A citation-based method for searching scientific literature

Yikai Shou, Feng Liang, Shunliang Xu, Xuekun Li. Front Cell Dev Biol 2020
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Cerebral organoids model human brain development and microcephaly.
Madeline A Lancaster, Magdalena Renner, Carol-Anne Martin, Daniel Wenzel, Louise S Bicknell, Matthew E Hurles, Tessa Homfray, Josef M Penninger, Andrew P Jackson, Juergen A Knoblich. Nature 2013
55

Brain organoids: advances, applications and challenges.
Xuyu Qian, Hongjun Song, Guo-Li Ming. Development 2019
145
44

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
22

Developmental disruptions underlying brain abnormalities in ciliopathies.
Jiami Guo, Holden Higginbotham, Jingjun Li, Jackie Nichols, Josua Hirt, Vladimir Ghukasyan, E S Anton. Nat Commun 2015
65
22

A transient role of the ciliary gene Inpp5e in controlling direct versus indirect neurogenesis in cortical development.
Kerstin Hasenpusch-Theil, Christine Laclef, Matt Colligan, Eamon Fitzgerald, Katherine Howe, Emily Carroll, Shaun R Abrams, Jeremy F Reiter, Sylvie Schneider-Maunoury, Thomas Theil. Elife 2020
5
40

Loss of the retrograde motor for IFT disrupts localization of Smo to cilia and prevents the expression of both activator and repressor functions of Gli.
Scott R May, Amir M Ashique, Mattias Karlen, Baolin Wang, Yiguo Shen, Kostantinos Zarbalis, Jeremy Reiter, Johan Ericson, Andrew S Peterson. Dev Biol 2005
319
22

Modeling microcephaly with cerebral organoids reveals a WDR62-CEP170-KIF2A pathway promoting cilium disassembly in neural progenitors.
Wei Zhang, Si-Lu Yang, Mei Yang, Stephanie Herrlinger, Qiang Shao, John L Collar, Edgar Fierro, Yanhong Shi, Aimin Liu, Hui Lu,[...]. Nat Commun 2019
45
22

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
157
22

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
843
22

Molecular regionalization of the neocortex is disrupted in Fgf8 hypomorphic mutants.
Sonia Garel, Kelly J Huffman, John L R Rubenstein. Development 2003
198
22

Meckel-Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research Advances.
Verity Hartill, Katarzyna Szymanska, Saghira Malik Sharif, Gabrielle Wheway, Colin A Johnson. Front Pediatr 2017
44
22

Bi-allelic Variations of SMO in Humans Cause a Broad Spectrum of Developmental Anomalies Due to Abnormal Hedgehog Signaling.
Thuy-Linh Le, Yunia Sribudiani, Xiaomin Dong, Céline Huber, Chelsea Kois, Geneviève Baujat, Christopher T Gordon, Valerie Mayne, Louise Galmiche, Valérie Serre,[...]. Am J Hum Genet 2020
10
22

Primary cilia and graded Sonic Hedgehog signaling.
Noriaki Sasai, James Briscoe. Wiley Interdiscip Rev Dev Biol 2012
50
22

Transventricular delivery of Sonic hedgehog is essential to cerebellar ventricular zone development.
Xi Huang, Jiang Liu, Tatiana Ketova, Jonathan T Fleming, Vandana K Grover, Michael K Cooper, Ying Litingtung, Chin Chiang. Proc Natl Acad Sci U S A 2010
96
22

ARL13B regulates Sonic hedgehog signaling from outside primary cilia.
Eduardo D Gigante, Megan R Taylor, Anna A Ivanova, Richard A Kahn, Tamara Caspary. Elife 2020
18
22

CPAP promotes timely cilium disassembly to maintain neural progenitor pool.
Elke Gabriel, Arpit Wason, Anand Ramani, Li Ming Gooi, Patrick Keller, Andrei Pozniakovsky, Ina Poser, Florian Noack, Narasimha Swamy Telugu, Federico Calegari,[...]. EMBO J 2016
112
22

Tangentially migrating neurons assemble a primary cilium that promotes their reorientation to the cortical plate.
Jean-Pierre Baudoin, Lucie Viou, Pierre-Serge Launay, Camilla Luccardini, Sergio Espeso Gil, Vera Kiyasova, Théano Irinopoulou, Chantal Alvarez, Jean-Paul Rio, Thomas Boudier,[...]. Neuron 2012
85
22

