A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
66

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
66


Systematic reanalysis of clinical exome data yields additional diagnoses: implications for providers.
Aaron M Wenger, Harendra Guturu, Jonathan A Bernstein, Gill Bejerano. Genet Med 2017
140
33

Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome.
John C Mulley, Bree Hodgson, Jacinta M McMahon, Xenia Iona, Susannah Bellows, Saul A Mullen, Kevin Farrell, Mark Mackay, Lynette Sadleir, Andrew Bleasel,[...]. Epilepsia 2013
41
33

Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsy.
Piero Perucca, Ingrid E Scheffer, A Simon Harvey, Paul A James, Sebastian Lunke, Natalie Thorne, Clara Gaff, Brigid M Regan, John A Damiano, Michael S Hildebrand,[...]. Epilepsy Res 2017
53
33

Utility of genetic testing for therapeutic decision-making in adults with epilepsy.
Katrine M Johannesen, Natalya Nikanorova, Dragan Marjanovic, Agnieszka Pavbro, Line H G Larsen, Guido Rubboli, Rikke S Møller. Epilepsia 2020
17
33


Epilepsy genetics: Current knowledge, applications, and future directions.
K A Myers, D L Johnstone, D A Dyment. Clin Genet 2019
44
33


Diagnostic Yield From 339 Epilepsy Patients Screened on a Clinical Gene Panel.
Kameryn M Butler, Cristina da Silva, John J Alexander, Madhuri Hegde, Andrew Escayg. Pediatr Neurol 2017
36
33

Novel mutation of SCN9A gene causing generalized epilepsy with febrile seizures plus in a Chinese family.
Tian Zhang, Mingwu Chen, Angang Zhu, Xiaoguang Zhang, Tao Fang. Neurol Sci 2020
6
33

Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG).
Joshua L Deignan, Wendy K Chung, Hutton M Kearney, Kristin G Monaghan, Catherine W Rehder, Elizabeth C Chao. Genet Med 2019
40
33

Advancing epilepsy genetics in the genomic era.
Candace T Myers, Heather C Mefford. Genome Med 2015
100
33

Advances in genetic testing and optimization of clinical management in children and adults with epilepsy.
Marcello Scala, Amedeo Bianchi, Francesca Bisulli, Antonietta Coppola, Maurizio Elia, Marina Trivisano, Dario Pruna, Tommaso Pippucci, Laura Canafoglia, Simona Lattanzi,[...]. Expert Rev Neurother 2020
15
33

Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.
Xing-Xing Xu, Xiao-Rong Liu, Cui-Ying Fan, Jin-Xing Lai, Yi-Wu Shi, Wei Yang, Tao Su, Jun-Yu Xu, Jian-Hong Luo, Wei-Ping Liao. Neurosci Bull 2018
9
33

Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort.
Anne Rochtus, Heather E Olson, Lacey Smith, Louisa G Keith, Christelle El Achkar, Alan Taylor, Sonal Mahida, Meredith Park, McKenna Kelly, Catherine Shain,[...]. Epilepsia 2020
25
33

Early-Life Epilepsies and the Emerging Role of Genetic Testing.
Anne T Berg, Jason Coryell, Russell P Saneto, Zachary M Grinspan, John J Alexander, Mariana Kekis, Joseph E Sullivan, Elaine C Wirrell, Renée A Shellhaas, John R Mytinger,[...]. JAMA Pediatr 2017
74
33

Clinical utility of multigene panel testing in adults with epilepsy and intellectual disability.
Felippe Borlot, Bruno Ivo de Almeida, Shari L Combe, Danielle M Andrade, Francis M Filloux, Kenneth A Myers. Epilepsia 2019
15
33

Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes.
Paul Dunn, Cassie L Albury, Neven Maksemous, Miles C Benton, Heidi G Sutherland, Robert A Smith, Larisa M Haupt, Lyn R Griffiths. Front Genet 2018
44
33

The role of nicotinic acetylcholine receptors in autosomal dominant nocturnal frontal lobe epilepsy.
Andrea Becchetti, Patrizia Aracri, Simone Meneghini, Simone Brusco, Alida Amadeo. Front Physiol 2015
55
33

Clinical Utility of Reinterpreting Previously Reported Genomic Epilepsy Test Results for Pediatric Patients.
Jeffrey A SoRelle, Drew M Thodeson, Susan Arnold, Garrett Gotway, Jason Y Park. JAMA Pediatr 2019
21
33

The Genetics of Epilepsy.
Piero Perucca, Melanie Bahlo, Samuel F Berkovic. Annu Rev Genomics Hum Genet 2020
16
33

The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric Patients.
Davide Mei, Elena Parrini, Carla Marini, Renzo Guerrini. Mol Diagn Ther 2017
30
33


Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis.
Sophie Nambot, Julien Thevenon, Paul Kuentz, Yannis Duffourd, Emilie Tisserant, Ange-Line Bruel, Anne-Laure Mosca-Boidron, Alice Masurel-Paulet, Daphné Lehalle, Nolwenn Jean-Marçais,[...]. Genet Med 2018
84
33

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
Ingrid E Scheffer, Samuel Berkovic, Giuseppe Capovilla, Mary B Connolly, Jacqueline French, Laura Guilhoto, Edouard Hirsch, Satish Jain, Gary W Mathern, Solomon L Moshé,[...]. Epilepsia 2017
33

A novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes.
Ann J Johnston, Jing-Qiong Kang, Wangzhen Shen, William O Pickrell, Thomas D Cushion, Jeffrey S Davies, Kristin Baer, Jonathan G L Mullins, Carrie L Hammond, Seo-Kyung Chung,[...]. Neurobiol Dis 2014
24
33


