A citation-based method for searching scientific literature

Evelina Siavrienė, Eglė Preikšaitienė, Živilė Maldžienė, Violeta Mikštienė, Tautvydas Rančelis, Laima Ambrozaitytė, Lucie Gueneau, Alexandre Reymond, Vaidutis Kučinskas. Gene 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


The renaissance of GSK3.
P Cohen, S Frame. Nat Rev Mol Cell Biol 2001
100

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
Suleyman Gulsuner, Tom Walsh, Amanda C Watts, Ming K Lee, Anne M Thornton, Silvia Casadei, Caitlin Rippey, Hashem Shahin, Vishwajit L Nimgaonkar, Rodney C P Go,[...]. Cell 2013
336
100

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
100

10q23.31 microduplication encompassing PTEN decreases mTOR signalling activity and is associated with autosomal dominant primary microcephaly.
Danyllo Oliveira, Gabriela Ferraz Leal, Andréa L Sertié, Luiz Carlos Caires, Ernesto Goulart, Camila Manso Musso, João Ricardo Mendes de Oliveira, Ana Cristina Victorino Krepischi, Angela Maria Vianna-Morgante, Mayana Zatz. J Med Genet 2019
3
100

Polymicrogyria with calcification in Pallister-Killian syndrome detected by microarray analysis.
Akiko Hiraiwa, Kou Matsui, Yumi Nakayama, Takao Komatsubara, Shinichi Magara, Yu Kobayashi, Moemi Hojo, Mitsuhiro Kato, Toshiyuki Yamamoto, Jun Tohyama. Brain Dev 2021
2
100

Duplication of AKT3 is associated with macrocephaly and speech delay.
Brian K Chung, Patrice Eydoux, Clara D Van Karnebeek, William T Gibson. Am J Med Genet A 2014
9
100

PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia.
Laura A Jansen, Ghayda M Mirzaa, Gisele E Ishak, Brian J O'Roak, Joseph B Hiatt, William H Roden, Sonya A Gunter, Susan L Christian, Sarah Collins, Carissa Adams,[...]. Brain 2015
166
100

Somatic activation of AKT3 causes hemispheric developmental brain malformations.
Annapurna Poduri, Gilad D Evrony, Xuyu Cai, Princess Christina Elhosary, Rameen Beroukhim, Maria K Lehtinen, L Benjamin Hills, Erin L Heinzen, Anthony Hill, R Sean Hill,[...]. Neuron 2012
278
100


Further phenotype description, genotype characterization in patients with de novo interstitial deletion on 2p23.2-24.1.
Mercedes Bloch, Anissa Leonard, Andreas A Diplas, Xavier Pepermans, Beverly S Emanuel, Maria Santa Rocca, Nicole Revencu, Yves Sznajer. Am J Med Genet A 2014
5
100

dbSNP: the NCBI database of genetic variation.
S T Sherry, M H Ward, M Kholodov, J Baker, L Phan, E M Smigielski, K Sirotkin. Nucleic Acids Res 2001
100

Mucinous cystadenoma of ovary in a patient with juvenile polyposis due to 10q23 microdeletion: expansion of phenotype.
Nikola Babovic, Patricia S Simmons, Christopher Moir, Erik C Thorland, Bernd Scheithauer, Troy J Gliem, Dusica Babovic-Vuksanovic. Am J Med Genet A 2010
8
100

Phenotypes of AKT3 deletion: a case report and literature review.
Dayu Gai, Eric Haan, Matthew Scholar, Jillian Nicholl, Sui Yu. Am J Med Genet A 2015
23
100

CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions.
Darci T Butcher, Cheryl Cytrynbaum, Andrei L Turinsky, Michelle T Siu, Michal Inbar-Feigenberg, Roberto Mendoza-Londono, David Chitayat, Susan Walker, Jerry Machado, Oana Caluseriu,[...]. Am J Hum Genet 2017
77
100

Bannayan-Riley-Ruvalcaba syndrome.
R J Gorlin, M M Cohen, L M Condon, B A Burke. Am J Med Genet 1992
195
100

Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes.
Erfan Aref-Eshghi, David I Rodenhiser, Laila C Schenkel, Hanxin Lin, Cindy Skinner, Peter Ainsworth, Guillaume Paré, Rebecca L Hood, Dennis E Bulman, Kristin D Kernohan,[...]. Am J Hum Genet 2018
55
100

The Role of AKT3 Copy Number Changes in Brain Abnormalities and Neurodevelopmental Disorders: Four New Cases and Literature Review.
Fátima Lopes, Fátima Torres, Gabriela Soares, Clara D van Karnebeek, Cecília Martins, Diana Antunes, João Silva, Lauren Muttucomaroe, Luís Filipe Botelho, Susana Sousa,[...]. Front Genet 2019
3
100

