizi, Thomas Renne, Myriam Poirier,[...]. Mol Psychiatry 2021
3
100

Mathematical learning disabilities in children with 22q11.2 deletion syndrome: a review.
Bert De Smedt, Ann Swillen, Lieven Verschaffel, Pol Ghesquière. Dev Disabil Res Rev 2009
37
100

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.
Natalie Cope, Denise Harold, Gary Hill, Valentina Moskvina, Jim Stevenson, Peter Holmans, Michael J Owen, Michael C O'Donovan, Julie Williams. Am J Hum Genet 2005
197
100

From BDNF to reading: Neural activation and phonological processing as multiple mediators.
Sara Mascheretti, Meaghan V Perdue, Bei Feng, Chiara Andreola, Ginette Dionne, Kaja K Jasińska, Kenneth R Pugh, Elena L Grigorenko, Nicole Landi. Behav Brain Res 2021
3
100

DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling.
Markus Schueler, Daniela A Braun, Gayathri Chandrasekar, Heon Yung Gee, Timothy D Klasson, Jan Halbritter, Andrea Bieder, Jonathan D Porath, Rannar Airik, Weibin Zhou,[...]. Am J Hum Genet 2015
51
100

Ancestral Variations of the PCDHG Gene Cluster Predispose to Dyslexia in a Multiplex Family.
Teesta Naskar, Mohammed Faruq, Priyajit Banerjee, Massarat Khan, Rashi Midha, Renu Kumari, Subhashree Devasenapathy, Bharat Prajapati, Sanghamitra Sengupta, Deepti Jain,[...]. EBioMedicine 2018
6
100

DCDC2 Mutations Cause Neonatal Sclerosing Cholangitis.
Muriel Girard, Albane A Bizet, Alain Lachaux, Emmanuel Gonzales, Emilie Filhol, Sophie Collardeau-Frachon, Cécile Jeanpierre, Charline Henry, Monique Fabre, Loic Viremouneix,[...]. Hum Mutat 2016
20
100

Examining and interpreting the female protective effect against autistic behavior.
Elise B Robinson, Paul Lichtenstein, Henrik Anckarsäter, Francesca Happé, Angelica Ronald. Proc Natl Acad Sci U S A 2013
189
100


A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5.
Ging-Yuek R Hsiung, Bonnie J Kaplan, Tracey L Petryshen, Shao Lu, L Leigh Field. Am J Med Genet B Neuropsychiatr Genet 2004
49
100

Genetic influences on reading difficulties in boys and girls: the Colorado twin study.
Jesse L Hawke, Sally J Wadsworth, John C DeFries. Dyslexia 2006
24
100

Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia.
Satu Massinen, Kristiina Tammimies, Isabel Tapia-Páez, Hans Matsson, Marie-Estelle Hokkanen, Ola Söderberg, Ulf Landegren, Eero Castrén, Jan-Ake Gustafsson, Eckardt Treuter,[...]. Hum Mol Genet 2009
43
100

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
Nuala H Simpson, Laura Addis, William M Brandler, Vicky Slonims, Ann Clark, Jocelynne Watson, Thomas S Scerri, Elizabeth R Hennessy, Patrick F Bolton, Gina Conti-Ramsden,[...]. Dev Med Child Neurol 2014
22
100

Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels.
S Poliak, L Gollan, R Martinez, A Custer, S Einheber, J L Salzer, J S Trimmer, P Shrager, E Peles. Neuron 1999
352
100

The effect of variation in expression of the candidate dyslexia susceptibility gene homolog Kiaa0319 on neuronal migration and dendritic morphology in the rat.
Veronica J Peschansky, Timothy J Burbridge, Amy J Volz, Christopher Fiondella, Zach Wissner-Gross, Albert M Galaburda, Joseph J Lo Turco, Glenn D Rosen. Cereb Cortex 2010
52
100

DYX1C1 is required for axonemal dynein assembly and ciliary motility.
Aarti Tarkar, Niki T Loges, Christopher E Slagle, Richard Francis, Gerard W Dougherty, Joel V Tamayo, Brett Shook, Marie Cantino, Daniel Schwartz, Charlotte Jahnke,[...]. Nat Genet 2013
160
100

The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function.
Gayathri Chandrasekar, Liselotte Vesterlund, Kjell Hultenby, Isabel Tapia-Páez, Juha Kere. PLoS One 2013
35
100

Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice.
Ozlem Bozdagi, Takeshi Sakurai, Nathan Dorr, Marion Pilorge, Nagahide Takahashi, Joseph D Buxbaum. PLoS One 2012
69
100

A new gene (DYX3) for dyslexia is located on chromosome 2.
T Fagerheim, P Raeymaekers, F E Tønnessen, M Pedersen, L Tranebjaerg, H A Lubs. J Med Genet 1999
138
100

Generalist genes and learning disabilities.
Robert Plomin, Yulia Kovas. Psychol Bull 2005
257
100

Evaluation of results from genome-wide studies of language and reading in a novel independent dataset.
A Carrion-Castillo, E van Bergen, A Vino, T van Zuijen, P F de Jong, C Francks, S E Fisher. Genes Brain Behav 2016
11
100

Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
Hans Matsson, Mikael Huss, Helena Persson, Elisabet Einarsdottir, Ettore Tiraboschi, Jaana Nopola-Hemmi, Johannes Schumacher, Nina Neuhoff, Andreas Warnke, Heikki Lyytinen,[...]. J Hum Genet 2015
12
100

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
202
100

Gene-environment interaction in the etiology of mathematical ability using SNP sets.
Sophia J Docherty, Yulia Kovas, Robert Plomin. Behav Genet 2011
12
100

