A citation-based method for searching scientific literature

Joseph T Glessner, Jin Li, Dai Wang, Michael March, Leandro Lima, Akshatha Desai, Dexter Hadley, Charlly Kao, Raquel E Gur, Nadine Cohen, Patrick M A Sleiman, Qingqin Li, Hakon Hakonarson. Genome Med 2017
Times Cited: 21







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



Times Cited
  Times     Co-cited
Similarity


Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders.
Danijela Krgovic, Nadja Kokalj Vokac, Andreja Zagorac, Hojka Gregoric Kumperscak. Sci Rep 2018
9
66

Dedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilities.
Bradley L Griggs, Sydney Ladd, Robert A Saul, Barbara R DuPont, Anand K Srivastava. Genomics 2008
74
23


Interstitial 9p24.3 deletion involving only DOCK8 and KANK1 genes in two patients with non-overlapping phenotypic traits.
Elisa Tassano, Andrea Accogli, Marco Pavanello, Claudio Bruno, Valeria Capra, Giorgio Gimelli, Cristina Cuoco. Eur J Med Genet 2016
9
44

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
614
14

Refining analyses of copy number variation identifies specific genes associated with developmental delay.
Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers,[...]. Nat Genet 2014
325
14

Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
14

The familial risk of autism.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Henrik Larsson, Christina M Hultman, Abraham Reichenberg. JAMA 2014
485
14

Heritability of autism spectrum disorders: a meta-analysis of twin studies.
Beata Tick, Patrick Bolton, Francesca Happé, Michael Rutter, Frühling Rijsdijk. J Child Psychol Psychiatry 2016
269
14

Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy.
Israela Lerer, Michal Sagi, Vardiella Meiner, Tirza Cohen, Joel Zlotogora, Dvorah Abeliovich. Hum Mol Genet 2005
84
14

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
14

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
516
14

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
14

Mapping a shared genetic basis for neurodevelopmental disorders.
Matthew Jensen, Santhosh Girirajan. Genome Med 2017
13
15

Psychiatric disorders in children with autism spectrum disorders: prevalence, comorbidity, and associated factors in a population-derived sample.
Emily Simonoff, Andrew Pickles, Tony Charman, Susie Chandler, Tom Loucas, Gillian Baird. J Am Acad Child Adolesc Psychiatry 2008
9

Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.
Chia-Lin Yin, Hsin-I Chen, Ling-Hui Li, Yi-Ling Chien, Hsiao-Mei Liao, Miao Chun Chou, Wen-Jiun Chou, Wen-Che Tsai, Yen-Nan Chiu, Yu-Yu Wu,[...]. Mol Autism 2016
36
9

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.
Hui Guo, Yu Peng, Zhengmao Hu, Ying Li, Guanglei Xun, Jianjun Ou, Liangdan Sun, Zhimin Xiong, Yanling Liu, Tianyun Wang,[...]. Sci Rep 2017
21
9


Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders.
Hjördis O Atladóttir, Poul Thorsen, Lars Østergaard, Diana E Schendel, Sanne Lemcke, Morsi Abdallah, Erik T Parner. J Autism Dev Disord 2010
471
9

Characteristics of fetal anticonvulsant syndrome associated autistic disorder.
A D Rasalam, H Hailey, J H G Williams, S J Moore, P D Turnpenny, D J Lloyd, J C S Dean. Dev Med Child Neurol 2005
249
9

Sex differences in the brain: implications for explaining autism.
Simon Baron-Cohen, Rebecca C Knickmeyer, Matthew K Belmonte. Science 2005
516
9

Advances in autism genetics: on the threshold of a new neurobiology.
Brett S Abrahams, Daniel H Geschwind. Nat Rev Genet 2008
9

Most genetic risk for autism resides with common variation.
Trent Gaugler, Lambertus Klei, Stephan J Sanders, Corneliu A Bodea, Arthur P Goldberg, Ann B Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert,[...]. Nat Genet 2014
543
9

