A citation-based method for searching scientific literature

A Skórka, J Bielicka-Cymermann, D Gieruszczak-Białek, L Korniszewski. Genet Couns 2005
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.
Cornelis A Albers, Dirk S Paul, Harald Schulze, Kathleen Freson, Jonathan C Stephens, Peter A Smethurst, Jennifer D Jolley, Ana Cvejic, Myrto Kostadima, Paul Bertone,[...]. Nat Genet 2012
251
44

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
Heather C Mefford, Andrew J Sharp, Carl Baker, Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv K Maloney, John A Crolla, Diana Baralle,[...]. N Engl J Med 2008
514
44

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi,[...]. Nat Genet 2008
389
44

Thrombocytopenia-absent radius syndrome: a clinical genetic study.
K L Greenhalgh, R T Howell, A Bottani, P J Ancliff, H G Brunner, C C Verschuuren-Bemelmans, E Vernon, K W Brown, R A Newbury-Ecob. J Med Genet 2002
93
33

Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome.
Eva Klopocki, Harald Schulze, Gabriele Strauss, Claus-Eric Ott, Judith Hall, Fabienne Trotier, Silke Fleischhauer, Lynn Greenhalgh, Ruth A Newbury-Ecob, Luitgard M Neumann,[...]. Am J Hum Genet 2007
198
33




The exon junction complex component Magoh controls brain size by regulating neural stem cell division.
Debra L Silver, Dawn E Watkins-Chow, Karisa C Schreck, Tarran J Pierfelice, Denise M Larson, Anthony J Burnetti, Hung-Jiun Liaw, Kyungjae Myung, Christopher A Walsh, Nicholas Gaiano,[...]. Nat Neurosci 2010
110
33

An alternative branch of the nonsense-mediated decay pathway.
Wai-Kin Chan, Lulu Huang, Jayanthi P Gudikote, Yao-Fu Chang, J Saadi Imam, James A MacLean, Miles F Wilkinson. EMBO J 2007
151
33

Translation is required to remove Y14 from mRNAs in the cytoplasm.
Josée Dostie, Gideon Dreyfuss. Curr Biol 2002
160
33

The exon junction complex controls the splicing of MAPK and other long intron-containing transcripts in Drosophila.
Dariel Ashton-Beaucage, Christian M Udell, Hugo Lavoie, Caroline Baril, Martin Lefrançois, Pierre Chagnon, Patrick Gendron, Olivier Caron-Lizotte, Eric Bonneil, Pierre Thibault,[...]. Cell 2010
91
33


Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling.
Yingwei Mao, Xuecai Ge, Christopher L Frank, Jon M Madison, Angela N Koehler, Mary Kathryn Doud, Carlos Tassa, Erin M Berry, Takahiro Soda, Karun K Singh,[...]. Cell 2009
573
33


Y14 and hUpf3b form an NMD-activating complex.
Niels H Gehring, Gabriele Neu-Yilik, Thomas Schell, Matthias W Hentze, Andreas E Kulozik. Mol Cell 2003
216
33

An EJC factor RBM8a regulates anxiety behaviors.
A Alachkar, D Jiang, M Harrison, Y Zhou, G Chen, Y Mao. Curr Mol Med 2013
28
33


Thrombocytopenia with absent radius (TAR).
J G Hall, J Levin, J P Kuhn, E J Ottenheimer, K A van Berkum, V A McKusick. Medicine (Baltimore) 1969
237
22

Existence of a differentiation blockage at the stage of a megakaryocyte precursor in the thrombocytopenia and absent radii (TAR) syndrome.
R Letestu, N Vitrat, A Massé, J P Le Couedic, V Lazar, P Rameau, F Wendling, J Vuillier, P Boutard, E Plouvier,[...]. Blood 2000
47
22

Mutational screening of thrombopoietin receptor gene (c-mpl) in patients with congenital thrombocytopenia and absent radii (TAR).
P Strippoli, A Savoia, A Iolascon, R Tonelli, M Savino, P Giordano, M D'Avanzo, F Massolo, F Locatelli, C Borgna,[...]. Br J Haematol 1998
35
22

Bilaterally cleft lip, limb defects, and haematological manifestations: Roberts syndrome versus TAR syndrome.
M Urban, C Opitz, C Bommer, H Enders, S Tinschert, R Witkowski. Am J Med Genet 1998
14
22

Absence of mutations in the HoxA10, HoxA11 and HoxD11 nucleotide coding sequences in thrombocytopenia with absent radius syndrome.
Roger A Fleischman, Rémi Letestu, Xiafang Mi, David Stevens, Jeffrey Winters, Najet Debili, William Vainchenker. Br J Haematol 2002
20
22

Congenital leukemia.
W G BERNHARD, I GORE, R A KILBY. Blood 1951
83
22


Identification of mutations in the c-mpl gene in congenital amegakaryocytic thrombocytopenia.
K Ihara, E Ishii, M Eguchi, H Takada, A Suminoe, R A Good, T Hara. Proc Natl Acad Sci U S A 1999
174
22

A hematopoietic growth factor, thrombopoietin, has a proapoptotic role in the brain.
Hannelore Ehrenreich, Martin Hasselblatt, Friederike Knerlich, Nico von Ahsen, Sonja Jacob, Swetlana Sperling, Helge Woldt, Katalin Vehmeyer, Klaus-Armin Nave, Anna-Leena Sirén. Proc Natl Acad Sci U S A 2005
68
22


