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Maja Bućan

Showing results (1-10 of 19) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 31, 2016
Expanding the phenotype half of the genotype-phenotype spaceMaja Bućan
Nature Reviews. Genetics|February 12, 2002
The mouse: genetics meets behaviourMaja Bućan, Ted Abel
Plos Genetics|May 16, 2013
From mouse to human: evolutionary genomics analysis of human orthologs of essential genesBenjamin Georgi, Benjamin F Voight, Maja Bućan
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2016
Increased burden of deleterious variants in essential genes in autism spectrum disorderXiao Ji, Rachel L Kember, Christopher D Brown, et al.
Genome Biology|November 14, 2006
Patterns of sequence conservation in presynaptic neural genesDexter Hadley, Tara Murphy, Otto Valladares, et al.
BMC Genetics|April 19, 2015
Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorderRachel L Kember, Benjamin Georgi, Joan E Bailey-Wilson, et al.
Plos Genetics|August 26, 2017
Functional significance of rare neuroligin 1 variants found in autismMoe Nakanishi, Jun Nomura, Xiao Ji, et al.
Plos Genetics|October 4, 2017
Correction: Functional significance of rare neuroligin 1 variants found in autismMoe Nakanishi, Jun Nomura, Xiao Ji, et al.
Nature Genetics|September 24, 2002
Mutations in Rab3a alter circadian period and homeostatic response to sleep loss in the mouseDavid Kapfhamer, Otto Valladares, Yi Sun, et al.
Plos Genetics|March 15, 2014
Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolateBenjamin Georgi, David Craig, Rachel L Kember, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Proceedings of the National Academy of Sciences of the United States of America|January 31, 2016
Expanding the phenotype half of the genotype-phenotype spaceMaja Bućan
Nature Reviews. Genetics|February 12, 2002
The mouse: genetics meets behaviourMaja Bućan, Ted Abel
Plos Genetics|May 16, 2013
From mouse to human: evolutionary genomics analysis of human orthologs of essential genesBenjamin Georgi, Benjamin F Voight, Maja Bućan
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2016
Increased burden of deleterious variants in essential genes in autism spectrum disorderXiao Ji, Rachel L Kember, Christopher D Brown, et al.
Genome Biology|November 14, 2006
Patterns of sequence conservation in presynaptic neural genesDexter Hadley, Tara Murphy, Otto Valladares, et al.
BMC Genetics|April 19, 2015
Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorderRachel L Kember, Benjamin Georgi, Joan E Bailey-Wilson, et al.
Plos Genetics|August 26, 2017
Functional significance of rare neuroligin 1 variants found in autismMoe Nakanishi, Jun Nomura, Xiao Ji, et al.
Plos Genetics|October 4, 2017
Correction: Functional significance of rare neuroligin 1 variants found in autismMoe Nakanishi, Jun Nomura, Xiao Ji, et al.
Nature Genetics|September 24, 2002
Mutations in Rab3a alter circadian period and homeostatic response to sleep loss in the mouseDavid Kapfhamer, Otto Valladares, Yi Sun, et al.
Plos Genetics|March 15, 2014
Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolateBenjamin Georgi, David Craig, Rachel L Kember, et al.
Pageof 2