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

par Sharp, Andrew J
Publié 2009

Screening for rare epigenetic variations in autism and schizophrenia

par Garg, Paras, Sharp, Andrew J.
Publié dans Hum Mutat (2019)

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

par Garg, Paras, Borel, Christelle, Sharp, Andrew J.
Publié 2012

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

par Watson, Corey T., Garg, Paras, Sharp, Andrew J.
Publié 2013

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

par Garg, Paras, Joshi, Ricky S., Watson, Corey, Sharp, Andrew J.
Publié dans PLoS Genet (2018)

MsPAC: a tool for haplotype-phased structural variant detection

par Rodriguez, Oscar L, Ritz, Anna, Sharp, Andrew J, Bashir, Ali
Publié dans Bioinformatics (2020)

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

par Guilmatre, Audrey, Highnam, Gareth, Borel, Christelle, Mittelman, David, Sharp, Andrew J.
Publié 2013

The Genetics of Microdeletion and Microduplication Syndromes: An Update

par Watson, Corey T., Marques-Bonet, Tomas, Sharp, Andrew J., Mefford, Heather C.
Publié dans Annu Rev Genomics Hum Genet (2014)

DNA Methylation: Insights into Human Evolution

par Hernando-Herraez, Irene, Garcia-Perez, Raquel, Sharp, Andrew J., Marques-Bonet, Tomas
Publié dans PLoS Genet (2015)

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

par Barber, John C K, Sharp, Andrew J, Hollox, Edward J, Tyson, Christine
Publié dans Eur J Hum Genet (2017)

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

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

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

par Forni, Diego, Martin, Diana, Abujaber, Razan, Sharp, Andrew J., Sironi, Manuela, Hollox, Edward J.
Publié dans BMC Genomics (2015)

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

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

DNA methylation profiles of human active and inactive X chromosomes

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

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

par Watson, Corey T, Szutorisz, Henrietta, Garg, Paras, Martin, Qammarah, Landry, Joseph A, Sharp, Andrew J, Hurd, Yasmin L
Publié dans Neuropsychopharmacology (2015)

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

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

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

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

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

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

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

Placental expression profile of imprinted genes impacts birth weight

par Kappil, Maya A, Green, Benjamin B, Armstrong, David A, Sharp, Andrew J, Lambertini, Luca, Marsit, Carmen J, Chen, Jia
Publié dans Epigenetics (2015)