A citation-based method for searching scientific literature

Jennifer L Fish, Yoichi Kosodo, Wolfgang Enard, Svante Pääbo, Wieland B Huttner. Proc Natl Acad Sci U S A 2006
Times Cited: 284







List of co-cited articles
1172 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


ASPM is a major determinant of cerebral cortical size.
Jacquelyn Bond, Emma Roberts, Ganesh H Mochida, Daniel J Hampshire, Sheila Scott, Jonathan M Askham, Kelly Springell, Meera Mahadevan, Yanick J Crow, Alexander F Markham,[...]. Nat Genet 2002
408
35

Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors.
Sofia B Lizarraga, Steven P Margossian, Marian H Harris, Dean R Campagna, An-Ping Han, Sherika Blevins, Raksha Mudbhary, Jane E Barker, Christopher A Walsh, Mark D Fleming. Development 2010
184
29

Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline.
Jeremy N Pulvers, Jarosław Bryk, Jennifer L Fish, Michaela Wilsch-Bräuninger, Yoko Arai, Dora Schreier, Ronald Naumann, Jussi Helppi, Bianca Habermann, Johannes Vogt,[...]. Proc Natl Acad Sci U S A 2010
130
24

A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size.
Jacquelyn Bond, Emma Roberts, Kelly Springell, Sofia B Lizarraga, Sheila Scott, Julie Higgins, Daniel J Hampshire, Ewan E Morrison, Gabriella F Leal, Elias O Silva,[...]. Nat Genet 2005
394
21

Cortical neurogenesis in the absence of centrioles.
Ryan Insolera, Hisham Bazzi, Wei Shao, Kathryn V Anderson, Song-Hai Shi. Nat Neurosci 2014
111
20

The cell biology of neurogenesis.
Magdalena Götz, Wieland B Huttner. Nat Rev Mol Cell Biol 2005
19

Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis.
Daijiro Konno, Go Shioi, Atsunori Shitamukai, Asako Mori, Hiroshi Kiyonari, Takaki Miyata, Fumio Matsuzaki. Nat Cell Biol 2008
363
19

WDR62 is associated with the spindle pole and is mutated in human microcephaly.
Adeline K Nicholas, Maryam Khurshid, Julie Désir, Ofélia P Carvalho, James J Cox, Gemma Thornton, Rizwana Kausar, Muhammad Ansar, Wasim Ahmad, Alain Verloes,[...]. Nat Genet 2010
207
19

Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate.
Divya Jayaraman, Andrew Kodani, Dilenny M Gonzalez, Joseph D Mancias, Ganeshwaran H Mochida, Cristiana Vagnoni, Jeffrey Johnson, Nevan Krogan, J Wade Harper, Jeremy F Reiter,[...]. Neuron 2016
71
26

MCPH1 regulates the neuroprogenitor division mode by coupling the centrosomal cycle with mitotic entry through the Chk1-Cdc25 pathway.
Ralph Gruber, Zhongwei Zhou, Mikhail Sukchev, Tjard Joerss, Pierre-Olivier Frappart, Zhao-Qi Wang. Nat Cell Biol 2011
159
18

Cdk5rap2 interacts with pericentrin to maintain the neural progenitor pool in the developing neocortex.
Joshua J Buchman, Huan-Chung Tseng, Ying Zhou, Christopher L Frank, Zhigang Xie, Li-Huei Tsai. Neuron 2010
125
18

Human ASPM participates in spindle organisation, spindle orientation and cytokinesis.
Julie Higgins, Carol Midgley, Anna-Maria Bergh, Sandra M Bell, Jonathan M Askham, Emma Roberts, Ruth K Binns, Saghira M Sharif, Christopher Bennett, David M Glover,[...]. BMC Cell Biol 2010
75
24

Protein-truncating mutations in ASPM cause variable reduction in brain size.
Jacquelyn Bond, Sheila Scott, Daniel J Hampshire, Kelly Springell, Peter Corry, Marc J Abramowicz, Ganesh H Mochida, Raoul C M Hennekam, Eamonn R Maher, Jean-Pierre Fryns,[...]. Am J Hum Genet 2003
128
18

A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function.
Muhammad Sajid Hussain, Shahid Mahmood Baig, Sascha Neumann, Gudrun Nürnberg, Muhammad Farooq, Ilyas Ahmad, Thomas Alef, Hans Christian Hennies, Martin Technau, Janine Altmüller,[...]. Am J Hum Genet 2012
120
17

