A citation-based method for searching scientific literature

Jihoon G Yoon, Hyung Min Hahn, Sungkyoung Choi, Soo Jung Kim, Sowon Aum, Jung Woo Yu, Eun Kyung Park, Kyu Won Shim, Min Goo Lee, Yong Oock Kim. Neurosurgery 2020
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations.
Eric Lee, Trang Le, Ying Zhu, George Elakis, Anne Turner, William Lo, Hanka Venselaar, Carol-Ann Verrenkamp, Nicole Snow, David Mowat,[...]. Genet Med 2018
22
66

Clinical genetics of craniosynostosis.
Andrew O M Wilkie, David Johnson, Steven A Wall. Curr Opin Pediatr 2017
53
50

Heterozygous mutations in ERF cause syndromic craniosynostosis with multiple suture involvement.
Ayeshah Chaudhry, Peter Sabatini, Liping Han, Peter N Ray, Christopher Forrest, Sarah Bowdin. Am J Med Genet A 2015
16
33

Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis.
Stephen R F Twigg, Elena Vorgia, Simon J McGowan, Ioanna Peraki, Aimée L Fenwick, Vikram P Sharma, Maryline Allegra, Andreas Zaragkoulias, Elham Sadighi Akha, Samantha J L Knight,[...]. Nat Genet 2013
94
33

The transcriptional ETS2 repressor factor associates with active and inactive Erks through distinct FXF motifs.
Sarantis Polychronopoulos, Mihalis Verykokakis, Mustafa N Yazicioglu, Maria Sakarellos-Daitsiotis, Melanie H Cobb, George Mavrothalassitis. J Biol Chem 2006
19
33

De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis.
Andrew T Timberlake, Charuta G Furey, Jungmin Choi, Carol Nelson-Williams, Erin Loring, Amy Galm, Kristopher T Kahle, Derek M Steinbacher, Dawid Larysz, John A Persing,[...]. Proc Natl Acad Sci U S A 2017
43
33

ERF nuclear shuttling, a continuous monitor of Erk activity that links it to cell cycle progression.
Lionel Le Gallic, Laura Virgilio, Philip Cohen, Benoit Biteau, George Mavrothalassitis. Mol Cell Biol 2004
46
33

A progressive and complex clinical course in two family members with ERF-related craniosynostosis: a case report.
Izabella Körberg, Daniel Nowinski, Marie-Louise Bondeson, Malin Melin, Lars Kölby, Eva-Lena Stattin. BMC Med Genet 2020
3
66

ERF-related craniosynostosis: The phenotypic and developmental profile of a new craniosynostosis syndrome.
Graeme E Glass, Justine O'Hara, Natalie Canham, Deirdre Cilliers, David Dunaway, Aimee L Fenwick, Noor-Owase Jeelani, David Johnson, Tracy Lester, Helen Lord,[...]. Am J Med Genet A 2019
15
33

Cell fate decisions are specified by the dynamic ERK interactome.
Alex von Kriegsheim, Daniela Baiocchi, Marc Birtwistle, David Sumpton, Willy Bienvenut, Nicholas Morrice, Kayo Yamada, Angus Lamond, Gabriella Kalna, Richard Orton,[...]. Nat Cell Biol 2009
195
33

Gene/environment interactions in craniosynostosis: A brief review.
E L Durham, R N Howie, J J Cray. Orthod Craniofac Res 2017
9
16

Genetic advances in craniosynostosis.
Wanda Lattanzi, Marta Barba, Lorena Di Pietro, Simeon A Boyadjiev. Am J Med Genet A 2017
43
16


Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes.
Erik Engelen, Umut Akinci, Jan Christian Bryne, Jun Hou, Cristina Gontan, Maaike Moen, Dorota Szumska, Christel Kockx, Wilfred van Ijcken, Dick H W Dekkers,[...]. Nat Genet 2011
164
16

