A citation-based method for searching scientific literature

Christina Blagojevic, Tracy Heung, Mylene Theriault, Aoy Tomita-Mitchell, Pranesh Chakraborty, Kristin Kernohan, Dennis E Bulman, Anne S Bassett. CMAJ Open 2021
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
469
71

Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Francesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, Celine Dupont, Viola Alesi, Laetitia Gouas, Nina Horelli-Kuitunen, Kwong Wai Choy, Sandra García-Herrero, Alberto Gonzalez de la Vega,[...]. Prenat Diagn 2015
170
28

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study.
Line Olsen, Thomas Sparsø, Shantel M Weinsheimer, Marcelo Bertalan Quintanilha Dos Santos, Wiktor Mazin, Anders Rosengren, Xabier Calle Sanchez, Louise K Hoeffding, Henriette Schmock, Marie Baekvad-Hansen,[...]. Lancet Psychiatry 2018
56
28

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
Lorenzo D Botto, Kristin May, Paul M Fernhoff, Adolfo Correa, Karlene Coleman, Sonja A Rasmussen, Robert K Merritt, Leslie A O'Leary, Lee-Yang Wong, E Marsha Elixson,[...]. Pediatrics 2003
425
28

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Anne S Bassett, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W C Chow, Therese van Amelsvoort, Donna McDonald-McGinn, Raquel E Gur, Ann Swillen, Marianne Van den Bree,[...]. Am J Psychiatry 2017
48
28

Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms.
Alina Guna, Nancy J Butcher, Anne S Bassett. J Neurodev Disord 2015
57
28

Prevalence of adolescent idiopathic scoliosis in Turkey: an epidemiological study.
Hurriyet Yılmaz, Coskun Zateri, Aslihan Kusvuran Ozkan, Gulseren Kayalar, Haluk Berk. Spine J 2020
13
14

Congenital heart disease and idiopathic scoliosis.
R K Beals, K H Kenney, M H Lees. Clin Orthop Relat Res 1972
21
14

Animal models of scoliosis.
Justin D Bobyn, David G Little, Randolph Gray, Aaron Schindeler. J Orthop Res 2015
13
14

Scoliosis in association with the 22q11.2 deletion syndrome: an observational study.
Jelle F Homans, Vyaas G M Baldew, Rob C Brink, Moyo C Kruyt, Tom P C Schlösser, Michiel L Houben, Vincent F X Deeney, Terrence B Crowley, René M Castelein, Donna M McDonald-McGinn. Arch Dis Child 2019
12
14

Adolescent idiopathic scoliosis.
Jack C Cheng, René M Castelein, Winnie C Chu, Aina J Danielsson, Matthew B Dobbs, Theodoros B Grivas, Christina A Gurnett, Keith D Luk, Alain Moreau, Peter O Newton,[...]. Nat Rev Dis Primers 2015
193
14

Prevalence and risk factors for neural axis anomalies in idiopathic scoliosis: a systematic review.
Johan L Heemskerk, Moyo C Kruyt, Dino Colo, René M Castelein, Diederik H R Kempen. Spine J 2018
13
14

Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Anne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Solveig Oskarsdottir, Nicole Philip, Kathleen Sullivan,[...]. J Pediatr 2011
317
14

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium.
R E Gur, A S Bassett, D M McDonald-McGinn, C E Bearden, E Chow, B S Emanuel, M Owen, A Swillen, M Van den Bree, J Vermeesch,[...]. Mol Psychiatry 2017
42
14

What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia.
Ian M Campbell, Sarah E Sheppard, T Blaine Crowley, Daniel E McGinn, Alice Bailey, Michael J McGinn, Marta Unolt, Jelle F Homans, Erin Y Chen, Harold I Salmons,[...]. Am J Med Genet A 2018
41
14

The Natural History of Idiopathic Scoliosis During Growth: A Meta-Analysis.
Francesca Di Felice, Fabio Zaina, Sabrina Donzelli, Stefano Negrini. Am J Phys Med Rehabil 2018
10
14


Thoracic Idiopathic Scoliosis Severity Is Highly Correlated with 3D Measures of Thoracic Kyphosis.
T Barrett Sullivan, Fredrick G Reighard, Emily J Osborn, Kevin C Parvaresh, Peter O Newton. J Bone Joint Surg Am 2017
21
14

Sagittal curvature of the spine as a predictor of the pediatric spinal deformity development.
Saba Pasha, Steven de Reuver, Jelle F Homans, René M Castelein. Spine Deform 2021
2
50

The association between Chiari malformation Type I, spinal syrinx, and scoliosis.
Jennifer Strahle, Brandon W Smith, Melaine Martinez, J Rajiv Bapuraj, Karin M Muraszko, Hugh J L Garton, Cormac O Maher. J Neurosurg Pediatr 2015
43
14

An experimental study in chickens for the pathogenesis of idiopathic scoliosis.
M Machida, J Dubousset, Y Imamura, T Iwaya, T Yamada, J Kimura. Spine (Phila Pa 1976) 1993
122
14

Variations in the sagittal spinal profile precede the development of scoliosis: a pilot study of a new approach.
Jelle F Homans, Tom P C Schlösser, Saba Pasha, Moyo C Kruyt, René M Castelein. Spine J 2021
6
16

Understanding Idiopathic Scoliosis: A New Zebrafish School of Thought.
Curtis W Boswell, Brian Ciruna. Trends Genet 2017
51
14


Trabecular bone mineral density in idiopathic scoliosis.
S D Cook, A F Harding, E L Morgan, R J Nicholson, K A Thomas, T S Whitecloud, E S Ratner. J Pediatr Orthop 1987
84
14

