A citation-based method for searching scientific literature

Ake Tzu-Hui Lu, Xiaoxian Dai, Julian A Martinez-Agosto, Rita M Cantor. Mol Autism 2012
Times Cited: 48







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



Times Cited
  Times     Co-cited
Similarity


Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.
Igor Splawski, Katherine W Timothy, Leah M Sharpe, Niels Decher, Pradeep Kumar, Raffaella Bloise, Carlo Napolitano, Peter J Schwartz, Robert M Joseph, Karen Condouris,[...]. Cell 2004
54


CACNA1H mutations in autism spectrum disorders.
Igor Splawski, Dana S Yoo, Stephanie C Stotz, Allison Cherry, David E Clapham, Mark T Keating. J Biol Chem 2006
145
31

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
29

High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene.
S P Strom, J L Stone, J R Ten Bosch, B Merriman, R M Cantor, D H Geschwind, S F Nelson. Mol Psychiatry 2010
45
28

CACNA1D de novo mutations in autism spectrum disorders activate Cav1.3 L-type calcium channels.
Alexandra Pinggera, Andreas Lieb, Bruno Benedetti, Michaela Lampert, Stefania Monteleone, Klaus R Liedl, Petronel Tuluc, Jörg Striessnig. Biol Psychiatry 2015
95
27

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
27

De novo gene disruptions in children on the autistic spectrum.
Ivan Iossifov, Michael Ronemus, Dan Levy, Zihua Wang, Inessa Hakker, Julie Rosenbaum, Boris Yamrom, Yoon-Ha Lee, Giuseppe Narzisi, Anthony Leotta,[...]. Neuron 2012
931
25


Mouse model of Timothy syndrome recapitulates triad of autistic traits.
Patrick L Bader, Mehrdad Faizi, Leo H Kim, Scott F Owen, Michael R Tadross, Ronald W Alfa, Glenna C L Bett, Richard W Tsien, Randall L Rasmusson, Mehrdad Shamloo. Proc Natl Acad Sci U S A 2011
125
20

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia.
E K Green, D Grozeva, I Jones, L Jones, G Kirov, S Caesar, K Gordon-Smith, C Fraser, L Forty, E Russell,[...]. Mol Psychiatry 2010
346
20

Rare mutations of CACNB2 found in autism spectrum disease-affected families alter calcium channel function.
Alexandra F S Breitenkamp, Jan Matthes, Robert Daniel Nass, Judith Sinzig, Gerd Lehmkuhl, Peter Nürnberg, Stefan Herzig. PLoS One 2014
30
33


Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.
L Palmieri, V Papaleo, V Porcelli, P Scarcia, L Gaita, R Sacco, J Hager, F Rousseau, P Curatolo, B Manzi,[...]. Mol Psychiatry 2010
134
18


Voltage-gated calcium channels.
William A Catterall. Cold Spring Harb Perspect Biol 2011
796
16

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.
Manuel A R Ferreira, Michael C O'Donovan, Yan A Meng, Ian R Jones, Douglas M Ruderfer, Lisa Jones, Jinbo Fan, George Kirov, Roy H Perlis, Elaine K Green,[...]. Nat Genet 2008
866
16

Genetic variation in CACNA1C affects brain circuitries related to mental illness.
Kristin L Bigos, Venkata S Mattay, Joseph H Callicott, Richard E Straub, Radhakrishna Vakkalanka, Bhaskar Kolachana, Thomas M Hyde, Barbara K Lipska, Joel E Kleinman, Daniel R Weinberger. Arch Gen Psychiatry 2010
210
16

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
16

Predicting the diagnosis of autism spectrum disorder using gene pathway analysis.
E Skafidas, R Testa, D Zantomio, G Chana, I P Everall, C Pantelis. Mol Psychiatry 2014
90
16

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.
Igor Splawski, Katherine W Timothy, Niels Decher, Pradeep Kumar, Frank B Sachse, Alan H Beggs, Michael C Sanguinetti, Mark T Keating. Proc Natl Acad Sci U S A 2005
417
16

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
557
16

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
16

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
783
14

Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome.
Sergiu P Paşca, Thomas Portmann, Irina Voineagu, Masayuki Yazawa, Aleksandr Shcheglovitov, Anca M Paşca, Branden Cord, Theo D Palmer, Sachiko Chikahisa, Seiji Nishino,[...]. Nat Med 2011
396
14

Molecular mechanisms of autism: a possible role for Ca2+ signaling.
Jocelyn F Krey, Ricardo E Dolmetsch. Curr Opin Neurobiol 2007
111
14