Prevalence and incidence of epilepsy: A systematic review and meta-analysis of international studies.
Kirsten M Fiest, Khara M Sauro, Samuel Wiebe, Scott B Patten, Churl-Su Kwon, Jonathan Dykeman, Tamara Pringsheim, Diane L Lorenzetti, Nathalie Jetté. Neurology 2017
464
33

Epilepsy and developmental disorders: Next generation sequencing in the clinic.
Joseph D Symonds, Amy McTague. Eur J Paediatr Neurol 2020
25
33


Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.
Johannes R Lemke, Dennis Lal, Eva M Reinthaler, Isabelle Steiner, Michael Nothnagel, Michael Alber, Kirsten Geider, Bodo Laube, Michael Schwake, Katrin Finsterwalder,[...]. Nat Genet 2013
249
33

A systematic approach to assessing the clinical significance of genetic variants.
H Duzkale, J Shen, H McLaughlin, A Alfares, M A Kelly, T J Pugh, B H Funke, H L Rehm, M S Lebo. Clin Genet 2013
110
33

Seizures and enhanced cortical GABAergic inhibition in two mouse models of human autosomal dominant nocturnal frontal lobe epilepsy.
Alwin Klaassen, Joseph Glykys, Jamie Maguire, Cesar Labarca, Istvan Mody, Jim Boulter. Proc Natl Acad Sci U S A 2006
139
33

Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits.
Maryam Al-Nabhani, Samiya Al-Rashdi, Fathiya Al-Murshedi, Adila Al-Kindi, Khalid Al-Thihli, Abeer Al-Saegh, Amna Al-Futaisi, Watfa Al-Mamari, Fahad Zadjali, Almundher Al-Maawali. Clin Genet 2018
27
33

Definition and diagnostic criteria of sleep-related hypermotor epilepsy.
Paolo Tinuper, Francesca Bisulli, J H Cross, Dale Hesdorffer, Philippe Kahane, Lino Nobili, Federica Provini, Ingrid E Scheffer, Laura Tassi, Luca Vignatelli,[...]. Neurology 2016
114
33

One gene, many neuropsychiatric disorders: lessons from Mendelian diseases.
Xiaolin Zhu, Anna C Need, Slavé Petrovski, David B Goldstein. Nat Neurosci 2014
78
33


Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment.
P Burda, A Kuster, O Hjalmarson, T Suormala, C Bürer, S Lutz, G Roussey, L Christa, J Asin-Cayuela, G Kollberg,[...]. J Inherit Metab Dis 2015
23
33

Insights into genetics, human biology and disease gleaned from family based genomic studies.
Jennifer E Posey, Anne H O'Donnell-Luria, Jessica X Chong, Tamar Harel, Shalini N Jhangiani, Zeynep H Coban Akdemir, Steven Buyske, Davut Pehlivan, Claudia M B Carvalho, Samantha Baxter,[...]. Genet Med 2019
71
33

Next-generation diagnostics and disease-gene discovery with the Exomiser.
Damian Smedley, Julius O B Jacobsen, Marten Jäger, Sebastian Köhler, Manuel Holtgrewe, Max Schubach, Enrico Siragusa, Tomasz Zemojtel, Orion J Buske, Nicole L Washington,[...]. Nat Protoc 2015
112
33

The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation.
Violeta Muñoz-Fuentes, Pilar Cacheiro, Terrence F Meehan, Juan Antonio Aguilar-Pimentel, Steve D M Brown, Ann M Flenniken, Paul Flicek, Antonella Galli, Hamed Haseli Mashhadi, Martin Hrabě de Angelis,[...]. Conserv Genet 2018
36
33

Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency.
William P Bone, Nicole L Washington, Orion J Buske, David R Adams, Joie Davis, David Draper, Elise D Flynn, Marta Girdea, Rena Godfrey, Gretchen Golas,[...]. Genet Med 2016
56
33

Phevor combines multiple biomedical ontologies for accurate identification of disease-causing alleles in single individuals and small nuclear families.
Marc V Singleton, Stephen L Guthery, Karl V Voelkerding, Karin Chen, Brett Kennedy, Rebecca L Margraf, Jacob Durtschi, Karen Eilbeck, Martin G Reese, Lynn B Jorde,[...]. Am J Hum Genet 2014
108
33


Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.
Allison A Regier, Yossi Farjoun, David E Larson, Olga Krasheninina, Hyun Min Kang, Daniel P Howrigan, Bo-Juen Chen, Manisha Kher, Eric Banks, Darren C Ames,[...]. Nat Commun 2018
57
33

The knockout mouse project.
Christopher P Austin, James F Battey, Allan Bradley, Maja Bucan, Mario Capecchi, Francis S Collins, William F Dove, Geoffrey Duyk, Susan Dymecki, Janan T Eppig,[...]. Nat Genet 2004
416
33

The NIH Roadmap Epigenomics Mapping Consortium.
Bradley E Bernstein, John A Stamatoyannopoulos, Joseph F Costello, Bing Ren, Aleksandar Milosavljevic, Alexander Meissner, Manolis Kellis, Marco A Marra, Arthur L Beaudet, Joseph R Ecker,[...]. Nat Biotechnol 2010
33

Genomic Data Sharing for Novel Mendelian Disease Gene Discovery: The Matchmaker Exchange.
Danielle R Azzariti, Ada Hamosh. Annu Rev Genomics Hum Genet 2020
7
33


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.