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Andrew J Sharp

Showing results (21-30 of 85) with videos related to

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Human Molecular Genetics|August 30, 2007
Optimal design of oligonucleotide microarrays for measurement of DNA copy-numberAndrew J Sharp, Andy Itsara, Ze Cheng, et al.
BMC Genomics|November 4, 2015
Determining multiallelic complex copy number and sequence variation from high coverage exome sequencing dataDiego Forni, Diana Martin, Razan Abujaber, et al.
American Journal of Human Genetics|May 24, 2022
A phenome-wide association study identifies effects of copy-number variation of VNTRs and multicopy genes on multiple human traitsParas Garg, Bharati Jadhav, William Lee, et al.
Plos Genetics|June 20, 2014
Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeatsManisha Brahmachary, Audrey Guilmatre, Javier Quilez, et al.
Human Molecular Genetics|November 22, 2002
Molecular and cytogenetic analysis of the spreading of X inactivation in X;autosome translocationsAndrew J Sharp, Hugh T Spotswood, David O Robinson, et al.
Clinical Dysmorphology|June 11, 2008
Potocki-Lupski syndrome mimicking a connective tissue disorderJudy Martin, Samantha J L Knight, Andrew J Sharp, et al.
Genome Research|August 25, 2011
DNA methylation profiles of human active and inactive X chromosomesAndrew J Sharp, Elisavet Stathaki, Eugenia Migliavacca, et al.
Human Molecular Genetics|February 25, 2010
A recurrent 14q32.2 microdeletion mediated by expanded TGG repeatsFrédérique Béna, Stefania Gimelli, Eugenia Migliavacca, et al.
Iscience|January 3, 2024
Feeder-free generation and characterization of endocardial and cardiac valve cells from human pluripotent stem cellsClifford Z Liu, Aditi Prasad, Bharati Jadhav, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2024
A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK BiobankCeline A Manigbas, Bharati Jadhav, Paras Garg, et al.
Pageof 9

Showing results (21-30 of 85) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|August 30, 2007
Optimal design of oligonucleotide microarrays for measurement of DNA copy-numberAndrew J Sharp, Andy Itsara, Ze Cheng, et al.
BMC Genomics|November 4, 2015
Determining multiallelic complex copy number and sequence variation from high coverage exome sequencing dataDiego Forni, Diana Martin, Razan Abujaber, et al.
American Journal of Human Genetics|May 24, 2022
A phenome-wide association study identifies effects of copy-number variation of VNTRs and multicopy genes on multiple human traitsParas Garg, Bharati Jadhav, William Lee, et al.
Plos Genetics|June 20, 2014
Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeatsManisha Brahmachary, Audrey Guilmatre, Javier Quilez, et al.
Human Molecular Genetics|November 22, 2002
Molecular and cytogenetic analysis of the spreading of X inactivation in X;autosome translocationsAndrew J Sharp, Hugh T Spotswood, David O Robinson, et al.
Clinical Dysmorphology|June 11, 2008
Potocki-Lupski syndrome mimicking a connective tissue disorderJudy Martin, Samantha J L Knight, Andrew J Sharp, et al.
Genome Research|August 25, 2011
DNA methylation profiles of human active and inactive X chromosomesAndrew J Sharp, Elisavet Stathaki, Eugenia Migliavacca, et al.
Human Molecular Genetics|February 25, 2010
A recurrent 14q32.2 microdeletion mediated by expanded TGG repeatsFrédérique Béna, Stefania Gimelli, Eugenia Migliavacca, et al.
Iscience|January 3, 2024
Feeder-free generation and characterization of endocardial and cardiac valve cells from human pluripotent stem cellsClifford Z Liu, Aditi Prasad, Bharati Jadhav, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2024
A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK BiobankCeline A Manigbas, Bharati Jadhav, Paras Garg, et al.
Pageof 9