A citation-based method for searching scientific literature

Yumi Ueki, Grisela Ramirez, Ernesto Salcedo, Maureen E Stabio, Frances Lefcort. eNeuro 2016
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


A neuron autonomous role for the familial dysautonomia gene ELP1 in sympathetic and sensory target tissue innervation.
Marisa Z Jackson, Katherine A Gruner, Charles Qin, Warren G Tourtellotte. Development 2014
40
58

Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia.
S A Slaugenhaupt, A Blumenfeld, S P Gill, M Leyne, J Mull, M P Cuajungco, C B Liebert, B Chadwick, M Idelson, L Reznik,[...]. Am J Hum Genet 2001
411
58

Familial dysautonomia: History, genotype, phenotype and translational research.
Lucy Norcliffe-Kaufmann, Susan A Slaugenhaupt, Horacio Kaufmann. Prog Neurobiol 2017
54
50

A Dynamic Unfolded Protein Response Contributes to the Control of Cortical Neurogenesis.
Sophie Laguesse, Catherine Creppe, Danny D Nedialkova, Pierre-Paul Prévot, Laurence Borgs, Sandra Huysseune, Bénédicte Franco, Guérin Duysens, Nathalie Krusy, Gabsang Lee,[...]. Dev Cell 2015
110
50

Familial dysautonomia is caused by mutations of the IKAP gene.
S L Anderson, R Coli, I W Daly, E A Kichula, M J Rork, S A Volpi, J Ekstein, B Y Rubin. Am J Hum Genet 2001
301
50

Selective retinal ganglion cell loss in familial dysautonomia.
Carlos E Mendoza-Santiesteban, Thomas R Hedges Iii, Lucy Norcliffe-Kaufmann, Felicia Axelrod, Horacio Kaufmann. J Neurol 2014
20
41

Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).
Lisa J Strug, Tara Clarke, Theodore Chiang, Minchen Chien, Zeynep Baskurt, Weili Li, Ruslan Dorfman, Bhavna Bali, Elaine Wirrell, Steven L Kugler,[...]. Eur J Hum Genet 2009
130
41

Tissue-specific reduction in splicing efficiency of IKBKAP due to the major mutation associated with familial dysautonomia.
Math P Cuajungco, Maire Leyne, James Mull, Sandra P Gill, Weining Lu, David Zagzag, Felicia B Axelrod, Channa Maayan, James F Gusella, Susan A Slaugenhaupt. Am J Hum Genet 2003
95
41

Familial dysautonomia model reveals Ikbkap deletion causes apoptosis of Pax3+ progenitors and peripheral neurons.
Lynn George, Marta Chaverra, Lindsey Wolfe, Julian Thorne, Mattheson Close-Davis, Amy Eibs, Vickie Riojas, Andrea Grindeland, Miranda Orr, George A Carlson,[...]. Proc Natl Acad Sci U S A 2013
40
41

Clinical neuro-ophthalmic findings in familial dysautonomia.
Carlos E Mendoza-Santiesteban, Thomas R Hedges, Lucy Norcliffe-Kaufmann, Floyd Warren, Shantan Reddy, Felicia B Axelrod, Horacio Kaufmann. J Neuroophthalmol 2012
27
41

Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration.
Claire L Simpson, Robin Lemmens, Katarzyna Miskiewicz, Wendy J Broom, Valerie K Hansen, Paul W J van Vught, John E Landers, Peter Sapp, Ludo Van Den Bosch, Joanne Knight,[...]. Hum Mol Genet 2009
182
41

ELP2 is a novel gene implicated in neurodevelopmental disabilities.
Julie S Cohen, Siddharth Srivastava, Kelly D Farwell, Hsiao-Mei Lu, Wenqi Zeng, Hong Lu, Elizabeth C Chao, Ali Fatemi. Am J Med Genet A 2015
41
41

IKAP/Elp1 is required in vivo for neurogenesis and neuronal survival, but not for neural crest migration.
Barbara J Hunnicutt, Marta Chaverra, Lynn George, Frances Lefcort. PLoS One 2012
25
41

The familial dysautonomia disease gene IKBKAP is required in the developing and adult mouse central nervous system.
Marta Chaverra, Lynn George, Marc Mergy, Hannah Waller, Katharine Kujawa, Connor Murnion, Ezekiel Sharples, Julian Thorne, Nathaniel Podgajny, Andrea Grindeland,[...]. Dis Model Mech 2017
17
41

Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy.
Eva M Reinthaler, Dennis Lal, Wiktor Jurkowski, Martha Feucht, Hannelore Steinböck, Ursula Gruber-Sedlmayr, Gabriel M Ronen, Julia Geldner, Edda Haberlandt, Birgit Neophytou,[...]. Epilepsia 2014
40
33

Familial Dysautonomia: Mechanisms and Models.
Paula Dietrich, Ioannis Dragatsis. Genet Mol Biol 2016
15
33