The Ca(V)3.3 calcium channel is the major sleep spindle pacemaker in thalamus.
Simone Astori, Ralf D Wimmer, Haydn M Prosser, Corrado Corti, Mauro Corsi, Nicolas Liaudet, Andrea Volterra, Paul Franken, John P Adelman, Anita Lüthi. Proc Natl Acad Sci U S A 2011
128
14

Role of hippocampal Cav1.2 Ca2+ channels in NMDA receptor-independent synaptic plasticity and spatial memory.
Sven Moosmang, Nicole Haider, Norbert Klugbauer, Helmuth Adelsberger, Nicolas Langwieser, Jochen Müller, Michael Stiess, Else Marais, Verena Schulla, Lubica Lacinova,[...]. J Neurosci 2005
302
14

A de novo convergence of autism genetics and molecular neuroscience.
Niklas Krumm, Brian J O'Roak, Jay Shendure, Evan E Eichler. Trends Neurosci 2014
291
14

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
14

Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism.
Jun Li, Linnan Zhao, Yang You, Tianlan Lu, Meixiang Jia, Hao Yu, Yanyan Ruan, Weihua Yue, Jing Liu, Lin Lu,[...]. PLoS One 2015
40
17

Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders.
Samuel Heyes, Wendy S Pratt, Elliott Rees, Shehrazade Dahimene, Laurent Ferron, Michael J Owen, Annette C Dolphin. Prog Neurobiol 2015
121
14

Sodium channels SCN1A, SCN2A and SCN3A in familial autism.
L A Weiss, A Escayg, J A Kearney, M Trudeau, B T MacDonald, M Mori, J Reichert, J D Buxbaum, M H Meisler. Mol Psychiatry 2003
208
12

Mitochondrial and ion channel gene alterations in autism.
Moyra Smith, Pamela L Flodman, John J Gargus, Mariella T Simon, Kimberley Verrell, Richard Haas, Gail E Reiner, Robert Naviaux, Katherine Osann, M Anne Spence,[...]. Biochim Biophys Acta 2012
35
17

Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
Irina Voineagu, Xinchen Wang, Patrick Johnston, Jennifer K Lowe, Yuan Tian, Steve Horvath, Jonathan Mill, Rita M Cantor, Benjamin J Blencowe, Daniel H Geschwind. Nature 2011
12

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
Brian J O'Roak, Laura Vives, Wenqing Fu, Jarrett D Egertson, Ian B Stanaway, Ian G Phelps, Gemma Carvill, Akash Kumar, Choli Lee, Katy Ankenman,[...]. Science 2012
810
12

Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder.
Santhosh Girirajan, Megan Y Dennis, Carl Baker, Maika Malig, Bradley P Coe, Catarina D Campbell, Kenneth Mark, Tiffany H Vu, Can Alkan, Ze Cheng,[...]. Am J Hum Genet 2013
194
12

Timothy syndrome is associated with activity-dependent dendritic retraction in rodent and human neurons.
Jocelyn F Krey, Sergiu P Paşca, Aleksandr Shcheglovitov, Masayuki Yazawa, Rachel Schwemberger, Randall Rasmusson, Ricardo E Dolmetsch. Nat Neurosci 2013
168
12

International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels.
William A Catterall, Edward Perez-Reyes, Terrance P Snutch, Joerg Striessnig. Pharmacol Rev 2005
853
12

Mechanisms by which a CACNA1H mutation in epilepsy patients increases seizure susceptibility.
Veit-Simon Eckle, Aleksandr Shcheglovitov, Iuliia Vitko, Deblina Dey, Chan Choo Yap, Bettina Winckler, Edward Perez-Reyes. J Physiol 2014
54
12

Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy.
Houman Khosravani, Christophe Altier, Brett Simms, Kevin S Hamming, Terrance P Snutch, Janette Mezeyova, John E McRory, Gerald W Zamponi. J Biol Chem 2004
133
12


Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels.
J Platzer, J Engel, A Schrott-Fischer, K Stephan, S Bova, H Chen, H Zheng, J Striessnig. Cell 2000
623
12


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
12

Shared functional defect in IP₃R-mediated calcium signaling in diverse monogenic autism syndromes.
G Schmunk, B J Boubion, I F Smith, I Parker, J J Gargus. Transl Psychiatry 2015
23
26

Activity-dependent neuronal signalling and autism spectrum disorder.
Daniel H Ebert, Michael E Greenberg. Nature 2013
390
10

A genome-wide scan for common alleles affecting risk for autism.
Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams, Nuala Sykes, Alistair T Pagnamenta,[...]. Hum Mol Genet 2010
408
10

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
10

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
139
10


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.