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations.
S Passemard, L Titomanlio, M Elmaleh, A Afenjar, J-L Alessandri, G Andria, T Billette de Villemeur, O Boespflug-Tanguy, L Burglen, E Del Giudice,[...]. Neurology 2009
78
21

The Genetics of Primary Microcephaly.
Divya Jayaraman, Byoung-Il Bae, Christopher A Walsh. Annu Rev Genomics Hum Genet 2018
112
17

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
16

Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases.
Stephen C Noctor, Verónica Martínez-Cerdeño, Lidija Ivic, Arnold R Kriegstein. Nat Neurosci 2004
16

Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiation.
Yawei J Yang, Andrew E Baltus, Rebecca S Mathew, Elisabeth A Murphy, Gilad D Evrony, Dilenny M Gonzalez, Estee P Wang, Christine A Marshall-Walker, Brenda J Barry, Jernej Murn,[...]. Cell 2012
106
16

Asymmetric distribution of the apical plasma membrane during neurogenic divisions of mammalian neuroepithelial cells.
Yoichi Kosodo, Katja Röper, Wulf Haubensak, Anne-Marie Marzesco, Denis Corbeil, Wieland B Huttner. EMBO J 2004
321
16


Primary microcephaly: do all roads lead to Rome?
Gemma K Thornton, C Geoffrey Woods. Trends Genet 2009
279
16

Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture.
Timothy W Yu, Ganeshwaran H Mochida, David J Tischfield, Sema K Sgaier, Laura Flores-Sarnat, Consolato M Sergi, Meral Topçu, Marie T McDonald, Brenda J Barry, Jillian M Felie,[...]. Nat Genet 2010
205
15

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations.
Kaya Bilgüvar, Ali Kemal Oztürk, Angeliki Louvi, Kenneth Y Kwan, Murim Choi, Burak Tatli, Dilek Yalnizoğlu, Beyhan Tüysüz, Ahmet Okay Cağlayan, Sarenur Gökben,[...]. Nature 2010
353
15

Microcephaly disease gene Wdr62 regulates mitotic progression of embryonic neural stem cells and brain size.
Jian-Fu Chen, Ying Zhang, Jonathan Wilde, Kirk C Hansen, Fan Lai, Lee Niswander. Nat Commun 2014
95
15

The cell biology of neurogenesis: toward an understanding of the development and evolution of the neocortex.
Elena Taverna, Magdalena Götz, Wieland B Huttner. Annu Rev Cell Dev Biol 2014
385
15

The molecular landscape of ASPM mutations in primary microcephaly.
A K Nicholas, E A Swanson, J J Cox, G Karbani, S Malik, K Springell, D Hampshire, M Ahmed, J Bond, D Di Benedetto,[...]. J Med Genet 2009
72
20

Neurogenic radial glia in the outer subventricular zone of human neocortex.
David V Hansen, Jan H Lui, Philip R L Parker, Arnold R Kriegstein. Nature 2010
774
14

The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle protein.
Natalay Kouprina, Adam Pavlicek, N Keith Collins, Megumi Nakano, Vladimir N Noskov, Jun-Ichirou Ohzeki, Ganeshwaran H Mochida, John I Risinger, Paul Goldsmith, Michelle Gunsior,[...]. Hum Mol Genet 2005
135
14

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
312
14

Identification of microcephalin, a protein implicated in determining the size of the human brain.
Andrew P Jackson, Helen Eastwood, Sandra M Bell, Jimi Adu, Carmel Toomes, Ian M Carr, Emma Roberts, Daniel J Hampshire, Yanick J Crow, Alan J Mighell,[...]. Am J Hum Genet 2002
300
14



Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: a major site of neurogenesis.
Wulf Haubensak, Alessio Attardo, Winfried Denk, Wieland B Huttner. Proc Natl Acad Sci U S A 2004
662
13

CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly.
Muhammad S Hussain, Shahid M Baig, Sascha Neumann, Vivek S Peche, Sandra Szczepanski, Gudrun Nürnberg, Muhammad Tariq, Muhammad Jameel, Tahir N Khan, Ambrin Fatima,[...]. Hum Mol Genet 2013
75
17

