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
0

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
15

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
21

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
21

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
38

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