A citation-based method for searching scientific literature

Reza Asadollahi, Beatrice Oneda, Pascal Joset, Silvia Azzarello-Burri, Deborah Bartholdi, Katharina Steindl, Marie Vincent, Joana Cobilanschi, Heinrich Sticht, Rosa Baldinger, Regina Reissmann, Irene Sudholt, Christian T Thiel, Arif B Ekici, André Reis, Emilia K Bijlsma, Joris Andrieux, Anne Dieux, David FitzPatrick, Susanne Ritter, Alessandra Baumer, Beatrice Latal, Barbara Plecko, Oskar G Jenni, Anita Rauch. J Med Genet 2014
Times Cited: 57







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



Times Cited
  Times     Co-cited
Similarity


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
208
3

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
Silvia Paracchini, Ankur Thomas, Sandra Castro, Cecilia Lai, Murugan Paramasivam, Yu Wang, Brendan J Keating, Jennifer M Taylor, Douglas F Hacking, Thomas Scerri,[...]. Hum Mol Genet 2006
173
3

Clinical diagnosis by whole-genome sequencing of a prenatal sample.
Michael E Talkowski, Zehra Ordulu, Vamsee Pillalamarri, Carol B Benson, Ian Blumenthal, Susan Connolly, Carrie Hanscom, Naveed Hussain, Shahrin Pereira, Jonathan Picker,[...]. N Engl J Med 2012
119
3

DCDC2 is associated with reading disability and modulates neuronal development in the brain.
Haiying Meng, Shelley D Smith, Karl Hager, Matthew Held, Jonathan Liu, Richard K Olson, Bruce F Pennington, John C DeFries, Joel Gelernter, Thomas O'Reilly-Pol,[...]. Proc Natl Acad Sci U S A 2005
257
3

Genome-wide screening for DNA variants associated with reading and language traits.
A Gialluisi, D F Newbury, E G Wilcutt, R K Olson, J C DeFries, W M Brandler, B F Pennington, S D Smith, T S Scerri, N H Simpson,[...]. Genes Brain Behav 2014
59
3

Genome-wide association study of shared components of reading disability and language impairment.
J D Eicher, N R Powers, L L Miller, N Akshoomoff, D G Amaral, C S Bloss, O Libiger, N J Schork, B F Darst, B J Casey,[...]. Genes Brain Behav 2013
55
3

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.
Mikko Taipale, Nina Kaminen, Jaana Nopola-Hemmi, Tuomas Haltia, Birgitta Myllyluoma, Heikki Lyytinen, Kurt Muller, Minna Kaaranen, Perttu J Lindsberg, Katariina Hannula-Jouppi,[...]. Proc Natl Acad Sci U S A 2003
224
3

Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization.
Jm Friedman, Shelin Adam, Laura Arbour, Linlea Armstrong, Agnes Baross, Patricia Birch, Cornelius Boerkoel, Susanna Chan, David Chai, Allen D Delaney,[...]. BMC Genomics 2009
27
7

Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes.
Tracy Tucker, Farah R Zahir, Malachi Griffith, Allen Delaney, David Chai, Erica Tsang, Emmanuelle Lemyre, Sylvia Dobrzeniecka, Marco Marra, Patrice Eydoux,[...]. Eur J Hum Genet 2014
29
6

Somatic mutation, genomic variation, and neurological disease.
Annapurna Poduri, Gilad D Evrony, Xuyu Cai, Christopher A Walsh. Science 2013
326
3


Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
3

Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalities.
Heather Mason-Suares, Wayne Kim, Leslie Grimmett, Eli S Williams, Vanessa L Horner, Dawn Kunig, Ian S Goldlust, Bai-Lin Wu, Yiping Shen, David T Miller,[...]. Genet Med 2013
20
10

Mapping copy number variation by population-scale genome sequencing.
Ryan E Mills, Klaudia Walter, Chip Stewart, Robert E Handsaker, Ken Chen, Can Alkan, Alexej Abyzov, Seungtai Chris Yoon, Kai Ye, R Keira Cheetham,[...]. Nature 2011
707
3

The diverse genetic landscape of neurodevelopmental disorders.
Wen F Hu, Maria H Chahrour, Christopher A Walsh. Annu Rev Genomics Hum Genet 2014
100
3