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

IMP 2.0: a multi-species functional genomics portal for integration, visualization and prediction of protein functions and networks.
Aaron K Wong, Arjun Krishnan, Victoria Yao, Alicja Tadych, Olga G Troyanskaya. Nucleic Acids Res 2015
35
16

Clinical spectrum and outcomes in families with coronal synostosis and TCF12 mutations.
Federico di Rocco, Geneviève Baujat, Eric Arnaud, Dominique Rénier, Jean-Louis Laplanche, Valérie Cormier Daire, Corinne Collet. Eur J Hum Genet 2014
20
16

The zebrafish as a model system for forebrain GnRH neuronal development.
Eytan Abraham, Ori Palevitch, Yoav Gothilf, Yonathan Zohar. Gen Comp Endocrinol 2009
42
16

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome.
M Muenke, U Schell, A Hehr, N H Robin, H W Losken, A Schinzel, L J Pulleyn, P Rutland, W Reardon, S Malcolm. Nat Genet 1994
488
16

GEMINI: integrative exploration of genetic variation and genome annotations.
Umadevi Paila, Brad A Chapman, Rory Kirchner, Aaron R Quinlan. PLoS Comput Biol 2013
236
16

Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans.
Daniel Kelberman, Karine Rizzoti, Ariel Avilion, Maria Bitner-Glindzicz, Stefano Cianfarani, Julie Collins, W Kling Chong, Jeremy M W Kirk, John C Achermann, Richard Ross,[...]. J Clin Invest 2006
207
16

CHIP is a chaperone-dependent E3 ligase that ubiquitylates unfolded protein.
S Murata, Y Minami, M Minami, T Chiba, K Tanaka. EMBO Rep 2001
405
16

NGS targeted screening of 100 Scandinavian patients with coronal synostosis.
Alexandra Topa, Anna Rohlin, Mattias K Andersson, André Fehr, Lovisa Lovmar, Göran Stenman, Lars Kölby. Am J Med Genet A 2020
3
33




Two novel variants in the TCF12 gene identified in cases with craniosynostosis.
Athanasios Goumenos, Eirini Tsoutsou, Joanne Traeger-Synodinos, Dimitrios Petychakis, Maria Gavra, Aggeliki Kolialexi, Helena Frysira. Appl Clin Genet 2019
2
50


SoxB1 transcription factors and Notch signaling use distinct mechanisms to regulate proneural gene function and neural progenitor differentiation.
Johan Holmberg, Emil Hansson, Michal Malewicz, Magnus Sandberg, Thomas Perlmann, Urban Lendahl, Jonas Muhr. Development 2008
47
16

GeneMatcher: a matching tool for connecting investigators with an interest in the same gene.
Nara Sobreira, François Schiettecatte, David Valle, Ada Hamosh. Hum Mutat 2015
589
16


CHOPCHOP v2: a web tool for the next generation of CRISPR genome engineering.
Kornel Labun, Tessa G Montague, James A Gagnon, Summer B Thyme, Eivind Valen. Nucleic Acids Res 2016
401
16

Co-occurrence of frameshift mutations in SMAD6 and TCF12 in a child with complex craniosynostosis.
Andrew T Timberlake, Robin Wu, Carol Nelson-Williams, Charuta G Furey, Kristi I Hildebrand, Scott W Elton, Jeyhan S Wood, John A Persing, Richard P Lifton. Hum Genome Var 2018
8
16

Widespread defects in the primary olfactory pathway caused by loss of Mash1 function.
Richard C Murray, Daniel Navi, John Fesenko, Arthur D Lander, Anne L Calof. J Neurosci 2003
80
16

TRIM33 switches off Ifnb1 gene transcription during the late phase of macrophage activation.
Federica Ferri, Aude Parcelier, Vanessa Petit, Anne-Sophie Gallouet, Daniel Lewandowski, Marion Dalloz, Anita van den Heuvel, Petros Kolovos, Eric Soler, Mario Leonardo Squadrito,[...]. Nat Commun 2015
22
16


