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



Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura, Naoyuki Kamatani, Kazuo Momma, Atsuyoshi Takao, Makoto Nakazawa, Nobuyoshi Shimizu, Rumiko Matsuoka. Lancet 2003
Times Cited: 524




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
2

Care of Children with DiGeorge Before and After Cultured Thymus Tissue Implantation.
Stephanie E Gupton, Elizabeth A McCarthy, M Louise Markert. J Clin Immunol 2021
0


The Genetics and Epigenetics of 22q11.2 Deletion Syndrome.
Qiumei Du, M Teresa de la Morena, Nicolai S C van Oers. Front Genet 2020
19

Clinical application of chromosomal microarray analysis for fetuses with craniofacial malformations.
Chenyang Xu, Yanbao Xiang, Xueqin Xu, Lili Zhou, Huanzheng Li, Xueqin Dong, Shaohua Tang. Mol Cytogenet 2020
1

Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.
Ikuyo Kou, Nao Otomo, Kazuki Takeda, Yukihide Momozawa, Hsing-Fang Lu, Michiaki Kubo, Yoichiro Kamatani, Yoji Ogura, Yohei Takahashi, Masahiro Nakajima,[...]. Nat Commun 2019
14

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
17

De novo unbalanced translocation t(15;22)(q26.2;q12) with velo-cardio-facial syndrome: A case report and review of the literature.
Cristina Gug, Delia Huțanu, Monica Vaida, Gabriela Doroş, Cristina Popa, Ramona Stroescu, Gheorghe Furău, Cristian Furău, Laura Grigoriță, Ioana Mozos. Exp Ther Med 2018
4

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
Esther Lopez-Rivera, Yangfan P Liu, Miguel Verbitsky, Blair R Anderson, Valentina P Capone, Edgar A Otto, Zhonghai Yan, Adele Mitrotti, Jeremiah Martino, Nicholas J Steers,[...]. N Engl J Med 2017
65