A citation-based method for searching scientific literature

S Oskarsdóttir, M Vujic, A Fasth. Arch Dis Child 2004
Times Cited: 277

A S Bassett, E W C Chow, J Husted, K A Hodgkinson, E Oechslin, L Harris, C Silversides. J Med Genet 2009
Times Cited: 60

List of shared articles

Times cited

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

The psychosocial impact of 22q11 deletion syndrome on patients and families: A systematic review.
Oanh Kieu Vo, Alisdair McNeill, Katharina Sophie Vogt. 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

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

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