Familial dysautonomia (FD) patients have reduced levels of the modified wobble nucleoside mcm(5)s(2)U in tRNA.
Tony Karlsborn, Hasan Tükenmez, Changchun Chen, Anders S Byström. Biochem Biophys Res Commun 2014
53
33

Elevated levels of two tRNA species bypass the requirement for elongator complex in transcription and exocytosis.
Anders Esberg, Bo Huang, Marcus J O Johansson, Anders S Byström. Mol Cell 2006
207
33

Elongator controls the migration and differentiation of cortical neurons through acetylation of alpha-tubulin.
Catherine Creppe, Lina Malinouskaya, Marie-Laure Volvert, Magali Gillard, Pierre Close, Olivier Malaise, Sophie Laguesse, Isabelle Cornez, Souad Rahmouni, Sandra Ormenese,[...]. Cell 2009
333
33

Genome-wide analysis of familial dysautonomia and kinetin target genes with patient olfactory ecto-mesenchymal stem cells.
Nathalie Boone, Aurélie Bergon, Béatrice Loriod, Arnaud Devèze, Catherine Nguyen, Felicia B Axelrod, El Chérif Ibrahim. Hum Mutat 2012
20
33

Rectifier of aberrant mRNA splicing recovers tRNA modification in familial dysautonomia.
Mayumi Yoshida, Naoyuki Kataoka, Kenjyo Miyauchi, Kenji Ohe, Kei Iida, Suguru Yoshida, Takayuki Nojima, Yukiko Okuno, Hiroshi Onogi, Tomomi Usui,[...]. Proc Natl Acad Sci U S A 2015
59
33

Sensory and autonomic deficits in a new humanized mouse model of familial dysautonomia.
Elisabetta Morini, Paula Dietrich, Monica Salani, Heather M Downs, Gregory R Wojtkiewicz, Shanta Alli, Anthony Brenner, Mats Nilbratt, John W LeClair, Anne Louise Oaklander,[...]. Hum Mol Genet 2016
22
33

Loss of mouse Ikbkap, a subunit of elongator, leads to transcriptional deficits and embryonic lethality that can be rescued by human IKBKAP.
Yei-Tsung Chen, Matthew M Hims, Ranjit S Shetty, James Mull, Lijuan Liu, Maire Leyne, Susan A Slaugenhaupt. Mol Cell Biol 2009
80
33

Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.
Laura Addis, Joo Wook Ahn, Richard Dobson, Abhishek Dixit, Caroline M Ogilvie, Dalila Pinto, Andrea K Vaags, Hilary Coon, Pauline Chaste, Scott Wilson,[...]. Hum Mutat 2015
21
33

IKAP expression levels modulate disease severity in a mouse model of familial dysautonomia.
Paula Dietrich, Shanta Alli, Revathi Shanmugasundaram, Ioannis Dragatsis. Hum Mol Genet 2012
32
33

Familial Dysautonomia (FD) Human Embryonic Stem Cell Derived PNS Neurons Reveal that Synaptic Vesicular and Neuronal Transport Genes Are Directly or Indirectly Affected by IKBKAP Downregulation.
Sharon Lefler, Malkiel A Cohen, Gal Kantor, David Cheishvili, Aviel Even, Anastasya Birger, Tikva Turetsky, Yaniv Gil, Sharona Even-Ram, Einat Aizenman,[...]. PLoS One 2015
13
33

Phosphatidylserine Ameliorates Neurodegenerative Symptoms and Enhances Axonal Transport in a Mouse Model of Familial Dysautonomia.
Shiran Naftelberg, Ziv Abramovitch, Shani Gluska, Sivan Yannai, Yuvraj Joshi, Maya Donyo, Keren Ben-Yaakov, Tal Gradus, Jonathan Zonszain, Chen Farhy,[...]. PLoS Genet 2016
18
33

Involvement of IKAP in peripheral target innervation and in specific JNK and NGF signaling in developing PNS neurons.
Anastasia Abashidze, Veronica Gold, Yaron Anavi, Hayit Greenspan, Miguel Weil. PLoS One 2014
21
33

Transcription impairment and cell migration defects in elongator-depleted cells: implication for familial dysautonomia.
Pierre Close, Nicola Hawkes, Isabelle Cornez, Catherine Creppe, Charles A Lambert, Bernard Rogister, Ulrich Siebenlist, Marie-Paule Merville, Susan A Slaugenhaupt, Vincent Bours,[...]. Mol Cell 2006
150
33

Anatomy and spatial organization of Müller glia in mouse retina.
Jingjing Wang, Matthew L O'Sullivan, Dibyendu Mukherjee, Vanessa M Puñal, Sina Farsiu, Jeremy N Kay. J Comp Neurol 2017
30
33

