A citation-based method for searching scientific literature

Brett Trost, Susan Walker, Zhuozhi Wang, Bhooma Thiruvahindrapuram, Jeffrey R MacDonald, Wilson W L Sung, Sergio L Pereira, Joe Whitney, Ada J S Chan, Giovanna Pellecchia, Miriam S Reuter, Si Lok, Ryan K C Yuen, Christian R Marshall, Daniele Merico, Stephen W Scherer. Am J Hum Genet 2018
Times Cited: 74



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: 172




List of shared articles



Times cited

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
9

A novel intronic variant in UBE3A identified by genome sequencing in a patient with an atypical presentation of Angelman syndrome.
Meredith Curtis, Danielle Baribeau, Susan Walker, Melissa Carter, Gregory Costain, Sylvia Lamoureux, Eriskay Liston, Christian R Marshall, Miriam S Reuter, Meaghan Snell,[...]. Am J Med Genet A 2020
1

Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies.
Vaidehi Jobanputra, Peter Andrews, Vanessa Felice, Avinash Abhyankar, Lukasz Kozon, Dino Robinson, Ferrah London, Inessa Hakker, Kazimierz Wrzeszczynski, Michael Ronemus. J Mol Diagn 2020
0

Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype.
Farah Qaiser, Yue Yin, Carolyn B Mervis, Colleen A Morris, Bonita P Klein-Tasman, Elaine Tam, Lucy R Osborne, Ryan K C Yuen. Orphanet J Rare Dis 2021
2

4

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
7

Whole genome analysis identifies the association of TP53 genomic deletions with lower survival in Stage III colorectal cancer.
Li C Xia, Paul Van Hummelen, Matthew Kubit, HoJoon Lee, John M Bell, Susan M Grimes, Christina Wood-Bouwens, Stephanie U Greer, Tyler Barker, Derrick S Haslem,[...]. Sci Rep 2020
1

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.
Miriam S Reuter, Susan Walker, Bhooma Thiruvahindrapuram, Joe Whitney, Iris Cohn, Neal Sondheimer, Ryan K C Yuen, Brett Trost, Tara A Paton, Sergio L Pereira,[...]. CMAJ 2018
30

Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants.
Sjors Middelkamp, Judith M Vlaar, Jacques Giltay, Jerome Korzelius, Nicolle Besselink, Sander Boymans, Roel Janssen, Lisanne de la Fonteijne, Ellen van Binsbergen, Markus J van Roosmalen,[...]. Genome Med 2019
7

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.
Gregory Costain, Susan Walker, Bob Argiropoulos, Danielle A Baribeau, Anne S Bassett, Erik Boot, Koen Devriendt, Barbara Kellam, Christian R Marshall, Aparna Prasad,[...]. J Neurodev Disord 2019
5