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

অনুযায়ী Sharp, Andrew J
প্রকাশিত 2009

Screening for rare epigenetic variations in autism and schizophrenia

অনুযায়ী Garg, Paras, Sharp, Andrew J.
প্রকাশিত Hum Mutat (2019)

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

অনুযায়ী Garg, Paras, Borel, Christelle, Sharp, Andrew J.
প্রকাশিত 2012

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

অনুযায়ী Watson, Corey T., Garg, Paras, Sharp, Andrew J.
প্রকাশিত 2013

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

অনুযায়ী Garg, Paras, Joshi, Ricky S., Watson, Corey, Sharp, Andrew J.
প্রকাশিত PLoS Genet (2018)

MsPAC: a tool for haplotype-phased structural variant detection

অনুযায়ী Rodriguez, Oscar L, Ritz, Anna, Sharp, Andrew J, Bashir, Ali
প্রকাশিত Bioinformatics (2020)

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

অনুযায়ী Guilmatre, Audrey, Highnam, Gareth, Borel, Christelle, Mittelman, David, Sharp, Andrew J.
প্রকাশিত 2013

The Genetics of Microdeletion and Microduplication Syndromes: An Update

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

DNA Methylation: Insights into Human Evolution

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

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

অনুযায়ী Barber, John C K, Sharp, Andrew J, Hollox, Edward J, Tyson, Christine
প্রকাশিত Eur J Hum Genet (2017)

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

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

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

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

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

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

DNA methylation profiles of human active and inactive X chromosomes

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

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

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

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

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

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

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

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

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

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

Placental expression profile of imprinted genes impacts birth weight

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