A citation-based method for searching scientific literature

Marc Kschonsak, Han Chow Chua, Claudia Weidling, Nourdine Chakouri, Cameron L Noland, Katharina Schott, Timothy Chang, Christine Tam, Nidhi Patel, Christopher P Arthur, Alexander Leitner, Manu Ben-Johny, Claudio Ciferri, Stephan Alexander Pless, Jian Payandeh. Nature 2022
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


UCSF Chimera--a visualization system for exploratory research and analysis.
Eric F Pettersen, Thomas D Goddard, Conrad C Huang, Gregory S Couch, Daniel M Greenblatt, Elaine C Meng, Thomas E Ferrin. J Comput Chem 2004
100

cryoSPARC: algorithms for rapid unsupervised cryo-EM structure determination.
Ali Punjani, John L Rubinstein, David J Fleet, Marcus A Brubaker. Nat Methods 2017
100

Highly accurate protein structure prediction with AlphaFold.
John Jumper, Richard Evans, Alexander Pritzel, Tim Green, Michael Figurnov, Olaf Ronneberger, Kathryn Tunyasuvunakool, Russ Bates, Augustin Žídek, Anna Potapenko,[...]. Nature 2021
100

A putative cation channel, NCA-1, and a novel protein, UNC-80, transmit neuronal activity in C. elegans.
Edward Yeh, Sharon Ng, Mi Zhang, Magali Bouhours, Ying Wang, Min Wang, Wesley Hung, Kyota Aoyagi, Katya Melnik-Martinez, Michelle Li,[...]. PLoS Biol 2008
88
66

The neuronal channel NALCN contributes resting sodium permeability and is required for normal respiratory rhythm.
Boxun Lu, Yanhua Su, Sudipto Das, Jin Liu, Jingsheng Xia, Dejian Ren. Cell 2007
221
66


PHENIX: a comprehensive Python-based system for macromolecular structure solution.
Paul D Adams, Pavel V Afonine, Gábor Bunkóczi, Vincent B Chen, Ian W Davis, Nathaniel Echols, Jeffrey J Headd, Li-Wei Hung, Gary J Kapral, Ralf W Grosse-Kunstleve,[...]. Acta Crystallogr D Biol Crystallogr 2010
66

Identification of a novel homozygous UNC80 variant in a child with infantile hypotonia with psychomotor retardation and characteristic facies-2 (IHPRF2).
Tasneem Obeid, Abdul Rezzak Hamzeh, Fatima Saif, Pratibha Nair, Madiha Mohamed, Mahmoud Taleb Al-Ali, Fatma Bastaki. Metab Brain Dis 2018
7
66


Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy.
Hanan E Shamseldin, Eissa Faqeih, Ali Alasmari, Maha S Zaki, Joseph G Gleeson, Fowzan S Alkuraya. Am J Hum Genet 2016
28
66


Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay.
Moeenaldeen D Al-Sayed, Hamad Al-Zaidan, Albandary Albakheet, Hana Hakami, Rosan Kenana, Yusra Al-Yafee, Mazhor Al-Dosary, Alya Qari, Tarfa Al-Sheddi, Muhammed Al-Muheiza,[...]. Am J Hum Genet 2013
61
66

De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay.
Jessica X Chong, Margaret J McMillin, Kathryn M Shively, Anita E Beck, Colby T Marvin, Jose R Armenteros, Kati J Buckingham, Naomi T Nkinsi, Evan A Boyle, Margaret N Berry,[...]. Am J Hum Genet 2015
90
66

Extracellular calcium controls background current and neuronal excitability via an UNC79-UNC80-NALCN cation channel complex.
Boxun Lu, Qi Zhang, Haikun Wang, Yan Wang, Manabu Nakayama, Dejian Ren. Neuron 2010
122
66

Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability.
Asbjørg Stray-Pedersen, Jan-Maarten Cobben, Trine E Prescott, Sora Lee, Chunlei Cang, Kimberly Aranda, Sohnee Ahmed, Marielle Alders, Thorsten Gerstner, Kathinka Aslaksen,[...]. Am J Hum Genet 2016
34
66

Contribution of next generation sequencing in pediatric practice in Lebanon. A Study on 213 cases.
Pratibha Nair, Sandra Sabbagh, Hicham Mansour, Ali Fawaz, Ghassan Hmaimess, Peter Noun, Rawane Dagher, Hala Megarbane, Sayeeda Hana, Saada Alame,[...]. Mol Genet Genomic Med 2018
13
66

