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: 778







List of shared articles



Times cited

Clinical and Neurobiological Aspects of TAO Kinase Family in Neurodevelopmental Disorders.
Chun Hu, Pan Feng, Qian Yang, Lin Xiao. Front Mol Neurosci 2021
0

Bcl11 Transcription Factors Regulate Cortical Development and Function.
Ruth Simon, Christoph Wiegreffe, Stefan Britsch. Front Mol Neurosci 2020
3

Exon-focused targeted oligonucleotide microarray design increases detection of clinically relevant variants across multiple NHS genomic centres.
Jana Jezkova, Jade Heath, Angharad Williams, Deborah Barrell, Jessica Norton, Morag N Collinson, Sarah J Beal, Sian Corrin, Sian Morgan. NPJ Genom Med 2020
1

A Bibliometric Insight of Genetic Factors in ASD: Emerging Trends and New Developments.
Kang Wang, Weicheng Duan, Yijie Duan, Yuxin Yu, Xiuyi Chen, Yinhui Xu, Haihong Chen, Hongzhi Huang, Bo Xiong. Brain Sci 2020
0


Analysis of GWAS-Derived Schizophrenia Genes for Links to Ischemia-Hypoxia Response of the Brain.
Rainald Schmidt-Kastner, Sinan Guloksuz, Thomas Kietzmann, Jim van Os, Bart P F Rutten. Front Psychiatry 2020
3

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
0

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
20

Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease.
David B Beck, Marcela A Ferrada, Keith A Sikora, Amanda K Ombrello, Jason C Collins, Wuhong Pei, Nicholas Balanda, Daron L Ross, Daniela Ospina Cardona, Zhijie Wu,[...]. N Engl J Med 2020
25

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
11

Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.
Bradley P Coe, Holly A F Stessman, Arvis Sulovari, Madeleine R Geisheker, Trygve E Bakken, Allison M Lake, Joseph D Dougherty, Ed S Lein, Fereydoun Hormozdiari, Raphael A Bernier,[...]. Nat Genet 2019
83