A citation-based method for searching scientific literature

Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers, Anne-Marie Laberge, Jacek Majewski, Roberto Mendoza-Londono, M Stephen Meyn, Jacques L Michaud, Tanya N Nelson, Julie Richer, Bekim Sadikovic, David L Skidmore, Tracy Stockley, Sherry Taylor, Clara van Karnebeek, Ma'n H Zawati, Julie Lauzon, Christine M Armour. J Med Genet 2015
Times Cited: 104



Anath C Lionel, Gregory Costain, Nasim Monfared, Susan Walker, Miriam S Reuter, S Mohsen Hosseini, Bhooma Thiruvahindrapuram, Daniele Merico, Rebekah Jobling, Thomas Nalpathamkalam, Giovanna Pellecchia, Wilson W L Sung, Zhuozhi Wang, Peter Bikangaga, Cyrus Boelman, Melissa T Carter, Dawn Cordeiro, Cheryl Cytrynbaum, Sharon D Dell, Priya Dhir, James J Dowling, Elise Heon, Stacy Hewson, Linda Hiraki, Michal Inbar-Feigenberg, Regan Klatt, Jonathan Kronick, Ronald M Laxer, Christoph Licht, Heather MacDonald, Saadet Mercimek-Andrews, Roberto Mendoza-Londono, Tino Piscione, Rayfel Schneider, Andreas Schulze, Earl Silverman, Komudi Siriwardena, O Carter Snead, Neal Sondheimer, Joanne Sutherland, Ajoy Vincent, Jonathan D Wasserman, Rosanna Weksberg, Cheryl Shuman, Chris Carew, Michael J Szego, Robin Z Hayeems, Raveen Basran, Dimitri J Stavropoulos, Peter N Ray, Sarah Bowdin, M Stephen Meyn, Ronald D Cohn, Stephen W Scherer, Christian R Marshall. Genet Med 2018
Times Cited: 154




List of shared articles



Times cited

Improving diagnostics of rare genetic diseases with NGS approaches.
Mateja Vinkšel, Karin Writzl, Aleš Maver, Borut Peterlin. J Community Genet 2021
0

Please give me a copy of my child's raw genomic data.
Lauren Chad, Michael J Szego. NPJ Genom Med 2021
0

Primary care provider perspectives on using genomic sequencing in the care of healthy children.
Esha Joshi, Chloe Mighton, Marc Clausen, Selina Casalino, Theresa H M Kim, Christine Kowal, Catherine Birken, Jonathon L Maguire, Yvonne Bombard. Eur J Hum Genet 2020
0

Exome sequencing in genetic disease: recent advances and considerations.
Jay P Ross, Patrick A Dion, Guy A Rouleau. F1000Res 2020
1

Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease.
Christian R Marshall, Shimul Chowdhury, Ryan J Taft, Mathew S Lebo, Jillian G Buchan, Steven M Harrison, Ross Rowsey, Eric W Klee, Pengfei Liu, Elizabeth A Worthey,[...]. NPJ Genom Med 2020
3

Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatrics.
M J Szego, M S Meyn, C Shuman, R Zlotnik Shaul, J A Anderson, S Bowdin, N Monfared, R Z Hayeems. Eur J Med Genet 2019
2

Paediatric genomics: diagnosing rare disease in children.
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat Rev Genet 2018
111

Genome-wide sequencing technologies: A primer for paediatricians.
Robin Z Hayeems, Kym M Boycott. Paediatr Child Health 2018
4

Genome-wide Sequencing in Rheumatic Diseases.
Linda T Hiraki. J Rheumatol 2018
0