Ikbkap/Elp1 deficiency causes male infertility by disrupting meiotic progression.
Fu-Jung Lin, Li Shen, Chuan-Wei Jang, Pål Ø Falnes, Yi Zhang. PLoS Genet 2013
38
25

Can loss of muscle spindle afferents explain the ataxic gait in Riley-Day syndrome?
Vaughan G Macefield, Lucy Norcliffe-Kaufmann, Joel Gutiérrez, Felicia B Axelrod, Horacio Kaufmann. Brain 2011
39
25

Neuroimaging supports central pathology in familial dysautonomia.
Felicia B Axelrod, Max J Hilz, Dena Berlin, Po Lai Yau, David Javier, Victoria Sweat, Hannah Bruehl, Antonio Convit. J Neurol 2010
20
25

Purification and characterization of the human elongator complex.
Nicola A Hawkes, Gabriel Otero, G Sebastiaan Winkler, Nick Marshall, Michael E Dahmus, Daniel Krappmann, Claus Scheidereit, Claire L Thomas, Giampietro Schiavo, Hediye Erdjument-Bromage,[...]. J Biol Chem 2002
186
25


A world without pain or tears.
Felicia B Axelrod. Clin Auton Res 2006
26
25

Afferent baroreflex failure in familial dysautonomia.
Lucy Norcliffe-Kaufmann, Felicia Axelrod, Horacio Kaufmann. Neurology 2010
71
25


A high-density genome-wide association screen of sporadic ALS in US veterans.
Lydia Coulter Kwee, Yutao Liu, Carol Haynes, Jason R Gibson, Annjanette Stone, Steven A Schichman, Freya Kamel, Lorene M Nelson, Barbara Topol, Stephen K Van den Eeden,[...]. PLoS One 2012
41
25

Association of brain-derived neurotrophic factor (BDNF) and elongator protein complex 4 (ELP4) polymorphisms with benign epilepsy with centrotemporal spikes in a Greek population.
Anastasia Gkampeta, Liana Fidani, Jordi Clarimón, Kallirhoe Kalinderi, Teodora Katopodi, Dimitrios Zafeiriou, Evangelos Pavlou. Epilepsy Res 2014
13
25



Current treatments in familial dysautonomia.
Jose-Alberto Palma, Lucy Norcliffe-Kaufmann, Cristina Fuente-Mora, Leila Percival, Carlos Mendoza-Santiesteban, Horacio Kaufmann. Expert Opin Pharmacother 2014
35
25

Increased frequency of rhabdomyolysis in familial dysautonomia.
Jose-Alberto Palma, Ricardo Roda, Lucy Norcliffe-Kaufmann, Horacio Kaufmann. Muscle Nerve 2015
7
42

Modelling pathogenesis and treatment of familial dysautonomia using patient-specific iPSCs.
Gabsang Lee, Eirini P Papapetrou, Hyesoo Kim, Stuart M Chambers, Mark J Tomishima, Christopher A Fasano, Yosif M Ganat, Jayanthi Menon, Fumiko Shimizu, Agnes Viale,[...]. Nature 2009
583
25

Olfactory stem cells, a new cellular model for studying molecular mechanisms underlying familial dysautonomia.
Nathalie Boone, Béatrice Loriod, Aurélie Bergon, Oualid Sbai, Christine Formisano-Tréziny, Jean Gabert, Michel Khrestchatisky, Catherine Nguyen, François Féron, Felicia B Axelrod,[...]. PLoS One 2010
38
25

Capturing the biology of disease severity in a PSC-based model of familial dysautonomia.
Nadja Zeltner, Faranak Fattahi, Nicole C Dubois, Nathalie Saurat, Fabien Lafaille, Lei Shang, Bastian Zimmer, Jason Tchieu, Mohamed A Soliman, Gabsang Lee,[...]. Nat Med 2016
24
25

Dimerization of elongator protein 1 is essential for Elongator complex assembly.
Huisha Xu, Zhijie Lin, Fengzhi Li, Wentao Diao, Chunming Dong, Hao Zhou, Xingqiao Xie, Zheng Wang, Yuequan Shen, Jiafu Long. Proc Natl Acad Sci U S A 2015
27
25

The Caenorhabditis elegans Elongator complex regulates neuronal alpha-tubulin acetylation.
Jachen A Solinger, Roberta Paolinelli, Holger Klöss, Francesco Berlanda Scorza, Stefano Marchesi, Ursula Sauder, Dai Mitsushima, Fabrizio Capuani, Stephen R Stürzenbaum, Giuseppe Cassata. PLoS Genet 2010
76
25

IKAP localizes to membrane ruffles with filamin A and regulates actin cytoskeleton organization and cell migration.
Lars Dan Johansen, Tiina Naumanen, Astrid Knudsen, Nina Westerlund, Irina Gromova, Melissa Junttila, Christina Nielsen, Trine Bøttzauw, Aviva Tolkovsky, Jukka Westermarck,[...]. J Cell Sci 2008
80
25


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.