A citation-based method for searching scientific literature

Dimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, Sarah Bowdin, Nasim Monfared, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Giovanna Pellecchia, Ryan K C Yuen, Michael J Szego, Robin Z Hayeems, Randi Zlotnik Shaul, Michael Brudno, Marta Girdea, Brendan Frey, Babak Alipanahi, Sohnee Ahmed, Riyana Babul-Hirji, Ramses Badilla Porras, Melissa T Carter, Lauren Chad, Ayeshah Chaudhry, David Chitayat, Soghra Jougheh Doust, Cheryl Cytrynbaum, Lucie Dupuis, Resham Ejaz, Leona Fishman, Andrea Guerin, Bita Hashemi, Mayada Helal, Stacy Hewson, Michal Inbar-Feigenberg, Peter Kannu, Natalya Karp, Raymond Kim, Jonathan Kronick, Eriskay Liston, Heather MacDonald, Saadet Mercimek-Mahmutoglu, Roberto Mendoza-Londono, Enas Nasr, Graeme Nimmo, Nicole Parkinson, Nada Quercia, Julian Raiman, Maian Roifman, Andreas Schulze, Andrea Shugar, Cheryl Shuman, Pierre Sinajon, Komudi Siriwardena, Rosanna Weksberg, Grace Yoon, Chris Carew, Raith Erickson, Richard A Leach, Robert Klein, Peter N Ray, M Stephen Meyn, Stephen W Scherer, Ronald D Cohn, Christian R Marshall. NPJ Genom Med 2016
Times Cited: 165



Caroline F Wright, Tomas W Fitzgerald, Wendy D Jones, Stephen Clayton, Jeremy F McRae, Margriet van Kogelenberg, Daniel A King, Kirsty Ambridge, Daniel M Barrett, Tanya Bayzetinova, A Paul Bevan, Eugene Bragin, Eleni A Chatzimichali, Susan Gribble, Philip Jones, Netravathi Krishnappa, Laura E Mason, Ray Miller, Katherine I Morley, Vijaya Parthiban, Elena Prigmore, Diana Rajan, Alejandro Sifrim, G Jawahar Swaminathan, Adrian R Tivey, Anna Middleton, Michael Parker, Nigel P Carter, Jeffrey C Barrett, Matthew E Hurles, David R FitzPatrick, Helen V Firth. Lancet 2015
Times Cited: 363




List of shared articles



Times cited

Cost-effectiveness of genome-wide sequencing for unexplained developmental disabilities and multiple congenital anomalies.
Chunmei Li, Stacey Vandersluis, Corinne Holubowich, Wendy J Ungar, Elaine S Goh, Kym M Boycott, Nancy Sikich, Irfan Dhalla, Vivian Ng. Genet Med 2021
4


Next-generation sequencing approaches and challenges in the diagnosis of developmental anomalies and intellectual disability.
Ange-Line Bruel, Antonio Vitobello, Frédéric Tran Mau-Them, Sophie Nambot, Arthur Sorlin, Anne-Sophie Denommé-Pichon, Julian Delanne, Sébastien Moutton, Patrick Callier, Yannis Duffourd,[...]. Clin Genet 2020
1

The frontiers of sequencing in undiagnosed neurodevelopmental diseases.
Hane Lee, Stanley F Nelson. Curr Opin Genet Dev 2020
0

Young people's understanding, attitudes and involvement in decision-making about genome sequencing for rare diseases: A qualitative study with participants in the UK 100, 000 Genomes Project.
Celine Lewis, Jennifer Hammond, Melissa Hill, Beverly Searle, Amy Hunter, Christine Patch, Lyn S Chitty, Saskia C Sanderson. Eur J Med Genet 2020
2

Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity.
Gregory Costain, Susan Walker, Maria Marano, Danielle Veenma, Meaghan Snell, Meredith Curtis, Stephanie Luca, Jason Buera, Danielle Arje, Miriam S Reuter,[...]. JAMA Netw Open 2020
6

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
7

Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases.
David Bick, Marilyn Jones, Stacie L Taylor, Ryan J Taft, John Belmont. J Med Genet 2019
24