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



Caterina Cancrini, Pamela Puliafito, Maria Cristina Digilio, Annarosa Soresina, Silvana Martino, Roberto Rondelli, Rita Consolini, Ezia Maria Ruga, Fabio Cardinale, Andrea Finocchi, Maria Luisa Romiti, Baldassarre Martire, Rosa Bacchetta, Veronica Albano, Adriano Carotti, Fernando Specchia, Davide Montin, Emilia Cirillo, Guido Cocchi, Antonino Trizzino, Grazia Bossi, Ornella Milanesi, Chiara Azzari, Giovanni Corsello, Claudio Pignata, Alessandro Aiuti, Maria Cristina Pietrogrande, Bruno Marino, Alberto Giovanni Ugazio, Alessandro Plebani, Paolo Rossi. J Pediatr 2014
Times Cited: 78




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

Clinical Features in a Large Cohort of Patients With 22q11.2 Deletion Syndrome.
Ella Nissan, Uriel Katz, Yael Levy-Shraga, Shirly Frizinsky, Eldar Carmel, Doron Gothelf, Raz Somech. J Pediatr 2021
0

Pediatric endocrinology through syndromes.
Gianluca Tornese, Maria Chiara Pellegrin, Egidio Barbi, Alessandro Ventura. Eur J Med Genet 2020
4

Clinical and immunophenotypic characteristics of patients with chromosome 22q11.2 deletion syndrome: a single institution's experience.
Serdar Nepesov, Fatma Deniz Aygün, Umut Küçüksezer, Emre Taşdemir, Haluk Çokuğraş, Yıldız Camcıoğlu. Turk Pediatri Ars 2019
0

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
19


Delayed diagnosis of 22q11 deletion syndrome due to late onset hypocalcemia in a 11-year-old girl with imperforated anus.
Dong-Yoon Yoo, Hae Jung Kim, Kee Hyun Cho, Eun Byul Kwon, Eun-Gyong Yoo. Ann Pediatr Endocrinol Metab 2017
4

Post-childhood Presentation and Diagnosis of DiGeorge Syndrome.
Nir Friedman, Shlomit Rienstein, Yonatan Yeshayahu, Doron Gothelf, Raz Somech. Clin Pediatr (Phila) 2016
5

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
22