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Nature
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May 19, 2012
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant
Christelle Golzio, Jason Willer, Michael E Talkowski, et al.
European Journal of Human Genetics : EJHG
|
December 19, 2022
Correction to: Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'
Francesca Forzano, Olga Antonova, Angus Clarke, et al.
Genome Research
|
December 15, 2017
Slightly deleterious genomic variants and transcriptome perturbations in Down syndrome embryonic selection
Konstantin Popadin, Stephan Peischl, Marco Garieri, et al.
American Journal of Human Genetics
|
October 3, 2017
The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs
Maria Nicla Loviglio, Thomas Arbogast, Aia Elise Jønch, et al.
Bioinformatics (Oxford, England)
|
November 21, 2013
Identification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data
Sebastian M Waszak, Helena Kilpinen, Andreas R Gschwind, et al.
Genome Biology
|
September 7, 2012
The GENCODE pseudogene resource
Baikang Pei, Cristina Sisu, Adam Frankish, et al.
Human Mutation
|
June 30, 2009
Variation in novel exons (RACEfrags) of the MECP2 gene in Rett syndrome patients and controls
Periklis Makrythanasis, Philipp Kapranov, Lucia Bartoloni, et al.
Genome Biology
|
August 24, 2006
GENCODE: producing a reference annotation for ENCODE
Jennifer Harrow, France Denoeud, Adam Frankish, et al.
BMC Bioinformatics
|
June 1, 2005
Gene finding in the chicken genome
Eduardo Eyras, Alexandre Reymond, Robert Castelo, et al.
Genome Biology
|
December 6, 2008
Assaying the regulatory potential of mammalian conserved non-coding sequences in human cells
Catia Attanasio, Alexandre Reymond, Richard Humbert, et al.
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of 17
Search research articles
Search
Showing results (81-90 of 169) with videos related to
Sort By:
Page
of 17
Nature
|
May 19, 2012
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant
Christelle Golzio, Jason Willer, Michael E Talkowski, et al.
European Journal of Human Genetics : EJHG
|
December 19, 2022
Correction to: Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'
Francesca Forzano, Olga Antonova, Angus Clarke, et al.
Genome Research
|
December 15, 2017
Slightly deleterious genomic variants and transcriptome perturbations in Down syndrome embryonic selection
Konstantin Popadin, Stephan Peischl, Marco Garieri, et al.
American Journal of Human Genetics
|
October 3, 2017
The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs
Maria Nicla Loviglio, Thomas Arbogast, Aia Elise Jønch, et al.
Bioinformatics (Oxford, England)
|
November 21, 2013
Identification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data
Sebastian M Waszak, Helena Kilpinen, Andreas R Gschwind, et al.
Genome Biology
|
September 7, 2012
The GENCODE pseudogene resource
Baikang Pei, Cristina Sisu, Adam Frankish, et al.
Human Mutation
|
June 30, 2009
Variation in novel exons (RACEfrags) of the MECP2 gene in Rett syndrome patients and controls
Periklis Makrythanasis, Philipp Kapranov, Lucia Bartoloni, et al.
Genome Biology
|
August 24, 2006
GENCODE: producing a reference annotation for ENCODE
Jennifer Harrow, France Denoeud, Adam Frankish, et al.
BMC Bioinformatics
|
June 1, 2005
Gene finding in the chicken genome
Eduardo Eyras, Alexandre Reymond, Robert Castelo, et al.
Genome Biology
|
December 6, 2008
Assaying the regulatory potential of mammalian conserved non-coding sequences in human cells
Catia Attanasio, Alexandre Reymond, Richard Humbert, et al.
Page
of 17