4
100

Cyclin D2 and the CDK substrate p220(NPAT) are required for self-renewal of human embryonic stem cells.
Klaus A Becker, Prachi N Ghule, Jane B Lian, Janet L Stein, Andre J van Wijnen, Gary S Stein. J Cell Physiol 2010
25
100

Generation of the Sotos syndrome deletion in mice.
Anna M Migdalska, Louise van der Weyden, Ozama Ismail, Alistair G Rust, Mamunur Rashid, Jacqueline K White, Gabriela Sánchez-Andrade, James R Lupski, Darren W Logan, Mark J Arends,[...]. Mamm Genome 2012
12
100

Direct induction of cyclin D2 by Myc contributes to cell cycle progression and sequestration of p27.
C Bouchard, K Thieke, A Maier, R Saffrich, J Hanley-Hyde, W Ansorge, S Reed, P Sicinski, J Bartek, M Eilers. EMBO J 1999
381
100

Pten regulates neuronal soma size: a mouse model of Lhermitte-Duclos disease.
C H Kwon, X Zhu, J Zhang, L L Knoop, R Tharp, R J Smeyne, C G Eberhart, P C Burger, S J Baker. Nat Genet 2001
334
100

Dosage-dependent effects of Akt1/protein kinase Balpha (PKBalpha) and Akt3/PKBgamma on thymus, skin, and cardiovascular and nervous system development in mice.
Zhong-Zhou Yang, Oliver Tschopp, Nicolas Di-Poï, Elisabeth Bruder, Anne Baudry, Bettina Dümmler, Walter Wahli, Brian A Hemmings. Mol Cell Biol 2005
164
100

mTORC1 is necessary but mTORC2 and GSK3β are inhibitory for AKT3-induced axon regeneration in the central nervous system.
Linqing Miao, Liu Yang, Haoliang Huang, Feisi Liang, Chen Ling, Yang Hu. Elife 2016
54
100

Role for Akt3/protein kinase Bgamma in attainment of normal brain size.
Rachael M Easton, Han Cho, Kristin Roovers, Diana W Shineman, Moshe Mizrahi, Mark S Forman, Virginia M-Y Lee, Matthias Szabolcs, Ron de Jong, Tilman Oltersdorf,[...]. Mol Cell Biol 2005
445
100


Severe presentation and complex brain malformations in an individual carrying a CCND2 variant.
Gerarda Cappuccio, Lorenzo Ugga, Elena Parrini, Alessandra D'Amico, Nicola Brunetti-Pierri. Mol Genet Genomic Med 2019
5
100


Reinforcing the association between distal 1q CNVs and structural brain disorder: A case of a complex 1q43-q44 CNV and a review of the literature.
Isabel A Hemming, Alistair R R Forrest, Peter Shipman, Karen J Woodward, Peter Walsh, David G Ravine, Julian Ik-Tsen Heng. Am J Med Genet B Neuropsychiatr Genet 2016
17
100

Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans.
Loïc de Pontual, Evelyn Yao, Patrick Callier, Laurence Faivre, Valérie Drouin, Sandra Cariou, Arie Van Haeringen, David Geneviève, Alice Goldenberg, Myriam Oufadem,[...]. Nat Genet 2011
196
100

Ezh2 Mutations Found in the Weaver Overgrowth Syndrome Cause a Partial Loss of H3K27 Histone Methyltransferase Activity.
Julian C Lui, Kevin M Barnes, Lijin Dong, Shanna Yue, Evan Graber, Robert Rapaport, Andrew Dauber, Ola Nilsson, Jeffrey Baron. J Clin Endocrinol Metab 2018
15
100

Migratory localization of cyclin D2-Cdk4 complex suggests a spatial regulation of the G1-S transition.
Zizhang Wang, Yongli Xie, Lixia Zhang, Haiwen Zhang, Xiaojing An, Tai Wang, Anming Meng. Cell Struct Funct 2008
13
100

Ventricular noncompaction and absent thumbs in a newborn with tetrasomy 5q35.2-5q35.3: an association with Hunter-McAlpine syndrome?
Elizabeth A Sellars, Sarah L Zimmerman, Teresa Smolarek, Robert J Hopkin. Am J Med Genet A 2011
10
100

Reversed clinical phenotype due to a microduplication of Sotos syndrome region detected by array CGH: microcephaly, developmental delay and delayed bone age.
Han Zhang, Xianglan Lu, Julie Beasley, John J Mulvihill, Ruizhi Liu, Shibo Li, Ji-Yun Lee. Am J Med Genet A 2011
20
100

