A citation-based method for searching scientific literature

David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein, W Andrew Faucett, Lars Feuk, Jan M Friedman, Ada Hamosh, Laird Jackson, Erin B Kaminsky, Klaas Kok, Ian D Krantz, Robert M Kuhn, Charles Lee, James M Ostell, Carla Rosenberg, Stephen W Scherer, Nancy B Spinner, Dimitri J Stavropoulos, James H Tepperberg, Erik C Thorland, Joris R Vermeesch, Darrel J Waggoner, Michael S Watson, Christa Lese Martin, David H Ledbetter. Am J Hum Genet 2010
Times Cited: 1485



Agatino Battaglia, Viola Doccini, Laura Bernardini, Antonio Novelli, Sara Loddo, Anna Capalbo, Tiziana Filippi, John C Carey. Eur J Paediatr Neurol 2013
Times Cited: 118




List of shared articles



Times cited

Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project.
Huijun Wang, Feifan Xiao, Xinran Dong, Yulan Lu, Guoqiang Cheng, Laishuan Wang, Wei Lu, Lin Yang, Liping Chen, Wenqing Kang,[...]. Hum Mutat 2021
0

Genetic Testing in Neurodevelopmental Disorders.
Juliann M Savatt, Scott M Myers. Front Pediatr 2021
5

Genetic and metabolic investigations for individuals with neurodevelopmental disorders: A survey of Canadian geneticists' practices.
Melissa T Carter, Mireille Cloutier, Anne Tsampalieros, Richard Webster. Am J Med Genet A 2021
0

Next-generation gene panel testing in adolescents and adults in a medical neuropsychiatric genetics clinic.
Y Trakadis, A Accogli, B Qi, D Bloom, R Joober, E Levy, K Tabbane. Neurogenetics 2021
0

Optimizing the Diagnostic Strategy to Identify Genetic Abnormalities in Miscarriage.
Jong-Mi Lee, So Young Shin, Guk Won Kim, Woo Jeng Kim, Jeong Ha Wie, Subeen Hong, Dain Kang, Hayoung Choi, Jisook Yim, Yonggoo Kim,[...]. Mol Diagn Ther 2021
0

Exome Sequencing in 200 Intellectual Disability/Autistic Patients: New Candidates and Atypical Presentations.
Floriana Valentino, Lucia Pia Bruno, Gabriella Doddato, Annarita Giliberti, Rossella Tita, Sara Resciniti, Chiara Fallerini, Mirella Bruttini, Caterina Lo Rizzo, Maria Antonietta Mencarelli,[...]. Brain Sci 2021
0

Comparison of the diagnostic yield of aCGH and genome-wide sequencing across different neurodevelopmental disorders.
Francisco Martinez-Granero, Fiona Blanco-Kelly, Carolina Sanchez-Jimeno, Almudena Avila-Fernandez, Ana Arteche, Ana Bustamante-Aragones, Cristina Rodilla, Elvira Rodríguez-Pinilla, Rosa Riveiro-Alvarez, Saoud Tahsin-Swafiri,[...]. NPJ Genom Med 2021
1

Parental stress and adjustment in the context of rare genetic syndromes: A scoping review.
Jacqueline Fitzgerald, Louise Gallagher. J Intellect Disabil 2021
0