A citation-based method for searching scientific literature

Anthony A Philippakis, Danielle R Azzariti, Sergi Beltran, Anthony J Brookes, Catherine A Brownstein, Michael Brudno, Han G Brunner, Orion J Buske, Knox Carey, Cassie Doll, Sergiu Dumitriu, Stephanie O M Dyke, Johan T den Dunnen, Helen V Firth, Richard A Gibbs, Marta Girdea, Michael Gonzalez, Melissa A Haendel, Ada Hamosh, Ingrid A Holm, Lijia Huang, Matthew E Hurles, Ben Hutton, Joel B Krier, Andriy Misyura, Christopher J Mungall, Justin Paschall, Benedict Paten, Peter N Robinson, François Schiettecatte, Nara L Sobreira, Ganesh J Swaminathan, Peter E Taschner, Sharon F Terry, Nicole L Washington, Stephan Züchner, Kym M Boycott, Heidi L Rehm. Hum Mutat 2015
Times Cited: 271



Lina Basel-Salmon, Naama Orenstein, Keren Markus-Bustani, Noa Ruhrman-Shahar, Yael Kilim, Nurit Magal, Monika Weisz Hubshman, Lily Bazak. Genet Med 2019
Times Cited: 41




List of shared articles



Times cited

Lessons learnt from multifaceted diagnostic approaches to the first 150 families in Victoria's Undiagnosed Diseases Program.
Thomas Cloney, Lyndon Gallacher, Lynn S Pais, Natalie B Tan, Alison Yeung, Zornitza Stark, Natasha J Brown, George McGillivray, Martin B Delatycki, Michelle G de Silva,[...]. J Med Genet 2022
0

Re-analysis of genomic data: An overview of the mechanisms and complexities of clinical adoption.
Alan J Robertson, Natalie B Tan, Amanda B Spurdle, Alejandro Metke-Jimenez, Clair Sullivan, Nicola Waddell. Genet Med 2022
3

Methods to Improve Molecular Diagnosis in Genomic Cold Cases in Pediatric Neurology.
Magda K Kadlubowska, Isabelle Schrauwen. Genes (Basel) 2022
0

How to proceed after "negative" exome: A review on genetic diagnostics, limitations, challenges, and emerging new multiomics techniques.
Saskia B Wortmann, Machteld M Oud, Mariëlle Alders, Karlien L M Coene, Saskia N van der Crabben, René G Feichtinger, Alejandro Garanto, Alex Hoischen, Mirjam Langeveld, Dirk Lefeber,[...]. J Inherit Metab Dis 2022
0

Genetic Testing in Neurodevelopmental Disorders.
Juliann M Savatt, Scott M Myers. Front Pediatr 2021
31

New Diagnostic Approaches for Undiagnosed Rare Genetic Diseases.
Taila Hartley, Gabrielle Lemire, Kristin D Kernohan, Heather E Howley, David R Adams, Kym M Boycott. Annu Rev Genomics Hum Genet 2020
22