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American Journal of Human Genetics
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April 9, 2011
Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research
Michael E Talkowski, Carl Ernst, Adrian Heilbut, et al.
Scientific Reports
|
January 26, 2017
Potential molecular consequences of transgene integration: The R6/2 mouse example
Jessie C Jacobsen, Serkan Erdin, Colby Chiang, et al.
Nature
|
October 13, 2017
The impact of rare variation on gene expression across tissues
Xin Li, Yungil Kim, Emily K Tsang, et al.
Human Genetics
|
January 29, 2013
Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate
Amelia M Lindgren, Tatiana Hoyos, Michael E Talkowski, et al.
Nature
|
May 28, 2020
Mapping and characterization of structural variation in 17,795 human genomes
Haley J Abel, David E Larson, Allison A Regier, et al.
American Journal of Human Genetics
|
April 2, 2021
Association of structural variation with cardiometabolic traits in Finns
Lei Chen, Haley J Abel, Indraniel Das, et al.
Nature Genetics
|
March 6, 2012
Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration
Colby Chiang, Jessie C Jacobsen, Carl Ernst, et al.
Archives of General Psychiatry
|
October 10, 2012
Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity
Carl Ernst, Christian R Marshall, Yiping Shen, et al.
American Journal of Human Genetics
|
December 11, 2012
Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities
Michael E Talkowski, Gilles Maussion, Liam Crapper, et al.
American Journal of Medical Genetics. Part A
|
October 21, 2016
Implication of LRRC4C and DPP6 in neurodevelopmental disorders
Gilles Maussion, Cristiana Cruceanu, Jill A Rosenfeld, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
American Journal of Human Genetics
|
April 9, 2011
Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research
Michael E Talkowski, Carl Ernst, Adrian Heilbut, et al.
Scientific Reports
|
January 26, 2017
Potential molecular consequences of transgene integration: The R6/2 mouse example
Jessie C Jacobsen, Serkan Erdin, Colby Chiang, et al.
Nature
|
October 13, 2017
The impact of rare variation on gene expression across tissues
Xin Li, Yungil Kim, Emily K Tsang, et al.
Human Genetics
|
January 29, 2013
Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate
Amelia M Lindgren, Tatiana Hoyos, Michael E Talkowski, et al.
Nature
|
May 28, 2020
Mapping and characterization of structural variation in 17,795 human genomes
Haley J Abel, David E Larson, Allison A Regier, et al.
American Journal of Human Genetics
|
April 2, 2021
Association of structural variation with cardiometabolic traits in Finns
Lei Chen, Haley J Abel, Indraniel Das, et al.
Nature Genetics
|
March 6, 2012
Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration
Colby Chiang, Jessie C Jacobsen, Carl Ernst, et al.
Archives of General Psychiatry
|
October 10, 2012
Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity
Carl Ernst, Christian R Marshall, Yiping Shen, et al.
American Journal of Human Genetics
|
December 11, 2012
Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities
Michael E Talkowski, Gilles Maussion, Liam Crapper, et al.
American Journal of Medical Genetics. Part A
|
October 21, 2016
Implication of LRRC4C and DPP6 in neurodevelopmental disorders
Gilles Maussion, Cristiana Cruceanu, Jill A Rosenfeld, et al.
Page
of 3