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



Nilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, Sumit Middha, Shannon K McDonnell, Saurabh Baheti, Anthony Musolf, Qing Li, Emily Holzinger, Danielle Karyadi, Lisa A Cannon-Albright, Craig C Teerlink, Janet L Stanford, William B Isaacs, Jianfeng Xu, Kathleen A Cooney, Ethan M Lange, Johanna Schleutker, John D Carpten, Isaac J Powell, Olivier Cussenot, Geraldine Cancel-Tassin, Graham G Giles, Robert J MacInnis, Christiane Maier, Chih-Lin Hsieh, Fredrik Wiklund, William J Catalona, William D Foulkes, Diptasri Mandal, Rosalind A Eeles, Zsofia Kote-Jarai, Carlos D Bustamante, Daniel J Schaid, Trevor Hastie, Elaine A Ostrander, Joan E Bailey-Wilson, Predrag Radivojac, Stephen N Thibodeau, Alice S Whittemore, Weiva Sieh. Am J Hum Genet 2016
Times Cited: 709




List of shared articles



Times cited


Computational and experimental methods for classifying variants of unknown clinical significance.
Malte Spielmann, Martin Kircher. Cold Spring Harb Mol Case Stud 2022
1

Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability.
Arisha Rasheed, Evren Gumus, Maha Zaki, Katherine Johnson, Humera Manzoor, Geneva LaForce, Danica Ross, Jennifer McEvoy-Venneri, Valentina Stanley, Sangmoon Lee,[...]. J Med Genet 2021
3

Identification of missense MAB21L1 variants in microphthalmia and aniridia.
Sarah E Seese, Linda M Reis, Brett Deml, Christopher Griffith, Adi Reich, Robyn V Jamieson, Elena V Semina. Hum Mutat 2021
3

Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & Immunology.
Ivan K Chinn, Alice Y Chan, Karin Chen, Janet Chou, Morna J Dorsey, Joud Hajjar, Artemio M Jongco, Michael D Keller, Lisa J Kobrynski, Attila Kumanovics,[...]. J Allergy Clin Immunol 2020
33