MotionCor2: anisotropic correction of beam-induced motion for improved cryo-electron microscopy.
Shawn Q Zheng, Eugene Palovcak, Jean-Paul Armache, Kliment A Verba, Yifan Cheng, David A Agard. Nat Methods 2017
66

Structure of voltage-modulated sodium-selective NALCN-FAM155A channel complex.
Yunlu Kang, Jing-Xiang Wu, Lei Chen. Nat Commun 2020
6
66

Structure of the human sodium leak channel NALCN.
Marc Kschonsak, Han Chow Chua, Cameron L Noland, Claudia Weidling, Thomas Clairfeuille, Oskar Ørts Bahlke, Aishat Oluwanifemi Ameen, Zhong Rong Li, Christopher P Arthur, Claudio Ciferri,[...]. Nature 2020
16
66

UNC-80 and the NCA ion channels contribute to endocytosis defects in synaptojanin mutants.
Maelle Jospin, Shigeki Watanabe, Deepa Joshi, Sean Young, Kevin Hamming, Colin Thacker, Terrance P Snutch, Erik M Jorgensen, Kim Schuske. Curr Biol 2007
70
66

Structure of the human sodium leak channel NALCN in complex with FAM155A.
Jiongfang Xie, Meng Ke, Lizhen Xu, Shiyi Lin, Jin Huang, Jiabei Zhang, Fan Yang, Jianping Wu, Zhen Yan. Nat Commun 2020
10
66

The NALCN channel complex is voltage sensitive and directly modulated by extracellular calcium.
H C Chua, M Wulf, C Weidling, L P Rasmussen, S A Pless. Sci Adv 2020
25
66

UCSF ChimeraX: Structure visualization for researchers, educators, and developers.
Eric F Pettersen, Thomas D Goddard, Conrad C Huang, Elaine C Meng, Gregory S Couch, Tristan I Croll, John H Morris, Thomas E Ferrin. Protein Sci 2021
66

Real-space refinement in PHENIX for cryo-EM and crystallography.
Pavel V Afonine, Billy K Poon, Randy J Read, Oleg V Sobolev, Thomas C Terwilliger, Alexandre Urzhumtsev, Paul D Adams. Acta Crystallogr D Struct Biol 2018
924
66

Features and development of Coot.
P Emsley, B Lohkamp, W G Scott, K Cowtan. Acta Crystallogr D Biol Crystallogr 2010
66

De novo missense mutations in NALCN cause developmental and intellectual impairment with hypotonia.
Ryoko Fukai, Hirotomo Saitsu, Nobuhiko Okamoto, Yasunari Sakai, Aviva Fattal-Valevski, Shiina Masaaki, Yukihiro Kitai, Michiko Torio, Kanako Kojima-Ishii, Kenji Ihara,[...]. J Hum Genet 2016
24
33

Elevated Expression and Activity of Sodium Leak Channel Contributes to Neuronal Sensitization of Inflammatory Pain in Rats.
Jia Li, Yali Chen, Jin Liu, Donghang Zhang, Peng Liang, Peilin Lu, Jiefei Shen, Changhong Miao, Yunxia Zuo, Cheng Zhou. Front Mol Neurosci 2021
3
33

A high-speed search engine pLink 2 with systematic evaluation for proteome-scale identification of cross-linked peptides.
Zhen-Lin Chen, Jia-Ming Meng, Yong Cao, Ji-Li Yin, Run-Qian Fang, Sheng-Bo Fan, Chao Liu, Wen-Feng Zeng, Yue-He Ding, Dan Tan,[...]. Nat Commun 2019
146
33

Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex.
Jinhong Wie, Apoorva Bharthur, Morgan Wolfgang, Vinodh Narayanan, Keri Ramsey, Kimberly Aranda, Qi Zhang, Yandong Zhou, Dejian Ren. Nat Commun 2020
10
33

The ion channel narrow abdomen is critical for neural output of the Drosophila circadian pacemaker.
Bridget C Lear, Jui-Ming Lin, J Russel Keath, Jermaine J McGill, Indira M Raman, Ravi Allada. Neuron 2005
77
33

Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies).
Nuria C Bramswig, Aida M Bertoli-Avella, Beate Albrecht, Aida I Al Aqeel, Amal Alhashem, Nouriya Al-Sannaa, Maissa Bah, Katharina Bröhl, Christel Depienne, Nathalie Dorison,[...]. Hum Genet 2018
23
33


