A citation-based method for searching scientific literature

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden.
S Oskarsdóttir, M Vujic, A Fasth. Arch Dis Child 2004
Times Cited: 277



Prevalence of 22q11 microdeletion.
S Tézenas Du Montcel, H Mendizabai, S Aymé, A Lévy, N Philip. J Med Genet 1996
Times Cited: 196




List of shared articles



Times cited

Inborn errors of thymic stromal cell development and function.
Alexandra Y Kreins, Stefano Maio, Fatima Dhalla. Semin Immunopathol 2021
4

Long Noncoding RNA lnc-TSSK2-8 Activates Canonical Wnt/β-Catenin Signaling Through Small Heat Shock Proteins HSPA6 and CRYAB.
Jingjing Fa, Xiaoqing Zhang, Xiaoping Zhang, Ming Qi, Xingyu Zhang, Qihua Fu, Zhuoming Xu, Yunqian Gao, Bo Wang. Front Cell Dev Biol 2021
1

Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screening.
Christina Blagojevic, Tracy Heung, Mylene Theriault, Aoy Tomita-Mitchell, Pranesh Chakraborty, Kristin Kernohan, Dennis E Bulman, Anne S Bassett. CMAJ Open 2021
6

A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort.
Lisa Hui, Alice Poulton, Eliza Kluckow, Anthea Lindquist, Briohny Hutchinson, Mark D Pertile, Leonard Bonacquisto, Lucy Gugasyan, Abhijit Kulkarni, James Harraway,[...]. Hum Reprod 2020
2

Clinical Features to Predict 22q11.2 Deletion Syndrome Proven by Molecular Genetic Testing.
Kitiwan Rojnueangit, Thanitchet Khetkham, Preyaporn Onsod, Takol Chareonsirisuthigul. J Pediatr Genet 2020
1

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

Chromosome 22q11.2 deletion syndrome and DiGeorge syndrome.
Kathleen E Sullivan. Immunol Rev 2019
34

Palatal evaluation and treatment in 22q11.2 deletion syndrome.
Oksana Jackson, T Blaine Crowley, Robert Sharkus, Robert Smith, Stephanie Jeong, Cynthia Solot, Donna McDonald-Mcginn. Am J Med Genet A 2019
7

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

Speech-Language Disorders in 22q11.2 Deletion Syndrome: Best Practices for Diagnosis and Management.
Cynthia B Solot, Debbie Sell, Anne Mayne, Adriane L Baylis, Christina Persson, Oksana Jackson, Donna M McDonald-McGinn. Am J Speech Lang Pathol 2019
14

Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions.
K Martin, S Iyengar, A Kalyan, C Lan, A L Simon, M Stosic, K Kobara, H Ravi, T Truong, A Ryan,[...]. Clin Genet 2018
46

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

Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2.
Tingwei Guo, Alexander Diacou, Hiroko Nomaru, Donna M McDonald-McGinn, Matthew Hestand, Wolfram Demaerel, Liangtian Zhang, Yingjie Zhao, Francisco Ujueta, Jidong Shan,[...]. Hum Mol Genet 2018
14

Developmental Delay, Treatment-Resistant Psychosis, and Early-Onset Dementia in a Man With 22q11 Deletion Syndrome and Huntington's Disease.
Martilias Farrell, Maya Lichtenstein, James J Crowley, Dawn M Filmyer, Gabriel Lázaro-Muñoz, Rita A Shaughnessy, Ian R Mackenzie, Veronica Hirsch-Reinshagen, Robert Stowe, James P Evans,[...]. Am J Psychiatry 2018
6

22q and two: 22q11.2 deletion syndrome and coexisting conditions.
Jennifer L Cohen, Terrence B Crowley, Daniel E McGinn, Carey McDougall, Marta Unolt, Michele P Lambert, Beverly S Emanuel, Elaine H Zackai, Donna M McDonald-McGinn. Am J Med Genet A 2018
9

Club foot in association with the 22q11.2 deletion syndrome: An observational study.
Jelle F Homans, Terrence B Crowley, Erin Chen, Daniel E McGinn, Vincent F X Deeney, Ralph J B Sakkers, Richard S Davidson, René M Castelein, Donna M McDonald-McGinn. Am J Med Genet A 2018
2

The benefits and limitations of cell-free DNA screening for 22q11.2 deletion syndrome.
Lorraine Dugoff, Michael T Mennuti, Donna M McDonald-McGinn. Prenat Diagn 2017
17

Resolution of Primary Immune Defect in 22q11.2 Deletion Syndrome.
Yiwa Suksawat, Achara Sathienkijkanchai, Jittima Veskitkul, Orathai Jirapongsananuruk, Nualanong Visitsunthorn, Pakit Vichyanond, Punchama Pacharn. J Clin Immunol 2017
5

Examining the Overlap between Autism Spectrum Disorder and 22q11.2 Deletion Syndrome.
Opal Ousley, A Nichole Evans, Samuel Fernandez-Carriba, Erica L Smearman, Kimberly Rockers, Michael J Morrier, David W Evans, Karlene Coleman, Joseph Cubells. Int J Mol Sci 2017
15

Neuroradiographic findings in 22q11.2 deletion syndrome.
Lauren A Bohm, Tom C Zhou, Tyler J Mingo, Sarah L Dugan, Richard J Patterson, James D Sidman, Brianne B Roby. Am J Med Genet A 2017
13


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