A citation-based method for searching scientific literature

Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi, Joseph Shen, Sung-Hae L Kang, Amber Pursley, Timothy Lotze, Gail Kennedy, Susan Lansky-Shafer, Christine Weaver, Elizabeth R Roeder, Theresa A Grebe, Georgianne L Arnold, Terry Hutchison, Tyler Reimschisel, Stephen Amato, Michael T Geragthy, Jeffrey W Innis, Ewa Obersztyn, Beata Nowakowska, Sally S Rosengren, Patricia I Bader, Dorothy K Grange, Sayed Naqvi, Adolfo D Garnica, Saunder M Bernes, Chin-To Fong, Anne Summers, W David Walters, James R Lupski, Pawel Stankiewicz, Sau Wai Cheung, Ankita Patel. Nat Genet 2008
Times Cited: 389



Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson, Christopher E Mason, Kaya Bilguvar, Patricia B S Celestino-Soper, Murim Choi, Emily L Crawford, Lea Davis, Nicole R Davis Wright, Rahul M Dhodapkar, Michael DiCola, Nicholas M DiLullo, Thomas V Fernandez, Vikram Fielding-Singh, Daniel O Fishman, Stephanie Frahm, Rouben Garagaloyan, Gerald S Goh, Sindhuja Kammela, Lambertus Klei, Jennifer K Lowe, Sabata C Lund, Anna D McGrew, Kyle A Meyer, William J Moffat, John D Murdoch, Brian J O'Roak, Gordon T Ober, Rebecca S Pottenger, Melanie J Raubeson, Youeun Song, Qi Wang, Brian L Yaspan, Timothy W Yu, Ilana R Yurkiewicz, Arthur L Beaudet, Rita M Cantor, Martin Curland, Dorothy E Grice, Murat Günel, Richard P Lifton, Shrikant M Mane, Donna M Martin, Chad A Shaw, Michael Sheldon, Jay A Tischfield, Christopher A Walsh, Eric M Morrow, David H Ledbetter, Eric Fombonne, Catherine Lord, Christa Lese Martin, Andrew I Brooks, James S Sutcliffe, Edwin H Cook, Daniel Geschwind, Kathryn Roeder, Bernie Devlin, Matthew W State. Neuron 2011
Times Cited: 802




List of shared articles



Times cited


Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.
Lisa-Marie Niestroj, Eduardo Perez-Palma, Daniel P Howrigan, Yadi Zhou, Feixiong Cheng, Elmo Saarentaus, Peter Nürnberg, Remi Stevelink, Mark J Daly, Aarno Palotie,[...]. Brain 2020
5

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, Priya Krithivasan, Adele Mitrotti, David A Fasel, Ekaterina Batourina, Matthew G Sampson,[...]. Nat Genet 2019
46


Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.
Rebecca M Pollak, Melissa M Murphy, Michael P Epstein, Michael E Zwick, Cheryl Klaiman, Celine A Saulnier, Jennifer G Mulle. Mol Autism 2019
10

Genetic basis of human congenital anomalies of the kidney and urinary tract.
Simone Sanna-Cherchi, Rik Westland, Gian Marco Ghiggeri, Ali G Gharavi. J Clin Invest 2018
33

Repint of "Reframing autism as a behavioral syndrome and not a specific mental disorder: Implications of genetic and phenotypic heterogeneity".
S Tordjman, D Cohen, G M Anderson, M Botbol, R Canitano, N Coulon, P L Roubertoux. Neurosci Biobehav Rev 2018
17


Effects of pathogenic CNVs on physical traits in participants of the UK Biobank.
David Owen, Mathew Bracher-Smith, Kimberley M Kendall, Elliott Rees, Mark Einon, Valentina Escott-Price, Michael J Owen, Michael C O'Donovan, George Kirov. BMC Genomics 2018
14

Reframing autism as a behavioral syndrome and not a specific mental disorder: Implications of genetic and phenotypic heterogeneity.
S Tordjman, D Cohen, N Coulon, G M Anderson, M Botbol, R Canitano, P L Roubertoux. Neurosci Biobehav Rev 2017
14

Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy.
Cyrille Robert, Laurent Pasquier, David Cohen, Mélanie Fradin, Roberto Canitano, Léna Damaj, Sylvie Odent, Sylvie Tordjman. Int J Mol Sci 2017
12