A citation-based method for searching scientific literature

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: 518



Christos Kopanos, Vasilis Tsiolkas, Alexandros Kouris, Charles E Chapple, Monica Albarca Aguilera, Richard Meyer, Andreas Massouras. Bioinformatics 2019
Times Cited: 387




List of shared articles



Times cited

MobiDetails: online DNA variants interpretation.
David Baux, Charles Van Goethem, Olivier Ardouin, Thomas Guignard, Anne Bergougnoux, Michel Koenig, Anne-Françoise Roux. Eur J Hum Genet 2021
2

Mutational spectrum of GNAL, THAP1 and TOR1A genes in isolated dystonia: study in a population from Spain and systematic literature review.
Pilar Gómez-Garre, Silvia Jesús, María Teresa Periñán, Astrid Adarmes, Araceli Alonso-Canovas, Alberto Blanco-Ollero, Dolores Buiza-Rueda, Fátima Carrillo, María José Catalán-Alonso, Javier Del Val,[...]. Eur J Neurol 2021
1

New clinical and molecular evidence linking mutations in ARSG to Usher syndrome type IV.
Virginie G Peter, Mathieu Quinodoz, Silvia Sadio, Sebastian Held, Márcia Rodrigues, Marta Soares, Ana Berta Sousa, Luisa Coutinho Santos, Markus Damme, Carlo Rivolta. Hum Mutat 2021
4

Functional and clinical implications of genetic structure in 1686 Italian exomes.
Giovanni Birolo, Serena Aneli, Cornelia Di Gaetano, Giovanni Cugliari, Alessia Russo, Alessandra Allione, Elisabetta Casalone, Elisa Giorgio, Elvezia M Paraboschi, Diego Ardissino,[...]. Hum Mutat 2021
0

Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing.
Shalini S Nayak, Pauline E Schneeberger, Siddaramappa J Patil, Karegowda M Arun, Pujar V Suresh, Viralam S Kiran, Sateesh Siddaiah, Shreesha Maiya, Shrikanth K Venkatachalagupta, Neethukrishna Kausthubham,[...]. Sci Rep 2021
0

A novel variant in the COX15 gene causing a fatal infantile cardioencephalomyopathy: A case report with clinical and molecular review.
Manuella Galvão de Oliveira, Célia Tengan, Cecília Micheletti, Paloma Ramos de Macedo, Mirlene Cecília Soares Pinho Cernach, Thiago Rodrigues Cavole, Marina de França Basto, Joselito Sobreira Filho, Luiza Amaral Virmond, Fernanda Milanezi,[...]. Eur J Med Genet 2021
0

Genetic Causes of Oculocutaneous Albinism in Pakistani Population.
Zureesha Sajid, Sairah Yousaf, Yar M Waryah, Tauqeer A Mughal, Tasleem Kausar, Mohsin Shahzad, Ali R Rao, Ansar A Abbasi, Rehan S Shaikh, Ali M Waryah,[...]. Genes (Basel) 2021
0