Coronal craniosynostosis due to TCF12 mutations in patients from Turkey.
Elanur Yilmaz, Ercan Mihci, Banu Nur, Ozgul M Alper. Am J Med Genet A 2019
1
100

Neural crest and olfactory system: new prospective.
Paolo E Forni, Susan Wray. Mol Neurobiol 2012
45
16

FGFs, their receptors, and human limb malformations: clinical and molecular correlations.
Andrew O M Wilkie, Susannah J Patey, Shih-Hsin Kan, Ans M W van den Ouweland, Ben C J Hamel. Am J Med Genet 2002
136
16

The Molecular Signatures Database (MSigDB) hallmark gene set collection.
Arthur Liberzon, Chet Birger, Helga Thorvaldsdóttir, Mahmoud Ghandi, Jill P Mesirov, Pablo Tamayo. Cell Syst 2015
16

Olfactory phenotypic spectrum in idiopathic hypogonadotropic hypogonadism: pathophysiological and genetic implications.
Hilana M Lewkowitz-Shpuntoff, Virginia A Hughes, Lacey Plummer, Margaret G Au, Richard L Doty, Stephanie B Seminara, Yee-Ming Chan, Nelly Pitteloud, William F Crowley, Ravikumar Balasubramanian. J Clin Endocrinol Metab 2012
58
16

Prokineticin 2 is a target gene of proneural basic helix-loop-helix factors for olfactory bulb neurogenesis.
Chengkang Zhang, Kwan L Ng, Jia-Da Li, Fei He, David J Anderson, Yi E Sun, Qun-Yong Zhou. J Biol Chem 2007
30
16

Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletion.
D Bick, C J Curry, J R McGill, D F Schorderet, R C Bux, C M Moore. Am J Med Genet 1989
60
16

GeNets: a unified web platform for network-based genomic analyses.
Taibo Li, April Kim, Joseph Rosenbluh, Heiko Horn, Liraz Greenfeld, David An, Andrew Zimmer, Arthur Liberzon, Jon Bistline, Ted Natoli,[...]. Nat Methods 2018
26
16

TCF12 microdeletion in a 72-year-old woman with intellectual disability.
Juliette Piard, Virginie Rozé, Alain Czorny, Marion Lenoir, Mylène Valduga, Aimée L Fenwick, Andrew O M Wilkie, Lionel Van Maldergem. Am J Med Genet A 2015
9
16

Ataxia, dementia, and hypogonadotropism caused by disordered ubiquitination.
David H Margolin, Maria Kousi, Yee-Ming Chan, Elaine T Lim, Jeremy D Schmahmann, Marios Hadjivassiliou, Janet E Hall, Ibrahim Adam, Andrew Dwyer, Lacey Plummer,[...]. N Engl J Med 2013
123
16

Interactions between heterologous helix-loop-helix proteins generate complexes that bind specifically to a common DNA sequence.
C Murre, P S McCaw, H Vaessin, M Caudy, L Y Jan, Y N Jan, C V Cabrera, J N Buskin, S D Hauschka, A B Lassar. Cell 1989
16

CHIP is a U-box-dependent E3 ubiquitin ligase: identification of Hsc70 as a target for ubiquitylation.
J Jiang, C A Ballinger, Y Wu, Q Dai, D M Cyr, J Höhfeld, C Patterson. J Biol Chem 2001
435
16

Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.
Ravikumar Balasubramanian, Jin-Ho Choi, Ludmila Francescatto, Jason Willer, Edward R Horton, Eleni P Asimacopoulos, Konstantina M Stankovic, Lacey Plummer, Cassandra L Buck, Richard Quinton,[...]. Proc Natl Acad Sci U S A 2014
38
16

E proteins in lymphocyte development and lymphoid diseases.
Ian Belle, Yuan Zhuang. Curr Top Dev Biol 2014
21
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.