A citation-based method for searching scientific literature

Kyle Retterer, Jane Juusola, Megan T Cho, Patrik Vitazka, Francisca Millan, Federica Gibellini, Annette Vertino-Bell, Nizar Smaoui, Julie Neidich, Kristin G Monaghan, Dianalee McKnight, Renkui Bai, Sharon Suchy, Bethany Friedman, Jackie Tahiliani, Daniel Pineda-Alvarez, Gabriele Richard, Tracy Brandt, Eden Haverfield, Wendy K Chung, Sherri Bale. Genet Med 2016
Times Cited: 433



Geraldine A Van der Auwera, Mauricio O Carneiro, Christopher Hartl, Ryan Poplin, Guillermo Del Angel, Ami Levy-Moonshine, Tadeusz Jordan, Khalid Shakir, David Roazen, Joel Thibault, Eric Banks, Kiran V Garimella, David Altshuler, Stacey Gabriel, Mark A DePristo. Curr Protoc Bioinformatics 2013
Times Cited: 2433




List of shared articles



Times cited

Successful application of genome sequencing in a diagnostic setting: 1007 index cases from a clinically heterogeneous cohort.
Aida M Bertoli-Avella, Christian Beetz, Najim Ameziane, Maria Eugenia Rocha, Pilar Guatibonza, Catarina Pereira, Maria Calvo, Natalia Herrera-Ordonez, Monica Segura-Castel, Dan Diego-Alvarez,[...]. Eur J Hum Genet 2021
6

Genome sequencing increases diagnostic yield in clinically diagnosed Alagille syndrome patients with previously negative test results.
Ramakrishnan Rajagopalan, Melissa A Gilbert, Deborah A McEldrew, James A Nassur, Kathleen M Loomes, David A Piccoli, Ian D Krantz, Laura K Conlin, Nancy B Spinner. Genet Med 2021
2

Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities.
Kimia Najafi, Zohreh Mehrjoo, Fariba Ardalani, Siavash Ghaderi-Sohi, Ariana Kariminejad, Roxana Kariminejad, Hossein Najmabadi. Sci Rep 2021
0

Clinical application of whole-exome sequencing: A retrospective, single-center study.
Qiang Zhang, Zailong Qin, Shang Yi, Hao Wei, Xun Zhao Zhou, Jiasun Su. Exp Ther Med 2021
0

Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.
Miriam S Reuter, Rajiv R Chaturvedi, Rebekah K Jobling, Giovanna Pellecchia, Omar Hamdan, Wilson W L Sung, Thomas Nalpathamkalam, Pratyusha Attaluri, Candice K Silversides, Rachel M Wald,[...]. Circ Genom Precis Med 2021
0