A citation-based method for searching scientific literature

Juliann M Savatt, Scott M Myers. Front Pediatr 2021
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders.
Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, David H Ledbetter, Christa L Martin, Wendy K Chung, Helen V Firth, Thomas Frazier, Robin L Hansen, Lisa Prock,[...]. Genet Med 2019
98
80

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
920
40


Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
310
40


A Causal and Mediation Analysis of the Comorbidity Between Attention Deficit Hyperactivity Disorder (ADHD) and Autism Spectrum Disorder (ASD).
Elena Sokolova, Anoek M Oerlemans, Nanda N Rommelse, Perry Groot, Catharina A Hartman, Jeffrey C Glennon, Tom Claassen, Tom Heskes, Jan K Buitelaar. J Autism Dev Disord 2017
43
20

Insufficient Evidence for "Autism-Specific" Genes.
Scott M Myers, Thomas D Challman, Raphael Bernier, Thomas Bourgeron, Wendy K Chung, John N Constantino, Evan E Eichler, Sebastien Jacquemont, David T Miller, Kevin J Mitchell,[...]. Am J Hum Genet 2020
24
20

ClinVar: improvements to accessing data.
Melissa J Landrum, Shanmuga Chitipiralla, Garth R Brown, Chao Chen, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang, Kuljeet Kaur, Chunlei Liu,[...]. Nucleic Acids Res 2020
61
20

A large data resource of genomic copy number variation across neurodevelopmental disorders.
Mehdi Zarrei, Christie L Burton, Worrawat Engchuan, Edwin J Young, Edward J Higginbotham, Jeffrey R MacDonald, Brett Trost, Ada J S Chan, Susan Walker, Sylvia Lamoureux,[...]. NPJ Genom Med 2019
31
20

The Heritability of Autism Spectrum Disorder.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Christina Hultman, Henrik Larsson, Abraham Reichenberg. JAMA 2017
183
20

Analysis of shared heritability in common disorders of the brain.
Verneri Anttila, Brendan Bulik-Sullivan, Hilary K Finucane, Raymond K Walters, Jose Bras, Laramie Duncan, Valentina Escott-Price, Guido J Falcone, Padhraig Gormley, Rainer Malik,[...]. Science 2018
622
20

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
20

SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse.
Frank Koopmans, Pim van Nierop, Maria Andres-Alonso, Andrea Byrnes, Tony Cijsouw, Marcelo P Coba, L Niels Cornelisse, Ryan J Farrell, Hana L Goldschmidt, Daniel P Howrigan,[...]. Neuron 2019
79
20

The familial risk of autism.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Henrik Larsson, Christina M Hultman, Abraham Reichenberg. JAMA 2014
482
20

Prevalence and cumulative incidence of autism spectrum disorders and the patterns of co-occurring neurodevelopmental disorders in a total population sample of 5-year-old children.
Manabu Saito, Tomoya Hirota, Yui Sakamoto, Masaki Adachi, Michio Takahashi, Ayako Osato-Kaneda, Young Shin Kim, Bennett Leventhal, Amy Shui, Sumi Kato,[...]. Mol Autism 2020
15
20

The prevalence of psychiatric disorders among students aged 6~ 16 years old in central Hunan, China.
Yan-Mei Shen, Bella Siu Man Chan, Jian-Bo Liu, Yuan-Yue Zhou, Xi-Long Cui, Yu-Qiong He, Yu-Min Fang, Yu-Tao Xiang, Xue-Rong Luo. BMC Psychiatry 2018
14
20

Lafora progressive Myoclonus Epilepsy mutation database-EPM2A and NHLRC1 (EPM2B) genes.
Leonarda Ianzano, Junjun Zhang, Elayne M Chan, Xiao-Chu Zhao, Hannes Lohi, Stephen W Scherer, Berge A Minassian. Hum Mutat 2005
35
20

Prevalence and Trends of Developmental Disabilities among Children in the United States: 2009-2017.
Benjamin Zablotsky, Lindsey I Black, Matthew J Maenner, Laura A Schieve, Melissa L Danielson, Rebecca H Bitsko, Stephen J Blumberg, Michael D Kogan, Coleen A Boyle. Pediatrics 2019
124
20

Prevalence of autism spectrum disorders in an Icelandic birth cohort.
Evald Saemundsen, Páll Magnússon, Ingibjörg Georgsdóttir, Erlendur Egilsson, Vilhjálmur Rafnsson. BMJ Open 2013
50
20

Epidemiology and classification of epilepsy: gender comparisons.
John C McHugh, Norman Delanty. Int Rev Neurobiol 2008
69
20

A Cross-Disorder Method to Identify Novel Candidate Genes for Developmental Brain Disorders.
Andrea J Gonzalez-Mantilla, Andres Moreno-De-Luca, David H Ledbetter, Christa Lese Martin. JAMA Psychiatry 2016
59
20


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
262
20

Prevalence of autism-spectrum conditions: UK school-based population study.
Simon Baron-Cohen, Fiona J Scott, Carrie Allison, Joanna Williams, Patrick Bolton, Fiona E Matthews, Carol Brayne. Br J Psychiatry 2009
385
20

