A citation-based method for searching scientific literature

Robert J Shprintzen. Dev Disabil Res Rev 2008
Times Cited: 271



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, William T Mahle, Robert M Campbell. Pediatrics 2003
Times Cited: 411




List of shared articles



Times cited

The Oral Health of Patients with DiGeorge Syndrome (22q11) Microdeletion: A Case Report.
Estephania Candelo, Maria Alejandra Estrada-Mesa, Adriana Jaramillo, Carlos Humberto Martinez-Cajas, Julio Cesar Osorio, Harry Pachajoa. Appl Clin Genet 2021
0

CNVs in the 22q11.2 Chromosomal Region Should Be an Early Suspect in Infants with Congenital Cardiac Disease.
Tatiana Pineda, Ignacio Zarante, Angela Camila Paredes, Juan Pablo Rozo, Martha C Reyes, Olga María Moreno-Niño. Clin Med Insights Cardiol 2021
0

Reflections of parents of children with 22q11.2 Deletion Syndrome on the experience of receiving psychiatric genetic counseling: 'Awareness to Act'.
Prescilla Carrion, Alicia Semaka, Rolan Batallones, Caitlin Slomp, Emily Morris, Angela Inglis, Marlene Moretti, Jehannine Austin. J Genet Couns 2021
0

Second instance of co-occurring 22q11.2 deletion syndrome and Williams syndrome.
Crescenda L Uhles, Shirelle Barnes, Naseem Uddin, Luis A Umaña. Am J Med Genet A 2021
0

Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil.
Bruna Lixinski Diniz, Andressa Schneiders Santos, Andressa Barreto Glaeser, Bruna Baierle Guaraná, Cláudia Fernandes Lorea, Juliana Alves Josahkian, Janaína Huber, Rafael Fabiano Machado Rosa, Paulo Ricardo Gazzola Zen. J Pediatr Genet 2020
0

Magnetic resonance angiography (MRA) in preoperative planning for patients with 22q11.2 deletion syndrome undergoing craniofacial and otorhinolaryngologic procedures.
Rotem Kimia, Lisa Elden, Julia Dailey, Mallika Kodavatiganti, T Blaine Crowley, Daniel E McGinn, Alice Bailey, Elaine H Zackai, Donna M McDonald-McGinn, Oksana A Jackson. Int J Pediatr Otorhinolaryngol 2020
0

Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array.
Meiying Cai, Na Lin, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Ying Li, Yuan Lin, Hailong Huang, Liangpu Xu. Mol Biol Rep 2020
0


Immune system defects in DiGeorge syndrome and association with clinical course.
Ercan Nain, Ayca Kiykim, Ismail Ogulur, Nurhan Kasap, Elif Karakoc-Aydiner, Ahmet Ozen, Safa Baris. Scand J Immunol 2019
2

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
10

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


Comparing the broad socio-cognitive profile of youth with Williams syndrome and 22q11.2 deletion syndrome.
O Weisman, R Feldman, M Burg-Malki, M Keren, R Geva, G Diesendruck, D Gothelf. J Intellect Disabil Res 2017
4

Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndrome.
Arnaud Leleu, Guillaume Saucourt, Caroline Rigard, Gabrielle Chesnoy, Jean-Yves Baudouin, Massimiliano Rossi, Patrick Edery, Nicolas Franck, Caroline Demily. Eur Child Adolesc Psychiatry 2016
14


The use of two different MLPA kits in 22q11.2 deletion syndrome.
L J M Evers, J J M Engelen, L M H Houben, L M G Curfs, T A M J van Amelsvoort. Eur J Med Genet 2016
3