A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Racial and ethnic disparities in awareness of genetic testing for cancer risk.
José A Pagán, Dejun Su, Lifeng Li, Katrina Armstrong, David A Asch. Am J Prev Med 2009
68
25

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
573
25


ZNHIT3 is defective in PEHO syndrome, a severe encephalopathy with cerebellar granule neuron loss.
Anna-Kaisa Anttonen, Anni Laari, Maria Kousi, Yawei J Yang, Tiina Jääskeläinen, Mirja Somer, Eija Siintola, Eveliina Jakkula, Mikko Muona, Saara Tegelberg,[...]. Brain 2017
15
12

Seizure variables and their relationship to genotype and functional abilities in the CDKL5 disorder.
Stephanie Fehr, Kingsley Wong, Richard Chin, Simon Williams, Nick de Klerk, David Forbes, Rahul Krishnaraj, John Christodoulou, Jenny Downs, Helen Leonard. Neurology 2016
45
12



Human iPSC-Derived Cerebral Organoids Model Cellular Features of Lissencephaly and Reveal Prolonged Mitosis of Outer Radial Glia.
Marina Bershteyn, Tomasz J Nowakowski, Alex A Pollen, Elizabeth Di Lullo, Aishwarya Nene, Anthony Wynshaw-Boris, Arnold R Kriegstein. Cell Stem Cell 2017
250
12

Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early death.
Siqi Cao, Laura L Smith, Sergio R Padilla-Lopez, Brandon S Guida, Elizabeth Blume, Jiahai Shi, Sarah U Morton, Catherine A Brownstein, Alan H Beggs, Michael C Kruer,[...]. Hum Mol Genet 2017
17
12

The Human Phenotype Ontology in 2017.
Sebastian Köhler, Nicole A Vasilevsky, Mark Engelstad, Erin Foster, Julie McMurry, Ségolène Aymé, Gareth Baynam, Susan M Bello, Cornelius F Boerkoel, Kym M Boycott,[...]. Nucleic Acids Res 2017
408
12

Variable clinical expression in patients with mosaicism for KCNQ2 mutations.
Mathieu Milh, Caroline Lacoste, Pierre Cacciagli, Affef Abidi, Julie Sutera-Sardo, Ilias Tzelepis, Estelle Colin, Catherine Badens, Alexandra Afenjar, Anne Dieux Coeslier,[...]. Am J Med Genet A 2015
23
12

Neuronal hyperexcitability in a mouse model of SCN8A epileptic encephalopathy.
Luis F Lopez-Santiago, Yukun Yuan, Jacy L Wagnon, Jacob M Hull, Chad R Frasier, Heather A O'Malley, Miriam H Meisler, Lori L Isom. Proc Natl Acad Sci U S A 2017
44
12

Neurodegeneration and Epilepsy in a Zebrafish Model of CLN3 Disease (Batten Disease).
Kim Wager, Anselm A Zdebik, Sonia Fu, Jonathan D Cooper, Robert J Harvey, Claire Russell. PLoS One 2016
21
12

Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits.
Francesco Miceli, Maria Virginia Soldovieri, Paolo Ambrosino, Michela De Maria, Michele Migliore, Rosanna Migliore, Maurizio Taglialatela. J Neurosci 2015
89
12

Low-dose fenfluramine significantly reduces seizure frequency in Dravet syndrome: a prospective study of a new cohort of patients.
A Schoonjans, B P Paelinck, F Marchau, B Gunning, A Gammaitoni, B S Galer, L Lagae, B Ceulemans. Eur J Neurol 2017
55
12

Establishment of isogenic iPSCs from an individual with SCN1A mutation mosaicism as a model for investigating neurocognitive impairment in Dravet syndrome.
Hiroshi Maeda, Tomohiro Chiyonobu, Michiko Yoshida, Satoshi Yamashita, Masashi Zuiki, Satoshi Kidowaki, Kenichi Isoda, Kazuhiro Yamakawa, Masafumi Morimoto, Tatsutoshi Nakahata,[...]. J Hum Genet 2016
13
12

Nav1.2 is expressed in caudal ganglionic eminence-derived disinhibitory interneurons: Mutually exclusive distributions of Nav1.1 and Nav1.2.
Tetsushi Yamagata, Ikuo Ogiwara, Emi Mazaki, Yuchio Yanagawa, Kazuhiro Yamakawa. Biochem Biophys Res Commun 2017
23
12

Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H.
Sarah B Mulkey, Bruria Ben-Zeev, Joost Nicolai, John L Carroll, Sabine Grønborg, Yong-Hui Jiang, Nishtha Joshi, Megan Kelly, David A Koolen, Mohamad A Mikati,[...]. Epilepsia 2017
33
12

Precision therapy for epilepsy due to KCNT1 mutations: A randomized trial of oral quinidine.
Saul A Mullen, Patrick W Carney, Annie Roten, Michael Ching, Paul A Lightfoot, Leonid Churilov, Umesh Nair, Melody Li, Samuel F Berkovic, Steven Petrou,[...]. Neurology 2018
51
12

CDKL5, a novel MYCN-repressed gene, blocks cell cycle and promotes differentiation of neuronal cells.
Emanuele Valli, Stefania Trazzi, Claudia Fuchs, Daniela Erriquez, Renata Bartesaghi, Giovanni Perini, Elisabetta Ciani. Biochim Biophys Acta 2012
20
12

A state-wide initiative to promote genetic testing in an underserved population.
Meghan L Underhill, Traci M Blonquist, Karleen Habin, Debra Lundquist, Kristen Shannon, Kathryn Robinson, Mary-Lou Woodford, Jean Boucher. Cancer Med 2017
6
16


Deep phenotyping for precision medicine.
Peter N Robinson. Hum Mutat 2012
181
12

Sleep impairment and reduced interneuron excitability in a mouse model of Dravet Syndrome.
Franck Kalume, John C Oakley, Ruth E Westenbroek, Jennifer Gile, Horacio O de la Iglesia, Todd Scheuer, William A Catterall. Neurobiol Dis 2015
50
12

High-Throughput Screening Using iPSC-Derived Neuronal Progenitors to Identify Compounds Counteracting Epigenetic Gene Silencing in Fragile X Syndrome.
Markus Kaufmann, Ansgar Schuffenhauer, Isabelle Fruh, Jessica Klein, Anke Thiemeyer, Pierre Rigo, Baltazar Gomez-Mancilla, Valerie Heidinger-Millot, Tewis Bouwmeester, Ulrich Schopfer,[...]. J Biomol Screen 2015
57
12

DNA sequencing: bench to bedside and beyond.
Clyde A Hutchison. Nucleic Acids Res 2007
106
12


Microarray Noninvasive Neuronal Seizure Recordings from Intact Larval Zebrafish.
Michaela Meyer, Sameer C Dhamne, Christopher M LaCoursiere, Dimira Tambunan, Annapurna Poduri, Alexander Rotenberg. PLoS One 2016
14
12

Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy.
Amy McTague, Umesh Nair, Sony Malhotra, Esther Meyer, Natalie Trump, Elena V Gazina, Apostolos Papandreou, Adeline Ngoh, Sally Ackermann, Gautam Ambegaonkar,[...]. Neurology 2018
42
12

Recurrent mutations in the CDKL5 gene: genotype-phenotype relationships.
Nadia Bahi-Buisson, Nathalie Villeneuve, Emilie Caietta, Aurélia Jacquette, Helene Maurey, Gert Matthijs, Hilde Van Esch, Andrée Delahaye, Anne Moncla, Mathieu Milh,[...]. Am J Med Genet A 2012
31
12

Transcriptional landscape of a RETC634Y-mutated iPSC and its CRISPR-corrected isogenic control reveals the putative role of EGR1 transcriptional program in the development of multiple endocrine neoplasia type 2A-associated cancers.
Julien Hadoux, Christophe Desterke, Olivier Féraud, Mathieu Guibert, Roberta Francesca De Rose, Paule Opolon, Dominique Divers, Emilie Gobbo, Frank Griscelli, Martin Schlumberger,[...]. Stem Cell Res 2018
10
12

Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A.
Maria Virginia Soldovieri, Nadia Boutry-Kryza, Mathieu Milh, Diane Doummar, Benedicte Heron, Emilie Bourel, Paolo Ambrosino, Francesco Miceli, Michela De Maria, Nathalie Dorison,[...]. Hum Mutat 2014
54
12

Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy.
Federico Sicca, Elena Ambrosini, Maria Marchese, Luigi Sforna, Ilenio Servettini, Giulia Valvo, Maria Stefania Brignone, Angela Lanciotti, Francesca Moro, Alessandro Grottesi,[...]. Sci Rep 2016
41
12

Induction of pluripotent stem cells from adult human fibroblasts by defined factors.
Kazutoshi Takahashi, Koji Tanabe, Mari Ohnuki, Megumi Narita, Tomoko Ichisaka, Kiichiro Tomoda, Shinya Yamanaka. Cell 2007
12

hVGAT-mCherry: A novel molecular tool for analysis of GABAergic neurons derived from human pluripotent stem cells.
Brooke A DeRosa, Kinsley C Belle, Blake J Thomas, Holly N Cukier, Margaret A Pericak-Vance, Jeffery M Vance, Derek M Dykxhoorn. Mol Cell Neurosci 2015
12
12


Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome.
Moran Rubinstein, Ruth E Westenbroek, Frank H Yu, Christina J Jones, Todd Scheuer, William A Catterall. Neurobiol Dis 2015
47
12

Characterisation of CDKL5 Transcript Isoforms in Human and Mouse.
Ralph D Hector, Owen Dando, Nicoletta Landsberger, Charlotte Kilstrup-Nielsen, Peter C Kind, Mark E S Bailey, Stuart R Cobb. PLoS One 2016
30
12

CDKL5 ensures excitatory synapse stability by reinforcing NGL-1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons.
Sara Ricciardi, Federica Ungaro, Melanie Hambrock, Nils Rademacher, Gilda Stefanelli, Dario Brambilla, Alessandro Sessa, Cinzia Magagnotti, Angela Bachi, Elisa Giarda,[...]. Nat Cell Biol 2012
163
12


Disparities in genetics assessment for women with ovarian cancer: Can we do better?
Erica Manrriquez, Jocelyn S Chapman, Julie Mak, Amie M Blanco, Lee-May Chen. Gynecol Oncol 2018
25
12

Generation of the SCN1A epilepsy mutation in hiPS cells using the TALEN technique.
Wanjuan Chen, Jingxin Liu, Longmei Zhang, Huijuan Xu, Xiaogang Guo, Sihao Deng, Lipeng Liu, Daiguan Yu, Yonglong Chen, Zhiyuan Li. Sci Rep 2014
15
12

Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant.
John J Millichap, Francesco Miceli, Michela De Maria, Cynthia Keator, Nishtha Joshi, Baouyen Tran, Maria Virginia Soldovieri, Paolo Ambrosino, Vandana Shashi, Mohamad A Mikati,[...]. Epilepsia 2017
37
12

Rapid Generation of Human Genetic Loss-of-Function iPSC Lines by Simultaneous Reprogramming and Gene Editing.
Andrew M Tidball, Louis T Dang, Trevor W Glenn, Emma G Kilbane, Daniel J Klarr, Joshua L Margolis, Michael D Uhler, Jack M Parent. Stem Cell Reports 2017
17
12

Axonal Kv7.2/7.3 channels: caught in the act.
Maarten H P Kole, Edward C Cooper. Channels (Austin) 2014
4
25


Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.
Linda S Weaving, John Christodoulou, Sarah L Williamson, Kathie L Friend, Olivia L D McKenzie, Hayley Archer, Julie Evans, Angus Clarke, Gregory J Pelka, Patrick P L Tam,[...]. Am J Hum Genet 2004
319
12

Metabolic Dysfunction and Oxidative Stress in Epilepsy.
Jennifer N Pearson-Smith, Manisha Patel. Int J Mol Sci 2017
91
12

Developmental changes in KCNQ2 and KCNQ3 expression in human brain: possible contribution to the age-dependent etiology of benign familial neonatal convulsions.
Takeshi Kanaumi, Sachio Takashima, Hiroshi Iwasaki, Masayuki Itoh, Akihisa Mitsudome, Shinichi Hirose. Brain Dev 2008
44
12

The intolerance to functional genetic variation of protein domains predicts the localization of pathogenic mutations within genes.
Ayal B Gussow, Slavé Petrovski, Quanli Wang, Andrew S Allen, David B Goldstein. Genome Biol 2016
74
12


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.