A citation-based method for searching scientific literature

Ash Zawerton, Cyril Mignot, Ashley Sigafoos, Patrick R Blackburn, Abdul Haseeb, Kirsty McWalter, Shoji Ichikawa, Caroline Nava, Boris Keren, Perrine Charles, Isabelle Marey, Anne-Claude Tabet, Jonathan Levy, Laurence Perrin, Andreas Hartmann, Gaetan Lesca, Caroline Schluth-Bolard, Pauline Monin, Sophie Dupuis-Girod, Maria J Guillen Sacoto, Rhonda E Schnur, Zehua Zhu, Alice Poisson, Salima El Chehadeh, Yves Alembik, Ange-Line Bruel, Daphné Lehalle, Sophie Nambot, Sébastien Moutton, Sylvie Odent, Sylvie Jaillard, Christèle Dubourg, Yvonne Hilhorst-Hofstee, Tina Barbaro-Dieber, Lucia Ortega, Elizabeth J Bhoj, Diane Masser-Frye, Lynne M Bird, Kristin Lindstrom, Keri M Ramsey, Vinodh Narayanan, Emily Fassi, Marcia Willing, Trevor Cole, Claire G Salter, Rhoda Akilapa, Anthony Vandersteen, Natalie Canham, Patrick Rump, Erica H Gerkes, Jolien S Klein Wassink-Ruiter, Emilia Bijlsma, Mariëtte J V Hoffer, Marcelo Vargas, Antonina Wojcik, Florian Cherik, Christine Francannet, Jill A Rosenfeld, Keren Machol, Daryl A Scott, Carlos A Bacino, Xia Wang, Gary D Clark, Marta Bertoli, Simon Zwolinski, Rhys H Thomas, Ela Akay, Richard C Chang, Rebekah Bressi, Rossana Sanchez Russo, Myriam Srour, Laura Russell, Anne-Marie E Goyette, Lucie Dupuis, Roberto Mendoza-Londono, Catherine Karimov, Maries Joseph, Mathilde Nizon, Benjamin Cogné, Alma Kuechler, Amélie Piton, Eric W Klee, Véronique Lefebvre, Karl J Clark, Christel Depienne. Genet Med 2020
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features.
Allen N Lamb, Jill A Rosenfeld, Nicholas J Neill, Michael E Talkowski, Ian Blumenthal, Santhosh Girirajan, Debra Keelean-Fuller, Zheng Fan, Jill Pouncey, Cathy Stevens,[...]. Hum Mutat 2012
58
66

SOXopathies: Growing Family of Developmental Disorders Due to SOX Mutations.
Marco Angelozzi, Véronique Lefebvre. Trends Genet 2019
11
50


Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome.
Annmarie Hempel, Alistair T Pagnamenta, Moira Blyth, Sahar Mansour, Vivienne McConnell, Ikuyo Kou, Shiro Ikegawa, Yoshinori Tsurusaki, Naomichi Matsumoto, Adriana Lo-Castro,[...]. J Med Genet 2016
40
50



De novo SOX11 mutations cause Coffin-Siris syndrome.
Yoshinori Tsurusaki, Eriko Koshimizu, Hirofumi Ohashi, Shubha Phadke, Ikuyo Kou, Masaaki Shiina, Toshifumi Suzuki, Nobuhiko Okamoto, Shintaro Imamura, Michiaki Yamashita,[...]. Nat Commun 2014
73
33

Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations.
J Meyer, P Südbeck, M Held, T Wagner, M L Schmitz, F D Bricarelli, E Eggermont, U Friedrich, O A Haas, A Kobelt,[...]. Hum Mol Genet 1997
133
33


A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes.
J Gubbay, J Collignon, P Koopman, B Capel, A Economou, A Münsterberg, N Vivian, P Goodfellow, R Lovell-Badge. Nature 1990
33


The transcription factors L-Sox5 and Sox6 are essential for cartilage formation.
P Smits, P Li, J Mandel, Z Zhang, J M Deng, R R Behringer, B de Crombrugghe, V Lefebvre. Dev Cell 2001
424
33

De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.
Ash Zawerton, Baojin Yao, J Paige Yeager, Tommaso Pippucci, Abdul Haseeb, Joshua D Smith, Lisa Wischmann, Susanne J Kühl, John C S Dean, Daniela T Pilz,[...]. Am J Hum Genet 2019
13
33

Clinical and genetic characterization of a patient with SOX5 haploinsufficiency caused by a de novo balanced reciprocal translocation.
Daisuke Fukushi, Kenichiro Yamada, Kaoru Suzuki, Mie Inaba, Noriko Nomura, Yasuyo Suzuki, Kimiko Katoh, Seiji Mizuno, Nobuaki Wakamatsu. Gene 2018
6
33