The Central domain of RyR1 is the transducer for long-range allosteric gating of channel opening.
Xiao-Chen Bai, Zhen Yan, Jianping Wu, Zhangqiang Li, Nieng Yan. Cell Res 2016
74
33

Structure of the rabbit ryanodine receptor RyR1 at near-atomic resolution.
Zhen Yan, Xiaochen Bai, Chuangye Yan, Jianping Wu, Zhangqiang Li, Tian Xie, Wei Peng, Changcheng Yin, Xueming Li, Sjors H W Scheres,[...]. Nature 2015
303
33

The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane.
A H Chishti, A C Kim, S M Marfatia, M Lutchman, M Hanspal, H Jindal, S C Liu, P S Low, G A Rouleau, N Mohandas,[...]. Trends Biochem Sci 1998
426
33

UNC79 and UNC80, putative auxiliary subunits of the NARROW ABDOMEN ion channel, are indispensable for robust circadian locomotor rhythms in Drosophila.
Bridget C Lear, Eric J Darrah, Benjamin T Aldrich, Senetibeb Gebre, Robert L Scott, Howard A Nash, Ravi Allada. PLoS One 2013
33
33

Coot: model-building tools for molecular graphics.
Paul Emsley, Kevin Cowtan. Acta Crystallogr D Biol Crystallogr 2004
33

UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCN.
Yonatan Perez, Rotem Kadir, Michael Volodarsky, Iris Noyman, Hagit Flusser, Zamir Shorer, Libe Gradstein, Ramon Y Birnbaum, Ohad S Birk. J Med Genet 2016
33
33

A gene-targeting approach for functional characterization of KIAA genes encoding extremely large proteins.
Manabu Nakayama, Midori Iida, Haruhiko Koseki, Osamu Ohara. FASEB J 2006
23
33

The NALCN ion channel is activated by M3 muscarinic receptors in a pancreatic beta-cell line.
Leigh Anne Swayne, Alexandre Mezghrani, Annie Varrault, Jean Chemin, Gyslaine Bertrand, Stephane Dalle, Emmanuel Bourinet, Philippe Lory, Richard J Miller, Joel Nargeot,[...]. EMBO Rep 2009
83
33

An unusual cation channel mediates photic control of locomotion in Drosophila.
Howard A Nash, Robert L Scott, Bridget C Lear, Ravi Allada. Curr Biol 2002
71
33

NALCN channelopathies: Distinguishing gain-of-function and loss-of-function mutations.
Eric G Bend, Yue Si, David A Stevenson, Pinar Bayrak-Toydemir, Tara M Newcomb, Erik M Jorgensen, Kathryn J Swoboda. Neurology 2016
22
33


Phenotypic evolution of UNC80 loss of function.
Elise Valkanas, Katherine Schaffer, Christopher Dunham, Valerie Maduro, Christèle du Souich, Rosemarie Rupps, David R Adams, Alireza Baradaran-Heravi, Elise Flynn, May C Malicdan,[...]. Am J Med Genet A 2016
12
33

Modulation of protein properties in living cells using nanobodies.
Axel Kirchhofer, Jonas Helma, Katrin Schmidthals, Carina Frauer, Sheng Cui, Annette Karcher, Mireille Pellis, Serge Muyldermans, Corella S Casas-Delucchi, M Cristina Cardoso,[...]. Nat Struct Mol Biol 2010
349
33


Forward-genetics analysis of sleep in randomly mutagenized mice.
Hiromasa Funato, Chika Miyoshi, Tomoyuki Fujiyama, Takeshi Kanda, Makito Sato, Zhiqiang Wang, Jing Ma, Shin Nakane, Jun Tomita, Aya Ikkyu,[...]. Nature 2016
140
33


High-resolution noise substitution to measure overfitting and validate resolution in 3D structure determination by single particle electron cryomicroscopy.
Shaoxia Chen, Greg McMullan, Abdul R Faruqi, Garib N Murshudov, Judith M Short, Sjors H W Scheres, Richard Henderson. Ultramicroscopy 2013
554
33

NLF-1 delivers a sodium leak channel to regulate neuronal excitability and modulate rhythmic locomotion.
Lin Xie, Shangbang Gao, Salvador M Alcaire, Kyota Aoyagi, Ying Wang, Jennifer K Griffin, Igor Stagljar, Shinya Nagamatsu, Mei Zhen. Neuron 2013
53
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.