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
924
9

The maternal interleukin-17a pathway in mice promotes autism-like phenotypes in offspring.
Gloria B Choi, Yeong S Yim, Helen Wong, Sangdoo Kim, Hyunju Kim, Sangwon V Kim, Charles A Hoeffer, Dan R Littman, Jun R Huh. Science 2016
434
9





A sociability gene? Meta-analysis of oxytocin receptor genotype effects in humans.
Marian J Bakermans-Kranenburg, Marinus H van Ijzendoorn. Psychiatr Genet 2014
133
9

Genetics of autism spectrum disorders.
Daniel H Geschwind. Trends Cogn Sci 2011
313
9

Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder.
Sergio I Nemirovsky, Marta Córdoba, Jonathan J Zaiat, Sabrina P Completa, Patricia A Vega, Dolores González-Morón, Nancy M Medina, Mónica Fabbro, Soledad Romero, Bianca Brun,[...]. PLoS One 2015
32
9

The valproic acid-induced rodent model of autism.
Chiara Nicolini, Margaret Fahnestock. Exp Neurol 2018
145
9



Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorder.
Thorsten M Kranz, Marnie Kopp, Regina Waltes, Michael Sachse, Eftichia Duketis, Tomasz A Jarczok, Franziska Degenhardt, Katharina Görgen, Jobst Meyer, Christine M Freitag,[...]. Autism Res 2016
23
9

Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
9

Maternal immune activation yields offspring displaying mouse versions of the three core symptoms of autism.
Natalia V Malkova, Collin Z Yu, Elaine Y Hsiao, Marlyn J Moore, Paul H Patterson. Brain Behav Immun 2012
344
9

Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints.
Scott Newman, Karen E Hermetz, Brooke Weckselblatt, M Katharine Rudd. Am J Hum Genet 2015
80
9

Familial KANK1 deletion that does not follow expected imprinting pattern.
Rena J Vanzo, Megan M Martin, Mallory R Sdano, Sarah T South. Eur J Med Genet 2013
13
15

Copy number variations in cryptogenic cerebral palsy.
Reeval Segel, Hilla Ben-Pazi, Sharon Zeligson, Aviva Fatal-Valevski, Adi Aran, Varda Gross-Tsur, Nira Schneebaum-Sender, Dorit Shmueli, Dorit Lev, Shira Perlberg,[...]. Neurology 2015
45
9

Combined immunodeficiency associated with DOCK8 mutations.
Qian Zhang, Jeremiah C Davis, Ian T Lamborn, Alexandra F Freeman, Huie Jing, Amanda J Favreau, Helen F Matthews, Joie Davis, Maria L Turner, Gulbu Uzel,[...]. N Engl J Med 2009
436
9

A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation.
Khaled K Abu-Amero, Ali M Hellani, Mustafa A Salih, Mohammad Z Seidahmed, Tageldin S Elmalik, Ghassan Zidan, Thomas M Bosley. BMC Med Genet 2010
27
9

Kank proteins: structure, functions and diseases.
N Kakinuma, Y Zhu, Y Wang, B C Roy, R Kiyama. Cell Mol Life Sci 2009
59
9



Simplified molecular diagnosis of fragile X syndrome by fluorescent methylation-specific PCR and GeneScan analysis.
Youyou Zhou, Josephine M S Lum, Gare-Hoon Yeo, Jennifer Kiing, Stacey K H Tay, Samuel S Chong. Clin Chem 2006
31
9

Dock-family exchange factors in cell migration and disease.
Gilles Gadea, Anne Blangy. Eur J Cell Biol 2014
110
9

Patterns of genic intolerance of rare copy number variation in 59,898 human exomes.
Douglas M Ruderfer, Tymor Hamamsy, Monkol Lek, Konrad J Karczewski, David Kavanagh, Kaitlin E Samocha, Mark J Daly, Daniel G MacArthur, Menachem Fromer, Shaun M Purcell. Nat Genet 2016
108
9



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.