A citation-based method for searching scientific literature

Anne S Bassett, Eva W C Chow, Janice Husted, Rosanna Weksberg, Oana Caluseriu, Gary D Webb, Michael A Gatzoulis. Am J Med Genet A 2005
Times Cited: 285

S Oskarsdóttir, M Vujic, A Fasth. Arch Dis Child 2004
Times Cited: 270

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

Sexual knowledge and behaviour in 22q11.2 deletion syndrome, a complex care condition.
Lisa D Palmer, Tracy Heung, Maria Corral, Erik Boot, Stephanie G Brooks, Anne S Bassett. J Appl Res Intellect Disabil 2021

Evaluation and Maintenance of Behavioral Interventions for 22q11.2 Deletion Syndrome.
Louis Busch, Valdeep Saini, Sidrah Karim, Roland Jones. Dev Neurorehabil 2021

Lower [18F]fallypride binding to dopamine D2/3 receptors in frontal brain areas in adults with 22q11.2 deletion syndrome: a positron emission tomography study.
Esther D A van Duin, Jenny Ceccarini, Jan Booij, Zuzana Kasanova, Claudia Vingerhoets, Jytte van Huijstee, Alexander Heinzel, Siamak Mohammadkhani-Shali, Oliver Winz, Felix Mottaghy,[...]. Psychol Med 2020

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

22q11 microdeletion syndrome and ultra-high risk for psychosis: The role of neurological soft signs as an independent marker of vulnerability for psychosis.
Mariabernarda Pitzianti, Maria Pontillo, Stefano Vicari, Marco Armando, Augusto Pasini. Early Interv Psychiatry 2019

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

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

Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome.
Lisa D Palmer, Nancy J Butcher, Erik Boot, Kathleen A Hodgkinson, Tracy Heung, Eva W C Chow, Alina Guna, T Blaine Crowley, Elaine Zackai, Donna M McDonald-McGinn,[...]. Am J Med Genet A 2018

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.
Marta Unolt, Paolo Versacci, Silvia Anaclerio, Caterina Lambiase, Giulio Calcagni, Matteo Trezzi, Adriano Carotti, Terrence Blaine Crowley, Elaine H Zackai, Elizabeth Goldmuntz,[...]. Am J Med Genet A 2018

Signs of dysarthria in adults with 22q11.2 deletion syndrome.
Christina Persson, Katja Laakso, Hannah Edwardsson, Johanna Lindblom, Lena Hartelius. Am J Med Genet A 2017

High prevalence of fatigue in adults with a 22q11.2 deletion syndrome.
Elfi Vergaelen, Stephan Claes, Stefan Kempke, Ann Swillen. Am J Med Genet A 2017

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

Post-childhood Presentation and Diagnosis of DiGeorge Syndrome.
Nir Friedman, Shlomit Rienstein, Yonatan Yeshayahu, Doron Gothelf, Raz Somech. Clin Pediatr (Phila) 2016

A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH.
Céline Poirsier, Justine Besseau-Ayasse, Caroline Schluth-Bolard, Jérôme Toutain, Chantal Missirian, Cédric Le Caignec, Anne Bazin, Marie Christine de Blois, Paul Kuentz, Marie Catty,[...]. Eur J Hum Genet 2016