A citation-based method for searching scientific literature

Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow, Peter J Scambler, Anne S Bassett. Nat Rev Dis Primers 2015
Times Cited: 381



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: 523




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
1

Current and Future Therapeutic Approaches for Thymic Stromal Cell Defects.
Alexandra Y Kreins, Paola Bonfanti, E Graham Davies. Front Immunol 2021
0

Palatoschisis, Schizophrenia and Hypocalcaemia: Phenotypic Expression of 22q11.2 Deletion Syndrome (DiGeorge Syndrome) in an Adult.
Melissa Elise van der Meijs, Dave Henri Schweitzer, Henk Boom. Eur J Case Rep Intern Med 2021
0

Congenital Athymia: Genetic Etiologies, Clinical Manifestations, Diagnosis, and Treatment.
Cathleen Collins, Emily Sharpe, Abigail Silber, Sarah Kulke, Elena W Y Hsieh. J Clin Immunol 2021
1

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

Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center.
Tugba Sarac Sivrikoz, Seher Basaran, Recep Has, Birsen Karaman, Ibrahim Halil Kalelioglu, Melike Kirgiz, Umut Altunoglu, Atil Yuksel. Arch Gynecol Obstet 2021
0

Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights.
Giulio Calcagni, Flaminia Pugnaloni, Maria Cristina Digilio, Marta Unolt, Carolina Putotto, Marcello Niceta, Anwar Baban, Francesca Piceci Sparascio, Fabrizio Drago, Alessandro De Luca,[...]. Genes (Basel) 2021
0

DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosis.
Barbara Rivera, Javad Nadaf, Somayyeh Fahiminiya, Maria Apellaniz-Ruiz, Avi Saskin, Anne-Sophie Chong, Sahil Sharma, Rabea Wagener, Timothée Revil, Vincenzo Condello,[...]. J Clin Invest 2020
5

Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
Yingjie Zhao, Alexander Diacou, H Richard Johnston, Fadi I Musfee, Donna M McDonald-McGinn, Daniel McGinn, T Blaine Crowley, Gabriela M Repetto, Ann Swillen, Jeroen Breckpot,[...]. Am J Hum Genet 2020
14

Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx.
Noritaka Adachi, Marchesa Bilio, Antonio Baldini, Robert G Kelly. Development 2020
6