An evaluation of copy number variation detection tools from whole-exome sequencing data.
Renjie Tan, Yadong Wang, Sarah E Kleinstein, Yongzhuang Liu, Xiaolin Zhu, Hongzhe Guo, Qinghua Jiang, Andrew S Allen, Mingfu Zhu. Hum Mutat 2014
124
3

Rare copy number variation in cerebral palsy.
Gai McMichael, Santhosh Girirajan, Andres Moreno-De-Luca, Jozef Gecz, Chloe Shard, Lam Son Nguyen, Jillian Nicholl, Catherine Gibson, Eric Haan, Evan Eichler,[...]. Eur J Hum Genet 2014
38
5

Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disability.
Ilaria Gandin, Flavio Faletra, Francesca Faletra, Massimo Carella, Vanna Pecile, Giovanni B Ferrero, Elisa Biamino, Pietro Palumbo, Orazio Palumbo, Paolo Bosco,[...]. Genet Med 2015
16
12


Genome structural variation discovery and genotyping.
Can Alkan, Bradley P Coe, Evan E Eichler. Nat Rev Genet 2011
749
3

Delta-catenin at the synaptic-adherens junction.
Kenneth S Kosik, Christine P Donahue, Inbal Israely, Xin Liu, Tomoyo Ochiishi. Trends Cell Biol 2005
50
4

δ-Catenin is genetically and biologically associated with cortical cataract and future Alzheimer-related structural and functional brain changes.
Gyungah Jun, Juliet A Moncaster, Carolina Koutras, Sudha Seshadri, Jacqueline Buros, Ann C McKee, Georges Levesque, Philip A Wolf, Peter St George-Hyslop, Lee E Goldstein,[...]. PLoS One 2012
40
5

Discovery and Replication of Gene Influences on Brain Structure Using LASSO Regression.
Omid Kohannim, Derrek P Hibar, Jason L Stein, Neda Jahanshad, Xue Hua, Priya Rajagopalan, Arthur W Toga, Clifford R Jack, Michael W Weiner, Greig I de Zubicaray,[...]. Front Neurosci 2012
59
3

Cohort profile: the study of health in Pomerania.
Henry Völzke, Dietrich Alte, Carsten Oliver Schmidt, Dörte Radke, Roberto Lorbeer, Nele Friedrich, Nicole Aumann, Katharina Lau, Michael Piontek, Gabriele Born,[...]. Int J Epidemiol 2011
643
3

Enrichr: interactive and collaborative HTML5 gene list enrichment analysis tool.
Edward Y Chen, Christopher M Tan, Yan Kou, Qiaonan Duan, Zichen Wang, Gabriela Vaz Meirelles, Neil R Clark, Avi Ma'ayan. BMC Bioinformatics 2013
3

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
529
3

A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders.
Sébastien Jacquemont, Bradley P Coe, Micha Hersch, Michael H Duyzend, Niklas Krumm, Sven Bergmann, Jacques S Beckmann, Jill A Rosenfeld, Evan E Eichler. Am J Hum Genet 2014
257
3

Population analysis of large copy number variants and hotspots of human genetic disease.
Andy Itsara, Gregory M Cooper, Carl Baker, Santhosh Girirajan, Jun Li, Devin Absher, Ronald M Krauss, Richard M Myers, Paul M Ridker, Daniel I Chasman,[...]. Am J Hum Genet 2009
419
3

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.
Carolien G F de Kovel, Holger Trucks, Ingo Helbig, Heather C Mefford, Carl Baker, Costin Leu, Christian Kluck, Hiltrud Muhle, Sarah von Spiczak, Philipp Ostertag,[...]. Brain 2010
315
3

Principal components analysis corrects for stratification in genome-wide association studies.
Alkes L Price, Nick J Patterson, Robert M Plenge, Michael E Weinblatt, Nancy A Shadick, David Reich. Nat Genet 2006
3

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Erin L Heinzen, Rodney A Radtke, Thomas J Urban, Gianpiero L Cavalleri, Chantal Depondt, Anna C Need, Nicole M Walley, Paola Nicoletti, Dongliang Ge, Claudia B Catarino,[...]. Am J Hum Genet 2010
176
3

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009.
Anne T Berg, Samuel F Berkovic, Martin J Brodie, Jeffrey Buchhalter, J Helen Cross, Walter van Emde Boas, Jerome Engel, Jacqueline French, Tracy A Glauser, Gary W Mathern,[...]. Epilepsia 2010
3