Does scoliosis causes low bone mass? A comparative study between siblings.
Mir Sadat-Ali, Abdallah Al-Othman, Dalal Bubshait, Dakheel Al-Dakheel. Eur Spine J 2008
40
14

Adolescent idiopathic scoliosis: a new classification to determine extent of spinal arthrodesis.
L G Lenke, R R Betz, J Harms, K H Bridwell, D H Clements, T G Lowe, K Blanke. J Bone Joint Surg Am 2001
887
14

Effects of dorsal versus ventral shear loads on the rotational stability of the thoracic spine: a biomechanical porcine and human cadaveric study.
Jan-Willem M Kouwenhoven, Theo H Smit, Albert J van der Veen, Idsart Kingma, Jaap H van Dieën, René M Castelein. Spine (Phila Pa 1976) 2007
54
14

The selection of fusion levels in thoracic idiopathic scoliosis.
H A King, J H Moe, D S Bradford, R B Winter. J Bone Joint Surg Am 1983
580
14

Thyroid function and morphology in subjects with microdeletion of chromosome 22q11 (del(22)(q11)).
Stefano Stagi, Elisabetta Lapi, Eleonora Gambineri, Roberto Salti, Maurizio Genuardi, Gloria Colarusso, Camilla Conti, Rita Jenuso, Francesco Chiarelli, Chiara Azzari,[...]. Clin Endocrinol (Oxf) 2010
19
14

Generalized low areal and volumetric bone mineral density in adolescent idiopathic scoliosis.
J C Cheng, L Qin, C S Cheung, A H Sher, K M Lee, S W Ng, X Guo. J Bone Miner Res 2000
127
14

Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.
Jelle F Homans, Isabel N Tromp, Dino Colo, Tom P C Schlösser, Moyo C Kruyt, Vincent F X Deeney, Terrence B Crowley, Donna M McDonald-McGinn, René M Castelein. Am J Med Genet A 2018
9
14

Incidence and Surgery Rate of Idiopathic Scoliosis: A Nationwide Database Study.
Sahyun Sung, Hyun-Wook Chae, Hye Sun Lee, Sinae Kim, Ji-Won Kwon, Soo-Bin Lee, Seong-Hwan Moon, Hwan-Mo Lee, Byung Ho Lee. Int J Environ Res Public Health 2021
2
50

How 'idiopathic' is adolescent idiopathic scoliosis? A systematic review on associated abnormalities.
Tom P C Schlösser, Geert J M G van der Heijden, Anne L Versteeg, René M Castelein. PLoS One 2014
32
14


The 22q11.2 deletion syndrome as a model for idiopathic scoliosis - A hypothesis.
Jelle F Homans, Steven de Reuver, Elemi J Breetvelt, Jacob A S Vorstman, Vincent F X Deeney, John M Flynn, Donna M McDonald-McGinn, Moyo C Kruyt, René M Castelein. Med Hypotheses 2019
4
25

Differences in early sagittal plane alignment between thoracic and lumbar adolescent idiopathic scoliosis.
Tom P C Schlösser, Suken A Shah, Samantha J Reichard, Kenneth Rogers, Koen L Vincken, René M Castelein. Spine J 2014
44
14

The pathogenesis of adolescent idiopathic scoliosis: review of the literature.
Jan-Willem M Kouwenhoven, René M Castelein. Spine (Phila Pa 1976) 2008
140
14

Experimental animal models in scoliosis research: a review of the literature.
Michiel M A Janssen, Roeland F de Wilde, Jan-Willem M Kouwenhoven, René M Castelein. Spine J 2011
42
14

An assessment of maturity from anthropometric measurements.
Robert L Mirwald, Adam D G Baxter-Jones, Donald A Bailey, Gaston P Beunen. Med Sci Sports Exerc 2002
14

The genetic epidemiology of idiopathic scoliosis.
Kristen Fay Gorman, Cédric Julien, Alain Moreau. Eur Spine J 2012
62
14

The scoliosis of congenital heart disease.
C E Jordan, R I White, K C Fischer, C Neill, J P Dorst. Am Heart J 1972
36
14

The role of 22q11.2 deletion syndrome in the relationship between congenital heart disease and scoliosis.
Jelle F Homans, Steven de Reuver, Tracy Heung, Candice K Silversides, Erwin N Oechslin, Michiel L Houben, Donna M McDonald-McGinn, Moyo C Kruyt, René M Castelein, Anne S Bassett. Spine J 2020
1
100

Osteoporosis and acquired back deformities.
W L Burner, V M Badger, F C Sherman. J Pediatr Orthop 1982
56
14


Idiopathic Scoliosis as a Rotatory Decompensation of the Spine.
René M Castelein, Saba Pasha, Jack Cy Cheng, Jean Dubousset. J Bone Miner Res 2020
7
14

Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples.
Harini Ravi, Gabriel McNeill, Shruti Goel, Steven D Meltzer, Nathan Hunkapiller, Allison Ryan, Brynn Levy, Zachary P Demko. PLoS One 2018
21
14

Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
715
14

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!
D M McDonald-McGinn, M K Tonnesen, A Laufer-Cahana, B Finucane, D A Driscoll, B S Emanuel, E H Zackai. Genet Med 2001
203
14

Molecular genetics of 22q11.2 deletion syndrome.
Bernice E Morrow, Donna M McDonald-McGinn, Beverly S Emanuel, Joris R Vermeesch, Peter J Scambler. Am J Med Genet A 2018
41
14


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.