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

di Sharp, Andrew J
Pubblicazione 2009

Screening for rare epigenetic variations in autism and schizophrenia

di Garg, Paras, Sharp, Andrew J.
Pubblicato in Hum Mutat (2019)

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

di Garg, Paras, Borel, Christelle, Sharp, Andrew J.
Pubblicazione 2012

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

di Watson, Corey T., Garg, Paras, Sharp, Andrew J.
Pubblicazione 2013

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

di Garg, Paras, Joshi, Ricky S., Watson, Corey, Sharp, Andrew J.
Pubblicato in PLoS Genet (2018)

MsPAC: a tool for haplotype-phased structural variant detection

di Rodriguez, Oscar L, Ritz, Anna, Sharp, Andrew J, Bashir, Ali
Pubblicato in Bioinformatics (2020)

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

di Guilmatre, Audrey, Highnam, Gareth, Borel, Christelle, Mittelman, David, Sharp, Andrew J.
Pubblicazione 2013

The Genetics of Microdeletion and Microduplication Syndromes: An Update

di Watson, Corey T., Marques-Bonet, Tomas, Sharp, Andrew J., Mefford, Heather C.
Pubblicato in Annu Rev Genomics Hum Genet (2014)

DNA Methylation: Insights into Human Evolution

di Hernando-Herraez, Irene, Garcia-Perez, Raquel, Sharp, Andrew J., Marques-Bonet, Tomas
Pubblicato in PLoS Genet (2015)

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

di Barber, John C K, Sharp, Andrew J, Hollox, Edward J, Tyson, Christine
Pubblicato in Eur J Hum Genet (2017)

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

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

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

di Forni, Diego, Martin, Diana, Abujaber, Razan, Sharp, Andrew J., Sironi, Manuela, Hollox, Edward J.
Pubblicato in BMC Genomics (2015)

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

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

DNA methylation profiles of human active and inactive X chromosomes

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

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

di Watson, Corey T, Szutorisz, Henrietta, Garg, Paras, Martin, Qammarah, Landry, Joseph A, Sharp, Andrew J, Hurd, Yasmin L
Pubblicato in Neuropsychopharmacology (2015)

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

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

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

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

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

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

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

Placental expression profile of imprinted genes impacts birth weight

di Kappil, Maya A, Green, Benjamin B, Armstrong, David A, Sharp, Andrew J, Lambertini, Luca, Marsit, Carmen J, Chen, Jia
Pubblicato in Epigenetics (2015)