The use of brain organoids to investigate neural development and disease.
Elizabeth Di Lullo, Arnold R Kriegstein. Nat Rev Neurosci 2017
255
22

The primary cilium as a Hedgehog signal transduction machine.
Sarah C Goetz, Polloneal J R Ocbina, Kathryn V Anderson. Methods Cell Biol 2009
103
22

The Ciliary Protein Arl13b Functions Outside of the Primary Cilium in Shh-Mediated Axon Guidance.
Julien Ferent, Sandii Constable, Eduardo D Gigante, Patricia T Yam, Laura E Mariani, Emilie Legué, Karel F Liem, Tamara Caspary, Frédéric Charron. Cell Rep 2019
17
22

Reality check for organoids in neuroscience.
Vivien Marx. Nat Methods 2020
7
28

Generation of cerebral organoids from human pluripotent stem cells.
Madeline A Lancaster, Juergen A Knoblich. Nat Protoc 2014
556
22

Modeling G2019S-LRRK2 Sporadic Parkinson's Disease in 3D Midbrain Organoids.
Hongwon Kim, Hyeok Ju Park, Hwan Choi, Yujung Chang, Hanseul Park, Jaein Shin, Junyeop Kim, Christopher J Lengner, Yong Kyu Lee, Jongpil Kim. Stem Cell Reports 2019
98
22

Functional cortical neurons and astrocytes from human pluripotent stem cells in 3D culture.
Anca M Paşca, Steven A Sloan, Laura E Clarke, Yuan Tian, Christopher D Makinson, Nina Huber, Chul Hoon Kim, Jin-Young Park, Nancy A O'Rourke, Khoa D Nguyen,[...]. Nat Methods 2015
649
22

The human brain in a dish: the promise of iPSC-derived neurons.
Ricardo Dolmetsch, Daniel H Geschwind. Cell 2011
179
22

A three-dimensional human neural cell culture model of Alzheimer's disease.
Se Hoon Choi, Young Hye Kim, Matthias Hebisch, Christopher Sliwinski, Seungkyu Lee, Carla D'Avanzo, Hechao Chen, Basavaraj Hooli, Caroline Asselin, Julien Muffat,[...]. Nature 2014
612
22

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
22

Modeling Neurological Diseases With Human Brain Organoids.
Hansen Wang. Front Synaptic Neurosci 2018
59
22

Midbrain-like Organoids from Human Pluripotent Stem Cells Contain Functional Dopaminergic and Neuromelanin-Producing Neurons.
Junghyun Jo, Yixin Xiao, Alfred Xuyang Sun, Engin Cukuroglu, Hoang-Dai Tran, Jonathan Göke, Zi Ying Tan, Tzuen Yih Saw, Cheng-Peow Tan, Hidayat Lokman,[...]. Cell Stem Cell 2016
330
22

Brain-Region-Specific Organoids Using Mini-bioreactors for Modeling ZIKV Exposure.
Xuyu Qian, Ha Nam Nguyen, Mingxi M Song, Christopher Hadiono, Sarah C Ogden, Christy Hammack, Bing Yao, Gregory R Hamersky, Fadi Jacob, Chun Zhong,[...]. Cell 2016
952
22

Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.
Margaret W Leigh, Jessica E Pittman, Johnny L Carson, Thomas W Ferkol, Sharon D Dell, Stephanie D Davis, Michael R Knowles, Maimoona A Zariwala. Genet Med 2009
240
11

Ciliary transition zone activation of phosphorylated Tctex-1 controls ciliary resorption, S-phase entry and fate of neural progenitors.
Aiqun Li, Masaki Saito, Jen-Zen Chuang, Yun-Yu Tseng, Carlos Dedesma, Kazuhito Tomizawa, Taku Kaitsuka, Ching-Hwa Sung. Nat Cell Biol 2011
157
11

Altered GLI3 and FGF8 signaling underlies acrocallosal syndrome phenotypes in Kif7 depleted mice.
Audrey Putoux, Dominique Baas, Marie Paschaki, Laurette Morlé, Charline Maire, Tania Attié-Bitach, Sophie Thomas, Bénédicte Durand. Hum Mol Genet 2019
11
11