Exome sequencing expands the mechanism of SOX5-associated intellectual disability: A case presentation with review of sox-related disorders.
Addie Nesbitt, Elizabeth J Bhoj, Kristin McDonald Gibson, Zhenming Yu, Elizabeth Denenberg, Mahdi Sarmady, Tanya Tischler, Kajia Cao, Holly Dubbs, Elaine H Zackai,[...]. Am J Med Genet A 2015
17
33

Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness.
Veronique Pingault, Virginie Bodereau, Viviane Baral, Severine Marcos, Yuli Watanabe, Asma Chaoui, Corinne Fouveaut, Chrystel Leroy, Odile Vérier-Mine, Christine Francannet,[...]. Am J Hum Genet 2013
118
16

Characterization of tumor-suppressive function of SOX6 in human esophageal squamous cell carcinoma.
Yan-Ru Qin, Hong Tang, Fajun Xie, Haibo Liu, Yinghui Zhu, Jiaoyu Ai, Leilei Chen, Yan Li, Dora L Kwong, Li Fu,[...]. Clin Cancer Res 2011
59
16

Expression of SoxE and SoxD genes in human gliomas.
B Schlierf, R P Friedrich, P Roerig, J Felsberg, G Reifenberger, M Wegner. Neuropathol Appl Neurobiol 2007
34
16

SoxD proteins influence multiple stages of oligodendrocyte development and modulate SoxE protein function.
C Claus Stolt, Anita Schlierf, Petra Lommes, Simone Hillgärtner, Torsten Werner, Thomas Kosian, Elisabeth Sock, Nicoletta Kessaris, William D Richardson, Veronique Lefebvre,[...]. Dev Cell 2006
187
16

Genetic evidence equating SRY and the testis-determining factor.
P Berta, J R Hawkins, A H Sinclair, A Taylor, B L Griffiths, P N Goodfellow, M Fellous. Nature 1990
694
16

Regulation of Sox6 by cyclin dependent kinase 5 in brain.
Parvathi Rudrabhatla, Elias Utreras, Howard Jaffe, Ashok B Kulkarni. PLoS One 2014
7
16

Loci influencing blood pressure identified using a cardiovascular gene-centric array.
Santhi K Ganesh, Vinicius Tragante, Wei Guo, Yiran Guo, Matthew B Lanktree, Erin N Smith, Toby Johnson, Berta Almoguera Castillo, John Barnard, Jens Baumert,[...]. Hum Mol Genet 2013
101
16

Sry: the master switch in mammalian sex determination.
Kenichi Kashimada, Peter Koopman. Development 2010
190
16

Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesis.
Claire Bastian, Jean-Baptiste Muller, Stephen Lortat-Jacob, Claire Nihoul-Fékété, Joelle Bignon-Topalovic, Ken McElreavey, Anu Bashamboo, Raja Brauner. Fertil Steril 2015
10
16

Genomewide linkage and peakwide association analyses of carotid plaque in Caribbean Hispanics.
Chuanhui Dong, Ashley Beecham, Susan Slifer, Liyong Wang, Susan H Blanton, Clinton B Wright, Tatjana Rundek, Ralph L Sacco. Stroke 2010
26
16

Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia.
N Chassaing, A Causse, A Vigouroux, A Delahaye, J-L Alessandri, O Boespflug-Tanguy, O Boute-Benejean, H Dollfus, B Duban-Bedu, B Gilbert-Dussardier,[...]. Clin Genet 2014
69
16


De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.
Ash Zawerton, Baojin Yao, J Paige Yeager, Tommaso Pippucci, Abdul Haseeb, Joshua D Smith, Lisa Wischmann, Susanne J Kühl, John C S Dean, Daniela T Pilz,[...]. Am J Hum Genet 2019
2
50



Disruption of SOX6 is associated with a rapid-onset dopa-responsive movement disorder, delayed development, and dysmorphic features.
Darius Ebrahimi-Fakhari, Bianca Maas, Christian Haneke, Tim Niehues, Katrin Hinderhofer, Birgit E Assmann, Heiko Runz. Pediatr Neurol 2015
7
16

MicroRNA-1 and -499 regulate differentiation and proliferation in human-derived cardiomyocyte progenitor cells.
Joost P G Sluijter, Alain van Mil, Patrick van Vliet, Corina H G Metz, Jia Liu, Pieter A Doevendans, Marie-José Goumans. Arterioscler Thromb Vasc Biol 2010
237
16

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif.
A H Sinclair, P Berta, M S Palmer, J R Hawkins, B L Griffiths, M J Smith, J W Foster, A M Frischauf, R Lovell-Badge, P N Goodfellow. Nature 1990
16

