The 2009 European Society of Human Genetics Meeting: novel technologies driving change

द्वारा Sharp, Andrew J
प्रकाशित 2009

Screening for rare epigenetic variations in autism and schizophrenia

द्वारा Garg, Paras, Sharp, Andrew J.
में प्रकाशित Hum Mutat (2019)

Detection of Parent-of-Origin Specific Expression Quantitative Trait Loci by Cis-Association Analysis of Gene Expression in Trios

द्वारा Garg, Paras, Borel, Christelle, Sharp, Andrew J.
प्रकाशित 2012

Comment on “Genomic Hypomethylation in the Human Germline Associates with Selective Structural Mutability in the Human Genome”

द्वारा Watson, Corey T., Garg, Paras, Sharp, Andrew J.
प्रकाशित 2013

A survey of inter-individual variation in DNA methylation identifies environmentally responsive co-regulated networks of epigenetic variation in the human genome

द्वारा Garg, Paras, Joshi, Ricky S., Watson, Corey, Sharp, Andrew J.
में प्रकाशित PLoS Genet (2018)

MsPAC: a tool for haplotype-phased structural variant detection

द्वारा Rodriguez, Oscar L, Ritz, Anna, Sharp, Andrew J, Bashir, Ali
में प्रकाशित Bioinformatics (2020)

Rapid multiplexed genotyping of simple tandem repeats using capture and high-throughput sequencing

द्वारा Guilmatre, Audrey, Highnam, Gareth, Borel, Christelle, Mittelman, David, Sharp, Andrew J.
प्रकाशित 2013

The Genetics of Microdeletion and Microduplication Syndromes: An Update

द्वारा Watson, Corey T., Marques-Bonet, Tomas, Sharp, Andrew J., Mefford, Heather C.
में प्रकाशित Annu Rev Genomics Hum Genet (2014)

DNA Methylation: Insights into Human Evolution

द्वारा Hernando-Herraez, Irene, Garcia-Perez, Raquel, Sharp, Andrew J., Marques-Bonet, Tomas
में प्रकाशित PLoS Genet (2015)

Copy number variation of the REXO1L1 gene cluster; euchromatic deletion variant or susceptibility factor?

द्वारा Barber, John C K, Sharp, Andrew J, Hollox, Edward J, Tyson, Christine
में प्रकाशित Eur J Hum Genet (2017)

Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome

द्वारा Duchon, Arnaud, Raveau, Matthieu, Chevalier, Claire, Nalesso, Valérie, Sharp, Andrew J., Herault, Yann
प्रकाशित 2011

Determining multiallelic complex copy number and sequence variation from high coverage exome sequencing data

द्वारा Forni, Diego, Martin, Diana, Abujaber, Razan, Sharp, Andrew J., Sironi, Manuela, Hollox, Edward J.
में प्रकाशित BMC Genomics (2015)

Digital Genotyping of Macrosatellites and Multicopy Genes Reveals Novel Biological Functions Associated with Copy Number Variation of Large Tandem Repeats

द्वारा Brahmachary, Manisha, Guilmatre, Audrey, Quilez, Javier, Hasson, Dan, Borel, Christelle, Warburton, Peter, Sharp, Andrew J.
प्रकाशित 2014

DNA methylation profiles of human active and inactive X chromosomes

द्वारा Sharp, Andrew J., Stathaki, Elisavet, Migliavacca, Eugenia, Brahmachary, Manisha, Montgomery, Stephen B., Dupre, Yann, Antonarakis, Stylianos E.
प्रकाशित 2011

Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated With Cross-Generational Effects of Adolescent THC Exposure

द्वारा Watson, Corey T, Szutorisz, Henrietta, Garg, Paras, Martin, Qammarah, Landry, Joseph A, Sharp, Andrew J, Hurd, Yasmin L
में प्रकाशित Neuropsychopharmacology (2015)

Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2

द्वारा Tyson, Christine, Sharp, Andrew J, Hrynchak, Monica, Yong, Siu L, Hollox, Edward J, Warburton, Peter, Barber, John CK
प्रकाशित 2014

Detection of Genomic Variation by Selection of a 9 Mb DNA Region and High Throughput Sequencing

द्वारा Nikolaev, Sergey I., Iseli, Christian, Sharp, Andrew J., Robyr, Daniel, Rougemont, Jacques, Gehrig, Corinne, Farinelli, Laurent, Antonarakis, Stylianos E.
प्रकाशित 2009

The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndrome

द्वारा Duchon, Arnaud, Pothion, Stéphanie, Brault, Véronique, Sharp, Andrew J., Tybulewicz, Victor L.J., Fisher, Elizabeth M.C., Herault, Yann
प्रकाशित 2011

DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation

द्वारा Bala Tannan, Neeta, Brahmachary, Manisha, Garg, Paras, Borel, Christelle, Alnefaie, Randah, Watson, Corey T., Thomas, N. Simon, Sharp, Andrew J.
प्रकाशित 2014

Placental expression profile of imprinted genes impacts birth weight

द्वारा Kappil, Maya A, Green, Benjamin B, Armstrong, David A, Sharp, Andrew J, Lambertini, Luca, Marsit, Carmen J, Chen, Jia
में प्रकाशित Epigenetics (2015)