Generation of mice with functional inactivation of talpid3, a gene first identified in chicken.
Fiona Bangs, Nicole Antonio, Peerapat Thongnuek, Monique Welten, Megan G Davey, James Briscoe, Cheryll Tickle. Development 2011
49
11

Evolution and development of interhemispheric connections in the vertebrate forebrain.
Rodrigo Suárez, Ilan Gobius, Linda J Richards. Front Hum Neurosci 2014
76
11

Loss of Bardet-Biedl syndrome protein-8 (BBS8) perturbs olfactory function, protein localization, and axon targeting.
Abigail L D Tadenev, Heather M Kulaga, Helen L May-Simera, Matthew W Kelley, Nicholas Katsanis, Randall R Reed. Proc Natl Acad Sci U S A 2011
67
11

Ofd1 controls dorso-ventral patterning and axoneme elongation during embryonic brain development.
Anna D'Angelo, Amalia De Angelis, Bice Avallone, Immacolata Piscopo, Roberta Tammaro, Michèle Studer, Brunella Franco. PLoS One 2012
18
11

Spatial and temporal requirements for sonic hedgehog in the regulation of thalamic interneuron identity.
Yongsu Jeong, Diane K Dolson, Ronald R Waclaw, Michael P Matise, Lori Sussel, Kenneth Campbell, Klaus H Kaestner, Douglas J Epstein. Development 2011
53
11

Asymmetric centrosome inheritance maintains neural progenitors in the neocortex.
Xiaoqun Wang, Jin-Wu Tsai, Janice H Imai, Wei-Nan Lian, Richard B Vallee, Song-Hai Shi. Nature 2009
304
11

Joubert syndrome: neuroimaging findings in 110 patients in correlation with cognitive function and genetic cause.
Andrea Poretti, Joseph Snow, Angela C Summers, Aylin Tekes, Thierry A G M Huisman, Nafi Aygun, Kathryn A Carson, Dan Doherty, Melissa A Parisi, Camilo Toro,[...]. J Med Genet 2017
31
11

Haploinsufficiency of Six3 fails to activate Sonic hedgehog expression in the ventral forebrain and causes holoprosencephaly.
Xin Geng, Christina Speirs, Oleg Lagutin, Adi Inbal, Wei Liu, Lilianna Solnica-Krezel, Yongsu Jeong, Douglas J Epstein, Guillermo Oliver. Dev Cell 2008
120
11

Gene regulatory logic for reading the Sonic Hedgehog signaling gradient in the vertebrate neural tube.
Nikolaos Balaskas, Ana Ribeiro, Jasmina Panovska, Eric Dessaud, Noriaki Sasai, Karen M Page, James Briscoe, Vanessa Ribes. Cell 2012
274
11

A developmental ontology for the mammalian brain based on the prosomeric model.
Luis Puelles, Megan Harrison, George Paxinos, Charles Watson. Trends Neurosci 2013
120
11

Recent advances in understanding inheritance of holoprosencephaly.
Christèle Dubourg, Artem Kim, Erwan Watrin, Marie de Tayrac, Sylvie Odent, Véronique David, Valérie Dupé. Am J Med Genet C Semin Med Genet 2018
22
11

Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse.
Heather M Kulaga, Carmen C Leitch, Erica R Eichers, Jose L Badano, Alysa Lesemann, Bethan E Hoskins, James R Lupski, Philip L Beales, Randall R Reed, Nicholas Katsanis. Nat Genet 2004
242
11

Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
Jennifer J Johnston, Isabelle Olivos-Glander, Christina Killoran, Emma Elson, Joyce T Turner, Kathryn F Peters, Margaret H Abbott, David J Aughton, Arthur S Aylsworth, Michael J Bamshad,[...]. Am J Hum Genet 2005
168
11

A TCTN2 mutation defines a novel Meckel Gruber syndrome locus.
Ranad Shaheen, Eissa Faqeih, Mohammed Z Seidahmed, Asma Sunker, Faten Ezzat Alali, Khadijah AlQahtani, Fowzan S Alkuraya. Hum Mutat 2011
58
11

The molecular basis of oral-facial-digital syndrome, type 1.
Marina Macca, Brunella Franco. Am J Med Genet C Semin Med Genet 2009
66
11

Making sense of cilia in disease: the human ciliopathies.
Kate Baker, Philip L Beales. Am J Med Genet C Semin Med Genet 2009
218
11



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.