Aberrant expression of microRNA 155 may accelerate cell proliferation by targeting sex-determining region Y box 6 in hepatocellular carcinoma.
Qing Xie, Xiangmei Chen, Fengmin Lu, Ting Zhang, Meili Hao, Yongfeng Wang, Jingmin Zhao, Malcolm A McCrae, Hui Zhuang. Cancer 2012
99
16

Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations.
G Scherer, M Held, M Erdel, D Meschede, J Horst, R Lesniewicz, A T Midro. Cytogenet Cell Genet 1998
49
16

Cloning, characterization and chromosome mapping of the human SOX6 gene.
O Cohen-Barak, N Hagiwara, M F Arlt, J P Horton, M H Brilliant. Gene 2001
34
16

PEP-FOLD3: faster de novo structure prediction for linear peptides in solution and in complex.
Alexis Lamiable, Pierre Thévenet, Julien Rey, Marek Vavrusa, Philippe Derreumaux, Pierre Tufféry. Nucleic Acids Res 2016
250
16

Decreased expression of SOX6 confers a poor prognosis in hepatocellular carcinoma.
Xiaodong Guo, Mei Yang, Hao Gu, Jingmin Zhao, Lin Zou. Cancer Epidemiol 2013
29
16

Sox6 and Otx2 control the specification of substantia nigra and ventral tegmental area dopamine neurons.
Lia Panman, Maria Papathanou, Ariadna Laguna, Tony Oosterveen, Nikolaos Volakakis, Dario Acampora, Idha Kurtsdotter, Takashi Yoshitake, Jan Kehr, Eliza Joodmardi,[...]. Cell Rep 2014
72
16


Concerted regulation of myofiber-specific gene expression and muscle performance by the transcriptional repressor Sox6.
Daniel Quiat, Kevin A Voelker, Jimin Pei, Nick V Grishin, Robert W Grange, Rhonda Bassel-Duby, Eric N Olson. Proc Natl Acad Sci U S A 2011
87
16

SOX6 controls dorsal progenitor identity and interneuron diversity during neocortical development.
Eiman Azim, Denis Jabaudon, Ryann M Fame, Jeffrey D Macklis. Nat Neurosci 2009
127
16

High-resolution genome-wide copy-number analyses identify localized copy-number alterations in Ewing sarcoma.
Miriam Lynn, Yuexiang Wang, Jaime Slater, Naisha Shah, Judith Conroy, Sean Ennis, Thomas Morris, David R Betts, Jonathan A Fletcher, Maureen J O'Sullivan. Diagn Mol Pathol 2013
16
16

Transcriptional landscape of the prenatal human brain.
Jeremy A Miller, Song-Lin Ding, Susan M Sunkin, Kimberly A Smith, Lydia Ng, Aaron Szafer, Amanda Ebbert, Zackery L Riley, Joshua J Royall, Kaylynn Aiona,[...]. Nature 2014
589
16

Genetic variants in the SOX6 gene are associated with bone mineral density in both Caucasian and Chinese populations.
T-L Yang, Y Guo, Y-J Liu, H Shen, Y-Z Liu, S-F Lei, J Li, Q Tian, H-W Deng. Osteoporos Int 2012
29
16

SOX6 attenuates glucose-stimulated insulin secretion by repressing PDX1 transcriptional activity and is down-regulated in hyperinsulinemic obese mice.
Haruhisa Iguchi, Yukio Ikeda, Masashi Okamura, Toshiya Tanaka, Yasuyo Urashima, Hiroto Ohguchi, Shinobu Takayasu, Noriaki Kojima, Satoshi Iwasaki, Riuko Ohashi,[...]. J Biol Chem 2005
62
16

Sox6 cell-autonomously stimulates erythroid cell survival, proliferation, and terminal maturation and is thereby an important enhancer of definitive erythropoiesis during mouse development.
Bogdan Dumitriu, Michael R Patrick, Jane P Petschek, Srujana Cherukuri, Ursula Klingmuller, Paul L Fox, Véronique Lefebvre. Blood 2006
59
16

Global developmental delay, progressive relapsing-remitting parkinsonism, and spinal syrinx in a child with SOX6 mutation.
Ori Scott, Jeffrey Pugh, Darcie Kiddoo, Lyn K Sonnenberg, Steven Bamforth, Helly R Goez. J Child Neurol 2014
8
16

The cell-intrinsic requirement of Sox6 for cortical interneuron development.
Renata Batista-Brito, Elsa Rossignol, Jens Hjerling-Leffler, Myrto Denaxa, Michael Wegner, Véronique Lefebvre, Vassilis Pachnis, Gord Fishell. Neuron 2009
137
16


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.