Haploinsufficiency of NSD1 causes Sotos syndrome.
Naohiro Kurotaki, Kiyoshi Imaizumi, Naoki Harada, Mitsuo Masuno, Tatsuro Kondoh, Toshiro Nagai, Hirofumi Ohashi, Kenji Naritomi, Masato Tsukahara, Yoshio Makita,[...]. Nat Genet 2002
377
100

Mutations in EZH2 cause Weaver syndrome.
William T Gibson, Rebecca L Hood, Shing Hei Zhan, Dennis E Bulman, Anthony P Fejes, Richard Moore, Andrew J Mungall, Patrice Eydoux, Riyana Babul-Hirji, Jianghong An,[...]. Am J Hum Genet 2012
153
100

The PI3K/AKT/mTOR interactive pathway.
Tulin Ersahin, Nurcan Tuncbag, Rengul Cetin-Atalay. Mol Biosyst 2015
144
100

DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes.
Sanaa Choufani, William T Gibson, Andrei L Turinsky, Brian H Y Chung, Tianren Wang, Kopal Garg, Alessandro Vitriolo, Ana S A Cohen, Sharri Cyrus, Sarah Goodman,[...]. Am J Hum Genet 2020
17
100

A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly.
Yutaka Negishi, Fuyuki Miya, Ayako Hattori, Yoshikazu Johmura, Motoo Nakagawa, Naoki Ando, Ikumi Hori, Takao Togawa, Kohei Aoyama, Kei Ohashi,[...]. BMC Med Genet 2017
12
100

An allelic series of miR-17 ∼ 92-mutant mice uncovers functional specialization and cooperation among members of a microRNA polycistron.
Yoon-Chi Han, Joana A Vidigal, Ping Mu, Evelyn Yao, Irtisha Singh, Alvaro J González, Carla P Concepcion, Ciro Bonetti, Paul Ogrodowski, Brett Carver,[...]. Nat Genet 2015
65
100

Akt2 and Akt3 play a pivotal role in malignant gliomas.
Hideo Mure, Kazuhito Matsuzaki, Keiko T Kitazato, Yoshifumi Mizobuchi, Kazuyuki Kuwayama, Teruyoshi Kageji, Shinji Nagahiro. Neuro Oncol 2010
76
100

MYCN promotes neuroblastoma malignancy by establishing a regulatory circuit with transcription factor AP4.
Chengyuan Xue, Denise M T Yu, Samuele Gherardi, Jessica Koach, Giorgio Milazzo, Laura Gamble, Bing Liu, Emanuele Valli, Amanda J Russell, Wendy B London,[...]. Oncotarget 2016
11
100

Genotype-phenotype correlations in MYCN-related Feingold syndrome.
Carlo L M Marcelis, Frans A Hol, Gail E Graham, Paul N M A Rieu, Richard Kellermayer, Rowdy P P Meijer, Dorien Lugtenberg, Hans Scheffer, Hans van Bokhoven, Han G Brunner,[...]. Hum Mutat 2008
57
100

AKT3 and PIK3R2 mutations in two patients with megalencephaly-related syndromes: MCAP and MPPH.
K Nakamura, M Kato, J Tohyama, T Shiohama, K Hayasaka, K Nishiyama, H Kodera, M Nakashima, Y Tsurusaki, N Miyake,[...]. Clin Genet 2014
21
100

MYCN de novo gain-of-function mutation in a patient with a novel megalencephaly syndrome.
Kohji Kato, Fuyuki Miya, Nanako Hamada, Yutaka Negishi, Yoko Narumi-Kishimoto, Hiroshi Ozawa, Hidenori Ito, Ikumi Hori, Ayako Hattori, Nobuhiko Okamoto,[...]. J Med Genet 2019
4
100

Germline activating AKT3 mutation associated with megalencephaly, polymicrogyria, epilepsy and hypoglycemia.
Mark Nellist, Rachel Schot, Marianne Hoogeveen-Westerveld, Rinze F Neuteboom, Elles J T M van der Louw, Maarten H Lequin, Karen Bindels-de Heus, Barbara J Sibbles, René de Coo, Alice Brooks,[...]. Mol Genet Metab 2015
31
100

Craniosynostosis associated with distal 5q-trisomy: further evidence that extra copy of MSX2 gene leads to craniosynostosis.
Jia-Chi Wang, Michelle Steinraths, Linda Dang, Brenda Lomax, Patrice Eydoux, Tracy Stockley, Siu-Li Yong, Margot I Van Allen. Am J Med Genet A 2007
18
100


Deconstructing myc.
R N Eisenman. Genes Dev 2001
308
100

Distinct functional roles of Akt isoforms for proliferation, survival, migration and EGF-mediated signalling in lung cancer derived disseminated tumor cells.
Nicole Grabinski, Kai Bartkowiak, Katharina Grupp, Burkhard Brandt, Klaus Pantel, Manfred Jücker. Cell Signal 2011
65
100


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.