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: 387



Laura J Dumas, Majesta S O'Bleness, Jonathan M Davis, C Michael Dickens, Nathan Anderson, J G Keeney, Jay Jackson, Megan Sikela, Armin Raznahan, Jay Giedd, Judith Rapoport, Sandesh S C Nagamani, Ayelet Erez, Nicola Brunetti-Pierri, Rachel Sugalski, James R Lupski, Tasha Fingerlin, Sau Wai Cheung, James M Sikela. Am J Hum Genet 2012
Times Cited: 65




List of shared articles



Times cited

The psychiatric phenotypes of 1q21 distal deletion and duplication.
Stefanie C Linden, Cameron J Watson, Jacqueline Smith, Samuel J R A Chawner, Thomas M Lancaster, Ffion Evans, Nigel Williams, David Skuse, F Lucy Raymond, Jeremy Hall,[...]. Transl Psychiatry 2021
1

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
Ida E S√łnderby, Dennis van der Meer, Clara Moreau, Tobias Kaufmann, G Bragi Walters, Maria Ellegaard, Abdel Abdellaoui, David Ames, Katrin Amunts, Micael Andersson,[...]. Transl Psychiatry 2021
2


The Driver of Extreme Human-Specific Olduvai Repeat Expansion Remains Highly Active in the Human Genome.
Ilea E Heft, Yulia Mostovoy, Michal Levy-Sakin, Walfred Ma, Aaron J Stevens, Steven Pastor, Jennifer McCaffrey, Dario Boffelli, David I Martin, Ming Xiao,[...]. Genetics 2020
1

The N-terminal of NBPF15 causes multiple types of aggregates and mediates phase transition.
Han Wu, Liu-Tao Zhai, Xue-Xue Guo, Stephane Rety, Xu-Guang Xi. Biochem J 2020
1

Disorders Associated With Diverse, Recurrent Deletions and Duplications at 1q21.1.
Hui Pang, Xiaowei Yu, Young Mi Kim, Xianfu Wang, Jeremy K Jinkins, Jianing Yin, Shibo Li, Hongcang Gu. Front Genet 2020
1

A Third Linear Association Between Olduvai (DUF1220) Copy Number and Severity of the Classic Symptoms of Inherited Autism.
Jonathan M Davis, Ilea Heft, Stephen W Scherer, James M Sikela. Am J Psychiatry 2019
6

An eight-case 1q21 region series: novel aberrations and clinical variability with new features.
A C Ceylan, I Sahin, H B Erdem, G Kayhan, P O Simsek-Kiper, G E Utine, F Percin, K Boduroglu, M Alikasifoglu. J Intellect Disabil Res 2019
2


Paired involvement of human-specific Olduvai domains and NOTCH2NL genes in human brain evolution.
Ian T Fiddes, Alex A Pollen, Jonathan M Davis, James M Sikela. Hum Genet 2019
7

Mutations in ANKLE2, a ZIKA Virus Target, Disrupt an Asymmetric Cell Division Pathway in Drosophila Neuroblasts to Cause Microcephaly.
Nichole Link, Hyunglok Chung, Angad Jolly, Marjorie Withers, Burak Tepe, Benjamin R Arenkiel, Priya S Shah, Nevan J Krogan, Hatip Aydin, Bilgen B Geckinli,[...]. Dev Cell 2019
14


Recurrent homozygous deletion of DROSHA and microduplication of PDE4DIP in pineoblastoma.
Matija Snuderl, Kasthuri Kannan, Elke Pfaff, Shiyang Wang, James M Stafford, Jonathan Serrano, Adriana Heguy, Karina Ray, Arline Faustin, Olga Aminova,[...]. Nat Commun 2018
23