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

por Sharp, Andrew J
Publicado 2009

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

por Garg, Paras, Borel, Christelle, Sharp, Andrew J.
Publicado 2012

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

por Watson, Corey T., Garg, Paras, Sharp, Andrew J.
Publicado 2013

Limitations of lymphoblastoid cell lines for establishing genetic reference datasets in the immunoglobulin loci

por Rodriguez, Oscar L., Sharp, Andrew J., Watson, Corey T.
Publicado 2021

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

por Garg, Paras, Joshi, Ricky S., Watson, Corey, Sharp, Andrew J.
Publicado 2018

Genome-wide evaluation of the effect of short tandem repeat variation on local DNA methylation

por Martin-Trujillo, Alejandro, Garg, Paras, Patel, Nihir, Jadhav, Bharati, Sharp, Andrew J.
Publicado 2023

Small open reading frames: a comparative genetics approach to validation

por Jain, Niyati, Richter, Felix, Adzhubei, Ivan, Sharp, Andrew J., Gelb, Bruce D.
Publicado 2023

DNA Methylation: Insights into Human Evolution

por Hernando-Herraez, Irene, Garcia-Perez, Raquel, Sharp, Andrew J., Marques-Bonet, Tomas
Publicado 2015

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

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

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

por Forni, Diego, Martin, Diana, Abujaber, Razan, Sharp, Andrew J., Sironi, Manuela, Hollox, Edward J.
Publicado 2015

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

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

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

por Watson, Corey T, Szutorisz, Henrietta, Garg, Paras, Martin, Qammarah, Landry, Joseph A, Sharp, Andrew J, Hurd, Yasmin L
Publicado 2015

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

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

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

Genome-wide12 DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer’s disease

por Watson, Corey T., Roussos, Panos, Garg, Paras, Ho, Daniel J., Azam, Nidha, Katsel, Pavel L., Haroutunian, Vahram, Sharp, Andrew J.
Publicado 2016

Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans

por Quilez, Javier, Guilmatre, Audrey, Garg, Paras, Highnam, Gareth, Gymrek, Melissa, Erlich, Yaniv, Joshi, Ricky S., Mittelman, David, Sharp, Andrew J.
Publicado 2016

The App-Runx1 Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in a Down Syndrome Mouse Model

por Raveau, Matthieu, Lignon, Jacques M., Nalesso, Valérie, Duchon, Arnaud, Groner, Yoram, Sharp, Andrew J., Dembele, Doulaye, Brault, Véronique, Hérault, Yann
Publicado 2012

The interplay between DNA methylation and sequence divergence in recent human evolution

por Hernando-Herraez, Irene, Heyn, Holger, Fernandez-Callejo, Marcos, Vidal, Enrique, Fernandez-Bellon, Hugo, Prado-Martinez, Javier, Sharp, Andrew J., Esteller, Manel, Marques-Bonet, Tomas
Publicado 2015

Dynamics of DNA Methylation in Recent Human and Great Ape Evolution

por Hernando-Herraez, Irene, Prado-Martinez, Javier, Garg, Paras, Fernandez-Callejo, Marcos, Heyn, Holger, Hvilsom, Christina, Navarro, Arcadi, Esteller, Manel, Sharp, Andrew J., Marques-Bonet, Tomas
Publicado 2013

Foxa2 identifies a cardiac progenitor population with ventricular differentiation potential

por Bardot, Evan, Calderon, Damelys, Santoriello, Francis, Han, Songyan, Cheung, Kakit, Jadhav, Bharati, Burtscher, Ingo, Artap, Stanley, Jain, Rajan, Epstein, Jonathan, Lickert, Heiko, Gouon-Evans, Valerie, Sharp, Andrew J., Dubois, Nicole C.
Publicado 2017