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.
Jack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, Stephan J Sanders, Kamil Slowikowski, Monkol Lek, Konrad J Karczewski, David J Cutler, Bernie Devlin, Kathryn Roeder,[...]. Nat Genet 2017
152
20


Neurodevelopmental disorders: prevalence and comorbidity in children referred to mental health services.
Berit Hjelde Hansen, Beate Oerbeck, Benedicte Skirbekk, Beáta Éva Petrovski, Hanne Kristensen. Nord J Psychiatry 2018
25
20

Autism spectrum disorders in the Stockholm Youth Cohort: design, prevalence and validity.
Selma Idring, Dheeraj Rai, Henrik Dal, Christina Dalman, Harald Sturm, Eric Zander, Brian K Lee, Eva Serlachius, Cecilia Magnusson. PLoS One 2012
149
20

Epilepsy-associated genes.
Jie Wang, Zhi-Jian Lin, Liu Liu, Hai-Qing Xu, Yi-Wu Shi, Yong-Hong Yi, Na He, Wei-Ping Liao. Seizure 2017
117
20

Describing the genetic architecture of epilepsy through heritability analysis.
Doug Speed, Terence J O'Brien, Aarno Palotie, Kirill Shkura, Anthony G Marson, David J Balding, Michael R Johnson. Brain 2014
50
20

Tiered analysis of whole-exome sequencing for epilepsy diagnosis.
Paul J Dunn, Bridget H Maher, Cassie L Albury, Shani Stuart, Heidi G Sutherland, Neven Maksemous, Miles C Benton, Robert A Smith, Larisa M Haupt, Lyn R Griffiths. Mol Genet Genomics 2020
3
33


Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.
Korinna Kochinke, Christiane Zweier, Bonnie Nijhof, Michaela Fenckova, Pavel Cizek, Frank Honti, Shivakumar Keerthikumar, Merel A W Oortveld, Tjitske Kleefstra, Jamie M Kramer,[...]. Am J Hum Genet 2016
116
20

Human disease genes website series: An international, open and dynamic library for up-to-date clinical information.
Alexander J M Dingemans, Diante E Stremmelaar, Lisenka E L M Vissers, Sandra Jansen, Maria J Nabais Sá, Angela van Remortele, Noraly Jonis, Kim Truijen, Sam van de Ven, Jeroen Ewals,[...]. Am J Med Genet A 2021
2
50


SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).
Brett S Abrahams, Dan E Arking, Daniel B Campbell, Heather C Mefford, Eric M Morrow, Lauren A Weiss, Idan Menashe, Tim Wadkins, Sharmila Banerjee-Basu, Alan Packer. Mol Autism 2013
250
20

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources.
Da Wei Huang, Brad T Sherman, Richard A Lempicki. Nat Protoc 2009
20

Etiology of Autism Spectrum Disorders and Autistic Traits Over Time.
Mark J Taylor, Mina A Rosenqvist, Henrik Larsson, Christopher Gillberg, Brian M D'Onofrio, Paul Lichtenstein, Sebastian Lundström. JAMA Psychiatry 2020
13
20

Genetic and environmental factors in epilepsy: a population-based study of 11900 Danish twin pairs.
M J Kjeldsen, K O Kyvik, K Christensen, M L Friis. Epilepsy Res 2001
62
20


Analytical approaches to RNA profiling data for the identification of genes enriched in specific cells.
Joseph D Dougherty, Eric F Schmidt, Miho Nakajima, Nathaniel Heintz. Nucleic Acids Res 2010
139
20

Evidence for 28 genetic disorders discovered by combining healthcare and research data.
Joanna Kaplanis, Kaitlin E Samocha, Laurens Wiel, Zhancheng Zhang, Kevin J Arvai, Ruth Y Eberhardt, Giuseppe Gallone, Stefan H Lelieveld, Hilary C Martin, Jeremy F McRae,[...]. Nature 2020
36
20


Identification of epilepsy-associated neuronal subtypes and gene expression underlying epileptogenesis.
Ulrich Pfisterer, Viktor Petukhov, Samuel Demharter, Johanna Meichsner, Jonatan J Thompson, Mykhailo Y Batiuk, Andrea Asenjo-Martinez, Navneet A Vasistha, Ashish Thakur, Jens Mikkelsen,[...]. Nat Commun 2020
10
20


Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
20


Mutations in RAI1 associated with Smith-Magenis syndrome.
Rebecca E Slager, Tiffany Lynn Newton, Christopher N Vlangos, Brenda Finucane, Sarah H Elsea. Nat Genet 2003
202
20

Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases.
E A Edelman, S Girirajan, B Finucane, P I Patel, J R Lupski, A C M Smith, S H Elsea. Clin Genet 2007
88
20

Evolution of genetic techniques: past, present, and beyond.
Asude Alpman Durmaz, Emin Karaca, Urszula Demkow, Gokce Toruner, Jacqueline Schoumans, Ozgur Cogulu. Biomed Res Int 2015
25
20


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.