A citation-based method for searching scientific literature

Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig, Hoda Abdel-Hamid, Patricia Bader, Elizabeth McCracken, Dmitriy Niyazov, Kathleen Leppig, Heidi Thiese, Marybeth Hummel, Nora Alexander, Jerome Gorski, Jennifer Kussmann, Vandana Shashi, Krys Johnson, Catherine Rehder, Blake C Ballif, Lisa G Shaffer, Evan E Eichler. Nat Genet 2011
Times Cited: 794

List of shared articles

Times cited

Spatiotemporal 7q11.23 protein network analysis implicates the role of DNA repair pathway during human brain development.
Liang Chen, Weidi Wang, Wenxiang Cai, Weichen Song, Wei Qian, Guan Ning Lin. Sci Rep 2021

Clinical and Neurobiological Aspects of TAO Kinase Family in Neurodevelopmental Disorders.
Chun Hu, Pan Feng, Qian Yang, Lin Xiao. Front Mol Neurosci 2021

Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN Mutations.
Lamis Yehia, Marilyn Seyfi, Lisa-Marie Niestroj, Roshan Padmanabhan, Ying Ni, Thomas W Frazier, Dennis Lal, Charis Eng. JAMA Netw Open 2020

Genetic mechanisms of neurodevelopmental disorders.
P Y Billie Au, Alison Eaton, David A Dyment. Handb Clin Neurol 2020

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020

Impairments in sensory-motor gating and information processing in a mouse model of Ehmt1 haploinsufficiency.
Brittany A Davis, Fran├žois David, Ciara O'Regan, Manal A Adam, Adrian J Harwood, Vincenzo Crunelli, Anthony R Isles. Brain Neurosci Adv 2020

Evidence for 28 genetic disorders discovered by combining healthcare and research data.
Joanna Kaplanis, Kaitlin E Samocha, Laurens Wiel, Zhancheng Zhang, Kevin J Arvai, Ruth Y Eberhardt, Giuseppe Gallone, Stefan H Lelieveld, Hilary C Martin, Jeremy F McRae,[...]. Nature 2020

Haploinsufficiency of ATP6V0C possibly underlies 16p13.3 deletions that cause microcephaly, seizures, and neurodevelopmental disorder.
Rory J Tinker, George J Burghel, Shruti Garg, Maggie Steggall, Sara Cuvertino, Siddharth Banka. Am J Med Genet A 2020

A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.
Bettina E Mucha, Siddharth Banka, Norbert Fonya Ajeawung, Sirinart Molidperee, Gary G Chen, Mary Kay Koenig, Rhamat B Adejumo, Marianne Till, Michael Harbord, Renee Perrier,[...]. Genet Med 2019