Copy number variations in neurodevelopmental disorders.
Hannah M Grayton, Cathy Fernandes, Dan Rujescu, David A Collier. Prog Neurobiol 2012
106
3

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
929
3

Accuracy of CNV Detection from GWAS Data.
Dandan Zhang, Yudong Qian, Nirmala Akula, Ney Alliey-Rodriguez, Jinsong Tang, Elliot S Gershon, Chunyu Liu. PLoS One 2011
60
3

Investigation of NRXN1 deletions: clinical and molecular characterization.
Mindy Preston Dabell, Jill A Rosenfeld, Patricia Bader, Luis F Escobar, Dima El-Khechen, Stephanie E Vallee, Mary Beth Palko Dinulos, Cynthia Curry, Jamie Fisher, Raymond Tervo,[...]. Am J Med Genet A 2013
70
3

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
Ingo Helbig, Heather C Mefford, Andrew J Sharp, Michel Guipponi, Marco Fichera, Andre Franke, Hiltrud Muhle, Carolien de Kovel, Carl Baker, Sarah von Spiczak,[...]. Nat Genet 2009
396
3

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance.
Leanne M Dibbens, Saul Mullen, Ingo Helbig, Heather C Mefford, Marta A Bayly, Susannah Bellows, Costin Leu, Holger Trucks, Tanja Obermeier, Michael Wittig,[...]. Hum Mol Genet 2009
165
3

Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption.
Alex R Paciorkowski, Kim Keppler-Noreuil, Luther Robinson, Christopher Sullivan, Samin Sajan, Susan L Christian, Polina Bukshpun, Stacy B Gabriel, Joseph G Gleeson, Elliott H Sherr,[...]. Am J Med Genet A 2013
42
4

The first three mosaic cri du chat syndrome patients with two rearranged cell lines.
C Perfumo, P Cerruti Mainardi, A Calí, G Coucourde, F Zara, S Cavani, J Overhauser, F D Bricarelli, M Pierluigi. J Med Genet 2000
23
8

Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion.
J-S Fang, K-F Lee, C-T Huang, C-L Syu, K-J Yang, L-H Wang, D-L Liao, C-H Chen. Clin Genet 2008
10
20

Whole exome sequencing in females with autism implicates novel and candidate genes.
Merlin G Butler, Syed K Rafi, Waheeda Hossain, Dietrich A Stephan, Ann M Manzardo. Int J Mol Sci 2015
48
4

An association between a dopamine transporter gene (SLC6A3) haplotype and ADHD symptom measures in nonclinical adults.
Janette H S Tong, Tarrant D R Cummins, Beth P Johnson, Leigh-Anne McKinley, Hayley E Pickering, Peter Fanning, Nicole R Stefanac, Daniel P Newman, Ziarih Hawi, Mark A Bellgrove. Am J Med Genet B Neuropsychiatr Genet 2015
11
18

Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bucan, Joseph T Glessner, Brett S Abrahams, Daria Salyakina, Marcin Imielinski, Jonathan P Bradfield, Patrick M A Sleiman,[...]. Nature 2009
667
3

Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p- syndrome.
Hong-Yan Du, Rachel Idol, Sara Robledo, Jennifer Ivanovich, Ping An, Arturo Londono-Vallejo, David B Wilson, Philip J Mason, Monica Bessler. Aging Cell 2007
16
12

[3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].
J LEJEUNE, J LAFOURCADE, R BERGER, J VIALATTE, M BOESWILLWALD, P SERINGE, R TURPIN. C R Hebd Seances Acad Sci 1963
323
3

Novelty seeking and stereotypic activation of behavior in mice with disruption of the Dat1 gene.
Vladimir M Pogorelov, Ramona M Rodriguiz, Megan L Insco, Marc G Caron, William C Wetsel. Neuropsychopharmacology 2005
100
3

Evidence for a distinct region causing a cat-like cry in patients with 5p deletions.
M Gersh, S A Goodart, L M Pasztor, D J Harris, L Weiss, J Overhauser. Am J Hum Genet 1995
71
3

Cadherin-9 regulates synapse-specific differentiation in the developing hippocampus.
Megan E Williams, Scott A Wilke, Anthony Daggett, Elizabeth Davis, Stefanie Otto, Deepak Ravi, Beth Ripley, Eric A Bushong, Mark H Ellisman, Gerd Klein,[...]. Neuron 2011
143
3


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.