A citation-based method for searching scientific literature

Maria Lisa Dentici, Sabina Barresi, Marta Nardella, Emanuele Bellacchio, Paolo Alfieri, Alessandro Bruselles, Francesca Pantaleoni, Alberto Danieli, Giancarlo Iarossi, Marco Cappa, Enrico Bertini, Marco Tartaglia, Ginevra Zanni. Gene 2017
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


Mechanism of ER stress-induced brain damage by IP(3) receptor.
Takayasu Higo, Kozo Hamada, Chihiro Hisatsune, Nobuyuki Nukina, Tsutomu Hashikawa, Mitsuharu Hattori, Takeshi Nakamura, Katsuhiko Mikoshiba. Neuron 2010
100
18


Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage.
Masato Obayashi, Kinya Ishikawa, Yuishin Izumi, Makoto Takahashi, Yusuke Niimi, Nozomu Sato, Osamu Onodera, Ryuji Kaji, Masatoyo Nishizawa, Hidehiro Mizusawa. J Hum Genet 2012
17
18

The type 1 inositol 1,4,5-trisphosphate receptor gene is altered in the opisthotonos mouse.
V A Street, M M Bosma, V P Demas, M R Regan, D D Lin, L C Robinson, W S Agnew, B L Tempel. J Neurosci 1997
93
18

Putative receptor for inositol 1,4,5-trisphosphate similar to ryanodine receptor.
G A Mignery, T C Südhof, K Takei, P De Camilli. Nature 1989
482
18

Toward a high-resolution structure of IP₃R channel.
Irina I Serysheva. Cell Calcium 2014
22
18

Huntingtin and huntingtin-associated protein 1 influence neuronal calcium signaling mediated by inositol-(1,4,5) triphosphate receptor type 1.
Tie-Shan Tang, Huiping Tu, Edmond Y W Chan, Anton Maximov, Zhengnan Wang, Cheryl L Wellington, Michael R Hayden, Ilya Bezprozvanny. Neuron 2003
354
18

Gain-of-function enhancement of IP3 receptor modal gating by familial Alzheimer's disease-linked presenilin mutants in human cells and mouse neurons.
King-Ho Cheung, Lijuan Mei, Don-On Daniel Mak, Ikuo Hayashi, Takeshi Iwatsubo, David E Kang, J Kevin Foskett. Sci Signal 2010
147
18

Expression of inositol trisphosphate receptors.
C W Taylor, A A Genazzani, S A Morris. Cell Calcium 1999
218
18

Ocular findings in Gillespie-like syndrome: association with a new PAX6 mutation.
Benjamin H Ticho, Clair Hilchie-Schmidt, Robert T Egel, Elias I Traboulsi, Rachel J Howarth, David Robinson. Ophthalmic Genet 2006
27
18

Roles of inositol 1,4,5-trisphosphate receptors in spinocerebellar ataxias.
Masayoshi Tada, Masatoyo Nishizawa, Osamu Onodera. Neurochem Int 2016
29
18

Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII.
Namik Kaya, Hesham Aldhalaan, Banan Al-Younes, Dilek Colak, Taghreed Shuaib, Fahad Al-Mohaileb, Abdulaziz Al-Sugair, Michael Nester, Suad Al-Yamani, Albandary Al-Bakheet,[...]. Am J Med Genet B Neuropsychiatr Genet 2011
48
18

Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1.
Velina Guergueltcheva, Dimitar N Azmanov, Dora Angelicheva, Katherine R Smith, Teodora Chamova, Laura Florez, Michael Bynevelt, Thai Nguyen, Sylvia Cherninkova, Veneta Bojinova,[...]. Am J Hum Genet 2012
57
18

CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait.
Seval Türkmen, Gao Guo, Masoud Garshasbi, Katrin Hoffmann, Amjad J Alshalah, Claudia Mischung, Andreas Kuss, Nicholas Humphrey, Stefan Mundlos, Peter N Robinson. PLoS Genet 2009
88
18

Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia.
Lorena Travaglini, Marta Nardella, Emanuele Bellacchio, Adele D'Amico, Alessandro Capuano, Roberto Frusciante, Matteo Di Capua, Raffaella Cusmai, Sabina Barresi, Silvia Morlino,[...]. Eur J Paediatr Neurol 2017
27
18


The type III inositol 1,4,5-trisphosphate receptor is associated with aggressiveness of colorectal carcinoma.
Kazunori Shibao, Michael J Fiedler, Jun Nagata, Noritaka Minagawa, Keiji Hirata, Yoshifumi Nakayama, Yasuko Iwakiri, Michael H Nathanson, Koji Yamaguchi. Cell Calcium 2010
73
18

Widespread expression of inositol 1,4,5-trisphosphate receptor type 1 gene (Insp3r1) in the mouse central nervous system.
T Furuichi, D Simon-Chazottes, I Fujino, N Yamada, M Hasegawa, A Miyawaki, S Yoshikawa, J L Guénet, K Mikoshiba. Recept Channels 1993
187
18

IRBIT suppresses IP3 receptor activity by competing with IP3 for the common binding site on the IP3 receptor.
Hideaki Ando, Akihiro Mizutani, Hélène Kiefer, Dai Tsuzurugi, Takayuki Michikawa, Katsuhiko Mikoshiba. Mol Cell 2006
119
18

Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma.
Matthew L Hedberg, Gerald Goh, Simion I Chiosea, Julie E Bauman, Maria L Freilino, Yan Zeng, Lin Wang, Brenda B Diergaarde, William E Gooding, Vivian W Y Lui,[...]. J Clin Invest 2016
96
18

Aniridia.
Melanie Hingorani, Isabel Hanson, Veronica van Heyningen. Eur J Hum Genet 2012
116
18



Iris development in vertebrates; genetic and molecular considerations.
Noa Davis-Silberman, Ruth Ashery-Padan. Brain Res 2008
48
18

Linking structure to function: Recent lessons from inositol 1,4,5-trisphosphate receptor mutagenesis.
David I Yule, Matthew J Betzenhauser, Suresh K Joseph. Cell Calcium 2010
53
18


Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series.
Joyce van de Leemput, Fabienne Wavrant-De Vrièze, Ian Rafferty, Jose M Bras, Paola Giunti, Elizabeth M C Fisher, John A Hardy, Andrew B Singleton, Henry Houlden. Mov Disord 2010
11
18



HAP1 facilitates effects of mutant huntingtin on inositol 1,4,5-trisphosphate-induced Ca release in primary culture of striatal medium spiny neurons.
Tie-Shan Tang, Huiping Tu, Paul C Orban, Edmond Y W Chan, Michael R Hayden, Ilya Bezprozvanny. Eur J Neurosci 2004
49
12

Aberrant calcium signaling by transglutaminase-mediated posttranslational modification of inositol 1,4,5-trisphosphate receptors.
Kozo Hamada, Akiko Terauchi, Kyoko Nakamura, Takayasu Higo, Nobuyuki Nukina, Nagisa Matsumoto, Chihiro Hisatsune, Takeshi Nakamura, Katsuhiko Mikoshiba. Proc Natl Acad Sci U S A 2014
32
12

Functional characterization of the type 1 inositol 1,4,5-trisphosphate receptor coupling domain SII(+/-) splice variants and the Opisthotonos mutant form.
Huiping Tu, Tomoya Miyakawa, Zhengnan Wang, Lyuba Glouchankova, Masamitsu Iino, Ilya Bezprozvanny. Biophys J 2002
42
12

Bcl-2 functionally interacts with inositol 1,4,5-trisphosphate receptors to regulate calcium release from the ER in response to inositol 1,4,5-trisphosphate.
Rui Chen, Ignacio Valencia, Fei Zhong, Karen S McColl, H Llewelyn Roderick, Martin D Bootman, Michael J Berridge, Stuart J Conway, Andrew B Holmes, Gregory A Mignery,[...]. J Cell Biol 2004
310
12