A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q.
Tiemo Grimm, Masoud Garshasbi, Lucia Puettmann, Wei Chen, Reinhard Ullmann, Bertram Müller-Myhsok, Eva Klopocki, Lina Herbst, Janina Haug, Lars R Jensen,[...]. Z Kinder Jugendpsychiatr Psychother 2020
1
100

Sex Differences in Autism Spectrum Disorder: a Review.
Sarah L Ferri, Ted Abel, Edward S Brodkin. Curr Psychiatry Rep 2018
61
100

Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family.
Elisabet Einarsdottir, Idor Svensson, Fahimeh Darki, Myriam Peyrard-Janvid, Jessica M Lindvall, Adam Ameur, Christer Jacobsson, Torkel Klingberg, Juha Kere, Hans Matsson. Hum Genet 2015
13
100

Association of short-term memory with a variant within DYX1C1 in developmental dyslexia.
C Marino, A Citterio, R Giorda, A Facoetti, G Menozzi, L Vanzin, M L Lorusso, M Nobile, M Molteni. Genes Brain Behav 2007
59
100

Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics.
Avinash M Veerappa, Marita Saldanha, Prakash Padakannaya, Nallur B Ramachandra. Am J Med Genet B Neuropsychiatr Genet 2014
8
100

The Influence of Dyslexia Candidate Genes on Reading Skill in Old Age.
Michelle Luciano, Alan J Gow, Alison Pattie, Timothy C Bates, Ian J Deary. Behav Genet 2018
4
100

A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study.
Simon Baron-Cohen, Laura Murphy, Bhismadev Chakrabarti, Ian Craig, Uma Mallya, Silvia Lakatošová, Karola Rehnstrom, Leena Peltonen, Sally Wheelwright, Carrie Allison,[...]. PLoS One 2014
11
100

Developmental dyscalculia is a familial learning disability.
R S Shalev, O Manor, B Kerem, M Ayali, N Badichi, Y Friedlander, V Gross-Tsur. J Learn Disabil 2001
55
100

On the "specifics" of specific reading disability and specific language impairment.
G M McArthur, J H Hogben, V T Edwards, S M Heath, E D Mengler. J Child Psychol Psychiatry 2000
195
100

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia.
Katariina Hannula-Jouppi, Nina Kaminen-Ahola, Mikko Taipale, Ranja Eklund, Jaana Nopola-Hemmi, Helena Kääriäinen, Juha Kere. PLoS Genet 2005
203
100


Identification of NCAN as a candidate gene for developmental dyslexia.
Elisabet Einarsdottir, Myriam Peyrard-Janvid, Fahimeh Darki, Jetro J Tuulari, Harri Merisaari, Linnea Karlsson, Noora M Scheinin, Jani Saunavaara, Riitta Parkkola, Katri Kantojärvi,[...]. Sci Rep 2017
10
100

CEP63 deficiency promotes p53-dependent microcephaly and reveals a role for the centrosome in meiotic recombination.
Marko Marjanović, Carlos Sánchez-Huertas, Berta Terré, Rocío Gómez, Jan Frederik Scheel, Sarai Pacheco, Philip A Knobel, Ana Martínez-Marchal, Suvi Aivio, Lluís Palenzuela,[...]. Nat Commun 2015
39
100

The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults.
Catherine Doust, Scott D Gordon, Natalie Garden, Simon E Fisher, Nicholas G Martin, Timothy C Bates, Michelle Luciano. Twin Res Hum Genet 2020
3
100

Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples.
Sara Mascheretti, Vittoria Trezzi, Roberto Giorda, Michel Boivin, Vickie Plourde, Frank Vitaro, Mara Brendgen, Ginette Dionne, Cecilia Marino. J Child Psychol Psychiatry 2017
13
100

Understanding Comorbidity Between Specific Learning Disabilities.
Erik G Willcutt, Lauren M McGrath, Bruce F Pennington, Janice M Keenan, John C DeFries, Richard K Olson, Sally J Wadsworth. New Dir Child Adolesc Dev 2019
6
100

Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families.
M Huc-Chabrolle, C Charon, A Guilmatre, P Vourc'h, G Tripi, M A Barthez, E Sizaret, R A Thepault, S Le Gallic, J Hager,[...]. Behav Genet 2013
5
100

Dysfunctional neural network of spatial working memory contributes to developmental dyscalculia.
S Rotzer, T Loenneker, K Kucian, E Martin, P Klaver, M von Aster. Neuropsychologia 2009
75
100

Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia.
T L Petryshen, B J Kaplan, M Fu Liu, N S de French, R Tobias, M L Hughes, L L Field. Am J Med Genet 2001
57
100

Mutations in the pericentrin (PCNT) gene cause primordial dwarfism.
Anita Rauch, Christian T Thiel, Detlev Schindler, Ursula Wick, Yanick J Crow, Arif B Ekici, Anthonie J van Essen, Timm O Goecke, Lihadh Al-Gazali, Krystyna H Chrzanowska,[...]. Science 2008
263
100

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
D F Newbury, S Paracchini, T S Scerri, L Winchester, L Addis, Alex J Richardson, J Walter, J F Stein, J B Talcott, A P Monaco. Behav Genet 2011
131
100

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
Clyde Francks, Silvia Paracchini, Shelley D Smith, Alex J Richardson, Tom S Scerri, Lon R Cardon, Angela J Marlow, I Laurence MacPhie, Janet Walter, Bruce F Pennington,[...]. Am J Hum Genet 2004
166
100

Dyslexia Candidate Gene and Ciliary Gene Expression Dynamics During Human Neuronal Differentiation.
Andrea Bieder, Masahito Yoshihara, Shintaro Katayama, Kaarel Krjutškov, Anna Falk, Juha Kere, Isabel Tapia-Páez. Mol Neurobiol 2020
2
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.