A citation-based method for searching scientific literature

Agne Liedén, Malin Kvarnung, Daniel Nilssson, Ellika Sahlin, Elisabeth Syk Lundberg. Am J Med Genet A 2014
Times Cited: 25







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



Times Cited
  Times     Co-cited
Similarity


SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation.
Gergana Dobreva, Maria Chahrour, Marcel Dautzenberg, Laura Chirivella, Benoit Kanzler, Isabel Fariñas, Gerard Karsenty, Rudolf Grosschedl. Cell 2006
348
36

Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.
Petcharat Leoyklang, Kanya Suphapeetiporn, Pichit Siriwan, Tayard Desudchit, Pattraporn Chaowanapanja, William A Gahl, Vorasuk Shotelersuk. Hum Mutat 2007
93
36

Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome.
Jill A Rosenfeld, Blake C Ballif, Ann Lucas, Edward J Spence, Cynthia Powell, Arthur S Aylsworth, Beth A Torchia, Lisa G Shaffer. PLoS One 2009
78
32

SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations.
Yuri A Zarate, Jennifer L Fish. Am J Med Genet A 2017
43
32

Further delineation of the SATB2 phenotype.
Dennis Döcker, Max Schubach, Moritz Menzel, Marita Munz, Christiane Spaich, Saskia Biskup, Deborah Bartholdi. Eur J Hum Genet 2014
48
28

Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing.
Yuri A Zarate, Hazel Perry, Tawfeg Ben-Omran, Elizabeth A Sellars, Quinn Stein, Mariam Almureikhi, Kirk Simmons, Ophir Klein, Jennifer Fish, Murray Feingold,[...]. Am J Med Genet A 2015
27
28

Satb2 regulates callosal projection neuron identity in the developing cerebral cortex.
Elizabeth A Alcamo, Laura Chirivella, Marcel Dautzenberg, Gergana Dobreva, Isabel Fariñas, Rudolf Grosschedl, Susan K McConnell. Neuron 2008
405
28

Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype.
M Balasubramanian, K Smith, L Basel-Vanagaite, M F Feingold, P Brock, G C Gowans, P C Vasudevan, L Cresswell, E J Taylor, C J Harris,[...]. J Med Genet 2011
38
24

Identification of SATB2 as the cleft palate gene on 2q32-q33.
David R FitzPatrick, Ian M Carr, Lorna McLaren, Jack P Leek, Patrick Wightman, Kathy Williamson, Philippe Gautier, Niolette McGill, Caroline Hayward, Helen Firth,[...]. Hum Mol Genet 2003
188
24

Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development.
Olga Britanova, Michael J Depew, Manuela Schwark, Bethan L Thomas, Isabelle Miletich, Paul Sharpe, Victor Tarabykin. Am J Hum Genet 2006
120
24

Satb2 is a postmitotic determinant for upper-layer neuron specification in the neocortex.
Olga Britanova, Camino de Juan Romero, Amanda Cheung, Kenneth Y Kwan, Manuela Schwark, Andrea Gyorgy, Tanja Vogel, Sergey Akopov, Miso Mitkovski, Denes Agoston,[...]. Neuron 2008
416
24

Genome sequencing identifies major causes of severe intellectual disability.
Christian Gilissen, Jayne Y Hehir-Kwa, Djie Tjwan Thung, Maartje van de Vorst, Bregje W M van Bon, Marjolein H Willemsen, Michael Kwint, Irene M Janssen, Alexander Hoischen, Annette Schenck,[...]. Nature 2014
624
20

Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.
Michael E Talkowski, Jill A Rosenfeld, Ian Blumenthal, Vamsee Pillalamarri, Colby Chiang, Adrian Heilbut, Carl Ernst, Carrie Hanscom, Elizabeth Rossin, Amelia M Lindgren,[...]. Cell 2012
380
20

The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
20

Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontia.
Ann-Sophie Kaiser, Bianca Maas, Anna Wolff, Christian Sutter, Johannes W G Janssen, Katrin Hinderhofer, Ute Moog. Eur J Hum Genet 2015
6
83



Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration.
Colby Chiang, Jessie C Jacobsen, Carl Ernst, Carrie Hanscom, Adrian Heilbut, Ian Blumenthal, Ryan E Mills, Andrew Kirby, Amelia M Lindgren, Skye R Rudiger,[...]. Nat Genet 2012
169
16

A network of genetic repression and derepression specifies projection fates in the developing neocortex.
Karpagam Srinivasan, Dino P Leone, Rosalie K Bateson, Gergana Dobreva, Yoshinori Kohwi, Terumi Kohwi-Shigematsu, Rudolf Grosschedl, Susan K McConnell. Proc Natl Acad Sci U S A 2012
98
16

The role of SATB2 in skeletogenesis and human disease.
Xiaoying Zhao, Zhihu Qu, Jennifer Tickner, Jiake Xu, Kerong Dai, Xiaoling Zhang. Cytokine Growth Factor Rev 2014
45
16

Satb2 Regulates the Differentiation of Both Callosal and Subcerebral Projection Neurons in the Developing Cerebral Cortex.
Dino P Leone, Whitney E Heavner, Emily A Ferenczi, Gergana Dobreva, John R Huguenard, Rudolf Grosschedl, Susan K McConnell. Cereb Cortex 2015
73
16

4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate.
Jill Urquhart, Graeme C M Black, Jill Clayton-Smith. Eur J Med Genet 2009
29
16

Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene.
Petcharat Leoyklang, Kanya Suphapeetiporn, Chalurmpon Srichomthong, Siraprapa Tongkobpetch, Stefanie Fietze, Heidi Dorward, Andrew R Cullinane, William A Gahl, Marjan Huizing, Vorasuk Shotelersuk. Hum Genet 2013
18
22

Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence.
Jacqueline K Rainger, Shipra Bhatia, Hemant Bengani, Philippe Gautier, Joe Rainger, Matt Pearson, Morad Ansari, Jayne Crow, Felicity Mehendale, Bozena Palinkasova,[...]. Hum Mol Genet 2014
43
16

SATB2-associated syndrome presenting with Rett-like phenotypes.
J S Lee, Y Yoo, B C Lim, K J Kim, M Choi, J-H Chae. Clin Genet 2016
21
19




TIDDIT, an efficient and comprehensive structural variant caller for massive parallel sequencing data.
Jesper Eisfeldt, Francesco Vezzi, Pall Olason, Daniel Nilsson, Anna Lindstrand. F1000Res 2017
31
16

Mutation update for the SATB2 gene.
Yuri A Zarate, Katherine A Bosanko, Aisling R Caffrey, Jonathan A Bernstein, Donna M Martin, Marc S Williams, Elizabeth M Berry-Kravis, Paul R Mark, Melanie A Manning, Vikas Bhambhani,[...]. Hum Mutat 2019
15
26

Circos: an information aesthetic for comparative genomics.
Martin Krzywinski, Jacqueline Schein, Inanç Birol, Joseph Connors, Randy Gascoyne, Doug Horsman, Steven J Jones, Marco A Marra. Genome Res 2009
12

The clinical significance of small copy number variants in neurodevelopmental disorders.
Reza Asadollahi, Beatrice Oneda, Pascal Joset, Silvia Azzarello-Burri, Deborah Bartholdi, Katharina Steindl, Marie Vincent, Joana Cobilanschi, Heinrich Sticht, Rosa Baldinger,[...]. J Med Genet 2014
55
12

Clinical diagnosis by whole-genome sequencing of a prenatal sample.
Michael E Talkowski, Zehra Ordulu, Vamsee Pillalamarri, Carol B Benson, Ian Blumenthal, Susan Connolly, Carrie Hanscom, Naveed Hussain, Shahrin Pereira, Jonathan Picker,[...]. N Engl J Med 2012
118
12

Replicative mechanisms for CNV formation are error prone.
Claudia M B Carvalho, Davut Pehlivan, Melissa B Ramocki, Ping Fang, Benjamin Alleva, Luis M Franco, John W Belmont, P J Hastings, James R Lupski. Nat Genet 2013
89
12

Human induced rotation and reorganization of the brain of domestic dogs.
Taryn Roberts, Paul McGreevy, Michael Valenzuela. PLoS One 2010
51
12

The shape of the human language-ready brain.
Cedric Boeckx, Antonio Benítez-Burraco. Front Psychol 2014
54
12

Brain development after birth differs between Neanderthals and modern humans.
Philipp Gunz, Simon Neubauer, Bruno Maureille, Jean-Jacques Hublin. Curr Biol 2010
110
12



Human-specific transcriptional regulation of CNS development genes by FOXP2.
Genevieve Konopka, Jamee M Bomar, Kellen Winden, Giovanni Coppola, Zophonias O Jonsson, Fuying Gao, Sophia Peng, Todd M Preuss, James A Wohlschlegel, Daniel H Geschwind. Nature 2009
216
12

Foxp1/2/4 regulate endochondral ossification as a suppresser complex.
Haixia Zhao, Wenrong Zhou, Zhengju Yao, Yong Wan, Jingjing Cao, Lingling Zhang, Jianzhi Zhao, Hanjun Li, Rujiang Zhou, Baojie Li,[...]. Dev Biol 2015
37
12

Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: further clinical and molecular delineation of del(2q32) syndrome.
Laila Rifai, Marylin Port-Lis, Anne-Claude Tabet, Isabelle Bailleul-Forestier, Brigitte Benzacken, Séverine Drunat, Suzanne Kuzbari, Sandrine Passemard, Alain Verloes, Azzedine Aboura. Am J Med Genet A 2010
18
16

Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase.
I A Glass, C A Swindlehurst, D A Aitken, W McCrea, E Boyd. J Med Genet 1989
31
12

Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort.
Julia Baptista, Catherine Mercer, Elena Prigmore, Susan M Gribble, Nigel P Carter, Viv Maloney, N Simon Thomas, Patricia A Jacobs, John A Crolla. Am J Hum Genet 2008
115
12

Toriello-Carey syndrome in a patient with a de novo balanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2.
D H Tegay, K K Chan, L Leung, C Wang, S Burkett, G Stone, R Stanyon, H V Toriello, E Hatchwell. Clin Genet 2009
23
13

A cross-species analysis of Satb2 expression suggests deep conservation across vertebrate lineages.
Kelly Sheehan-Rooney, Božena Pálinkášová, Johann K Eberhart, Michael J Dixon. Dev Dyn 2010
46
12

SATB2 interacts with chromatin-remodeling molecules in differentiating cortical neurons.
Andrea B Gyorgy, Marianna Szemes, Camino de Juan Romero, Victor Tarabykin, Denes V Agoston. Eur J Neurosci 2008
92
12


Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.
Shen Gu, Bo Yuan, Ian M Campbell, Christine R Beck, Claudia M B Carvalho, Sandesh C S Nagamani, Ayelet Erez, Ankita Patel, Carlos A Bacino, Chad A Shaw,[...]. Hum Mol Genet 2015
53
12

The structural basis for the oligomerization of the N-terminal domain of SATB1.
Zheng Wang, Xue Yang, Xinlei Chu, Jinxiu Zhang, Hao Zhou, Yuequan Shen, Jiafu Long. Nucleic Acids Res 2012
20
15


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.