Spinocerebellar ataxia type 15.
Elsdon Storey, R J McKinlay Gardner. Handb Clin Neurol 2012
15
13


Calcium--a life and death signal.
M J Berridge, M D Bootman, P Lipp. Nature 1998
12

Mechanism of Ca2+ disruption in Alzheimer's disease by presenilin regulation of InsP3 receptor channel gating.
King-Ho Cheung, Diana Shineman, Marioly Müller, César Cárdenas, Lijuan Mei, Jun Yang, Taisuke Tomita, Takeshi Iwatsubo, Virginia M-Y Lee, J Kevin Foskett. Neuron 2008
340
12


Identification of functionally critical residues in the channel domain of inositol trisphosphate receptors.
Cunnigaiper Bhanumathy, Paula C A da Fonseca, Edward P Morris, Suresh K Joseph. J Biol Chem 2012
13
15


Neuroprotective effects of inositol 1,4,5-trisphosphate receptor C-terminal fragment in a Huntington's disease mouse model.
Tie-Shan Tang, Caixia Guo, Hongyu Wang, Xi Chen, Ilya Bezprozvanny. J Neurosci 2009
75
12

Analyzing and Quantifying the Gain-of-Function Enhancement of IP3 Receptor Gating by Familial Alzheimer's Disease-Causing Mutants in Presenilins.
Don-On Daniel Mak, King-Ho Cheung, Patrick Toglia, J Kevin Foskett, Ghanim Ullah. PLoS Comput Biol 2015
23
12

CaBP1, a neuronal Ca2+ sensor protein, inhibits inositol trisphosphate receptors by clamping intersubunit interactions.
Congmin Li, Masahiro Enomoto, Ana M Rossi, Min-Duk Seo, Taufiq Rahman, Peter B Stathopulos, Colin W Taylor, Mitsuhiko Ikura, James B Ames. Proc Natl Acad Sci U S A 2013
30
12

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
S M Pulst, A Nechiporuk, T Nechiporuk, S Gispert, X N Chen, I Lopes-Cendes, S Pearlman, S Starkman, G Orozco-Diaz, A Lunkes,[...]. Nat Genet 1996
873
12

Suppression of InsP3 receptor-mediated Ca2+ signaling alleviates mutant presenilin-linked familial Alzheimer's disease pathogenesis.
Dustin Shilling, Marioly Müller, Hajime Takano, Don-On Daniel Mak, Ted Abel, Douglas A Coulter, J Kevin Foskett. J Neurosci 2014
65
12

Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome.
Morad Ansari, Jacqueline Rainger, Isabel M Hanson, Kathleen A Williamson, Freddie Sharkey, Louise Harewood, Angela Sandilands, Jill Clayton-Smith, Helene Dollfus, Pierre Bitoun,[...]. PLoS One 2016
29
12

Gillespie syndrome: a report of two further cases.
J Nelson, M Flaherty, P Grattan-Smith. Am J Med Genet 1997
18
12

Gillespie syndrome: additional findings and parental consanguinity.
Daniela Varela Luquetti, Ruy Pires Oliveira-Sobrinho, Vera Lúcia Gil-da-Silva-Lopes. Ophthalmic Genet 2007
8
25

Absence of PAX6 gene mutations in Gillespie syndrome (partial aniridia, cerebellar ataxia, and mental retardation).
T Glaser, C C Ton, R Mueller, M L Petzl-Erler, C Oliver, N C Nevin, D E Housman, R L Maas. Genomics 1994
48
12

Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations.
Solaf M Elsayed, Raoul Heller, Michaela Thoenes, Maha S Zaki, Daniel Swan, Ezzat Elsobky, Christine Zühlke, Inga Ebermann, Gudrun Nürnberg, Peter Nürnberg,[...]. Eur J Hum Genet 2014
27
12


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.