The ever-increasing complexities of the exon junction complex.
Thomas Ø Tange, Ajit Nott, Melissa J Moore. Curr Opin Cell Biol 2004
220
22

A UPF3-mediated regulatory switch that maintains RNA surveillance.
Wai-Kin Chan, Angela D Bhalla, Hervé Le Hir, Lam Son Nguyen, Lulu Huang, Jozef Gécz, Miles F Wilkinson. Nat Struct Mol Biol 2009
78
22

Large recurrent microdeletions associated with schizophrenia.
Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp,[...]. Nature 2008
22

Upf1 phosphorylation triggers translational repression during nonsense-mediated mRNA decay.
Olaf Isken, Yoon Ki Kim, Nao Hosoda, Greg L Mayeur, John W B Hershey, Lynne E Maquat. Cell 2008
203
22

NMD factors UPF2 and UPF3 bridge UPF1 to the exon junction complex and stimulate its RNA helicase activity.
Hala Chamieh, Lionel Ballut, Fabien Bonneau, Hervé Le Hir. Nat Struct Mol Biol 2008
193
22



The nonsense-mediated decay RNA surveillance pathway.
Yao-Fu Chang, J Saadi Imam, Miles F Wilkinson. Annu Rev Biochem 2007
843
22

Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders.
Lam S Nguyen, Hyung-Goo Kim, Jill A Rosenfeld, Yiping Shen, James F Gusella, Yves Lacassie, Lawrence C Layman, Lisa G Shaffer, Jozef Gécz. Hum Mol Genet 2013
73
22

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.
A M Addington, J Gauthier, A Piton, F F Hamdan, A Raymond, N Gogtay, R Miller, J Tossell, J Bakalar, G Inoff-Germain,[...]. Mol Psychiatry 2011
69
22

The surveillance complex interacts with the translation release factors to enhance termination and degrade aberrant mRNAs.
K Czaplinski, M J Ruiz-Echevarria, S V Paushkin, X Han, Y Weng, H A Perlick, H C Dietz, M D Ter-Avanesyan, S W Peltz. Genes Dev 1998
278
22

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
Patrick S Tarpey, F Lucy Raymond, Lam S Nguyen, Jayson Rodriguez, Anna Hackett, Lucianne Vandeleur, Raffaella Smith, Cheryl Shoubridge, Sarah Edkins, Claire Stevens,[...]. Nat Genet 2007
166
22

An RNA biding protein, Y14 interacts with and modulates STAT3 activation.
Norihiko Ohbayashi, Naohisa Taira, Shiho Kawakami, Sumihito Togi, Noriko Sato, Osamu Ikeda, Shinya Kamitani, Ryuta Muromoto, Yuichi Sekine, Tadashi Matsuda. Biochem Biophys Res Commun 2008
17
22

Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism.
F Laumonnier, C Shoubridge, C Antar, L S Nguyen, H Van Esch, T Kleefstra, S Briault, J P Fryns, B Hamel, J Chelly,[...]. Mol Psychiatry 2010
71
22

hSMG-1 and ATM sequentially and independently regulate the G1 checkpoint during oxidative stress.
S C Gehen, R J Staversky, R A Bambara, P C Keng, M A O'Reilly. Oncogene 2008
38
22

The EJC factor eIF4AIII modulates synaptic strength and neuronal protein expression.
Corinna Giorgi, Gene W Yeo, Martha E Stone, Donald B Katz, Christopher Burge, Gina Turrigiano, Melissa J Moore. Cell 2007
204
22

Binding of a novel SMG-1-Upf1-eRF1-eRF3 complex (SURF) to the exon junction complex triggers Upf1 phosphorylation and nonsense-mediated mRNA decay.
Isao Kashima, Akio Yamashita, Natsuko Izumi, Naoyuki Kataoka, Ryo Morishita, Shinichi Hoshino, Mutsuhito Ohno, Gideon Dreyfuss, Shigeo Ohno. Genes Dev 2006
385
22

A novel role for the SMG-1 kinase in lifespan and oxidative stress resistance in Caenorhabditis elegans.
Ingrid Masse, Laurent Molin, Laurent Mouchiroud, Philippe Vanhems, Francesca Palladino, Marc Billaud, Florence Solari. PLoS One 2008
44
22

Nonsense surveillance regulates expression of diverse classes of mammalian transcripts and mutes genomic noise.
Joshua T Mendell, Neda A Sharifi, Jennifer L Meyers, Francisco Martinez-Murillo, Harry C Dietz. Nat Genet 2004
582
22

Knockdown of COPA, identified by loss-of-function screen, induces apoptosis and suppresses tumor growth in mesothelioma mouse model.
Hitomi Sudo, Atsushi B Tsuji, Aya Sugyo, Masakazu Kohda, Chizuru Sogawa, Chisato Yoshida, Yoshi-nobu Harada, Okio Hino, Tsuneo Saga. Genomics 2010
46
22

Proteins associated with the exon junction complex also control the alternative splicing of apoptotic regulators.
Laetitia Michelle, Alexandre Cloutier, Johanne Toutant, Lulzim Shkreta, Philippe Thibault, Mathieu Durand, Daniel Garneau, Daniel Gendron, Elvy Lapointe, Sonia Couture,[...]. Mol Cell Biol 2012
77
22



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.