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Bioinformatics (Oxford, England)|April 6, 2021
Customized de novo mutation detection for any variant calling pipeline: SynthDNMAojie Lian, James Guevara, Kun Xia, et al.Cell|September 7, 2019
Getting to the Cores of AutismLilia M Iakoucheva, Alysson R Muotri, Jonathan SebatTrends in Genetics : TIG|November 4, 2009
Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disordersJonathan Sebat, Deborah L Levy, Shane E McCarthyHuman Mutation|April 27, 2018
Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypesChristopher M Grochowski, Shen Gu, Bo Yuan, et al.Molecular Psychiatry|August 30, 2024
Integrative genetic analysis: cornerstone of precision psychiatryJacob Vorstman, Jonathan Sebat, Vincent-Raphaël Bourque, et al.Annales De Genetique|June 9, 2004
A novel promoter polymorphism (-71C>T) in KRTHB6 gene in Indian populationNarendra K Bairwa, Dheeraj Malhotra, Anjana Saha, et al.European Journal of Human Genetics : EJHG|March 31, 2011
Reduced transcript expression of genes affected by inherited and de novo CNVs in autismAlex S Nord, Wendy Roeb, Diane E Dickel, et al.Current Opinion in Genetics & Development|February 14, 2026
Convergence and divergence of molecular phenotypes in iPSC-derived models of 16p11.2 and 22q11.2 reciprocal copy number variantsSandeep Rajkumar, Carrie E Bearden, Jonathan Sebat, et al.Genome Research|August 7, 2009
Sensitive and accurate detection of copy number variants using read depth of coverageSeungtai Yoon, Zhenyu Xuan, Vladimir Makarov, et al.Critical Reviews in Microbiology|November 26, 2003
How far have we reached in tuberculosis vaccine development?Himanshu Kumar, Dheeraj Malhotra, Sanjeev Goswami, et al.Pageof 12