Molecular genetics of human primary microcephaly: an overview.
Muhammad Faheem, Muhammad Imran Naseer, Mahmood Rasool, Adeel G Chaudhary, Taha A Kumosani, Asad Muhammad Ilyas, Peter Pushparaj, Farid Ahmed, Hussain A Algahtani, Mohammad H Al-Qahtani,[...]. BMC Med Genomics 2015
134
13

Autosomal recessive primary microcephaly due to ASPM mutations: An update.
Pascaline Létard, Séverine Drunat, Yoann Vial, Sarah Duerinckx, Anais Ernault, Daniel Amram, Stéphanie Arpin, Marta Bertoli, Tiffany Busa, Berten Ceulemans,[...]. Hum Mutat 2018
30
43

Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division.
Jessica Yingling, Yong Ha Youn, Dawn Darling, Kazuhito Toyo-Oka, Tiziano Pramparo, Shinji Hirotsune, Anthony Wynshaw-Boris. Cell 2008
202
12

OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling.
Simone A Fietz, Iva Kelava, Johannes Vogt, Michaela Wilsch-Bräuninger, Denise Stenzel, Jennifer L Fish, Denis Corbeil, Axel Riehn, Wolfgang Distler, Robert Nitsch,[...]. Nat Neurosci 2010
498
12

Asymmetric inheritance of centrosome-associated primary cilium membrane directs ciliogenesis after cell division.
Judith T M L Paridaen, Michaela Wilsch-Bräuninger, Wieland B Huttner. Cell 2013
183
12

ASPM and CITK regulate spindle orientation by affecting the dynamics of astral microtubules.
Marta Gai, Federico T Bianchi, Cristiana Vagnoni, Fiammetta Vernì, Silvia Bonaccorsi, Selina Pasquero, Gaia E Berto, Francesco Sgrò, Alessandra Ma Chiotto, Laura Annaratone,[...]. EMBO Rep 2016
38
31

Many roads lead to primary autosomal recessive microcephaly.
Angela M Kaindl, Sandrine Passemard, Pavan Kumar, Nadine Kraemer, Lina Issa, Angelika Zwirner, Benedicte Gerard, Alain Verloes, Shyamala Mani, Pierre Gressens. Prog Neurobiol 2010
139
12

Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis.
Salma Awad, Mohammed S Al-Dosari, Nadya Al-Yacoub, Dilek Colak, Mustafa A Salih, Fowzan S Alkuraya, Coralie Poizat. Hum Mol Genet 2013
60
20

Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size.
Matthew B Johnson, Xingshen Sun, Andrew Kodani, Rebeca Borges-Monroy, Kelly M Girskis, Steven C Ryu, Peter P Wang, Komal Patel, Dilenny M Gonzalez, Yu Mi Woo,[...]. Nature 2018
72
16

A primary microcephaly protein complex forms a ring around parental centrioles.
Joo-Hee Sir, Alexis R Barr, Adeline K Nicholas, Ofelia P Carvalho, Maryam Khurshid, Alex Sossick, Stefanie Reichelt, Clive D'Santos, C Geoffrey Woods, Fanni Gergely. Nat Genet 2011
151
11

Asymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells.
Takaki Miyata, Ayano Kawaguchi, Kanako Saito, Masako Kawano, Tetsuji Muto, Masaharu Ogawa. Development 2004
527
11

A role for intermediate radial glia in the tangential expansion of the mammalian cerebral cortex.
Isabel Reillo, Camino de Juan Romero, Miguel Ángel García-Cabezas, Víctor Borrell. Cereb Cortex 2011
371
11

Precursor diversity and complexity of lineage relationships in the outer subventricular zone of the primate.
Marion Betizeau, Veronique Cortay, Dorothée Patti, Sabina Pfister, Elodie Gautier, Angèle Bellemin-Ménard, Marielle Afanassieff, Cyril Huissoud, Rodney J Douglas, Henry Kennedy,[...]. Neuron 2013
265
11

A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family.
Muzammil A Khan, Verena M Rupp, Meritxell Orpinell, Muhammad S Hussain, Janine Altmüller, Michel O Steinmetz, Christian Enzinger, Holger Thiele, Wolfgang Höhne, Gudrun Nürnberg,[...]. Hum Mol Genet 2014
47
23

Centrosome amplification causes microcephaly.
Véronique Marthiens, Maria A Rujano, Carole Pennetier, Sarah Tessier, Perrine Paul-Gilloteaux, Renata Basto. Nat Cell Biol 2013
164
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.